category_class	label	harrisons_view	mondo_txgnn	mondo_top_grouping	medical_specialization	txgnn	anatomical	is_pathogen_caused	is_cancer	is_glucose_dysfunction	tag_existing_treatment	tag_qaly_lost
MONDO:0000004	adrenocortical insufficiency	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology	adrenal_gland_disease|metabolic_disorder	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0000005	alopecia, isolated	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	low
MONDO:0000009	inherited bleeding disorder, platelet-type	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	inherited_bleeding_disorders_often_fall_under_more_specific_categories_but_the_closest_is_anemia_as_it_s_a_disorder_related_to_blood_components|metabolic_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0000014	colorblindness, partial	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0000015	classic complement early component deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|allergy_and_immunology|immunology|hematology	inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0000022	nocturnal enuresis	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|urology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	low
MONDO:0000023	infantile liver failure	endocrine_system_disorder|hereditary_disease|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|hereditary_disease|endocrine_system_disorder	gastroenterology|hepatology|pediatric	metabolic_disorder|neonatal_disorders	biliary_disorder|liver_disorder	true	false	false	true	very_high
MONDO:0000030	familial sleep-related hypermotor epilepsy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric	neurodegenerative_disease|mental_health_disorder|inflammatory_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0000032	febrile seizures, familial	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|vascular_disorder	false	false	false	true	low
MONDO:0000044	hereditary hypophosphatemic rickets	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology|pediatric|orthopaedic	metabolic_disorder|hereditary_disease	endocrine_disorder|kidney_disorder|bone_disorder	false	false	false	true	medium
MONDO:0000045	hypothyroidism, congenital, nongoitrous	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|autoimmune_diseases	endocrine_disorder|congenital_disorder|thyroid_disorder	false	false	false	true	medium
MONDO:0000050	isolated congenital growth hormone deficiency	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder|nervous_system_disorder	endocrine_system_disorder	reproductive_system_disorder|nervous_system_disorder|hereditary_disease|endocrine_system_disorder	endocrinology|pediatric	congenital_growth_hormone_deficiency|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0000060	microcephalic osteodysplastic primordial dwarfism	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	orthopaedic|pediatric|endocrinology|genetics_and_genomics	genetic_disorder|metabolic_disorder	skeletal_system_disorder|bone_disorder|lower_body_disorder	false	false	false	false	high
MONDO:0000062	isolated microphthalmia	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	pediatric|ophthalmology|genetics_and_genomics	genetic_disorder|developmental_disorder|neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0000066	mitochondrial respiratory chain complex deficiency	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetic_and_genomics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	high
MONDO:0000078	acrocephalopolysyndactyly	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0000079	nephrolithiasis/osteoporosis, hypophosphatemic	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	endocrinology|urology|renal_medicine	metabolic_disorder|osteoporosis	kidney_disorder|bone_disorder	false	false	false	true	medium
MONDO:0000082	pelvic organ prolapse	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|gastroenterology	pelvic_floor_disorder|urological_disease|gynecological_disease|inflammatory_disease	reproductive_system_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0000087	polymicrogyria	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0000088	precocious puberty	endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder	pediatric|endocrinology	metabolic_disorder|autoimmune_diseases|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0000090	progressive external ophthalmoplegia with mitochondrial DNA deletions	mitochondrial_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|musculoskeletal_system_disorder	neurology|ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0000104	anemia, hypochromic microcytic with iron overload	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	hematology|gastroenterology	anemia|metabolic_disorder	liver_disorder|iron_overload_is_not_a_category_so_it_has_been_removed|blood_bone_marrow_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0000105	anemia, nonspherocytic hemolytic	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases|anemia	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0000107	auriculocondylar syndrome	hereditary_disease	other	hereditary_disease	pediatric|otolaryngology|orthopaedic|genetics_and_genomics	inflammatory_disease|other___corrected_answer___autoimmune_diseases|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0000110	bifid nose	otorhinolaryngologic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|otorhinolaryngologic_disease	pediatric|otolaryngology	developmental_disorder|congenital_disorder|neurodegenerative_disease	muscle_disorder|nose_disorder	false	false	false	false	low
MONDO:0000111	camptodactyly syndrome, Guadalajara	hereditary_disease	other	hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0000114	cerebelloparenchymal disorder	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	cerebellarparenchymal_disorder_is_a_type_of_brain_disease__but_it_does_not_fit_perfectly_into_the_provided_category_list|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0000115	Chiari malformation	hereditary_disease	other	hereditary_disease	pediatric|neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0000118	reticulate pigment disorder	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	anemia|metabolic_disorder|autoimmune_diseases	skin_disorder|immune_disorder|eye_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0000119	congenital heart defects, multiple types	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|pediatric	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0000127	geleophysic dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	genetic_disorder|metabolic_disorder|genetic_disorder___corrected_to_fit_the_format___metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0000128	giant axonal neuropathy	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	gastroenterology|genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0000129	glutaric aciduria	metabolic_disease	metabolic_disease	metabolic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	true	high
MONDO:0000133	immunodeficiency-centromeric instability-facial anomalies syndrome	premature_aging_syndrome|hereditary_disease	other	hereditary_disease|premature_aging_syndrome	genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease|metabolic_disorder|cancer	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0000136	keratosis follicularis spinulosa decalvans	integumentary_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	integumentary_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	scalp_disorder|hair_loss_disorder|skin_disorder	false	false	false	false	high
MONDO:0000137	leukoencephalopathy, megalencephalic	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|hematology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0000138	metaphyseal chondrodysplasia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|rheumatology|genetics_and_genomics	genetic_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0000141	mosaic variegated aneuploidy syndrome	cancer_or_benign_tumor|chromosomal_disorder|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|chromosomal_disorder|hereditary_disease|syndromic_disease	oncology|genetics_and_genomics|neurology|pediatric	genetic_disorder|neurodegenerative_disease	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0000147	polyposis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|gastroenterology|genetics_and_genomics	inflammatory_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0000148	pulmonary fibrosis and/or bone marrow failure, telomere-related	respiratory_system_disorder|premature_aging_syndrome|hereditary_disease	other	respiratory_system_disorder|hereditary_disease|premature_aging_syndrome	pulmonology|hematology|oncology|genetics_and_genomics|pediatric	metabolic_disorder|cancer|anemia	blood_bone_marrow_disorder|lung_disorder	false	false	false	true	high
MONDO:0000151	symphalangism	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|neurology|rheumatology	musculoskeletal_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0000152	thiamine-responsive dysfunction syndrome	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|nerve_disorder	false	false	false	true	high
MONDO:0000153	transposition of the great arteries	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|pediatric	congenital_heart_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0000155	triglyceride storage disease	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|hepatology|genetics_and_genomics|cardiology	metabolic_disorder|cardiovascular_disorder	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0000156	trigonocephaly	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000158	developmental dysplasia of the hip	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|developmental_disorder	bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0000159	bone marrow failure syndrome	hematologic_disorder|hereditary_disease|musculoskeletal_system_disorder|immune_system_disorder	other	hematologic_disorder|hereditary_disease|immune_system_disorder|musculoskeletal_system_disorder	hematology|oncology|genetics_and_genomics	metabolic_disorder|cancer|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0000160	epilepsy, familial adult myoclonic	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0000166	encephalopathy, acute, infection-induced	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|acute_disease|post_infectious_disorder	infectious_diseases|pediatrics|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	infection_induced_disorders|immune_disorder|brain_disorder	true	false	false	false	high
MONDO:0000167	Huntington disease and related disorders	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0000170	microphthalmia, isolated, with coloboma	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	genetics_and_genomics|ophthalmology|pediatric	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0000171	muscular dystrophy-dystroglycanopathy, type A	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0000172	muscular dystrophy-dystroglycanopathy, type B	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	high
MONDO:0000173	muscular dystrophy-dystroglycanopathy, type C	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|neurology|pediatric	muscular_dystrophy_is_a_muscle_disorder_but_there_s_no_separate_category_for_it__so_the_closest_ones_were_used|metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0000179	Neu-Laxova syndrome	nervous_system_disorder|integumentary_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	metabolic_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|syndromic_disease|integumentary_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder|brain_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0000181	microcephaly and chorioretinopathy	nervous_system_disorder|disorder_of_visual_system|inflammatory_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	nervous_system_disorder|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|inflammatory_disease|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	true	false	false	false	high
MONDO:0000182	congenital myasthenic syndrome with tubular aggregates	nervous_system_disorder|hereditary_disease|syndromic_disease	other	nervous_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0000188	GLUT1 deficiency syndrome	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	true	true	high
MONDO:0000190	ventricular fibrillation	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic|pulmonology|renal_medicine	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0000192	polyglucosan body myopathy	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	medium
MONDO:0000193	cortisone reductase deficiency	endocrine_system_disorder|reproductive_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease|endocrine_system_disorder	metabolic_disease|hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	pediatrics|endocrinology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|inflammatory_disease	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0000200	Zimmermann-Laband syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|joint_disorder	false	false	false	false	medium
MONDO:0000208	microcephaly, short stature, and impaired glucose metabolism 1	hereditary_disease	other	hereditary_disease	endocrinology|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	growth_disorder|endocrine_disorder|brain_disorder	false	false	true	false	high
MONDO:0000209	prenatal-onset spinal muscular atrophy with congenital bone fractures	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric|obstetrics_and_gynecology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0000210	thiopurine metabolic disease	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|oncology|gastroenterology|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|immune_disorder	false	false	false	true	high
MONDO:0000211	striatal degeneration, autosomal dominant	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease|neurodegenerative_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	autosomal_dominant_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0000212	hypercalcemia, infantile	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|pediatric	metabolic_disorder|autoimmune_diseases	kidney_disorder|bone_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0000213	autoimmune disease, multisystem, infantile-onset	hereditary_disease|immune_system_disorder	autoimmune_disease	immune_system_disorder|hereditary_disease	rheumatology|genetics_and_genomics|allergy_and_immunology|pediatric	inflammatory_disease|multisystem_disease|autoimmune_diseases	multisystem_disorder____note__the_term__multisystem__is_a_broader_category_that_encompasses_autoimmune_diseases__but_i_have_included_it_as_per_your_request_since_the_disease_is_described_as_having_infantile_onset_and_affecting_multiple_systems|immune_disorder	false	false	false	false	very_high
MONDO:0000214	hypermanganesemia with dystonia	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|metabolic_disorder	metabolic_disorder|anemia|neurodegenerative_disease	muscle_disorder|endocrine_disorder	true	false	false	true	high
MONDO:0000222	seminal vesicle acute gonorrhea	infectious_disease|reproductive_system_disorder|endocrine_system_disorder|inflammatory_disease	endocrine_system_disorder|infectious_disease	acute_disease|reproductive_system_disorder|endocrine_system_disorder|inflammatory_disease|infectious_disease	urology|obstetrics_and_gynecology	inflammatory_disease|urological_disorder|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	false	medium
MONDO:0000224	acquired carbohydrate metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	endocrinology|genetics_and_genomics	metabolic_disorder|acquired_diseases	upper_gastrointestinal_disorder|liver_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0000225	human monocytic ehrlichiosis	immune_system_disorder|infectious_disease|hematologic_disorder	infectious_disease	immune_system_disorder|hematologic_disorder|infectious_disease	infectious_diseases|hematology	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0000226	mineral metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	endocrinology|genetics_and_genomics|renal_medicine	mineral_metabolism_disease|adrenal_gland_disease|metabolic_disorder	mineral_metabolism_disease_is_not_in_the_list_so_that_one_does_not_get_included|endocrine_disorder	false	false	false	false	high
MONDO:0000227	African tick-bite fever	infectious_disease	infectious_disease	infectious_disease	hepatology|dermatology|hematology	inflammatory_disease|allergy|autoimmune_diseases	lymphatic_disorder|skin_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0000229	Indian tick typhus	infectious_disease	infectious_disease	infectious_disease	dermatology|pediatrics	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0000230	Israeli tick typhus	infectious_disease	infectious_disease	infectious_disease	pulmonology|hematology|dermatology	autoimmune_diseases|inflammatory_disease	vascular_disorder|skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0000231	Far eastern spotted fever	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0000232	Flinders island spotted fever	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|dermatology|other____corrected_answer____dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder	true	false	false	false	medium
MONDO:0000233	Japanese spotted fever	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|pediatrics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0000234	Rickettsia parkeri spotted fever	infectious_disease	infectious_disease	infectious_disease	pediatrics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0000236	oropharyngeal anthrax	respiratory_system_disorder|digestive_system_disorder|otorhinolaryngologic_disease|infectious_disease	infectious_disease	digestive_system_disorder|respiratory_system_disorder|infectious_disease|otorhinolaryngologic_disease	pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease	lung_disorder|upper_gastrointestinal_disorder|throat_disorder	true	false	false	true	high
MONDO:0000239	adiaspiromycosis	respiratory_system_disorder|infectious_disease	infectious_disease	respiratory_system_disorder|infectious_disease	pulmonology|allergy_and_immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	lung_disorder|respiratory_system_disorder	true	false	false	true	medium
MONDO:0000240	invasive aspergillosis	respiratory_system_disorder|infectious_disease	infectious_disease	respiratory_system_disorder|infectious_disease	pulmonology|invasive_aspergillosis_is_most_commonly_associated_with_pulmonary_disease	autoimmune_diseases|inflammatory_disease|cancer	lung_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0000241	Keshan disease	nutritional_disorder|infectious_disease|musculoskeletal_system_disorder|cardiovascular_disorder	infectious_disease|cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|infectious_disease|nutritional_disorder	pediatric|hepatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	liver_disorder|endocrine_disorder	true	false	false	true	high
MONDO:0000242	tinea barbae	infectious_disease|integumentary_system_disorder|inflammatory_disease	infectious_disease	inflammatory_disease|infectious_disease|integumentary_system_disorder	dermatology	allergy|autoimmune_diseases|inflammatory_disease	skin_disorder|lower_gastrointestinal_disorder|nose_disorder	true	false	false	true	low
MONDO:0000243	ectothrix infectious disease	infectious_disease|integumentary_system_disorder|inflammatory_disease	infectious_disease	inflammatory_disease|infectious_disease|integumentary_system_disorder	infectious_diseases|dermatology|allergy_and_immunology	autoimmune_diseases|neurodegenerative_disease	brain_disorder|ear_disorder	true	false	false	true	medium
MONDO:0000244	endothrix infectious disease	infectious_disease|integumentary_system_disorder|inflammatory_disease	infectious_disease	inflammatory_disease|infectious_disease|integumentary_system_disorder	pulmonology|pediatrics|infectious_disease|allergy_and_immunology|dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|cancer	vascular_disorder|immune_disorder	true	false	false	false	low
MONDO:0000245	tinea imbricata	infectious_disease|integumentary_system_disorder|inflammatory_disease	infectious_disease	inflammatory_disease|infectious_disease|integumentary_system_disorder	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|fungus_disorder	true	false	false	true	low
MONDO:0000248	dengue shock syndrome	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric|hematology	cardiovascular_disorder|inflammatory_disease	vascular_disorder|immune_disorder	true	false	false	true	high
MONDO:0000249	secretory diarrhea	digestive_system_disorder	other	digestive_system_disorder	hepatology|hematology|allergy_and_immunology|gastroenterology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0000250	osmotic diarrheal disease	digestive_system_disorder	other	digestive_system_disorder	pediatric|gastroenterology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0000251	diarrheal disease secondary to altered bowel motility	digestive_system_disorder	other	digestive_system_disorder	neurology|gastroenterology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0000252	inflammatory diarrhea	digestive_system_disorder|inflammatory_disease	other	digestive_system_disorder|inflammatory_disease	pediatrics|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	high
MONDO:0000253	piedra	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	urology|dermatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	urinary_tract_disorder|skin_disorder|kidney_disorder	true	false	false	true	low
MONDO:0000254	cutaneous mycosis	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	allergy_and_immunology|dermatology	allergy|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0000255	subcutaneous mycosis	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology	allergy|autoimmune_diseases|inflammatory_disease	skin_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0000256	systemic mycosis	infectious_disease	infectious_disease	infectious_disease	dermatology|immunology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0000257	acute diarrhea	digestive_system_disorder	other	acute_disease|digestive_system_disorder	pediatric|gastroenterology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0000259	asymptomatic dengue	infectious_disease	infectious_disease	infectious_disease	pediatric|hematology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder	true	false	false	true	low
MONDO:0000261	adenoiditis	immune_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease|inflammatory_disease	other	inflammatory_disease|respiratory_system_disorder|otorhinolaryngologic_disease|immune_system_disorder	pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease	throat_disorder|nose_disorder	true	false	false	true	medium
MONDO:0000262	otomycosis	auditory_system_disorder|otorhinolaryngologic_disease|infectious_disease|integumentary_system_disorder|inflammatory_disease	infectious_disease	auditory_system_disorder|inflammatory_disease|infectious_disease|otorhinolaryngologic_disease|post_infectious_disorder|integumentary_system_disorder	otolaryngology|dermatology	allergy|autoimmune_diseases|inflammatory_disease	skin_disorder|ear_disorder|nose_disorder	true	false	false	true	medium
MONDO:0000263	laryngotracheitis	respiratory_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	inflammatory_disease|infectious_disease|respiratory_system_disorder	pulmonology|pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease	lung_disorder|throat_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0000265	aspiration pneumonia	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|respiratory	cardiovascular_disorder|respiratory_disease|inflammatory_disease	lung_disorder|lower_gastrointestinal_disorder|throat_disorder	true	false	false	true	high
MONDO:0000266	pulmonary aspergilloma	respiratory_system_disorder|infectious_disease	infectious_disease	infectious_disease|respiratory_system_disorder	pulmonology|oncology|cardiothoracic	cancer|inflammatory_disease	lung_disorder|immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0000270	lower respiratory tract disorder	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|pulmonology	autoimmune_diseases|lower_respiratory_tract_disorder|inflammatory_disease	lung_disorder|lower_respiratory_tract_disorder	true	false	false	false	high
MONDO:0000271	tuberculous salpingitis	infectious_disease|inflammatory_disease|reproductive_system_disorder	infectious_disease	reproductive_system_disorder|inflammatory_disease|infectious_disease	obstetrics_and_gynecology|pulmonology	autoimmune_diseases|inflammatory_disease	lung_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0000273	Kunjin virus infectous disease	infectious_disease|nervous_system_disorder|inflammatory_disease	infectious_disease	acute_disease|inflammatory_disease|infectious_disease|nervous_system_disorder	pediatric|infectious_disease|virology	autoimmune_diseases|adrenal_gland_disease|cardiovascular_disorder|inflammatory_disease	immune_disorder|liver_disorder	true	false	false	false	medium
MONDO:0000276	Powassan encephalitis	infectious_disease|nervous_system_disorder|inflammatory_disease	infectious_disease	inflammatory_disease|acute_disease|infectious_disease|nervous_system_disorder	neurology|infectious_diseases|epidemiology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder|lymphatic_disorder	true	false	false	false	medium
MONDO:0000282	Whitewater Arroyo hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	hepatology|pulmonology|hematology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	vascular_disorder|liver_disorder	true	false	false	false	medium
MONDO:0000283	Hantavirus hemorrhagic fever with renal syndrome, Seoul virus type	infectious_disease|urinary_system_disorder	infectious_disease	urinary_system_disorder|infectious_disease	renal_medicine|hematology	inflammatory_disease|autoimmune_diseases	vascular_disorder|kidney_disorder|immune_disorder	true	false	false	false	medium
MONDO:0000284	Hantavirus hemorrhagic fever with renal syndrome, Puumala virus type	infectious_disease|urinary_system_disorder	infectious_disease	urinary_system_disorder|infectious_disease	hepatology|renal_medicine|pulmonology|hematology	inflammatory_disease|autoimmune_diseases	vascular_disorder|kidney_disorder	true	false	false	false	medium
MONDO:0000286	Epstein-Barr virus hepatitis	digestive_system_disorder|infectious_disease|integumentary_system_disorder|inflammatory_disease|endocrine_system_disorder	endocrine_system_disorder|infectious_disease	endocrine_system_disorder|inflammatory_disease|digestive_system_disorder|infectious_disease|integumentary_system_disorder	pediatric|hepatology	inflammatory_disease|autoimmune_diseases|cancer	immune_disorder|liver_disorder	true	false	false	true	medium
MONDO:0000288	polycystic echinococcosis	digestive_system_disorder|infectious_disease|endocrine_system_disorder	endocrine_system_disorder|infectious_disease	endocrine_system_disorder|digestive_system_disorder|infectious_disease	hepatology|renal_medicine|pulmonology|endocrinology|gastroenterology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	kidney_disorder|liver_disorder	true	false	false	true	medium
MONDO:0000290	primary amebic meningoencephalitis	infectious_disease|nervous_system_disorder|inflammatory_disease	infectious_disease	acute_disease|inflammatory_disease|infectious_disease|nervous_system_disorder	pediatric|neurology	inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0000291	granulomatous amebic encephalitis	infectious_disease|nervous_system_disorder|inflammatory_disease	infectious_disease	acute_disease|inflammatory_disease|infectious_disease|nervous_system_disorder	pediatric|neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder|immune_disorder	true	false	false	false	very_high
MONDO:0000292	philophthalmiasis	infectious_disease	infectious_disease	infectious_disease	ophthalmology	inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder	true	false	false	false	medium
MONDO:0000293	coenurosis	digestive_system_disorder|infectious_disease	infectious_disease	digestive_system_disorder|infectious_disease	pulmonology|zoology|dermatology|entomology	autoimmune_diseases|neurodegenerative_disease	vascular_disorder|skin_disorder|ear_disorder	true	false	false	true	medium
MONDO:0000294	mesocestoidiasis	infectious_disease	infectious_disease	infectious_disease	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	joint_disorder|skin_disorder|spinal_disorder|muscle_disorder	true	false	false	false	low
MONDO:0000295	acanthocephaliasis	infectious_disease	infectious_disease	infectious_disease	pediatric|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	intestinal_disorder|lower_gastrointestinal_disorder	true	false	false	false	low
MONDO:0000297	baylisascariasis	infectious_disease	infectious_disease	infectious_disease	neurology|infectious_diseases	inflammatory_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder	true	false	false	false	high
MONDO:0000298	dioctophymiasis	infectious_disease	infectious_disease	infectious_disease	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	liver_disorder|eye_disorder|upper_gastrointestinal_disorder	true	false	false	false	medium
MONDO:0000299	thelaziasis	infectious_disease	infectious_disease	infectious_disease	hepatology|pulmonology|urology|genetics_and_genomics|dermatology|hematology	autoimmune_diseases	liver_disorder	true	false	false	false	medium
MONDO:0000301	ophthalmomyiasis	integumentary_system_disorder|infectious_disease	infectious_disease	infectious_disease|integumentary_system_disorder	ophthalmology|otolaryngology	autoimmune_diseases|inflammatory_disease	eye_disorder|nose_disorder	true	false	false	true	medium
MONDO:0000302	basidiobolomycosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|immunology|infectious_disease|dermatology|mycology	autoimmune_diseases|inflammatory_disease|cancer	skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0000303	conidiobolomycosis	integumentary_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|inflammatory_disease|integumentary_system_disorder	pulmonology|allergy_and_immunology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|fungal_infection	true	false	false	false	medium
MONDO:0000304	penicilliosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0000306	trichosporonosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|lung_disorder	true	false	false	true	medium
MONDO:0000307	parasitic Ichthyosporea infectious disease	infectious_disease	infectious_disease	infectious_disease	infectious_disease|dermatology	inflammatory_disease|infectious_disease	skin_disorder|liver_disorder	true	false	false	false	low
MONDO:0000308	primary systemic mycosis	infectious_disease	infectious_disease	infectious_disease	immunology|hematology	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder__skin_disorder	true	false	false	false	high
MONDO:0000309	aniseikonia	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	mental_health_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000310	Alkhurma hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	pulmonology|hematology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	true	false	false	false	high
MONDO:0000313	hypophosphatemia	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|renal_medicine|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	true	medium
MONDO:0000314	primary bacterial infectious disease	infectious_disease	infectious_disease	infectious_disease	allergy_and_immunology|infectious_diseases|pediatric	primary|bacterial|infectious_disease	immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0000315	commensal bacterial infectious disease	infectious_disease	infectious_disease	infectious_disease	gastroenterology|infectious_diseases|pediatric	inflammatory_disease|commensal_bacterial_infectious_disease	skin_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	false	medium
MONDO:0000316	opportunistic bacterial infectious disease	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	inflammatory_disease|bacterial_infectious_disease	lung_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0000320	glandular tularemia	infectious_disease|immune_system_disorder	infectious_disease	immune_system_disorder|infectious_disease	pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|upper_gastrointestinal_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0000321	typhoidal tularemia	infectious_disease	infectious_disease	infectious_disease	hematology|gastroenterology|renal_medicine|pediatrics|infectious_diseases	inflammatory_disease|autoimmune_diseases	immune_disorder|upper_gastrointestinal_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0000327	Buruli ulcer disease	infectious_disease	infectious_disease	infectious_disease	dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	true	false	false	true	medium
MONDO:0000328	hyperphosphatemia	metabolic_disease	metabolic_disease	metabolic_disease	endocrinology|renal_medicine	adrenal_gland_disease|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0000330	endemic typhus	infectious_disease	infectious_disease	infectious_disease	infectious_disease|pediatric|hematology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	medium
MONDO:0000331	Rickettsia helvetica spotted fever	infectious_disease	infectious_disease	infectious_disease	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|vascular_disorder|immune_disorder	true	false	false	true	medium
MONDO:0000332	sennetsu fever	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	biliary_disorder|upper_gastrointestinal_disorder|liver_disorder	true	false	false	false	low
MONDO:0000333	early congenital syphilis	reproductive_system_disorder|disorder_of_development_or_morphogenesis|infectious_disease	infectious_disease	infectious_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis	otolaryngology|pediatric|obstetrics_and_gynecology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	ear_disorder|vascular_disorder|birth_disorder_is_not_in_the_list_so__ear_disorder	true	false	false	true	very_high
MONDO:0000334	multinodular goiter	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	thyroid|endocrinology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|thyroid_disorder	false	false	false	false	medium
MONDO:0000335	parenchymatous neurosyphilis	reproductive_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease	psychiatry|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder_spinal_disorder	true	false	false	true	very_high
MONDO:0000336	meningovascular neurosyphilis	reproductive_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease	psychiatry|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|vascular_disorder|brain_disorder	true	false	false	true	high
MONDO:0000337	exanthema subitum	integumentary_system_disorder|infectious_disease	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0000338	variola major infectious disease	integumentary_system_disorder|infectious_disease	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0000339	spinal polio	nervous_system_disorder|inflammatory_disease|infectious_disease	neurodegenerative_disease|infectious_disease	infectious_disease|acute_disease|inflammatory_disease|nervous_system_disorder	neurology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder|brain_disorder	true	false	false	true	high
MONDO:0000340	bulbospinal polio	nervous_system_disorder|inflammatory_disease|infectious_disease	neurodegenerative_disease|infectious_disease	acute_disease|inflammatory_disease|nervous_system_disorder|infectious_disease	neurology|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder	true	false	false	false	high
MONDO:0000341	paralytic poliomyelitis	nervous_system_disorder|inflammatory_disease|infectious_disease	neurodegenerative_disease|infectious_disease	acute_disease|inflammatory_disease|nervous_system_disorder|infectious_disease	neurology|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0000342	O'nyong'nyong fever	infectious_disease	infectious_disease	infectious_disease	pediatric|infectious_diseases	autoimmune_diseases|inflammatory_disease	vascular_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0000343	Barmah forest virus disease	infectious_disease	infectious_disease	infectious_disease	neurology|virology__note__i_had_to_add_the_category__virology__which_is_not_in_the_original_list__but_it_s_the_most_relevant_one_for_this_disease|hematology	autoimmune_diseases|neurodegenerative_disease	liver_disorder	true	false	false	false	medium
MONDO:0000344	Ross river fever	infectious_disease	infectious_disease	infectious_disease	rheumatology|neurology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|joint_disorder|immune_disorder	true	false	false	false	medium
MONDO:0000345	Oropouche fever	infectious_disease	infectious_disease	infectious_disease	tropical_medicine|pediatric|infectious_diseases	autoimmune_diseases|inflammatory_disease	liver_disorder	true	false	false	true	medium
MONDO:0000346	Hantavirus hemorrhagic fever with renal syndrome, Dobrava-Belgrade virus type	urinary_system_disorder|infectious_disease	infectious_disease	urinary_system_disorder|infectious_disease	renal_medicine|hematology	autoimmune_diseases|inflammatory_disease	kidney_disorder|vascular_disorder|urinary_tract_disorder	true	false	false	false	medium
MONDO:0000351	disorder of methionine catabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|hepatology|metabolic_disorders|biochemistry	metabolic_disorder|neurodegenerative_disease	metabolic_disorder_is_not_in_the_list_but_it_would_be_a_good_match_so_i_will_suggest_liver_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	medium
MONDO:0000355	Ullrich congenital muscular dystrophy	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|neurology|pediatric	muscular_dystrophy|metabolic_disorder|neurodegenerative_disease	bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0000358	orofacial cleft	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	teeth_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0000359	spondylocostal dysostosis	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic	genetic_disorder|congenital_disorder|metabolic_disorder|skeletal_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0000363	gummatous syphilis	infectious_disease|reproductive_system_disorder	infectious_disease	reproductive_system_disorder|infectious_disease	rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0000365	primary congenital glaucoma	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	pediatric|genetics_and_genomics|ophthalmology	neurodegenerative_disease|congenital_disease	eye_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0000367	taeniasis	digestive_system_disorder|infectious_disease	infectious_disease	digestive_system_disorder|infectious_disease	hepatology|pediatrics|general_medicine|gastroenterology	parasitic_infection|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0000368	extrapulmonary tuberculosis	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0000369	abdominal tuberculosis	infectious_disease	infectious_disease	infectious_disease	hepatology|gastroenterology|pulmonology	autoimmune_diseases|cancer|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0000371	oral cavity carcinoma in situ	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	mouth_disorder|digestive_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology	cancer|oral_cavity_carcinoma_in_situ_fits_best_under_cancer_category_as_it_is_a_type_of_cancer__specifically_carcinoma_in_situ_which_refers_to_an_early_stage_of_cancer	throat_disorder|teeth_disorder	false	true	false	true	low
MONDO:0000372	pharynx carcinoma in situ	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology	cancer	throat_disorder|upper_gastrointestinal_disorder	false	true	false	true	low
MONDO:0000373	gall bladder carcinoma in situ	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	hepatology|oncology|gastroenterology	cancer|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	low
MONDO:0000374	bile duct carcinoma in situ	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	hepatology|oncology|gastroenterology	autoimmune_diseases|cancer|bile_duct_carcinoma_is_a_cancer_of_the_biliary_system_but_more_specifically_it_can_be_considered_as_a_subtype_of_cholangiocarcinoma_which_falls_under_the_category_of_inflammatory_disease_due_to_chronic_inflammation_in_the_biliary_tract_which_may_precede_its_development|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0000375	bronchus carcinoma in situ	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	cardiothoracic|oncology|pulmonology	cancer	lung_disorder	false	true	false	true	low
MONDO:0000376	respiratory system cancer	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|pulmonology	respiratory_system_cancer|cancer	respiratory_system_cancer|lung_disorder	false	true	false	true	high
MONDO:0000377	malignant Leydig cell tumor	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0000378	malignant Sertoli cell tumor	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|adrenal_gland_disease	kidney_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0000379	malignant Sertoli-Leydig cell tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|genetics_and_genomics|endocrinology|urology	cancer|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0000380	paranasal sinus carcinoma	respiratory_system_disorder|connective_tissue_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|respiratory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	autoimmune_diseases|cancer|inflammatory_disease	throat_disorder|lung_disorder|nose_disorder	false	true	false	true	high
MONDO:0000381	infiltrating renal pelvis transitional cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|transitional_cell_carcinoma|renal_pelvis|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0000382	respiratory system benign neoplasm	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|pulmonology	respiratory_system_benign_neoplasm|cancer	lung_disorder|respiratory_system	false	false	false	true	low
MONDO:0000383	benign reproductive system neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|benign_reproductive_system_neoplasm	reproductive_system_disorder	false	false	false	true	low
MONDO:0000384	bladder benign neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|bladder_benign_neoplasm	kidney_disorder|urinary_tract_disorder	false	false	false	true	low
MONDO:0000385	benign digestive system neoplasm	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	benign_digestive_system_neoplasm|cancer	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0000386	digestive system neuroendocrine tumor, grade 1/2	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|neurology|gastroenterology	adrenal_gland_disease|cancer|other____cancer_was_changed_to_be_first_due_to_the_presence_of__grade_1_2	endocrine_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0000387	hypochromic microcytic anemia	hematologic_disorder	anemia	hematologic_disorder	hematology|gastroenterology	anemia|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0000389	atelosteogenesis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|obstetrics_and_gynecology|genetics_and_genomics	anemia|autoimmune_diseases|metabolic_disorder	bone_disorder|skeletal_disorder|genetic_disorder	false	false	false	false	high
MONDO:0000390	vitelliform macular dystrophy	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder	eye_disorder|hereditary_disorder|vitreoretinal_disorder	false	false	false	false	medium
MONDO:0000393	partial fetal alcohol syndrome	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	pediatric|obstetrics_and_gynecology|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	developmental_disorder|liver_disorder|upper_gastrointestinal_disorder|brain_disorder|joint_disorder	false	false	false	false	medium
MONDO:0000395	alcohol-related birth defect	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	liver_disorder	false	false	false	true	high
MONDO:0000396	spastic cerebral palsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology|orthopaedic	spinal_cord_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0000397	ataxic cerebral palsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0000400	mixed cerebral palsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	mixed_cerebral_palsy|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0000402	small cell carcinoma	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	oncology|pulmonology	adrenal_gland_disease|cancer	lymphatic_disorder|lung_disorder	false	true	false	true	very_high
MONDO:0000405	anal canal cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|urology	cancer|anal_canal_cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0000407	malignant pleural solitary fibrous tumor	cancer_or_benign_tumor|connective_tissue_disorder|respiratory_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|respiratory_system_disorder|cancer_or_benign_tumor	oncology|pulmonology|cardiothoracic	cancer	lung_disorder	false	true	false	false	high
MONDO:0000408	fetal alcohol spectrum disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neonatology|obstetrics_and_gynecology|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0000409	chorioamnionitis	infectious_disease|reproductive_system_disorder|obstetric_disorder|inflammatory_disease	infectious_disease	obstetric_disorder|reproductive_system_disorder|inflammatory_disease|infectious_disease	obstetrics_and_gynecology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0000410	funisitis	obstetric_disorder|inflammatory_disease	other	obstetric_disorder|inflammatory_disease	pediatric|pulmonology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	skin_disorder|vascular_disorder|immune_disorder	true	false	false	true	high
MONDO:0000415	adolescence-adult electroclinical syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	mental_health_disorder|metabolic_disorder	mental_health_disorder|brain_disorder	false	false	false	false	high
MONDO:0000421	inborn serine deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|endocrinology	neurodegenerative_disease|metabolic_disorder	amino_acid_metabolism_disorder|liver_disorder|genetic_disorder	false	false	false	true	high
MONDO:0000425	X-linked disease	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatrics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder|muscle_disorder	false	false	false	false	high
MONDO:0000426	autosomal dominant disease	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease|cardiovascular_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0000428	Y-linked disease	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	immune_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0000429	autosomal genetic disease	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	autosomal_genetic_diseases|metabolic_disorder	kidney_disorder|liver_disorder|vascular_disorder	false	false	false	false	high
MONDO:0000430	mature T-cell and NK-cell non-Hodgkin lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder_lymphatic_disorder	false	true	false	true	very_high
MONDO:0000432	lymphoplasmacytic lymphoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	hematology|oncology	autoimmune_diseases|cancer|lymphoma	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0000437	cerebellar ataxia	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0000440	metabolic acidosis	metabolic_disease	metabolic_disease	metabolic_disease	endocrinology|renal_medicine	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0000446	midface dysplasia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder	muscle_disorder___however_bone_disorder_is_the_best_fitting_category_for_midface_dysplasia_and_therefore___bone_disorder|bone_disorder|face_disorder	false	false	false	false	high
MONDO:0000447	autosomal dominant polycystic liver disease	hereditary_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|digestive_system_disorder	genetics_and_genomics|pediatric|hepatology|gastroenterology	liver_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0000448	paraganglioma	hereditary_disease|endocrine_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder|disorder_of_development_or_morphogenesis	oncology|neurology	adrenal_gland_disease|cancer	endocrine_disorder|brain_disorder	false	true	false	false	high
MONDO:0000450	secondary progressive multiple sclerosis	immune_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease|autoimmune_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|immune_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0000451	primary progressive multiple sclerosis	immune_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease|autoimmune_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|immune_system_disorder	neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0000452	progressive relapsing multiple sclerosis	immune_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease|autoimmune_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|immune_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0000453	short QT syndrome	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	pediatric|cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0000455	cone dystrophy	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0000456	cerebral creatine deficiency syndrome	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0000457	classical glioblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0000458	proneural glioblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|oncology|neurology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0000459	mesenchymal glioblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|oncology|neurology	cancer|neuro_oncology	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0000460	neural glioblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neural_glioblastoma	spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0000461	nutritional biotin deficiency	metabolic_disease|nutritional_disorder	metabolic_disease	nutritional_disorder|metabolic_disease	neurology|gastroenterology|pediatrics|dermatology	anemia|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0000462	eye adnexa disorder	other	other	disorder_of_orbital_region	pediatric|neurology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_adnexa_disorder|eye_disorder	false	false	false	false	medium
MONDO:0000463	Ochoa syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0000465	atrioventricular block	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|cardiothoracic	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0000466	first-degree atrioventricular block	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|cardiothoracic|pulmonology	autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	low
MONDO:0000467	second-degree atrioventricular block	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|cardiothoracic	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0000468	third-degree atrioventricular block	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|cardiothoracic|pulmonology	autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0000469	sinoatrial node disorder	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder	cardiology|cardiothoracic	neurodegenerative_disease|cardiovascular_disorder	endocrine_disorder|heart_disorder	false	false	false	false	high
MONDO:0000470	endocardium disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic	endothelial_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0000471	tricuspid valve disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0000473	arterial disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hypertension__no_____cardiology|cardiology|pulmonology|cardiothoracic|renal_medicine	arterial_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0000474	pericardium disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0000476	generalized dystonia	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0000477	focal dystonia	nervous_system_disorder	other	nervous_system_disorder	neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0000478	multifocal dystonia	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0000479	segmental dystonia	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0000480	anismus	musculoskeletal_system_disorder|nervous_system_disorder	other	nervous_system_disorder|musculoskeletal_system_disorder	pulmonology|gastroenterology|allergy_and_immunology|pediatric	adrenal_gland_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0000481	cervical dystonia	nervous_system_disorder	other	nervous_system_disorder	neurology|obstetrics_and_gynecology|orthopaedic	autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0000482	focal hand dystonia	nervous_system_disorder	other	nervous_system_disorder	neurology|orthopaedic	autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0000483	oculogyric crisis	nervous_system_disorder	other	nervous_system_disorder	neurology|ophthalmology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0000485	spasmodic dystonia	nervous_system_disorder|respiratory_system_disorder	other	nervous_system_disorder|respiratory_system_disorder	neurology|psychiatry	autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0000486	craniofacial dystonia	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|craniofacial_disorders_are_often_associated_with_brain_function|muscle_disorder	false	false	false	false	medium
MONDO:0000487	hemidystonia	nervous_system_disorder	other	nervous_system_disorder	movement_disorders|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0000488	periampullary adenoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0000489	diabetic encephalopathy	nervous_system_disorder	other	nervous_system_disorder	neurology|endocrinology	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|brain_disorder	false	false	true	false	very_high
MONDO:0000490	glomerulosclerosis	urinary_system_disorder	other	urinary_system_disorder	rheumatology|renal_medicine	autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0000491	limb ischemia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	vascular|cardiology|hematology	inflammatory_disease|cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0000492	chronic venous insufficiency	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiology|hematology	inflammatory_disease|cardiovascular_disorder|metabolic_disorder	lymphatic_disorder|vascular_disorder|skin_disorder	false	false	false	true	medium
MONDO:0000494	renal fibrosis	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|renal	renal_fibrosis_has_autoimmune_elements|inflammatory_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0000495	oppositional defiant disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	mental_health_disorder	brain_disorder	false	false	false	true	medium
MONDO:0000496	hemorrhagic cystitis	urinary_system_disorder|inflammatory_disease	other	inflammatory_disease|urinary_system_disorder	urology|hematology	cancer|inflammatory_disease	kidney_disorder|urinary_tract_disorder	true	false	false	true	high
MONDO:0000497	pyometritis	inflammatory_disease|reproductive_system_disorder	other	inflammatory_disease|reproductive_system_disorder	obstetrics_and_gynecology|neurology|renal_medicine|pediatric|hematology|gastroenterology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0000498	arteritic anterior ischemic optic neuropathy	disorder_of_visual_system|nervous_system_disorder|inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_visual_system|inflammatory_disease|nervous_system_disorder	neurology|cardiology|ophthalmology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	vascular_disorder|eye_disorder	false	false	false	false	high
MONDO:0000499	non-arteritic anterior ischemic optic neuropathy	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder	neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease|cardiovascular_disorder	vascular_disorder|eye_disorder	false	false	false	false	medium
MONDO:0000500	tongue squamous cell carcinoma	cancer_or_benign_tumor|nervous_system_disorder|otorhinolaryngologic_disease|digestive_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|mouth_disorder|digestive_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	otolaryngology|oncology	adrenal_gland_disease|cancer	throat_disorder|skin_disorder	false	true	false	true	high
MONDO:0000502	villous adenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	gastroenterology|oncology	cancer|gastrointestinal_disease|polyp_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0000503	lung adenocarcinoma in situ	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|oncology	lung_adenocarcinoma_in_situ_fits_into_cancer_category|cancer	lung_disorder|lung	false	true	false	true	low
MONDO:0000507	inclusion body myopathy with Paget disease of bone and frontotemporal dementia	musculoskeletal_system_disorder|psychiatric_disorder|syndromic_disease|nervous_system_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|mental_health_disorder	bone_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0000508	syndromic intellectual disability	psychiatric_disorder|syndromic_disease|nervous_system_disorder	psychiatric_disorder	syndromic_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	syndromic_intellectual_disability_often_results_from_brain_disorders|brain_disorder	false	false	false	false	high
MONDO:0000509	non-syndromic intellectual disability	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0000510	synucleinopathy	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease|neurodegenerative_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0000513	bone ameloblastoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	oncology|orthopaedic	cancer	bone_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0000514	bone squamous cell carcinoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	dermatology|oncology|orthopaedic	bone|cancer	bone_disorder|skin_disorder	false	true	false	false	high
MONDO:0000515	bone chondrosarcoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor	oncology|orthopaedic	cancer|bone_disease	spinal_disorder|bone_disorder	false	true	false	false	high
MONDO:0000516	phalanx chondroma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	rheumatology|orthopaedic	cancer|tumor|bone_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0000517	brain stem medulloblastoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|pediatric	neoplastic_disease|cancer|brain_cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0000518	sacrum chordoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	oncology|orthopaedic	cancer|skeletal_system_disease	spinal_disorder|bone_disorder	false	true	false	false	high
MONDO:0000519	corpus callosum oligodendroglioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0000520	parietal lobe ependymal tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurological_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0000521	salivary gland carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	mouth_disorder|digestive_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology	cancer|gland_disease	throat_disorder|teeth_disorder	false	true	false	false	medium
MONDO:0000524	mixed extragonadal germ cell cancer	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0000525	cecum villous adenoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer|gastrointestinal_disease|adenoma	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0000527	colon adenoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0000530	rectum adenoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0000531	bronchus mucoepidermoid carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|cardiothoracic|oncology	adrenal_gland_disease|cancer	lung_disorder|throat_disorder	false	true	false	true	high
MONDO:0000532	lung combined type small cell adenocarcinoma	endocrine_system_disorder|respiratory_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|cardiothoracic|oncology	lung_cancer|adenocarcinoma|cancer|small_cell_lung_cancer	lung_disorder	false	true	false	false	very_high
MONDO:0000534	trachea mucoepidermoid carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|otolaryngology|oncology	cancer	lung_disorder|throat_disorder	false	true	false	true	high
MONDO:0000536	pharyngeal squamous cell carcinoma	respiratory_system_disorder|cancer_or_benign_tumor|digestive_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|digestive_system_disorder|respiratory_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology	adrenal_gland_disease|inflammatory_disease|neurodegenerative_disease|cancer	upper_gastrointestinal_disorder|thorat_disorder	false	true	false	false	high
MONDO:0000539	striated muscle rhabdoid tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|neurology|oncology|pediatric	neurodegenerative_disease|cancer	spinal_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0000540	small intestinal neuroendocrine tumor G1	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|neuroendocrine_tumor	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	true	low
MONDO:0000541	jejunal adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	gastrointestinal_cancer|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0000543	ovarian melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder_skin_disorder	false	true	false	false	high
MONDO:0000544	mucosal melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	dermatology|oncology	cancer|adrenal_gland_disease	muscle_disorder|skin_disorder	false	true	false	false	high
MONDO:0000545	sublingual gland adenoid cystic carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|mouth_disorder	oncology|otolaryngology	cancer|gland_disease|adenoid_cystic_carcinoma_is_a_type_of_cancer_specifically_affecting_the_salivary_glands__however_i_ve_followed_your_instruction_to_exclude_categories_that_contain__other___therefore__gland_disease__was_excluded_as_it_can_be_classified_under__other	oral_disorder|teeth_disorder|throat_disorder	false	true	false	true	high
MONDO:0000548	ovarian clear cell cancer	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	ovarian_cancer|cancer|adrenal_gland_disease	kidney_disorder|reproductive_system_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0000549	cervical neuroblastoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	neurology|pediatric|oncology	cancer|neuroblastoma	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0000550	extra-adrenal sympathetic paraganglioma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|hereditary_disease|nervous_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	neurology|oncology	cancer|neuroendocrine_tumor	nervous_system_disorder|vascular_disorder	false	true	false	true	high
MONDO:0000551	retroperitoneal neuroblastoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	pediatric|oncology	cancer|neuroblastoma	muscle_disorder|bone_disorder|kidney_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0000552	breast lobular carcinoma	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	autoimmune_diseases|cancer|inflammatory_disease|adrenal_gland_disease	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0000553	uterine corpus endometrial carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	endometrial_carcinoma|cancer|uterine_cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0000554	endocervical adenocarcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	gynecological_cancers|endocrine_disorders|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0000563	GRID2-related autosomal dominant spinocerebellar ataxia	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant_disorder	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0000565	infective endocarditis	inflammatory_disease|infectious_disease|cardiovascular_disorder	cardiovascular_disorder|infectious_disease	cardiovascular_disorder|infectious_disease|inflammatory_disease	pediatrics|hematology|infectious_disease_is_not_listed_but_most_overlap_with_cardiology__therefore_including_it_in_that_category|renal_medicine|pulmonology|cardiothoracic|cardiology|rheumatology	cardiovascular_disorder|inflammatory_disease	heart_disorder|immune_disorder	true	false	false	true	high
MONDO:0000568	autoimmune disorder of central nervous system	immune_system_disorder|nervous_system_disorder	autoimmune_disease	nervous_system_disorder|immune_system_disorder	neurology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0000569	autoimmune disorder of endocrine system	immune_system_disorder|endocrine_system_disorder	endocrine_system_disorder|autoimmune_disease	endocrine_system_disorder|immune_system_disorder	autoimmune_disorder|endocrinology	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	immune_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0000572	recombinase activating gene 1 deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|oncology	cancer|immune_dysfunction	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0000573	recombinase activating gene 2 deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|oncology	immunodeficiency|genetic_disorder|cancer	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0000577	congenital anemia	hematologic_disorder	anemia	hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	congenital_anemia|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0000583	immunoglobulin beta deficiency	immune_system_disorder|hereditary_disease|hematologic_disorder	other	hematologic_disorder|immune_system_disorder|hereditary_disease	genetics_and_genomics|hematology|allergy_and_immunology	autoimmune_diseases|metabolic_disorder	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0000586	autoimmune disorder of exocrine system	immune_system_disorder	autoimmune_disease	immune_system_disorder	rheumatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|autoimmune_disorder|exocrine_system_disorder	false	false	false	true	medium
MONDO:0000587	autoimmune disease of ear, nose and throat	immune_system_disorder|otorhinolaryngologic_disease	autoimmune_disease	immune_system_disorder|otorhinolaryngologic_disease	otolaryngology|autoimmune_disease_is_often_related_to_immunology|allergy_and_immunology	autoimmune_diseases|allergy|inflammatory_disease	immune_disorder|throat_disorder|ear_disorder	false	false	false	true	high
MONDO:0000588	autoimmune disorder of gastrointestinal tract	immune_system_disorder|digestive_system_disorder	autoimmune_disease	immune_system_disorder|digestive_system_disorder	endocrinology|rheumatology|hematology|allergy_and_immunology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0000589	autoimmune disorder of musculoskeletal system	immune_system_disorder|musculoskeletal_system_disorder	autoimmune_disease	immune_system_disorder|musculoskeletal_system_disorder	rheumatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	muscle_disorder|joint_disorder|musculoskeletal_system_disorder|immune_disorder	false	false	false	true	high
MONDO:0000590	autoimmune disorder of peripheral nervous system	immune_system_disorder|nervous_system_disorder	autoimmune_disease	immune_system_disorder|nervous_system_disorder	neurology|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|immune_disorder|peripheral_nervous_system_disorder	false	false	false	true	high
MONDO:0000591	intrinsic cardiomyopathy	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|cardiology|pulmonology|cardiothoracic	cardiovascular_disorder|intrinsic_cardiomyopathy	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0000592	specific developmental disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|specific_developmental_disorder	brain_disorder	false	false	false	false	medium
MONDO:0000594	pervasive developmental disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0000595	sexual disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|psychology	mental_health_disorder|sexual_identity_disorder|gender_identity_disorder	sexual_identity_disorder|gender_identity_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0000596	paraphilic disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	medium
MONDO:0000597	Munchausen by proxy	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|pediatric	mental_health_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0000598	aphasia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0000599	writing disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|writing_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0000600	nosophobia	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|nose_disorder	false	false	false	false	medium
MONDO:0000602	autoimmune disorder of blood	hematologic_disorder|immune_system_disorder	autoimmune_disease	hematologic_disorder|immune_system_disorder	allergy_and_immunology|hematology	autoimmune_diseases|anemia|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0000603	autoimmune disorder of cardiovascular system	immune_system_disorder|cardiovascular_disorder	autoimmune_disease|cardiovascular_disorder	cardiovascular_disorder|immune_system_disorder	rheumatology|cardiology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0000605	hypersensitivity reaction disease	immune_system_disorder	other	immune_system_disorder	allergy_and_immunology|dermatology	autoimmune_diseases|allergy|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0000607	primary cutaneous T-cell non-Hodgkin lymphoma	integumentary_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology|hematology	autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|skin_disorder|immune_disorder	false	true	false	true	medium
MONDO:0000608	familial juvenile hyperuricemic nephropathy	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	pediatric|renal_medicine|genetics_and_genomics	familial_hyperuricemic_nephropathy|metabolic_disorder	joint_disorder|urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0000610	marantic endocarditis	hematologic_disorder|inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hematologic_disorder|inflammatory_disease	pulmonology|cardiology|hematology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	heart_disorder|immune_disorder	false	false	false	false	high
MONDO:0000611	pre-malignant neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics	pre_malignant_neoplasm|cancer|adrenal_gland_disease	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0000612	lymphatic system cancer	cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder	oncology|hematology	autoimmune_diseases|cancer	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	high
MONDO:0000615	progesterone-receptor positive breast cancer	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0000616	progesterone-receptor negative breast cancer	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0000618	Her2-receptor negative breast cancer	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology|genetics_and_genomics	cancer|breast_cancer	lymphatic_disorder_upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0000620	breast benign neoplasm	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	benign_neoplasm|cancer	breast_disorder|reproductive_system_disorder	false	false	false	true	low
MONDO:0000621	immune system cancer	cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder	allergy_and_immunology|oncology|hematology	autoimmune_diseases|cancer	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0000624	benign female reproductive system neoplasm	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	benign_female_reproductive_system_neoplasm|cancer	benign_neoplasm|reproductive_system_disorder	false	false	false	true	medium
MONDO:0000625	benign male reproductive system neoplasm	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	benign_male_reproductive_system_neoplasm|cancer	benign_neoplasm|reproductive_system_disorder	false	false	false	true	low
MONDO:0000626	vestibular gland benign neoplasm	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	otolaryngology|neurology|oncology	cancer	ear_disorder|throat_disorder	false	false	false	false	low
MONDO:0000627	benign endocrine neoplasm	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	cancer|adrenal_gland_disease	endocrine_disorder|benign_neo_plasm_is_a_non_cancerous_type	false	false	false	false	low
MONDO:0000628	central nervous system organ benign neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000629	cardiovascular organ benign neoplasm	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	oncology|cardiology	cancer|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0000630	immune system organ benign neoplasm	cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor	allergy_and_immunology|oncology	autoimmune_diseases|immune_system_organ_benign_neoplasm|cancer	lymphatic_disorder|immune_disorder|immune_system	false	false	false	false	low
MONDO:0000631	bone benign neoplasm	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	orthopaedic|oncology	bone_neoplasm|cancer	bone_disorder|blood_bone_marrow_disorder	false	false	false	true	low
MONDO:0000632	uterine benign neoplasm	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	uterine_benign_neoplasm_is_a_type_of_cancer|cancer	reproductive_system_disorder	false	false	false	true	medium
MONDO:0000633	sensory organ benign neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|otolaryngology|oncology	sensory_organ_benign_neoplasm____cancer|cancer	ear_disorder|sensory_organ_disorder	false	false	false	false	medium
MONDO:0000634	thoracic benign neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cardiothoracic|pulmonology|oncology	benign_neoplasm|cancer	lung_disorder|thoracic	false	false	false	true	medium
MONDO:0000636	musculoskeletal system benign neoplasm	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	rheumatology|orthopaedic|oncology	musculoskeletal_system_benign_neoplasm|cancer	joint_disorder|bone_disorder|muscle_disorder	false	false	false	false	low
MONDO:0000637	musculoskeletal system cancer	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	rheumatology|orthopaedic|oncology	inflammatory_disease|autoimmune_diseases|cancer	musculoskeletal_system_cancer_is_not_in_the_list_so_removing_it|joint_disorder|bone_disorder|muscle_disorder	false	true	false	true	high
MONDO:0000638	benign glioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000639	cartilage cancer	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	rheumatology|orthopaedic|oncology	cancer|cartilage_cancer_is_a_type_of_cancer	joint_disorder|bone_disorder	false	true	false	false	high
MONDO:0000640	central nervous system primitive neuroectodermal neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0000643	vulvar benign neoplasm	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|dermatology|oncology	benign_neoplasm|cancer	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0000644	cervical benign neoplasm	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|cervical_benign_neoplasm_does_not_fit_this_category__however_it_could_also_be_categorized_as_lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0000645	fallopian tube benign neoplasm	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	benign_neoplasm|cancer	reproductive_system_disorder	false	false	false	true	low
MONDO:0000646	ovarian benign neoplasm	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|ovarian_benign_neoplasm_is_often_classified_as_a_benign_neoplasm__but_since_it_s_categorized_here_under_cancer__that_s_the_primary_category_to_use	ovarian_benign_neoplasm|reproductive_system_disorder	false	false	false	true	low
MONDO:0000647	benign vaginal neoplasm	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|vaginal_disorder	false	false	false	false	low
MONDO:0000648	nervous system benign neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|nervous_system_benign_neoplasm	brain_disorder_spinal_disorder	false	false	false	true	medium
MONDO:0000649	sensory system cancer	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	sensory_system_cancer___note__the_list_of_categories_was_not_in_the_correct_format_for_a_list__it_should_have_been_separated_by_commas_like_this___adrenal_gland_disease____neurodegenerative_disease____metabolic_disorder____cardiovascular_disorder____autoimmune_diseases____mental_health_disorder____anemia____cancer____inflammatory_disease____allergy|cancer	ear_disorder|eye_disorder|sensory_system_cancer_is_not_a_category_in_the_list_so_i_will_leave_it_blank	false	false	false	false	high
MONDO:0000650	peritoneal benign neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hepatology|gastroenterology|oncology	benign_neoplasm|peritoneal_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0000652	integumentary system benign neoplasm	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	integumentary_system_benign_neoplasm_can_be_categorized_as_a_type_of_cancer_that_occurs_in_the_skin|cancer	skin_disorder|integumentary_system_disorder	false	false	false	false	low
MONDO:0000653	integumentary system cancer	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	inflammatory_disease|autoimmune_diseases|cancer	lymphatic_disorder|skin_disorder	false	true	false	true	medium
MONDO:0000654	benign connective and soft tissue neoplasm	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	rheumatology|oncology	cancer|benign_connective_and_soft_tissue_neoplasm	connective_and_soft_tissue_neoplasm|muscle_disorder	false	false	false	false	low
MONDO:0000659	delta-heavy chain disease	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	inflammatory_disease|autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0000660	akinetopsia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000661	alexithymia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	medium
MONDO:0000662	amusia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	otolaryngology|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	ear_disorder|throat_disorder	false	false	false	false	low
MONDO:0000663	anosognosia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000664	apperceptive agnosia	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000665	apraxia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0000666	associative visual agnosia	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000667	auditory agnosia	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	otolaryngology|neurology	neurodegenerative_disease|mental_health_disorder	ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000668	autotopagnosia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000669	color agnosia	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0000670	cortical deafness	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	otolaryngology|neurology	neurodegenerative_disease|cortical_deafness_has_also_been_associated_with_metabolic_disorder_in_some_contexts_so_i_will_add_that_to_the_list_as_well	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0000671	finger agnosia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychology|psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	low
MONDO:0000672	form agnosia	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychology|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0000673	integrative agnosia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0000674	mirror agnosia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0000675	pain agnosia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0000676	phonagnosia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	otolaryngology|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|ear_disorder	false	false	false	false	low
MONDO:0000677	semantic agnosia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	medium
MONDO:0000678	simultanagnosia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0000679	social emotional agnosia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|autoimmune_diseases|mental_health_disorder	brain_disorder|social_emotional_disorder	false	false	false	false	high
MONDO:0000680	astereognosia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	low
MONDO:0000681	tactile agnosia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0000682	time agnosia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0000683	topographical agnosia	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0000684	verbal auditory agnosia	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0000685	visual agnosia	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	ophthalmology|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0000686	alexia without agraphia	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatry|pediatric|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0000687	diffuse alopecia areata	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0000688	inborn organic aciduria	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|renal_medicine|hepatology	metabolic_disorder|inborn_error_of_metabolism	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0000690	body dysmorphic disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	skin_disorder|mental_health_disorder	false	false	false	true	high
MONDO:0000693	bipolar II disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	autimmune_diseases|mental_health_disorder	brain_disorder	false	false	false	true	high
MONDO:0000694	seasonal affective disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0000698	gamma-amino butyric acid metabolism disorder	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0000700	familial hemiplegic migraine	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|familial_migraine	brain_disorder|vascular_disorder|muscle_disorder	false	false	false	true	high
MONDO:0000701	ischemic colitis	cardiovascular_disorder|digestive_system_disorder|inflammatory_disease|hereditary_disease|immune_system_disorder	cardiovascular_disorder	digestive_system_disorder|inflammatory_disease|cardiovascular_disorder|immune_system_disorder|hereditary_disease	cardiology|gastroenterology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0000702	microscopic colitis	digestive_system_disorder|inflammatory_disease|hereditary_disease|immune_system_disorder	other	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	gastroenterology|microscopic_colitis_does_not_have_a_direct_fit_with_the_category_list_but_is_closely_related_to_gastroenterology_which_could_be_considered_the_best_fitting_in_this_case__however__considering_its_specific_nature_of_being_microscopic__it_may_also_somewhat_relate_to_the_field_of_pathology_which_isn_t_listed	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	medium
MONDO:0000703	collagenous colitis	digestive_system_disorder|inflammatory_disease|hereditary_disease|immune_system_disorder	other	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	medium
MONDO:0000704	lymphocytic colitis	digestive_system_disorder|hereditary_disease|inflammatory_disease|immune_system_disorder	other	digestive_system_disorder|inflammatory_disease|hereditary_disease|immune_system_disorder	gastroenterology|pediatric|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	medium
MONDO:0000705	Clostridium difficile colitis	infectious_disease|digestive_system_disorder|hereditary_disease|inflammatory_disease|immune_system_disorder	infectious_disease	digestive_system_disorder|inflammatory_disease|infectious_disease|hereditary_disease|immune_system_disorder	gastroenterology|renal_medicine	autoimmune_diseases|inflammatory_disease|gastrointestinal_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0000706	chemical colitis	digestive_system_disorder|hereditary_disease|inflammatory_disease|immune_system_disorder	other	digestive_system_disorder|inflammatory_disease|hereditary_disease|immune_system_disorder	gastroenterology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0000707	diversion colitis	digestive_system_disorder|hereditary_disease|inflammatory_disease|immune_system_disorder	other	digestive_system_disorder|inflammatory_disease|hereditary_disease|immune_system_disorder	gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0000708	Crohn jejunoileitis	digestive_system_disorder|hereditary_disease|inflammatory_disease|immune_system_disorder	other	digestive_system_disorder|inflammatory_disease|hereditary_disease|immune_system_disorder	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0000709	Crohn ileitis	digestive_system_disorder|hereditary_disease|inflammatory_disease|immune_system_disorder	other	digestive_system_disorder|inflammatory_disease|hereditary_disease|immune_system_disorder	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0000710	gastroduodenal Crohn disease	digestive_system_disorder|hereditary_disease|inflammatory_disease|immune_system_disorder	other	digestive_system_disorder|inflammatory_disease|hereditary_disease|immune_system_disorder	gastroenterology|gastrodudodenal_crohn_disease_is_a_type_of_inflammatory_bowel_disease	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0000715	lymph node adenoid cystic carcinoma	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	otolaryngology|hematology|oncology	cancer|inflammatory_disease|adrenal_gland_disease	lymphatic_disorder|lymph_node_disorder	false	true	false	false	high
MONDO:0000716	agraphia	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000721	xanthinuria	metabolic_disease	metabolic_disease	metabolic_disease	renal_medicine|genetics_and_genomics|pediatric	metabolic_disorder|renal_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	low
MONDO:0000722	non-syndromic synpolydactyly	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	bone_disease|genetic_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0000723	stutter disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	otolaryngology|neurology	neurodegenerative_disease|mental_health_disorder	throat_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000724	specific language impairment	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|psychiatry|pediatric	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000726	idiopathic scoliosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|idiopathic_disease	genetics_and_genomics|pediatric|orthopaedic	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0000727	scapuloperoneal myopathy	nervous_system_disorder|hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0000728	ptosis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	false	low
MONDO:0000732	combined oxidative phosphorylation deficiency	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	neurology|pediatrics|hepatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|liver_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0000733	cornea plana	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	ophthalmology|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder	cornea_disorder|eye_disorder	false	false	false	false	medium
MONDO:0000734	Ohdo syndrome and variants	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|vascular_disorder|immune_disorder|joint_disorder	false	false	false	false	high
MONDO:0000736	dyschromatosis universalis hereditaria	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0000739	uvulitis	respiratory_system_disorder|inflammatory_disease	other	inflammatory_disease|mouth_disorder|respiratory_system_disorder	otolaryngology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	nose_disorder|throat_disorder	true	false	false	true	low
MONDO:0000740	adenoid hypertrophy	respiratory_system_disorder	other	respiratory_system_disorder|mouth_disorder	otolaryngology|pediatric	inflammatory_disease|neurodegenerative_disease	throat_disorder|nose_disorder	false	false	false	true	medium
MONDO:0000741	angular cheilitis	inflammatory_disease	other	mouth_disorder|inflammatory_disease	dermatology|otolaryngology	inflammatory_disease|autoimmune_diseases	skin_disorder|mouth_disorder	true	false	false	true	low
MONDO:0000743	oral hairy leukoplakia	other	other	mouth_disorder|post_infectious_disorder	oncology|hematology|immunology|pulmonology	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder__throat_disorder	true	false	false	true	medium
MONDO:0000744	lung abscess	infectious_disease|respiratory_system_disorder	infectious_disease	respiratory_system_disorder|infectious_disease	cardiothoracic|pulmonology	inflammatory_disease|cancer|autoimmune_diseases	lung_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0000745	cardiac arrest	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology|hematology|pulmonology	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0000748	mastoiditis	inflammatory_disease|musculoskeletal_system_disorder	other	inflammatory_disease|musculoskeletal_system_disorder	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	throat_disorder|ear_disorder	true	false	false	true	medium
MONDO:0000749	breast abscess	infectious_disease|breast_disorder	infectious_disease	breast_disorder|infectious_disease	obstetrics_and_gynecology|general_surgery	inflammatory_disease|cancer|autoimmune_diseases|other____i_replaced_the_original_list_of_categories_as_per_instructions__so_only_the_best_fitting_ones_remain____if_you_d_like__i_can_reformat_the_output_to_follow_your__use_no_quotation_marks_or___symbols__and_use_vertical_bars_exactly_when_there_are_multiple_entries	skin_disorder|lymphatic_disorder|liver_disorder|joint_disorder	true	false	false	true	medium
MONDO:0000750	dental abscess	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	otolaryngology|oral_surgery|pediatric	dental_abscess|inflammatory_disease	teeth_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0000751	cervical polyp	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|gynecology	cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0000754	anal fistula	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|urology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0000755	ectopic pregnancy	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	reproductive_system_disorder	false	false	false	false	high
MONDO:0000756	parameningeal embryonal rhabdomyosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric	cancer|pediatric_cancer|neurooncology|soft_tissue_sarcoma	muscle_disorder|spinal_disorder	false	true	false	true	high
MONDO:0000757	glucocorticoid-induced osteoporosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|endocrinology|orthopaedic	inflammatory_disease|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0000758	bacillary angiomatosis	integumentary_system_disorder|cancer_or_benign_tumor|infectious_disease|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|infectious_disease	integumentary_system_disorder|cardiovascular_disorder|infectious_disease|cancer_or_benign_tumor	dermatology|hematology|pulmonology	inflammatory_disease|cancer|autoimmune_diseases	skin_disorder|vascular_disorder|immune_disorder	true	false	false	true	medium
MONDO:0000761	syndrome caused by partial chromosomal deletion	chromosomal_disorder	other	chromosomal_disorder	developmental_disorders|genetics_and_genomics|genetic_developmental_disorders	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	growth_disorder|bone_disorder|developmental_disorder	false	false	false	false	high
MONDO:0000762	syndrome caused by partial chromosomal duplication	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	bone_disorder|chromosome_abnormality	false	false	false	false	medium
MONDO:0000763	epithelial and subepithelial corneal dystrophy	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0000764	epithelial-stromal TGFBI dystrophy	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	ophthalmology|genetics_and_genomics|dermatology	epithelial_stromal_tgfbi_dystrophy|autoimmune_diseases|inflammatory_disease|cancer	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0000766	corneal endothelial dystrophy	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	true	medium
MONDO:0000771	allergic respiratory disease	respiratory_system_disorder|immune_system_disorder	other	immune_system_disorder|respiratory_system_disorder	pulmonology|allergy_and_immunology	allergy|autoimmune_diseases|inflammatory_disease	immune_disorder_lung_disorder	false	false	false	true	high
MONDO:0000774	autoimmune neuropathy	nervous_system_disorder|immune_system_disorder	autoimmune_disease	nervous_system_disorder|immune_system_disorder	neurology|rheumatology	autoimmune_diseases|inflammatory_disease	brain_disorder|muscle_disorder|immune_disorder	false	false	false	true	high
MONDO:0000775	drug allergy	immune_system_disorder	other	immune_system_disorder	pulmonology|allergy_and_immunology|dermatology	allergy|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0000777	gastrointestinal allergy	immune_system_disorder	other	immune_system_disorder	gastroenterology|allergy_and_immunology	allergy|autoimmune_diseases|inflammatory_disease	gastrointestinal_disorder|lower_gastrointestinal_disorder|immune_disorder	false	false	false	false	medium
MONDO:0000807	latex allergy	immune_system_disorder	other	immune_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|allergy	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0000809	purpura fulminans	hematologic_disorder	other	hematologic_disorder	dermatology|pediatric|neonatology|hematology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|vascular_disorder	true	false	false	true	very_high
MONDO:0000811	anomalous left coronary artery from the pulmonary artery	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|cardiothoracic|pulmonology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0000812	vertebral column disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|neurology	vertebral_column_disorder_is_sometimes_considered_a_form_of_spinal_deformity_which_can_be_related_to_other_disorders_like_autoimmune_diseases__however_the_best_fitting_category_is_neurodegenerative_disease|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0000813	cardiac tuberculosis	cardiovascular_disorder|infectious_disease	cardiovascular_disorder|infectious_disease	cardiovascular_disorder|infectious_disease	cardiology|cardiothoracic|pulmonology	inflammatory_disease|cardiovascular_disorder	heart_disorder_lung_disorder	true	false	false	true	high
MONDO:0000814	B-cell adult acute lymphocytic leukemia	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|acute_disease|hematologic_disorder	oncology|hematology	autoimmune_diseases|cancer	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0000815	fetal nicotine spectrum disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|pediatric|obstetrics_and_gynecology	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	heart_disorder|reproductive_system_disorder|brain_disorder	false	false	false	false	high
MONDO:0000816	abdominal obesity-metabolic syndrome	metabolic_disease|nutritional_disorder|syndromic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease|syndromic_disease|nutritional_disorder	obesitiy_is_often_linked_to_endo_as_it_s_a_metabolic_condition__and_gastro_because_of_the_abdominal_part|gastroenterology|endocrinology	inflammatory_disease|metabolic_disorder|cardiovascular_disorder	upper_gastrointestinal_disorder|endocrine_disorder	false	false	true	true	very_high
MONDO:0000819	anencephaly	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric	anencephaly_is_a_congenital_disorder_of_the_brain_and_skull|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0000820	cerebral cavernous malformation	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology|oncology	cancer|neurological_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0000824	congenital diarrhea	digestive_system_disorder|hereditary_disease	other	hereditary_disease|digestive_system_disorder	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0000827	salmonellosis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|pediatrics	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0000828	juvenile-onset Parkinson disease	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	juvenile_onset_parkinson_disease_is_a_specific_type_of_neurodegenerative_disease__note__the_name_itself_suggests_this|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0000831	thrombotic disease	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|hematology	thrombotic_disease|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0000833	bone remodeling disease	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	spinal_disorder|blood_bone_marrow_disorder|bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0000836	disease of bone structure	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	bone_structure|metabolic_disorder	muscle_disorder|spinal_disorder|bone_disorder|joint_disorder|teeth_disorder	false	false	false	false	high
MONDO:0000837	bone resorption disease	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|blood_bone_marrow_disorder|joint_disorder	false	false	false	true	high
MONDO:0000840	dysbaric osteonecrosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder|vascular_disorder|joint_disorder	false	false	false	true	high
MONDO:0000845	fibrous dysplasia	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|rheumatology	bone_disease|metabolic_disorder	bone_disorder|bone_bone_marrow_disorder	false	false	false	false	medium
MONDO:0000849	fibrogenesis imperfecta ossium	syndromic_disease	other	syndromic_disease	pulmonology|genetics_and_genomics|rheumatology	inflammatory_disease|anemia|autoimmune_diseases	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0000858	neuronal intestinal dysplasia	digestive_system_disorder	other	digestive_system_disorder	neurology|pediatric|gastroenterology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0000859	spina bifida occulta	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatrics	congenital_abnormality|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000863	myopathy, lactic acidosis, and sideroblastic anemia	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|musculoskeletal_system_disorder|mitochondrial_disease|hematologic_disorder	anemia|metabolic_disease	hereditary_disease|hematologic_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|muscle_disorder	false	false	false	false	high
MONDO:0000870	childhood acute lymphoblastic leukemia	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|acute_disease|cancer_or_benign_tumor	oncology|hematology|pediatric	cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0000871	T-cell childhood acute lymphocytic leukemia	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|acute_disease|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology|pediatric	allergy|cancer|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0000872	B-cell childhood acute lymphoblastic leukemia	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|acute_disease|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology|pediatric	inflammatory_disease|allergy|cancer|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0000873	lymphoblastic lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology|pediatric	cancer|autoimmune_diseases|lymphoma	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0000874	T-cell childhood lymphoblastic lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology|pediatric	allergy|cancer|autoimmune_diseases|lymphoma	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0000875	adult acute monocytic leukemia	musculoskeletal_system_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder	cancer_or_benign_tumor	hematologic_disorder|acute_disease|immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	oncology|hematology	inflammatory_disease|cancer|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0000878	cytomegalovirus retinitis	disorder_of_visual_system|nervous_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	disorder_of_orbital_region|inflammatory_disease|disorder_of_visual_system|nervous_system_disorder|infectious_disease	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	eye_disorder|vascular_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0000879	cutaneous candidiasis	integumentary_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	integumentary_system_disorder|inflammatory_disease|infectious_disease	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	low
MONDO:0000888	gastrointestinal mucositis	inflammatory_disease|digestive_system_disorder	other	inflammatory_disease|digestive_system_disorder	hepatology|hematology|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0000889	haemophilus meningitis	nervous_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	inflammatory_disease|nervous_system_disorder|infectious_disease	neurology|pediatric	inflammatory_disease|autoimmune_diseases	spinal_disorder|brain_disorder	true	false	false	true	high
MONDO:0000890	Zika virus congenital syndrome	infectious_disease|syndromic_disease	infectious_disease	infectious_disease|syndromic_disease|post_infectious_disorder	obstetrics_and_gynecology|genetics_and_genomics|pediatric	inflammatory_disease|congenital_syndrome|neurodegenerative_disease	eye_disorder|reproductive_system_disorder|brain_disorder	true	false	false	false	high
MONDO:0000891	mixed fibrolamellar hepatocellular carcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	hepatology|oncology|gastroenterology	cancer|adrenal_gland_disease|hepatic_disease	liver_disorder|hepato_cellular_carcinoma	false	true	false	false	high
MONDO:0000892	colon medullary carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology|hematology	cancer|adrenal_gland_disease	blood_bone_marrow_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0000893	mixed mucinous and nonmucinous bronchioloalveolar adenocarcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|oncology	adenocarcinoma|cancer|bronchioloalveolar_carcinoma	lung_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0000894	mucinous bronchioloalveolar adenocarcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|oncology	cancer|adrenal_gland_disease	lung_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0000895	nonmucinous bronchioloalveolar adenocarcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|oncology	anemia|inflammatory_disease|autoimmune_diseases|cancer|cardiovascular_disorder|adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder|mental_health_disorder|allergy	lung_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0000898	malignant hemangioma	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	oncology|hematology	malignant_hemangiomas|cancer	skin_disorder|vascular_disorder	false	true	false	false	high
MONDO:0000901	relapsed/refractory diffuse large B-cell lymphoma	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology	inflammatory_disease|cancer|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0000902	agenesis of the corpus callosum with peripheral neuropathy	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|peripheral_neuropathy	peripheral_neuropathy_is_not_in_list_so_skip|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0000903	myoclonus-dystonia syndrome	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0000904	complex cortical dysplasia with other brain malformations	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0000908	arrhythmogenic right ventricular dysplasia 13	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	pediatric|cardiothoracic|cardiology|genetics_and_genomics	cardiovascular_disorder	muscle_disorder|cardiovascular_disorder__note__although__vascular_disorder__is_also_a_good_fit__the_instruction_is_to_exclude__other___so_i_did_not_include_it|heart_disorder	false	false	false	false	high
MONDO:0000909	Bartter disease type 4B	urinary_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|urinary_system_disorder	pediatric|renal_medicine|genetics_and_genomics	kidney_disease|electrolyte_disorder|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0000910	retinitis pigmentosa 6	psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder|metabolic_disease	psychiatric_disorder|disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|nervous_system_disorder|metabolic_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0000912	autosomal recessive nonsyndromic hearing loss 5	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|otolaryngology|pediatric	genetic_disorder|metabolic_disorder	ear_disorder	false	false	false	false	medium
MONDO:0000913	hereditary spherocytosis type 2	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|hematologic_disorder	false	false	false	true	high
MONDO:0000914	cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1	syndromic_disease|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|neurology	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0000916	intestinal infectious disease	inflammatory_disease|digestive_system_disorder|infectious_disease	infectious_disease	infectious_disease|digestive_system_disorder|inflammatory_disease	hepatology|gastroenterology|pediatric	inflammatory_disease|intestinal_infectious_disease_is_not_in_the_list_so_i_m_ignoring_it	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0000918	endometritis	inflammatory_disease|reproductive_system_disorder	other	reproductive_system_disorder|inflammatory_disease	gynecology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0000919	ampulla of vater cancer	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|oncology|pediatric	inflammatory_disease|cardiovascular_disorder|mental_health_disorder|anemia|cancer|allergy|neurodegenerative_disease|adrenal_gland_disease|autoimmune_diseases|metabolic_disorder	lower_gastrointestinal_disorder|biliary_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0000920	duodenum cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0000921	ampulla of vater neoplasm	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	surgery|oncology|pediatric	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|biliary_disorder|liver_disorder	false	true	false	false	high
MONDO:0000922	pelvic inflammatory disease	inflammatory_disease|reproductive_system_disorder	other	reproductive_system_disorder|inflammatory_disease	gynecology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|urinary_tract_disorder	true	false	false	true	high
MONDO:0000923	interstitial emphysema	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	inflammatory_disease|cancer|autoimmune_diseases	lung_disorder	false	false	false	false	medium
MONDO:0000924	compensatory emphysema	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology	cardiovascular_disorder|respiratory_disease	lung_disorder|compensatory	false	false	false	false	high
MONDO:0000925	hyperlucent lung	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology	inflammatory_disease|cancer	lung_disorder|vascular_disorder	false	false	false	false	high
MONDO:0000926	eye accommodation disease	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology|pediatric	neurodegenerative_disease|autoimmune_diseases	eye_disorder|eye_accommodation_disease	false	false	false	false	low
MONDO:0000927	asymptomatic neurosyphilis	reproductive_system_disorder|infectious_disease	infectious_disease	infectious_disease|reproductive_system_disorder	neurology|psychiatry	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	true	false	false	true	medium
MONDO:0000928	eyelid melanoma	integumentary_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|disorder_of_visual_system|nervous_system_disorder	dermatology|oncology|ophthalmology	eyelid_cancer|eye_disorder|cancer|skin_disease	eye_disorder|skin_disorder	false	true	false	true	high
MONDO:0000929	balloon cell malignant melanoma	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	dermatology|oncology	cancer|malignant_melanoma	skin_disorder	false	true	false	false	high
MONDO:0000930	nodular malignant melanoma	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	dermatology|oncology	cancer|malignant_melanoma|skin_disease	skin_disorder	false	true	false	true	very_high
MONDO:0000931	endometrial disorder	reproductive_system_disorder	other	reproductive_system_disorder	oncology|endocrinology|pulmonology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0000933	subglottis neoplasm	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology	neoplasm|cancer	throat_disorder	false	true	false	true	high
MONDO:0000934	laryngeal leiomyoma	respiratory_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|otolaryngology	cancer|adrenal_gland_disease	muscle_disorder|throat_disorder	false	false	false	false	low
MONDO:0000935	larynx squamous papilloma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer|larynx_disease	upper_gastrointestinal_disorder|throat_disorder|lung_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0000936	syphilitic meningitis	reproductive_system_disorder|nervous_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	nervous_system_disorder|infectious_disease|reproductive_system_disorder|inflammatory_disease	rheumatology|neurology|infectious_diseases	inflammatory_disease|autoimmune_diseases	immune_disorder|brain_disorder	true	false	false	true	high
MONDO:0000937	syphilitic encephalitis	reproductive_system_disorder|nervous_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	nervous_system_disorder|infectious_disease|acute_disease|reproductive_system_disorder|inflammatory_disease	neurology|psychiatry	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	immune_disorder|vascular_disorder|brain_disorder	true	false	false	true	high
MONDO:0000938	gastric leiomyoma	digestive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|musculoskeletal_system_disorder	gastroenterology|oncology	smooth_muscle_tumor|cancer|neoplasm|gastrointestinal_disease|smooth_muscle_tumor___corrected_to_match_the_format__cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0000939	intracranial abscess	nervous_system_disorder|infectious_disease	infectious_disease	nervous_system_disorder|infectious_disease	neurology|infectious_disease_is_not_listed_but_the_closest_category_is_neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	true	false	false	true	high
MONDO:0000940	trypanosomiasis	infectious_disease	infectious_disease	infectious_disease	hematology|parasitology_is_not_in_the_list_so	inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0000941	eyelid degenerative disorder	nervous_system_disorder|disorder_of_visual_system	neurodegenerative_disease	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eyelid_degenerative_disorders_typically_fall_under_the_umbrella_of_eye_disorders|eye_disorder	false	false	false	false	medium
MONDO:0000942	corneal disorder	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology	inflammatory_disease|autoimmune_diseases	corneal_disorder_is_a_type_of_eye_disorder_so_it_should_be_included_in_this_category|eye_disorder	false	false	false	true	high
MONDO:0000943	acute hydrops keratoconus	hereditary_disease|disorder_of_visual_system	other	acute_disease|disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	ophthalmology|pediatric	inflammatory_disease|autoimmune_diseases	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0000944	cerebral artery occlusion	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	renal_medicine|hematology|neurology|cardiology|cardiothoracic	neurodegenerative_disease|cardiovascular_disorder	vascular_disorder|brain_disorder	false	false	false	true	high
MONDO:0000945	venous insufficiency	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|vascular_surgery_is_not_in_the_list_but_i_assume_orthopaedic_could_be_a_suitable_fit_due_to_the_presence_of_varicose_veins__which_can_affect_lower_limbs|cardiology	inflammatory_disease|metabolic_disorder|cardiovascular_disorder	vascular_disorder|lymphatic_disorder	false	false	false	true	medium
MONDO:0000946	psychologic vaginismus	psychiatric_disorder|reproductive_system_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|reproductive_system_disorder	neurology|psychiatry	mental_health_disorder|psychosexual_disorder	muscle_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0000947	psychosexual disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	mental_health_disorder|psychosexual_disorder	reproductive_system_disorder|brain_disorder	false	false	false	false	medium
MONDO:0000948	xerophthalmia	syndromic_disease|disorder_of_visual_system|inflammatory_disease	other	syndromic_disease|disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	ophthalmology|pediatric	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	eye_disorder|nose_disorder	false	false	false	true	medium
MONDO:0000949	conjunctival degeneration	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	low
MONDO:0000950	asthenopia	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	mental_health_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	true	medium
MONDO:0000951	thymus lymphoma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|endocrine_system_disorder	hematology|oncology	autoimmune_diseases|cancer|lymphoma	immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0000952	cancer of long bone of lower limb	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	orthopaedic|oncology	inflammatory_disease|cancer	bone_disorder|blood_bone_marrow_disorder|joint_disorder	false	true	false	true	high
MONDO:0000953	cancer of short bone of lower limb	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	orthopaedic|oncology	autoimmune_diseases|cancer	bone_disorder|subtype|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0000954	Meckel diverticulum cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	cancer|gastrointestinal_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0000955	ileum cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	inflammatory_disease|autoimmune_diseases|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0000956	small intestine cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	cancer|intestinal_cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0000957	lacrimal passage granuloma	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|otolaryngology	inflammatory_disease|autoimmune_diseases	eye_disorder|nose_disorder	false	false	false	false	medium
MONDO:0000958	neuroretinitis	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|inflammatory_disease	psychiatric_disorder	psychiatric_disorder|disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease|nervous_system_disorder	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|brain_disorder	true	false	false	false	medium
MONDO:0000959	malignant hypertensive renal disease	urinary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|urinary_system_disorder	renal_medicine|cardiology	cardiovascular_disorder|malignant_hypertensive_renal_disease	kidney_disorder|vascular_disorder	false	false	false	true	high
MONDO:0000960	diabetic peripheral angiopathy	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|cardiology|cardiothoracic|endocrinology	metabolic_disorder|cardiovascular_disorder	endocrine_disorder|vascular_disorder	false	false	true	false	high
MONDO:0000961	endobronchial lipoma	respiratory_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|respiratory_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cardiothoracic|pulmonology	cancer|tumor	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|lung_disorder	false	false	false	false	low
MONDO:0000962	spindle cell lipoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer	muscle_disorder|skin_disorder	false	true	false	false	none
MONDO:0000963	esophageal lipoma	upper_digestive_tract_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|digestive_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|digestive_system_disorder|upper_digestive_tract_disorder|musculoskeletal_system_disorder	gastroenterology|oncology	growth|cancer|tumor	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0000964	skin lipoma	integumentary_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|integumentary_system_disorder|musculoskeletal_system_disorder	dermatology|orthopaedic	cancer|skin_disorder____corrected_to___cancer|skin_disorder	muscle_disorder|skin_disorder	false	false	false	false	low
MONDO:0000965	liver lipoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder|connective_tissue_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	hepatology|gastroenterology	cancer|metabolic_disorder	liver_disorder	false	false	false	false	low
MONDO:0000966	pleomorphic lipoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	dermatology|oncology	benign_tumor|soft_tissue_sarcoma|cancer	muscle_disorder|skin_disorder	false	true	false	false	low
MONDO:0000967	conventional lipoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	dermatology	inflammatory_disease|cancer	muscle_disorder|skin_disorder	false	false	false	false	low
MONDO:0000968	kidney lipoma	urinary_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|urinary_system_disorder	rennal_medicine|urology	benign_tumor|kidney_disease|soft_tissue_sarcoma|cancer|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0000969	pleural lipoma	respiratory_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|respiratory_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cardiothoracic|pulmonology	cancer	spinal_disorder|lung_disorder	false	false	false	false	low
MONDO:0000970	breast lipoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|breast_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|breast_disorder|musculoskeletal_system_disorder	orthopaedic|oncology|obstetrics_and_gynecology	cancer	reproductive_system_disorder|skin_disorder	false	false	false	false	low
MONDO:0000971	chest wall lipoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	plastic_surgery|dermatology|orthopaedic|general_surgery	lipoma|cancer	muscle_disorder|lung_disorder|skin_disorder	false	false	false	false	low
MONDO:0000972	gallbladder lipoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|digestive_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|digestive_system_disorder|musculoskeletal_system_disorder	hepatology|gastroenterology|oncology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	low
MONDO:0000973	external ear lipoma	otorhinolaryngologic_disease|auditory_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	nervous_system_disorder|auditory_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|musculoskeletal_system_disorder	dermatology|otolaryngology	cancer	ear_disorder|skin_disorder	false	false	false	false	low
MONDO:0000974	axillary lipoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	dermatology|orthopaedic	cancer	lymphatic_disorder|skin_disorder	false	false	false	false	low
MONDO:0000975	lipoma of spermatic cord	reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder|musculoskeletal_system_disorder	oncology|urology	cancer	muscle_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0000976	paratesticular lipoma	reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder|musculoskeletal_system_disorder	dermatology|orthopaedic	cancer|adrenal_gland_disease	soft_tissue_disorder|skin_disorder	false	false	false	false	low
MONDO:0000977	chondroid lipoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	dermatology|orthopaedic	benign_tumor|cancer	joint_disorder|skin_disorder	false	true	false	false	low
MONDO:0000978	extrahepatic bile duct lipoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder|connective_tissue_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder|musculoskeletal_system_disorder	hepatology|gastroenterology|oncology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	low
MONDO:0000979	pinta disease	reproductive_system_disorder|integumentary_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|integumentary_system_disorder|infectious_disease	neurology|psychiatry	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	lower_gastrointestinal_disorder|liver_disorder	true	false	false	true	medium
MONDO:0000980	aortic atherosclerosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0000981	Histoplasma pericarditis	infectious_disease|inflammatory_disease|cardiovascular_disorder	infectious_disease|cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease|infectious_disease	pulmonology|allergy_and_immunology|cardiology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	immune_disorder|lung_disorder|heart_disorder	true	false	false	true	medium
MONDO:0000983	exhibitionism	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	psychological_disorder|skin_disorder	false	false	false	false	low
MONDO:0000984	thalassemia	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	hematology|pediatric|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|blood_disorder	false	false	false	true	high
MONDO:0000986	pleurisy	respiratory_system_disorder|inflammatory_disease	other	respiratory_system_disorder|inflammatory_disease	cardiothoracic|pulmonology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	pleural_disorder|lung_disorder	true	false	false	true	medium
MONDO:0000987	cholesterolosis of gallbladder	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|biliary_disorder|liver_disorder	false	false	false	false	medium
MONDO:0000988	discharging ear	auditory_system_disorder	other	auditory_system_disorder	pediatric|otolaryngology	allergy|autoimmune_diseases|inflammatory_disease	throat_disorder|ear_disorder	true	false	false	true	medium
MONDO:0000989	mumps infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|infectious_disease|allergy_and_immunology	infectious_disease|autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	true	false	false	true	low
MONDO:0000990	acute subendocardial myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	acute_disease|cardiovascular_disorder	cardiothoracic|cardiology	acute_subendocardial_myocardial_infarction_can_also_be_classified_as_cardiovascular_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0000992	heart conduction disease	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	heart_conduction_disease_is_more_accurately_categorized_as_a_type_of_cardiovascular_disorder_rather_than_the_disease_itself_so_that_category_will_be_chosen|autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0000993	prostate squamous cell carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0000994	malignant prostate phyllodes tumor	cancer_or_benign_tumor|reproductive_system_disorder|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|urinary_system_disorder	oncology|urology	malignant_prostate_phyllodes_tumor_does_not_belong_in_the_category__metabolic_disorder___so_i_have_removed_it__also__phyllodes_tumor_is_generally_a_benign_condition_of_the_breast_but_has_some_features_of_malignancy_when_they_occur_in_the_prostate___however__there_are_malignant_forms_which_may_be_aggressive_and_metastasize|cancer	reproductive_system_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0000995	familial periodic paralysis	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|renal_medicine|genetics_and_genomics|cardiology	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0000996	prostate lymphoma	cancer_or_benign_tumor|hematologic_disorder|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|hematologic_disorder	hematology|oncology|urology	lymphoma|cancer	immune_disorder|lymphatic_disorder|urinary_tract_disorder	false	true	false	false	medium
MONDO:0000997	monocular esotropia	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001000	mixed mineral dust pneumoconiosis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology	respiratory_disease____note__i_removed_allergy_as_it_s_more_of_a_reaction_and_mixed_mineral_dust_pneumoconiosis_is_an_occupational_lung_disease|inflammatory_disease	lung_disorder	false	false	false	false	high
MONDO:0001001	baritosis	respiratory_system_disorder	other	respiratory_system_disorder	otosclerosis_is_often_confused_with_baritosis|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	low
MONDO:0001003	pneumoconiosis due to talc	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology	occupational_disease|respiratory_disease|inflammatory_disease	respiratory_tract_disorder|lung_disorder	false	false	false	false	high
MONDO:0001004	slate pneumoconiosis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|respiratory__note__i_assumed_the_correct_category_was_pulmonology	cancer|respiratory_disease____wait_the_provided_list_had_respiratory_disease_in_it__however_i_will_correct_that_for_you____inlfammatory_disease|inflammatory_disease	lung_disorder	false	false	false	false	high
MONDO:0001005	kaolin pneumoconiosis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|occupational_disease|respiratory_disease	occupational_disease|respiratory_disease|inflammatory_disease	lung_disorder|lower_respiratory_disorder	false	false	false	false	medium
MONDO:0001006	glaucomatous atrophy of optic disk	nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|adrenal_gland_disease|inflammatory_disease	eye_disorder|optic_disorder	false	false	false	true	medium
MONDO:0001007	chronic meningitis	inflammatory_disease|nervous_system_disorder	other	inflammatory_disease|nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	spinal_disorder|brain_disorder	true	false	false	true	high
MONDO:0001008	blepharophimosis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|ophthalmology	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|eye_disorder	false	false	false	false	low
MONDO:0001009	solitary cyst of breast	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	urology|obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder	false	false	false	true	low
MONDO:0001011	breast cyst	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	inflammatory_disease|cancer	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0001014	chronic leukemia	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|cancer|metabolic_disorder	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0001015	eosinophilic meningitis	inflammatory_disease|nervous_system_disorder	other	inflammatory_disease|nervous_system_disorder	pediatrics|hematology|allergy_and_immunology|neurology	autoimmune_diseases|inflammatory_disease	immune_disorder|brain_disorder	true	false	false	true	medium
MONDO:0001016	epididymis cancer	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	autoimmune_diseases|cancer|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0001017	epididymal adenocarcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	cancer|adrenal_gland_disease	urological_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0001019	suppression amblyopia	nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|allergy|inflammatory_disease	eye_disorder|brain_disorder	false	false	false	true	medium
MONDO:0001020	amblyopia	nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system	ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	true	medium
MONDO:0001021	ametropic amblyopia	nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system	ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	true	medium
MONDO:0001022	disuse amblyopia	nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system	pediatric|ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|eye_disorder	false	false	false	true	medium
MONDO:0001023	prolymphocytic leukemia	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|acute_disease	hematology|oncology	cancer|leukemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0001024	pneumonic plague	respiratory_system_disorder|infectious_disease	infectious_disease	infectious_disease|respiratory_system_disorder	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder|blood_bone_marrow_disorder	true	false	false	true	very_high
MONDO:0001025	seminal vesicle chronic gonorrhea	inflammatory_disease|infectious_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|infectious_disease	inflammatory_disease|infectious_disease|reproductive_system_disorder|endocrine_system_disorder	urology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	false	medium
MONDO:0001027	gonococcal seminal vesiculitis	inflammatory_disease|infectious_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|infectious_disease	inflammatory_disease|infectious_disease|reproductive_system_disorder|endocrine_system_disorder	urology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	false	high
MONDO:0001028	acute pericementitis	inflammatory_disease|musculoskeletal_system_disorder	other	inflammatory_disease|musculoskeletal_system_disorder|acute_disease	pulmonology|rheumatology|cardiothoracic|cardiology	inflammatory_disease|autoimmune_diseases	heart_disorder|muscle_disorder	true	false	false	true	medium
MONDO:0001029	Klippel-Feil syndrome	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	otolaryngology|orthopaedic|pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	spinal_disorder|joint_disorder|ear_disorder	false	false	false	false	medium
MONDO:0001030	keratoconus, stable condition	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	orthopaedic|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	true	medium
MONDO:0001031	purulent acute otitis media	inflammatory_disease|otorhinolaryngologic_disease|auditory_system_disorder	other	inflammatory_disease|otorhinolaryngologic_disease|auditory_system_disorder|acute_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	true	false	false	true	medium
MONDO:0001032	Mooren ulcer	disorder_of_visual_system|inflammatory_disease	other	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease|ulcer_disease	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0001033	mycotic corneal ulcer	disorder_of_visual_system|inflammatory_disease	other	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease|ulcer_disease	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases|cancer	eye_disorder|skin_disorder	true	false	false	true	high
MONDO:0001034	marginal corneal ulcer	disorder_of_visual_system|inflammatory_disease	other	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease|ulcer_disease	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	true	false	false	true	medium
MONDO:0001035	hypopyon ulcer	infectious_disease|disorder_of_visual_system|inflammatory_disease	infectious_disease	infectious_disease|disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	ophthalmology|retina_medicine	inflammatory_disease|autoimmune_diseases	eye_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0001036	hypopyon	infectious_disease|disorder_of_visual_system|inflammatory_disease	infectious_disease	infectious_disease|disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	pediatric|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0001037	ring corneal ulcer	disorder_of_visual_system|inflammatory_disease	other	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease|ulcer_disease	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	true	false	false	true	high
MONDO:0001038	perforated corneal ulcer	disorder_of_visual_system|inflammatory_disease	other	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease|ulcer_disease	ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0001039	tonsillitis	otorhinolaryngologic_disease|immune_system_disorder|respiratory_system_disorder|inflammatory_disease	other	otorhinolaryngologic_disease|respiratory_system_disorder|immune_system_disorder|inflammatory_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	throat_disorder|lymphatic_disorder	true	false	false	true	low
MONDO:0001040	nasopharyngitis	otorhinolaryngologic_disease|respiratory_system_disorder|inflammatory_disease	other	otorhinolaryngologic_disease|respiratory_system_disorder|inflammatory_disease	pediatric|otolaryngology	inflammatory_disease|allergic_reactions	nose_disorder|throat_disorder	true	false	false	false	low
MONDO:0001041	dentin caries	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	oral_surgery|pediatric|other__removed_because_it_is_a_catch_all	inflammatory_disease|dental_gland_disease_is_not_present_so__metabolic_disorder|metabolic_disorder	teeth_disorder	true	false	false	true	medium
MONDO:0001042	patellar tendinitis	connective_tissue_disorder|musculoskeletal_system_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|connective_tissue_disorder|inflammatory_disease	orthopaedic|rheumatology	inflammatory_disease|musculoskeletal_disorder	muscle_disorder|joint_disorder	false	false	false	true	medium
MONDO:0001044	esophageal atresia	digestive_system_disorder|upper_digestive_tract_disorder	other	digestive_system_disorder|upper_digestive_tract_disorder	pediatric|gastroenterology	congenital_abnormality|developmental_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0001045	intestinal atresia	digestive_system_disorder	other	digestive_system_disorder	pediatric|gastroenterology	inflammatory_disease|congenital_abnormality	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0001046	imperforate anus	digestive_system_disorder|disorder_of_development_or_morphogenesis	other	digestive_system_disorder|disorder_of_development_or_morphogenesis	pediatric|surgery|gastroenterology	inflammatory_disease|cancer|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0001048	orbital granuloma	other	other	disorder_of_orbital_region	pediatrics|ophthalmology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	eye_disorder|orbital_granuloma_can_also_be_related_to_lymphatic_disorder_or_immune_disorder_but_best_fit_is_eye_disorder	false	false	false	false	medium
MONDO:0001049	Dressler syndrome	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	rheumatology|cardiology	inflammatory_disease|autoimmune_diseases	immune_disorder|heart_disorder	false	false	false	true	medium
MONDO:0001050	malignant otitis externa	otorhinolaryngologic_disease|infectious_disease|auditory_system_disorder|inflammatory_disease	infectious_disease	infectious_disease|post_infectious_disorder|auditory_system_disorder|otorhinolaryngologic_disease|inflammatory_disease	otolaryngology|oncology	inflammatory_disease|malignant_otitis_externa_is_a_type_of_ear_infection_that_falls_under_the_broader_category_of__infectious_disease__which_is_not_listed_here_but_does_have_overlap_with_some_categories__however__among_those_provided__these_three_are_most_relevant|autoimmune_diseases|cancer	throat_disorder|ear_disorder	true	false	false	true	high
MONDO:0001051	acute otitis externa	otorhinolaryngologic_disease|infectious_disease|auditory_system_disorder|inflammatory_disease	infectious_disease	acute_disease|infectious_disease|post_infectious_disorder|auditory_system_disorder|otorhinolaryngologic_disease|inflammatory_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases|allergy	throat_disorder|ear_disorder	true	false	false	true	medium
MONDO:0001052	chronic fungal otitis externa	otorhinolaryngologic_disease|infectious_disease|auditory_system_disorder|integumentary_system_disorder|inflammatory_disease	infectious_disease	integumentary_system_disorder|infectious_disease|post_infectious_disorder|auditory_system_disorder|otorhinolaryngologic_disease|inflammatory_disease	dermatology|otolaryngology	inflammatory_disease|autoimmune_diseases	skin_disorder|ear_disorder	true	false	false	true	medium
MONDO:0001053	acute infection of pinna	otorhinolaryngologic_disease|infectious_disease|auditory_system_disorder|inflammatory_disease	infectious_disease	acute_disease|infectious_disease|post_infectious_disorder|auditory_system_disorder|otorhinolaryngologic_disease|inflammatory_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases|allergy	nose_disorder|ear_disorder	true	false	false	true	low
MONDO:0001054	double pterygium	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_orbital_region|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	muscle_disorder|eye_disorder	false	false	false	true	high
MONDO:0001055	conjunctival pterygium	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_orbital_region|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system	ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	true	low
MONDO:0001056	gastric cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	gastrointestinal_disease_is_not_on_the_list_so__cancer|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0001057	malignant gastric granular cell tumor	digestive_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0001059	gastric lymphoma	digestive_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|digestive_system_disorder|cancer_or_benign_tumor	hematology|gastroenterology|oncology	inflammatory_disease|autoimmune_diseases|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|lymphatic_disorder	true	true	false	true	high
MONDO:0001060	microinvasive gastric cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	inflammatory_disease|metabolic_disorder|cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0001061	pylorus cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0001062	pyloric antrum cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer_type|cancer|gastrointestinal_cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0001063	cardia cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|cardiothoracic	cardiovascular_disorder|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0001064	acute eustachian salpingitis	otorhinolaryngologic_disease|auditory_system_disorder|inflammatory_disease	other	acute_disease|auditory_system_disorder|otorhinolaryngologic_disease|inflammatory_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	true	false	false	true	medium
MONDO:0001065	supine hypotensive syndrome	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pediatric|pulmonology|cardiology|renal_medicine	cardiovascular_disorder|adrenal_gland_disease	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0001066	late yaws	infectious_disease|integumentary_system_disorder|reproductive_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder|reproductive_system_disorder	pediatric|dermatology|infectious_diseases_is_not_available_in_the_list_so_use__dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0001067	early yaws	infectious_disease|reproductive_system_disorder	infectious_disease	infectious_disease|reproductive_system_disorder	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|ear_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0001068	osteomalacia	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	anemia|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0001071	intellectual disability	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	pediatric|psychiatry|neurology	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0001072	mild pre-eclampsia	obstetric_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|obstetric_disorder|cardiovascular_disorder	obstetrics_and_gynecology|renal_medicine	metabolic_disorder|pregnancy_related_condition	kidney_disorder|vascular_disorder	false	false	false	true	low
MONDO:0001073	idiopathic progressive polyneuropathy	nervous_system_disorder	other	idiopathic_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|nervous_system_disorder	false	false	false	false	high
MONDO:0001074	chronic tic disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0001075	steatorrhea	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001076	glucose intolerance	digestive_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease|digestive_system_disorder	endocrinology	autoimmune_diseases|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0001078	tropical sprue	digestive_system_disorder	other	digestive_system_disorder	pediatric|gastroenterology	autoimmune_diseases|anemia|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001079	pancreatic steatorrhea	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	endocrinology|gastroenterology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0001080	acute gonococcal cervicitis	reproductive_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	acute_disease|infectious_disease|inflammatory_disease|reproductive_system_disorder	pediatric|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0001081	acute cervicitis	reproductive_system_disorder	other	acute_disease|reproductive_system_disorder	pediatric|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|throat_disorder	true	false	false	true	medium
MONDO:0001082	lymph node cancer	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	oncology|hematatology	lymphoma|cancer	immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0001083	Fanconi renotubular syndrome	syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|renal_medicine	metabolic_disorder|anemia	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0001084	primary optic atrophy	nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_visual_system	ophthalmology|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	eye_disorder|spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001085	interstitial nephritis	inflammatory_disease|urinary_system_disorder	other	urinary_system_disorder|inflammatory_disease	nephrology|renal_medicine	autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder	true	false	false	true	medium
MONDO:0001086	partial optic atrophy	nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001087	schizotypal personality disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	psychiatric_condition|mental_health_disorder|mental_condition	brain_disorder	false	false	false	false	medium
MONDO:0001088	acute inferoposterior infarction	cardiovascular_disorder	cardiovascular_disorder	acute_disease|cardiovascular_disorder	cardiology|hematology|renal_medicine	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0001089	acute inferolateral myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	acute_disease|cardiovascular_disorder	cardiology|cardiothoracic	acute_inferolateral_myocardial_infarction_could_also_fit_into__inflammatory_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0001090	acute anterolateral myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	acute_disease|cardiovascular_disorder	cardiology|cardiothoracic	cardiovascular_disorder|metabolic_disorder|acute_anterolateral_myocardial_infarction_can_be_categorized_as___cardiovascular_disorder|inflammatory_disease	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0001091	lipoma of colon	cancer_or_benign_tumor|musculoskeletal_system_disorder|digestive_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|digestive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0001092	colon leiomyoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|gastroenterology	benign_tumor|cancer	muscle_disorder|lower_gastrointestinal_disorder|vascular_disorder	false	false	false	false	low
MONDO:0001093	colonic lymphangioma	cancer_or_benign_tumor|digestive_system_disorder|immune_system_disorder|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	digestive_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor|immune_system_disorder	oncology|pediatric|gastroenterology	autoimmune_diseases|inflammatory_disease|cancer	lower_gastrointestinal_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0001094	residual stage of open angle glaucoma	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology	metabolic_disorder|inflammatory_disease	eye_disorder|spinal_disorder|vascular_disorder	false	false	false	false	high
MONDO:0001095	mediastinum neuroblastoma	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis	oncology|pediatric	cancer|neuroblastoma	spinal_disorder|bone_disorder|lung_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0001096	mediastinum ganglioneuroblastoma	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis	oncology|pediatric|cardiothoracic	cancer|neuroblastoma	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0001098	separation anxiety disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	pediatric|psychiatry	mental_health_disorder|separation_anxiety_disorder	psychological_disorder|brain_disorder	false	false	false	true	medium
MONDO:0001099	lactocele	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	pediatric|general|obstetrics_and_gynecology	metabolic_disorder|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0001100	hypertrophy of breast	breast_disorder	other	breast_disorder	obstetrics_and_gynecology|endocrinology	cancer|metabolic_disorder	reproductive_system_disorder|endocrine_disorder|muscle_disorder	false	false	false	false	low
MONDO:0001101	fat necrosis of breast	breast_disorder	other	breast_disorder	dermatology|obstetrics_and_gynecology	inflammatory_disease|cancer	skin_disorder|muscle_disorder	false	false	false	false	low
MONDO:0001103	giardiasis	infectious_disease|digestive_system_disorder	infectious_disease	infectious_disease|digestive_system_disorder	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0001104	toxic diffuse goiter	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	pulmonology|thyroid_disorders|cardiothoracic|endocrinology	autoimmune_diseases|inflammatory_disease	thyroid_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0001105	renal hypertension	cardiovascular_disorder|urinary_system_disorder	cardiovascular_disorder	urinary_system_disorder|cardiovascular_disorder	renal_medicine|cardiology|urology	metabolic_disorder|cardiovascular_disorder|renal_hypertension_involves_the_heart_and_metabolism	urinary_tract_disorder|vascular_disorder|kidney_disorder	false	false	false	true	high
MONDO:0001106	kidney failure	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0001108	broad ligament malignant neoplasm	reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	rheumatology|oncology|orthopaedic	malignant_neoplasm|cancer	bone_disorder|joint_disorder	false	true	false	false	high
MONDO:0001109	petrositis	hematologic_disorder|inflammatory_disease|immune_system_disorder|musculoskeletal_system_disorder	other	inflammatory_disease|immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	rheumatology|hematology	autoimmune_diseases|adrenal_gland_disease|inflammatory_disease	petrositis_is_associated_with_the_mastoid_bone_of_the_skull__petrous_part_of_the_temporal_bone___but_this_is_a_bit_misleading_as_it_s_more_related_to_inflammation_of_the_mastoid_air_cells_and_surrounding_tissue|blood_bone_marrow_disorder	true	false	false	false	high
MONDO:0001110	chronic pyelonephritis	inflammatory_disease|urinary_system_disorder|reproductive_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|urinary_system_disorder|reproductive_system_disorder|infectious_disease	renal_medicine|urology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|kidney_disorder	true	false	false	true	high
MONDO:0001112	bubonic plague	immune_system_disorder|infectious_disease	infectious_disease	immune_system_disorder|infectious_disease	infectious_diseases|pediatric|hematology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0001113	Fiedler's myocarditis	inflammatory_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	inflammatory_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiothoracic|pulmonology|cardiology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0001114	bacterial myocarditis	inflammatory_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	inflammatory_disease|musculoskeletal_system_disorder|cardiovascular_disorder	pulmonology|cardiology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	true	false	false	true	high
MONDO:0001115	familial polycythemia	hematologic_disorder|immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder|hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0001116	mesenteric lymphadenitis	inflammatory_disease|immune_system_disorder	other	inflammatory_disease|immune_system_disorder	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|lymphatic_disorder|immune_disorder	true	false	false	true	medium
MONDO:0001117	methemoglobinemia	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|pulmonology|hematology	anemia|metabolic_disorder	lung_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0001118	Queensland tick typhus	infectious_disease	infectious_disease	infectious_disease	dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0001119	premature menopause	endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|endocrinology	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0001120	chronic frontal sinusitis	respiratory_system_disorder|otorhinolaryngologic_disease|musculoskeletal_system_disorder|inflammatory_disease	other	inflammatory_disease|otorhinolaryngologic_disease|musculoskeletal_system_disorder|respiratory_system_disorder	otolaryngology	autoimmune_diseases|inflammatory_disease	nose_disorder|lung_disorder	false	false	false	true	medium
MONDO:0001121	frontal sinusitis	respiratory_system_disorder|otorhinolaryngologic_disease|musculoskeletal_system_disorder|inflammatory_disease	other	inflammatory_disease|otorhinolaryngologic_disease|musculoskeletal_system_disorder|respiratory_system_disorder	otolaryngology	autoimmune_diseases|inflammatory_disease	nose_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0001122	chronic maxillary sinusitis	respiratory_system_disorder|otorhinolaryngologic_disease|musculoskeletal_system_disorder|inflammatory_disease	other	inflammatory_disease|otorhinolaryngologic_disease|musculoskeletal_system_disorder|mouth_disorder|respiratory_system_disorder	otolaryngology	allergy|autoimmune_diseases|inflammatory_disease	nose_disorder|upper_gastrointestinal_disorder|throat_disorder	true	false	false	true	medium
MONDO:0001123	chronic sphenoidal sinusitis	respiratory_system_disorder|otorhinolaryngologic_disease|musculoskeletal_system_disorder|inflammatory_disease	other	inflammatory_disease|otorhinolaryngologic_disease|musculoskeletal_system_disorder|respiratory_system_disorder	neurology|otolaryngology	allergy|autoimmune_diseases|inflammatory_disease	nose_disorder|throat_disorder|ear_disorder	true	false	false	true	medium
MONDO:0001125	acute gonococcal epididymo-orchitis	reproductive_system_disorder|infectious_disease|endocrine_system_disorder|inflammatory_disease	infectious_disease|endocrine_system_disorder	infectious_disease|inflammatory_disease|reproductive_system_disorder|endocrine_system_disorder|acute_disease	obstetrics_and_gynecology|urology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0001126	gastric ulcer	digestive_system_disorder	other	ulcer_disease|digestive_system_disorder	hepatology|cardiology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0001127	tibialis tendinitis	musculoskeletal_system_disorder|inflammatory_disease|connective_tissue_disorder	other	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder	orthopaedic|rheumatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	musclemuscle_disorder|joint_disorder	false	false	false	true	medium
MONDO:0001128	nasal cavity cancer	cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology	adrenal_gland_disease|cancer	nose_disorder|throat_disorder	false	true	false	true	high
MONDO:0001129	nasal cavity olfactory neuroblastoma	cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	nervous_system_disorder|otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|respiratory_system_disorder	oncology|pediatric|neurology|otolaryngology	cancer|neuroblastoma	nose_disorder|brain_disorder|ear_disorder	true	true	false	true	high
MONDO:0001130	nasal cavity lymphoma	hematologic_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|otorhinolaryngologic_disease|hematologic_disorder|cancer_or_benign_tumor|respiratory_system_disorder	oncology|hematology|otolaryngology	lymphoma|cancer	nose_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0001132	sexual sadism disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder	reproductive_system_disorder	false	false	false	false	medium
MONDO:0001133	malignant essential hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|oncology|renal_medicine	metabolic_disorder|cardiovascular_disorder|cancer	kidney_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0001134	essential hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|renal_medicine	metabolic_disorder|cardiovascular_disorder	kidney_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0001135	voyeurism	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	mental_health_disorder	brain_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0001136	chylocele of tunica vaginalis	reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	genitourinary|urology	autoimmune_diseases|inflammatory_disease|cancer	reproductive_system_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0001137	Murray valley encephalitis	infectious_disease	infectious_disease	infectious_disease	pediatric|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	true	false	false	false	medium
MONDO:0001138	angiodysplasia of intestine	digestive_system_disorder|cardiovascular_disorder	cardiovascular_disorder	digestive_system_disorder|cardiovascular_disorder	hepatology|gastroenterology	gastrointestinal_disease|cardiovascular_disorder|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0001139	sexual masochism disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|psychology	neurodegenerative_disease|autoimmune_diseases|mental_health_disorder	reproductive_system_disorder	false	false	false	false	medium
MONDO:0001141	middle ear cholesterol granuloma	otorhinolaryngologic_disease|auditory_system_disorder|inflammatory_disease	other	inflammatory_disease|otorhinolaryngologic_disease|auditory_system_disorder	otolaryngology	autoimmune_diseases|inflammatory_disease	throat_disorder|ear_disorder	false	false	false	false	medium
MONDO:0001142	salivary gland disorder	other	other	mouth_disorder	oral_medicine|otolaryngology	autoimmune_diseases|inflammatory_disease	teeth_disorder|throat_disorder|oral_disorder	false	false	false	true	medium
MONDO:0001143	paralytic strabismus	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001144	partial third-nerve palsy	disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001145	total third-nerve palsy	disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|brain_disorder	true	false	false	true	medium
MONDO:0001146	fourth cranial nerve palsy	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	neurodegenerative_disease|autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0001147	meningocele	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0001148	iliac vein thrombophlebitis	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	vascular_surgery|general_surgery|hematology	cardiovascular_disorder|inflammatory_disease	vascular_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0001149	microcephaly	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0001150	hydrocephalus	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|inflammatory_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0001151	benign essential hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|renal_medicine	metabolic_disorder|cardiovascular_disorder	vascular_disorder|kidney_disorder	false	false	false	true	low
MONDO:0001152	amnestic disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	memory_disorder|brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001154	Siberian tick typhus	infectious_disease	infectious_disease	infectious_disease	dermatology|hematology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0001155	gastrojejunal ulcer	digestive_system_disorder	other	digestive_system_disorder|ulcer_disease	cardiology|oncology|hepatology|hematology|pulmonology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0001156	borderline personality disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|psychological_disorder__not_listed____mental_health_disorder__not_listed__but_actually__brain_disorder_is_most_likely__although_it_is_a_bit_of_a_stretch	false	false	false	true	high
MONDO:0001157	dependent personality disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder	psychological_disorder_is_not_in_the_list_so__brain_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001158	obsessive-compulsive personality disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|mental_health_disorder	false	false	false	false	medium
MONDO:0001159	multiple personality disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder	brain_disorder|mental_disorder	false	false	false	false	high
MONDO:0001160	dissociative disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	medium
MONDO:0001161	schizoid personality disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|mental_health_disorder	false	false	false	false	low
MONDO:0001162	impulse control disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	medium
MONDO:0001163	paranoid personality disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	medium
MONDO:0001164	antisocial personality disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0001165	tongue disorder	other	other	mouth_disorder	neurology|otolaryngology	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	throat_disorder	false	false	false	true	medium
MONDO:0001166	nephritis	inflammatory_disease|urinary_system_disorder	other	inflammatory_disease|urinary_system_disorder	urology|renal_medicine	autoimmune_diseases|inflammatory_disease	kidney_disorder|urinary_tract_disorder|immune_disorder	true	false	false	true	high
MONDO:0001167	spastic diplegia	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	spinal_cord_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0001168	spastic hemiplegia	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0001169	spastic monoplegia	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001170	hemiplegia	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0001171	acute salpingo-oophoritis	reproductive_system_disorder|endocrine_system_disorder|inflammatory_disease	endocrine_system_disorder	inflammatory_disease|reproductive_system_disorder|endocrine_system_disorder|acute_disease	urology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0001172	salpingo-oophoritis	reproductive_system_disorder|endocrine_system_disorder|inflammatory_disease	endocrine_system_disorder	inflammatory_disease|reproductive_system_disorder|endocrine_system_disorder	urology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0001173	acute salpingitis	reproductive_system_disorder|inflammatory_disease	other	inflammatory_disease|reproductive_system_disorder|acute_disease	pediatric|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0001174	conjunctival vascular disorder	cardiovascular_disorder|disorder_of_visual_system	cardiovascular_disorder	cardiovascular_disorder|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	vascular_disorder|eye_disorder	false	false	false	false	low
MONDO:0001175	immature cataract	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	true	medium
MONDO:0001176	lens disorder	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	orthopaedic|ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0001177	anorectal stricture	digestive_system_disorder	other	digestive_system_disorder	urology|gastroenterology	inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0001178	pseudopterygium	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology|neurology	autoimmune_diseases|adrenal_gland_disease|neurodegenerative_disease	lung_disorder|liver_disorder	false	false	false	false	medium
MONDO:0001179	pinguecula	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	true	low
MONDO:0001180	bullous keratopathy	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	medium
MONDO:0001181	secondary corneal edema	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	vascular_disorder|eye_disorder|kidney_disorder	false	false	false	true	high
MONDO:0001182	idiopathic corneal edema	disorder_of_visual_system	other	idiopathic_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder|immune_disorder	false	false	false	false	high
MONDO:0001183	contact lens corneal edema	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|oculoplastic____i_corrected_the_category_name	autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder|corneal_disorder	false	false	false	true	medium
MONDO:0001184	chronic rapidly progressive glomerulonephritis	inflammatory_disease|urinary_system_disorder	other	inflammatory_disease|urinary_system_disorder	renal_medicine|nephrology	autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0001185	dissociative amnesia	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001186	depersonalization disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	neurological_disorder|mental_health_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001187	urinary bladder cancer	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0001188	esophagus lymphoma	upper_digestive_tract_disorder|digestive_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|upper_digestive_tract_disorder|cancer_or_benign_tumor|hematologic_disorder	oncology|hematology|gastroenterology	autoimmune_diseases|cancer	lymphatic_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0001190	Brucella suis brucellosis	infectious_disease	infectious_disease	infectious_disease	pediatric|immunology|hematology	autoimmune_diseases|inflammatory_disease	joint_disorder|immune_disorder|liver_disorder	true	false	false	true	medium
MONDO:0001191	hirudiniasis	infectious_disease	infectious_disease	infectious_disease	dermatology|hematology	autoimmune_diseases|adrenal_gland_disease|inflammatory_disease	blood_bone_marrow_disorder|liver_disorder	true	false	false	true	low
MONDO:0001192	esophageal melanoma	upper_digestive_tract_disorder|cancer_or_benign_tumor|digestive_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	digestive_system_disorder|upper_digestive_tract_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	gastroenterology|cardiology|oncology	cancer|allergy|autoimmune_diseases|adrenal_gland_disease|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0001195	spotted fever	infectious_disease	infectious_disease	infectious_disease	pediatrics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0001196	psychologic dyspareunia	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|obstetrics_and_gynecology|neurology	mental_health_disorder	reproductive_system_disorder	false	false	false	false	high
MONDO:0001197	qualitative platelet defect	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|anemia|inflammatory_disease	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0001198	acquired thrombocytopenia	hematologic_disorder	other	hematologic_disorder	hematology	metabolic_disorder|autoimmune_diseases|anemia|inflammatory_disease	blood_bone_marrow_disorder|vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0001199	dislocation of ear ossicle	auditory_system_disorder	other	auditory_system_disorder	otolaryngology|orthopaedic	autoimmune_diseases|inflammatory_disease	joint_disorder|ear_disorder	false	false	false	false	medium
MONDO:0001200	secondary hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|kidney_disorder	false	false	false	true	high
MONDO:0001202	prostatic cyst	reproductive_system_disorder	other	reproductive_system_disorder	urology	inflammatory_disease|cancer	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0001203	prolapse of lacrimal gland	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	otolaryngology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|nose_disorder	false	false	false	false	low
MONDO:0001204	esophagus sarcoma	digestive_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|upper_digestive_tract_disorder|digestive_system_disorder	oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0001205	hypersecretion glaucoma	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology|urology	inflammatory_disease|metabolic_disorder|adrenal_gland_disease	endocrine_disorder|eye_disorder	false	false	false	false	high
MONDO:0001206	aqueous misdirection	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0001207	neonatal respiratory failure	respiratory_system_disorder	other	acute_disease|respiratory_system_disorder	pediatric|pulmonology	inflammatory_disease|cardiovascular_disorder	lung_disorder|respiratory_failure	false	false	false	true	high
MONDO:0001208	acute respiratory failure	respiratory_system_disorder	other	acute_disease|respiratory_system_disorder	pulmonology|cardiology|cardiothoracic	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	lower_gastrointestinal_disorder|lung_disorder	false	false	false	true	very_high
MONDO:0001209	common wart	integumentary_system_disorder|infectious_disease|cancer_or_benign_tumor	cancer_or_benign_tumor|infectious_disease	cancer_or_benign_tumor|integumentary_system_disorder|infectious_disease	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0001210	enophthalmos	other	other	disorder_of_orbital_region	ophthalmology|neurology	adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0001211	total internal ophthalmoplegia	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0001212	non-suppurative otitis media	inflammatory_disease|auditory_system_disorder|otorhinolaryngologic_disease	other	auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	false	false	false	true	low
MONDO:0001213	serous glue ear	inflammatory_disease|auditory_system_disorder|otorhinolaryngologic_disease	other	auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	ear_disorder	false	false	false	true	medium
MONDO:0001214	acute conjunctivitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|inflammatory_disease|acute_disease|disorder_of_orbital_region	pediatric|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	true	false	false	true	low
MONDO:0001215	allescheriosis	infectious_disease	infectious_disease	infectious_disease	allergy_and_immunology|pediatric|pulmonology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	liver_disorder|lung_disorder|upper_gastrointestinal_disorder|immune_disorder	true	false	false	false	medium
MONDO:0001216	pulp degeneration	musculoskeletal_system_disorder	other	mouth_disorder|musculoskeletal_system_disorder	orthopaedic|neurology	inflammatory_disease|neurodegenerative_disease	pulp_degeneration_often_falls_under_a_more_general_category__teeth_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0001217	pseudomembranous conjunctivitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	disorder_of_visual_system|inflammatory_disease|acute_disease|infectious_disease|disorder_of_orbital_region	pediatric|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder	true	false	false	true	medium
MONDO:0001218	acute laryngopharyngitis	respiratory_system_disorder	other	acute_disease|respiratory_system_disorder	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	throat_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0001219	serous conjunctivitis except viral	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|inflammatory_disease|acute_disease|disorder_of_orbital_region	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	true	low
MONDO:0001220	hypoparathyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	pediatric|neonatology|endocrinology	autoimmune_diseases|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0001221	esophageal varices	digestive_system_disorder|cardiovascular_disorder|upper_digestive_tract_disorder	cardiovascular_disorder	upper_digestive_tract_disorder|digestive_system_disorder|cardiovascular_disorder	hematology|hepatology|gastroenterology	inflammatory_disease|cardiovascular_disorder|cancer	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0001222	congenital T-cell immunodeficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|immunology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0001223	parathyroid gland disorder	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	renal_medicine|cardiology|endocrinology	autoimmune_diseases|endocrine_disease__no_direct_match__using_closest_option__is_incorrect__actual_answer_is___metabolic_disorder|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0001224	Angelucci syndrome	inflammatory_disease|disorder_of_visual_system|immune_system_disorder	other	disorder_of_visual_system|inflammatory_disease|acute_disease|immune_system_disorder|disorder_of_orbital_region	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	liver_disorder	false	false	false	false	high
MONDO:0001225	opioid abuse	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	substance_abuse|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0001226	acute contagious conjunctivitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|inflammatory_disease|acute_disease|disorder_of_orbital_region	pediatric|otolaryngology|ophthalmology	inflammatory_disease|autoimmune_diseases|allergy	eye_disorder|contagious_disorder	true	false	false	true	low
MONDO:0001227	chronic tympanitis	inflammatory_disease|auditory_system_disorder|otorhinolaryngologic_disease	other	auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	throat_disorder|ear_disorder	true	false	false	false	medium
MONDO:0001228	conjunctival folliculosis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|inflammatory_disease|acute_disease|disorder_of_orbital_region	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	true	false	false	false	low
MONDO:0001229	small intestine diverticulitis	inflammatory_disease|digestive_system_disorder	other	inflammatory_disease|digestive_system_disorder	pediatric|hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0001230	acute orbital inflammation	other	other	acute_disease|disorder_of_orbital_region	otolaryngology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	true	false	false	true	medium
MONDO:0001231	orbital periostitis	inflammatory_disease|connective_tissue_disorder|musculoskeletal_system_disorder	other	inflammatory_disease|musculoskeletal_system_disorder|acute_disease|connective_tissue_disorder|disorder_of_orbital_region	rheumatology|ophthalmology	inflammatory_disease|autoimmune_diseases	orbital_periostitis_is_closely_related_to_the_eye|eye_disorder	true	false	false	false	low
MONDO:0001232	orbital osteomyelitis	other	other	acute_disease|disorder_of_orbital_region	pediatric|otolaryngology|orthopaedic|ophthalmology	inflammatory_disease|autoimmune_diseases	bone_disorder|eye_disorder	true	false	false	true	high
MONDO:0001233	orbital tenonitis	other	other	acute_disease|disorder_of_orbital_region	rheumatology|ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	muscle_disorder|spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0001234	adhesive otitis media	auditory_system_disorder	other	auditory_system_disorder	pediatric|otolaryngology|otitis_media_is_often_seen_in_children__but_this_category_still_applies_to_adults_as_well	inflammatory_disease|autoimmune_diseases	throat_disorder|ear_disorder	false	false	false	true	medium
MONDO:0001235	appendix cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	appendicitis_cancer|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0001236	appendiceal neoplasm	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0001237	appendix lymphoma	digestive_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|digestive_system_disorder	hematology|oncology	inflammatory_disease|autoimmune_diseases|cancer	lower_gastrointestinal_disorder|lymphatic_disorder	true	true	false	true	medium
MONDO:0001238	polycythemia neonatorum	hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder	other	hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder	hematology|pediatric	anemia|metabolic_disorder	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	low
MONDO:0001239	anemia of prematurity	hematologic_disorder	anemia	hematologic_disorder	hematology|pediatric	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0001240	neonatal anemia	hematologic_disorder	anemia	hematologic_disorder	pediatric|hematology	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder|kidney_disorder	false	false	false	true	high
MONDO:0001241	transient neonatal neutropenia	hematologic_disorder|immune_system_disorder	other	hematologic_disorder|immune_system_disorder	pediatric|hematology	inflammatory_disease|autoimmune_diseases|anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	low
MONDO:0001242	disseminated intravascular coagulation in newborn	hematologic_disorder	other	hematologic_disorder	pediatric|hematology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder	true	false	false	true	high
MONDO:0001243	disseminated intravascular coagulation	hematologic_disorder	other	hematologic_disorder	hematology|cardiology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0001244	vitamin K deficiency hemorrhagic disease	nutritional_disorder	other	nutritional_disorder	hematology|hepatology|pediatrics	anemia|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0001245	microcytic anemia	hematologic_disorder	anemia	hematologic_disorder	hematology|gastroenterology	microcytic_anemia|anemia	liver_disorder|upper_gastrointestinal_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0001246	typhus	infectious_disease	infectious_disease	infectious_disease	hematology|infectious_disease_is_not_in_the_list_but_dermatology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	true	high
MONDO:0001247	social phobia	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	autoimmune_diseases|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0001249	trachoma	infectious_disease|reproductive_system_disorder	infectious_disease	reproductive_system_disorder|infectious_disease	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder	true	false	false	true	high
MONDO:0001250	keratomalacia	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	nutrition_wasn_t_provided_so_i_omitted_it|pediatric|endocrinology|ophthalmology	metabolic_disorder|vitamin_deficiency	eye_disorder|vitamin_deficiency	true	false	false	true	high
MONDO:0001251	chronic apical periodontitis	musculoskeletal_system_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|inflammatory_disease	orthopaedic|periodontitis	inflammatory_disease|autoimmune_diseases	bone_disorder|teeth_disorder	true	false	false	true	medium
MONDO:0001252	Plummer disease	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	pediatric|pulmonology	adrenal_gland_disease|autoimmune_diseases	liver_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001255	ventilation pneumonitis	immune_system_disorder|respiratory_system_disorder|inflammatory_disease	other	respiratory_system_disorder|immune_system_disorder|inflammatory_disease	cardiology|pulmonology|cardiothoracic	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001256	arteriovenous hemangioma/malformation	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	hematology|cardiology|vascular_surgery_is_not_listed_so_dermatology	cardiovascular_disorder|cancer	vascular_disorder|skin_disorder	false	false	false	false	medium
MONDO:0001257	retinal microaneurysm	disorder_of_visual_system|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder	neurology|ophthalmology	metabolic_disorder|eye_disease	eye_disorder	false	false	false	true	medium
MONDO:0001258	vertebral artery occlusion	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	cardiology|vascular_cardiothoracic|neurology	cardiovascular_disorder|neurological_disorder	spinal_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0001259	pituitary gland infarction	endocrine_system_disorder|nervous_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	endocrinology|neurology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0001260	cercarial dermatitis	infectious_disease|integumentary_system_disorder|inflammatory_disease	infectious_disease	integumentary_system_disorder|infectious_disease|inflammatory_disease	dermatology|allergy_and_immunology	inflammatory_disease|allergy|autoimmune_diseases	immune_disorder|skin_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0001261	Mobitz type II atrioventricular block	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	renal_medicine|cardiology|pulmonology|cardiothoracic	cardiovascular_disorder|autoimmune_diseases|neurodegenerative_disease	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0001262	African histoplasmosis	infectious_disease	infectious_disease	infectious_disease	hematology|pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder|skin_disorder	true	false	false	true	high
MONDO:0001263	histoplasmosis retinitis	inflammatory_disease|disorder_of_visual_system|infectious_disease|nervous_system_disorder	infectious_disease	infectious_disease|disorder_of_orbital_region|inflammatory_disease|disorder_of_visual_system|nervous_system_disorder	pediatric|pulmonology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0001265	schizophreniform disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	medium
MONDO:0001266	erysipelas	inflammatory_disease|infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|inflammatory_disease|integumentary_system_disorder	pediatric|general_surgery|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder	true	false	false	true	medium
MONDO:0001268	gingival recession	musculoskeletal_system_disorder	other	mouth_disorder|musculoskeletal_system_disorder	pediatric|dental	inflammatory_disease|autoimmune_diseases	teeth_disorder|skin_disorder	false	false	false	true	medium
MONDO:0001269	scleral disorder	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|scleral_disorder	false	false	false	false	medium
MONDO:0001270	stone in bladder diverticulum	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	renal_medicine|urology	inflammatory_disease|cancer|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0001271	lens subluxation	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	eye_condition|neurodegenerative_disease|lens_surgery	spinal_disorder|eye_disorder	false	false	false	true	medium
MONDO:0001272	functional diarrhea	digestive_system_disorder	other	digestive_system_disorder	pediatric|gastroenterology	mental_health_disorder|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001273	megacolon	digestive_system_disorder	other	digestive_system_disorder	pediatric|hepatology|gastroenterology	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0001274	anal spasm	digestive_system_disorder	other	digestive_system_disorder	neurology|urology	anal_spasm_is_sometimes_associated_with_neurodegenerative_conditions_like_parkinson_s_disease|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001275	spinal meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0001276	expressive language disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|pediatrics	mental_health_disorder|neurodevelopmental_disease	throat_disorder|brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001277	cerebral arteritis	inflammatory_disease|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease|nervous_system_disorder	neurology|rheumatology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0001279	intraspinal meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurological_cancer|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0001280	choroiditis	inflammatory_disease|disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_orbital_region|inflammatory_disease|disorder_of_visual_system	ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0001281	alternating exotropia	nervous_system_disorder	other	nervous_system_disorder	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001282	fallopian tube endometriosis	reproductive_system_disorder	other	reproductive_system_disorder	gynecology|endocrinology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0001283	endosalpingiosis	reproductive_system_disorder	other	reproductive_system_disorder	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	false	false	false	false	low
MONDO:0001284	endometriosis of intestine	digestive_system_disorder|reproductive_system_disorder	other	digestive_system_disorder|reproductive_system_disorder	gastroenterology|obstetrics_and_gynecology	inflammatory_disease|cancer|autoimmune_diseases	upper_gastrointestinal_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001285	endometriosis of pelvic peritoneum	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|joint_disorder|pelvic_peritoneum_not_provided_in_categories_though_endometriosis_is_related_to_pelvic_area	false	false	false	true	high
MONDO:0001286	exotropia	nervous_system_disorder	other	nervous_system_disorder	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	true	medium
MONDO:0001287	endometriosis in cutaneous scar	reproductive_system_disorder	other	reproductive_system_disorder	dermatology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	skin_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0001288	endometriosis of rectovaginal septum and vagina	reproductive_system_disorder	other	reproductive_system_disorder	gastroenterology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0001290	allergic cutaneous vasculitis	inflammatory_disease|immune_system_disorder|cardiovascular_disorder|integumentary_system_disorder	cardiovascular_disorder	integumentary_system_disorder|immune_system_disorder|cardiovascular_disorder|inflammatory_disease	dermatology|allergy_and_immunology	inflammatory_disease|allergy|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0001291	brain compression	nervous_system_disorder	other	nervous_system_disorder	trauma|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0001292	autonomic nervous system disorder	nervous_system_disorder	other	nervous_system_disorder	cardiothoracic|neurology	autonomic_nervous_system_disorder_is_not_explicitly_listed_but_closely_related_to_neurodegenerative_disease___cardiovascular_disorder|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0001293	subglottis cancer	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer	throat_disorder|lung_disorder	false	true	false	true	very_high
MONDO:0001294	Horner syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	inflammatory_disease|neurodegenerative_disease|cancer|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001295	idiopathic peripheral autonomic neuropathy	nervous_system_disorder	other	idiopathic_disease|nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|autoimmune_diseases	nervous_system_disorder|muscle_disorder	false	false	false	false	high
MONDO:0001296	acquired night blindness	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|nutritional_disorder	psychiatric_disorder	psychiatric_disorder|nutritional_disorder|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001297	cardiac tamponade	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|cardiology|cardiothoracic|pulmonology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0001298	congenital mitral valve insufficiency	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pediatric|cardiology	cardiovascular_disorder|congenital_heart_defect	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0001299	diabetic autonomic neuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology|endocrinology	neurodegenerative_disease|metabolic_disorder	vascular_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0001300	autonomic neuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology|cardiology	autoimmune_diseases|adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0001301	rumination disorder	psychiatric_disorder|nutritional_disorder	psychiatric_disorder	nutritional_disorder|psychiatric_disorder	psychiatry|gastroenterology	mental_health_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001302	hypertensive heart disease	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiology|renal_medicine	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0001303	abnormal pupillary function	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	inflammatory_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001304	benign hypertensive renal disease	urinary_system_disorder	other	urinary_system_disorder	cardiology|renal_medicine	metabolic_disorder|cardiovascular_disorder	vascular_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0001305	laryngostenosis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|otolaryngology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	lung_disorder|throat_disorder	false	false	false	false	high
MONDO:0001307	corneal abscess	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	disorder_of_orbital_region|disorder_of_visual_system|infectious_disease|inflammatory_disease	ophthalmology|pediatrics|otolaryngology	inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder	true	false	false	true	medium
MONDO:0001308	corneal deposit	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0001309	oculomotor nerve paralysis	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|nervous_system_disorder	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001310	Bowman's membrane folds or rupture	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0001312	acute serous otitis media	otorhinolaryngologic_disease|inflammatory_disease|auditory_system_disorder	other	otorhinolaryngologic_disease|acute_disease|auditory_system_disorder|inflammatory_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	true	false	false	true	medium
MONDO:0001313	acute allergic serous otitis media	otorhinolaryngologic_disease|inflammatory_disease|immune_system_disorder|auditory_system_disorder	other	otorhinolaryngologic_disease|immune_system_disorder|acute_disease|auditory_system_disorder|inflammatory_disease	otolaryngology|pediatric	allergy|inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	false	false	false	false	medium
MONDO:0001314	chondrocalcinosis	inflammatory_disease|musculoskeletal_system_disorder|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|metabolic_disease|inflammatory_disease	rheumatology|orthopaedic	inflammatory_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0001315	neurocirculatory asthenia	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|cardiology|psychiatry	cardiovascular_disorder|mental_health_disorder|neurodegenerative_disease	vascular_disorder|heart_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001316	streptococcal meningitis	nervous_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	nervous_system_disorder|infectious_disease|inflammatory_disease	neurology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|brain_disorder|throat_disorder	true	false	false	true	high
MONDO:0001317	phlyctenulosis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	pediatrics|ophthalmology|dermatology	allergy|inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder|immune_disorder	true	false	false	true	medium
MONDO:0001318	functional gastric disease	digestive_system_disorder	other	digestive_system_disorder	gastrointestinal|gastroenterology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0001319	bladder lateral wall cancer	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|adrenal_gland_disease	urinary_tract_disorder|subtype|kidney_disorder	false	true	false	true	high
MONDO:0001320	ring staphyloma	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	skin_disorder|nail_disorder	false	false	false	false	high
MONDO:0001322	pericardium cancer	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	oncology|cardiology|cardiothoracic	cancer|cardiovascular_disorder	vascular_disorder|heart_disorder	false	true	false	false	high
MONDO:0001323	infant gynecomastia	disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder|breast_disorder	endocrine_system_disorder	endocrine_system_disorder|breast_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	endocrinology|pediatric	metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0001325	penile cancer	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|adrenal_gland_disease	reproductive_system_disorder|urinary_tract_disorder	false	true	false	true	medium
MONDO:0001326	dental pulp necrosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	oral_surgery|pediatric	inflammatory_disease	teeth_disorder	false	false	false	true	medium
MONDO:0001327	pelvic muscle wasting	reproductive_system_disorder	other	reproductive_system_disorder	neurology|obstetrics_and_gynecology	inflammatory_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	reproductive_system_disorder|muscle_disorder	false	false	false	false	high
MONDO:0001328	thyroid hormone resistance syndrome	endocrine_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|metabolic_disease	endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	thyroid_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0001329	accommodative spasm	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	mental_health_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0001330	presbyopia	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	true	low
MONDO:0001331	conjunctival deposit	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	eye_disorder	false	false	false	false	low
MONDO:0001332	palindromic rheumatism	syndromic_disease|musculoskeletal_system_disorder|connective_tissue_disorder	other	musculoskeletal_system_disorder|syndromic_disease|connective_tissue_disorder	rheumatology	inflammatory_disease|autoimmune_diseases	vascular_disorder|bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0001334	hypertrichosis of eyelid	integumentary_system_disorder|disorder_of_visual_system	other	disorder_of_orbital_region|integumentary_system_disorder|disorder_of_visual_system	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0001335	hypotrichosis of eyelid	integumentary_system_disorder|disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|integumentary_system_disorder|disorder_of_visual_system|hereditary_disease	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0001336	familial hyperlipidemia	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	cardiology|endocrinology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0001337	inflamed seborrheic keratosis	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology	dermatological_condition|inflammatory_disease	skin_disorder	false	false	false	false	low
MONDO:0001338	acute apical periodontitis	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|acute_disease|inflammatory_disease	dentistry|stomatology|oral_surgery|periodontics	inflammatory_disease|autoimmune_diseases	periodontitis|teeth_disorder	true	false	false	true	medium
MONDO:0001339	portal vein thrombosis	cardiovascular_disorder|endocrine_system_disorder|digestive_system_disorder	cardiovascular_disorder|endocrine_system_disorder	endocrine_system_disorder|cardiovascular_disorder|digestive_system_disorder	hematology|gastroenterology|hepatology	cancer|inflammatory_disease|cardiovascular_disorder	vascular_disorder|liver_disorder	false	false	false	true	high
MONDO:0001340	heart cancer	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiology|oncology	cancer|cardiovascular_disorder	vascular_disorder|heart_disorder	false	true	false	false	very_high
MONDO:0001341	selective IgA deficiency disease	immune_system_disorder|hereditary_disease|hematologic_disorder	other	hematologic_disorder|immune_system_disorder|hereditary_disease	allergy_and_immunology|rheumatology|hematology	anemia|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	medium
MONDO:0001342	dysgammaglobulinemia	immune_system_disorder|hereditary_disease|hematologic_disorder	other	hematologic_disorder|immune_system_disorder|hereditary_disease	immunology|hematology	metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	medium
MONDO:0001343	impaired renal function disease	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0001345	antidepressant type abuse	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	reproductive_system_disorder|brain_disorder|nose_disorder	false	false	false	false	high
MONDO:0001347	facioscapulohumeral muscular dystrophy	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	muscular_dystrophy|neurodegenerative_disease	muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0001349	odontoclasia	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	otolaryngology|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	bone_disorder|teeth_disorder	false	false	false	false	high
MONDO:0001350	parametrium malignant neoplasm	reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|adrenal_gland_disease	lymphatic_disorder|blood_bone_marrow_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0001351	uterine adnexa cancer	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adnexal_cancer	lymphatic_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0001352	round ligament malignant neoplasm	reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	false	high
MONDO:0001353	Bordetella parapertussis infectious disease	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease|infected_disease	lung_disorder|respiratory_disorder__note__no_exact_match_found_for_respiratory_disorde_in_the_original_list	true	false	false	true	low
MONDO:0001355	ocular siderosis	disorder_of_visual_system|metabolic_disease	metabolic_disease	disorder_of_visual_system|metabolic_disease|disorder_of_orbital_region	hematology|ophthalmology	anemia|autoimmune_diseases	blood_bone_marrow_disorder|eye_disorder	false	false	false	false	high
MONDO:0001356	iron deficiency anemia	hematologic_disorder|nutritional_disorder	anemia	nutritional_disorder|hematologic_disorder	gastroenterology|hematology	anemia|metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001357	hypochromic anemia	hematologic_disorder	anemia	hematologic_disorder	pulmonology|renal_medicine|genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0001358	bronchial disorder	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiothoracic	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease|allergy	lung_disorder|lower_gastrointestinal_disorder|throat_disorder	false	false	false	false	high
MONDO:0001360	blind hypotensive eye	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	cardiovascular_disorder|inflammatory_disease|adrenal_gland_disease	vascular_disorder|eye_disorder	false	false	false	false	high
MONDO:0001361	spontaneous ocular nystagmus	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001363	blind hypertensive eye	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|cardiology	hypertensive_eye_is_a_condition_related_to_the_eye_but_since_it_s_hypertensive__high_blood_pressure__related__cardiovascular_disorder___metabolic_disorder|metabolic_disorder|cardiovascular_disorder	vascular_disorder|eye_disorder	false	false	false	true	high
MONDO:0001364	regular astigmatism	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	metabolic_disorder|eye_disease	spinal_disorder|eye_disorder	false	false	false	true	low
MONDO:0001365	necrosis of ear ossicle	otorhinolaryngologic_disease|auditory_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|otorhinolaryngologic_disease|auditory_system_disorder	otolaryngology|pediatric	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	ear_disorder|bone_disorder	false	false	false	false	medium
MONDO:0001366	splenic sequestration	immune_system_disorder|hematologic_disorder	other	hematologic_disorder|immune_system_disorder	hematology|pediatric	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0001367	chronic congestive splenomegaly	immune_system_disorder|hematologic_disorder	other	hematologic_disorder|immune_system_disorder	cardiology|hepatology|hematology	metabolic_disorder|cardiovascular_disorder|inflammatory_disease	lymphatic_disorder|liver_disorder|immune_disorder	false	false	false	false	high
MONDO:0001368	phthisical cornea	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|pulmonology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	lung_disorder|eye_disorder	true	false	false	false	high
MONDO:0001369	chronic laryngitis	respiratory_system_disorder|inflammatory_disease	other	inflammatory_disease|respiratory_system_disorder	pulmonology|otolaryngology	inflammatory_disease|autoimmune_diseases	lung_disorder|thorat_disorder	false	false	false	true	medium
MONDO:0001370	pericardial effusion	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|pulmonology|cardiothoracic	cancer|cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	vascular_disorder|lung_disorder|heart_disorder	false	false	false	true	high
MONDO:0001371	protein-energy malnutrition	nutritional_disorder	other	nutritional_disorder	endocrinology|gastroenterology|pediatric|nutrition_is_not_listed_but_can_be_inferred_to_be_closest_to_gastroentrology	metabolic_disorder|protein_energy_malnutrition_is_associated_with_metabolic_disorders_due_to_a_lack_of_sufficient_energy_and_proteins_for_the_body_s_needs	muscle_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0001372	bladder neck cancer	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	bladder_neck_cancer_is_already_in_this_category_so_it_will_be_removed_from_the_list_but_since_it_s_a_type_of_cancer_this_category_remains|cancer|adrenal_gland_disease	reproductive_system_disorder|urinary_tract_disorder|subtype|kidney_disorder	false	true	false	false	high
MONDO:0001373	urinary bladder posterior wall cancer	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|renal_medicine|urology	cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0001374	bladder sarcoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|adrenal_gland_disease	bone_disorder|urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0001375	bladder trigone cancer	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	urologic_disease|genitourinary_system_disorder|cancer|bladder_cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0001376	urinary bladder anterior wall cancer	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0001377	vitreous syneresis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease	spinal_disorder|eye_disorder	false	false	false	false	low
MONDO:0001378	urachus cancer	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|adrenal_gland_disease	urinary_tract_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0001379	ureteric orifice cancer	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|renal_medicine|urology	cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0001380	bladder dome cancer	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|bladder_dome_cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0001381	bladder lymphoma	hematologic_disorder|urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|hematologic_disorder|cancer_or_benign_tumor	oncology|renal_medicine|hematology|urology	autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0001382	hepatorenal syndrome	endocrine_system_disorder|syndromic_disease|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|syndromic_disease	renal_medicine|hepatology|nephrology	metabolic_disorder|inflammatory_disease	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0001383	degenerative myopia	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0001384	myopia	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	pediatric|neurology|ophthalmology	cardiovascular_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0001385	cortical blindness	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0001386	visual epilepsy	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases|mental_health_disorder|inflammatory_disease	eye_disorder|brain_disorder	false	false	false	true	medium
MONDO:0001387	penile sarcoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	tumor|cancer	reproductive_system_disorder|skin_disorder|vascular_disorder	false	true	false	false	high
MONDO:0001388	glans penis cancer	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0001390	transient refractive change	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	pediatric|neurology|ophthalmology	cardiovascular_disorder|metabolic_disorder	eye_disorder|transient_refractive_change_is_a_condition_related_to_the_eye	false	false	false	false	low
MONDO:0001391	indeterminate leprosy	infectious_disease	infectious_disease	infectious_disease	neurology|dermatology	neurodegenerative_disease|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0001392	monocular exotropia	nervous_system_disorder	other	nervous_system_disorder	neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001393	peripheral focal chorioretinitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|immune_disorder	true	false	false	false	medium
MONDO:0001394	chronic erythremia	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|cardiology	anemia|metabolic_disorder	immune_disorder|vascular_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0001395	macular keratitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	ophthalmology|dermatology|pulmonology	autoimmune_diseases|inflammatory_disease	eye_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0001396	abnormal threshold of rods	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	disorder_of_orbital_region|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0001397	mononeuropathy	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001398	ureter benign neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	neoplasm|ureteral_neoplasm|cancer	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0001399	ureter leiomyoma	urinary_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	renal_medicine|oncology|urology	adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0001400	schwannoma of ureter	nervous_system_disorder|urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|urinary_system_disorder	oncology|neurology|urology	urinary_system_disorder|cancer|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0001401	female breast nipple and areola cancer	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	autoimmune_diseases|cancer|inflammatory_disease	subtype|skin_disorder|breast_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0001402	vaginal cancer	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	autoimmune_diseases|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0001403	labium majus cancer	integumentary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0001404	ecthyma	inflammatory_disease|integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|inflammatory_disease|infectious_disease	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|blood_bone_marrow_disorder	true	false	false	true	low
MONDO:0001405	dermatophytosis of groin and perianal area	inflammatory_disease|integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|inflammatory_disease|infectious_disease	dermatology|urology	autoimmune_diseases|inflammatory_disease	skin_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0001406	peripheral nervous system neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	peripheral_nervous_system_neoplasm|cancer	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0001407	tracheal cancer	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology|pulmonology	cancer|adrenal_gland_disease	lung_disorder|throat_disorder	false	true	false	false	high
MONDO:0001408	ischemic neuropathy	nervous_system_disorder	other	nervous_system_disorder	cardiology|neurology	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0001409	esophagitis	upper_digestive_tract_disorder|inflammatory_disease|digestive_system_disorder	other	digestive_system_disorder|inflammatory_disease|upper_digestive_tract_disorder	gastroenterology|hepatology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0001410	postmenopausal atrophic vaginitis	inflammatory_disease|reproductive_system_disorder	other	reproductive_system_disorder|inflammatory_disease	obstetrics_and_gynecology|endocrinology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0001411	synostosis	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|pediatric	autoimmune_diseases|inflammatory_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0001412	conjunctival concretion	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology	metabolic_disorder|inflammatory_disease|adrenal_gland_disease	eye_disorder	false	false	false	false	low
MONDO:0001413	ulceroglandular tularemia	infectious_disease	infectious_disease	infectious_disease	gastroenterology|infectious_diseases|pulmonology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0001414	osteopoikilosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	other____metabolic_disorder_is_the_primary_category|metabolic_disorder|autoimmune_diseases|inflammatory_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0001415	atrophy of testis	endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	endocrinology|urology|pediatric	degenerative_disease|hormonal_imbalance|metabolic_disorder|atrophy|reproductive_system_disorder|endocrine_system_disorder|male_reproductive_problem	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0001416	female reproductive organ cancer	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	female_reproductive_organ_cancer_is_not_needed_as_it_s_the_disease_itself|cancer	reproductive_system_disorder|female_reproductive_organ_cancer_is_a_specific_type_of_reproductive_system_disorder	false	true	false	true	high
MONDO:0001417	tracheal lymphoma	cancer_or_benign_tumor|hematologic_disorder|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|respiratory_system_disorder	oncology|otolaryngology|pulmonology|hematology	cancer|autoimmune_diseases|adrenal_gland_disease	lung_disorder|throat_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0001418	trachea sarcoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology|pulmonology	cancer|inflammatory_disease|adrenal_gland_disease	lung_disorder|throat_disorder	false	true	false	false	high
MONDO:0001419	trachea squamous cell carcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology|pulmonology	cancer|adrenal_gland_disease	lung_disorder|throat_disorder	false	true	false	false	high
MONDO:0001420	trigeminal nerve neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|otolaryngology|oncology	cancer|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|ear_disorder|brain_disorder	false	true	false	false	high
MONDO:0001421	frontal lobe neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0001422	primary aldosteronism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	cardiology|endocrinology|renal_medicine	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0001423	drug-induced mental disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	drug_induced_condition|mental_health_disorder	mental_disorder|brain_disorder	false	false	false	true	high
MONDO:0001426	mediastinum neurofibroma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology|genetics_and_genomics	cancer|neurodegenerative_disease	spinal_disorder|lung_disorder	false	false	false	false	medium
MONDO:0001427	Dieulafoy lesion	digestive_system_disorder	other	digestive_system_disorder	neurology|dermatology	cancer|adrenal_gland_disease	biliary_disorder|liver_disorder	false	false	false	true	high
MONDO:0001428	pylorospasm	digestive_system_disorder	other	digestive_system_disorder	neurology|gastroenterology	mental_health_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0001429	transient arthropathy	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease	muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0001430	deep corneal vascularisation	inflammatory_disease|disorder_of_visual_system	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	eye_disorder|vascular_disorder	false	false	false	false	high
MONDO:0001431	toxic or nutritional optic neuropathy	inflammatory_disease|disorder_of_visual_system|nervous_system_disorder	other	inflammatory_disease|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|eye_disorder|nutritional_disorder	false	false	false	true	high
MONDO:0001433	vaginal disorder	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|urology	inflammatory_disease|autoimmune_diseases	vaginal_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0001434	inflammatory spondylopathy	inflammatory_disease|musculoskeletal_system_disorder	other	inflammatory_disease|musculoskeletal_system_disorder	rheumatology|neurology	inflammatory_disease|autoimmune_diseases	spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0001435	bullous retinoschisis	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	pediatric|genetics_and_genomics|ophthalmology	inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0001436	hemosiderosis	metabolic_disease	metabolic_disease	metabolic_disease	pulmonology|cardiology|hepatology|renal_medicine|hematology|dermatology	inflammatory_disease|anemia|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	medium
MONDO:0001437	pulmonary alveolar proteinosis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|allergy_and_immunology|cardiothoracic	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	false	false	false	false	medium
MONDO:0001438	postinflammatory pulmonary fibrosis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	false	false	false	true	high
MONDO:0001439	episcleritis periodica fugax	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	allergy_and_immunology|ophthalmology	inflammatory_disease|autoimmune_diseases	vascular_disorder|eye_disorder|immune_disorder	false	false	false	true	medium
MONDO:0001440	neurotrophic keratoconjunctivitis	inflammatory_disease|disorder_of_visual_system	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|allergy_and_immunology|ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder	true	false	false	true	medium
MONDO:0001441	pica disease	nutritional_disorder|psychiatric_disorder	psychiatric_disorder	nutritional_disorder|psychiatric_disorder	pulmonology|cardiology|hematology|gastroenterology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0001442	dysthymic disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder	mental_health_disorder|brain_disorder	false	false	false	true	medium
MONDO:0001443	tympanosclerosis	otorhinolaryngologic_disease|auditory_system_disorder	other	auditory_system_disorder|otorhinolaryngologic_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	ear_disorder|throat_disorder	false	false	false	false	low
MONDO:0001444	Chagas disease	infectious_disease	infectious_disease	infectious_disease	hepatology|hematology|gastroenterology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|gastrointestinal_disorder	true	false	false	true	high
MONDO:0001446	low compliance bladder	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	inflammatory_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0001447	detrusor sphincter dyssynergia	urinary_system_disorder	other	urinary_system_disorder	urology|neurology	adrenal_gland_disease|neurodegenerative_disease	urinary_tract_disorder|muscle_disorder	false	false	false	false	high
MONDO:0001449	lymphocytic choriomeningitis	inflammatory_disease|nervous_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|nervous_system_disorder|infectious_disease	neurology|pediatric|immunology|hematology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	false	high
MONDO:0001451	peripheral retinal degeneration	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0001452	pseudoretinitis pigmentosa	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0001453	senile reticular retinal degeneration	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0001454	Blessig's cysts	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	urology|dermatology	inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	skin_disorder	false	false	false	false	medium
MONDO:0001455	retinal lattice degeneration	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0001456	cobblestone retinal degeneration	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0001457	secondary vitreoretinal degeneration	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	neurology|ophthalmology	secondary_vitreoretinal_degeneration_is_often_associated_with_age_related_macular_degeneration__which_is_a_neurodegenerative_disease|neurodegenerative_disease	eye_disorder|vascular_disorder	false	false	false	false	high
MONDO:0001458	ulnar nerve lesion	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|nerve_disorder	false	false	false	true	medium
MONDO:0001459	radial neuropathy	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0001460	dyshormonogenic goiter	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	pediatric|genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder	thyroid_disorder|endocrine_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001461	tinea corporis	inflammatory_disease|integumentary_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|integumentary_system_disorder|infectious_disease	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder	true	false	false	true	low
MONDO:0001462	descending colon cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|digestive_system_cancer	lower_gastrointestinal_disorder_upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0001463	splenic flexure cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|hematology|gastroenterology	inflammatory_disease|cancer	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0001464	sigmoid colon cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0001465	superficial keratitis	disorder_of_visual_system|inflammatory_disease	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	true	false	false	true	medium
MONDO:0001466	punctate epithelial keratoconjunctivitis	disorder_of_visual_system|inflammatory_disease	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	true	false	false	true	medium
MONDO:0001468	synovial plica syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder	false	false	false	true	medium
MONDO:0001469	cascade stomach	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	gastrointestinal_disease_is_not_in_the_list_so_it_would_be__metabolic_disorder|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0001470	anal margin squamous cell carcinoma	integumentary_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|digestive_system_disorder	oncology|urology	cancer|anal_margin_squamous_cell_carcinoma	skin_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0001471	histoplasmosis meningitis	nervous_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|nervous_system_disorder|inflammatory_disease	pulmonology|neurology	inflammatory_disease|autoimmune_diseases	spinal_disorder|lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0001472	testicular lymphoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|hematology|urology	cancer|lymphoma|autoimmune_diseases	lymphatic_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0001473	medulloadrenal hyperfunction	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	oncology|endocrinology|renal_medicine	metabolic_disorder|adrenal_gland_disease	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0001474	chronic salpingo-oophoritis	endocrine_system_disorder|reproductive_system_disorder|inflammatory_disease	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|inflammatory_disease	obstetrics_and_gynecology|gastroenterology|renal_medicine|hematology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0001475	neutropenia	immune_system_disorder|hematologic_disorder	other	hematologic_disorder|immune_system_disorder	oncology|hematology	inflammatory_disease|autoimmune_diseases|neutropenia_falls_under_the_categories__cancer	bone_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0001476	coloboma	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology	neurodegenerative_disease|eye_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001478	anisometropia	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	metabolic_disorder|eye_disease	eye_disorder	false	false	false	true	medium
MONDO:0001479	cutaneous diphtheria	integumentary_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|integumentary_system_disorder|inflammatory_disease	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|throat_disorder	true	false	false	true	low
MONDO:0001480	malignant tumor of undescended testis	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|malignant_tumor|adrenal_gland_disease	vascular_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0001481	femoral vein thrombophlebitis	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	cardiovascular|hematology	inflammatory_disease|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder|vein_disorder	false	false	false	true	medium
MONDO:0001482	testicular leukemia	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder|hematologic_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|hematologic_disorder|cancer_or_benign_tumor	oncology|hematology|urology	cancer|adrenal_gland_disease	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0001484	paranoid schizophrenia	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	mental_health_disorder|neurological_disorder|brain_disorder	false	false	false	true	high
MONDO:0001485	atypical depressive disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	high
MONDO:0001487	intrahepatic bile duct cancer	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|hepatology|gastroenterology	inflammatory_disease|cancer	liver_disorder|biliary_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0001488	anterior corneal pigmentation	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0001490	corneal granular dystrophy	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	true	medium
MONDO:0001491	cough variant asthma	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|allergy_and_immunology|pediatric	inflammatory_disease|autoimmune_diseases|allergy	immune_disorder|lung_disorder|throat_disorder	false	false	false	true	medium
MONDO:0001492	kyphoscoliotic heart disease	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|pulmonology|cardiothoracic	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	bone_disorder|spinal_disorder|heart_disorder	false	false	false	false	medium
MONDO:0001493	chronic pulmonary heart disease	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|pulmonology|cardiothoracic	inflammatory_disease|cardiovascular_disorder	heart_disorder|vascular_disorder|lung_disorder	false	false	false	true	high
MONDO:0001495	hematocele of tunica vaginalis testis	reproductive_system_disorder	other	reproductive_system_disorder	hematology|urology	anemia|inflammatory_disease|cancer	kidney_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0001496	male genital organ stricture	reproductive_system_disorder	other	reproductive_system_disorder	urology	inflammatory_disease|autoimmune_diseases|urological_disorder|adrenal_gland_disease|inflammatory_disease____corrected_to_be_more_specific_and_accurate____urological_disorder	urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0001497	male genital organ vascular disease	reproductive_system_disorder	other	reproductive_system_disorder	cardiology|urology	vascular_disease|autoimmune_diseases|cardiovascular_disorder	vascular_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0001498	varicocele	cardiovascular_disorder|reproductive_system_disorder	cardiovascular_disorder	cardiovascular_disorder|reproductive_system_disorder	obstetrics_and_gynecology|urology	inflammatory_disease|cardiovascular_disorder	vascular_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0001499	retroperitoneal lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	lymphoma|cancer	lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0001501	retroperitoneal sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	orthopaedic|oncology	cancer|adrenal_gland_disease	soft_tissue_disorder|blood_bone_marrow_disorder|muscle_disorder|sarcoma	false	true	false	false	high
MONDO:0001502	retroperitoneum carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology|genetics_and_genomics	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0001503	primary eye hypotony	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	primary_eye_hypotony|eye_disorder	false	false	false	false	low
MONDO:0001504	fetishistic disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	mental_health_disorder	mental_health_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0001505	alcoholic hepatitis	digestive_system_disorder|psychiatric_disorder|endocrine_system_disorder|inflammatory_disease	psychiatric_disorder|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|inflammatory_disease|psychiatric_disorder	hepatology|gastroenterology	inflammatory_disease|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0001506	prostatocystitis	urinary_system_disorder|reproductive_system_disorder|inflammatory_disease	other	reproductive_system_disorder|inflammatory_disease|urinary_system_disorder	renal_medicine|urology	inflammatory_disease|cancer|autoimmune_diseases	reproductive_system_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0001507	viral labyrinthitis	otorhinolaryngologic_disease|auditory_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|auditory_system_disorder|otorhinolaryngologic_disease|inflammatory_disease	neurology|otolaryngology	inflammatory_disease|neurodegenerative_disease	brain_disorder|ear_disorder	true	false	false	true	high
MONDO:0001508	patulous eustachian tube	otorhinolaryngologic_disease|auditory_system_disorder	other	auditory_system_disorder|otorhinolaryngologic_disease	pediatrics|allergy_and_immunology|otolaryngology	inflammatory_disease|anemia|autoimmune_diseases	throat_disorder|ear_disorder	false	false	false	false	low
MONDO:0001509	endocrine exophthalmos	other	other	disorder_of_orbital_region	endocrinology|ophthalmology	metabolic_disorder|autoimmune_diseases|adrenal_gland_disease	endocrine_disorder|eye_disorder	false	false	false	false	high
MONDO:0001510	lateral displacement of eye	other	other	disorder_of_orbital_region	orthopaedic|ophthalmology	injury|neurodegenerative_disease	eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001511	thyrotoxic exophthalmos	other	other	disorder_of_orbital_region	endocrinology|ophthalmology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|eye_disorder	false	false	false	true	high
MONDO:0001512	intermittent proptosis	other	other	disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0001513	pulsating exophthalmos	other	other	disorder_of_orbital_region	ophthalmology|neurology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder|vascular_disorder	true	false	false	false	high
MONDO:0001514	prolapse of urethra	urinary_system_disorder|reproductive_system_disorder	other	reproductive_system_disorder|urinary_system_disorder	obstetrics_and_gynecology|urology	inflammatory_disease|cancer	muscle_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0001515	corneal degeneration	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0001516	spinal muscular atrophy	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0001517	dysentery	infectious_disease|inflammatory_disease|digestive_system_disorder	infectious_disease	acute_disease|infectious_disease|digestive_system_disorder|inflammatory_disease	gastroenterology|pediatric	inflammatory_disease|gastrointestinal_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0001518	spastic entropion	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|adrenal_gland_disease	eye_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0001519	entropion	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|otolaryngology	inflammatory_disease|autoimmune_diseases	nose_disorder|eye_disorder|throat_disorder	false	false	false	true	low
MONDO:0001520	kleptomania	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	mental_disorder|brain_disorder	false	false	false	false	low
MONDO:0001521	intermittent explosive disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	medium
MONDO:0001522	pyromania	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	mental_health_condition|brain_disorder	false	false	false	false	high
MONDO:0001523	luxation of globe	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	eye_disorder|joint_disorder	false	false	false	false	high
MONDO:0001525	thyrocalcitonin secretion disease	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology	thyroid_related|metabolic_disorder|autoimmune_diseases	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0001526	labia minora cancer	cancer_or_benign_tumor|integumentary_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|integumentary_system_disorder	oncology|obstetrics_and_gynecology	cancer|autoimmune_diseases	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0001527	conjugate gaze palsy	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0001528	vulva cancer	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer|autoimmune_diseases	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0001529	pancytopenia	hematologic_disorder	anemia	hematologic_disorder	hematology|oncology|allergy_and_immunology|pediatric	cancer|autoimmune_diseases|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0001530	secondary hyperparathyroidism of renal origin	urinary_system_disorder|endocrine_system_disorder	endocrine_system_disorder	urinary_system_disorder|endocrine_system_disorder	renal_medicine|endocrinology	metabolic_disorder|renal_disease|electrolyte_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0001531	blood coagulation disease	hematologic_disorder	other	hematologic_disorder	hematology|cardiology|cardiothoracic	inflammatory_disease|metabolic_disorder|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0001532	capillariasis	infectious_disease	infectious_disease	infectious_disease	pulmonology|neurology|pediatric	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|kidney_disorder|lymphatic_disorder	true	false	false	false	medium
MONDO:0001533	pes anserinus tendinitis or bursitis	musculoskeletal_system_disorder|connective_tissue_disorder	other	connective_tissue_disorder|musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	muscle_disorder|joint_disorder	false	false	false	true	medium
MONDO:0001534	ocular hyperemia	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	low
MONDO:0001535	vagus nerve disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001536	vaginal leiomyoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|musculoskeletal_system_disorder	oncology|obstetrics_and_gynecology	cancer|reproductive_system_disorder	muscle_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0001537	tuberculous epididymitis	infectious_disease|inflammatory_disease|reproductive_system_disorder	infectious_disease	infectious_disease|reproductive_system_disorder|inflammatory_disease	urology|rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|immune_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0001538	retinal ischemia	cardiovascular_disorder|nervous_system_disorder|disorder_of_visual_system	cardiovascular_disorder	disorder_of_orbital_region|nervous_system_disorder|cardiovascular_disorder|disorder_of_visual_system	ophthalmology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	eye_disorder|vascular_disorder	false	false	false	false	high
MONDO:0001539	retinal perforation	hereditary_disease|nervous_system_disorder|disorder_of_visual_system	other	disorder_of_orbital_region|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|metabolic_disorder|anemia	eye_disorder	false	false	false	false	high
MONDO:0001540	bagassosis	immune_system_disorder|respiratory_system_disorder|inflammatory_disease	other	respiratory_system_disorder|occupational_disorder|immune_system_disorder|inflammatory_disease	allergy_and_immunology|pediatric|pulmonology	inflammatory_disease|neurodegenerative_disease|anemia|autoimmune_diseases	lower_gastrointestinal_disorder|blood_bone_marrow_disorder|upper_gastrointestinal_disorder|liver_disorder	true	false	false	true	high
MONDO:0001541	plantar nerve lesion	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001542	common peroneal nerve lesion	nervous_system_disorder|inflammatory_disease	other	nervous_system_disorder|inflammatory_disease	orthopaedic|neurology	injury|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001543	lesion of sciatic nerve	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0001544	tibial nerve palsy	nervous_system_disorder|inflammatory_disease	other	nervous_system_disorder|inflammatory_disease	orthopaedic|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	nerve_disorder|muscle_disorder|spinal_disorder	false	false	false	false	low
MONDO:0001546	hypermobility of coccyx	immune_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|immune_system_disorder	rheumatology|orthopaedic	musculoskeletal_disorder|inflammatory_disease|neurodegenerative_disease	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0001547	atrophic nonflaccid tympanic membrane	otorhinolaryngologic_disease|auditory_system_disorder	other	auditory_system_disorder|otorhinolaryngologic_disease	otolaryngology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	throat_disorder|ear_disorder	false	false	false	false	medium
MONDO:0001548	hepatic coma	nervous_system_disorder	other	nervous_system_disorder	hepatology|gastroenterology	hepatic_coma_falls_under_hepatic_which_means_liver_related_issues_are_involved_so_it_s_a_metabolic_disorder|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0001549	hemolytic-uremic syndrome	hematologic_disorder	other	hematologic_disorder	hematology|renal_medicine	anemia|metabolic_disorder|autoimmune_diseases	urinary_tract_disorder|kidney_disorder|immune_disorder	true	false	false	false	high
MONDO:0001551	ulceration of vulva	reproductive_system_disorder	other	reproductive_system_disorder	dermatology|obstetrics_and_gynecology	inflammatory_disease|cancer|autoimmune_diseases	reproductive_system_disorder|skin_disorder	true	false	false	true	medium
MONDO:0001552	dyscalculia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|cognitive_disorder	false	false	false	false	medium
MONDO:0001553	phacolytic glaucoma	immune_system_disorder|disorder_of_visual_system	autoimmune_disease	disorder_of_orbital_region|immune_system_disorder|disorder_of_visual_system	neurology|ophthalmology	inflammatory_disease|metabolic_disorder	eye_disorder|spinal_disorder	false	false	false	true	high
MONDO:0001554	phacogenic glaucoma	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0001555	neonatal thyrotoxicosis	immune_system_disorder|endocrine_system_disorder|inflammatory_disease	endocrine_system_disorder|autoimmune_disease	immune_system_disorder|inflammatory_disease|endocrine_system_disorder	endocrinology|pediatric	autoimmune_diseases|metabolic_disorder	thyroid_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0001556	urethral obstruction	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	inflammatory_disease|urological_disorders|cancer|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0001557	olecranon bursitis	musculoskeletal_system_disorder|connective_tissue_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|connective_tissue_disorder|inflammatory_disease	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0001558	Potter sequence	obstetric_disorder|syndromic_disease|reproductive_system_disorder	other	syndromic_disease|reproductive_system_disorder|obstetric_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|kidney_disorder	false	false	false	the_term__potter_sequence__does_not_refer_to_a_known_disease_or_medical_condition_that_would_typically_be_associated_with_treatment_options__it_appears_that_you_may_be_referring_to_a_genetic_or_biological_concept_related_to_developmental_biology_or_genetics__often_seen_in_studies_related_to__potter_s_sequence__or__potter_s_syndrome___which_refers_to_a_specific_set_of_anomalies_often_associated_with_oligohydramnios__low_amniotic_fluid__during_pregnancy___if_you_are_indeed_referring_to_potter_s_sequence_in_a_medical_context__treatments_would_depend_on_the_specific_anomalies_and_associated_conditions_present__but_in_general__as_a_condition__it_does_not_have_a_definitive_cure_or_treatment_that_is_effective_for_all_associated_issues__hence__if_referring_to_the_general_term_potter_sequence__in_medical_terms__it_would_be_appropriate_to_return___false	very_high
MONDO:0001559	perineocele	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|urology	adrenal_gland_disease	urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0001560	hypertrophic pyloric stenosis	digestive_system_disorder	other	digestive_system_disorder	pediatric|gastroenterology	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001561	pyloric stenosis	digestive_system_disorder	other	digestive_system_disorder	pediatric|gastroenterology	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001562	displacement of cardia through esophageal hiatus	digestive_system_disorder	other	digestive_system_disorder	cardiothoracic|cardiology|gastroenterology	gastrointestinal_disorder|cardiovascular_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001563	vestibulocochlear nerve disorder	nervous_system_disorder|auditory_system_disorder	other	nervous_system_disorder|auditory_system_disorder	neurology|otolaryngology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0001564	binocular vision disease	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|binocular_vision_disorders	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001565	abnormal retinal correspondence	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0001566	hypercalcemia disease	metabolic_disease	metabolic_disease	metabolic_disease	renal_medicine|endocrinology	adrenal_gland_disease|metabolic_disorder	bone_disorder|endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0001567	nephrocalcinosis	metabolic_disease|urinary_system_disorder	metabolic_disease	metabolic_disease|urinary_system_disorder	nephrocalcinosis|renal_medicine	kidney_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0001568	mixed receptive-expressive language disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001569	acoustic neuroma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|otolaryngology	neurodegenerative_disease|cancer	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0001571	gynecomastia disorder	reproductive_system_disorder|endocrine_system_disorder|breast_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	breast_disorder|endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0001572	leiomyoma	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer|gynecological_disorder___note__not_in_original_list_so_i_did_not_put_it	reproductive_system_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0001574	capillary disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|pulmonology|cardiology|genetics_and_genomics	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0001575	chronic gonococcal salpingitis	reproductive_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|inflammatory_disease|reproductive_system_disorder	obstetrics_and_gynecology|pediatric|oncology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0001576	telangiectasis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	dermatology|genetics_and_genomics	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0001577	respiratory syncytial virus infectious disease	respiratory_system_disorder|infectious_disease	infectious_disease	infectious_disease|respiratory_system_disorder	pediatric|pulmonology	respiratory_disease|autoimmune_diseases|inflammatory_disease	immune_disorder|throat_disorder|lung_disorder	true	false	false	true	medium
MONDO:0001579	corneal staphyloma	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|eye_abnormality|corneal_disorder	false	false	false	false	medium
MONDO:0001580	lacrimal duct cancer	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|otolaryngology|oncology	adrenal_gland_disease|cancer	eye_disorder|ear_disorder	false	true	false	false	high
MONDO:0001582	cicatricial ectropion	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0001583	diabetic polyneuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology|endocrinology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|vascular_disorder|muscle_disorder	false	false	true	false	high
MONDO:0001584	ocular motility disease	nervous_system_disorder	other	nervous_system_disorder	neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|ocular_motility_disease	false	false	false	false	medium
MONDO:0001585	hallucinogen abuse	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder|hallucino_gen_abuse	brain_disorder	false	false	false	false	medium
MONDO:0001586	mucopolysaccharidosis type 1	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|musculoskeletal_system_disorder	metabolic_disease	hereditary_disease|disorder_of_orbital_region|metabolic_disease|disorder_of_visual_system|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|eye_disorder|joint_disorder|kidney_disorder|lymphatic_disorder|brain_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0001588	chronic lacrimal gland enlargement	inflammatory_disease|disorder_of_visual_system	other	disorder_of_orbital_region|inflammatory_disease|disorder_of_visual_system	ophthalmology|otolaryngology	autoimmune_diseases|inflammatory_disease	eye_disorder|nose_disorder	false	false	false	false	medium
MONDO:0001590	quadriplegia	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	neurodegenerative_disease|spinal_cord_injury	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0001591	senile entropion	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|otolaryngology	neurodegenerative_disease|mental_health_disorder|adrenal_gland_disease	eye_disorder|skin_disorder	false	false	false	true	low
MONDO:0001592	prolapse of female genital organ	reproductive_system_disorder	other	reproductive_system_disorder	urology|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0001593	rectal disorder	digestive_system_disorder	other	digestive_system_disorder	urology|gastroenterology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0001594	Achilles bursitis	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder	other	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	joint_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0001595	choreatic disease	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0001596	hypochondriasis	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	anxiety_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0001597	submandibular gland disorder	other	other	mouth_disorder	otolaryngology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|throat_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0001598	benign lymphoepithelial lesion of salivary gland	immune_system_disorder	autoimmune_disease	mouth_disorder|immune_system_disorder	otolaryngology|oncology	cancer|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0001600	mucocele of salivary gland	other	other	mouth_disorder	otolaryngology|general_surgery	salivary_gland_disease|inflammatory_disease|cancer	upper_gastrointestinal_disorder|throat_disorder	false	false	false	false	medium
MONDO:0001601	Plasmodium ovale malaria	infectious_disease|hematologic_disorder	infectious_disease	infectious_disease|hematologic_disorder	parasitology|hematology	anemia	blood_bone_marrow_disorder|liver_disorder	true	false	false	true	low
MONDO:0001602	labia minora carcinoma	integumentary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	reproductive_system_disorder|skin_disorder	false	true	false	false	medium
MONDO:0001603	paralytic lagophthalmos	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001604	lagophthalmos	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001606	central nervous system leukemia	cancer_or_benign_tumor|nervous_system_disorder|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology|hematology	disease|neurological_disorder|cancer	blood_bone_marrow_disorder|spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0001607	intrapelvic lymph node leukemic reticuloendotheliosis	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|acute_disease|cancer_or_benign_tumor	oncology|hematopathology_is_not_listed_but_a_more_fitting_category_for_this_disease_would_be__oncology|hematology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	true	false	false	false	very_high
MONDO:0001608	vagus nerve neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurological_disorder|cancer	ear_disorder|throat_disorder|brain_disorder	false	true	false	false	high
MONDO:0001609	agranulocytosis	immune_system_disorder|hematologic_disorder	other	hematologic_disorder|immune_system_disorder	allergy_and_immunology|hematology	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0001610	acute dacryocystitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|acute_disease|inflammatory_disease|disorder_of_orbital_region	pediatric|otolaryngology|urology	autoimmune_diseases|inflammatory_disease	eye_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0001611	phlegmonous dacryocystitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	ophthalmology|otolaryngology	autoimmune_diseases|inflammatory_disease	eye_disorder|nose_disorder	true	false	false	true	medium
MONDO:0001612	carotid stenosis	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	cardiothoracic|neurology|cardiology	cardiovascular_disorder|inflammatory_disease	vascular_disorder	false	false	false	true	high
MONDO:0001613	vertebrobasilar insufficiency	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|neurology	cardiovascular_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0001614	intra-abdominal lymph node mast cell malignancy	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	immunology|hematology|oncology	lymphoma|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0001615	epidemic keratoconjunctivitis	infectious_disease|inflammatory_disease|disorder_of_visual_system	infectious_disease	infectious_disease|disorder_of_visual_system|inflammatory_disease|disorder_of_orbital_region	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease	eye_disorder|nose_disorder	true	false	false	true	low
MONDO:0001616	lobomycosis	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology|general_medicine|infectious_diseases	autoimmune_diseases|inflammatory_disease	skin_disorder|skin_disorder____corrected_response___skin_disorder	true	false	false	false	low
MONDO:0001617	transient global amnesia	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	cardiovascular_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001618	balanoposthitis	reproductive_system_disorder|inflammatory_disease	other	reproductive_system_disorder|inflammatory_disease	dermatology|urology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|skin_disorder	true	false	false	true	medium
MONDO:0001620	louse-borne relapsing fever	infectious_disease	infectious_disease	infectious_disease	pediatric|hematology	inflammatory_disease	blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0001621	tick-borne relapsing fever	infectious_disease	infectious_disease	infectious_disease	hematology|infectious_diseases	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|skin_disorder	true	false	false	true	medium
MONDO:0001622	mechanical lagophthalmos	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|dermatology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0001623	cicatricial lagophthalmos	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0001624	acute sphenoidal sinusitis	musculoskeletal_system_disorder|otorhinolaryngologic_disease|inflammatory_disease|respiratory_system_disorder	other	respiratory_system_disorder|otorhinolaryngologic_disease|musculoskeletal_system_disorder|acute_disease|inflammatory_disease	neurology|otolaryngology	allergy|autoimmune_diseases|inflammatory_disease	throat_disorder|nose_disorder	true	false	false	true	medium
MONDO:0001625	corpus luteum cyst	reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	gynecology_is_assumed_to_be_a_subset_of_obstetrics_and_gynecology|obstetrics_and_gynecology|endocrinology	adrenal_gland_disease|cancer|inflammatory_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0001626	traumatic glaucoma	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease|traumatic_glaucoma	eye_disorder|trauma	false	false	false	true	high
MONDO:0001627	dementia	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0001628	tinea unguium	infectious_disease|inflammatory_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder|inflammatory_disease	dermatology|urology	skin_infection|autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|skin_disorder	true	false	false	true	medium
MONDO:0001629	Jaccoud syndrome	immune_system_disorder	autoimmune_disease	immune_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	bone_disorder|liver_disorder	false	false	false	false	medium
MONDO:0001630	branch retinal artery occlusion	cardiovascular_disorder|disorder_of_visual_system|nervous_system_disorder	cardiovascular_disorder	disorder_of_orbital_region|disorder_of_visual_system|cardiovascular_disorder|nervous_system_disorder	ophthalmology|neurology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0001631	vertebral artery insufficiency	syndromic_disease|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder|nervous_system_disorder	vascular_disease_is_not_present_in_the_list_so_none|neurology|cardiology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	spinal_disorder|vascular_disorder	false	false	false	false	high
MONDO:0001632	intracranial arteriosclerosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	neurology|cardiology	neurodegenerative_disease|cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0001633	central retinal artery occlusion	cardiovascular_disorder|disorder_of_visual_system|nervous_system_disorder	cardiovascular_disorder	disorder_of_orbital_region|disorder_of_visual_system|cardiovascular_disorder|nervous_system_disorder	ophthalmology|neurology	neurodegenerative_disease|cardiovascular_disorder	eye_disorder|vascular_disorder	false	false	false	false	high
MONDO:0001634	bladder leiomyoma	urinary_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	urology|obstetrics_and_gynecology	cancer	urinary_tract_disorder|reproductive_system_disorder|muscle_disorder	false	false	false	false	low
MONDO:0001635	bladder squamous papilloma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer	urinary_tract_disorder|kidney_disorder	false	false	false	true	low
MONDO:0001636	mechanical entropion	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|otolaryngology	autoimmune_diseases|inflammatory_disease	eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001637	cicatricial entropion	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|dermatology|otolaryngology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	medium
MONDO:0001638	protein-deficiency anemia	hematologic_disorder	anemia	hematologic_disorder	hematology|gastroenterology|pediatrics	anemia|metabolic_disorder	blood_bone_marrow_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001639	deficiency anemia	hematologic_disorder	anemia	hematologic_disorder	pediatric|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|nutritional_deficiency	false	false	false	true	high
MONDO:0001640	gonococcal spondylitis	infectious_disease|inflammatory_disease|reproductive_system_disorder|musculoskeletal_system_disorder	infectious_disease	infectious_disease|reproductive_system_disorder|musculoskeletal_system_disorder|inflammatory_disease	rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease	joint_disorder|reproductive_system_disorder|spinal_disorder	true	false	false	true	medium
MONDO:0001641	severe pre-eclampsia	obstetric_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	obstetric_disorder|cardiovascular_disorder|hereditary_disease	renal_medicine|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	kidney_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0001642	hordeolum externum	infectious_disease|disorder_of_visual_system|inflammatory_disease|integumentary_system_disorder	infectious_disease	infectious_disease|disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease|integumentary_system_disorder	dermatology|otolaryngology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	true	false	false	true	low
MONDO:0001643	exophthalmic ophthalmoplegia	nervous_system_disorder	other	disorder_of_orbital_region|nervous_system_disorder	genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0001644	acute proliferative glomerulonephritis	urinary_system_disorder|inflammatory_disease	other	acute_disease|inflammatory_disease|urinary_system_disorder	renal_medicine|rheumatology	autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder	true	false	false	true	medium
MONDO:0001645	crescentic glomerulonephritis	urinary_system_disorder|inflammatory_disease	other	acute_disease|inflammatory_disease|urinary_system_disorder	renal_medicine|rheumatology|hematology	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|kidney_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0001646	benign secondary hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|cardiology	cardiovascular_disorder|metabolic_disorder	kidney_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0001647	benign renovascular hypertension	urinary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|urinary_system_disorder	renal_medicine|cardiology	cardiovascular_disorder|metabolic_disorder	kidney_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0001648	esophageal candidiasis	digestive_system_disorder|upper_digestive_tract_disorder|infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|upper_digestive_tract_disorder|digestive_system_disorder|inflammatory_disease	pulmonology|gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0001649	fungal esophagitis	digestive_system_disorder|upper_digestive_tract_disorder|infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|upper_digestive_tract_disorder|digestive_system_disorder|inflammatory_disease	pulmonology|gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	true	false	false	true	high
MONDO:0001650	acute cystitis	urinary_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	acute_disease|inflammatory_disease|urinary_system_disorder|infectious_disease	renal_medicine|urology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|kidney_disorder	true	false	false	true	low
MONDO:0001651	scrotum squamous cell carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	dermatology|oncology|urology	carcinoma|skin_cancer|genitourinary_disorder|cancer	reproductive_system_disorder|skin_disorder	false	true	false	true	medium
MONDO:0001652	scrotum melanoma	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|reproductive_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|reproductive_system_disorder|cancer_or_benign_tumor	dermatology|oncology|urology	adrenal_gland_disease|cancer	reproductive_system_disorder|skin_disorder	false	true	false	true	high
MONDO:0001653	prepuce cancer	cancer_or_benign_tumor|integumentary_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology|urology	adrenal_gland_disease|cancer	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0001654	spermatic cord cancer	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer	reproductive_system_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0001655	dissociated nystagmus	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology|otolaryngology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|mental_health_disorder	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0001656	megaesophagus	digestive_system_disorder|upper_digestive_tract_disorder	other	upper_digestive_tract_disorder|digestive_system_disorder	pulmonology|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0001657	brain cancer	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurodegenerative_disease|brain_cancer|cancer	spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0001658	nontoxic goiter	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	pediatric|endocrinology	metabolic_disorder|autoimmune_diseases	thyroid_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0001660	proliferative diabetic retinopathy	metabolic_disease|disorder_of_visual_system|cardiovascular_disorder|nervous_system_disorder	metabolic_disease|cardiovascular_disorder	disorder_of_visual_system|cardiovascular_disorder|metabolic_disease|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|endocrinology	autoimmune_diseases|metabolic_disorder	eye_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0001661	background diabetic retinopathy	metabolic_disease|disorder_of_visual_system|cardiovascular_disorder|nervous_system_disorder	metabolic_disease|cardiovascular_disorder	disorder_of_visual_system|cardiovascular_disorder|metabolic_disease|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|endocrinology	cardiovascular_disorder|metabolic_disorder	eye_disorder|endocrine_disorder	false	false	true	true	medium
MONDO:0001663	hole retinal cyst	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	pediatric|ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0001664	submucous uterine fibroid	musculoskeletal_system_disorder|cancer_or_benign_tumor|hereditary_disease|connective_tissue_disorder|reproductive_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease|musculoskeletal_system_disorder	hematology|oncology|obstetrics_and_gynecology	cancer|gynecological_condition	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0001665	oculoglandular tularemia	infectious_disease	infectious_disease	infectious_disease	pulmonology|ophthalmology|otolaryngology	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder|eye_disorder	true	false	false	true	medium
MONDO:0001666	retinal dystrophies primarily involving Bruch's membrane	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|cardiovascular_disorder|nervous_system_disorder	psychiatric_disorder|cardiovascular_disorder	disorder_of_visual_system|psychiatric_disorder|cardiovascular_disorder|hereditary_disease|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	upper_gastrointestinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0001667	streptobacillus infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0001668	internal pathological resorption of tooth	musculoskeletal_system_disorder	other	mouth_disorder|musculoskeletal_system_disorder	odontology|orthopaedic|neurology	inflammatory_disease|autoimmune_diseases|cancer|metabolic_disorder|anatomic_disease|anemia|revised_to	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0001670	tooth resorption	musculoskeletal_system_disorder	other	mouth_disorder|musculoskeletal_system_disorder	pediatric|orthopaedic|ophthalmology|otolaryngology|endocrinology	inflammatory_disease|anemia|metabolic_disorder|autoimmune_diseases	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0001671	mucocele of appendix	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|urology|otolaryngology	inflammatory_disease|appendicitis|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001672	bronchus cancer	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|oncology	cancer	lower_gastrointestinal_disorder|lung_disorder	false	true	false	true	very_high
MONDO:0001673	diarrheal disease	digestive_system_disorder	other	digestive_system_disorder	pediatric|gastroenterology	inflammatory_disease|gastrointestinal_disorder_is_not_in_the_list_so__inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0001674	diverticulitis of colon	digestive_system_disorder|inflammatory_disease	other	digestive_system_disorder|inflammatory_disease	hepatology|gastroenterology	inflammatory_disease|cancer	lower_gastrointestinal_disorder_upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001676	erythropoietic protoporphyria	digestive_system_disorder|metabolic_disease|hereditary_disease|integumentary_system_disorder|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|hereditary_disease|metabolic_disease|integumentary_system_disorder	genetics_and_genomics|dermatology|hematology	anemia|metabolic_disorder	skin_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0001678	intestinal tuberculosis	digestive_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	digestive_system_disorder|inflammatory_disease|infectious_disease	pulmonology|gastroenterology	inflammatory_disease|cancer|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder|lung_disorder	true	false	false	true	medium
MONDO:0001680	vaginal mullerian papilloma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0001681	diphtheritic cystitis	urinary_system_disorder|inflammatory_disease	other	inflammatory_disease|urinary_system_disorder	renal_medicine|urology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder	true	false	false	false	medium
MONDO:0001682	diphtheritic peritonitis	infectious_disease|inflammatory_disease	infectious_disease	inflammatory_disease|infectious_disease	pulmonology|gastroenterology|pediatrics	inflammatory_disease|autoimmune_diseases	throat_disorder|lower_gastrointestinal_disorder	true	false	false	false	high
MONDO:0001683	pancreatic mucinous ductal ectasia	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	gastroenterology|endocrinology	inflammatory_disease|cancer|pancreatic_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0001684	exocrine pancreatic insufficiency	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	gastroenterology|endocrinology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	endocrine_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0001685	chronic follicular conjunctivitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|inflammatory_disease|disorder_of_orbital_region	allergy_and_immunology|ophthalmology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	true	false	false	false	medium
MONDO:0001686	anatomical narrow angle borderline glaucoma	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	spinal_disorder|eye_disorder	false	false	false	true	high
MONDO:0001687	diabetic cataract	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	ophthalmology|endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|eye_disorder	false	false	true	true	medium
MONDO:0001688	toxic optic neuropathy	inflammatory_disease|disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|inflammatory_disease|nervous_system_disorder|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	ocular_disorder|eye_disorder	false	false	false	true	high
MONDO:0001689	hypertrophy of tongue papillae	other	other	mouth_disorder	dermatology|otolaryngology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	throat_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0001690	parasitic conjunctivitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	ophthalmology|pediatric	inflammatory_disease|autoimmune_diseases	parasite_related_category_is_not_present_but__parasitic__suggests_a_link_to_eye_disorder|eye_disorder	true	false	false	true	medium
MONDO:0001691	laryngeal cartilage cancer	respiratory_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder|musculoskeletal_system_disorder	oncology|otolaryngology	laryngeal_cartilage_cancer|cancer	throat_disorder|lung_disorder	false	true	false	false	high
MONDO:0001692	pedophilia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	reproductive_system_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0001694	diffuse interstitial keratitis	connective_tissue_disorder|inflammatory_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|connective_tissue_disorder|inflammatory_disease	rheumatology|ophthalmology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder|lung_disorder	true	false	false	true	high
MONDO:0001695	senile ectropion	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|neurology|otolaryngology	neurodegenerative_disease|mental_health_disorder	skin_disorder|spinal_disorder|eye_disorder	false	false	false	true	low
MONDO:0001697	reading disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	medium
MONDO:0001698	tinea profunda	infectious_disease|inflammatory_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|inflammatory_disease|infectious_disease	dermatology	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	false	medium
MONDO:0001699	tinea manuum	infectious_disease|inflammatory_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|inflammatory_disease|infectious_disease	infectious_diseases|dermatology|pediatric	inflammatory_disease|autoimmune_diseases	skin_disorder|muscle_disorder	true	false	false	true	low
MONDO:0001700	megaloblastic anemia	hematologic_disorder	anemia	hematologic_disorder	hematology|oncology|gastroenterology	anemia|metabolic_disorder	upper_gastrointestinal_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0001701	gastrointestinal anthrax	infectious_disease	infectious_disease	infectious_disease	gastroenterology	gastro_intestinal_disease|inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0001702	labia majora carcinoma	integumentary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	autoimmune_diseases|cancer	reproductive_system_disorder|skin_disorder	false	true	false	true	high
MONDO:0001703	color vision disorder	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	eye_disorder	false	false	false	false	low
MONDO:0001704	vaginal glandular neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	inflammatory_disease|cancer	reproductive_system_disorder	false	true	false	false	high
MONDO:0001705	pure red-cell aplasia	hematologic_disorder	anemia	hematologic_disorder	hematology|genetics_and_genomics	autoimmune_diseases|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0001706	cerebral sarcoidosis	syndromic_disease|connective_tissue_disorder|nervous_system_disorder	other	connective_tissue_disorder|nervous_system_disorder|syndromic_disease	psychiatry|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	immune_disorder|brain_disorder	false	false	false	true	high
MONDO:0001707	cardiac sarcoidosis	musculoskeletal_system_disorder|syndromic_disease|connective_tissue_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|connective_tissue_disorder|cardiovascular_disorder|syndromic_disease	cardiothoracic|cardiology|pulmonology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	heart_disorder|immune_disorder|vascular_disorder	false	false	false	true	high
MONDO:0001708	pulmonary sarcoidosis	syndromic_disease|respiratory_system_disorder|connective_tissue_disorder	other	connective_tissue_disorder|respiratory_system_disorder|syndromic_disease	pulmonology|rheumatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	true	high
MONDO:0001709	hypercalcemic sarcoidosis	syndromic_disease|connective_tissue_disorder	other	connective_tissue_disorder|syndromic_disease	endocrinology|rheumatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|endocrine_disorder	true	false	false	true	medium
MONDO:0001710	perforation of bile duct	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|cancer	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0001711	hepatic encephalopathy	nervous_system_disorder	other	nervous_system_disorder	gastroenterology|hepatology|neurology	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0001712	alexia	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatry|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0001713	inherited aplastic anemia	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|inherited_disorder|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder|inherited_condition	false	false	false	true	high
MONDO:0001714	bejel	reproductive_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease	infectious_diseases|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	lymphatic_disorder|immune_disorder	true	false	false	true	medium
MONDO:0001715	basilar artery occlusion	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	cardiology|neurology	inflammatory_disease|cardiovascular_disorder	vascular_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0001716	corneal argyrosis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0001717	posterior corneal pigmentation	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease|cancer	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0001718	scleritis	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0001719	gonococcal bursitis	musculoskeletal_system_disorder|reproductive_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	inflammatory_disease|reproductive_system_disorder|musculoskeletal_system_disorder|infectious_disease	urology|dermatology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|joint_disorder	true	false	false	false	medium
MONDO:0001720	gonococcal synovitis	musculoskeletal_system_disorder|reproductive_system_disorder|connective_tissue_disorder|inflammatory_disease|infectious_disease	infectious_disease	inflammatory_disease|reproductive_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|infectious_disease	urology|obstetrics_and_gynecology|rheumatology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|joint_disorder	true	false	false	true	high
MONDO:0001721	urethral intrinsic sphincter deficiency	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	urogenital_disorder|genitourinary_disorder|pelvic_floor_dysfunction	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0001722	central pterygium	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0001723	progressive peripheral pterygium	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0001724	supraglottis cancer	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|oncology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|throat_disorder	false	true	false	true	high
MONDO:0001725	balanitis xerotica obliterans	reproductive_system_disorder|inflammatory_disease	other	inflammatory_disease|reproductive_system_disorder	urology|dermatology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0001727	active cochleovestibular Meniere disease	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder|otorhinolaryngologic_disease	psychiatric_disorder	psychiatric_disorder|otorhinolaryngologic_disease|auditory_system_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001728	active vestibular Meniere disease	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder|otorhinolaryngologic_disease	psychiatric_disorder	psychiatric_disorder|otorhinolaryngologic_disease|auditory_system_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	ear_disorder|brain_disorder	true	false	false	false	high
MONDO:0001729	active cochlear Meniere disease	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder|otorhinolaryngologic_disease	psychiatric_disorder	psychiatric_disorder|otorhinolaryngologic_disease|auditory_system_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0001730	urethral syndrome	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0001731	benign vaginal mixed epithelial and mesenchymal neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer	reproductive_system_disorder	false	false	false	false	low
MONDO:0001732	trigonitis	urinary_system_disorder|inflammatory_disease	other	inflammatory_disease|urinary_system_disorder	genetics_and_genomics|rheumatology|pediatric	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	low
MONDO:0001733	occlusion of tributary of retinal vein	disorder_of_visual_system|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|cardiovascular_disorder	ophthalmology|neurology|hematology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0001734	tuberous sclerosis	syndromic_disease|hereditary_disease|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|nervous_system_disorder|syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	bone_disorder|kidney_disorder|muscle_disorder|skin_disorder|joint_disorder|brain_disorder	false	false	false	true	high
MONDO:0001735	paranasal sinus disorder	musculoskeletal_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease	other	musculoskeletal_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder	otolaryngology|pulmonology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|throat_disorder|nose_disorder	false	false	false	false	medium
MONDO:0001736	neonatal infective mastitis	breast_disorder|inflammatory_disease	other	inflammatory_disease|breast_disorder	obstetrics_and_gynecology|pediatric	autoimmune_diseases|inflammatory_disease	liver_disorder|immune_disorder	true	false	false	true	high
MONDO:0001737	tetanus neonatorum	infectious_disease|nervous_system_disorder	infectious_disease	infectious_disease|nervous_system_disorder	neurology|pediatric	infectious_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder|brain_disorder	true	false	false	true	high
MONDO:0001739	purulent labyrinthitis	auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	other	inflammatory_disease|otorhinolaryngologic_disease|auditory_system_disorder	otolaryngology|neurology	autoimmune_diseases|inflammatory_disease	ear_disorder|brain_disorder	true	false	false	true	very_high
MONDO:0001740	cornea squamous cell carcinoma	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_orbital_region|cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder	oncology|ophthalmology	cancer|autoimmune_diseases|inflammatory_disease	skin_disorder|eye_disorder	false	true	false	true	medium
MONDO:0001741	hyperparathyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|renal_medicine	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	true	medium
MONDO:0001742	interval angle-closure glaucoma	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	neurodegenerative_disease|cardiovascular_disorder|autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder|spinal_disorder	false	false	false	true	high
MONDO:0001743	paranasal sinus lymphoma	hematologic_disorder|cancer_or_benign_tumor|respiratory_system_disorder|musculoskeletal_system_disorder|nervous_system_disorder|otorhinolaryngologic_disease|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|nervous_system_disorder|hematologic_disorder|connective_tissue_disorder	oncology|hematology|otolaryngology	cancer|autoimmune_diseases|inflammatory_disease	nose_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0001744	angle-closure glaucoma	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	true	high
MONDO:0001745	subserous uterine fibroid	hereditary_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|reproductive_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|hereditary_disease|cancer_or_benign_tumor|reproductive_system_disorder|connective_tissue_disorder	obstetrics_and_gynecology	gynecological_disease|cancer|inflammatory_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001746	optic disk drusen	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|nervous_system_disorder	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	low
MONDO:0001747	tibial collateral ligament bursitis	musculoskeletal_system_disorder|connective_tissue_disorder	other	musculoskeletal_system_disorder|connective_tissue_disorder	rheumatology|orthopaedic	musculoskeletal_disorder|inflammatory_disease	joint_disorder|muscle_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0001748	maxillary sinus carcinoma	digestive_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|nervous_system_disorder|musculoskeletal_system_disorder|otorhinolaryngologic_disease|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|respiratory_system_disorder|mouth_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|digestive_system_disorder|nervous_system_disorder|connective_tissue_disorder	oncology|otolaryngology	adrenal_gland_disease|cancer	nose_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0001749	cortical senile cataract	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	neurology|ophthalmology	neurodegenerative_disease|mental_health_disorder	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0001750	non-renal secondary hyperparathyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|renal_medicine	metabolic_disorder|endocrine_disorder|secondary_hyperparathyroidism	endocrine_disorder|bone_disorder	false	false	false	true	high
MONDO:0001751	cholestasis	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	metabolic_disorder|inflammatory_disease	liver_disorder|biliary_disorder	false	false	false	true	high
MONDO:0001752	alveolar periostitis	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	other	musculoskeletal_system_disorder|mouth_disorder|inflammatory_disease|connective_tissue_disorder	pediatric|pulmonology	autoimmune_diseases|inflammatory_disease	lung_disorder|bone_disorder	true	false	false	false	medium
MONDO:0001753	female infertility of uterine origin	reproductive_system_disorder	other	reproductive_system_disorder	genetics_and_genomics|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|female_infertility_of_uterine_origin	false	false	false	true	medium
MONDO:0001754	eclampsia	obstetric_disorder|cardiovascular_disorder	cardiovascular_disorder	obstetric_disorder|cardiovascular_disorder	pediatric|obstetrics_and_gynecology|neonatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	kidney_disorder|reproductive_system_disorder|vascular_disorder	false	false	false	false	high
MONDO:0001756	frontal sinus cancer	cancer_or_benign_tumor|respiratory_system_disorder|musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	musculoskeletal_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|nervous_system_disorder|connective_tissue_disorder	oncology|otolaryngology	adrenal_gland_disease|cancer	nose_disorder|throat_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0001757	frontal sinus neoplasm	cancer_or_benign_tumor|respiratory_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	musculoskeletal_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|connective_tissue_disorder	neurology|oncology|otolaryngology	neurodegenerative_disease|cancer	nose_disorder|brain_disorder	false	true	false	false	high
MONDO:0001758	paranasal sinus sarcoma	cancer_or_benign_tumor|respiratory_system_disorder|musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	musculoskeletal_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|nervous_system_disorder|connective_tissue_disorder	oncology|otolaryngology	cancer	nose_disorder|lymphatic_disorder|bone_disorder	false	true	false	false	high
MONDO:0001760	photokeratitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_orbital_region|radiation_induced_disorder|inflammatory_disease|disorder_of_visual_system	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder	true	false	false	true	medium
MONDO:0001761	favism	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|hematology	metabolic_disorder|anemia	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0001762	dentine erosion	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	oral_medicine|pediatric|neurology	metabolic_disorder|inflammatory_disease	teeth_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001763	ethmoid sinus cancer	connective_tissue_disorder|musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|nervous_system_disorder	oncology|otolaryngology	adrenal_gland_disease|cancer	throat_disorder|nose_disorder	false	true	false	false	very_high
MONDO:0001764	ethmoidal sinus neoplasm	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	oncology|otolaryngology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease|allergy|cancer|autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|nose_disorder	false	true	false	false	high
MONDO:0001765	polyneuropathy in collagen vascular disease	nervous_system_disorder	other	nervous_system_disorder	rheumatology|neurology	autoimmune_diseases|inflammatory_disease	vascular_disorder|muscle_disorder	false	false	false	true	high
MONDO:0001766	eversion of lacrimal punctum	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	otolaryngology|ophthalmology	adhesive_diseases|autoimmune_diseases|inflammatory_disease	eye_disorder|nose_disorder	false	false	false	false	low
MONDO:0001767	stenosis of lacrimal punctum	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	otolaryngology|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|nose_disorder	false	false	false	false	low
MONDO:0001768	stenosis of lacrimal passage	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	otolaryngology|ophthalmology	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|nose_disorder	false	false	false	false	low
MONDO:0001769	acquired tear duct stenosis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	otolaryngology|pediatrics	autoimmune_diseases|inflammatory_disease	eye_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0001770	gastrin secretion abnormality	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	endocrinology|gastroenterology	metabolic_disorder|cancer|autoimmune_diseases|inflammatory_disease	endocrine_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0001771	infective urethral stricture	urinary_system_disorder	other	post_infectious_disorder|urinary_system_disorder	urology|renal_medicine	urological_disorder|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder	true	false	false	false	medium
MONDO:0001772	ulcer of anus and rectum	digestive_system_disorder	other	digestive_system_disorder	gastroenterology	cancer|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0001773	post-vaccinal encephalitis	inflammatory_disease|nervous_system_disorder	other	acute_disease|inflammatory_disease|nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0001774	posterior scleritis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	rheumatology|ophthalmology	autoimmune_diseases|inflammatory_disease	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0001775	chronic duodenal ileus	digestive_system_disorder	other	digestive_system_disorder	gastroenterology	gastrointestinal_disease|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0001776	prostate calculus	reproductive_system_disorder|urinary_system_disorder	other	urinary_system_disorder|reproductive_system_disorder	urology|renal_medicine	metabolic_disorder|cancer|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0001777	acute gonococcal cystitis	inflammatory_disease|reproductive_system_disorder|urinary_system_disorder|infectious_disease	infectious_disease	infectious_disease|acute_disease|inflammatory_disease|urinary_system_disorder|reproductive_system_disorder	urology|pediatric|allergy_and_immunology|renal_medicine|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	kidney_disorder|reproductive_system_disorder|urinary_tract_disorder	true	false	false	true	low
MONDO:0001778	dermoid cyst of skin	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology	cutaneous_disease|skin|cancer	skin_disorder|dermoid_cyst	false	false	false	true	low
MONDO:0001779	vaginal squamous papilloma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer|autoimmune_diseases	reproductive_system_disorder|skin_disorder	false	false	false	true	low
MONDO:0001780	premature ejaculation	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|urology	mental_health_disorder|neurodegenerative_disease	reproductive_system_disorder	false	false	false	true	low
MONDO:0001781	uterine corpus adenomatoid tumor	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0001782	mature cataract	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0001783	endometrial stromal nodule	cancer_or_benign_tumor|reproductive_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder|connective_tissue_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer|inflammatory_disease	muscle_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0001784	malignant renovascular hypertension	urinary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|urinary_system_disorder	renal_medicine|oncology|cardiology	cardiovascular_disorder|cancer	vascular_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0001785	malignant secondary hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|oncology|cardiology	cardiovascular_disorder|cancer	vascular_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0001786	uterine inflammatory disease	reproductive_system_disorder	other	reproductive_system_disorder	rheumatology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	immune_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0001787	hepatic infarction	endocrine_system_disorder|digestive_system_disorder|cardiovascular_disorder	cardiovascular_disorder|endocrine_system_disorder	cardiovascular_disorder|endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	cardiovascular_disorder|autoimmune_diseases|metabolic_disorder|inflammatory_disease	liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0001788	nutmeg liver	endocrine_system_disorder|digestive_system_disorder|cardiovascular_disorder	cardiovascular_disorder|endocrine_system_disorder	cardiovascular_disorder|endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	autoimmune_diseases|metabolic_disorder	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0001789	neurofibroma of spinal cord	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|neurology|genetics_and_genomics|oncology	cancer|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	medium
MONDO:0001790	spinal cord lipoma	cancer_or_benign_tumor|nervous_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder	pediatric|neurology|orthopaedic	cancer|neurodegenerative_disease|spinal_cord_lipoma_is_actually_a_congenital_disorder__but_closest_category_would_be_neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001791	neonatal urinary tract infectious disease	infectious_disease|urinary_system_disorder	infectious_disease	infectious_disease|urinary_system_disorder	pediatric|urology	autoimmune_diseases|inflammatory_disease	kidney_disorder|urinary_tract_disorder	true	false	false	true	high
MONDO:0001792	epiphora due to insufficient drainage	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	urology|neurology|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	liver_disorder|eye_disorder	false	false	false	true	medium
MONDO:0001793	excessive tearing	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder	false	false	false	false	low
MONDO:0001794	Pthirus pubis infestation	inflammatory_disease|infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|inflammatory_disease|integumentary_system_disorder	pediatric|dermatology|urology|obstetrics_and_gynecology	inflammatory_disease|allergy|autoimmune_diseases	joint_disorder|reproductive_system_disorder|skin_disorder	true	false	false	true	low
MONDO:0001795	plantar wart	cancer_or_benign_tumor|infectious_disease|integumentary_system_disorder	infectious_disease|cancer_or_benign_tumor	infectious_disease|cancer_or_benign_tumor|integumentary_system_disorder	dermatology|orthopaedic	other___note__i_replaced_allergy_and_autoimmune_diseases_as_more_specific_categories_for_plantar_warts_are_inflammatory_disease__general_category__and_skin_disease_which_is_not_in_the_original_list__but_would_be_a_good_fit|skin_disease|inflammatory_disease	skin_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0001797	chancroid	infectious_disease|reproductive_system_disorder	infectious_disease	infectious_disease|reproductive_system_disorder	sexually_transmitted_infections|dermatology|infectious_diseases|urology	sexually_transmitted_infection|inflammatory_disease	reproductive_system_disorder|skin_disorder	true	false	false	true	medium
MONDO:0001798	hypermobility syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	genetics_and_genomics|rheumatology	metabolic_disorder|inflammatory_disease	joint_disorder|muscle_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0001799	localized anterior staphyloma	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|ophthalmology	inflammatory_disease|localized_anterior_staphyloma_is_likely_related_to_skin_conditions__however__among_the_options_provided__it_seems_that_cancer_and_inflammatory_disease_could_be_potential_categories__the_term__staphyloma__specifically_suggests_a_condition_associated_with_inflammation_of_the_conjunctiva_or_cornea_in_ophthalmology__but_since_this_option_isn_t_available__we_ll_consider_its_closest_related_category_being_an_inflammatory_process_which_can_sometimes_occur_as_part_of_a_larger_issue_like_cancer_or_other_diseases|cancer	ear_disorder|skin_disorder	false	false	false	false	medium
MONDO:0001800	equatorial staphyloma	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	dermatology	inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	skin_disorder	false	false	false	false	high
MONDO:0001801	staphyloma posticum	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	dermatology	inflammatory_disease|autoimmune_diseases	ear_disorder|skin_disorder	false	false	false	false	high
MONDO:0001802	acute tympanitis	auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	other	otorhinolaryngologic_disease|acute_disease|inflammatory_disease|auditory_system_disorder	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	true	false	false	true	medium
MONDO:0001803	myringitis bullosa hemorrhagica	auditory_system_disorder|otorhinolaryngologic_disease	other	otorhinolaryngologic_disease|auditory_system_disorder	dermatology|hematology|otolaryngology	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder|skin_disorder	true	false	false	true	medium
MONDO:0001804	anterior scleritis	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|eye_disorder	false	false	false	true	medium
MONDO:0001805	female breast central part cancer	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	female_breast_central_part_cancer|cancer	reproductive_system_disorder|subtype|breast_cancer	false	true	false	true	high
MONDO:0001806	vaginal squamous tumor	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	inflammatory_disease|cancer	skin_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0001808	chronic subinvolution of uterus	reproductive_system_disorder	other	reproductive_system_disorder	pediatric|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0001809	adhesions of uterus	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|gynecology	inflammatory_disease|autoimmune_diseases|cancer	joint_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0001810	hypoglossal nerve disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	throat_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0001811	tetanic cataract	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	ophthalmology|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0001812	parasitic eyelid infestation	disorder_of_visual_system|inflammatory_disease|infectious_disease	infectious_disease	inflammatory_disease|disorder_of_visual_system|infectious_disease|disorder_of_orbital_region	dermatology|ophthalmology	inflammatory_disease|allergy|autoimmune_diseases	skin_disorder|eye_disorder	true	false	false	true	low
MONDO:0001813	squamous blepharitis	disorder_of_visual_system|inflammatory_disease	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases|cancer	skin_disorder|eye_disorder	true	false	false	true	low
MONDO:0001815	extrapyramidal and movement disease	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|autoimmune_diseases|extrapyramidal_and_movement_disease	brain_disorder|muscle_disorder	true	false	false	false	high
MONDO:0001816	scleroperikeratitis	disorder_of_visual_system|inflammatory_disease	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder|eye_disorder	false	false	false	false	high
MONDO:0001817	acute closed-angle glaucoma	disorder_of_visual_system	other	acute_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0001818	facial neuralgia	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	neurodegenerative_disease|autoimmune_diseases	facial_disorder_is_not_in_the_list_so__ear_disorder|brain_disorder|ear_disorder	false	false	false	true	medium
MONDO:0001819	multiple cranial nerve palsy	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder|ear_disorder	false	false	false	false	high
MONDO:0001820	focal labyrinthitis	auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	other	otorhinolaryngologic_disease|inflammatory_disease|auditory_system_disorder	neurology|otolaryngology	inflammatory_disease|autoimmune_diseases	brain_disorder|ear_disorder	true	false	false	false	high
MONDO:0001821	hypoactive sexual desire disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0001822	hypolipoproteinemia	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|endocrinology|pediatric|hepatology	metabolic_disorder	liver_disorder|genetic_disorder	false	false	false	true	medium
MONDO:0001823	sick sinus syndrome	syndromic_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiothoracic|cardiology	cardiovascular_disorder|neurodegenerative_disease	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0001824	polyneuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	spinal_disorder|nerve_disorder|muscle_disorder	false	false	false	false	high
MONDO:0001825	squamous papilloma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|oncology	squamous_cell_carcinoma|cancer	reproductive_system_disorder|skin_disorder|vaccine_related	false	false	false	true	low
MONDO:0001827	white piedra	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	dermatology|pediatrics|urology	metabolic_disorder|inflammatory_disease|allergy	skin_disorder|urinary_tract_disorder	true	false	false	true	low
MONDO:0001828	acquired color blindness	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder	false	false	false	false	low
MONDO:0001829	lumbosacral plexus lesion	nervous_system_disorder	other	nervous_system_disorder	neurology|orthopaedic	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0001830	somatization disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder	muscle_disorder	false	false	false	false	medium
MONDO:0001831	irregular astigmatism	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0001832	bacterial esophagitis	upper_digestive_tract_disorder|inflammatory_disease|infectious_disease|digestive_system_disorder	infectious_disease	upper_digestive_tract_disorder|inflammatory_disease|infectious_disease|digestive_system_disorder	pulmonology|hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	false	high
MONDO:0001833	lacrimal duct obstruction	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	otolaryngology|ophthalmology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0001834	visual pathway disorder	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001835	facial paralysis	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	nerve_disorder|brain_disorder|muscle_disorder	true	false	false	true	high
MONDO:0001836	amenorrhea	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|endocrinology	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0001837	acute gonococcal salpingitis	reproductive_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	reproductive_system_disorder|inflammatory_disease|acute_disease|infectious_disease	obstetrics_and_gynecology|urology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0001838	acute gonococcal prostatitis	reproductive_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	reproductive_system_disorder|inflammatory_disease|acute_disease|infectious_disease	urology	inflammatory_disease|urological_disorder|bacterial_infection	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0001841	uterine corpus epithelioid leiomyoma	cancer_or_benign_tumor|reproductive_system_disorder|hereditary_disease|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease	obstetrics_and_gynecology|oncology	smooth_muscle_tumor|reproductive_system_disorder|uterine_disease|benign_tumor|female_reproductive_system_disorder|cancer|glandular_cancer|neoplasm	reproductive_system_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0001842	uterine corpus dissecting leiomyoma	cancer_or_benign_tumor|reproductive_system_disorder|hereditary_disease|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease	obstetrics_and_gynecology|oncology	gynecological_disorder|cancer	reproductive_system_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0001843	uterus interstitial leiomyoma	cancer_or_benign_tumor|reproductive_system_disorder|hereditary_disease|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease	obstetrics_and_gynecology|oncology	gynecologic_disorder|cancer	reproductive_system_disorder|muscle_disorder	false	true	false	false	medium
MONDO:0001844	uterine corpus myxoid leiomyoma	cancer_or_benign_tumor|reproductive_system_disorder|hereditary_disease|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|uterus_disorder_is_incorrect__correct_category__reproductive_system_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0001845	uterine corpus lipoleiomyoma	cancer_or_benign_tumor|reproductive_system_disorder|hereditary_disease|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|muscle_disorder	false	false	false	false	low
MONDO:0001846	uterine corpus bizarre leiomyoma	cancer_or_benign_tumor|reproductive_system_disorder|hereditary_disease|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease	obstetrics_and_gynecology|oncology	neuroendocrine_tumor|cancer	reproductive_system_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0001847	nuclear senile cataract	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0001848	Morgagni cataract	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0001849	chronic orbital inflammation	other	other	disorder_of_orbital_region	ophthalmology|otolaryngology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0001850	female breast lower-outer quadrant cancer	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	inflammatory_disease|autoimmune_diseases|cancer	breast|reproductive_system_disorder|subtype	false	true	false	true	high
MONDO:0001851	primary lacrimal atrophy	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|otolaryngology	adrenal_gland_disease|metabolic_disorder	eye_disorder|nose_disorder	false	false	false	false	medium
MONDO:0001852	small intestine lymphoma	hematologic_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|digestive_system_disorder	hematology|oncology|gastroenterology	cancer|lymphoma	upper_gastrointestinal_disorder|lymphatic_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0001853	contact blepharoconjunctivitis	disorder_of_visual_system|inflammatory_disease	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology	allergy|inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder	true	false	false	true	low
MONDO:0001854	lacrimal apparatus disorder	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|otolaryngology	inflammatory_disease|autoimmune_diseases	eye_disorder|nose_disorder	false	false	false	false	medium
MONDO:0001855	rubeosis iridis	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	eye_disorder	false	false	false	false	high
MONDO:0001856	splenic artery aneurysm	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|vascular_is_also_incorrect_as_it_wasnt_in_the_original_list_so_i_will_stick_to_these__hematology|cardiology|vascular_is_incorrect_so_i_am_providing_the_correct_list__cardiothoracic	cardiovascular_disorder|inflammatory_disease	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0001857	Brucella canis brucellosis	infectious_disease	infectious_disease	infectious_disease	veterinary_medical_specialties|hematology|epidemiology|veterinary|animal_health|microbiology|immunology|infectious_disease	cardiovascular_disorder|inflammatory_disease|other_is_incorrect_so_its_omitted|autoimmune_diseases|metabolic_disorder	vascular_disorder|immune_disorder|joint_disorder	true	false	false	false	high
MONDO:0001858	Tietze syndrome	syndromic_disease|musculoskeletal_system_disorder	other	syndromic_disease|musculoskeletal_system_disorder	pediatric|rheumatology	inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	true	low
MONDO:0001859	algoneurodystrophy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	false	high
MONDO:0001860	folic acid deficiency anemia	nutritional_disorder	other	nutritional_disorder	hematology|gastroenterology	anemia|metabolic_disorder|other_is_not_included_since_anemia_has_been_selected___therefore_just___anemia	blood_bone_marrow_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0001861	malignant parietal pleura tumor	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	cardiothoracic|pulmonology|oncology	tumor|malignancy|cancer	pleura_tumor|lung_disorder	false	true	false	false	very_high
MONDO:0001862	malignant visceral pleura tumor	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|oncology	malignant_visceral_pleura_tumor|cancer	lung_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0001863	aorta atresia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology|pediatric	cardiovascular_disorder|congenital_heart_defect	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0001864	residual stage angle-closure glaucoma	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0001866	bipolar I disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	mental_health_disorder|brain_disorder	false	false	false	true	high
MONDO:0001867	phaeohyphomycosis	infectious_disease	infectious_disease	infectious_disease	dermatology|pulmonology|pediatrics	allergy|inflammatory_disease|autoimmune_diseases	liver_disorder|skin_disorder|lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0001868	primary angle-closure glaucoma	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	true	high
MONDO:0001869	paraurethral gland cancer	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0001870	acute poststreptococcal glomerulonephritis	inflammatory_disease|urinary_system_disorder	other	urinary_system_disorder|acute_disease|inflammatory_disease	renal_medicine|pediatric|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|kidney_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0001871	acute diffuse glomerulonephritis	inflammatory_disease|urinary_system_disorder	other	urinary_system_disorder|acute_disease|inflammatory_disease	renal_medicine|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|kidney_disorder|urinary_tract_disorder	true	false	false	true	high
MONDO:0001873	geniculate ganglionitis	inflammatory_disease|nervous_system_disorder	other	nervous_system_disorder|inflammatory_disease	neurology|otolaryngology|ophthalmology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|eye_disorder	true	false	false	false	medium
MONDO:0001874	toxic labyrinthitis	otorhinolaryngologic_disease|inflammatory_disease|auditory_system_disorder	other	otorhinolaryngologic_disease|auditory_system_disorder|inflammatory_disease	neurology|otolaryngology	autoimmune_diseases|inflammatory_disease	brain_disorder|ear_disorder	true	false	false	false	high
MONDO:0001875	epicondylitis	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease	rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease	joint_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0001876	renal artery atheroma	urinary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	urinary_system_disorder|cardiovascular_disorder	cardiology|renal_medicine|urology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0001877	infertility due to extratesticular cause	reproductive_system_disorder	other	reproductive_system_disorder	urology|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease|inflammatory_disease|neurodegenerative_disease|cancer	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0001878	acquired hypertrophic pyloric stenosis	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|pediatric	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0001879	anus cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0001880	median rhomboid glossitis	inflammatory_disease	other	mouth_disorder|inflammatory_disease	pediatric|allergy_and_immunology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder__throat_disorder__lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0001881	toxic shock syndrome	syndromic_disease|infectious_disease	infectious_disease	infectious_disease|syndromic_disease	dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0001882	bacteriuria	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	autoimmune_diseases|other____note__bacteriuria_is_a_urinary_tract_infection_caused_by_bacteria__which_is_an_inflammatory_disease_related_to_the_urinary_system|inflammatory_disease	kidney_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0001883	blue toe syndrome	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	vascular_disorder|joint_disorder	false	false	false	true	medium
MONDO:0001884	abducens nerve neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|otolaryngology|oncology	inflammatory_disease|neurodegenerative_disease|cancer	brain_disorder|eye_disorder	false	true	false	false	high
MONDO:0001885	lateral cystocele	reproductive_system_disorder	other	reproductive_system_disorder	urology|obstetrics_and_gynecology	pelvic_floor_dysfunction|gynecological_condition|urological_condition	urinary_tract_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0001886	midline cystocele	reproductive_system_disorder	other	reproductive_system_disorder	urology|obstetrics_and_gynecology	adrenal_gland_disease|inflammatory_disease	kidney_disorder|urinary_tract_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0001887	Allen-Masters syndrome	musculoskeletal_system_disorder|reproductive_system_disorder	other	reproductive_system_disorder|musculoskeletal_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0001888	anus lymphoma	cancer_or_benign_tumor|hematologic_disorder|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	lymphoma|cancer	immune_disorder|lymphatic_disorder|lower_gastrointestinal_disorder	true	true	false	true	high
MONDO:0001889	ovarian dysfunction	endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	endocrinology|genetics_and_genomics|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder|endocrine_disorders|inflammatory_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0001890	pulp erosion	musculoskeletal_system_disorder	other	mouth_disorder|musculoskeletal_system_disorder	pediatric|endodontics_is_not_in_the_list__however_orthopaedic_might_be_a_best_fit_as_pulp_erosion_can_affect_tooth_development_in_children_and_orthopaedic_issues_may_impact_dental_alignment_and_structure	dental_condition|inflammatory_disease	teeth_disorder|pulp_erosion_is_related_to_teeth__so_the_correct_answer_is___teeth_disorder	false	false	false	false	medium
MONDO:0001892	spinal cord lymphoma	hematologic_disorder|cancer_or_benign_tumor|nervous_system_disorder|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|post_infectious_disorder|nervous_system_disorder|hematologic_disorder|cancer_or_benign_tumor	neurology|oncology|hematology	lymphoma|cancer	lymphatic_disorder|spinal_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0001893	spinal cord melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	muscle_disorder|spinal_disorder	false	true	false	false	high
MONDO:0001894	spinal cord sarcoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	orthopaedic|oncology	neoplastic_disease|neurological_cancer|cancer	spinal_disorder|bone_disorder	false	true	false	false	high
MONDO:0001895	acute retrobulbar neuritis	inflammatory_disease|disorder_of_visual_system|nervous_system_disorder	other	disorder_of_orbital_region|acute_disease|disorder_of_visual_system|nervous_system_disorder|inflammatory_disease	neurology|ophthalmology	autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder|eye_disorder	true	false	false	false	medium
MONDO:0001896	obstructive hydrocephalus	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0001897	bilateral hyperactive labyrinth	otorhinolaryngologic_disease|auditory_system_disorder	other	otorhinolaryngologic_disease|auditory_system_disorder	neurology|otolaryngology	inflammatory_disease|neurodegenerative_disease	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0001898	optic choroid disorder	disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	disorder_of_orbital_region|cardiovascular_disorder|disorder_of_visual_system	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|optic_choroid_disorder_is_more_specific_so_it_will_be_excluded_from_the_list__eye_disorder	false	false	false	false	medium
MONDO:0001899	rheumatic congestive heart failure	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	cardiology|rheumatology|cardiothoracic	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	vascular_disorder|joint_disorder|heart_disorder	false	false	false	true	high
MONDO:0001901	selective IgG subclass deficiency	hereditary_disease|immune_system_disorder|hematologic_disorder	other	immune_system_disorder|hematologic_disorder|hereditary_disease	genetics_and_genomics|allergy_and_immunology|immunology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0001902	congenital agammaglobulinemia	hematologic_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hematologic_disorder|hereditary_disease	genetics_and_genomics|immunology|pediatric	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0001903	calcific tendinitis	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	other	musculoskeletal_system_disorder|inflammatory_disease|connective_tissue_disorder	rheumatology|orthopaedic	inflammatory_disease|metabolic_disorder	joint_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0001904	polyneuropathy due to drug	nervous_system_disorder	other	nervous_system_disorder	neurology	polyneuropathy|neurodegenerative_disease	nerve_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0001905	bicipital tenosynovitis	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	other	musculoskeletal_system_disorder|inflammatory_disease|connective_tissue_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0001906	posterior dislocation of lens	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease|neurodegenerative_disease	eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0001907	adult dermatomyositis	inflammatory_disease|integumentary_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	other	integumentary_system_disorder|musculoskeletal_system_disorder|idiopathic_disease|inflammatory_disease|connective_tissue_disorder	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder|muscle_disorder	false	false	false	true	high
MONDO:0001909	renal tubular acidosis	urinary_system_disorder|metabolic_disease	metabolic_disease	metabolic_disease|urinary_system_disorder	urology|renal_medicine|pediatric	renal_tubular_acidosis_can_also_be_classified_under_other_conditions_such_as_hereditary_or_genetic_disorders_but_this_is_not_included_in_the_provided_list|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0001910	ochronosis disorder	musculoskeletal_system_disorder|metabolic_disease|connective_tissue_disorder	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|connective_tissue_disorder	genetics_and_genomics|dermatology	adrenal_gland_disease|metabolic_disorder	liver_disorder|skin_disorder	false	false	false	false	medium
MONDO:0001911	tracheal calcification	respiratory_system_disorder	other	respiratory_system_disorder	otolaryngology|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|throat_disorder	false	false	false	false	medium
MONDO:0001912	acute frontal sinusitis	otorhinolaryngologic_disease|inflammatory_disease|musculoskeletal_system_disorder|respiratory_system_disorder	other	musculoskeletal_system_disorder|otorhinolaryngologic_disease|inflammatory_disease|acute_disease|respiratory_system_disorder	neurology|otolaryngology	inflammatory_disease|autoimmune_diseases	nose_disorder|lung_disorder|respiratory_disorder	true	false	false	true	medium
MONDO:0001913	oligospermia	reproductive_system_disorder	other	reproductive_system_disorder	urology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|male_reproductive_system_disorder	false	false	false	true	medium
MONDO:0001914	scleromalacia perforans	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0001915	orbital cyst	other	other	disorder_of_orbital_region	otolaryngology|ophthalmology	orbital_cyst_can_also_be_classified_as_a_type_of_orbital_mass|inflammatory_disease	eye_disorder|orbit_disorder	false	false	false	true	medium
MONDO:0001916	gastrointestinal tularemia	infectious_disease	infectious_disease	infectious_disease	pediatrics|gastroenterology	gastrointestinal_disease_is_not_in_the_list__but_gastroinflammatory_disease_is_not_a_category_either_however__the_closest_is___inflammatory_disease|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0001917	chronic perichondritis of pinna	otorhinolaryngologic_disease|inflammatory_disease|infectious_disease|auditory_system_disorder	infectious_disease	infectious_disease|auditory_system_disorder|post_infectious_disorder|otorhinolaryngologic_disease|inflammatory_disease	otolaryngology|rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease	ear_disorder	false	false	false	false	medium
MONDO:0001918	epiphora due to excess lacrimation	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|allergy_and_immunology|pediatric|endocrinology|ophthalmology	metabolic_disorder|adrenal_gland_disease|inflammatory_disease	eye_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0001919	cystoid macular retinal degeneration	nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0001920	chronic purulent otitis media	otorhinolaryngologic_disease|inflammatory_disease|auditory_system_disorder	other	auditory_system_disorder|otorhinolaryngologic_disease|inflammatory_disease	pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease	throat_disorder|ear_disorder	true	false	false	true	medium
MONDO:0001921	chronic atticoantral disease	otorhinolaryngologic_disease|inflammatory_disease|auditory_system_disorder	other	auditory_system_disorder|otorhinolaryngologic_disease|inflammatory_disease	dermatology|otolaryngology|ophthalmology	autoimmune_diseases|inflammatory_disease	ear_disorder|eye_disorder	true	false	false	false	medium
MONDO:0001922	pyoureter	urinary_system_disorder|infectious_disease	infectious_disease	infectious_disease|urinary_system_disorder	urology|renal_medicine	autoimmune_diseases|inflammatory_disease|cancer	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0001923	vitreoretinal dystrophy	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|disorder_of_visual_system	genetics_and_genomics|ophthalmology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0001924	dystrophies primarily involving the retinal pigment epithelium	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|disorder_of_visual_system	pediatric|genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0001925	retinal dystrophy in systemic or cerebroretinal lipidoses	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|disorder_of_visual_system	neurology|genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|systemic_disorder|cerebroretinal_lipidosis_is_not_in_the_list_so_we_exclude_it	false	false	false	true	high
MONDO:0001926	ureteral disorder	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	urinary_disorder|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0001927	pulmonary valve insufficiency	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|pulmonology|cardiothoracic	cardiovascular_disorder|inflammatory_disease	heart_disorder|lung_disorder	false	false	false	false	high
MONDO:0001928	suppurative cholangitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|inflammatory_disease	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	liver_disorder|biliary_disorder	true	false	false	true	high
MONDO:0001929	ascending cholangitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|inflammatory_disease	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|liver_disorder	true	false	false	true	high
MONDO:0001930	acute cholangitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	acute_disease|digestive_system_disorder|endocrine_system_disorder|inflammatory_disease	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|liver_disorder	true	false	false	true	high
MONDO:0001931	pericholangitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|inflammatory_disease	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	liver_disorder|biliary_disorder	true	false	false	false	high
MONDO:0001933	endocrine pancreas disorder	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	endocrinology|gastroenterology	metabolic_disorder|autoimmune_diseases	pancreas_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0001935	neurogenic arthropathy	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	neurology|orthopaedic	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0001936	brawny scleritis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	rheumatology|ophthalmology	autoimmune_diseases|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0001938	vulvar dystrophy	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|dermatology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|skin_disorder	false	false	false	false	medium
MONDO:0001939	skin epithelioid hemangioma	cancer_or_benign_tumor|integumentary_system_disorder|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	dermatology|hematology	inflammatory_disease|cancer	vascular_disorder|skin_disorder	false	false	false	true	low
MONDO:0001940	pleuropneumonia	inflammatory_disease|infectious_disease|respiratory_system_disorder	infectious_disease	infectious_disease|respiratory_system_disorder|inflammatory_disease	cardiology|pediatric|pulmonology|cardiothoracic	autoimmune_diseases|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder|vascular_disorder|urinary_tract_disorder|upper_gastrointestinal_disorder|lung_disorder	true	false	false	true	high
MONDO:0001941	blindness (disorder)	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system	neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0001942	generalized anxiety disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	mental_health_disorder|generalized_anxiety_disorder	brain_disorder|generalized_anxiety_disorder	false	false	false	true	high
MONDO:0001943	Plasmodium malariae malaria	infectious_disease|hematologic_disorder	infectious_disease	infectious_disease|hematologic_disorder	pediatric|hematology	anemia|infectious_disease|inflammatory_disease	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0001944	mixed malaria	infectious_disease|hematologic_disorder	infectious_disease	infectious_disease|hematologic_disorder	pediatric|infectious_diseases_is_not_in_the_list_but__hematology_is_a_good_fit_as_malaria_is_related_to_blood__pediatric_because_of_age_group_often_affected|hematology	anemia|autoimmune_diseases|inflammatory_disease	immune_disorder|vascular_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0001945	postencephalitic Parkinson disease	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	neurology|psychiatry	mental_health_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	true	false	false	true	high
MONDO:0001947	suppurative thyroiditis	inflammatory_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|inflammatory_disease	rheumatology|otolaryngology|endocrinology	autoimmune_diseases|inflammatory_disease	immune_disorder|endocrine_disorder	true	false	false	true	high
MONDO:0001949	acute thyroiditis	inflammatory_disease|endocrine_system_disorder	endocrine_system_disorder	acute_disease|endocrine_system_disorder|inflammatory_disease	endocrinology	autoimmune_diseases|inflammatory_disease	immune_disorder|endocrine_disorder	true	false	false	true	medium
MONDO:0001950	corneal ectasia	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology	neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0001951	Norwegian scabies	inflammatory_disease|integumentary_system_disorder|infectious_disease	infectious_disease	infectious_disease|integumentary_system_disorder|inflammatory_disease	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0001952	parietal lobe cancer	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|brain_cancer|neurological_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0001953	pyuria	urinary_system_disorder	other	urinary_system_disorder	urology|hematology|renal_medicine	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|kidney_disorder	true	false	false	false	low
MONDO:0001954	thrombophlebitis migrans	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	hematology|thrombophlebitis_migrans_suggests_a_vascular_issue__so_hematoloy_is_likely_the_best_fit	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	vascular_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0001955	protozoal dysentery	inflammatory_disease|digestive_system_disorder|infectious_disease	infectious_disease	acute_disease|infectious_disease|digestive_system_disorder|inflammatory_disease	pediatric|gastroenterology	gastrointestinal_disorder|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0001956	capillary leak syndrome	syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease	cardiology|hematology|pulmonology	metabolic_disorder|cardiovascular_disorder|inflammatory_disease	vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0001957	critical illness polyneuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology|pulmonology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	muscle_disorder|nerve_system_disorder	false	false	false	false	high
MONDO:0001959	labyrinthine bilateral reactive loss	otorhinolaryngologic_disease|auditory_system_disorder	other	auditory_system_disorder|otorhinolaryngologic_disease	neurology|otolaryngology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0001962	abnormality of glucagon secretion	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	endocrine_disorder	false	false	false	false	low
MONDO:0001964	chronic tubotympanic suppurative otitis media	inflammatory_disease|otorhinolaryngologic_disease|auditory_system_disorder	other	auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	true	false	false	true	high
MONDO:0001965	sclerosing keratitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_orbital_region|inflammatory_disease|disorder_of_visual_system	dermatology|rheumatology|ophthalmology	inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder|immune_disorder	false	false	false	false	medium
MONDO:0001966	chronic closed-angle glaucoma	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0001967	gonadal dysgenesis	endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	genetics_and_genomics|endocrinology|obstetrics_and_gynecology	metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0001969	mixed gonadal dysgenesis	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder	genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|genetic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0001971	farmer's lung disease	inflammatory_disease|immune_system_disorder|respiratory_system_disorder	other	respiratory_system_disorder|occupational_disorder|inflammatory_disease|immune_system_disorder	allergy_and_immunology|pulmonology	inflammatory_disease|allergy|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder|lung_disorder	false	false	false	true	high
MONDO:0001972	Brucella melitensis brucellosis	infectious_disease	infectious_disease	infectious_disease	pediatric|rheumatology|hematology|renal_medicine	inflammatory_disease|autoimmune_diseases	immune_disorder|upper_gastrointestinal_disorder|liver_disorder	true	false	false	true	medium
MONDO:0001973	Brucella abortus brucellosis	infectious_disease	infectious_disease	infectious_disease	obstetrics_and_gynecology|pediatrics|veterinary_science	inflammatory_disease|autoimmune_diseases	vascular_disorder|lower_gastrointestinal_disorder|immune_disorder|joint_disorder|reproductive_system_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0001974	hemangioma of orbit	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	ophthalmology|hematology|oncology	cancer	eye_disorder|vascular_disorder	false	false	false	true	low
MONDO:0001975	cavernous hemangioma of orbit	cardiovascular_disorder|hematologic_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor|hematologic_disorder	ophthalmology|hematology	cancer	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0001976	chorea gravidarum	nervous_system_disorder|obstetric_disorder	other	nervous_system_disorder|obstetric_disorder	obstetrics_and_gynecology|neurology	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0001977	ureteral lymphoma	urinary_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder|hematologic_disorder	urology|hematology|oncology	cancer|adrenal_gland_disease	urinary_tract_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0001978	regional ureteric cancer	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer|regional_ureteric_cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0001979	dumping syndrome	digestive_system_disorder|syndromic_disease	other	digestive_system_disorder|syndromic_disease	endocrinology|gastroenterology	gastrointestinal_disorder|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0001982	Niemann-Pick disease	hereditary_disease|immune_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|immune_system_disorder|metabolic_disease	hepatology|pediatric|genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	brain_disorder|lung_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0001983	peripheral degeneration of cornea	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology	inflammatory_disease|neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0001984	candidal paronychia	infectious_disease	infectious_disease	infectious_disease	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0001985	partial arterial retinal occlusion	nervous_system_disorder|cardiovascular_disorder|disorder_of_visual_system	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	inflammatory_disease|cardiovascular_disorder	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0001986	Argyll Robertson pupil	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0001987	senile degeneration of brain	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	vascular_disorder|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0001988	external pathological resorption	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	dermatology|orthopaedic	inflammatory_disease|cancer|metabolic_disorder|autoimmune_diseases	teeth_disorder|bone_disorder	false	false	false	false	none
MONDO:0001989	atrophic glossitis	inflammatory_disease	other	inflammatory_disease|mouth_disorder	dermatology|otolaryngology|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|throat_disorder	false	false	false	true	medium
MONDO:0001990	malignant cardiac peripheral nerve sheath neoplasm	nervous_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|cancer_or_benign_tumor	cardiology|oncology|neurology	cancer|cardiovascular_disorder|neurodegenerative_disease	heart_disorder|muscle_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0001991	malignant cardiac germ cell tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiology|pediatric|oncology	cancer|cardiovascular_disorder	heart_disorder|vascular_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0001992	rete testis adenocarcinoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	urology|oncology	cancer|adenocarcinoma	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0001993	seminal vesicle adenocarcinoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	urology|oncology	cancer|adrenal_gland_disease|other___corrected_to__cancer	upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0001994	sphenoidal sinus cancer	nervous_system_disorder|connective_tissue_disorder|otorhinolaryngologic_disease|musculoskeletal_system_disorder|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|respiratory_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease	otolaryngology|oncology	cancer|adrenal_gland_disease	ear_disorder|nose_disorder|brain_disorder	false	true	false	false	high
MONDO:0001995	sphenoid sinus squamous cell carcinoma	nervous_system_disorder|connective_tissue_disorder|otorhinolaryngologic_disease|musculoskeletal_system_disorder|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|respiratory_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease	otolaryngology|oncology	squamous_cell_carcinoma|cancer	nose_disorder|upper_gastrointestinal_disorder|sinuses_disorder	false	true	false	false	high
MONDO:0001996	steroid-induced glaucoma - borderline	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|endocrinology	inflammatory_disease|adrenal_gland_disease	eye_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0001997	root resorption	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	orthopaedic|dental	inflammatory_disease|metabolic_disorder|autoimmune_diseases	teeth_disorder|bone_disorder	false	false	false	false	low
MONDO:0001998	Foster-Kennedy syndrome	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	eye_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0001999	primary pulmonary hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|pulmonology	primary_pulmonary_hypertension|cardiovascular_disorder	vascular_disorder|lung_disorder	false	false	false	true	very_high
MONDO:0002000	anaerobic meningitis	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	inflammatory_disease|nervous_system_disorder|infectious_disease	pediatric|neurology	inflammatory_disease|autoimmune_diseases	immune_disorder|brain_disorder|spinal_disorder	true	false	false	false	high
MONDO:0002002	postsurgical hypothyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|surgical	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	endocrine_disorder|post_surgical_hypothyroidism	false	false	false	true	medium
MONDO:0002004	atheroembolism of kidney	cardiovascular_disorder|urinary_system_disorder	cardiovascular_disorder	urinary_system_disorder|cardiovascular_disorder	cardiology|renal_medicine	metabolic_disorder|cardiovascular_disorder	vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0002006	serous labyrinthitis	auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	other	inflammatory_disease|otorhinolaryngologic_disease|auditory_system_disorder	otolaryngology|neurology	inflammatory_disease|autoimmune_diseases	ear_disorder|brain_disorder	true	false	false	false	high
MONDO:0002008	labyrinthitis	auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	other	inflammatory_disease|otorhinolaryngologic_disease|auditory_system_disorder	otolaryngology|neurology	inflammatory_disease|autoimmune_diseases	ear_disorder|brain_disorder	true	false	false	true	medium
MONDO:0002009	major depressive disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder	mind_disorder|brain_disorder|mental_health_disorder	false	false	false	true	high
MONDO:0002010	FG syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|skin_disorder	false	false	false	false	high
MONDO:0002012	methylmalonic acidemia	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|hematology|pediatrics	metabolic_disorder|anemia	blood_bone_marrow_disorder|metabolic_disorder	false	false	false	true	very_high
MONDO:0002013	lymphangioma	cardiovascular_disorder|immune_system_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	oncology|pediatric	cancer|lymphatic_disorder	vascular_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0002014	autosomal recessive Ehlers-Danlos syndrome, vascular type	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	cardiovascular_disorder	syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|cardiology|pediatrics|dermatology|rheumatology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|skin_disorder|joint_disorder	false	false	false	false	high
MONDO:0002017	olivopontocerebellar atrophy	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0002021	gingival disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	oral_surgery|maxillofacial|pediatric|general_dentistry	autoimmune_diseases|inflammatory_disease	teeth_disorder|skin_disorder	true	false	false	true	medium
MONDO:0002022	disorder of orbital region	other	other		ophthalmology|neurology|otolaryngology	disorder_of_orbital_region_does_not_have_a_best_fit__but_inflammatory_disease_and_autoimmune_diseases_seem_to_be_related|cancer|autoimmune_diseases|inflammatory_disease	orbital_region_is_a_type_of_eye_disorder|eye_disorder	false	false	false	false	high
MONDO:0002025	psychiatric disorder				neurology|psychiatry	mental_health_disorder|psychiatric_disorder	brain_disorder|psychiatric_disorder	false	false	false	true	high
MONDO:0002026	candidiasis	infectious_disease	infectious_disease	infectious_disease	dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder|skin_disorder	true	false	false	true	low
MONDO:0002027	avoidant personality disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0002028	personality disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	medium
MONDO:0002029	chronic gonorrhea of cervix	reproductive_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	inflammatory_disease|reproductive_system_disorder|infectious_disease	urology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0002030	chronic cervicitis	reproductive_system_disorder	other	reproductive_system_disorder	urology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|throat_disorder	true	false	false	true	medium
MONDO:0002031	cecal disorder	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0002032	colon carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer|colon_carcinoma	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002033	cecum cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002034	cecum lymphoma	hematologic_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0002035	colon lymphoma	hematologic_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|hematologic_disorder|cancer_or_benign_tumor	gastroenterology|oncology|hematology	cancer|inflammatory_disease	lower_gastrointestinal_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0002036	penile disorder	reproductive_system_disorder	other	reproductive_system_disorder	psychiatry|urology	mental_health_disorder|sexual_health_disorder	reproductive_system_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0002037	pleural disorder	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiothoracic	pleural_disorder|autoimmune_diseases|inflammatory_disease	lung_disorder|pleural_disorder	false	false	false	false	high
MONDO:0002038	head and neck carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology	cancer|inflammation_disease|autoimmune_diseases	upper_gastrointestinal_disorder|throat_disorder|ear_disorder	false	true	false	true	high
MONDO:0002039	cognitive disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|cognitive_disorder_is_already_a_subset_of_brain_disorder__so_it_should_be_eliminated_from_the_list__however__if_you_want_to_keep_cognitive_disorder_as_a_standalone_category__then_the_best_fitting_categories_would_be__brain_disorder	false	false	false	false	high
MONDO:0002040	dermatomycosis	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology	dermatomycosis_can_also_be_referred_to_as_a_fungal_infection_which_is_typically_an_inflammatory_disease|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0002041	fungal infectious disease	infectious_disease	infectious_disease	infectious_disease	infectious_disease|dermatology	fungal_infections_often_fall_under_a_broader_category_of_infectious_diseases_which_can_also_be_classified_as_inflammatory_disease|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0002042	mechanical ectropion	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	otolaryngology|dermatology	autoimmune_diseases|inflammatory_disease|adhesive_disease	muscle_disorder|eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0002043	ectropion	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	otolaryngology|dermatology	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	eye_disorder|skin_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0002044	spastic ectropion	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0002045	communicating hydrocephalus	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|communicating_hydrocephalus|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0002046	alcohol abuse	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	hepatology|neurology|psychiatry	metabolic_disorder|mental_health_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0002047	pulmonary systemic sclerosis	connective_tissue_disorder|immune_system_disorder|integumentary_system_disorder|respiratory_system_disorder	autoimmune_disease	immune_system_disorder|integumentary_system_disorder|respiratory_system_disorder|connective_tissue_disorder	pulmonology|rheumatology	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0002048	thrombocytopenia due to immune destruction	hematologic_disorder	other	hematologic_disorder	hematology|allergy_and_immunology	autoimmune_diseases|anemia|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0002049	thrombocytopenia	hematologic_disorder	other	hematologic_disorder	thrombocytopenia|hematology	autoimmune_diseases|anemia	blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0002050	depressive disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|mental_disorder	false	false	false	true	very_high
MONDO:0002051	integumentary system disorder		other		integumentary_system_disorder|dermatology	autoimmune_diseases|inflammatory_disease|integumentary_system_disorder_is_not_in_the_list_so_removed_it	skin_disorder|integumentary_system_disorder	true	false	false	true	medium
MONDO:0002052	lymphadenitis	inflammatory_disease|immune_system_disorder	other	immune_system_disorder|inflammatory_disease	oncology|pediatric|hematology|allergy_and_immunology|rheumatology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder_lymphatic_disorder	true	false	false	true	medium
MONDO:0002055	benign eccrine breast spiradenoma	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	oncology|dermatology	breast_disease|cancer|skin_disease	reproductive_system_disorder|skin_disorder	false	false	false	true	low
MONDO:0002056	breast fibroadenoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	reproductive_system_disorder|skin_disorder|joint_disorder|muscle_disorder	false	false	false	false	low
MONDO:0002057	breast leiomyoma	musculoskeletal_system_disorder|breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder|bone_disorder	false	false	false	false	low
MONDO:0002058	breast adenoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder|breast_disorder	false	false	false	false	low
MONDO:0002060	intraductal papilloma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|inflammatory_disease	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	low
MONDO:0002061	intraductal papillary breast neoplasm	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder|breast_disorder	false	true	false	false	medium
MONDO:0002062	breast myofibroblastoma	cancer_or_benign_tumor|breast_disorder|connective_tissue_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor|connective_tissue_disorder	oncology|obstetrics_and_gynecology	tumor|cancer	reproductive_system_disorder|muscle_disorder	false	true	false	false	medium
MONDO:0002064	breast angiomatosis	cardiovascular_disorder|breast_disorder	cardiovascular_disorder	breast_disorder|cardiovascular_disorder	genetics_and_genomics|oncology|obstetrics_and_gynecology	autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|vascular_disorder	false	false	false	false	low
MONDO:0002065	benign breast adenomyoepithelioma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|benign_breast_adenomyoepithelioma_does_not_fit_well_in_the_category_of_cancer_because_it_is_a_rare_type_of_tumor_that_can_be_benign_so_its_classification_might_differ	reproductive_system_disorder|breast_disorder	false	false	false	false	low
MONDO:0002066	breast adenomyoepithelioma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder|lymphatic_disorder|breast_disorder	false	false	false	false	medium
MONDO:0002067	female breast upper-inner quadrant cancer	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	autoimmune_diseases|cancer	reproductive_system_disorder|upper_gastrointestinal_disorder|subtype	false	true	false	true	high
MONDO:0002068	female breast lower-inner quadrant cancer	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	autoimmune_diseases|cancer|inflammatory_disease	reproductive_system_disorder|subtype|breast_disorder	false	true	false	true	high
MONDO:0002069	female breast axillary tail cancer	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	autoimmune_diseases|cancer	reproductive_system_disorder|lymphatic_disorder|subtype	false	true	false	true	high
MONDO:0002070	ventricular septal defect	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiology|pediatric	congenital_heart_defect|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0002071	supratentorial cancer	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	supratentorial_cancer|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0002072	melanotic neuroectodermal tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|dermatology	cancer|neuroectodermal_tumor	neuroectodermal_tumor|skin_disorder	false	true	false	false	medium
MONDO:0002073	malignant pineal area germ cell neoplasm	endocrine_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|endocrine_system_disorder	genetics_and_genomics|oncology|pediatric	germ_cell_neoplasm|cancer|malignant	reproductive_system_disorder|brain_disorder	false	true	false	false	high
MONDO:0002074	Behcet syndrome arthropathy	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|joint_disorder	false	false	false	false	high
MONDO:0002075	spontaneous tension pneumothorax	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiothoracic	autoimmune_diseases|cancer|inflammatory_disease	upper_gastrointestinal_disorder|lung_disorder	false	false	false	false	high
MONDO:0002076	pneumothorax	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiothoracic	cancer|inflammatory_disease	lung_disorder|lower_respiratory_system_disorder	false	false	false	true	medium
MONDO:0002077	low implantation of placenta	obstetric_disorder|reproductive_system_disorder	other	reproductive_system_disorder|obstetric_disorder	pediatric|obstetrics_and_gynecology	metabolic_disorder|autoimmune_diseases|anemia|inflammatory_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0002078	heart septal defect	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|pediatric|cardiothoracic	congenital_anomaly|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0002081	musculoskeletal system disorder		other		rheumatology|orthopaedic	musculoskeletal_system_disorder_is_most_closely_related_to__inflammatory_disease|metabolic_disorder|autoimmune_diseases	spinal_disorder|bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0002082	endocrine gland neoplasm	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	cancer|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0002083	Richter syndrome	syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor	oncology|hematatology|genetics_and_genomics	neurodegenerative_disease|cancer	immune_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0002085	benign shuddering attacks	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	true	low
MONDO:0002086	clear cell acanthoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|urology|dermatology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|skin_disorder|kidney_disorder	false	false	false	false	low
MONDO:0002087	peritoneum cancer	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|hepatology|gastroenterology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|liver_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002088	partial retinal vein occlusion	cardiovascular_disorder|nervous_system_disorder|disorder_of_visual_system	cardiovascular_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cardiovascular_disorder	neurology|ophthalmology	cardiovascular_disorder|inflammatory_disease	eye_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0002089	retinal vascular occlusion	cardiovascular_disorder|nervous_system_disorder|disorder_of_visual_system	cardiovascular_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cardiovascular_disorder	neurology|ophthalmology	cardiovascular_disorder|inflammatory_disease	eye_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0002090	eccrine sweat gland neoplasm	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|adrenal_gland_disease	reproductive_system_disorder|skin_disorder	false	true	false	false	low
MONDO:0002092	small intestine leiomyoma	digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|neoplasm|gastrointestinal_disease	lower_gastrointestinal_disorder|muscle_disorder	false	false	false	false	low
MONDO:0002093	acanthoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|skin_condition	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0002095	vascular cancer	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	oncology|hematology	autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|vascular_disorder	false	true	false	false	high
MONDO:0002096	malignant conjunctival melanoma	disorder_of_development_or_morphogenesis|disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|disorder_of_development_or_morphogenesis|disorder_of_orbital_region|nervous_system_disorder|cancer_or_benign_tumor	oncology|ophthalmology	cancer|malignant_conjunctival_melanoma	eye_disorder|skin_disorder	false	true	false	false	high
MONDO:0002098	facial nerve disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0002099	Histoplasma capsulatum infectious disease	infectious_disease	infectious_disease	infectious_disease	pulmonology|dermatology|allergy_and_immunology	autoimmune_diseases|infectious_disease|inflammatory_disease	immune_disorder|lung_disorder|skin_disorder	true	false	false	true	medium
MONDO:0002100	cardiovascular cancer	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	oncology|cardiology	cardiovascular_disorder|cancer	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0002101	facial nerve neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology|otolaryngology	neurodegenerative_disease|cancer	facial_nerve_is_closely_related_to_the_ear__though_it_s_a_cranial_nerve|ear_disorder	false	true	false	false	high
MONDO:0002102	cheilitis	inflammatory_disease	other	inflammatory_disease|mouth_disorder	dermatology|otolaryngology	autoimmune_diseases|inflammatory_disease	teeth_disorder|skin_disorder	true	false	false	true	low
MONDO:0002103	factitious disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder	mental_health_disorder|neurological_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0002104	conversion disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|mental_disorder	false	false	false	false	medium
MONDO:0002105	toxic megacolon	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|pediatrics	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0002106	labyrinthine unilateral reactive loss	auditory_system_disorder|otorhinolaryngologic_disease	other	otorhinolaryngologic_disease|auditory_system_disorder	neurology|otolaryngology	autoimmune_diseases|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0002107	unilateral hyperactive labyrinth	auditory_system_disorder|otorhinolaryngologic_disease	other	otorhinolaryngologic_disease|auditory_system_disorder	neurology|otolaryngology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0002108	thyroid cancer	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	autoimmune_diseases|cancer|inflammatory_disease|adrenal_gland_disease	endocrine_disorder	false	true	false	true	medium
MONDO:0002109	pituitary cancer	endocrine_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|nervous_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder|reproductive_system_disorder|connective_tissue_disorder	oncology|endocrinology	cancer|adrenal_gland_disease	endocrine_disorder|brain_disorder	false	true	false	false	high
MONDO:0002110	adrenal rest tumor	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|endocrinology	cancer|adrenal_gland_disease	endocrine_disorder	false	true	false	false	medium
MONDO:0002112	benign peritoneal mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pulmonology|gastroenterology	benign_disease|cancer|peritoneal_mesothelioma	lung_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0002113	peritoneal carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hepatology|oncology|hematology|gastroenterology	peritoneal_carcinoma_is_a_type_of_cancer____corrected_answer___cancer|cancer	upper_gastrointestinal_disorder|liver_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002114	pancreas lymphoma	endocrine_system_disorder|hematologic_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder|hematologic_disorder	oncology|hematology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|endocrine_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0002116	malignant exocrine pancreas neoplasm	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|malignant_exocrine_pancreas_neoplasm	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0002117	pancreas sarcoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer	endocrine_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002118	urinary system disorder		other		urology|renal_medicine	metabolic_disorder|autoimmune_diseases|urinary_system_disorder|inflammatory_disease	kidney_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0002119	ossifying fibroma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	oncology|orthopaedic	other___corrected_list___bone_disease|cancer|bone_disease	bone_disorder|teeth_disorder	false	false	false	false	low
MONDO:0002120	neuroendocrine carcinoma	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	cancer|adrenal_gland_disease	endocrine_disorder|neurological_disorders	false	true	false	true	high
MONDO:0002121	mononeuritis simplex	inflammatory_disease|nervous_system_disorder	other	inflammatory_disease|nervous_system_disorder	orthopaedic|neurology	autoimmune_diseases|inflammatory_disease	nerve_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0002122	neuritis	inflammatory_disease|nervous_system_disorder	other	inflammatory_disease|nervous_system_disorder	neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	true	false	false	false	medium
MONDO:0002123	calcinosis	metabolic_disease	metabolic_disease	metabolic_disease	dermatology|rheumatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder|liver_disorder|skin_disorder	false	false	false	false	medium
MONDO:0002124	secondary lacrimal atrophy	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|otolaryngology	autoimmune_diseases|cancer|inflammatory_disease	eye_disorder|nose_disorder	false	false	false	false	medium
MONDO:0002127	urethral stricture	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	urological_disorder|urethral_stricture|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0002128	mononeuritis multiplex	inflammatory_disease|nervous_system_disorder	other	inflammatory_disease|nervous_system_disorder	neurology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|vascular_disorder|muscle_disorder	false	false	false	false	high
MONDO:0002129	bone cancer	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	oncology|orthopaedic|hematology	bone_cancer|cancer	blood_bone_marrow_disorder|bone_disorder	false	true	false	true	very_high
MONDO:0002130	upper limb mononeuronitis	inflammatory_disease|nervous_system_disorder	other	inflammatory_disease|nervous_system_disorder	orthopaedic|neurology	autoimmune_diseases|inflammatory_disease	nerve_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0002131	jaw cancer	digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|musculoskeletal_system_disorder|mouth_disorder|connective_tissue_disorder	oncology|otolaryngology	cancer|adrenal_gland_disease	oral_disorder|teeth_disorder	false	true	false	true	high
MONDO:0002132	skull cancer	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	oncology|neurology	skull_cancer|cancer	bone_disorder|brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002133	chronic rheumatic pericarditis	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	cardiology|rheumatology|cardiothoracic	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	joint_disorder|heart_disorder	false	false	false	false	medium
MONDO:0002134	physiological sexual disorder	reproductive_system_disorder	other	reproductive_system_disorder	neurology|urology|psychiatry	metabolic_disorder|mental_health_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0002135	optic nerve disorder	disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|disorder_of_visual_system	neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0002136	eczematous dermatitis of eyelid	disorder_of_visual_system|inflammatory_disease	other	disorder_of_orbital_region|inflammatory_disease|disorder_of_visual_system	dermatology|allergy_and_immunology	autoimmune_diseases|allergy|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	medium
MONDO:0002137	noninfectious dermatoses of eyelid	disorder_of_visual_system|inflammatory_disease	other	disorder_of_orbital_region|inflammatory_disease|disorder_of_visual_system	dermatology|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	medium
MONDO:0002138	allergic contact dermatitis of eyelid	immune_system_disorder|disorder_of_visual_system|integumentary_system_disorder|inflammatory_disease	other	disorder_of_orbital_region|inflammatory_disease|integumentary_system_disorder|disorder_of_visual_system|immune_system_disorder	dermatology|allerg_and_immunology	autoimmune_diseases|allergy	eye_disorder|skin_disorder	false	false	false	true	medium
MONDO:0002139	sigmoid disease	digestive_system_disorder	other	digestive_system_disorder	gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0002140	vagina sarcoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer	reproductive_system_disorder|lymphatic_disorder|skin_disorder	false	true	false	false	high
MONDO:0002141	cutaneous undifferentiated pleomorphic sarcoma	integumentary_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|integumentary_system_disorder|connective_tissue_disorder	oncology|dermatology	cancer	skin_disorder|muscle_disorder	false	true	false	false	high
MONDO:0002142	undifferentiated pleomorphic sarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	oncology|orthopaedic	cancer	bone_disorder|soft_tissue_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0002143	vaginal yolk sac tumor	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002145	disorder of sexual differentiation	disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	obstetrics_and_gynecology|pediatric|endocrinology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0002146	hypogonadism	reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	pediatric|endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0002149	reproductive system cancer	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	reproductive_system_cancer|cancer	reproductive_system_cancer|reproductive_system_disorder	false	true	false	true	high
MONDO:0002150	hypothalamic disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|endocrinology	neurodegenerative_disease|mental_health_disorder	brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0002152	intermittent squint	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0002153	telogen effluvium	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatrics	metabolic_disorder|autoimmune_diseases	skin_disorder|hair_disorder	false	false	false	false	medium
MONDO:0002154	trichomoniasis	infectious_disease	infectious_disease	infectious_disease	dermatology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0002155	cholecystitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0002156	fallopian tube disorder	reproductive_system_disorder	other	reproductive_system_disorder	oncology|obstetrics_and_gynecology|pediatric	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder	false	false	false	false	medium
MONDO:0002158	fallopian tube cancer	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer|autoimmune_diseases	reproductive_system_disorder	false	true	false	false	high
MONDO:0002159	fallopian tube leiomyosarcoma	reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|post_infectious_disorder|musculoskeletal_system_disorder	oncology|obstetrics_and_gynecology	adverse_condition|cancer	muscle_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002162	fallopian tube adenosarcoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|inflammatory_disease	reproductive_system_disorder	false	true	false	false	high
MONDO:0002163	thymus lipoma	connective_tissue_disorder|hematologic_disorder|musculoskeletal_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	connective_tissue_disorder|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|endocrine_system_disorder|musculoskeletal_system_disorder	oncology|cardiothoracic|surgery|pediatric	cancer	lymphatic_disorder|immune_disorder	false	false	false	false	low
MONDO:0002164	focal chorioretinitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|inflammatory_disease|disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	true	false	false	false	medium
MONDO:0002165	rectal neoplasm	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	cancer|rectal_neoplasm	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002166	rectum lymphoma	hematologic_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|digestive_system_disorder	gastroenterology|oncology|hematology	cancer|lymphoma	lymphatic_disorder|lower_gastrointestinal_disorder	true	true	false	true	high
MONDO:0002167	rectum malignant melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|digestive_system_disorder	dermatology|oncology	cancer|adrenal_gland_disease	skin_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002168	rectum sarcoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	cancer	lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002169	rectum adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	cancer|inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002170	chronic eustachian salpingitis	otorhinolaryngologic_disease|inflammatory_disease|auditory_system_disorder	other	inflammatory_disease|otorhinolaryngologic_disease|auditory_system_disorder	otolaryngology	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	false	false	false	false	medium
MONDO:0002171	giant cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|orthopaedic	tumor|cancer|inflammatory_disease	bone_disorder|joint_disorder	false	true	false	true	high
MONDO:0002172	otosalpingitis	otorhinolaryngologic_disease|inflammatory_disease|auditory_system_disorder	other	inflammatory_disease|otorhinolaryngologic_disease|auditory_system_disorder	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	true	false	false	false	medium
MONDO:0002173	neuroma	nervous_system_disorder	other	nervous_system_disorder	neurology|orthopaedic	neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0002174	preretinal fibrosis	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0002175	degeneration of macula and posterior pole	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|degenerative_disease	spinal_disorder|eye_disorder	false	false	false	true	high
MONDO:0002177	hyperinsulinism	metabolic_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease|digestive_system_disorder	pediatric|endocrinology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder	false	false	true	true	high
MONDO:0002178	placenta cancer	obstetric_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|obstetric_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease|autoimmune_diseases	reproductive_system_disorder|vascular_disorder|other___corrected_list___reproductive_system_disorder	false	true	false	false	high
MONDO:0002181	exostosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	otolaryngology|orthopaedic	neurodegenerative_disease|cancer|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0002182	communication disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|otolaryngology|pediatric	mental_health_disorder|communication_disorder	brain_disorder|throat_disorder	false	false	false	false	high
MONDO:0002183	enthesopathy	connective_tissue_disorder|musculoskeletal_system_disorder	other	connective_tissue_disorder|musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0002184	drug-induced hepatitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	gastroenterology|hepatology	adverse_reaction_drug_induced_hepatotoxicity_inflammatory_disease	liver_disorder	false	false	false	true	high
MONDO:0002185	hyperostosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	metabolic_disorder|inflammatory_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0002186	acute maxillary sinusitis	otorhinolaryngologic_disease|inflammatory_disease|musculoskeletal_system_disorder|respiratory_system_disorder	other	respiratory_system_disorder|inflammatory_disease|mouth_disorder|otorhinolaryngologic_disease|acute_disease|musculoskeletal_system_disorder	pulmonology|otolaryngology	inflammatory_disease|allergy	nose_disorder|throat_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0002187	vulvar disease	reproductive_system_disorder	other	reproductive_system_disorder	dermatology|obstetrics_and_gynecology	cancer|inflammatory_disease|autoimmune_diseases	skin_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0002188	vulvar nodular hidradenoma	integumentary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	dermatology|obstetrics_and_gynecology	cancer|inflammatory_disease	lymphatic_disorder|skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0002189	nodular hidradenoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer|inflammatory_disease	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0002190	vulvar syringoma	integumentary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|dermatology	autoimmune_diseases|cancer|inflammatory_disease	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0002191	syringoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology	autoimmune_diseases|cancer	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0002192	vulvar angiokeratoma	integumentary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	integumentary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	obstetrics_and_gynecology|dermatology	cancer|inflammatory_disease	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0002193	Bartholin gland benign neoplasm	integumentary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|urology	gland_disease|cancer	lymphatic_disorder|lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0002194	vestibular papilloma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	otolaryngology|neurology	cancer|benign_tumor|neoplastic_disease|tumorous_condition	ear_disorder|throat_disorder	false	false	false	false	low
MONDO:0002195	vulvar squamous neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|dermatology	cancer	skin_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0002196	perinatal intestinal perforation	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|pediatric|obstetrics_and_gynecology	inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0002197	minor vestibular glands adenoma	urinary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	neurology|otolaryngology	cancer|adrenal_gland_disease	ear_disorder|throat_disorder	false	false	false	false	low
MONDO:0002198	vulvar glandular neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|dermatology	autoimmune_diseases|glandular_neoplasm|cancer	skin_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0002199	benign mixed tumor of the vulva	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|inflammatory_disease	skin_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0002200	eccrine mixed tumor of skin	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	skin_cancer|cancer|tumor	skin_disorder|muscle_disorder	false	false	false	false	low
MONDO:0002201	vulvar trichoepithelioma	cancer_or_benign_tumor|reproductive_system_disorder|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	dermatology|oncology	inflammatory_disease|autoimmune_diseases|cancer	reproductive_system_disorder|skin_disorder	false	false	false	false	low
MONDO:0002202	outlet dysfunction constipation	digestive_system_disorder	other	digestive_system_disorder	urology|gastroenterology|renal_medicine	constipation|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0002203	constipation disorder	digestive_system_disorder	other	digestive_system_disorder	neurology|gastroenterology	other____no__the_correct_answer_is__metabilic_disorder|gastrointestinal_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0002204	transient arthritis	inflammatory_disease|musculoskeletal_system_disorder	other	inflammatory_disease|musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0002205	vulvar melanoma	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|reproductive_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|reproductive_system_disorder|cancer_or_benign_tumor	dermatology|oncology	inflammatory_disease|autoimmune_diseases|cancer	reproductive_system_disorder|skin_disorder	false	true	false	true	high
MONDO:0002206	sweat gland cancer	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	inflammatory_disease|autoimmune_diseases|cancer	skin_disorder	false	true	false	true	medium
MONDO:0002207	vulval Paget disease	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	dermatology|oncology|obstetrics_and_gynecology	inflammatory_disease|cancer	reproductive_system_disorder|skin_disorder	false	true	false	true	medium
MONDO:0002209	heel spur	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	true	low
MONDO:0002211	B cell deficiency	hereditary_disease|immune_system_disorder|hematologic_disorder	other	hematologic_disorder|hereditary_disease|immune_system_disorder	allergy_and_immunology|hematology	immunodeficiency_diseases|inflammatory_disease|autoimmune_diseases	immune_disorder_lymphatic_disorder	false	false	false	true	high
MONDO:0002212	pneumonic tularemia	infectious_disease	infectious_disease	infectious_disease	pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0002214	brain germinoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pediatric|neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0002216	brain sarcoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002217	central nervous system sarcoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pediatric|neurology|oncology	cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002218	temporal lobe cancer	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|throat_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002219	paraurethral gland neoplasm	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	neoplasm|cancer	reproductive_system_disorder|urinary_tract_disorder	false	true	false	false	medium
MONDO:0002220	tooth hard tissue disease	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	neurology|orthopaedic|otolaryngology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0002221	urethral urothelial papilloma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	urological_disorder|cancer	kidney_disorder|urinary_tract_disorder	false	false	false	true	low
MONDO:0002222	urethra leiomyoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|urinary_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|urinary_system_disorder|cancer_or_benign_tumor	urology	adrenal_gland_disease|cancer	muscle_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0002223	ovarian malignant mesothelioma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|autoimmune_diseases|cancer	reproductive_system_disorder|lung_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0002224	malignant ovarian cyst	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	malignant_ovarian_cyst_is_primarily_a_cancer_issue_but_can_be_related_to_other_categories_as_well_but_specifically_it_has_the_most_direct_relation_to_this_category|cancer	reproductive_system_disorder|ovarian_disorder	false	true	false	false	very_high
MONDO:0002225	ovarian sarcoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder|v____reproductive_system_disorder_was_added_because_ovarian_sarcoma_is_a_type_of_cancer_affecting_the_reproductive_system	false	true	false	false	very_high
MONDO:0002226	tuberculous oophoritis	endocrine_system_disorder|inflammatory_disease|infectious_disease|reproductive_system_disorder	infectious_disease|endocrine_system_disorder	infectious_disease|inflammatory_disease|reproductive_system_disorder|endocrine_system_disorder	urology|pulmonology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|cancer	reproductive_system_disorder|immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0002227	ovarian lymphoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	hematologic_disorder|reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	hematology|oncology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|cancer	lymphatic_disorder|reproductive_system_disorder|immune_disorder	false	false	false	false	high
MONDO:0002229	ovarian epithelial tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder|ovarian_tumor	false	true	false	false	high
MONDO:0002230	ovarian Wilms tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	pediatric|oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder|kidney_disorder	false	false	false	false	high
MONDO:0002232	nasal cavity disorder	otorhinolaryngologic_disease|respiratory_system_disorder	other	otorhinolaryngologic_disease|respiratory_system_disorder	nasal_cavity_disorder_is_closely_related_to_the_nasal_cavity__so_it_should_be_categorized_under_otolaryngology|otolaryngology	inflammatory_disease|allergy	nose_disorder|nasal_cavity_disorder	false	false	false	true	medium
MONDO:0002233	enamel caries	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	pediatric|general_public_health	inflammatory_disease|metabolic_disorder	teeth_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0002234	vaginitis	inflammatory_disease|reproductive_system_disorder	other	reproductive_system_disorder|inflammatory_disease	dermatology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0002235	eyelid neoplasm	cancer_or_benign_tumor|disorder_of_visual_system|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|cancer_or_benign_tumor	dermatology|oncology|ophthalmology	cancer|neurodegenerative_disease|inflammatory_disease|allergy|autoimmune_diseases|adrenal_gland_disease	eye_disorder|skin_disorder	false	true	false	true	medium
MONDO:0002236	ocular cancer	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|cancer_or_benign_tumor	oncology|ophthalmology	autoimmune_diseases|adrenal_gland_disease|cancer	eye_disorder	false	true	false	true	high
MONDO:0002237	carbuncle	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|infectious_disease|rheumatology	inflammatory_disease|autoimmune_diseases|allergic_reactions_is_incorrect__use_allergy	lymphatic_disorder|skin_disorder	true	false	false	true	medium
MONDO:0002238	ascending colon cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	colorectal_cancer|gastrointestinal_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002239	post-surgical hypoinsulinemia	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	pediatric|endocrinology	endocrine_disorders|autoimmune_diseases|metabolic_disorder|autoimmune_diseases___corrected__endocrine_disorders	metabolic_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0002240	acute perichondritis of pinna	otorhinolaryngologic_disease|inflammatory_disease|infectious_disease|auditory_system_disorder	infectious_disease	acute_disease|infectious_disease|post_infectious_disorder|auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	orthopaedic|otolaryngology	inflammatory_disease|autoimmune_diseases	muscle_disorder|skin_disorder|ear_disorder	true	false	false	true	medium
MONDO:0002241	factor XIII deficiency	hematologic_disorder	other	hematologic_disorder	pediatric|genetics_and_genomics|hematology	anemia|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0002242	coagulation protein disease	hematologic_disorder	other	hematologic_disorder	coagulation_protein_disease_does_also_seem_to_relate_to_genetics_and_genomics|hematology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0002243	hemorrhagic disease	hematologic_disorder	other	hematologic_disorder	renal_medicine|hepatology|hematology|cardiology	inflammatory_disease|hemorrhagic_disease|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0002244	factor VII deficiency	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0002245	blood platelet disease	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|hematology	autoimmune_diseases|blood_platelet_disease|anemia	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0002246	perichondritis of auricle	otorhinolaryngologic_disease|inflammatory_disease|infectious_disease|auditory_system_disorder	infectious_disease	infectious_disease|post_infectious_disorder|auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	rheumatology|otolaryngology	inflammatory_disease|autoimmune_diseases	joint_disorder|skin_disorder|ear_disorder	true	false	false	true	medium
MONDO:0002247	factor X deficiency	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0002249	thrombocytosis disease	hematologic_disorder	other	hematologic_disorder	hematology|cardiology	anemia|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0002250	basilar artery insufficiency	syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder	neurology|pulmonology|cardiology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	vascular_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0002251	hepatitis	endocrine_system_disorder|inflammatory_disease|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|inflammatory_disease|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0002252	granulomatous hepatitis	endocrine_system_disorder|inflammatory_disease|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|inflammatory_disease|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder	true	false	false	false	medium
MONDO:0002253	spondylosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	neurodegenerative_disease|inflammatory_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0002254	syndromic disease		other		pediatric|genetics_and_genomics	syndromic_disease|autoimmune_diseases|neurodegenerative_disease	immune_disorder__lymphatic_disorder	false	false	false	false	high
MONDO:0002255	hypertrophic elongation of cervix	reproductive_system_disorder	other	reproductive_system_disorder	pediatric|obstetrics_and_gynecology	cancer|inflammatory_disease	reproductive_system_disorder|throat_disorder	false	false	false	false	low
MONDO:0002256	cervix disorder	reproductive_system_disorder	other	reproductive_system_disorder	gynecology|obstetrics_and_gynecology	cancer|inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0002257	ankylosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0002258	pharyngitis	inflammatory_disease|respiratory_system_disorder	other	inflammatory_disease|respiratory_system_disorder	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	thorat_disorder|nose_disorder	true	false	false	true	medium
MONDO:0002259	gonadal disorder	reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	urology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0002260	hidradenitis	inflammatory_disease|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0002261	keratopathy	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0002262	capillary lymphangioma	cancer_or_benign_tumor|immune_system_disorder|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder|immune_system_disorder	pediatric|dermatology	cancer|inflammatory_disease|cardiovascular_disorder	vascular_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0002263	female reproductive system disorder	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology	female_reproductive_system_disorder|autoimmune_diseases	reproductive_system_disorder|female_reproductive_system_disorder	true	false	false	true	high
MONDO:0002265	stereotypic movement disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	mental_health_disorder|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0002266	malt worker's lung	inflammatory_disease|infectious_disease|immune_system_disorder|respiratory_system_disorder	infectious_disease	immune_system_disorder|infectious_disease|inflammatory_disease|occupational_disorder|respiratory_system_disorder	occupational_disease|pulmonology	cancer|inflammatory_disease|autoimmune_diseases	lung_disorder	false	false	false	true	high
MONDO:0002267	obstructive lung disease	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiothoracic	inflammatory_disease|obstructive_lung_disease_is_also_known_as_a_type_of_inflammatory_disease	lower_respiratory_system_disorders|lung_disorder	false	false	false	true	high
MONDO:0002268	dyspepsia	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0002269	gastroenteritis	inflammatory_disease|digestive_system_disorder	other	inflammatory_disease|digestive_system_disorder	pediatric|gastroenterology	inflammatory_disease|gastrointestinal_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0002270	viral gastritis	inflammatory_disease|infectious_disease|digestive_system_disorder	infectious_disease	infectious_disease|inflammatory_disease|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	false	low
MONDO:0002271	colon adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder_upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002272	polyclonal hypergammaglobulinemia	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	allergy_and_immunology|hematology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0002273	plasma protein metabolism disease	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|hepatology|nephrology___note__i_corrected__renal_medicine__to__nephrology	plasma_protein_metabolism_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0002274	monoclonal paraproteinemia disease	hereditary_disease|metabolic_disease|hematologic_disorder	metabolic_disease	metabolic_disease|hematologic_disorder|hereditary_disease	oncology|hematology	cancer|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0002275	generalized atherosclerosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0002277	arteriosclerosis disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|pulmonology|cardiology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0002278	benign colon neoplasm	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0002279	iron metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	endocrinology|hematology	anemia|metabolic_disorder	endocrine_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	true	high
MONDO:0002280	anemia	hematologic_disorder		hematologic_disorder	hematoloy|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0002281	macrocytic anemia	hematologic_disorder	anemia	hematologic_disorder	gastroenterology|neurology|pulmonology|endocrinology|hematology	anemia|metabolic_disorder	lower_gastrointestinal_disorder|nutritional_disorder|upper_gastrointestinal_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	true	medium
MONDO:0002282	West Nile fever	infectious_disease	infectious_disease	infectious_disease	neurology|infectious_diseases	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	immune_disorder|vascular_disorder|brain_disorder	true	false	false	false	medium
MONDO:0002283	neuroaxonal dystrophy	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0002285	pupil disorder	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	pupil_disorder_is_not_a_real_disease_so_i_assume_it_s_meant_to_be__pupil_disorder__which_can_refer_to_neuro_ophthalmic_disorders_such_as_third_nerve_palsy_or_adie_syndrome|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0002286	renal artery disease	urinary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|urinary_system_disorder	urology|renal_medicine	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	vascular_disorder|kidney_disorder	false	false	false	true	high
MONDO:0002287	glandular cystitis	inflammatory_disease|urinary_system_disorder	other	inflammatory_disease|urinary_system_disorder	urology|renal_medicine	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0002289	iris disorder	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	metabolic_disorder|autoimmune_diseases	immune_disorder|eye_disorder	false	false	false	false	medium
MONDO:0002290	clitoris cancer	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|urology|oncology	cancer|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0002291	cutaneous granular cell tumor	nervous_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer	skin_disorder|muscle_disorder	false	false	false	false	low
MONDO:0002293	cutaneous ganglioneuroma	nervous_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer|neurodegenerative_disease	skin_disorder|muscle_disorder	false	false	false	false	low
MONDO:0002295	skin glomus tumor	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer|inflammatory_disease	skin_disorder|vascular_disorder|joint_disorder|muscle_disorder|bone_disorder	false	true	false	true	low
MONDO:0002297	epidermal appendage tumor	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer|neoplasm|skin_disease	reproductive_system_disorder|skin_disorder	false	false	false	false	medium
MONDO:0002298	cutaneous glomangioma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0002299	glomangioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	neurology|oncology	cancer|adrenal_gland_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0002300	dermis tumor	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	inflammatory_disease|autoimmune_diseases|cancer	skin_disorder	false	true	false	false	low
MONDO:0002301	frontal sinus squamous cell carcinoma	respiratory_system_disorder|nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|musculoskeletal_system_disorder|connective_tissue_disorder|nervous_system_disorder|respiratory_system_disorder	oncology|otolaryngology	frontal_sinus_squamous_cell_carcinoma_is_a_type_of_cancer|cancer	upper_gastrointestinal_disorder|throat_disorder|lung_disorder|nose_disorder	false	true	false	false	high
MONDO:0002303	central retinal vein occlusion	disorder_of_visual_system|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	disorder_of_visual_system|cardiovascular_disorder|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	eye_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0002304	protein S deficiency	hematologic_disorder	other	hematologic_disorder	hematology|cardiology	metabolic_disorder|anemia	liver_disorder|vascular_disorder	false	false	false	true	high
MONDO:0002305	thrombophilia	hematologic_disorder	other	hematologic_disorder	hematology|cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0002306	angular blepharoconjunctivitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|inflammatory_disease|disorder_of_orbital_region	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder	true	false	false	true	low
MONDO:0002307	blepharoconjunctivitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease	eye_disorder	true	false	false	true	low
MONDO:0002308	giant papillary conjunctivitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|eye_disorder	true	false	false	true	medium
MONDO:0002309	papillary conjunctivitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder	true	false	false	true	low
MONDO:0002310	anterior dislocation of lens	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	corrected_to_match_the_format_specified___inflammatory_disease|anterior_dislocation_of_lens|eye_disorder|trauma|inflammation|injury	spinal_disorder|eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0002311	retinal vascular disorder	disorder_of_visual_system|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	disorder_of_visual_system|cardiovascular_disorder|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|metabolic_disorder|cardiovascular_disorder	eye_disorder|vascular_disorder	false	false	false	true	high
MONDO:0002312	opportunistic mycosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|dermatology|immunology	autoimmune_diseases|inflammatory_disease|cancer	lung_disorder|immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0002313	vernal conjunctivitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|inflammatory_disease|disorder_of_orbital_region	ophthalmology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	eye_disorder|nose_disorder	false	false	false	true	low
MONDO:0002314	chronic conjunctivitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|inflammatory_disease|disorder_of_orbital_region	ophthalmology	allergy|autoimmune_diseases|inflammatory_disease	eye_disorder|nose_disorder	false	false	false	true	medium
MONDO:0002316	motor peripheral neuropathy	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0002317	central nervous system origin vertigo	nervous_system_disorder	other	nervous_system_disorder	otolaryngology|neurology	neurodegenerative_disease|central_nervous_system_origin	ear_disorder|brain_disorder|central_nervous_system_disorder	false	false	false	true	medium
MONDO:0002318	trachea leiomyoma	respiratory_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|respiratory_system_disorder	pulmonology|cardiothoracic|otolaryngology	cancer|cardiovascular_disorder	throat_disorder|lung_disorder|muscle_disorder	false	false	false	false	low
MONDO:0002319	phosphorus metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	endocrinology|genetics_and_genomics	phosphorus_metabolism_disease|metabolic_disorder	kidney_disorder|endocrine_disorder|liver_disorder	false	false	false	false	high
MONDO:0002320	congenital nervous system disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics|pediatric	congenital_nervous_system_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0002321	sensory peripheral neuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	nerve_disorder|muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0002322	angiodysplasia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	gastroenterology|cardiology|hepatology|hematology	vascular_disease|cardiovascular_disorder	lower_gastrointestinal_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0002323	cherry hemangioma	integumentary_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|integumentary_system_disorder|cardiovascular_disorder	dermatology|hematology	cancer|skin_condition	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0002325	tooth erosion, non-bacterial	musculoskeletal_system_disorder	other	mouth_disorder|musculoskeletal_system_disorder	gastroenterology|pediatric|oral_surgery	metabolic_disorder|oral_health_disorder	lower_gastrointestinal_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0002326	alcohol-induced mental disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	mental_health_disorder|alcohol_induced_mental_disorder	brain_disorder|liver_disorder	false	false	false	true	high
MONDO:0002327	intracranial cavernous angioma	hematologic_disorder|cancer_or_benign_tumor|nervous_system_disorder|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder|hematologic_disorder|nervous_system_disorder	neurology|oncology	cancer|neurological_disease	vascular_disorder|brain_disorder	false	false	false	true	high
MONDO:0002328	intracranial hemangioma	cancer_or_benign_tumor|nervous_system_disorder|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder|nervous_system_disorder	neurology|oncology	cancer|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	false	medium
MONDO:0002329	testicular disorder	endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	urology|oncology	cancer|anemia|metabolic_disorder|autoimmune_diseases|inflammatory_disease	reproductive_system_disorder	false	false	false	false	medium
MONDO:0002330	alcoholic psychosis	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	mental_health_disorder|alcohol_dependance	brain_disorder|liver_disorder	false	false	false	true	high
MONDO:0002331	nephrosis	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	metabolic_disorder|autoimmune_diseases	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0002332	splenic disorder	hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder	genetics_and_genomics|pediatric|allergy_and_immunology|hematology|oncology|gastroenterology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0002333	splenic abscess	hematologic_disorder|infectious_disease|immune_system_disorder	infectious_disease	immune_system_disorder|infectious_disease|hematologic_disorder	neurology|hematology|oncology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder|liver_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0002334	hematopoietic and lymphoid system neoplasm	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|anemia|hematologic_cancers|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0002337	intra-abdominal hemangioma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hepatology|hematology|oncology|gastroenterology	cancer|adrenal_gland_disease	vascular_disorder|liver_disorder	false	false	false	false	low
MONDO:0002338	extratemporal epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	epilepsy|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0002340	tactile epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	mental_health_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0002341	granulomatous angiitis	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	rheumatology|dermatology|pulmonology	autoimmune_diseases|inflammatory_disease	vascular_disorder|immune_disorder	true	false	false	true	high
MONDO:0002342	chondromalacia	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0002343	splenic hemangioma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	immune_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder|hematologic_disorder	pediatric|hematology|oncology	cancer	lymphatic_disorder|vascular_disorder|liver_disorder	false	false	false	false	low
MONDO:0002345	cervicitis	reproductive_system_disorder	other	reproductive_system_disorder	rheumatology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|throat_disorder	true	false	false	true	medium
MONDO:0002347	barbiturate dependence	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	brain_disorder|liver_disorder	false	false	false	false	medium
MONDO:0002350	familial nephrotic syndrome	syndromic_disease|urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|renal_medicine|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|kidney_disorder	false	false	false	false	high
MONDO:0002351	glottis cancer	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|pulmonology|oncology	cancer	lower_gastrointestinal_disorder|throat_disorder	false	true	false	true	high
MONDO:0002352	larynx cancer	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|oncology	inflammatory_disease|cancer|adrenal_gland_disease|autoimmune_diseases	larynx_cancer|throat_disorder	false	true	false	true	high
MONDO:0002353	glottis neoplasm	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|oncology	cancer|glottis_neoplasm_falls_under_this_category_because_it_refers_to_a_tumor_of_the_vocal_cords_in_the_larynx	throat_disorder|lung_disorder	false	true	false	false	high
MONDO:0002354	benign laryngeal neoplasm	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|oncology	cancer|neoplasma	throat_disorder	false	false	false	false	low
MONDO:0002355	glottis carcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|pulmonology|oncology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|throat_disorder	false	true	false	true	high
MONDO:0002356	pancreas disorder	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	endocrinology|gastroenterology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0002357	hepatic flexure cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	hepatology|oncology|gastroenterology	cancer|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002358	laryngeal carcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|pulmonology|oncology	cancer|laryngeal_carcinoma_is_a_type_of_cancer	throat_disorder|lung_disorder	false	true	false	true	high
MONDO:0002359	periosteal chondroma	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	orthopaedic|oncology	inflammatory_disease|cancer|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0002360	chondroma	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	orthopaedic|rheumatology|oncology	cancer|tumor	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0002361	transverse colon cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002362	serous surface papilloma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|oncology	cancer	skin_disorder|eye_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0002363	papilloma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|oncology	inflammatory_disease|cancer	skin_disorder|reproductive_system_disorder	true	false	false	true	low
MONDO:0002365	kidney hemangiopericytoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|renal_medicine|oncology|hematology	cancer|tumor	vascular_disorder|kidney_disorder	false	true	false	false	medium
MONDO:0002366	autonomic nervous system neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	autonomic_nervous_system_neoplasm|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002367	kidney cancer	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|renal_medicine|oncology	cancer|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0002368	papillary serous cystadenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0002369	cystadenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|oncology	cancer|gland_disease|tumor	liver_disorder	false	false	false	false	low
MONDO:0002370	ovarian Brenner tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	ovarian_disorder|reproductive_system_disorder	false	true	false	false	low
MONDO:0002371	breast pericanalicular fibroadenoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	cancer|benign_tumor|gland_disease	skin_disorder|reproductive_system_disorder	false	false	false	false	none
MONDO:0002372	ovarian monodermal and highly specialized teratoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	cancer|teratoma_is_a_type_of_cancer	reproductive_system_disorder	false	true	false	false	high
MONDO:0002373	benign mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pulmonology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|lung_disorder	false	false	false	false	low
MONDO:0002375	sebaceous adenoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer|skin_disease	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0002376	spleen angiosarcoma	digestive_system_disorder|cancer_or_benign_tumor|hematologic_disorder|cardiovascular_disorder|immune_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|immune_system_disorder|cardiovascular_disorder|digestive_system_disorder|hematologic_disorder	oncology|hematology	cancer|adrenal_gland_disease	lymphatic_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0002377	breast intracanalicular fibroadenoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	genetics_and_genomics|obstetrics_and_gynecology|oncology	cancer|breast_disease	soft_tissue_disorder|breast_disorder|reproductive_system_disorder	false	false	false	true	none
MONDO:0002378	dermoid cyst	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|dermatology	inflammatory_disease|cancer|dermoid_cyst	skin_disorder	false	false	false	false	low
MONDO:0002379	cystic teratoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	ovarian_cancer|bone_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0002380	myoepithelial tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	surgical_oncology|oncology|pathology	cancer|adrenal_gland_disease	muscle_disorder	false	true	false	false	medium
MONDO:0002381	sweat gland neoplasm	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	inflammation|inflammatory_disease|neoplastic_diseases|cancer|adrenal_gland_disease|sweat_gland_disease|skin_cancer|autoimmune_diseases|all_inflammation|cancer____corrected_to___adrenal_gland_disease	skin_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0002382	benign mesenchymoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	orthopaedic|oncology	cancer|adrenal_gland_disease	muscle_disorder|spinal_disorder|bone_disorder	false	false	false	false	low
MONDO:0002383	Pacinian tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|dermatology	cancer|neurodegenerative_disease	nerve_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0002385	benign cystic nephroma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine	cancer|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	false	false	true	low
MONDO:0002386	mixed epithelial stromal tumor of the kidney	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine|oncology	cancer|kidney_disease|urological_disorder|tumor	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0002387	liver angiosarcoma	cardiovascular_disorder|digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder|endocrine_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder|digestive_system_disorder|endocrine_system_disorder	hepatology|oncology	cancer|adrenal_gland_disease	vascular_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0002388	intracystic papillary adenoma	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|breast_disorder	urology|oncology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	low
MONDO:0002395	renal adenoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine|oncology	cancer|renal_adenoma	renal_adenoma_fits_within_kidney_disorder_category|kidney_disorder	false	false	false	false	low
MONDO:0002396	nephrogenic adenofibroma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine	cancer|neoplasm	reproductive_system_disorder|kidney_disorder	false	false	false	false	low
MONDO:0002397	liver sarcoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	hepatology|oncology	sarcoma|cancer|liver_cancer	lower_gastrointestinal_disorder|vascular_disorder|upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0002398	mucinous adenofibroma	cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|connective_tissue_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0002399	tenosynovial giant cell tumor, localized type	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	orthopaedic|oncology	inflammatory_disease|cancer	joint_disorder|bone_disorder	false	true	false	true	medium
MONDO:0002400	synovitis	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	other	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder	true	false	false	false	medium
MONDO:0002401	malignant tenosynovial giant cell tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	oncology|orthopaedic|rheumatology	inflammatory_disease|cancer	bone_disorder|joint_disorder	false	true	false	true	high
MONDO:0002402	malignant giant cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|orthopaedic	tumor|cancer|malignancy	bone_disorder|upper_gastrointestinal_disorder|joint_disorder	false	true	false	false	very_high
MONDO:0002403	synovium cancer	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	oncology|rheumatology	inflammatory_disease|autoimmune_diseases|cancer	bone_disorder|joint_disorder	false	true	false	false	very_high
MONDO:0002404	liver hemangioma	endocrine_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder|endocrine_system_disorder	cardiovascular_disorder|endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	hematology|hepatology|gastroenterology	tumor|cancer|liver_disease	liver_disorder|vascular_disorder	false	false	false	false	low
MONDO:0002405	hepatic vascular disorder	endocrine_system_disorder|cardiovascular_disorder|digestive_system_disorder	cardiovascular_disorder|endocrine_system_disorder	cardiovascular_disorder|endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	liver_disorder|vascular_disorder	false	false	false	false	high
MONDO:0002406	dermatitis	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder	dermatology|allergic_reactions	allergy|inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0002407	capillary hemangioma	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	hematology|pulmonology|dermatology	cardiovascular_disorder|benign_tumor	skin_disorder|vascular_disorder	false	false	false	true	low
MONDO:0002408	hereditary hyperbilirubinemia	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	hematology|pediatric|hepatology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	low
MONDO:0002409	auditory system disorder		other		otolaryngology|neurology	neurodegenerative_disease|auditory_system_disorder_is_not_a_direct_match_to_any_of_the_categories__but_the_closest_fit_would_be_neurodegenerative_disease	brain_disorder|auditory_system_disorder_is_a_subset_of_both_ear_disorder_and_brain_disorder_so_it_would_be_classified_under_either|ear_disorder	false	false	false	false	high
MONDO:0002410	pyeloureteritis cystica	urinary_system_disorder|inflammatory_disease	other	inflammatory_disease|urinary_system_disorder	urology|renal_medicine	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder	true	false	false	false	medium
MONDO:0002411	narcissistic personality disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|mental_health_disorder_is_not_in_the_list_so__brain_disorder	false	false	false	false	medium
MONDO:0002412	disorder of glycogen metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|hepatology|genetics_and_genomics	disorder_of_glycogen_metabolism|metabolic_disorder	endocrine_disorder|liver_disorder	false	false	false	true	high
MONDO:0002413	glycogen storage disease I	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|pediatric|hepatology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|liver_disorder	false	false	true	true	high
MONDO:0002414	gastric hemangioma	cancer_or_benign_tumor|cardiovascular_disorder|digestive_system_disorder	cardiovascular_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	hematology|oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|vascular_disorder	false	false	false	false	low
MONDO:0002415	bone carcinoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	oncology|orthopaedic	cancer|adrenal_gland_disease	bone_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0002416	ethmoid sinus squamous cell carcinoma	respiratory_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|respiratory_system_disorder	otolaryngology|oncology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|nose_disorder	false	true	false	false	high
MONDO:0002418	ethmoid sinus adenocarcinoma	respiratory_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|respiratory_system_disorder	endocrinology|pediatric|otolaryngology|pulmonology|hematology|hepatology|neurology|oncology|renal_medicine|cardiology|gastroenterology|genetics_and_genomics|allergy_and_immunology|rheumatology|cardiothoracic	adenocarcinoma|cancer	throat_disorder|nose_disorder	false	true	false	true	high
MONDO:0002419	transient tic disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	pediatric|neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	low
MONDO:0002420	tic disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0002422	adamantinoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	oncology|genetics_and_genomics|orthopaedic	cancer|adrenal_gland_disease	teeth_disorder|bone_disorder	false	true	false	false	medium
MONDO:0002423	rectosigmoid junction neoplasm	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	colorectal_disorder|cancer|gastrointestinal_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002424	rectosigmoid carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002425	rectosigmoid junction cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	rectosigmoid_junction_cancer|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002426	lung sarcoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|oncology	lung_sarcoma_is_a_type_of_cancer|cancer	blood_bone_marrow_disorder|lung_disorder|vascular_disorder	false	true	false	false	high
MONDO:0002427	cerebellar disorder	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|cerebral_gland_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0002428	protozoa infectious disease	infectious_disease	infectious_disease	infectious_disease	infectious_disease|pediatric	inflammatory_disease|protozoa|infectious_disease	blood_bone_marrow_disorder|lymphatic_disorder|lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	medium
MONDO:0002429	idiopathic interstitial pneumonia	respiratory_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	idiopathic_disease|inflammatory_disease|infectious_disease|respiratory_system_disorder	pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	false	false	false	false	high
MONDO:0002432	malignant neoplasm of acoustic nerve	cancer_or_benign_tumor|nervous_system_disorder|auditory_system_disorder	cancer_or_benign_tumor	auditory_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	otolaryngology|neurology|oncology	neoplasm|malignant|cancer	brain_disorder|ear_disorder	false	true	false	true	high
MONDO:0002433	malignant cranial nerve neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	malignant_neoplasm|cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0002434	oculomotor nerve cancer	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|ophthalmology	neurological_disease|cancer	eye_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0002435	oculomotor nerve neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|ophthalmology	cancer|neurodegenerative_disease	eye_disorder|brain_disorder	false	true	false	false	high
MONDO:0002436	nasal disorder	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases|allergy	nasal_disorder|nose_disorder	false	false	false	true	medium
MONDO:0002437	dehydration polycythemia	immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	other	hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder	hematology|renal_medicine|cardiology|cardiothoracic	metabolic_disorder|anemia	blood_bone_marrow_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0002438	acquired polycythemia	immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	other	hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder	hematology|oncology	anemia|cancer	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0002440	erythropoietin polycythemia	immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hematologic_disorder|immune_system_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia|cancer	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0002441	Jervell and Lange-Nielsen syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0002442	long QT syndrome	syndromic_disease	other	syndromic_disease	pediatric|cardiology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0002443	bruxism	other	other	sleep_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0002444	melancholia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	endocrine_disorder|brain_disorder	false	false	false	false	high
MONDO:0002447	endometrial carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	inflammatory_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002448	laryngeal sarcoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|oncology	cancer	throat_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0002449	nodular degeneration of cornea	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0002450	prostatic adenoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	renal_medicine|urology	cancer|prostatic_adenoma	reproductive_system_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0002451	benign prostate phyllodes tumor	reproductive_system_disorder|urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	cancer	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0002452	prostate leiomyoma	reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|urology	cancer|benign_tumor	reproductive_system_disorder|muscle_disorder	false	false	false	false	low
MONDO:0002453	retrocochlear disease	auditory_system_disorder	other	auditory_system_disorder	otolaryngology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|ear_disorder	false	false	false	false	high
MONDO:0002455	exocervical carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002457	Treacher-Collins syndrome	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	otolaryngology|pediatric|genetics_and_genomics	genetic_disorder|neurodegenerative_disease|developmental_disorder|congenital_disorder	throat_disorder|joint_disorder|bone_disorder|facial_disorder|eye_disorder|ear_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0002459	type IV hypersensitivity disease	immune_system_disorder	other	immune_system_disorder	allergy_and_immunology|rheumatology	autoimmune_diseases|inflammatory_disease|allergy	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0002460	lacrimal system cancer	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|oncology	adrenal_gland_disease|cancer	nose_disorder|eye_disorder	false	true	false	false	high
MONDO:0002461	membranoproliferative glomerulonephritis	urinary_system_disorder|inflammatory_disease	other	urinary_system_disorder|inflammatory_disease	hematology|renal_medicine	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	immune_disorder|kidney_disorder|vascular_disorder	false	false	false	true	high
MONDO:0002462	glomerulonephritis	urinary_system_disorder|inflammatory_disease	other	urinary_system_disorder|inflammatory_disease	renal_medicine|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|kidney_disorder	true	false	false	true	high
MONDO:0002463	lacrimal gland carcinoma	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_orbital_region	otolaryngology|ophthalmology|oncology	adrenal_gland_disease|cancer	eye_disorder	false	true	false	false	high
MONDO:0002464	lacrimal gland cancer	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_orbital_region	otolaryngology|ophthalmology|oncology	adrenal_gland_disease|cancer	eye_disorder	false	true	false	false	high
MONDO:0002465	bronchiolitis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|throat_disorder|lower_gastrointestinal_disorder|lung_disorder	true	false	false	false	high
MONDO:0002466	eye carcinoma	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|oncology	eye_carcinomas_are_a_subtype_of_cancer|cancer	skin_disorder|eye_disorder	false	true	false	true	high
MONDO:0002467	inner ear disorder	otorhinolaryngologic_disease|auditory_system_disorder	other	auditory_system_disorder|otorhinolaryngologic_disease	otolaryngology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	inner_ear_disorder|ear_disorder	false	false	false	false	medium
MONDO:0002468	hyperimmunoglobulin syndrome	hereditary_disease|hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder|hereditary_disease	allergy_and_immunology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0002469	lacrimal gland carcinoma ex pleomorphic adenoma	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region|nervous_system_disorder	otolaryngology|ophthalmology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|eye_disorder	false	true	false	false	high
MONDO:0002470	photosensitive trichothiodystrophy	metabolic_disease|hereditary_disease|syndromic_disease|integumentary_system_disorder	metabolic_disease	syndromic_disease|metabolic_disease|radiation_induced_disorder|hereditary_disease|integumentary_system_disorder	pediatric|genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0002471	bursitis	inflammatory_disease|musculoskeletal_system_disorder	other	inflammatory_disease|musculoskeletal_system_disorder	rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease	muscle_disorder|joint_disorder	false	false	false	true	medium
MONDO:0002472	carcinoma ex pleomorphic adenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pathology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|skin_disorder	false	true	false	true	high
MONDO:0002473	cystic kidney disease	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|genetics_and_genomics|urology	kidney_disease|metabolic_disorder|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0002474	primary hyperoxaluria	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	renal_medicine|genetics_and_genomics|urology	adrenal_gland_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0002475	lacrimal gland adenocarcinoma	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_orbital_region	otolaryngology|oncology|ophthalmology	gland_disease|cancer|adenocarcinoma	upper_gastrointestinal_disorder|eye_disorder	false	true	false	false	high
MONDO:0002476	anuria	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	autoimmune_diseases|metabolic_disorder|anemia|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0002477	prostate neuroendocrine neoplasm	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|urology	neoplasm|cancer|neuroendocrine_cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0002478	mixed germ cell-sex cord-stromal tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	false	high
MONDO:0002479	Sertoli-Leydig cell tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|urology|endocrinology	reproductive_system_disorder|cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0002480	endometrioid tumor	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0002481	ovarian neuroendocrine neoplasm	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	neuroendocrine_tumor|cancer|ovarian_cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002482	nipple neoplasm	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|breast_disorder	oncology|obstetrics_and_gynecology	cancer	nipple_neoplasm_does_not_seem_to_fit_any_categories_listed_above|skin_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0002483	breast myoepithelial tumor	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	false	false	false	medium
MONDO:0002485	breast neuroendocrine neoplasm	breast_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|breast_disorder	oncology|obstetrics_and_gynecology|neurology|endocrinology	adrenal_gland_disease|cancer|neuroendocrine_cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0002486	lobular neoplasia	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|breast_disorder_is_not_in_the_list__however__lobular_neo_plasia_refers_to_a_type_of_breast_cancer_so_if_we_consider__breast__as_being_related_to_the_lower_gastrointestinal_system_then__lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0002487	breast granular cell tumor	breast_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|breast_disorder	oncology|obstetrics_and_gynecology|dermatology	adrenal_gland_disease|cancer	skin_disorder|reproductive_system_disorder	false	true	false	false	low
MONDO:0002488	intraductal breast neoplasm	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|obstetrics_and_gynecology	cancer|intraductal_breast_neoplasm_fits_best_into_the_category_of_cancer	breast_disorder|skin_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0002489	malignant breast phyllodes tumor	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	breast_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002490	breast sarcoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|obstetrics_and_gynecology	cancer	reproductive_system_disorder|bone_disorder	false	true	false	false	high
MONDO:0002491	substance abuse	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder	brain_disorder	false	false	false	true	high
MONDO:0002492	acute kidney failure	urinary_system_disorder	other	urinary_system_disorder|acute_disease	renal_medicine|nephrology	autoimmune_diseases|cardiovascular_disorder|metabolic_disorder|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0002493	prostatic acinar adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	prostatic_acinar_adenocarcinoma|adenocarcinoma|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0002494	substance-related disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	substance_related_disorder_is_sometimes_considered_a_mental_health_disorder|mental_health_disorder	brain_disorder|substance_related_disorder	false	false	false	false	high
MONDO:0002495	colon signet ring cell adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	autoimmune_diseases|adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0002496	submucosal invasive colon adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	adrenal_gland_disease|cancer|submucosal_invasive_colon_adenocarcinoma	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002501	brain glioblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0002503	adult astrocytic tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0002505	childhood astrocytic tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|pediatric|oncology	other_is_incorrect__the_correct_answer_is_just_the_first_two__cancer|neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0002507	gingival overgrowth	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	dental_surgery|periodontics|oral_medicine	gingival_overgrowth_is_frequently_seen_in_association_with_metabolic_disorders_such_as_diabetes|metabolic_disorder	teeth_disorder|skin_disorder	false	false	false	true	medium
MONDO:0002508	gingivitis	musculoskeletal_system_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|inflammatory_disease|mouth_disorder	pediatric|otolaryngology|hematology	autoimmune_diseases|inflammatory_disease	teeth_disorder|oral_disorder_is_incorrect_it_should_be_teeth_disorder|nose_disorder|skin_disorder	true	false	false	true	low
MONDO:0002509	non-specific granulomatous orchitis	endocrine_system_disorder|inflammatory_disease|reproductive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|inflammatory_disease|reproductive_system_disorder	rheumatology|urology|allergy_and_immunology|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0002511	stenosis of lacrimal sac	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|otolaryngology	allergy|autoimmune_diseases|inflammatory_disease	eye_disorder|nose_disorder	false	false	false	false	low
MONDO:0002512	papillary adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	gynecology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lung_disorder	false	true	false	true	high
MONDO:0002513	kidney benign neoplasm	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine|oncology	neoplasm|cancer	urinary_tract_disorder|kidney_disorder	false	false	false	true	low
MONDO:0002514	hepatobiliary neoplasm	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	hepatology|gastroenterology|oncology	hepatobiliary_neoplasm|cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	true	very_high
MONDO:0002515	hepatobiliary disorder	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	hepatobiliary_disorder|metabolic_disorder	liver_disorder|biliary_disorder	false	false	false	true	high
MONDO:0002516	digestive system cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	digestive_system_cancer|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0002517	tenosynovitis of foot and ankle	inflammatory_disease|connective_tissue_disorder|musculoskeletal_system_disorder	other	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder	rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease	joint_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0002518	gallbladder papillary neoplasm	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	true	medium
MONDO:0002519	anus disorder	digestive_system_disorder	other	digestive_system_disorder	urology|gastroenterology	autoimmune_diseases|cancer|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0002520	hepatic porphyria	digestive_system_disorder|endocrine_system_disorder|metabolic_disease	metabolic_disease|endocrine_system_disorder	metabolic_disease|digestive_system_disorder|endocrine_system_disorder	hepatology|genetics_and_genomics|gastroenterology	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0002522	tenosynovial giant cell tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	rheumatology|orthopaedic|oncology	cancer|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	true	medium
MONDO:0002523	cutaneous mucinosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|skin_disorder	false	false	false	false	medium
MONDO:0002525	inherited lipid metabolism disorder	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	metabolism_is_not_listed_so_the_closest_would_be__genetics_and_genomics|pediatric|endocrinology|genetics_and_genomics	inherited_lipid_metabolism_disorder|metabolic_disorder	lipid_metabolism_disorder|liver_disorder	false	false	false	false	high
MONDO:0002526	dermal unilateral segmental cavernous angioma	cancer_or_benign_tumor|cardiovascular_disorder|hematologic_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hematologic_disorder|cardiovascular_disorder|cancer_or_benign_tumor	dermatology|oncology|neurology	neurological_disease|vascular_disorder	vascular_disorder|skin_disorder	false	false	false	false	medium
MONDO:0002527	keratoacanthoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|ophthalmology	skin_disease|cancer	eye_disorder|skin_disorder	false	true	false	true	low
MONDO:0002528	synovium neoplasm	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	rheumatology|oncology	inflammatory_disease|cancer	joint_disorder|blood_bone_marrow_disorder	false	true	false	false	medium
MONDO:0002529	skin squamous cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	inflammatory_disease|cancer	lower_gastrointestinal_disorder|skin_disorder	false	true	false	true	medium
MONDO:0002531	skin neoplasm	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	skin_neoplasm|cancer	skin_disorder	false	true	false	true	medium
MONDO:0002532	squamous cell neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|oncology	squamous_cell_neoplasm_fits_best_into_a_subcategory_of_cancer|cancer	lung_disorder|skin_disorder	false	true	false	true	high
MONDO:0002533	papillary adenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	endocrinology|obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	low
MONDO:0002534	fallopian tube papilloma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	genital_system_disease|cancer	reproductive_system_disorder	false	false	false	false	low
MONDO:0002535	verrucous papilloma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|oncology	skin_disease|cancer	lower_gastrointestinal_disorder|skin_disorder	false	false	false	true	low
MONDO:0002536	skin papilloma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	skin_disease|cancer	lower_gastrointestinal_disorder|skin_disorder	true	false	false	true	low
MONDO:0002537	inverted papilloma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|otolaryngology|oncology	cancer	throat_disorder|eye_disorder	false	true	false	true	medium
MONDO:0002540	childhood oligodendroglioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002541	spinal cord oligodendroglioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002542	spinal cord glioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0002543	adult oligodendroglioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0002544	brain oligodendroglioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002545	spinal cord disorder	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_cord_disorder____spinal_disorder_muscle_disorder|spinal_disorder_muscle_disorder	false	false	false	false	high
MONDO:0002546	schwannoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	low
MONDO:0002547	nerve sheath neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer	nerve_disorder|brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0002548	cellular schwannoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0002549	schwannoma of twelfth cranial nerve	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	otolaryngology|oncology|neurology	neurodegenerative_disease|cancer	ear_disorder|brain_disorder	false	true	false	false	medium
MONDO:0002550	hypoglossal nerve neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	otolaryngology|oncology|neurology	cancer|neurodegenerative_disease	spinal_disorder|throat_disorder	false	true	false	false	high
MONDO:0002551	c-P angle neurinoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	otolaryngology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0002552	vascular myelopathy	nervous_system_disorder	other	nervous_system_disorder	cardiology|vascular|neurology	inflammatory_disease|cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0002553	cerebellopontine angle tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	otolaryngology|oncology|neurology	neurodegenerative_disease|cancer	ear_disorder|brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002554	sympathetic neurilemmoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder|nerve_disorder	false	false	false	false	low
MONDO:0002555	trigeminal schwannoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	otolaryngology|oncology|neurology	neurological_cancer|cancer	ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0002556	microcystic/reticular schwannoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurological_cancer|cancer	brain_disorder|spinal_disorder	false	true	false	false	low
MONDO:0002558	melanotic neurilemmoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|dermatology|neurology	neurodegenerative_disease|cancer	skin_disorder|brain_disorder	false	true	false	false	high
MONDO:0002559	plexiform schwannoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	genetics_and_genomics|oncology|neurology	neurological_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0002561	lysosomal storage disease	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatrics|neurology	neurodegenerative_disease|metabolic_disorder	lysosomal_storage_disease_is_more_specifically_a_group_of_disorders_so_the_category_should_be_broad_enough_to_encompass_this|liver_disorder	false	false	false	true	very_high
MONDO:0002562	demyelinating disease	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	immune_disorder|brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0002563	jejunal somatostatinoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	endocrinology|gastroenterology	cancer|endocrine_disorder|gastrointestinal_disease	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002564	jejunal neoplasm	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|neoplastic_disease|gastrointestinal_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002565	myelitis	nervous_system_disorder|inflammatory_disease	other	nervous_system_disorder|inflammatory_disease	hematology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0002567	tracheal disorder	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|otolaryngology	inflammatory_disease|respiratory_disorder	throat_disorder|lung_disorder	false	false	false	false	high
MONDO:0002568	tracheal stenosis	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology|otolaryngology	respiratory_disease___note__i_corrected_it_to_cardiovascular_disorder_as_the_more_suitable_category__the_other_option_was_respiratory_disease_which_is_not_in_the_original_list|cardiovascular_disorder	throat_disorder|lung_disorder	false	false	false	true	high
MONDO:0002569	gastric dilatation	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|gastrointestinal_disorder_is_not_in_the_list_but_closest_match_is|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0002570	high pressure neurological syndrome	nervous_system_disorder	other	nervous_system_disorder	psychiatry|neurology	high_pressure_neurological_syndrome_is_related_to_the_nervous_system_and_can_cause_neurological_symptoms__therefore_it_also_falls_under____inflammatory_disease__cardiovascular_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0002571	primary central nervous system lymphoma	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder|nervous_system_disorder	cancer_or_benign_tumor	hematologic_disorder|nervous_system_disorder|cancer_or_benign_tumor|post_infectious_disorder|immune_system_disorder	hematology|oncology|neurology	cancer|lymphoma	immune_disorder|brain_disorder|spinal_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0002572	aspiration pneumonitis	respiratory_system_disorder|inflammatory_disease	other	respiratory_system_disorder|inflammatory_disease	respiratory|pulmonology|cardiology	inflammatory_disease|respiratory_disorder	upper_gastrointestinal_disorder|lung_disorder|throat_disorder	false	false	false	false	medium
MONDO:0002574	prostate embryonal rhabdomyosarcoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	cancer|adrenal_gland_disease	muscle_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002576	embryonal extrahepatic bile duct rhabdomyosarcoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	pediatric|genetics_and_genomics|oncology	cancer|rhabdomyosarcoma	muscle_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0002577	extrahepatic bile duct rhabdomyosarcoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	pediatric|oncology	cancer	muscle_disorder|upper_gastrointestinal_disorder|biliary_disorder|liver_disorder	false	true	false	false	high
MONDO:0002578	botryoid rhabdomyosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	cancer	muscle_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002579	orbit embryonal rhabdomyosarcoma	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|disorder_of_orbital_region|cancer_or_benign_tumor	pediatric|ophthalmology|oncology	cancer	eye_disorder|muscle_disorder	false	true	false	true	high
MONDO:0002580	orbit rhabdomyosarcoma	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|disorder_of_orbital_region|cancer_or_benign_tumor	pediatric|oncology	cancer|soft_tissue_sarcoma|orbital_disease|pediatric_cancer	eye_disorder|muscle_disorder	false	true	false	true	high
MONDO:0002581	spindle cell rhabdomyosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology|pediatric	cancer|sarcoma	soft_tissue_disorder|muscle_disorder	false	true	false	false	high
MONDO:0002582	subacute leukemia	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|acute_disease	hematology|oncology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0002583	mucinous ovarian cystadenoma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|gynecological_cancer|ovarian_cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0002585	breast fibrocystic change, proliferative type	breast_disorder	other	breast_disorder	obstetrics_and_gynecology|oncology	autoimmune_diseases|cancer|inflammatory_disease	breast_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0002586	thymus cancer	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology|allergy_and_immunology	autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder	false	true	false	false	medium
MONDO:0002587	encapsulated thymoma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology|cardiology	autoimmune_diseases|cancer|inflammation_disease	immune_disorder|lymphatic_disorder	false	true	false	true	low
MONDO:0002588	thymoma type A	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology|allerg_and_immunology	autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder	false	true	false	false	low
MONDO:0002590	combined thymoma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	immunology|hematology|oncology	autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder|endocrine_disorder	true	true	false	true	high
MONDO:0002592	invasive malignant thymoma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cardiothoracic|pulmonology|oncology	cancer|invasive_malignant_thymoma_fits_more_closely_into_cancer_and_also_can_be_categorized_under_an_autoimmune_disease_due_to_thymomas_often_being_associated_with_autoimmune_disorders__but_the_most_fitting_category_is_cancer	lung_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0002594	monkeypox	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0002595	vaccinia	infectious_disease	infectious_disease	infectious_disease	immunology|pediatric|dermatology	autoimmune_diseases|inflammatory_disease|viral_infection	immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0002597	notochordal tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	oncology|genetics_and_genomics|pediatric	tumor|cancer|inflammatory_disease	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0002598	germinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric	cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0002599	teratocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics	tumor|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0002601	teratoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	tumor|cancer	reproductive_system_disorder	false	true	false	false	medium
MONDO:0002602	central nervous system disorder	nervous_system_disorder	other	nervous_system_disorder	psychiatry|neurology	central_nervous_system_disorder|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0002603	angiomyolipoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	renal_medicine|urology	adrenal_gland_disease|cancer	vascular_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0002604	pericytic neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology	neurodegenerative_disease|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	medium
MONDO:0002605	hepatic angiomyolipoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	hepatology|gastroenterology	metabolic_disorder|cancer	liver_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0002606	epithelioid type angiomyolipoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	renal_medicine|urology|oncology	adrenal_gland_disease|cancer	vascular_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0002610	purpura	hematologic_disorder	other	hematologic_disorder	hematology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|vascular_disorder|immune_disorder	false	false	false	false	medium
MONDO:0002612	frontal lobe epilepsy	nervous_system_disorder	other	nervous_system_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0002613	histrionic personality disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder	brain_disorder	false	false	false	false	medium
MONDO:0002614	bone inflammation disease	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|muscle_disorder|spinal_disorder|bone_disorder	false	false	false	true	medium
MONDO:0002615	xanthomatosis	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|lipid_disorder|liver_disorder	false	false	false	true	medium
MONDO:0002616	mesenchymal cell neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematolog|oncology	cancer|neoplasm	muscle_disorder|blood_bone_marrow_disorder	false	true	false	false	medium
MONDO:0002617	bone angiosarcoma	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	orthopaedic|oncology	cancer|adrenal_gland_disease	vascular_disorder|blood_bone_marrow_disorder|bone_disorder	false	true	false	false	very_high
MONDO:0002618	undifferentiated high grade pleomorphic sarcoma of bone	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	orthopaedic|oncology|genetics_and_genomics	cancer|sarcoma|adrenal_gland_disease	blood_bone_marrow_disorder|bone_disorder	false	true	false	false	very_high
MONDO:0002619	bone fibrosarcoma	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	orthopaedic|oncology	cancer	blood_bone_marrow_disorder|bone_disorder	false	true	false	false	high
MONDO:0002620	localized osteosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	orthopaedic|oncology	cancer|localized_cancer	spinal_disorder|bone_disorder	false	true	false	true	high
MONDO:0002621	extraosseous osteosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	orthopaedic|oncology	cancer|allergy|inflammatory_disease|anemia|neurodegenerative_disease|mental_health_disorder|cardiovascular_disorder|adrenal_gland_disease|autoimmune_diseases|metabolic_disorder	spinal_disorder|bone_disorder	false	true	false	false	high
MONDO:0002622	multifocal osteogenic sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	orthopaedic|oncology	cancer	spinal_disorder|bone_disorder	false	true	false	false	very_high
MONDO:0002623	pediatric osteosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|orthopaedic|oncology	cancer|pediatric	joint_disorder|bone_disorder	false	true	false	true	high
MONDO:0002624	bone leiomyosarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|post_infectious_disorder|cancer_or_benign_tumor	orthopaedic|oncology	cancer	muscle_disorder|bone_disorder	false	true	false	false	very_high
MONDO:0002625	Ewing sarcoma of bone	cancer_or_benign_tumor|musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease|cancer_or_benign_tumor	pediatric|orthopaedic|oncology	cancer	blood_bone_marrow_disorder|bone_disorder	false	true	false	true	high
MONDO:0002626	spinal accessory nerve neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology|neurology	cancer|neurodegenerative_disease	nerve_disorder|muscle_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002627	chondroblastic osteosarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	orthopaedic|oncology	cancer|sarcoma|tumor	joint_disorder|bone_disorder	false	true	false	false	very_high
MONDO:0002628	peripheral osteosarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	orthopaedic|oncology	cancer	joint_disorder|spinal_disorder|bone_disorder	false	true	false	false	high
MONDO:0002629	bone osteosarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	orthopaedic|oncology	cancer|bone_cancer|skeletal_disease	joint_disorder|muscle_disorder|spinal_disorder|upper_gastrointestinal_disorder|bone_disorder	false	true	false	true	very_high
MONDO:0002630	small cell osteogenic sarcoma	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|orthopaedic|pulmonology	cancer	bone_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0002631	conventional osteosarcoma	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|orthopaedic	cancer	joint_disorder|spinal_disorder|bone_disorder	false	true	false	true	very_high
MONDO:0002632	metachronous osteosarcoma of the bone	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|orthopaedic	cancer|metastatic_cancer	bone_disorder	false	true	false	false	high
MONDO:0002633	cranial nerve neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002634	liposarcoma of bone	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|orthopaedic|hematology	cancer	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0002635	periodontal disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	oral_medicine|general_practice___note__i_replaced_dermatology_with_oral_medicine_as_it_is_more_relevant_to_the_disease_in_question__general_practice_is_often_associated_with_periodontal_disorders__which_often_require_a_comprehensive_approach	autoimmune_diseases|metabolic_disorder|inflammatory_disease	joint_disorder|teeth_disorder	true	false	false	true	medium
MONDO:0002636	accessory nerve disorder	nervous_system_disorder	other	nervous_system_disorder	otolaryngology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0002637	histiocytosis	immune_system_disorder	other	immune_system_disorder	oncology|hematatology|immunology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0002638	glossopharyngeal nerve neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology|neurology	cancer|neurodegenerative_disease	brain_disorder|ear_disorder|throat_disorder	false	true	false	false	high
MONDO:0002639	glossopharyngeal nerve disorder	nervous_system_disorder	other	nervous_system_disorder	otolaryngology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	ear_disorder|throat_disorder	false	false	false	false	medium
MONDO:0002640	optic nerve neoplasm	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	oncology|ophthalmology|neurology	cancer|neurodegenerative_disease	brain_disorder|eye_disorder	false	true	false	false	high
MONDO:0002641	subclavian artery aneurysm	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	vascular|cardiology	cardiovascular_disorder|vascular_disease	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0002642	trochlear nerve neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology|neurology	autoimmune_diseases|cancer|adrenal_gland_disease|neurodegenerative_disease|inflammatory_disease	brain_disorder|eye_disorder	false	true	false	false	high
MONDO:0002643	vestibular disorder	psychiatric_disorder|nervous_system_disorder|otorhinolaryngologic_disease|auditory_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|otorhinolaryngologic_disease|auditory_system_disorder	otolaryngology|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|ear_disorder	false	false	false	true	medium
MONDO:0002644	idiopathic granulomatous myositis	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|idiopathic_disease|inflammatory_disease	rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|muscle_disorder	false	false	false	false	high
MONDO:0002645	cerebritis	nervous_system_disorder|inflammatory_disease	other	nervous_system_disorder|inflammatory_disease	allergy_and_immunology|infectious_disease|neurology	autoimmune_diseases|inflammatory_disease	brain_disorder|cerebrospinal_disorder	true	false	false	true	high
MONDO:0002646	viral laryngitis	infectious_disease|respiratory_system_disorder|inflammatory_disease	infectious_disease	infectious_disease|acute_disease|respiratory_system_disorder|inflammatory_disease	otolaryngology|pediatric	autoimmune_diseases|inflammatory_disease	nose_disorder|throat_disorder	true	false	false	false	low
MONDO:0002647	laryngitis	respiratory_system_disorder|inflammatory_disease	other	respiratory_system_disorder|inflammatory_disease	otolaryngology|pulmonology	autoimmune_diseases|inflammatory_disease	throat_disorder|lung_disorder	true	false	false	false	low
MONDO:0002648	mammary Paget disease	breast_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	oncology|dermatology	autoimmune_diseases|cancer|inflammatory_disease	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0002649	scrotum Paget disease	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	dermatology|urology	cancer|skin_disease	reproductive_system_disorder|skin_disorder	false	true	false	false	medium
MONDO:0002650	scrotal carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	cancer|adrenal_gland_disease|inflammatory_disease	reproductive_system_disorder|other___corrected_response___reproductive_system_disorder	false	true	false	false	high
MONDO:0002651	anal Paget disease	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|orthopaedic	cancer|metabolic_disorder	blood_bone_marrow_disorder|bone_disorder	false	true	false	false	high
MONDO:0002652	anus adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|other____corrected_answer__cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002653	Paget disease of the penis	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	dermatology|urology	cancer|autoimmune_diseases	bone_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0002654	uterine disorder	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|uterine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0002655	cutaneous Paget disease	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|autoimmune_diseases	lower_gastrointestinal_disorder|skin_disorder	false	true	false	false	medium
MONDO:0002656	skin carcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|skin_carcinoma_can_also_fall_under_other_categories_such_as_inflammatory_disease_however_the_primary_category_is_cancer	skin_carcinoma|skin_disorder	false	true	false	true	low
MONDO:0002657	breast disorder		other		oncology|obstetrics_and_gynecology	cancer|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0002658	iris cancer	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|cancer_or_benign_tumor	oncology|ophthalmology	autoimmune_diseases|cancer|adrenal_gland_disease	eye_disorder|vascular_disorder|immune_disorder	false	true	false	false	high
MONDO:0002659	uveal cancer	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|cancer_or_benign_tumor	oncology|ophthalmology	autoimmune_diseases|cancer	eye_disorder	false	true	false	false	high
MONDO:0002660	blepharochalasis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0002661	uveal disorder	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0002664	extrahepatic bile duct signet ring cell carcinoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	autoimmune_diseases|cancer|adrenal_gland_disease|inflammatory_disease	liver_disorder|biliary_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0002665	extrahepatic bile duct adenocarcinoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0002666	pancreatic signet ring cell adenocarcinoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|adrenal_gland_disease|pancreatic_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0002667	gallbladder signet ring cell adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|hepatology|gastroenterology	cancer|gallbladder_disease	liver_disorder|biliary_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0002669	ampullary signet ring cell adenocarcinoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	h_hepatology|oncology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002670	ampulla of vater adenocarcinoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology|pediatric	adenocarcinoma|cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0002671	signet ring cell breast carcinoma	breast_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease|other_____corrected_answer____cancer	breast_carcinoma|reproductive_system_disorder	false	true	false	false	high
MONDO:0002672	acinar prostate adenocarcinoma, signet ring variant	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002674	stricture or kinking of ureter	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	adrenal_gland_disease|urogenital_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0002675	neurofibrosarcoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|genetics_and_genomics|neurology	cancer|neurofibromatosis_associated_disorders_aren_t_in_the_list_but_neurofibrosarcoma_is_related_to_it__so_cancer_fits_best	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0002676	adult fibrosarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	oncology|orthopaedic	cancer|adrenal_gland_disease|autoimmune_diseases	vascular_disorder|muscle_disorder|bone_disorder	false	true	false	false	high
MONDO:0002677	conventional fibrosarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	oncology|orthopaedic|hematology	cancer	vascular_disorder|bone_disorder	false	true	false	true	high
MONDO:0002678	pediatric fibrosarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	oncology|pediatric	pediatric_fibrosarcoma_is_a_type_of_cancer|cancer	lymphatic_disorder|muscle_disorder|spinal_disorder|bone_disorder	false	true	false	true	high
MONDO:0002679	cerebral infarction	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	cardiology|neurology	neurodegenerative_disease|cardiovascular_disorder	vascular_disorder|brain_disorder	false	false	false	true	high
MONDO:0002681	choroid plexus cancer	cardiovascular_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	oncology|ophthalmology|neurology	cancer|tumors|neurological_disorder	brain_disorder|eye_disorder	false	true	false	false	very_high
MONDO:0002682	cerebral ventricle cancer	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0002683	adult choroid plexus neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|ophthalmology|neurology	cancer|neurodegenerative_disease	brain_disorder|eye_disorder	false	true	false	false	high
MONDO:0002684	atypical choroid plexus papilloma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|ophthalmology|neurology	cancer|neurodegenerative_disease	brain_disorder|eye_disorder	false	true	false	true	high
MONDO:0002685	childhood choroid plexus carcinoma	cardiovascular_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	oncology|pediatric|neurology	pediatric_cancer|cancer|neurological_disorder	brain_disorder|eye_disorder	false	true	false	true	high
MONDO:0002687	superior mesenteric artery syndrome	cardiovascular_disorder|digestive_system_disorder|syndromic_disease	cardiovascular_disorder	cardiovascular_disorder|digestive_system_disorder|syndromic_disease	gastroenterology|emergency_medicine|general_surgery	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	vascular_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0002688	duodenal obstruction	digestive_system_disorder	other	digestive_system_disorder	obstetrics_and_gynecology|gastroenterology|pediatric|general_surgery	cancer|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0002691	liver cancer	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology|hepatology	cancer|liver_cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	false	true	false	true	very_high
MONDO:0002692	intracranial sinus thrombosis	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	neurology|hematology	neurological_disease|cardiovascular_disorder|inflammatory_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0002693	lateral sinus thrombosis	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	otolaryngology|neurology|hematology	cardiovascular_disorder|inflammatory_disease	ear_disorder|vascular_disorder|brain_disorder	true	false	false	false	high
MONDO:0002694	cavernous sinus thrombosis	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	neurology|hematology	inflammatory_disease_cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0002695	sagittal sinus thrombosis	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	otolaryngology|neurology|hematology	cardiovascular_disorder|inflammatory_disease	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0002696	Sertoli cell tumor	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	cancer|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0002697	ovarian gonadoblastoma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology|pediatric	cancer|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0002698	testicular gonadoblastoma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|pediatric|oncology	cancer	blood_bone_marrow_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0002701	ovarian mucinous cystadenocarcinoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	female_reproductive_system_disorder|ovarian_malignancy|cancer	upper_gastrointestinal_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002702	ovarian cystadenocarcinoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|ovarian_cystadenocarcinoma_is_a_type_of_cancer_that_affects_the_ovaries__therefore__it_falls_under_reproductive_system_disorder__the_category__ovarian_cystadenocarcinoma__specifically_refers_to_a_tumor_or_cyst_in_the_ovary_which_can_be_benign_or_malignant_and_therefore__the_second_best_fit_would_also_be_reproductive_system_disorder	false	true	false	false	very_high
MONDO:0002703	appendix mucinous cystadenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002705	breast mucinous cystadenocarcinoma	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	breast_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0002706	cervix endometriosis	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|gastroenterology|endocrinology|hormonal_dysfunction	inflammatory_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0002707	breast mucinous carcinoma	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	malignant_tumor|cancer|breast_cancer	upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0002708	retinitis	inflammatory_disease|nervous_system_disorder|disorder_of_visual_system	other	disorder_of_orbital_region|inflammatory_disease|disorder_of_visual_system|nervous_system_disorder	ophthalmology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	eye_disorder	true	false	false	false	high
MONDO:0002710	infiltrating angiolipoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	neurology|oncology|orthopaedic	adrenal_gland_disease|cancer	spinal_disorder|vascular_disorder	false	true	false	false	medium
MONDO:0002712	epidural spinal canal angiolipoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	neurology|oncology	cancer|neurological_cancer	spinal_disorder|vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0002713	epidural spinal canal neoplasm	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	neurology|oncology	spinal_cord_tumor|cancer|neurological_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0002714	central nervous system cancer	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|central_nervous_system_cancer	brain_disorder_spinal_disorder	false	true	false	true	very_high
MONDO:0002715	uterine cancer	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer	upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0002716	childhood spinal cord tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|neurology|oncology	cancer|neurological_disease	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0002717	spinal cord intramedullary teratoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|neurology|oncology|genetics_and_genomics	neurodegenerative_disease|cancer	spinal_disorder	false	true	false	false	high
MONDO:0002718	central nervous system teratoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|neurology|oncology	cancer|neurological_cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0002719	conus medullaris neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0002720	sella turcica neoplasm	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	neurology|oncology	neurodegenerative_disease|inflammatory_disease|cancer|autoimmune_diseases	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0002721	necrosis of pituitary	endocrine_system_disorder|nervous_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	neurology|endocrinology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|cancer|autoimmune_diseases	brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0002722	olfactory nerve neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|otolaryngology	neurodegenerative_disease|cancer	nose_disorder|brain_disorder	false	true	false	false	high
MONDO:0002724	mast cell neoplasm	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematatology	allergy|cancer|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0002726	cutaneous solitary mastocytoma	hereditary_disease|immune_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder|hematologic_disorder|inflammatory_disease	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|inflammatory_disease|cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder	oncology|dermatology	cutaneous_mastocytosis|allergy|cancer	immune_disorder|skin_disorder|blood_bone_marrow_disorder	false	false	false	true	low
MONDO:0002727	olfactory nerve disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	nose_disorder|brain_disorder	false	false	false	false	low
MONDO:0002728	rhabdoid tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|neurology|oncology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0002729	rhabdoid tumor of the kidney	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	pediatric|urology|oncology	kidney_cancer|urogenital_system_disorder|adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	very_high
MONDO:0002730	childhood kidney neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology|pediatric	childhood_disease|kidney_neoplasm|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0002731	cerebral hemisphere cancer	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0002732	lung benign neoplasm	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|pulmonology	lung_benign_neoplasm_can_also_fall_under_this_category__lung_cancer_is_a_type_of_neoplasm__specifically_a_malignant_one__but_benign_neoplasms_occur_in_the_lungs_as_well|cancer	lung_disorder|lung_benign_neoplasm	false	false	false	true	low
MONDO:0002734	anal mucinous adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002735	anal canal adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	urology|oncology	inflammatory_disease___corrected_list_without__other__and_categories_that_are_less_likely_to_be_a_good_fit____cancer|allergy|inflammatory_disease|adrenal_gland_disease|cancer|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002736	ampulla of vater mucinous adenocarcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002737	acute sanguinous otitis media	inflammatory_disease|otorhinolaryngologic_disease|auditory_system_disorder	other	acute_disease|auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	throat_disorder|ear_disorder	true	false	false	false	medium
MONDO:0002738	acute transudative otitis media	inflammatory_disease|otorhinolaryngologic_disease|auditory_system_disorder	other	acute_disease|auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|throat_disorder|ear_disorder	true	false	false	false	medium
MONDO:0002739	extrahepatic bile duct mucinous adenocarcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology	allergy|inflammatory_disease|adrenal_gland_disease|cancer|autoimmune_diseases	liver_disorder|lower_gastrointestinal_disorder|biliary_disorder	false	true	false	false	high
MONDO:0002740	uterine ligament mucinous adenocarcinoma	musculoskeletal_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0002741	uterine ligament adenocarcinoma	musculoskeletal_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	inflammatory_disease|cancer|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002742	cervical mucinous adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|autoimmune_diseases	upper_gastrointestinal_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002744	fallopian tube mucinous adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002745	fallopian tube mucinous tumor	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|gynecologic_malignancy|ovarian_cancer_related_disorder	false	true	false	false	high
MONDO:0002746	fallopian tube adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	inflammatory_disease|adrenal_gland_disease|cancer|autoimmune_diseases	reproductive_system_disorder|genital_disorder|gynecological_disorder	false	true	false	false	high
MONDO:0002747	endometrial mucinous adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	other___note__endometrial_mucinous_adenocarcinoma_is_a_type_of_cancer_that_affects_the_endometrium__which_is_an_adrenal_gland_related_disease_but_can_also_be_classified_as_a_cancer_itself__so_it_falls_under_both_categories|adrenal_gland_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0002748	rectum mucinous adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	allergy|inflammatory_disease|adrenal_gland_disease|cancer|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002749	extracranial neuroblastoma	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|nervous_system_disorder	oncology|pediatric	neuroblastoma|cancer	muscle_disorder|other____revised___lymphatic_disorder	false	true	false	true	high
MONDO:0002750	bladder colloid adenocarcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer|bladder_cancer|urological_disorder	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0002751	bladder adenocarcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	bladder_cancer_is_a_type_of_urological_cancer_which_can_be_subsumed_under_the_broader_category_of_cancer__but_bladder_adenocarcinoma_also_affects_the_bladder_which_would_put_it_in_adrenal_gland_disease_as_well|adrenal_gland_disease|cancer	urinary_tract_disorder|lower_gastrointestinal_disorder|kidney_disorder	false	true	false	false	high
MONDO:0002752	ovarian adenocarcinoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0002754	extramedullary plasmacytoma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	adrenal_gland_disease|cancer	plasma_cell_disorder|blood_bone_marrow_disorder	false	true	false	true	medium
MONDO:0002755	solitary osseous plasmacytoma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	oncology|hematology|orthopaedic	cancer	blood_bone_marrow_disorder|bone_disorder	false	true	false	true	medium
MONDO:0002756	solitary plasmacytoma of chest wall	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	adrenal_gland_disease|cancer	lung_disorder|blood_bone_marrow_disorder|bone_disorder	false	true	false	true	medium
MONDO:0002757	acute allergic sanguinous otitis media	inflammatory_disease|otorhinolaryngologic_disease|auditory_system_disorder	other	acute_disease|auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	allergy_and_immunology|otolaryngology	allergy|inflammatory_disease|anemia|autoimmune_diseases	throat_disorder|ear_disorder|immune_disorder	false	false	false	false	medium
MONDO:0002758	vulva verrucous carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology|dermatology	adrenal_gland_disease|cancer	reproductive_system_disorder|skin_disorder	false	true	false	true	low
MONDO:0002759	bladder verrucous carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0002760	bladder squamous cell carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0002761	cervical verrucous carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	inflammatory_disease|cancer	skin_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002762	esophagus verrucous carcinoma	digestive_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	cancer_or_benign_tumor	upper_digestive_tract_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	low
MONDO:0002763	urethral verrucous carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	genital_cancer|cancer|urological_cancer	urinary_tract_disorder|skin_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002764	urethra squamous cell carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	urological_disorder|cancer	urinary_tract_disorder|skin_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0002765	plantar verrucous skin carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer	skin_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0002766	larynx verrucous carcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|oncology	cancer_of_the_voice_box|neoplasms_of_the_larynx___corrected_to___cancer|cancer|cancer_of_the_larynx|larynx_disease|laryngeal_neoplasm	lung_disorder|throat_disorder	false	true	false	true	medium
MONDO:0002768	true hermaphroditism	disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	endocrinology|urology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0002769	leukorrhea	reproductive_system_disorder	other	reproductive_system_disorder	hematology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|reproductive_system_disorder	true	false	false	false	low
MONDO:0002770	vaginal discharge	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|gastroenterology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	false	medium
MONDO:0002771	pulmonary fibrosis	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0002772	intraventricular meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurological_cancer|cancer	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0002775	anovulation	endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder	endocrinology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0002776	external ear disorder	otorhinolaryngologic_disease|auditory_system_disorder	other	auditory_system_disorder|otorhinolaryngologic_disease	dermatology|otolaryngology	inflammatory_disease|autoimmune_diseases	external_disorder|ear_disorder	false	false	false	true	low
MONDO:0002778	epidural spinal canal meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neurological_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002779	central nervous system chondroma	musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0002781	glossopharyngeal nerve paralysis	nervous_system_disorder	other	nervous_system_disorder	otolaryngology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	nerve_disorder|throat_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0002782	cranial nerve palsy	nervous_system_disorder	other	nervous_system_disorder	otolaryngology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	ear_disorder|brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0002783	Shwartzman phenomenon	hematologic_disorder|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	hematologic_disorder|inflammatory_disease|cardiovascular_disorder	hematology|allergy_and_immunology|immunology	inflammatory_disease|autoimmune_diseases	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0002785	skull base neoplasm	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|otolaryngology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002786	diencephalic cancer	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0002787	adamantinous craniopharyngioma	nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder	pediatric|oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|throat_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002788	papillary craniopharyngioma	nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder	pediatric|oncology|neurology	neuro|cancer	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0002789	hemangiopericytic tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology	adrenal_gland_disease|cancer	brain_disorder|blood_bone_marrow_disorder|vascular_disorder	false	true	false	false	medium
MONDO:0002790	seminal vesicle tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	urology|oncology	adrenal_gland_disease|cancer	genitourinary_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002791	large cell medulloblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0002792	cerebellar vermis medulloblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0002794	adult medulloblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	hematology|pediatric|oncology|genetics_and_genomics|neurology	cancer	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0002795	adult central nervous system primitive neuroectodermal neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0002796	melanotic medulloblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|oncology|neurology	adrenal_gland_disease|cancer	skin_disorder|brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002797	childhood medulloblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|oncology|neurology	cancer|neurological_disease	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0002798	childhood central nervous system primitive neuroectodermal neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0002800	thrombophlebitis	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	cardiology|vascular|hematology	inflammatory_disease|cardiovascular_disorder	immune_disorder|blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0002801	colonic pseudo-obstruction	digestive_system_disorder	other	digestive_system_disorder	general_surgery|gastroenterology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0002802	functional colonic disease	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|pediatric	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0002803	intestinal pseudo-obstruction	digestive_system_disorder	other	digestive_system_disorder	neurology|gastroenterology|pediatric	neurodegenerative_disease|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0002804	apocrine adenoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	adrenal_gland_disease|cancer	endocrine_disorder|skin_disorder	false	false	false	false	low
MONDO:0002805	hidradenoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer|skin_disease|benign_tumor	skin_disorder	false	false	false	false	low
MONDO:0002806	bronchogenic carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|pulmonology|cardiothoracic	cancer	lower_gastrointestinal_disorder|lung_disorder	false	true	false	true	very_high
MONDO:0002807	bronchial neoplasm	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|pulmonology	cancer|bronchial_neoplasm	lung_disorder	false	true	false	false	high
MONDO:0002808	pancreatic serous cystadenoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|endocrinology	gland_disease|pancreatic_disease___corrected_answer_based_on_original_prompt___cancer|cancer|pancreatic_disease	upper_gastrointestinal_disorder|endocrine_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0002809	pancreatic cystadenoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	pancreatic_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0002810	pancreatic serous cystic neoplasm	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	hepatology|oncology|gastroenterology	neoplasm|pancreatic_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0002811	main bronchus cancer	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|cardiothoracic|oncology	lung_cancer|cancer|respiratory_system_cancers	lung_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002812	infectious otitis interna	otorhinolaryngologic_disease|infectious_disease|auditory_system_disorder|inflammatory_disease	infectious_disease	infectious_disease|otorhinolaryngologic_disease|auditory_system_disorder|inflammatory_disease|post_infectious_disorder	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	throat_disorder|ear_disorder	true	false	false	true	medium
MONDO:0002813	lipomatous cancer	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	general|oncology|dermatology	adrenal_gland_disease|cancer	skin_disorder|muscle_disorder	false	true	false	false	high
MONDO:0002814	adrenal carcinoma	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|oncology	adrenal_gland_disease|cancer	endocrine_disorder|cancer	false	true	false	false	high
MONDO:0002815	acute myocarditis	musculoskeletal_system_disorder|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|inflammatory_disease|acute_disease	pulmonology|renal_medicine|cardiothoracic|hematology|cardiology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	true	false	false	false	high
MONDO:0002816	adrenal cortex disorder	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology	adrenal_gland_disease|metabolic_disorder	adrenal_cortex_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0002817	adrenal gland cancer	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|oncology	adrenal_gland_disease|cancer	endocrine_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0002821	trabecular follicular adenocarcinoma	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002822	trabecular adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	lung_disorder|upper_gastrointestinal_disorder|bone_disorder	false	true	false	false	high
MONDO:0002824	extrinsic cardiomyopathy	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder	pulmonology|cardiothoracic|cardiology	inflammatory_disease|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0002828	Bartholin gland transitional cell carcinoma	integumentary_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	obstetrics_and_gynecology|oncology|urology	inflammatory_disease|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002829	bartholin gland carcinoma	integumentary_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	obstetrics_and_gynecology|oncology|urology	inflammatory_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002831	non-keratinizing sinonasal squamous cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology	cancer	upper_gastrointestinal_disorder|skin_disorder|nose_disorder	false	true	false	false	high
MONDO:0002832	endometrial transitional cell carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|endometrial_carcinoma_is_a_type_of_cancer_that_occurs_in_the_endometrium__so_it_fits_into_this_category_most_directly__it_can_also_be_related_to_the_adrenal_gland_as_endometrial_cancer_may_spread_to_or_originate_from_the_adrenal_gland__endometrioid_adenocarcinoma_of_the_broad_ligament_which_is_an_uncommon_but_malignant_tumor_which_arises_from_the_endometrium_and_spreads_to_the_adrenal_gland|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002833	fallopian tube transitional cell carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology|urology	adrenal_gland_disease|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002834	primary prostate urothelial carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002836	urethra transitional cell carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	urological_cancer|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0002837	sarcomatoid transitional cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0002840	eosinophilic gastritis	digestive_system_disorder|inflammatory_disease	other	inflammatory_disease|digestive_system_disorder	pediatrics|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0002842	bacterial gastritis	infectious_disease|digestive_system_disorder|inflammatory_disease	infectious_disease	infectious_disease|inflammatory_disease|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0002843	fungal gastritis	infectious_disease|digestive_system_disorder|inflammatory_disease	infectious_disease	infectious_disease|inflammatory_disease|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	false	medium
MONDO:0002844	lymphocytic gastritis	digestive_system_disorder|inflammatory_disease	other	inflammatory_disease|digestive_system_disorder	pediatric|allergy_and_immunology|gastroenterology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|upper_gastrointestinal_disorder|immune_disorder	false	false	false	false	medium
MONDO:0002845	necrotizing gastritis	digestive_system_disorder|inflammatory_disease	other	inflammatory_disease|digestive_system_disorder	pediatric|gastroenterology	inflammatory_disease|autoimmune_diseases|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	false	very_high
MONDO:0002846	granulomatous gastritis	digestive_system_disorder|inflammatory_disease	other	inflammatory_disease|digestive_system_disorder	hepatology|allergy_and_immunology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0002847	skeletal muscle cancer	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	oncology|orthopaedic|rheumatology	skeletal_muscle_cancer|cancer	blood_bone_marrow_disorder|bone_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0002848	skeletal muscle neoplasm	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	oncology|orthopaedic	neoplasm|cancer	bone_disorder|muscle_disorder	false	true	false	false	high
MONDO:0002849	liver rhabdomyosarcoma	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	pediatric|hepatology|oncology|hematology	cancer	liver_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0002850	central nervous system rhabdomyosarcoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pediatric|oncology|neurology	cancer	spinal_disorder|brain_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0002851	mediastinum rhabdomyosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	cancer	throat_disorder|muscle_disorder	false	true	false	false	high
MONDO:0002852	mediastinum sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cardiothoracic|oncology	cancer	lymphatic_disorder|lung_disorder	false	true	false	false	high
MONDO:0002853	rectum rhabdomyosarcoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	pediatric|general_surgery|oncology	cancer	muscle_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0002854	prostate sarcoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002855	ectomesenchymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0002856	gallbladder rhabdomyosarcoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	pediatric|oncology|gastroenterology	cancer	upper_gastrointestinal_disorder|liver_disorder|muscle_disorder	false	true	false	false	high
MONDO:0002857	gallbladder sarcoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0002858	ovary rhabdomyosarcoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	muscle_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002859	breast rhabdomyosarcoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	pediatric|oncology|obstetrics_and_gynecology	cancer	muscle_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0002860	testis rhabdomyosarcoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	urology|pediatric|oncology	cancer	muscle_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0002861	testis sarcoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	urology|oncology	cancer|sarcoma	bone_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0002862	bile duct sarcoma	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	hepatology|oncology|gastroenterology	cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0002863	rhabdomyosarcoma with mixed embryonal and alveolar features	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|genetics_and_genomics|oncology	adrenal_gland_disease|cancer|other___corrected_answer___cancer	muscle_disorder	false	true	false	true	high
MONDO:0002864	anus rhabdomyosarcoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	pediatric|genetics_and_genomics|oncology	cancer	muscle_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002865	anus sarcoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|hematology	sarcoma|cancer	bone_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002866	duodenal disorder	digestive_system_disorder	other	digestive_system_disorder	endocrinology|hepatology|cardiology|hematology|gastroenterology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0002867	pancreatic cystadenocarcinoma	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer___becomes_____cancer|pancreatic_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002868	bile duct mucinous cystic neoplasm with an associated invasive carcinoma	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	hepatology|oncology|gastroenterology	autoimmune_diseases|inflammatory_disease|metabolic_disorder|cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0002869	heart valve disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	heart_valve_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0002870	tricuspid valve insufficiency	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0002871	testicular trophoblastic tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	testicular_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0002872	trophoblastic neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|hematology|obstetrics_and_gynecology	neoplasm|adrenal_gland_disease|tumor|cancer	blood_bone_marrow_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0002874	testicular pure germ cell tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0002875	parasitic ectoparasitic infectious disease	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease	pulmonology|pediatric|parasitology_is_not_in_the_list_but_we_can_infer_pediatric_as_it_deals_with_ectoparasitic_infections__and_infectious_disease_fits_hematolgy_and_pulmonology|hematolgy	infectious_disease|parasitic_infectious_disease|ectoparasitic_disease	skin_disorder|parasite_infection	true	false	false	true	medium
MONDO:0002876	cervical adenosarcoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease|cancer	reproductive_system_disorder	false	true	false	false	high
MONDO:0002877	cervical carcinosarcoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	cervical_disorder|lower_gastrointestinal_disorder___note__the_correct_categorization_would_likely_be_reproductive_system_disorder__but_i_ve_included_cervical_disorder_for_specificity_to_the_condition_mentioned__cervical_carcinomas___and_lower_gastrointestinal_disorder_as_an_indirect_relation_due_to_its_proximity_to_the_cervix|reproductive_system_disorder	false	true	false	false	high
MONDO:0002878	uterine corpus adenosarcoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0002879	uterine body mixed cancer	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	uterine_body_cancer|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0002880	ovarian adenosarcoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	ovarian_adenocarcinoma_is_actually_an_adenocarcinoma__not_a_sarcoma__reproductive_system_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002881	vaginal adenosarcoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002882	colon neuroendocrine neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	neuroendocrine_neoplasm|cancer	endocrine_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0002883	intestinal neuroendocrine neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	intestinal_neuroendocrine_tumor|cancer	upper_gastrointestinal_disorder|endocrine_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002884	nail disorder	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|general_medicine	nail_disorders_are_also_classified_as_nail_disorder_under_the_broader_category_of_skin_disorders_which_can_fall_under_metabolic_disorder|metabolic_disorder	skin_disorder|nail_disorders_are_often_associated_with_skin_conditions	false	false	false	true	medium
MONDO:0002885	erythrasma	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder	true	false	false	true	low
MONDO:0002886	common bile duct disorder	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder|biliary_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0002887	bile duct disorder	digestive_system_disorder	other	digestive_system_disorder	gastroenterology_hepatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0002888	intraorbital meningioma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|disorder_of_orbital_region	oncology|ophthalmology|neurology	neurodegenerative_disease|cancer	eye_disorder|brain_disorder	false	true	false	true	high
MONDO:0002889	orbital cancer	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|disorder_of_orbital_region	oncology|ophthalmology	orbital_cancer_is_a_subset_of_this_category|cancer	eye_disorder|orbital_cancer_is_closely_related_to_the_eye	false	true	false	true	very_high
MONDO:0002892	skull base chordoma	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	otolaryngology|neurology|oncology	skull_base_chordoma_is_a_type_of_tumor_that_occurs_in_the_base_of_the_skull|cancer	bone_disorder|spinal_disorder|ear_disorder	false	true	false	false	high
MONDO:0002894	spinal chordoma	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	orthopaedic|neurology|oncology	neurodegenerative_disease|cancer	bone_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002896	primary syphilis	reproductive_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease	infectious_diseases|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0002897	secondary syphilis	reproductive_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease	obstetrics_and_gynecology|dermatology|pediatric	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0002898	skin cancer	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	autoimmune_diseases|inflammatory_disease|cancer	skin_disorder	false	true	false	true	medium
MONDO:0002899	differentiating neuroblastoma	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	pediatric|neurology|oncology	neuroblastoma|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0002900	cerebral neuroblastoma	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|pediatric	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0002901	blood group incompatibility	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics|immunology	inflammatory_disease|anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0002903	articulation disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	otolaryngology|orthopaedic|neurology	mental_health_disorder|inflammation|neurodegenerative_disease	joint_disorder|muscle_disorder|spinal_disorder	false	false	false	true	low
MONDO:0002904	echolalia	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	low
MONDO:0002905	mutism	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0002907	intracranial thrombosis	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	hematology|neurology	cardiovascular_disorder|neurological_disorder	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0002908	glucose metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	endocrinology|genetics_and_genomics	cardiovascular_disorder|inflammatory_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|glucose_metabolism_disease	false	false	true	true	high
MONDO:0002909	hyperglycemia	metabolic_disease	metabolic_disease	metabolic_disease	endocrinology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|vascular_disorder	false	false	true	true	high
MONDO:0002910	peroneal neuropathy	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0002911	brain stem glioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0002912	brainstem cancer	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0002913	cerebellar neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0002914	childhood brain stem neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|pediatric	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0002915	childhood infratentorial neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|pediatric	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0002916	brainstem intraparenchymal clear cell meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	brainstem|cancer|intracranial_meningioma	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0002917	disorder of pilosebaceous unit	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases|disorder_of_pilosebaceous_unit	skin_disorder	false	false	false	true	medium
MONDO:0002918	clear cell meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	adrenal_gland_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	medium
MONDO:0002919	posterior cranial fossa meningioma	nervous_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0002920	malignant ovarian Brenner tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|ovarian_cancer|cancer	blood_bone_marrow_disorder|lymphatic_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0002921	congenital structural myopathy	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|pediatric	congenital_structural_myopathy_is_not_a_clear_match_for_the_list_provided__however__based_on_available_information__it_seems_to_be_related_more_closely_to_genetic_conditions_rather_than_the_listed_categories_but_it_could_fit_into__metabolic_disorder__as_some_forms_are_associated_with_metabolic_disturbances_due_to_muscle_weakness_and_wasting|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0002922	pyoderma	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0002923	uterine corpus endometrial stromal sarcoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer	muscle_disorder|blood_bone_marrow_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002924	smooth muscle cancer	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	urology|oncology	adrenal_gland_disease|cancer	smooth_muscle_cancer_does_not_exist_as_a_category__muscle_disorder_is_the_closest_match__however__smooth_muscle_tumors_are_generally_categorized_under_this_category|muscle_disorder	false	true	false	true	high
MONDO:0002926	clear cell sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|oncology|renal_medicine	adrenal_gland_disease|cancer	kidney_disorder|renal_disorder	false	true	false	false	very_high
MONDO:0002927	spindle cell sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|orthopaedic|oncology	sarcoma|cancer	skin_disorder|muscle_disorder	false	true	false	false	high
MONDO:0002928	carcinosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology	cancer	lung_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0002929	pulmonary immaturity	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	lung_disorder|pulmonary_disorder	false	false	false	false	high
MONDO:0002930	kidney sarcoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology|renal_medicine	adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0002931	conjunctivochalasis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	oculoplastic_eye_surgery_is_not_listed_but_conjunctivochalasis_deals_with_eyes_so_its_closely_related_to_category_ophthalmology_and_also_partially_to_genetics_and_genomics|ophthalmology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	low
MONDO:0002933	osteosclerosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|genetics_and_genomics|orthopaedic	metabolic_disorder|autoimmune_diseases	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0002934	intravascular angioleiomyoma	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	urology|vascular_surgery|cardiology	cardiovascular_disorder|cancer	muscle_disorder|vascular_disorder	false	true	false	false	medium
MONDO:0002935	penis basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|dermatology|oncology	basal_cell_carcinoma|cancer	skin_disorder|reproductive_system_disorder	false	true	false	true	low
MONDO:0002936	scrotum basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|dermatology|oncology	basal_cell_carcinoma|skin_cancer|cancer	skin_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0002937	nodular basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	basal_cell_carcinoma|skin_disease|cancer	skin_disorder	false	true	false	true	low
MONDO:0002938	metatypical basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer_type|skin_cancer|cancer	lung_disorder|skin_disorder	false	true	false	true	medium
MONDO:0002939	skin pigmented basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	basal_cell_carcinoma|skin_disease|cancer	skin_disorder	false	true	false	true	low
MONDO:0002940	anal margin basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|skin_disorder	false	true	false	true	low
MONDO:0002941	anal margin carcinoma	cancer_or_benign_tumor|integumentary_system_disorder|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor	oncology|urology	anal_margin_carcinoma_is_a_type_of_cancer|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0002942	sebaceous basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	carcinoma|skin_disease|basal_cell_carcinoma|cancer	eye_disorder|skin_disorder	false	true	false	true	low
MONDO:0002943	external ear basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder|auditory_system_disorder|otorhinolaryngologic_disease|nervous_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|nervous_system_disorder|integumentary_system_disorder|auditory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology|dermatology	external_ear_disease|skin_disease|basal_cell_carcinoma|cancer	ear_disorder|skin_disorder	false	true	false	true	low
MONDO:0002944	external ear carcinoma	cancer_or_benign_tumor|auditory_system_disorder|otorhinolaryngologic_disease|nervous_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|nervous_system_disorder|auditory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	autoimmune_diseases|cancer	ear_disorder|skin_disorder	false	true	false	true	medium
MONDO:0002945	micronodular basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	adrenal_gland_disease|autoimmune_diseases|cancer	skin_disorder	false	true	false	true	low
MONDO:0002946	gynatresia	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|dermatology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	reproductive_system_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0002947	adamantinoid basal cell epithelioma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	carcinoma|skin_disease|basal_cell_carcinoma|epithelioma|cancer	teeth_disorder|skin_disorder	false	true	false	false	low
MONDO:0002948	skin fibroepithelial basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	skin_disease|basal_cell_carcinoma|cancer	skin_disorder	false	true	false	true	medium
MONDO:0002949	morpheaform basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	carcinoma|skin_cancer|cancer	lower_gastrointestinal_disorder|skin_disorder	false	true	false	true	medium
MONDO:0002950	skin clear cell basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	skin_cancer|basal_cell_carcinoma|cancer	basal_cell_carcinoma_is_a_type_of_skin_disorder_and_clear_cell_carcinoma_is_also_a_form_of_skin_cancer|skin_disorder	false	true	false	true	low
MONDO:0002951	skin adenoid basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	skin|cancer	skin_disorder	false	true	false	true	low
MONDO:0002952	follicular basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	adrenal_gland_disease|cancer	skin_disorder	false	true	false	true	low
MONDO:0002953	skin infiltrative basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	skin_disease|basal_cell_carcinoma|cancer	skin_disorder	false	true	false	true	medium
MONDO:0002954	superficial multifocal basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	skin_disease|basal_cell_carcinoma|cancer	superficial_multifocal_basal_cell_carcinoma_fits_into_the_category_of_such_disease_as_it_is_related_to_skin_and_can_be_classified_as_a_form_of_skin_disorder|skin_disorder	false	true	false	true	low
MONDO:0002955	vulva basal cell carcinoma	cancer_or_benign_tumor|reproductive_system_disorder|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|integumentary_system_disorder	oncology|obstetrics_and_gynecology|dermatology	skin_disease|basal_cell_carcinoma|cancer	reproductive_system_disorder|skin_disorder	false	true	false	true	medium
MONDO:0002956	skin cystic basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	skin_disease|carcinoma|cancer	skin_cystic_basal_cell_carcinoma_is_actually_basal_cell_carcinoma_which_fits_better_into_skin_disorder_category_as_well_but_it_s_more_specifically_categorized_as_a_type_of_non_melanoma_skin_cancer_under_the_broader__skin_disorder__category|skin_disorder	false	true	false	true	low
MONDO:0002957	sarcomatoid basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	adrenal_gland_disease|cancer	sarcoma|skin_disorder|muscle_disorder	false	true	false	false	medium
MONDO:0002958	signet ring basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	adrenal_gland_disease|cancer	skin_disorder	false	true	false	false	low
MONDO:0002959	radiculopathy	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|spinal_disorder	false	false	false	true	high
MONDO:0002960	polyradiculopathy	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0002961	large cell acanthoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	cancer|tumor|skin_disease	nose_disorder|skin_disorder	false	false	false	false	low
MONDO:0002962	epidermolytic acanthoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0002963	acantholytic acanthoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatopathology|dermatology	adrenal_gland_disease|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0002965	parovarian cyst	reproductive_system_disorder	other	reproductive_system_disorder	urology|obstetrics_and_gynecology	reproductive_system_disorder|gynecological_disease	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0002966	splenic manifestation of prolymphocytic leukemia	cancer_or_benign_tumor|hematologic_disorder|digestive_system_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|immune_system_disorder|acute_disease|hematologic_disorder	oncology|hematology	cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0002967	dermatophytosis of scalp or beard	integumentary_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	inflammatory_disease|infectious_disease|integumentary_system_disorder	dermatology	autoimmune_diseases|allergic|inflammatory_disease	skin_disorder	true	false	false	true	low
MONDO:0002968	lymphocele	immune_system_disorder	other	immune_system_disorder	oncology|hematology|pulmonology|urology|general_surgery	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|lymphocele_is_also_related_to_biliary_system_so_biliary_disorder|liver_disorder	false	false	false	false	medium
MONDO:0002969	ciliary body cancer	cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	oncology|ophthalmology	cancer	eye_disorder	false	true	false	false	high
MONDO:0002970	ciliary body disorder	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	otolaryngology|pulmonology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0002971	amelanotic melanoma	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	dermatology|oncology	cancer|adrenal_gland_disease	skin_disorder	false	true	false	true	high
MONDO:0002972	posterior mediastinum cancer	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonology|oncology	cancer|adrenal_gland_disease	lymphatic_disorder|lung_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0002973	epithelioid cell melanoma	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	dermatology|oncology	cancer|adrenal_gland_disease	lymphatic_disorder|skin_disorder|muscle_disorder	false	true	false	false	high
MONDO:0002974	cervical cancer	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0002975	malignant breast melanoma	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|breast_disorder	dermatology|oncology	cancer|malignant_breast_melanoma_fits_into_the_category_of_cancer_as_it_is_a_type_of_malignancy__but_melanoma_is_typically_associated_with_skin_cancer__not_breast_cancer__however__i_will_leave_the_response_as_is_since_that_was_the_direct_request___cancer	lymphatic_disorder|skin_disorder	false	true	false	false	high
MONDO:0002976	stomach diverticulosis	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	gastrointestinal_disorder_is_not_listed_so_use__inflammatory_disease|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0002977	autoimmune disorder of the nervous system	immune_system_disorder|nervous_system_disorder	autoimmune_disease	nervous_system_disorder|immune_system_disorder	rheumatology|neurology|immunology|allergy_and_immunology	autoimmune_diseases|nervous_system|inflammatory_disease	nervous_system_disorder|immune_disorder|brain_disorder	false	false	false	true	high
MONDO:0002978	orbit alveolar rhabdomyosarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_orbital_region|musculoskeletal_system_disorder|connective_tissue_disorder	pediatric|ophthalmology|oncology	cancer|adrenal_gland_disease	teeth_disorder|eye_disorder|muscle_disorder	false	true	false	true	high
MONDO:0002979	papillary squamous carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|oncology	cancer|squamous_carcinoma|adrenal_gland_disease	lung_disorder|skin_disorder	false	true	false	false	high
MONDO:0002981	peripheral primitive neuroectodermal tumor of bone	connective_tissue_disorder|musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	orthopaedic|neurology|oncology	cancer|neuroectodermal_tumor|bone_cancer	bone_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0002982	peripheral primitive neuroectodermal tumor of soft tissues	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neuroectodermal_tumor	soft_tissue_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0002984	reticulohistiocytic granuloma	immune_system_disorder	other	immune_system_disorder	hematology|dermatology	anemia|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0002987	spongiotic dermatitis	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|joint_disorder	false	false	false	true	medium
MONDO:0002988	cervix melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	skin_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0002989	benign fibrous histiocytoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|pathology|oncology	cancer	bone_disorder|soft_tissue_disorder	false	false	false	true	none
MONDO:0002990	benign deep fibrous histiocytoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematopathology_is_not_in_the_list_so__oncology|dermatology|oncology	cancer|adrenal_gland_disease	skin_disorder|soft_tissue_disorder__assuming_the_category_list_had_this_instead_of__muscle_disorder|bone_disorder	false	false	false	false	low
MONDO:0002991	adenocarcinofibroma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	lung_disorder|upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0002993	pancreatic somatostatinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrinology|gastroenterology	cancer|adrenal_gland_disease|metabolic_disorder	upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0002994	pancreatic delta cell neuroendocrine tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|neuroendocrine_tumor	upper_gastrointestinal_disorder|endocrine_disorder|liver_disorder	false	true	false	true	medium
MONDO:0002995	small intestine neuroendocrine tumor, well differentiated, low or intermediate grade	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0002996	cavernous sinus meningioma	connective_tissue_disorder|musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	nervous_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|cardiovascular_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	vascular_disorder|brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002997	anterior cranial fossa meningioma	musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0002998	skull base meningioma	connective_tissue_disorder|musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neuro	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0002999	central nervous system germinoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pediatric|neurology|oncology	tumor|cancer|neurological_disease	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0003000	central nervous system germ cell tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0003001	seminoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0003002	dysgerminoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric	adrenal_gland_disease|cancer	spinal_disorder|brain_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003003	cervical alveolar soft part sarcoma	cancer_or_benign_tumor|hereditary_disease|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|reproductive_system_disorder	oncology|obstetrics_and_gynecology	sarcoma|cancer	bone_disorder|teeth_disorder	false	true	false	false	high
MONDO:0003004	macular degeneration	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	true	high
MONDO:0003005	macular retinal edema	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|neurology|cardiology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	true	high
MONDO:0003007	childhood kidney cell carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology|pediatric|renal_medicine	childhood_kidney_cell_carcinoma_fits_best_under_this_category|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0003008	hereditary renal cell carcinoma	cancer_or_benign_tumor|hereditary_disease|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder|hereditary_disease	oncology|urology|genetics_and_genomics	cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0003009	hyperaldosteronism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|renal_medicine|cardiology	cardiovascular_disorder|metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0003010	multilocular clear cell renal cell carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology|renal_medicine	kidney_disease|renal_cell_carcinoma|cancer	urinary_tract_disorder|kidney_disorder|cancer__note__cancer_is_implied_but_not_in_the_list_so_best_fitting_from_the_list__lymphatic_disorder	false	true	false	false	medium
MONDO:0003011	mucinous tubular and spindle renal cell carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology|renal_medicine	urological_disorder|renal_cancer|oncology|adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	medium
MONDO:0003012	sarcomatoid renal cell carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	renal_cell_carcinoma|adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	very_high
MONDO:0003014	rhinitis	otorhinolaryngologic_disease|respiratory_system_disorder|inflammatory_disease	other	otorhinolaryngologic_disease|respiratory_system_disorder|inflammatory_disease	pulmonology|otolaryngology	autoimmune_diseases|allergy|inflammatory_disease	nose_disorder|immune_disorder|lung_disorder|throat_disorder	true	false	false	true	low
MONDO:0003017	malignant peritoneal solitary fibrous tumor	cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	oncology|hematology|genetics_and_genomics|gastroenterology	malignant_disease|cancer	lower_gastrointestinal_disorder|lymphatic_disorder|abdominal_disorder	false	true	false	false	high
MONDO:0003019	potassium deficiency disease	nutritional_disorder|metabolic_disease	metabolic_disease	metabolic_disease|nutritional_disorder	endocrinology|renal_medicine|cardiology|gastroenterology	metabolic_disorder|potassium_deficiency_is_related_to_the_way_body_uses__or_doesn_t_use__potassium__this_suggests_a_problem_with_how_body_functions_or_processes___therefore_metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0003021	central nervous system angiosarcoma	nervous_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	central_nervous_system_disease|tumor|cancer	spinal_disorder|brain_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0003022	pediatric angiosarcoma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	oncology|pediatric	pediatric_disease|cancer	skin_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0003023	aorta angiosarcoma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	oncology|cardiothoracic|cardiology	cardiovascular_disorder|cancer	heart_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0003024	breast angiosarcoma	cancer_or_benign_tumor|breast_disorder|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	breast_disorder|cardiovascular_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	skin_disorder|vascular_disorder	false	true	false	false	high
MONDO:0003025	conventional angiosarcoma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	oncology|hematology|cardiothoracic	cardiovascular_disorder|adrenal_gland_disease|cancer	skin_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0003026	gallbladder angiosarcoma	cancer_or_benign_tumor|cardiovascular_disorder|digestive_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	digestive_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	hepatology|oncology|gastroenterology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0003027	thyroid gland angiosarcoma	cancer_or_benign_tumor|cardiovascular_disorder|endocrine_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder|endocrine_system_disorder	cardiovascular_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	autoimmune_diseases|adrenal_gland_disease|inflammatory_disease|cancer	endocrine_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0003028	thyroid sarcoma	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	oncology|hematology|endocrinology|genetics_and_genomics	adrenal_gland_disease|cancer	endocrine_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0003029	skin angiosarcoma	cancer_or_benign_tumor|cardiovascular_disorder|integumentary_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	cancerous_diseases|malignant_neoplasms|skin_condition|skin_cancer|cancer	skin_disorder|vascular_disorder	false	true	false	true	high
MONDO:0003030	endometrioid stromal sarcoma of the cervix	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	bone_disorder|muscle_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0003031	endometrioid stromal and related neoplasms of the cervix	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	endocrine_disorder|reproductive_system_disorder|lymphatic_disorder	false	true	false	false	medium
MONDO:0003032	superior vena cava angiosarcoma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	oncology|hematology|cardiothoracic|cardiology	cancer|cardiovascular_disorder	lymphatic_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0003033	prostate angiosarcoma	cancer_or_benign_tumor|cardiovascular_disorder|reproductive_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	reproductive_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	oncology|urology	cancer|adrenal_gland_disease	reproductive_system_disorder|vascular_disorder	false	true	false	false	high
MONDO:0003034	mediastinum angiosarcoma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	oncology|pulmonology|cardiothoracic	cancer	lung_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0003035	ovarian angiosarcoma	cancer_or_benign_tumor|cardiovascular_disorder|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder|endocrine_system_disorder	reproductive_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0003036	mucoepidermoid carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology|dermatology	cancer|adrenal_gland_disease	nose_disorder|skin_disorder|ear_disorder	false	true	false	true	medium
MONDO:0003037	hypotrichosis	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases|adrenal_gland_disease	hair_disorder|skin_disorder	false	false	false	true	low
MONDO:0003038	dysgraphia	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodevelopmental_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0003039	nominal aphasia	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0003040	retrograde amnesia	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	medium
MONDO:0003041	pediatric mesenchymal chondrosarcoma	hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|hereditary_disease|cancer_or_benign_tumor	oncology|pediatric|orthopaedic	cancer|pediatric	spinal_disorder|bone_disorder|joint_disorder|muscle_disorder	false	true	false	false	high
MONDO:0003042	adult mesenchymal chondrosarcoma	hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|hereditary_disease|cancer_or_benign_tumor	oncology|orthopaedic	cancer	bone_disorder|muscle_disorder	false	true	false	false	high
MONDO:0003045	anal gland neoplasm	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|urology	cancer|gland_disease|neoplasm	lower_gastrointestinal_disorder|skin_disorder	false	true	false	false	high
MONDO:0003046	anus neoplasm	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology|urology	cancer|anus_neoplasm	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0003047	thymic large cell neuroendocrine carcinoma	endocrine_system_disorder|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	hematologic_disorder|immune_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	pulmonology|cardiothoracic|oncology|neuroendocrinology	cancer	endocrine_disorder|immune_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0003049	ovarian large-cell neuroendocrine carcinoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|neuroendocrine_carcinoma_category|adrenal_gland_disease|ovarian_cancer	reproductive_system_disorder|endocrine_disorder	false	true	false	false	very_high
MONDO:0003050	lung large cell carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|cardiothoracic|oncology	cancer|large_cell_carcinoma_is_a_type_of_lung_cancer	lung_disorder	false	true	false	false	very_high
MONDO:0003051	non specific chronic endometritis	reproductive_system_disorder|inflammatory_disease	other	reproductive_system_disorder|inflammatory_disease	gastroenterology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0003052	granulomatous endometritis	reproductive_system_disorder|inflammatory_disease	other	reproductive_system_disorder|inflammatory_disease	hematology|rheumatology|obstetrics_and_gynecology|gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder|immune_disorder	true	false	false	false	medium
MONDO:0003053	choroid plexus meningioma	nervous_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0003054	benign meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|brain_cancer	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0003055	secretory meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurooncology	spinal_disorder|brain_disorder	false	true	false	true	medium
MONDO:0003056	lymphoplasmacyte-rich meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	hematology|oncology|neurology	cancer|neuro	lymphatic_disorder|blood_bone_marrow_disorder|brain_disorder	false	true	false	false	medium
MONDO:0003057	pediatric meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0003058	microcystic meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|tumor	spinal_disorder|brain_disorder	false	true	false	false	medium
MONDO:0003059	bile duct cancer	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology|hepatology	cancer|inflammatory_disease|metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0003060	biliary tract cancer	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	gastroenterology|oncology|hepatology	cancer|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0003061	benign muscle neoplasm	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	rheumatology|oncology|orthopaedic	cancer|neoplasm	benign_muscle_neoplasm|muscle_disorder	false	false	false	false	low
MONDO:0003062	intestinal benign neoplasm	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	cancer|intestinal_benign_neoplasm_is_a_type_of_cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0003064	inverted transitional cell papilloma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|dermatology	adenocarcinoma|cancer|tumor|papilloma|carcinoma	throat_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|skin_disorder	false	true	false	false	low
MONDO:0003065	nasal cavity inverting papilloma	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	oncology|otolaryngology	cancer|inflammatory_disease|autoimmune_diseases	throat_disorder|nose_disorder	false	false	false	true	medium
MONDO:0003066	submandibular adenitis	inflammatory_disease|immune_system_disorder	other	inflammatory_disease|mouth_disorder|immune_system_disorder	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	throat_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0003067	cervical lymphadenitis	inflammatory_disease|immune_system_disorder	other	inflammatory_disease|immune_system_disorder	rheumatology|pediatrics|oncology|obstetrics_and_gynecology|allergy_and_immunology	cancer|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	true	medium
MONDO:0003068	postauricular lymphadenitis	inflammatory_disease|immune_system_disorder	other	inflammatory_disease|immune_system_disorder	general_surgery|otolaryngology	cancer|inflammatory_disease|autoimmune_diseases	ear_disorder|lymphatic_disorder|immune_disorder	true	false	false	true	medium
MONDO:0003069	suppurative lymphadenitis	inflammatory_disease|immune_system_disorder	other	inflammatory_disease|immune_system_disorder	rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	true	medium
MONDO:0003070	axillary lymphadenitis	inflammatory_disease|immune_system_disorder	other	inflammatory_disease|immune_system_disorder	pediatrics|general_medicine|dermatology	cancer|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	true	medium
MONDO:0003072	retinal cancer	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|oncology	cancer|inflammatory_disease	eye_disorder	false	true	false	true	high
MONDO:0003073	trilateral retinoblastoma	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|oncology|pediatric	cancer|neurodegenerative_disease	eye_disorder|brain_disorder	true	true	false	true	very_high
MONDO:0003075	bilateral retinoblastoma	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|oncology|pediatric	cancer|bilateral_retinoblastoma_is_a_type_of_eye_cancer_that_affects_both_eyes	eye_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0003076	unilateral retinoblastoma	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|oncology|pediatric	cancer|neurodegenerative_disease	eye_disorder|spinal_disorder|reproductive_system_disorder|muscle_disorder	false	true	false	true	high
MONDO:0003077	intraocular retinoblastoma	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|oncology	cancer|oncology|neoplasm	eye_disorder|spinal_disorder	false	true	false	true	high
MONDO:0003078	extraocular retinoblastoma	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|oncology	cancer|extraocular_retinoblastoma_can_also_be_classified_as_a_genetic_disorder_but_cancer_is_the_closest_match_in_this_list	eye_disorder|extraocular_disorder	false	true	false	true	very_high
MONDO:0003079	mastocytoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|adrenal_gland_disease	immune_disorder|blood_bone_marrow_disorder|skin_disorder	false	true	false	true	medium
MONDO:0003081	thalamic disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0003082	filamentary keratitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|inflammatory_disease|disorder_of_orbital_region	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	true	low
MONDO:0003083	venous hemangioma	cardiovascular_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	hematology|dermatology	cancer|vascular_disorder	skin_disorder|vascular_disorder	false	false	false	true	low
MONDO:0003084	uremic neuropathy	urinary_system_disorder|nervous_system_disorder	other	urinary_system_disorder|nervous_system_disorder	renal_medicine|neurology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	kidney_disorder|urinary_tract_disorder|muscle_disorder	false	false	false	true	high
MONDO:0003085	keratitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|inflammatory_disease|disorder_of_orbital_region	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	true	false	false	true	high
MONDO:0003086	thymic mucoepidermoid carcinoma	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	hematologic_disorder|immune_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	thoracic|oncology	cancer|thymic_mucopidermoid_carcinoma_does_fit_into_the_category_of_cancer_which_includes_carcinoma_so_other_categories_that_could_also_be_considered___cancer_is_a_broad_term_so_these_cancers_have_similar_characteristics_but_they_do_not_include_thymic_mucopidermoid_carcinoma	lymphatic_disorder|immune_disorder|throat_disorder	false	true	false	false	high
MONDO:0003087	mucoepidermoid breast carcinoma	integumentary_system_disorder|cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease|breast_carcinoma	skin_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0003088	intramuscular hemangioma	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	hematology|oncology|dermatology	cancer|cardiovascular_disorder	vascular_disorder|muscle_disorder	false	false	false	false	low
MONDO:0003089	extrahepatic bile duct mucoepidermoid carcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer|adrenal_gland_disease|autoimmune_diseases	biliary_disorder|liver_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003090	extrahepatic bile duct carcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003091	cutaneous mucoepidermoid carcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|skin_cancer|cutaneous_carcinoma	skin_disorder	false	true	false	false	medium
MONDO:0003092	lacrimal gland mucoepidermoid carcinoma	disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	disorder_of_visual_system|disorder_of_orbital_region|cancer_or_benign_tumor|nervous_system_disorder	oncology|otolaryngology|ophthalmology	cancer	eye_disorder	false	true	false	false	medium
MONDO:0003093	mucoepidermoid esophageal carcinoma	upper_digestive_tract_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|upper_digestive_tract_disorder|cancer_or_benign_tumor	oncology|gastroenterology|otolaryngology	cancer|esophageal_carcinoma	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003095	laryngeal mucoepidermoid carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer|laryngeal_mucoepidermoid_carcinoma	head_and_neck_disorder|throat_disorder	false	true	false	false	medium
MONDO:0003096	deep hemangioma	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	hematology|dermatology	cancer|hemangioma	skin_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0003097	childhood mediastinal neurogenic neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology|pediatric	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder|lung_disorder	false	true	false	false	high
MONDO:0003098	mediastinal neural neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|cardiothoracic|neurology	cancer|neurodegenerative_disease	lung_disorder|throat_disorder	false	false	false	false	high
MONDO:0003100	nerve plexus neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	spinal_disorder|nerve_plexus_neoplasm_is_closely_related_to_the_nervous_system_so_also_brain_disorder	false	true	false	false	high
MONDO:0003103	nerve root neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|nerve_root_neoplasm_does_not_fit_well_here_since_it_is_a_type_of_neoplasm___thus_also_fits__brain_disorder	false	true	false	false	medium
MONDO:0003104	epicardium cancer	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiology|oncology|cardiothoracic	cancer|cardiovascular_disorder	vascular_disorder|heart_disorder	false	true	false	false	very_high
MONDO:0003105	prostate disorder	reproductive_system_disorder	other	reproductive_system_disorder	urology	cancer|metabolic_disorder|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0003107	infratentorial cancer	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|infratentorial_cancer_is_actually_a_type_of_cancer_so_i_will_just_put_it_as_cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0003108	cervicomedullary junction neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0003109	foramen magnum meningioma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|nervous_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neuro__neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0003110	skin hemangioma	cancer_or_benign_tumor|cardiovascular_disorder|integumentary_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology|pediatric	cancer	vascular_disorder|skin_disorder	false	false	false	true	low
MONDO:0003111	gastric neuroendocrine neoplasm	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	cancer|neuroendocrine_cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0003112	malignant gastric germ cell tumor	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology|genetics_and_genomics	cancer|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003113	extragonadal germ cell cancer	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics|pediatric	cancer|adrenal_gland_disease	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0003115	subglottic hemangioma	cardiovascular_disorder|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	respiratory_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	hematology|otolaryngology|genetics_and_genomics|pediatric	neurovascular_disorder|cancer|anemia|cardiovascular_disorder|inflammatory_disease	vascular_disorder|throat_disorder	false	false	false	true	high
MONDO:0003117	somatoform disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0003118	testicular Brenner tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|urology	cancer|neoplastic_disease|adrenal_gland_disease	urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0003120	mixed testicular germ cell cancer	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	cancer|adrenal_gland_disease	reproductive_system_disorder|testicular_disorder	false	true	false	true	high
MONDO:0003121	middle cranial fossa meningioma	cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	medium
MONDO:0003122	striatonigral degeneration	nervous_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0003124	testicular Leydig cell tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	cancer|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0003125	testicular sex cord-stromal neoplasm	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	urology|oncology	cancer|sex_cord_stromal_neoplasm|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0003126	breast hemangioma	breast_disorder|cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder|breast_disorder	oncology|hematology|obstetrics_and_gynecology	cancer|tumor_disease	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0003128	classic pulmonary blastoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|pulmonology|pediatric	cancer|pulmonary_blastoma	lung_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0003129	epithelial predominant pulmonary blastoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology|pediatric	cancer|adrenal_gland_disease	lung_disorder	false	true	false	false	high
MONDO:0003130	mesoblastic nephroma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|hematology|renal_medicine	cancer|anemia	kidney_disorder|blood_bone_marrow_disorder	false	true	false	true	medium
MONDO:0003133	exudative glomerulonephritis	urinary_system_disorder|inflammatory_disease	other	inflammatory_disease|urinary_system_disorder	hematology|nephrology|renal_medicine	autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0003134	proliferative glomerulonephritis	urinary_system_disorder|inflammatory_disease	other	inflammatory_disease|urinary_system_disorder	renal_medicine|rheumatology	autoimmune_diseases|inflammatory_disease	vascular_disorder|kidney_disorder|immune_disorder	true	false	false	true	high
MONDO:0003135	focal embolic glomerulonephritis	urinary_system_disorder|inflammatory_disease	other	inflammatory_disease|urinary_system_disorder	hematology|nephrology|renal_medicine	autoimmune_diseases|inflammatory_disease	vascular_disorder|kidney_disorder|immune_disorder	true	false	false	false	medium
MONDO:0003136	anti-basement membrane glomerulonephritis	urinary_system_disorder|inflammatory_disease	other	inflammatory_disease|urinary_system_disorder	renal_medicine|rheumatology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|kidney_disorder|immune_disorder	false	false	false	true	high
MONDO:0003137	diffuse glomerulonephritis	urinary_system_disorder|inflammatory_disease	other	inflammatory_disease|urinary_system_disorder	renal_medicine|rheumatology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|kidney_disorder|immune_disorder	true	false	false	false	high
MONDO:0003138	subacute glomerulonephritis	urinary_system_disorder|inflammatory_disease	other	inflammatory_disease|acute_disease|urinary_system_disorder	renal_medicine|rheumatology	autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder	true	false	false	true	medium
MONDO:0003139	mesangial proliferative glomerulonephritis	urinary_system_disorder|inflammatory_disease	other	inflammatory_disease|urinary_system_disorder	hematology|allergy_and_immunology|renal_medicine|pediatrics	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|kidney_disorder|immune_disorder	false	false	false	true	medium
MONDO:0003140	immune-complex glomerulonephritis	urinary_system_disorder|inflammatory_disease	other	inflammatory_disease|urinary_system_disorder	allergy_and_immunology|renal_medicine|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder_kidney_disorder	false	false	false	true	medium
MONDO:0003141	cerebellopontine angle embryonal tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology|otolaryngology	cancer|neurodegenerative_disease	brain_disorder|ear_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003142	intracranial primitive neuroectodermal tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neuroectodermal_tumors	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0003143	angiokeratoma	cardiovascular_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder|integumentary_system_disorder	dermatology	tumor|neurocutaneous_disease|skin_condition	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0003144	medulloepithelioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|adrenal_gland_disease	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003145	supratentorial primitive neuroectodermal tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neuroectodermal_tumor	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003147	space motion sickness	auditory_system_disorder|hereditary_disease|otorhinolaryngologic_disease	other	hereditary_disease|otorhinolaryngologic_disease|auditory_system_disorder	neurology|otolaryngology	mental_health_disorder|neurodegenerative_disease	muscle_disorder|ear_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0003150	male reproductive system disorder	reproductive_system_disorder	other	reproductive_system_disorder	urology	male_reproductive_system_disorder|autoimmune_diseases|adrenal_gland_disease|inflammatory_disease	reproductive_system_disorder|male_reproductive_system_disorder	false	false	false	true	high
MONDO:0003152	adult brainstem gliosarcoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neuro_oncology_is_not_in_the_list_but_brainstem_gliosarcoma_could_be_classified_as_a__cancer_of_the_nervous_system	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003153	adult brainstem glioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003154	hemangioma of peripheral nerve	nervous_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology|hematology	cancer|neurodegenerative_disease	vascular_disorder|muscle_disorder	false	false	false	false	low
MONDO:0003155	cavernous hemangioma	cardiovascular_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	cancer|cardiovascular_disorder	vascular_disorder|skin_disorder	false	false	false	false	medium
MONDO:0003157	disappearing bone disease	syndromic_disease	other	syndromic_disease	orthopaedic|genetics_and_genomics|rheumatology	metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0003158	malignant myoepithelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|neurology	cancer|malignant_myoepithelioma_is_a_type_of_cancer__but_it_s_more_specific_than_the_category_so_i_ve_left_it_out	muscle_disorder|lung_disorder	false	true	false	false	high
MONDO:0003159	vascular hemostatic disease	cardiovascular_disorder|hematologic_disorder	cardiovascular_disorder	cardiovascular_disorder|hematologic_disorder	cardiology|vascular_hemostatic_disease_does_not_seem_to_be_an_issue_in_the_provided_category_list__so_i_will_leave_it_out|hematology	cardiovascular_disorder|vascular_hemostatic_disease	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0003163	cauda equina intradural extramedullary astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003164	cauda equina neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003165	cerebellar astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0003168	cerebellar pilocytic astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric|neurology	neuro_cancer|cancer	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0003169	diencephalic astrocytomas	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003170	gliofibroma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	tumor|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0003171	pineal gland astrocytoma	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|nervous_system_disorder	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0003172	glomeruloid hemangioma	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	renal_medicine|hematology|oncology	cancer|inflammatory_disease|metabolic_disorder	vascular_disorder|kidney_disorder	false	false	false	false	low
MONDO:0003173	brain stem astrocytic neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0003174	spinal cord astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neurodegenerative_disease	spinal_cord|brain_disorder	false	true	false	false	high
MONDO:0003175	salivary gland adenoid cystic carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	otolaryngology|oncology	cancer|adenoid_cystic_carcinoma_is_a_type_of_salivary_gland_cancer_so_this_category_fits_better_than_general__cancer__alone	ear_disorder|upper_gastrointestinal_disorder|throat_disorder	false	true	false	false	high
MONDO:0003177	prostate adenoid cystic carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|urinary_tract_disorder	false	true	false	false	medium
MONDO:0003180	cutaneous adenocystic carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	cancer|adrenal_gland_disease	skin_disorder	false	true	false	false	medium
MONDO:0003181	lung adenoid cystic carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	cardiothoracic|pulmonology|oncology	autoimmune_diseases|cancer|inflammatory_disease	lung_disorder	false	true	false	false	medium
MONDO:0003182	anterior horn disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|anterior_horn_disorder_is_related_to_the_motor_neurons_in_the_spinal_cord__which_is_part_of_the_nervous_system__so_it_fits_this_category__this_disorder_disrupts_the_normal_functioning_of_the_nerve_cells_in_the_anterior_horn_of_the_spinal_cord	brain_disorder_spinal_disorder	false	false	false	false	very_high
MONDO:0003184	trachea carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|otolaryngology|oncology	cancer	lung_disorder|upper_gastrointestinal_disorder|throat_disorder	false	true	false	false	very_high
MONDO:0003185	adenoid cystic breast carcinoma	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|breast_disorder	breast_cancer|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder__breast_carcinoma	false	true	false	false	low
MONDO:0003186	esophageal adenoid cystic carcinoma	digestive_system_disorder|upper_digestive_tract_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	upper_digestive_tract_disorder|cancer_or_benign_tumor|digestive_system_disorder	otolaryngology|gastroenterology|oncology	cancer|adenoid_cystic_carcinoma_is_a_subtype_of_cancer_that_primarily_occurs_in_the_salivary_glands_but_also_occasionally_in_other_locations_including_the_esophagus	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003187	Bartholin gland adenoid cystic carcinoma	reproductive_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|integumentary_system_disorder	obstetrics_and_gynecology|urology|oncology	cancer|inflammatory_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003189	middle ear adenocarcinoma	nervous_system_disorder|auditory_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|auditory_system_disorder|otorhinolaryngologic_disease|nervous_system_disorder	otolaryngology|oncology	cancer	ear_disorder|throat_disorder	false	true	false	false	high
MONDO:0003190	middle ear carcinoma	auditory_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|auditory_system_disorder|nervous_system_disorder|otorhinolaryngologic_disease	otolaryngology|oncology	cancer	ear_disorder|throat_disorder	false	true	false	false	high
MONDO:0003191	rete ovarii adenocarcinoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology|genetics_and_genomics	cancer|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003192	rete ovarii neoplasm	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	cancer|gynecological_cancer|ovarian_cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0003193	bile duct adenocarcinoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology|oncology	autoimmune_diseases|cancer|inflammatory_disease|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003194	hemangioma of lung	cardiovascular_disorder|respiratory_system_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder|cardiovascular_disorder	pulmonology|hematology|oncology	cancer	lung_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0003195	peritoneal serous adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|gynecology|oncology	cancer	reproductive_system_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003196	appendix carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003197	granular cell carcinoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|dermatology	cancer|adrenal_gland_disease	skin_disorder|nerve_system_disorder	false	true	false	true	medium
MONDO:0003198	small intestine adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	adenocarcinoma|cancer|gastrointestinal_cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003199	anal carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	urology|oncology	autoimmune_diseases|cancer|inflammatory_disease|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0003200	urethra adenocarcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	cancer|genitourinary_disease|urological_disease	lower_gastrointestinal_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0003202	pituitary gland basophilic carcinoma	connective_tissue_disorder|endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|reproductive_system_disorder|endocrine_system_disorder	oncology|endocrinology|neurology	neurodegenerative_disease|cancer	endocrine_disorder|brain_disorder	false	true	false	false	high
MONDO:0003204	villous adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|gastroenterology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003205	renal pelvis adenocarcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	renal_medicine|oncology|urology	cancer|renal_pelvis_adenocarcinoma_is_a_type_of_cancer	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0003206	acquired hemangioma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	hematology|dermatology|oncology	adrenal_gland_disease|cancer	vascular_disorder|skin_disorder	false	false	false	false	medium
MONDO:0003208	breast secretory carcinoma	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0003209	thymus gland adenocarcinoma	immune_system_disorder|hematologic_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|endocrine_system_disorder	immunology|hematology|oncology|pulmonology	gland_disease|autoimmune_diseases|cancer	endocrine_disorder|immune_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0003210	intrahepatic cholangiocarcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	hepatology|oncology	cancer|inflammatory_disease	biliary_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0003211	nasal cavity adenocarcinoma	respiratory_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	otolaryngology|oncology	cancer	nose_disorder|lung_disorder	false	true	false	false	high
MONDO:0003212	nasal cavity carcinoma	respiratory_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	otolaryngology|oncology	adrenal_gland_disease|cancer|allergy|inflammatory_disease	nose_disorder|lymphatic_disorder|throat_disorder|lung_disorder	false	true	false	true	high
MONDO:0003214	apocrine adenocarcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|pediatric|oncology	adrenal_gland_disease|cancer	endocrine_disorder|skin_disorder	false	true	false	false	high
MONDO:0003215	apocrine sweat gland cancer	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer|autoimmune_diseases	endocrine_disorder|skin_disorder	false	true	false	false	high
MONDO:0003216	ureter adenocarcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	adrenal_gland_disease|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0003218	adenocarcinoma in situ	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pathology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0003219	gastroesophageal junction adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	gastrointestinal_cancer|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003220	gallbladder carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|inflammatory_disease	upper_gastrointestinal_disorder|biliary_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0003222	central nervous system melanocytic neoplasm	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0003223	meninges hemangiopericytoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurological_cancer|cancer	spinal_disorder|brain_disorder|vascular_disorder	false	true	false	false	high
MONDO:0003225	bone marrow disorder	hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder	other	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder	genetics_and_genomics|hematology	cancer|anemia|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|bone_disorder	false	false	false	true	high
MONDO:0003227	prosopagnosia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0003231	acute nonparalytic poliomyelitis	infectious_disease|nervous_system_disorder|inflammatory_disease	neurodegenerative_disease|infectious_disease	acute_disease|nervous_system_disorder|infectious_disease|inflammatory_disease	pediatric|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	spinal_disorder|muscle_disorder	true	false	false	true	low
MONDO:0003232	alcoholic pancreatitis	digestive_system_disorder|psychiatric_disorder|endocrine_system_disorder|inflammatory_disease	psychiatric_disorder|endocrine_system_disorder	digestive_system_disorder|psychiatric_disorder|inflammatory_disease|endocrine_system_disorder	hepatology|gastroenterology	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0003233	essential tremor	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	general_practice|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0003234	optic nerve astrocytoma	psychiatric_disorder|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder|cancer_or_benign_tumor	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor|psychiatric_disorder	neurology|ophthalmology|oncology	neurodegenerative_disease|cancer	eye_disorder|brain_disorder	false	true	false	true	high
MONDO:0003235	optic nerve glioma	psychiatric_disorder|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder|cancer_or_benign_tumor	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor|psychiatric_disorder	neurology|ophthalmology|oncology	neurodegenerative_disease|cancer	eye_disorder|brain_disorder	false	true	false	false	high
MONDO:0003236	atypical polypoid adenomyoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	urology|obstetrics_and_gynecology|pathology|gynecologic_oncology_is_not_in_the_category_list_but_could_be_a_best_fit|oncology	adrenal_gland_disease|cancer	kidney_disorder|muscle_disorder|liver_disorder	false	false	false	false	medium
MONDO:0003237	adenomyoma of uterine corpus	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology	gynecologic_cancer|reproductive_system_disease	lower_gastrointestinal_disorder|reproductive_system_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0003238	cervical adenomyoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|gynecology_is_not_a_separate_category_in_the_list_so_obstetrics_and_gynecology_will_suffice|oncology	gynecological_cancer|cancer	reproductive_system_disorder|muscle_disorder	false	false	false	false	low
MONDO:0003240	thyroid gland disorder	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	thyroid_gland_disorder_is_actually_an_endocrine_disorder_so_it_might_be_a_better_match_than_the_first|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|thyroid_gland_disorder	false	false	false	true	medium
MONDO:0003241	central nervous system hemangioma	nervous_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	nervous_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	neurology|oncology	neurological_disorder|cancer	spinal_disorder|brain_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0003243	hepatocellular clear cell carcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	hepatology|oncology|gastroenterology	adrenal_gland_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003244	central nervous system mesenchymal non-meningothelial tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0003245	aflatoxin-related hepatocellular carcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	hepatology|oncology|gastroenterology	cancer|liver_disease	liver_disorder	false	true	false	false	high
MONDO:0003246	sclerosing hepatic carcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	hepatology|oncology|gastroenterology	adrenal_gland_disease|cancer|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0003248	adult pineal parenchymal tumor	cancer_or_benign_tumor|nervous_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|endocrine_disorder|brain_disorder	false	true	false	false	high
MONDO:0003249	pineal gland cancer	cancer_or_benign_tumor|nervous_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	neurology|oncology|endocrinology	adrenal_gland_disease|cancer	endocrine_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0003250	benign granular cell tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	dermatology|oncology	adrenal_gland_disease|cancer	skin_disorder	false	false	false	false	low
MONDO:0003251	esophageal granular cell tumor	digestive_system_disorder|upper_digestive_tract_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|digestive_system_disorder|upper_digestive_tract_disorder	oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	low
MONDO:0003252	granular cell cancer	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	dermatology|oncology	adrenal_gland_disease|cancer	skin_disorder	false	true	false	false	high
MONDO:0003253	vulvar granular cell tumor	cancer_or_benign_tumor|nervous_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer|inflammatory_disease	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0003254	cardiac granular cell neoplasm	cancer_or_benign_tumor|nervous_system_disorder|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	nervous_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cardiology|oncology	cardiovascular_disorder|cancer	heart_disorder|vascular_disorder	false	true	false	false	medium
MONDO:0003255	mediastinal granular cell myoblastoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	hematolgy|cardiothoracic|oncology|pulmonary	cancer	throat_disorder|lung_disorder	false	true	false	false	low
MONDO:0003256	neurohypophysis granular cell tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|nervous_system_disorder|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	connective_tissue_disorder|reproductive_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|endocrine_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	endocrine_disorder|brain_disorder	false	false	false	false	low
MONDO:0003257	posterior pituitary gland neoplasm	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|nervous_system_disorder|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	connective_tissue_disorder|reproductive_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|endocrine_system_disorder	neurology|oncology|endocrinology	neurological_cancer|cancer	endocrine_disorder|brain_disorder	false	true	false	false	medium
MONDO:0003258	hobnail hemangioma	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hematology|dermatology	tumor|anemia|cancer	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0003260	adult cerebellar neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0003261	papillary meningioma of the cerebellum	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neuro	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0003262	rhabdoid meningioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|neurology|oncology	nervous_system_cancer|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0003263	childhood cerebellar neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|neurology|oncology	neurodegenerative_disease|cancer	brain_disorder_spinal_disorder	false	true	false	true	high
MONDO:0003264	basosquamous carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	inflammatory_disease|autoimmune_diseases|cancer	lymphatic_disorder|skin_disorder	false	true	false	true	high
MONDO:0003265	adjustment disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|pediatric	mental_health_disorder	brain_disorder	false	false	false	true	medium
MONDO:0003266	ependymal tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|neurology|oncology	neurological_cancer|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0003268	mixed glioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurological_cancer|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0003271	iodine hypothyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|thyroid_disorder	false	false	false	true	high
MONDO:0003272	mixed epithelial stromal tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pathology	adrenal_gland_disease|cancer	kidney_disorder|liver_disorder	false	false	false	true	medium
MONDO:0003273	sternum cancer	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	pulmonology|oncology|cardiothoracic	inflammatory_disease|cardiovascular_disorder|cancer	bone_bone_marrow_disorder|bone_disorder	false	true	false	false	very_high
MONDO:0003274	thoracic cancer	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonology|cardiothoracic|oncology	thoracic_cancer|cancer	lower_gastrointestinal_disorder|lung_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0003275	middle ear cancer	auditory_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|auditory_system_disorder|nervous_system_disorder|otorhinolaryngologic_disease	otolaryngology|oncology	cancer	throat_disorder|ear_disorder	false	true	false	false	high
MONDO:0003276	middle ear disorder	auditory_system_disorder|otorhinolaryngologic_disease	other	auditory_system_disorder|otorhinolaryngologic_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	middle_ear_disorder|ear_disorder	true	false	false	true	medium
MONDO:0003277	malignant ear neoplasm	cancer_or_benign_tumor|nervous_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|otorhinolaryngologic_disease	otolaryngology|oncology	malignant_ear_neoplasm|cancer	malignant_neoplasm|ear_disorder	false	true	false	false	high
MONDO:0003278	inner ear cancer	auditory_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|auditory_system_disorder|nervous_system_disorder|otorhinolaryngologic_disease	neurology|otolaryngology|oncology	cancer|inner_ear_cancer	inner_ear_cancer|ear_disorder	false	true	false	false	high
MONDO:0003279	testicular infarct	endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder	urology|cardiothoracic|renal_medicine|hematology	inflammatory_disease|cardiovascular_disorder	reproductive_system_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0003281	ovarian cystic teratoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|ovarian_disorder	false	false	false	true	medium
MONDO:0003282	ovarian cyst	endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	inflammatory_disease|ovarian_cyst_is_a_type_of_cyst_which_is_usually_a_symptom_of_ovarian_cancer|cancer	gynecologic_disorder|reproductive_system_disorder|ovary_disorder	false	false	false	true	medium
MONDO:0003283	epididymal neoplasm	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0003284	mediastinum leiomyoma	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	pulmonology|oncology|cardiothoracic	inflammatory_disease|adrenal_gland_disease|cancer	muscle_disorder|lung_disorder	false	false	false	false	low
MONDO:0003285	fallopian tube leiomyoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	gynecologic_cancer|reproductive_system_disorder|cancer	reproductive_system_disorder|muscle_disorder	false	false	false	false	low
MONDO:0003286	extrahepatic bile duct leiomyoma	digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|musculoskeletal_system_disorder|digestive_system_disorder|endocrine_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer	liver_disorder|biliary_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0003287	central nervous system leiomyoma	musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|musculoskeletal_system_disorder	neurology|oncology	neurodegenerative_disease|anemia|cancer	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0003288	bizarre leiomyoma	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|muscle_disorder	false	false	false	true	high
MONDO:0003289	deep leiomyoma	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	subtype|reproductive_system_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0003290	simple partial epilepsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|mental_health_disorder|epilepsy	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0003291	leiomyoma cutis	musculoskeletal_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|integumentary_system_disorder	obstetrics_and_gynecology|dermatology|oncology	skin_disease|cancer	skin_disorder|muscle_disorder	false	false	false	false	low
MONDO:0003292	anus leiomyoma	digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|digestive_system_disorder	obstetrics_and_gynecology|oncology	soft_tissue_sarcoma|genitourinary_neoplasms|gynecological_cancer|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0003293	lung leiomyoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder|musculoskeletal_system_disorder	pulmonology|oncology	neoplasm|lung_disease|tumor|benign_tumor|cancer	lung_disorder	false	false	false	false	low
MONDO:0003294	pericardium leiomyoma	cardiovascular_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|musculoskeletal_system_disorder|cardiovascular_disorder	cardiology|oncology|cardiothoracic	cardiovascular_disorder|cancer	heart_disorder|muscle_disorder	false	false	false	false	low
MONDO:0003295	leiomyomatosis	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0003296	cellular leiomyoma	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|muscle_disorder	false	false	false	false	low
MONDO:0003297	gallbladder leiomyoma	digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|digestive_system_disorder	hepatology|oncology|gastroenterology	neoplastic_disease__tumor|gallbladder_leiomyoma_is_a_benign_tumor_cancer	muscle_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	low
MONDO:0003298	vulvar leiomyoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|muscle_disorder	false	false	false	false	low
MONDO:0003299	colorectal leiomyoma	digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|digestive_system_disorder	oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0003300	appendix leiomyoma	digestive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	obstetrics_and_gynecology|oncology|gastroenterology|urology	tumor|cancer	lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0003301	dartoic leiomyoma	integumentary_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder|connective_tissue_disorder	oncology|gynecology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|reproductive_system_disorder|liver_disorder	false	false	false	false	low
MONDO:0003302	epithelioid neurofibroma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	genetics_and_genomics|neurology|oncology	cancer|neurofibroma	nerve_disorder__note__i_added_the_correct_category_for_neurofibroma|skin_disorder	false	false	false	false	medium
MONDO:0003303	neurofibroma of gallbladder	digestive_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|nervous_system_disorder	oncology|hpatology|gastroenterology	cancer|neurofibroma	upper_gastrointestinal_disorder|biliary_disorder|liver_disorder	false	false	false	false	low
MONDO:0003304	plexiform neurofibroma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	genetics_and_genomics|neurology|oncology	cancer|neurofibromatosis	brain_disorder|skin_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0003305	cellular neurofibroma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	genetics_and_genomics|neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0003306	atypical neurofibroma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	genetics_and_genomics|neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|skin_disorder|bone_disorder	false	true	false	false	medium
MONDO:0003307	multiple mucosal neuroma	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	neurodegenerative_disease|cancer	nerve_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0003308	pleural mesothelioma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|pulmonology	inflammatory_disease|autoimmune_diseases|cancer	lung_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0003310	Monckeberg arteriosclerosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	low
MONDO:0003311	endometrial stromal tumor	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	gynecological_cancer|adnexal_tumor|cancer	reproductive_system_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0003312	ovarian endometrioid stromal and related neoplasms	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	ovarian_endometrioid_stromal_and_related_neoplasms_belong_to_this_category_as_well_as_the_other_category_however_since_you_requested_that_if_multiple_items__only_those_fitting_best_should_be_included_without__other__then__cancer|cancer	ovarian|reproductive_system_disorder	false	true	false	false	high
MONDO:0003313	endometrioid stromal sarcoma of the vagina	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	inflammatory_disease|other____replaced_with___cancer|adrenal_gland_disease|cancer	joint_disorder|reproductive_system_disorder|muscle_disorder	false	true	false	true	high
MONDO:0003314	endometrioid stromal and related neoplasms of the vagina	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	endometrial_cancer|cancer	reproductive_system_disorder|muscle_disorder|endocrine_disorder	false	true	false	false	low
MONDO:0003315	endometrium carcinoma in situ	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	inflammatory_disease|adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	low
MONDO:0003316	nonanaplastic kidney Wilms tumor	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	pediatric|oncology|urology	kidney_disease|childhood_cancer|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	medium
MONDO:0003317	metachronous kidney Wilms' tumor	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	pediatric|oncology|urology	kidney_disease|cancer|pediatric_cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0003318	mixed cell type kidney Wilms' tumor	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	pediatric|oncology|urology	kidney_cancer|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0003319	scrotum neoplasm	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	scrotum_neoplasm|cancer	reproductive_system_disorder|skin_disorder	false	true	false	true	medium
MONDO:0003320	blastema predominant kidney Wilms tumor	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	pediatric|renal_medicine|oncology|urology	kidney|tumor|cancer	kidney_disorder|urogenital_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0003321	hereditary Wilms tumor	hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease	pediatric|renal_medicine|genetics_and_genomics|oncology|urology	hereditary|cancer	kidney_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0003322	epithelial predominant Wilms' tumor	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	pediatric|oncology|urology	kidney_diseases|epithelial_tumors|cancer	kidney_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0003325	nodular ganglioneuroblastoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|neurology|oncology	adrenal_gland_disease|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0003326	intermixed schwannian stroma-rich ganglioneuroblastoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003327	peripheral ganglioneuroblastoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|oncology	neuroblastoma|cancer	nervous_system_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0003328	fallopian tube adenomatoid tumor	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	adenomatoid_tumor_is_a_subtype_of_cancer|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0003329	ureteral obstruction	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	inflammatory_disease|metabolic_disorder|anemia|autoimmune_diseases|cancer	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0003330	urinary tract obstruction	urinary_system_disorder	other	urinary_system_disorder	pediatric|renal_medicine|urology	adrenal_gland_disease|urinary_tract_obstruction|cancer	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0003331	ovarian monodermal teratoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	teeth_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0003332	malignant struma ovarii	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|ovarian_cancer|cancer	reproductive_system_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0003333	benign struma ovarii	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	gynecologic_disease|cancer	reproductive_system_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0003334	demyelinating polyneuropathy	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|immune_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0003335	chronic polyneuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0003336	acute necrotizing encephalitis	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	infectious_disease|acute_disease|inflammatory_disease|nervous_system_disorder	pediatric|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|immune_disorder|spinal_disorder	true	false	false	true	very_high
MONDO:0003337	acute hemorrhagic encephalitis	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	infectious_disease|acute_disease|inflammatory_disease|nervous_system_disorder	pediatric|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|vascular_disorder	true	false	false	false	very_high
MONDO:0003340	malignant glomus tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	neurology|oncology|general_surgery	neurodegenerative_disease|adrenal_gland_disease|cancer	ear_disorder|brain_disorder	false	true	false	false	high
MONDO:0003341	subungual glomus tumor	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	neurology|dermatology|otolaryngology	neurological_cancer|cancer	skin_disorder|muscle_disorder	false	true	false	true	medium
MONDO:0003342	benign perivascular tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pathology|neurology|oncology	adrenal_gland_disease|cancer	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	low
MONDO:0003343	retinal hemangioblastoma	cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder	cardiovascular_disorder|cancer_or_benign_tumor	nervous_system_disorder|disorder_of_orbital_region|cancer_or_benign_tumor|disorder_of_visual_system|cardiovascular_disorder	oncology|ophthalmology|genetics_and_genomics	cancer	eye_disorder|vascular_disorder	false	true	false	true	high
MONDO:0003345	hilar cholangiocarcinoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|hepatology|gastroenterology	pancreatic_cancer|cancer	biliary_disorder|upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0003346	central nervous system vasculitis	cardiovascular_disorder|inflammatory_disease|nervous_system_disorder	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder|nervous_system_disorder	neurology|rheumatology	autoimmune_diseases|inflammatory_disease	spinal_disorder|brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0003347	inflammatory leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor	oncology|hematology	inflammatory_disease|cancer	muscle_disorder|sarcoma	false	true	false	false	high
MONDO:0003348	conventional leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor	oncology|orthopaedic|urology	adrenal_gland_disease|cancer	muscle_disorder|vascular_disorder	false	true	false	false	high
MONDO:0003349	central nervous system leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor	oncology|neurology	neoplasm|tumor|cancer	muscle_disorder|brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003350	granular cell leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor	oncology|dermatology|neurology|pediatric|genetics_and_genomics	adrenal_gland_disease|cancer	muscle_disorder|sarcoma	false	true	false	false	high
MONDO:0003351	colon leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|hematology|gastroenterology	adrenal_gland_disease|cancer	muscle_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003352	colon sarcoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	adrenal_gland_disease|inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003353	heart leiomyosarcoma	musculoskeletal_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|cardiovascular_disorder	oncology|cardiology	cardiovascular_disorder|cancer	muscle_disorder|heart_disorder	false	true	false	false	very_high
MONDO:0003354	heart sarcoma	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	oncology|hematology|cardiology	cardiovascular_disorder|cancer	vascular|heart	false	true	false	false	high
MONDO:0003355	ovary leiomyosarcoma	endocrine_system_disorder|reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer|ovarian_cancer	muscle_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0003356	epithelioid leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor	oncology|hematology|genetics_and_genomics	adrenal_gland_disease|cancer	muscle_disorder|sarcoma	false	true	false	false	high
MONDO:0003357	lung leiomyosarcoma	respiratory_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology	adrenal_gland_disease|cancer	muscle_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0003358	anus leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|urology	adrenal_gland_disease|cancer	muscle_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003359	myxoid leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor	oncology|hematology|pediatric|neurology|genetics_and_genomics	cancer	muscle_disorder|soft_tissue_disorder	false	true	false	false	high
MONDO:0003360	small intestine leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer	muscle_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003361	small intestinal sarcoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	small_intestinal_sarcoma_is_a_type_of_cancer|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003362	cutaneous leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	cancer	muscle_disorder|skin_disorder	false	true	false	false	high
MONDO:0003363	malignant dermis tumor	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	malignant_dermis_tumor___note__based_on_the_description_of_malignant_dermis_tumor__it_is_a_type_of_cancer_affecting_the_skin__dermis|cancer	muscle_disorder|skin_disorder	false	true	false	false	high
MONDO:0003364	gallbladder leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|hepatology|gastroenterology|general_surgery	cancer	muscle_disorder|upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0003365	esophagus leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|digestive_system_disorder|upper_digestive_tract_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|digestive_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	oncology|gastroenterology	cancer	muscle_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0003366	hydrarthrosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0003367	gastric leiomyosarcoma	musculoskeletal_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|surgery|oncology	soft_tissue_sarcoma|gastrointestinal_cancer|cancer	muscle_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0003368	prostate leiomyosarcoma	reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	adrenal_gland_disease|cancer	muscle_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003369	vagina leiomyosarcoma	reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	muscle_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003370	retroperitoneal leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor	hematology|gastroenterology|genetics_and_genomics|renal_medicine|oncology	adrenal_gland_disease|cancer	muscle_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0003371	breast leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	cancer	muscle_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0003372	vulvar leiomyosarcoma	reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer	muscle_disorder|skin_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0003373	kidney leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	adrenal_gland_disease|cancer	muscle_disorder|urinary_tract_disorder|kidney_disorder	false	true	false	false	very_high
MONDO:0003374	laryngeal leiomyosarcoma	musculoskeletal_system_disorder|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|oncology	cancer	muscle_disorder|throat_disorder	false	true	false	false	very_high
MONDO:0003376	mediastinum leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor	cardiothoracic|oncology	soft_tissue_sarcoma|cancer	muscle_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0003377	extrahepatic bile duct leiomyosarcoma	musculoskeletal_system_disorder|digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer	muscle_disorder|lower_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0003378	liver leiomyosarcoma	musculoskeletal_system_disorder|digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	hepatology|gastroenterology|oncology	liver_disease|neoplasm|cancer	muscle_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0003379	rectum leiomyosarcoma	musculoskeletal_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|digestive_system_disorder|cancer_or_benign_tumor	gastrointestinal_system_is_a_subset_of_the_category_gastroenterology|urology|oncology	cancer	muscle_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003381	pituitary gland disorder	reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|nervous_system_disorder	endocrinology|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	endocrine_disorder|brain_disorder	false	false	false	true	medium
MONDO:0003382	eyelid disorder	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|ophthalmology	eyelid_disorder_is_also_sometimes_related_to_inflammatory_disease|autoimmune_diseases	eye_disorder|eyelid_disorder_is_a_subset_of_eye_disorder_so_it_can_be_removed	false	false	false	true	medium
MONDO:0003383	fallopian tube clear cell adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	kidney_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003384	uterine ligament clear cell adenocarcinoma	reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	uterine_ligament_clear_cell_adenocarcinoma_is_a_type_of_cancer|cancer	kidney_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003386	bladder clear cell adenocarcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003387	urethra clear cell adenocarcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0003388	ampulla of vater clear cell adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	hepatology|gastroenterology|pediatric|genetics_and_genomics|oncology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0003389	epithelial-myoepithelial carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pathology|urology|oncology	epithelial_myoepithelial_carcinoma_is_a_type_of_cancer__specifically_a_rare_salivary_gland_tumor|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0003390	glycogen-rich clear cell breast carcinoma	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	obstetrics_and_gynecology|oncology	cancer|metabolic_disorder	reproductive_system_disorder|breast_carcinoma	false	true	false	false	high
MONDO:0003391	vulvar alveolar soft part sarcoma	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|reproductive_system_disorder	dermatology|pediatric|oncology	cancer	teeth_disorder|skin_disorder	false	true	false	false	high
MONDO:0003392	fallopian tube germ cell tumor	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|germ_cell_tumor	reproductive_system_disorder	false	true	false	true	high
MONDO:0003393	thymus gland disorder	immune_system_disorder|hematologic_disorder|endocrine_system_disorder	endocrine_system_disorder	immune_system_disorder|endocrine_system_disorder|hematologic_disorder	pediatric|pulmonology|allergy_and_immunology|oncology	inflammatory_disease|thymus_gland_disorder|autoimmune_diseases	endocrine_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0003394	dental pulp disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	dentistry|orthopaedic|pediatric|corrected_list_to_reflect_actual_categories__neurology	metabolic_disorder	teeth_disorder|dental_pulp_disorder_is_not_in_the_list_so_i_ll_exclude_it_and_choose_only_teeth_disorder	false	false	false	true	medium
MONDO:0003395	testicular granulosa cell tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	urology|oncology	cancer|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0003396	epulis	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|mouth_disorder	dermatology|otolaryngology|oncology	cancer|adrenal_gland_disease	oral_disorder|teeth_disorder	true	false	false	false	low
MONDO:0003397	gingival hypertrophy	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	orthopaedic|pediatric|dental_surgery	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	oral_disorder|teeth_disorder	false	false	false	true	low
MONDO:0003398	anterograde amnesia	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology|psychology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0003399	pineal region yolk sac tumor	cancer_or_benign_tumor|nervous_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	neurology|pediatric|genetics_and_genomics|oncology	cancer	endocrine_disorder|brain_disorder	false	true	false	false	high
MONDO:0003400	childhood endodermal sinus tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric	endocrine_disorder|rare_disease|pediatric_cancer|cancer	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0003401	central nervous system endodermal sinus tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0003402	testicular yolk sac tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|urology|pediatric	tumor|cancer	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0003403	testicular non-seminomatous germ cell cancer	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0003404	adult yolk sac tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatrics|oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0003405	adult central nervous system germ cell tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	reproductive_system_disorder|brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0003406	sleep-wake disorder	other	other	sleep_disorder	neurology|psychiatry	mental_health_disorder|sleep_wake_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0003408	ovarian primitive germ cell tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder|ovarian_disorder	false	true	false	true	high
MONDO:0003409	colonic disorder	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|hepatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0003410	Wolffian duct adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	reproductive_system_disorder|kidney_disorder	false	true	false	false	high
MONDO:0003411	breast hemangiopericytoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|pediatric|obstetrics_and_gynecology|hematology	tumor|cancer	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0003412	retroperitoneal hemangiopericytoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric|hematology	adrenal_gland_disease|cancer	kidney_disorder|vascular_disorder	false	true	false	false	medium
MONDO:0003413	hair follicle neoplasm	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	hair_follicle_neoplasm_falls_under_the_category_of_cancer_as_it_refers_to_a_tumor_formed_from_hair_follicle_cells|cancer	skin_disorder|hair_follicle_neoplasm_does_not_fit_well_within_this_category_list_so_the_best_fitting_category_is_actually_missing_from_the_options_provided_however_if_we_were_to_select_a_single_one_it_would_be__skin_disorder	false	true	false	false	medium
MONDO:0003414	skin pilomatrix carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	tumor|skin_disease|cancer	skin_disorder|cancer_disorder	false	true	false	false	medium
MONDO:0003417	internuclear ophthalmoplegia	nervous_system_disorder	other	nervous_system_disorder	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	muscle_disorder|brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0003419	Bartholin gland adenoma	reproductive_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor	urology|obstetrics_and_gynecology	inflammatory_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0003420	bile duct cystadenoma	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	gastroenterology|hepatology|oncology	gland_disease|cancer	liver_disorder|upper_gastrointestinal_disorder|biliary_disorder	false	false	false	false	medium
MONDO:0003421	mixed cell adenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|endocrinology|hematology	adrenal_gland_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0003422	lung adenoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|oncology	adenoma|lung_disease|cancer	lung_disorder	false	false	false	false	low
MONDO:0003423	middle ear adenoma	auditory_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|nervous_system_disorder|auditory_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology	adenoma|cancer	throat_disorder|ear_disorder	false	false	false	false	medium
MONDO:0003424	oncocytic adenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics|neurology|ophthalmology|pediatric	adrenal_gland_disease|cancer	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0003425	ophthalmoplegia	nervous_system_disorder	other	nervous_system_disorder	neurology|ophthalmology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0003426	clear cell adenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	reproductive_system_disorder|kidney_disorder	false	false	false	false	low
MONDO:0003427	bronchus adenoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	cardiology|pulmonology|cardiothoracic|oncology	cancer	lung_disorder|throat_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0003428	brain hemangioma	cancer_or_benign_tumor|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder|cancer_or_benign_tumor	nervous_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0003429	functioning pituitary gland adenoma	reproductive_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|endocrine_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	musculoskeletal_system_disorder|reproductive_system_disorder|endocrine_system_disorder|connective_tissue_disorder|nervous_system_disorder|cancer_or_benign_tumor	neurology|endocrinology	adenoma|cancer	brain_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0003430	prolactin producing pituitary tumor	reproductive_system_disorder|musculoskeletal_system_disorder|nervous_system_disorder|endocrine_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|endocrine_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	oncology|endocrinology	endocrine_disorder|hormone_disorder|neuroendocrine_tumor|pituitary_disease|cancer	brain_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0003431	lipoadenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|endocrinology|dermatology	adrenal_gland_disease|inflammatory_disease|cancer	blood_bone_marrow_disorder|muscle_disorder	false	false	false	false	low
MONDO:0003432	strabismus	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder|brain_disorder|eye_disorder	false	false	false	true	medium
MONDO:0003433	water-clear cell adenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0003434	vaginal adenoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0003435	microcystic adenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	neurology|oncology	adrenal_gland_disease|cancer	liver_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0003437	occult small cell lung carcinoma	endocrine_system_disorder|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	respiratory_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|pulmonology	adrenal_gland_disease|cancer	lung_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0003438	combined small cell lung carcinoma	endocrine_system_disorder|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	respiratory_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|pulmonology	adrenal_gland_disease|cancer	lung_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0003439	urinary bladder villous adenoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|urinary_system_disease|glandular_disease|cancer	lower_gastrointestinal_disorder|urinary_tract_disorder|kidney_disorder	false	true	false	false	medium
MONDO:0003441	dystonic disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0003442	bladder papillary urothelial neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|urothelial_cancer|urinary_tract_neoplasm	urinary_tract_disorder|kidney_disorder	false	true	false	false	medium
MONDO:0003443	papillary urothelial neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|urotheleial_carcinoma	urinary_tract_disorder|kidney_disorder	false	true	false	true	medium
MONDO:0003444	intrahepatic bile duct adenoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	hepatology|oncology|gastroenterology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|liver_disorder|biliary_disorder	false	false	false	false	low
MONDO:0003445	extrahepatic bile duct adenoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	hepatology|oncology|gastroenterology	cancer|tumor|gastrointestinal_disease	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0003446	papillary hidradenoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|skin_disease____corrected_response___cancer|skin_disease	reproductive_system_disorder|skin_disorder	false	false	false	false	low
MONDO:0003447	clear cell hidradenoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|urology|dermatology	cancer|skin_disease	skin_disorder	false	false	false	false	low
MONDO:0003448	benign spiradenoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|neoplasm	skin_disorder|benign_tumor_disorder|muscle_disorder	false	false	false	false	low
MONDO:0003450	eccrine papillary adenoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|adrenal_gland_disease|skin_disease	skin_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0003452	cochlear disorder	otorhinolaryngologic_disease|auditory_system_disorder|musculoskeletal_system_disorder	other	otorhinolaryngologic_disease|musculoskeletal_system_disorder|auditory_system_disorder	neurology|otolaryngology	cochlear_disorder_is_related_to_hearing_so_it_could_also_be_classified_as_an_inflammatory_disease|neurodegenerative_disease	ear_disorder	false	false	false	false	high
MONDO:0003453	conjunctival intraepithelial neoplasm	cancer_or_benign_tumor|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_visual_system|disorder_of_orbital_region|cancer_or_benign_tumor	oncology|ophthalmology	cancer|inflammatory_disease	eye_disorder	false	true	false	true	medium
MONDO:0003454	conjunctival cancer	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cancer_or_benign_tumor	oncology|ophthalmology	autoimmune_diseases|cancer|inflammatory_disease|allergy	skin_disorder|eye_disorder	false	true	false	true	medium
MONDO:0003455	bile duct papillary neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|hepatology|gastroenterology	cancer|neoplasm	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0003458	uterine corpus adenofibroma	cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|uterine	reproductive_system_disorder|uterus_disorder	false	false	false	false	low
MONDO:0003459	cervical adenofibroma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|gynecology	cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0003460	clear cell adenofibroma	cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	oncology|urology|gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder|upper_gastrointestinal_disorder|kidney_disorder	false	false	false	false	low
MONDO:0003461	fallopian tube serous adenofibroma	cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	glandular_cancer|cancer|ovarian_adenoma_tumor|female_reproductive_system_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	none
MONDO:0003462	papillary adenofibroma	cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	pathology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|upper_gastrointestinal_disorder|bone_disorder	false	false	false	false	low
MONDO:0003463	ovarian endometrioid adenofibroma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder	false	false	false	false	low
MONDO:0003464	cystadenofibroma	cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|gastroenterology	cancer|adrenal_gland_disease	liver_disorder|kidney_disorder	false	false	false	false	low
MONDO:0003465	fibrous synovial sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	orthopaedic|oncology|rheumatology	cancer|inflammatory_disease	bone_disorder|joint_disorder|muscle_disorder	false	true	false	true	high
MONDO:0003466	spindle cell synovial sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	orthopaedic|oncology|rheumatology	cancer|sarcoma	joint_disorder|muscle_disorder	false	true	false	false	high
MONDO:0003467	mediastinum synovial sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pulmonology|cardiothoracic|rheumatology	cancer|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	true	false	false	high
MONDO:0003468	biphasic synovial sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	orthopaedic|oncology|rheumatology	cancer|sarcoma	bone_disorder|joint_disorder	false	true	false	false	high
MONDO:0003469	epithelioid cell synovial sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics|rheumatology	cancer|sarcoma	immune_disorder|connective_tissue_disorder|cancer|soft_tissue_disorder|joint_disorder	false	true	false	false	very_high
MONDO:0003470	cellular ependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|tumor	spinal_disorder|brain_disorder	false	true	false	true	medium
MONDO:0003471	Pediculus humanus capitis infestation	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	pediatric|dermatology	skin_disease|inflammatory_disease	reproductive_system_disorder|skin_disorder	true	false	false	true	low
MONDO:0003472	lice infestation	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	pediatric|dermatology	skin_disorder|parasitic_disease|inflammatory_disease	skin_disorder|scalp_disorder	true	false	false	true	low
MONDO:0003473	spinal cord ependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0003474	tanycytic ependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurological_cancer	spinal_disorder|brain_disorder	false	true	false	false	medium
MONDO:0003475	papillary ependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|adrenal_gland_disease	spinal_disorder|brain_disorder	false	true	false	true	medium
MONDO:0003476	clear cell ependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|pediatric	cancer|adrenal_gland_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0003477	brain stem ependymoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0003478	childhood ependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|pediatric	neurological_disorder|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0003479	toxic pneumonitis	inflammatory_disease|respiratory_system_disorder	other	inflammatory_disease|respiratory_system_disorder	pulmonology	autoimmune_diseases|inflammatory_disease	lung_disorder|lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0003480	pineal region dysgerminoma	endocrine_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neuroendocrine_system_disorder	brain_disorder|spinal_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0003481	dysgerminoma of ovary	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|gynecological_cancer|germ_cell_tumor|ovarian_cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0003482	Pediculus humanus corporis infestation	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease	dermatology|pediatric	autoimmune_diseases|inflammatory_disease	skin_disorder|reproductive_system_disorder	true	false	false	true	low
MONDO:0003486	basaloid squamous cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|dermatology	cancer|adrenal_gland_disease	throat_disorder|lower_gastrointestinal_disorder|skin_disorder	false	true	false	false	high
MONDO:0003487	pseudoglandular squamous cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology	cancer	throat_disorder|ear_disorder|upper_gastrointestinal_disorder|skin_disorder	false	true	false	false	high
MONDO:0003490	ampulla of vater squamous cell carcinoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology|surgical	cancer|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003492	lacrimal gland squamous cell carcinoma	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|oncology|otolaryngology	cancer|autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	eye_disorder|skin_disorder	false	true	false	false	high
MONDO:0003493	thymus squamous cell carcinoma	immune_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|pulmonology|cardiothoracic	cancer|squamous_cell_carcinoma	immune_disorder_lymphatic_disorder	false	true	false	false	high
MONDO:0003494	ovarian squamous cell carcinoma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	gynecological_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0003495	ovarian squamous cell neoplasm	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|ovarian_squamous_cell_neoplasm_is_a_type_of_cancer__therefore_it_fits_best_into_this_category	ovarian_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003497	renal pelvis squamous cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	renal_medicine|oncology|urology	cancer|renal_pelvis_carcinoma	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0003499	sarcomatoid squamous cell skin carcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	carcinoma|cancer|skin_cancer	muscle_disorder|lymphatic_disorder|skin_disorder	false	true	false	false	high
MONDO:0003500	squamous cell bile duct carcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	hepatology|oncology|gastroenterology	inflammatory_disease|cancer|adrenal_gland_disease|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0003501	external ear squamous cell carcinoma	auditory_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	auditory_system_disorder|nervous_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	otolaryngology|dermatology	skin_cancer|cancer|external_dermatological_disorders	ear_disorder|skin_disorder	false	true	false	true	medium
MONDO:0003502	ureter squamous cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	renal_cancer|cancer|genitourinary_disorder|urological_disorder	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0003503	fallopian tube squamous cell carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	inflammatory_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003504	anal canal neuroendocrine neoplasm	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	neurology|oncology|endocrinology	cancer|neuroendocrine_cancer	lower_gastrointestinal_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0003505	femoral cancer	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	urology|orthopaedic|oncology	cancer|femoral_cancer	blood_bone_marrow_disorder|bone_disorder	false	true	false	false	high
MONDO:0003506	pulmonary artery choriocarcinoma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiothoracic|pulmonology|oncology	cancer|adrenal_gland_disease|cardiovascular_disorder	vascular_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0003507	choriocarcinoma of ovary	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	true	high
MONDO:0003508	choriocarcinoma of testis	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0003509	pineal region choriocarcinoma	nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|adrenal_gland_disease	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003510	malignant testicular germ cell tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0003512	mediastinal mesenchymal tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|cardiothoracic|oncology	cancer	muscle_disorder|lung_disorder	false	true	false	false	high
MONDO:0003513	gastric teratoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|gastric_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0003514	malignant teratoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology|genetics_and_genomics	cancer|adrenal_gland_disease	reproductive_system_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0003515	fallopian tube teratoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|gynecological_disorder	false	true	false	false	medium
MONDO:0003516	adult teratoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|pediatric|oncology	cancer|adrenal_gland_disease|neurodegenerative_disease	reproductive_system_disorder	false	true	false	true	medium
MONDO:0003517	mature teratoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|obstetrics_and_gynecology|general|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|ovarian_disorder	false	true	false	false	medium
MONDO:0003518	mediastinum teratoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|cardiothoracic|oncology	cancer	throat_disorder|lung_disorder	false	true	false	true	medium
MONDO:0003519	malignant syringoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer|adrenal_gland_disease	skin_disorder|muscle_disorder	false	true	false	false	high
MONDO:0003522	male orgasm disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	urology|psychiatry	mental_health_disorder|neurodegenerative_disease	muscle_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0003523	gastrin-producing neuroendocrine tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer|neuroendocrine_tumor|endocrine_disorder	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0003524	gastric gastrin-producing neuroendocrine tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer|neuroendocrine_tumor	endocrine_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003525	pancreatic gastrin-producing neuroendocrine tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology|endocrinology	cancer|neuroendocrine_tumor	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0003528	Volkmann contracture	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	neurology|orthopaedic	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0003529	acute pyelonephritis	infectious_disease|inflammatory_disease|reproductive_system_disorder|urinary_system_disorder	infectious_disease	acute_disease|inflammatory_disease|urinary_system_disorder|infectious_disease|reproductive_system_disorder	urology|renal_medicine	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|kidney_disorder	true	false	false	true	medium
MONDO:0003531	papillary eccrine carcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer|adrenal_gland_disease	eye_disorder|upper_gastrointestinal_disorder|skin_disorder	false	true	false	false	medium
MONDO:0003532	breast papillary carcinoma	breast_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|breast_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	breast|reproductive_system_disorder	false	true	false	true	medium
MONDO:0003534	papillary thymic adenocarcinoma	hematologic_disorder|endocrine_system_disorder|immune_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|hematologic_disorder|immune_system_disorder	cardiothoracic|pulmonology|oncology	cancer|thymic_adenocarcinoma	lung_disorder|thyroid_disorder	false	true	false	false	medium
MONDO:0003535	fallopian tube papillary adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003537	precursor T-lymphoblastic lymphoma/leukemia	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	leukemia|cancer|lymphoma	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0003538	precursor lymphoblastic lymphoma/leukemia	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|pediatric|hematology	leukemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	true	true	false	true	very_high
MONDO:0003539	T-cell adult acute lymphocytic leukemia	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|acute_disease|hematologic_disorder|immune_system_disorder	oncology|hematology	cancer|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0003541	adult acute lymphoblastic leukemia	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|acute_disease|hematologic_disorder	oncology|hematology	cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0003542	dental pulp calcification	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	genetics_and_genomics|oral_surgery|orthopaedic	adrenal_gland_disease|metabolic_disorder|inflammatory_disease	bone_disorder|teeth_disorder	false	false	false	false	low
MONDO:0003543	trigeminal nerve disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	inflammatory_disease|neurodegenerative_disease	brain_disorder|nerve_disorder	false	false	false	false	medium
MONDO:0003544	spinal cord cancer	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0003545	intradural extramedullary spinal canal neoplasm	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003546	third cranial nerve disorder	nervous_system_disorder	other	nervous_system_disorder	otolaryngology|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder|ear_disorder	false	false	false	false	medium
MONDO:0003548	adenosquamous breast carcinoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|lung_disorder|breast_carcinoma	false	true	false	false	high
MONDO:0003549	adenosquamous bile duct carcinoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	gastroenterology|oncology|hepatology	adrenal_gland_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0003550	esophageal adenosquamous carcinoma	digestive_system_disorder|upper_digestive_tract_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	upper_digestive_tract_disorder|cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0003551	thymic adenosquamous carcinoma	hematologic_disorder|endocrine_system_disorder|immune_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	oncology|immunology|pediatric|hematology|cardiothoracic	adrenal_gland_disease|cancer	immune_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0003553	ampulla of vater adenosquamous carcinoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	gastroenterology|oncology|pediatric	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003554	adenosquamous colon carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	adrenal_gland_disease|cancer|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003555	Bartholin gland adenosquamous carcinoma	reproductive_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|integumentary_system_disorder	urology|obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer|other___corrected_answer__cancer	lymphatic_disorder|lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003556	endometrial adenosquamous carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003557	optic nerve sheath meningioma	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder	neurology|ophthalmology|oncology	cancer|neurological_cancer	brain_disorder|eye_disorder	false	true	false	false	medium
MONDO:0003558	adenosquamous prostate carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	adrenal_gland_disease|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003561	malignant giant cell tumor of soft parts	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	oncology|orthopaedic	adrenal_gland_disease|cancer	bone_disorder|joint_disorder	false	true	false	false	very_high
MONDO:0003562	rete testis neoplasm	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology|pediatric	cancer|neoplasm	reproductive_system_disorder|kidney_disorder	false	true	false	false	medium
MONDO:0003563	diffuse pulmonary fibrosis	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	false	high
MONDO:0003564	localized pulmonary fibrosis	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology	autoimmune_diseases|cancer|inflammatory_disease	vascular_disorder|lung_disorder	false	false	false	false	medium
MONDO:0003565	urethral villous adenoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	urologic_disease|cancer|anatomic_abnormality|gland_disease	lower_gastrointestinal_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0003567	bilateral hypoactive labyrinth	otorhinolaryngologic_disease|auditory_system_disorder	other	otorhinolaryngologic_disease|auditory_system_disorder	otolaryngology|neurology	adrenal_gland_disease|neurodegenerative_disease	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0003568	disorder of optic chiasm	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0003569	cranial nerve neuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0003570	lipid-rich carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|dermatology|pathology	cancer|lipid_rich_carcinoma_is_a_type_of_skin_cancer_therefore_also___adrenal_gland_disease__some_cases	liver_disorder|skin_disorder	false	true	false	false	high
MONDO:0003572	nasopharyngeal type undifferentiated carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	otolaryngology|oncology	cancer	throat_disorder|nose_disorder	false	true	false	true	high
MONDO:0003573	pleomorphic carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics	adrenal_gland_disease|autoimmune_diseases|cancer	lung_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0003574	external ear cancer	otorhinolaryngologic_disease|nervous_system_disorder|cancer_or_benign_tumor|auditory_system_disorder	cancer_or_benign_tumor	auditory_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease	otolaryngology|oncology	cancer|external_diseases_category_was_not_listed_but_could_be_included_if_it_existed	skin_disorder|ear_disorder	false	true	false	true	medium
MONDO:0003575	comedocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0003578	extragonadal nonseminomatous germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer|neoplasm	reproductive_system_disorder	false	true	false	true	high
MONDO:0003579	retinal nerve fiber layer disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	disorder_of_orbital_region|nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	ophthalmology|neurology	autoimmune_diseases|retinal_nerve_fiber_layer_disorder_does_not_fit_well_into_this_category_but_it_is_the_best_match|neurodegenerative_disease|inflammatory_disease	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0003581	ovarian embryonal carcinoma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	ovarian_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0003582	hereditary breast ovarian cancer syndrome	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology|genetics_and_genomics	adrenal_gland_disease|cancer|hereditary_cancer_syndrome	ovarian_cancer|breast_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0003584	visual cortex disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|visual_cortex_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0003585	adult liposarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	oncology|orthopaedic	adrenal_gland_disease|other_is_incorrect__as_we_need_to_exclude__other__if_it_s_the_best_fit|cancer	muscle_disorder|skin_disorder	false	true	false	false	high
MONDO:0003586	esophagus liposarcoma	digestive_system_disorder|connective_tissue_disorder|upper_digestive_tract_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|upper_digestive_tract_disorder|cancer_or_benign_tumor|digestive_system_disorder	cardiology|cardiothoracic|gastroenterology|oncology|pulmonology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003587	pediatric liposarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	oncology|pediatric	cancer|pediatric	muscle_disorder|bone_disorder|skin_disorder	false	true	false	false	very_high
MONDO:0003588	larynx liposarcoma	respiratory_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|respiratory_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology	cancer|larynx_tumor	muscle_disorder|throat_disorder	false	true	false	false	high
MONDO:0003589	liposarcoma of the ovary	reproductive_system_disorder|endocrine_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|inflammatory_disease	muscle_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003590	fibroblastic liposarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	oncology|orthopaedic	cancer	muscle_disorder|skin_disorder	false	true	false	false	high
MONDO:0003591	kidney liposarcoma	urinary_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0003592	gastric liposarcoma	digestive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology|hematology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003593	breast liposarcoma	breast_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|breast_disorder	oncology|orthopaedic	adrenal_gland_disease|cancer	muscle_disorder|bone_disorder	false	true	false	false	high
MONDO:0003594	mixed liposarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	oncology|surgical_oncology|hematology	adrenal_gland_disease|cancer	muscle_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0003595	sclerosing liposarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	oncology|orthopaedic|dermatology	adrenal_gland_disease|cancer	muscle_disorder|skin_disorder	false	true	false	false	high
MONDO:0003596	spindle cell liposarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|spindle_cell_carcinoma_is_a_rare_subtype_of_liposarcoma	muscle_disorder|skin_disorder	false	true	false	false	high
MONDO:0003598	median nerve neuropathy	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0003599	vulvar liposarcoma	reproductive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|dermatology	cancer	muscle_disorder|reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0003600	cutaneous liposarcoma	cancer_or_benign_tumor|connective_tissue_disorder|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|integumentary_system_disorder	dermatology|oncology	cancer	skin_disorder|muscle_disorder	false	true	false	true	medium
MONDO:0003601	mediastinum liposarcoma	cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	cardiothoracic|oncology	cancer|inflammatory_disease	bone_disorder|lung_disorder	false	true	false	false	high
MONDO:0003602	intracranial liposarcoma	cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003603	non-functioning pituitary gland neoplasm	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|endocrine_system_disorder|connective_tissue_disorder|reproductive_system_disorder	oncology|endocrinology	cancer|neuroendocrine_disorder	brain_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0003604	functioning pituitary gland neoplasm	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|endocrine_system_disorder|connective_tissue_disorder|reproductive_system_disorder	oncology|endocrinology|neurology	adrenal_gland_disease|cancer	brain_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0003606	adrenal medulla cancer	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	adrenal_gland_disease|cancer	endocrine_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0003607	neuritis of upper limb	inflammatory_disease|nervous_system_disorder	other	nervous_system_disorder|inflammatory_disease	orthopaedic|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|nerve_disorder__note__there_is_no_exact_match_in_the_list_provided__however__based_on_the_context_of_neuritis_which_affects_nerves__i_have_included_nerve_disorder|spinal_disorder|muscle_disorder	true	false	false	false	medium
MONDO:0003608	optic atrophy	disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|disorder_of_visual_system	ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0003609	seminal vesicle cystadenoma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	oncology|urology	cancer|urogenital_disorder|benign_tumor	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0003610	rete ovarii cystadenoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	oncology|obstetrics_and_gynecology	gynecologic_cancer|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	none
MONDO:0003611	uterine ligament papillary cystadenoma associated with von Hippel-Lindau disease	musculoskeletal_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|reproductive_system_disorder	genetics_and_genomics|oncology|obstetrics_and_gynecology	adrenal_gland_disease|neoplastic_disease|cancer	reproductive_system_disorder|kidney_disorder	false	false	false	false	low
MONDO:0003612	uterine ligament cancer	musculoskeletal_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|reproductive_system_disorder	oncology|obstetrics_and_gynecology	uterine_ligament_cancer|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003614	intravenous leiomyomatosis	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	obstetrics_and_gynecology|hematology|oncology	adrenal_gland_disease|cancer|inflammatory_disease|autoimmune_diseases	vascular_disorder|muscle_disorder	false	true	false	false	medium
MONDO:0003615	nerve compression syndrome	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	neurodegenerative_disease|inflammatory_disease	spinal_disorder|nerve_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0003616	salpingitis isthmica nodosa	inflammatory_disease|reproductive_system_disorder	other	reproductive_system_disorder|inflammatory_disease	obstetrics_and_gynecology|pediatric	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0003617	chronic salpingitis	inflammatory_disease|reproductive_system_disorder	other	reproductive_system_disorder|inflammatory_disease	obstetrics_and_gynecology|urology|rheumatology|gynecology|renal_medicine	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	false	medium
MONDO:0003618	pyosalpinx	inflammatory_disease|reproductive_system_disorder	other	reproductive_system_disorder|inflammatory_disease	obstetrics_and_gynecology|urology	cancer|inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|kidney_disorder	true	false	false	false	medium
MONDO:0003619	salpingitis	inflammatory_disease|reproductive_system_disorder	other	reproductive_system_disorder|inflammatory_disease	obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0003620	peripheral nervous system disorder	nervous_system_disorder	other	nervous_system_disorder	neurology	neurodegenerative_disease|peripheral_nervous_system_disorder|inflammatory_disease|autoimmune_diseases	peripheral_nervous_system_is_a_part_of_the_peripheral_nervous_system_so_it_fits_here_too|muscle_disorder	false	false	false	false	medium
MONDO:0003621	small intestinal vasoactive intestinal peptide producing tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003622	pancreatic vasoactive intestinal peptide producing tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|gastroenterology	tumor|cancer	upper_gastrointestinal_disorder|pancreatic_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0003624	acinic cell breast carcinoma	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	obstetrics_and_gynecology|dermatology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|skin_disorder	false	true	false	false	medium
MONDO:0003626	uterine ligament serous adenocarcinoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cardiovascular_disorder|adrenal_gland_disease|cancer|inflammatory_disease|autoimmune_diseases	reproductive_system_disorder	false	true	false	false	high
MONDO:0003627	rheumatic pulmonary valve disease	cardiovascular_disorder|connective_tissue_disorder|immune_system_disorder	autoimmune_disease|cardiovascular_disorder	connective_tissue_disorder|immune_system_disorder|cardiovascular_disorder	rheumatology|cardiothoracic|cardiology|pulmonology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	lung_disorder|heart_disorder	false	false	false	false	high
MONDO:0003628	pulmonary valve disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology|pulmonology	cardiovascular_disorder|pulmonary_valve_disorder	lung_disorder|heart_disorder	false	false	false	true	medium
MONDO:0003630	pancreatic serous cystadenocarcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|gastroenterology	endocrine_disorder|cancerous_tumor|cancer|pancreatic_disease	pancreatic_disorder|liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003631	cervical serous adenocarcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	autoimmune_diseases|adrenal_gland_disease|cancer|inflammatory_disease	upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003632	endocervicitis	inflammatory_disease|reproductive_system_disorder	other	inflammatory_disease|reproductive_system_disorder	rheumatology|obstetrics_and_gynecology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|immune_disorder	true	false	false	true	medium
MONDO:0003633	malignant mesenchymoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	orthopaedic|oncology	adrenal_gland_disease|cancer	bone_disorder|muscle_disorder	false	true	false	false	high
MONDO:0003634	proteinuria	urinary_system_disorder	other	urinary_system_disorder	nephrology_is_not_listed__but_renal_medicine_would_fit|renal_medicine|urology	metabolic_disorder|cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0003635	sebaceous breast carcinoma	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	dermatology|oncology	cancer|inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0003636	vulvar sebaceous carcinoma	cancer_or_benign_tumor|integumentary_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|reproductive_system_disorder	dermatology|oncology	autoimmune_diseases|cancer|inflammatory_disease	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0003637	clear cell-sugar-tumor of the lung	musculoskeletal_system_disorder|respiratory_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	neurology|pulmonology|oncology	other_is_incorrect___cancer|adrenal_gland_disease|cancer	lung_disorder|kidney_disorder	false	true	false	false	low
MONDO:0003638	lung meningioma	respiratory_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder	neurology|pulmonology|oncology	tumor|cancer|lung_cancer	lung_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0003639	lung hilum neoplasm	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|oncology	respiratory_disease|cancer|lung_cancer	lung_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0003640	verruciform xanthoma of skin	metabolic_disease	metabolic_disease	metabolic_disease	dermatology	skin_disease|cancer|inflammatory_disease	skin_disorder|liver_disorder	false	false	false	false	low
MONDO:0003641	central nervous system hematopoietic neoplasm	cancer_or_benign_tumor|hematologic_disorder|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|hematologic_disorder	neurology|hematatology|oncology	central_nervous_system|hematopoietic_neoplasm|cancer	brain_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0003643	giant hemangioma	cardiovascular_disorder|cancer_or_benign_tumor|hematologic_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder|hematologic_disorder	hematology|gastroenterology|hepatology	cardiovascular_disorder|cancer	liver_disorder|vascular_disorder	false	false	false	false	high
MONDO:0003644	cavernous hemangioma of colon	cardiovascular_disorder|cancer_or_benign_tumor|digestive_system_disorder|hematologic_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|cardiovascular_disorder|hematologic_disorder	hematology|oncology|gastroenterology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0003645	cavernous hemangioma of face	cardiovascular_disorder|cancer_or_benign_tumor|hematologic_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder|hematologic_disorder	dermatology|otolaryngology|oncology	cancer	skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0003646	rectum neuroendocrine neoplasm	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|gastroenterology	neuroendocrine_cancer|cancer	lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0003647	atrophic flaccid tympanic membrane	auditory_system_disorder|otorhinolaryngologic_disease	other	auditory_system_disorder|otorhinolaryngologic_disease	pediatric|neurology|otolaryngology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	throat_disorder|ear_disorder	false	false	false	false	low
MONDO:0003648	tympanic membrane disorder	auditory_system_disorder|otorhinolaryngologic_disease	other	auditory_system_disorder|otorhinolaryngologic_disease	pediatric|otolaryngology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	ear_disorder	false	false	false	false	medium
MONDO:0003649	esophageal neuroendocrine tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder|upper_digestive_tract_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|upper_digestive_tract_disorder|endocrine_system_disorder	neuroendocrinology_is_implied_in_the_name_but_this_category_does_not_exist_so_oncology_will_be_used_instead|oncology|gastroenterology	neuroendocrine_tumor_cancer|cancer	upper_gastrointestinal_disorder|endocrine_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0003650	mixed hepatoblastoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	hepatology|pediatric|oncology	cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	true	high
MONDO:0003651	macrotrabecular hepatoblastoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	pediatric|oncology	neurodegenerative_disease|cancer|adrenal_gland_disease	liver_disorder	false	true	false	false	very_high
MONDO:0003652	acute urate nephropathy	urinary_system_disorder	other	urinary_system_disorder|acute_disease	urology|renal_medicine	metabolic_disorder|autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	true	high
MONDO:0003653	stork bite	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	dermatology|pediatric	autoimmune_diseases|inflammatory_disease	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0003654	childhood parosteal osteosarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	orthopaedic|pediatric|oncology	cancer|adrenal_gland_disease	spinal_disorder|joint_disorder|bone_disorder	false	true	false	false	low
MONDO:0003655	cerebral lymphoma	immune_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|nervous_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|hematologic_disorder	neurology|hematology|oncology	cancer	immune_disorder|brain_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0003656	hemoglobinuria	urinary_system_disorder	other	urinary_system_disorder	hematology|cardiology|renal_medicine	metabolic_disorder|anemia	blood_bone_marrow_disorder|kidney_disorder	true	false	false	false	high
MONDO:0003658	B-cell lymphoma, unclassifiable, with features intermediate between diffuse large b-cell lymphoma and classical Hodgkin lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	autoimmune_diseases|cancer|allergy|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	true	true	false	true	high
MONDO:0003659	pediatric lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|pediatric|oncology	pediatric_lymphoma|cancer	immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0003660	adult lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	autoimmune_diseases|cancer	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0003661	breast lymphoma	breast_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|obstetrics_and_gynecology|oncology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0003663	uterine ligament endometrioid adenocarcinoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	obstetrics_and_gynecology|oncology	ovarian_cancer|adrenal_gland_disease|cancer|endometrial_cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003664	hemolytic anemia	hematologic_disorder	anemia	hematologic_disorder	hematolgoy|hematology	autoimmune_diseases|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0003665	cervical endometrioid adenocarcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0003666	fallopian tube endometrioid adenocarcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0003668	extragonadal seminoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0003669	testicular seminoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0003670	posteroinferior myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology|cardiovascular	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0003671	septal myocardial infarction	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder	cardiothoracic|cardiology	cardiovascular_disorder|septal_myocardial_infarction	subtype|heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0003672	posterior myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder|posterior_myocardial_infarction_is_a_cardiovascular_condition	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0003673	apical myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|pulmonology|cardiology	apical_myocardial_infarction|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0003674	subendocardial myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	subendocardial_myocardial_infarction|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0003675	posterolateral myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	adrenal_gland_disease_is_not_applicable_here_as_it_is_related_to_adrenal_gland_disease_so_i_will_remove_it|cardiovascular_disorder	subtype|heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0003676	inferolateral myocardial infarct	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder|inflammatory_disease	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0003677	lateral myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder|inflammatory_disease	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0003678	silent myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiology|cardiothoracic	cardiovascular_disorder|silent_myocardial_infarction_is_also_a_type_of_cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0003679	anteroseptal myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0003680	periosteal chondrosarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder	cancer_or_benign_tumor	hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	orthopaedic|oncology	cancer	spinal_disorder|joint_disorder|bone_disorder	false	true	false	false	high
MONDO:0003681	myxoid chondrosarcoma	cancer_or_benign_tumor|hereditary_disease|connective_tissue_disorder	cancer_or_benign_tumor	hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor	orthopaedic|oncology	cancer	joint_disorder|bone_disorder|muscle_disorder	false	true	false	false	high
MONDO:0003682	localized chondrosarcoma	cancer_or_benign_tumor|hereditary_disease|connective_tissue_disorder	cancer_or_benign_tumor	hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor	orthopaedic|oncology	cancer|localized_tumor	spinal_disorder|joint_disorder|bone_disorder	false	true	false	true	high
MONDO:0003684	clear cell chondrosarcoma	cancer_or_benign_tumor|hereditary_disease|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	orthopaedic|oncology	adrenal_gland_disease|cancer	spinal_disorder|joint_disorder|bone_disorder	false	true	false	false	medium
MONDO:0003685	retroperitoneal germ cell neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|kidney_disorder	false	true	false	true	high
MONDO:0003686	apocrine sweat gland neoplasm	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	neoplasm|cancer	skin_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0003687	endocardium cancer	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiology|oncology	cardiovascular_disorder|cancer	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0003688	well differentiated papillary mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonology|oncology|cardiothoracic	cancer	lung_disorder|mesothelioma	false	true	false	true	medium
MONDO:0003689	familial hemolytic anemia	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0003690	adult anaplastic ependymoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	adrenal_gland_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0003691	childhood malignant mesenchymoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	malignant_mezenchymoma_cancer|adrenal_gland_disease|cancer	bone_disorder|muscle_disorder	false	true	false	false	high
MONDO:0003692	adult malignant mesenchymoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|orthopaedic|oncology	adrenal_gland_disease|cancer	bone_disorder|muscle_disorder	false	true	false	false	high
MONDO:0003693	clear cell cystadenofibroma	cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	urology|obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|kidney_disorder	false	false	false	false	low
MONDO:0003694	ovarian clear cell cystadenofibroma	endocrine_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	female_reproductive_disorder|ovarian_disorder|reproductive_system_disorder	false	true	false	false	low
MONDO:0003695	ovarian clear cell adenofibroma	endocrine_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	tumor|cancer|ovarian_gland_disease	ovarian_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0003697	non-invasive verrucous carcinoma of the penis	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	dermatology|urology|oncology	cancer	skin_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0003698	penis verrucous carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	dermatology|urology|oncology	neoplastic_disease|cancer	skin_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0003699	phobic disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	mental_health_disorder|brain_disorder	false	false	false	true	medium
MONDO:0003700	brachial plexus neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neoplasm	muscle_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003701	thyroid gland diffuse sclerosing papillary carcinoma	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	autoimmune_diseases|cancer|thyroid_gland_disease	endocrine_disorder	false	true	false	true	high
MONDO:0003702	uterus intravascular leiomyomatosis	reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer	vascular_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0003704	uterine corpus diffuse leiomyomatosis	connective_tissue_disorder|reproductive_system_disorder|hereditary_disease|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease|reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|gynecologic_cancer	muscle_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0003705	adult brainstem mixed glioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003706	adult brainstem astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003707	distal biliary tract carcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	hepatology|oncology|gastroenterology	inflammatory_disease|cancer	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0003708	extrahepatic bile duct small cell adenocarcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	hepatology|oncology|gastroenterology	adrenal_gland_disease|cancer	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0003709	agoraphobia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	inflammatory_disease|mental_health_disorder|autoimmune_diseases	mental_health_condition|brain_disorder	false	false	false	true	high
MONDO:0003710	ovarian mixed germ cell neoplasm	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	germ_cell_neoplasm|cancer	lymphatic_disorder|immune_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003712	angiokeratoma of mibelli	integumentary_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|integumentary_system_disorder|cancer_or_benign_tumor	pediatric|general|dermatology	cutaneous_condition|epidermal_growth|dermatological_disease	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0003713	angiokeratoma circumscriptum	integumentary_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|integumentary_system_disorder|cancer_or_benign_tumor	pediatric|dermatology	dermatological_condition|cutaneous_condition|neurological_disease	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0003714	bladder urachal squamous cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	bladder_cancer|cancer|urological_disease	reproductive_system_disorder|urinary_tract_disorder	false	true	false	false	very_high
MONDO:0003715	bladder urachal carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	bladder_cancer|urinary_system_cancer|cancer|urological_cancer	reproductive_system_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0003716	renal pelvis papillary urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	renal_pelvis_papillary_urothelial_carcinoma_fits_best_in_category__cancer|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0003717	renal pelvis papillary tumor	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	renal_pelvis_papillary_tumor|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	medium
MONDO:0003718	occlusion precerebral artery	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	cardiology|neurology|pulmonology	neurodegenerative_disease|cardiovascular_disorder	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0003719	renal pelvis neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology|renal_medicine	cancer|renal_pelvis_neoplasm_falls_under_cancer_because_it_is_a_tumor_originating_in_the_kidney_s_pelvis	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0003720	kidney fibrosarcoma	urinary_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	oncology|urology|renal_medicine	adrenal_gland_disease|cancer|kidney_disease	kidney_disorder|urinary_tract_disorder	false	true	false	false	very_high
MONDO:0003721	kidney osteogenic sarcoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|orthopaedic|urology	cancer|sarcoma	kidney_disorder|bone_disorder	false	true	false	false	very_high
MONDO:0003722	internal auditory canal meningioma	auditory_system_disorder|nervous_system_disorder|musculoskeletal_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	auditory_system_disorder|otorhinolaryngologic_disease|musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	neurology|otolaryngology	cancer|neurodegenerative_disease|neurological_disease	brain_disorder|ear_disorder	false	true	false	false	medium
MONDO:0003723	blunt duct adenosis of breast	breast_disorder	other	breast_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|inflammatory_disease|cancer	lymphatic_disorder|breast_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0003724	non-proliferative fibrocystic change of the breast	breast_disorder	other	breast_disorder	oncology|endocrinology|obstetrics_and_gynecology	inflammatory_disease|cancer	breast_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0003725	breast adenosis	breast_disorder	other	breast_disorder	pediatrics|oncology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|cancer	reproductive_system_disorder	false	false	false	false	low
MONDO:0003726	apocrine adenosis of breast	breast_disorder	other	breast_disorder	dermatology|oncology|obstetrics_and_gynecology	adrenal_gland_disease|autoimmune_diseases|cancer	reproductive_system_disorder|endocrine_disorder|skin_disorder	false	false	false	false	low
MONDO:0003727	animal phobia	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|psychiatry	mental_health_disorder	brain_disorder	false	false	false	true	medium
MONDO:0003728	breast fibrosarcoma	connective_tissue_disorder|breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|breast_disorder|cancer_or_benign_tumor	genetics_and_genomics|oncology|obstetrics_and_gynecology	cancer	muscle_disorder|reproductive_system_disorder|bone_disorder	false	true	false	true	high
MONDO:0003729	aleukemic leukemia cutis	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	autoimmune_diseases|cancer|anemia	immune_disorder|blood_bone_marrow_disorder|skin_disorder	false	true	false	false	high
MONDO:0003730	aleukemic leukemia	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|leukemia|anemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	true	false	false	false	medium
MONDO:0003731	adult central nervous system teratoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	adrenal_gland_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003732	adult central nervous system mature teratoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer	brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0003733	central nervous system mature teratoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0003734	adult central nervous system immature teratoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0003735	central nervous system immature teratoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|oncology	cancer|neurological_disease	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003736	cancerophobia	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	oncology|psychiatry	mental_health_disorder	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0003737	malignant testicular Leydig cell tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	oncology|urology	adrenal_gland_disease|cancer	reproductive_system_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0003738	selective IgE deficiency disease	hematologic_disorder|immune_system_disorder|hereditary_disease	other	hematologic_disorder|immune_system_disorder|hereditary_disease	pediatrics|genetics_and_genomics|allergy_and_immunology	autoimmune_diseases|allergy	immune_disorder	false	false	false	false	medium
MONDO:0003739	selective immunoglobulin deficiency disease	hematologic_disorder|immune_system_disorder|hereditary_disease	other	hematologic_disorder|immune_system_disorder|hereditary_disease	pediatrics|immunology|genetics_and_genomics|hematopathology____corrected_list____allergy_and_immunology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0003740	AIDS phobia	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatry	psychological_condition|mental_health_disorder	lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0003741	juvenile type testicular granulosa cell tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	urology|pediatric|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0003742	heart fibrosarcoma	connective_tissue_disorder|cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cardiology|cardiothoracic|oncology|pulmonology	cancer|cardiovascular_disorder	vascular_disorder|heart_disorder	false	true	false	false	very_high
MONDO:0003743	heart malignant hemangiopericytoma	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiology|oncology|hematolgy	cancer|cardiovascular_disorder	vascular_disorder|heart_disorder	false	true	false	false	very_high
MONDO:0003744	spindle cell intraocular melanoma	disorder_of_visual_system|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	disorder_of_orbital_region|disorder_of_development_or_morphogenesis|disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder	oncology|ophthalmology	cancer|intraocular_melanoma	eye_disorder|skin_disorder	false	true	false	false	high
MONDO:0003745	choroid spindle cell melanoma	disorder_of_visual_system|disorder_of_development_or_morphogenesis|cardiovascular_disorder|cancer_or_benign_tumor|nervous_system_disorder	cardiovascular_disorder|cancer_or_benign_tumor	disorder_of_orbital_region|disorder_of_development_or_morphogenesis|disorder_of_visual_system|cancer_or_benign_tumor|cardiovascular_disorder|nervous_system_disorder	oncology|ophthalmology	adrenal_gland_disease|cancer	eye_disorder	false	true	false	false	high
MONDO:0003746	ciliary body spindle cell melanoma	disorder_of_visual_system|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	disorder_of_orbital_region|disorder_of_development_or_morphogenesis|disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder	dermatology|oncology|ophthalmology	adrenal_gland_disease|autoimmune_diseases|cancer	eye_disorder|skin_disorder	false	true	false	false	high
MONDO:0003747	telangiectatic glomangioma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer|cardiovascular_disorder	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0003748	flying phobia	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	anxiety_disorder|mental_health_disorder	brain_disorder|spinal_disorder|ear_disorder	false	false	false	true	medium
MONDO:0003749	esophageal disorder	upper_digestive_tract_disorder|digestive_system_disorder	other	digestive_system_disorder|upper_digestive_tract_disorder	pulmonary|gastroenterology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0003750	childhood central nervous system germ cell tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|neurology|oncology	childhood_disease|cancer|central_nervous_system_disease	reproductive_system_disorder|brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0003751	childhood germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|genetics_and_genomics|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|germ_cell_tumor_disorder|childhood_disorder	false	true	false	true	high
MONDO:0003752	frontal sinus Schneiderian papilloma	otorhinolaryngologic_disease|musculoskeletal_system_disorder|respiratory_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|otorhinolaryngologic_disease|musculoskeletal_system_disorder|connective_tissue_disorder|respiratory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	inflammatory_disease|cancer	nose_disorder|throat_disorder	false	false	false	false	medium
MONDO:0003753	nasal vestibule squamous papilloma	otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	oncology|otolaryngology	autoimmune_diseases|inflammatory_disease|cancer	nose_disorder|nasal_disorder	false	false	false	true	medium
MONDO:0003754	Brown-Sequard syndrome	syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder	neurology|orthopaedic	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0003755	urinary tract non-invasive transitional cell neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer|urinary_tract_disease|neoplasm	kidney_disorder|urinary_tract_disorder	false	true	false	false	medium
MONDO:0003756	ovarian mucinous neoplasm	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0003757	paraplegia	nervous_system_disorder	other	nervous_system_disorder	neurology|orthopaedic	neurodegenerative_disease|spinal_cord_damage	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0003758	childhood testicular germ cell tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	urology|pediatric|oncology	cancer	reproductive_system_disorder|kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0003759	childhood ovarian yolk sac tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	pediatric|obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0003760	pediatric ovarian germ cell tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	pediatric|oncology|obstetrics_and_gynecology	pediatric_disease|cancer	reproductive_system_disorder|kidney_disorder	false	true	false	true	high
MONDO:0003761	leptomeningeal melanoma	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	adrenal_gland_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003762	malignant leptomeningeal tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|malignant_tumor	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003763	acute stress disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	acute_disease|psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	inflammatory_disease|autoimmune_diseases|mental_health_disorder	brain_disorder|mental_disorder___note__i_ve_modified_the_list_to_accurately_reflect_that_acute_stress_disorder_falls_under_a_mental_health_category	false	false	false	true	medium
MONDO:0003764	pediatric leptomeningeal melanoma	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	pediatric|neurology|oncology	neurodegenerative_disease|cancer	lymphatic_disorder|brain_disorder	false	true	false	true	high
MONDO:0003765	adult leptomeningeal melanoma	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	inflammatory_disease|autoimmune_diseases|allergy|neurodegenerative_disease|mental_health_disorder|cancer	lymphatic_disorder|brain_disorder|skin_disorder	true	true	false	false	very_high
MONDO:0003766	thalamic cancer	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003767	mitral valve disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic	cardiovascular_disorder|mitral_valve_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0003768	signet ring cell variant cervical mucinous adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0003769	herpetic gastritis	inflammatory_disease|infectious_disease|digestive_system_disorder	infectious_disease	digestive_system_disorder|inflammatory_disease|infectious_disease	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder	true	false	false	true	medium
MONDO:0003770	thoracic spinal canal and spinal cord meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neuro|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0003771	jugular foramen meningioma	musculoskeletal_system_disorder|connective_tissue_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|nervous_system_disorder	neurology|otolaryngology	neurological_cancer|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003772	cerebral meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	brain_tumor|cancer|neoplasm|tumor|neurological_disease	brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0003773	intracerebral cystic meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurological_cancer|cancer	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0003774	cerebral convexity meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0003775	lateral ventricle meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neuro|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003776	renal pelvis inverted papilloma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	renal_medicine|urology	neoplastic_disease|inflammatory_disease|renal_pelvis_disease|cancer|urological_disease___corrected_list_based_on_the_original_instruction_to_provide_categories_from_the_given_list____cancer|urological_disease|urinary_system_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0003777	renal pelvis urothelial papilloma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	renal_medicine|urology	renal_pelvis|cancer|urothelial_cancer	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0003778	inborn error of immunity	immune_system_disorder	other	immune_system_disorder	pediatric|genetics_and_genomics|allergy_and_immunology	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0003780	T-cell immunodeficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|hematology|pediatric|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0003781	bronchitis	inflammatory_disease|respiratory_system_disorder	other	inflammatory_disease|respiratory_system_disorder	pulmonology|cardiothoracic	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lung_disorder|liver_disorder	true	false	false	true	high
MONDO:0003782	uterine corpus epithelioid leiomyosarcoma	reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|other____however__given_the_specificity_of_the_disease_name_and_its_relation_to_cancer__it_can_be_inferred_that__cancer__is_likely_a_more_specific_category_than_necessary_____cancer|cancer	muscle_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003783	lymphopenia	immune_system_disorder|hematologic_disorder	other	immune_system_disorder|hematologic_disorder	oncology|hematology	autoimmune_diseases|cancer|anemia	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0003784	nasal cavity carcinoma in situ	respiratory_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology	cancer	throat_disorder|nose_disorder	false	true	false	true	low
MONDO:0003785	leukopenia	immune_system_disorder|hematologic_disorder	other	immune_system_disorder|hematologic_disorder	oncology|hematology	autoimmune_diseases|cancer|anemia	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	true	medium
MONDO:0003786	childhood testicular choriocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|pediatric|urology	childhood_cancer|cancer	urinary_tract_disorder|reproductive_system_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0003787	childhood testicular mixed germ cell cancer	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|pediatric|urology	germ_cell_tumor_subcategory_is_part_of_the_cancer_category__so_that_is_the_best_fit_here__cancer|cancer	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0003788	childhood embryonal testis carcinoma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|pediatric	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0003789	hereditary papillary renal cell carcinoma	cancer_or_benign_tumor|hereditary_disease|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|hereditary_disease|cancer_or_benign_tumor	oncology|genetics_and_genomics|urology	adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0003790	prostatic urethra urothelial carcinoma	reproductive_system_disorder|cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	urothelial_carcinoma|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003791	prostatic urethral cancer	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003792	ovarian carcinosarcoma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|obstetrics_and_gynecology	ovarian_carcinosarcoma_is_actually_a_subtype_of_cancer|cancer	ovarian_carcinosarcoma_fits_into_this_category_as_it_is_a_type_of_cancer_originating_in_the_female_reproductive_system|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0003795	ovarian small cell carcinoma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	lung_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003796	rectum Kaposi sarcoma	cardiovascular_disorder|infectious_disease|cancer_or_benign_tumor|digestive_system_disorder	infectious_disease|cancer_or_benign_tumor|cardiovascular_disorder	digestive_system_disorder|cardiovascular_disorder|infectious_disease|post_infectious_disorder|cancer_or_benign_tumor	oncology|dermatology|hematology	autoimmune_diseases|inflammatory_disease|cancer	lower_gastrointestinal_disorder|skin_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0003799	conjunctivitis	disorder_of_visual_system|inflammatory_disease	other	inflammatory_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|pediatric	autoimmune_diseases|inflammatory_disease	eye_disorder	true	false	false	true	low
MONDO:0003800	conventional malignant hemangiopericytoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	hematology|oncology	adrenal_gland_disease|cancer	vascular_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0003801	corneal intraepithelial neoplasm	disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region	oncology|ophthalmology	intraepithelial_neoplasm_is_a_hallmark_of_cancer__the_term__intraepithelial__specifically_indicates_the_location_of_the_neoplasm_within_epithelial_tissues__which_are_one_of_the_primary_sites_where_cancers_originate|cancer	corneal_disorder|eye_disorder	false	true	false	true	medium
MONDO:0003802	cornea cancer	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_orbital_region	oncology|ophthalmology	autoimmune_diseases|cancer	eye_disorder	false	true	false	true	high
MONDO:0003803	aortic valve disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic	cardiovascular_disorder|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0003805	malignant pericardial mesothelioma	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiology|cardiothoracic|oncology	cancer|malignant_pericardial_mesothelioma_is_a_type_of_cancer	lung_disorder|heart_disorder	false	true	false	false	very_high
MONDO:0003806	thyroid hyalinizing trabecular adenoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	thyroid|cancer	thyroid_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0003808	mediastinal extraskeletal osteosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|orthopaedic	adrenal_gland_disease|cancer	spinal_disorder|bone_disorder|joint_disorder	false	true	false	false	very_high
MONDO:0003809	malignant mediastinum hemangiopericytoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	hematology|cardiothoracic|oncology	cancer|malignant_tumor	lung_disorder|vascular_disorder	false	true	false	false	high
MONDO:0003810	bladder diffuse clear cell adenocarcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	adrenal_gland_disease|cancer|other___note__bladder_diffuse_clear_cell_adenocarcinoma_is_a_type_of_cancer_that_affects_the_bladder__which_is_part_of_the_urinary_system_but_also_related_to_the_adrenal_gland_due_to_its_histological_classification	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0003811	ovarian seromucinous tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	ovarian_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0003812	ovarian endometrial cancer	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	ovarian_endometrial_cancer|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003813	ovarian papillary tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	malignant_neoplasm_of_ovary|cancer|epithelial_ovarian_cancer|ovarian_cancer|gynecologic_malignancy|ovarian_tumor	ovarian_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0003816	articular cartilage disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0003818	childhood mature teratoma of the ovary	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|pediatric|oncology	cancer	reproductive_system_disorder	false	true	false	true	medium
MONDO:0003819	childhood teratoma of the ovary	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|pediatric|oncology	cancer	ovarian_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0003820	mature ovarian teratoma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	ovarian_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0003821	ovarian biphasic or triphasic teratoma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	false	high
MONDO:0003822	non-invasive bladder papillary urothelial neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	cancer|neoplasm|urothelial_neoplasm	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0003824	hereditary kidney oncocytoma	hereditary_disease|urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder|hereditary_disease	oncology|renal_medicine|urology|genetics_and_genomics	cancer|hereditary_disease	urinary_tract_disorder|kidney_disorder	false	true	false	false	medium
MONDO:0003825	kidney oncocytoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	renal_medicine|urology	adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	low
MONDO:0003826	mediastinum seminoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	lung_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0003827	transient hypogammaglobulinemia	syndromic_disease|immune_system_disorder|hereditary_disease|hematologic_disorder	other	hematologic_disorder|syndromic_disease|hereditary_disease|immune_system_disorder	pediatric|hematology|allergy_and_immunology	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	medium
MONDO:0003828	growth hormone-producing pituitary gland carcinoma	musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder|reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	oncology|endocrinology	adrenal_gland_disease|cancer	endocrine_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0003829	chromophil adenoma of the kidney	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|renal_medicine|urology	kidney_disease|adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	false	false	false	low
MONDO:0003830	type 1 papillary adenoma of the kidney	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	renal_medicine|oncology|urology	adenoma|cancer|kidney_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0003831	type 2 papillary adenoma of the kidney	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	renal_medicine|oncology|urology	kidney_cancer|cancer	kidney_disorder|urinary_tract_disorder	false	false	false	true	low
MONDO:0003832	complement deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	rheumatology|allergy_and_immunology|hematology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0003834	gastric cardia carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	gastrointestinal_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003835	gastric cardia adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|gastrointestinal_cancer|adenocarcinoma	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003836	malignant thyroid stimulating hormone producing neoplasm of pituitary gland	reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder	neurology|oncology|endocrinology	cancer|neuroendocrine_disorder|pituitary_gland_disease	endocrine_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0003837	TSH producing pituitary tumor	reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder	oncology|endocrinology	autoimmune_diseases|cancer|pituitary_tumor	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0003839	ovarian mucinous adenocarcinofibroma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003840	epicardium lipoma	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	cardiothoracic|cardiology	cancer|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	none
MONDO:0003841	heart lipoma	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	cardiothoracic|cardiology	cancer|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	low
MONDO:0003842	childhood cerebellar astrocytic neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|pediatric|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0003843	cerebral hemisphere lipoma	nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder	neurology|pediatric|oncology	cancer|neurological_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0003844	central nervous system lipoma	nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	low
MONDO:0003845	corpus callosum lipoma	nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder	neurology|pediatric	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	low
MONDO:0003846	viral esophagitis	upper_digestive_tract_disorder|digestive_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	upper_digestive_tract_disorder|inflammatory_disease|digestive_system_disorder|infectious_disease	pulmonology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0003847	hereditary disease		other		genetics_and_genomics|pediatric	hereditary___note__hereditary_is_often_classified_as_a_type_of_metabolic_disorder_because_it_involves_genetic_factors_that_affect_the_body_s_metabolism__however__some_sources_might_categorize_it_differently_depending_on_the_specific_characteristics_of_the_disease|metabolic_disorder	blood_bone_marrow_disorder|hereditary_disease_is_not_in_the_list__assume_you_meant_to_say_it_matches_blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0003848	ectopic thymus	endocrine_system_disorder|hematologic_disorder|immune_system_disorder	endocrine_system_disorder	hematologic_disorder|endocrine_system_disorder|immune_system_disorder	genetics_and_genomics|pediatric	pediatric_disease|genetic_condition|autoimmune_diseases|developmental_disorder|rare_disease|congenital_anomalies	lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0003849	clivus chordoma	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	otolaryngology|neurology|oncology	neurosurgery|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003850	clivus chondroid chordoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	neurology|otolaryngology|orthopaedic|oncology	chordoma|cancer	bone_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003851	ovarian fetiform teratoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|pediatric|oncology	cancer|teratoma	ovarian_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0003852	ovarian solid teratoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|ovarian_disease_is_likely_cancer_which_encompasses_solid_teratomas|adrenal_gland_disease	ovarian_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0003853	Bartholin gland adenocarcinoma	integumentary_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology|urology	cancer|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003856	adult malignant hemangiopericytoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	oncology|hematology	cancer|adrenal_gland_disease	blood_bone_marrow_disorder|vascular_disorder	false	true	false	true	high
MONDO:0003857	adult intracranial malignant hemangiopericytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	inflammatory_disease|mental_health_disorder|neurodegenerative_disease|autoimmune_diseases|cancer|metabolic_disorder|adrenal_gland_disease	brain_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0003858	anterior optic tract meningioma	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor|psychiatric_disorder	cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	neurology|oncology|ophthalmology	neurodegenerative_disease|cancer	brain_disorder|eye_disorder	false	true	false	false	high
MONDO:0003859	bilateral meningioma of optic nerve	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor|psychiatric_disorder	cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	neurology|oncology|ophthalmology	neurodegenerative_disease|cancer	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0003860	cerebellopontine angle meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|otolaryngology	neurological_disorder|cancer|tumor	ear_disorder|brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003861	vulvar eccrine adenocarcinoma	integumentary_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|reproductive_system_disorder	oncology|dermatology	autoimmune_diseases|cancer|adrenal_gland_disease	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0003862	melanotic psammomatous malignant peripheral nerve sheath tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|dermatology	mental_health_disorder|neurodegenerative_disease|cancer	skin_disorder|nerve_disorder___note__i_have_modified_the_response_to_remove__peripheral__as_it_is_a_descriptive_term_rather_than_a_specific_category__and_added__nerve_disorder__as_malignant_peripheral_nerve_sheath_tumor_implies_involvement_of_nerves	false	true	false	false	high
MONDO:0003863	malignant melanocytic neoplasm of the peripheral nerve sheath	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|malignant_melanocytic_neoplasm_of_the_peripheral_nerve_sheath_fits_within_this_category_as_it_is_a_type_of_cancer	nervous_system_disorder|muscle_disorder|skin_disorder	false	true	false	false	high
MONDO:0003864	chronic lymphocytic leukemia/small lymphocytic lymphoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|acute_disease|cancer_or_benign_tumor|immune_system_disorder	oncology|hematology	autoimmune_diseases|cancer|lymphoma	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	medium
MONDO:0003865	acral lentiginous melanoma	disorder_of_development_or_morphogenesis|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	skin_cancer|cancer	skin_disorder|eye_disorder	false	true	false	true	high
MONDO:0003866	liver extraskeletal osteosarcoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	hepatology|orthopaedic|oncology	inflammatory_disease|autoimmune_diseases|cancer	liver_disorder|joint_disorder|bone_disorder	false	true	false	false	very_high
MONDO:0003867	diffuse meningeal melanocytosis	nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	inflammatory_disease|autoimmune_diseases|cancer	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0003868	anterior foramen magnum meningioma	nervous_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder	neurology|oncology	neurosurgery|cancer|brain_tumor	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0003869	childhood brain stem glioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|pediatric|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003870	childhood brainstem astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|pediatric|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003872	ovarian papillary cystadenoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|ovarian_cancer	ovarian_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0003873	ovarian surface papilloma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	inflammatory_disease|adrenal_gland_disease|cancer	ovarian_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0003874	ovarian serous surface papillary adenocarcinoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	inflammatory_disease|adrenal_gland_disease|allergy|neurodegenerative_disease|autoimmune_diseases|cancer	reproductive_system_disorder|gynecological_disorder	false	true	false	false	high
MONDO:0003875	childhood central nervous system mature teratoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|pediatric|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0003876	eyelid carcinoma	nervous_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region|cancer_or_benign_tumor	dermatology|oncology|ophthalmology	eyelid_carcinoma_falls_into_a_subcategory_of_skin_cancer_which_can_also_fall_under_this_category|cancer	eye_disorder|skin_disorder	false	true	false	true	medium
MONDO:0003878	malignant choroid melanoma	nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|cardiovascular_disorder|disorder_of_visual_system	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region|cancer_or_benign_tumor	oncology|ophthalmology	adrenal_gland_disease|cancer	eye_disorder|skin_disorder	false	true	false	false	high
MONDO:0003879	ovarian endometrioid adenocarcinofibroma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|ovarian	false	true	false	false	high
MONDO:0003880	ceruminous carcinoma	nervous_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|integumentary_system_disorder|auditory_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|integumentary_system_disorder|auditory_system_disorder|nervous_system_disorder	otolaryngology|dermatology|oncology	adrenal_gland_disease|cancer	nose_disorder|throat_disorder	false	true	false	false	high
MONDO:0003881	vulvar apocrine adenocarcinoma	cancer_or_benign_tumor|integumentary_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|dermatology|oncology	adrenal_gland_disease|autoimmune_diseases|cancer	reproductive_system_disorder|skin_disorder	false	true	false	false	medium
MONDO:0003882	central nervous system fibrosarcoma	nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder	neurology|oncology	cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003884	lipoma of the rectum	digestive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|digestive_system_disorder	oncology|gastroenterology	inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0003885	colorectal lipoma	digestive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|digestive_system_disorder	general_surgery_is_not_listed_but_would_be_a_best_fit|oncology|gastroenterology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0003886	mucinous cystadenofibroma	connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder	false	true	false	false	low
MONDO:0003887	ovarian mucinous adenofibroma	endocrine_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|connective_tissue_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|adenofibroma_is_a_type_of_tumor	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	low
MONDO:0003888	childhood testicular mixed embryonal carcinoma and teratoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	pediatric|oncology|urology	childhood_cancer|cancer	reproductive_system_disorder|genitourinary_disorder	false	true	false	true	high
MONDO:0003889	infiltrating bladder urothelial carcinoma, clear cell variant	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	adrenal_gland_disease|cancer|urological_disease	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0003890	infiltrating bladder urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	urothelial_carcinoma|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	very_high
MONDO:0003891	bladder signet ring cell adenocarcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	urological_cancer|cancer|bladder_disease	kidney_disorder|urinary_tract_disorder	false	true	false	false	very_high
MONDO:0003892	acinar lung adenocarcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	cardiothoracic|oncology|pulmonology	lung_cancer|adenocarcinoma|cancer	upper_gastrointestinal_disorder|lymphatic_disorder|lung_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003893	rete testis adenoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	genetics_and_genomics|oncology|urology	adrenal_gland_disease|cancer	reproductive_system_disorder|testis_adenoma	false	false	false	false	low
MONDO:0003894	mediastinal melanocytic neurilemmoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	cardiothoracic|neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|lung_disorder|skin_disorder	false	true	false	false	medium
MONDO:0003895	periosteal osteogenic sarcoma	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	oncology|orthopaedic	cancer	blood_bone_marrow_disorder|bone_disorder	false	true	false	true	high
MONDO:0003896	breast capillary hemangioma	breast_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder|breast_disorder	obstetrics_and_gynecology|oncology|hematology	cancer	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0003897	breast epithelioid hemangioma	breast_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder|breast_disorder	obstetrics_and_gynecology|dermatology|oncology	adrenal_gland_disease|cancer	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0003898	pediatric myxoid chondrosarcoma	connective_tissue_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|hereditary_disease	pediatric|oncology	cancer	bone_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003899	adult myxoid chondrosarcoma	connective_tissue_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|hereditary_disease	oncology|orthopaedic	adrenal_gland_disease|cancer	bone_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003900	connective tissue disorder		other		other_is_incorrect___rheumatology|genetics_and_genomics|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder|vascular_disorder	false	false	false	false	high
MONDO:0003901	cerebellar hemangioblastoma	nervous_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|cancer_or_benign_tumor	neurology|pediatric|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0003902	brain stem hemangioblastoma	nervous_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|cancer_or_benign_tumor	neurology|pediatric|oncology	cancer|brain_stem_tumors	brain_disorder|vascular_disorder	false	true	false	false	high
MONDO:0003903	benign vaginal mixed tumor	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	neoplastic_disease|cancer	reproductive_system_disorder|muscle_disorder	false	false	false	false	low
MONDO:0003904	lung occult squamous cell carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|cardiothoracic|oncology	cancer|squamous_cell_carcinoma|lung_cancer	lower_gastrointestinal_disorder|lung_disorder	false	true	false	true	high
MONDO:0003905	ovarian yolk sac tumor, glandular pattern	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disorder|cancer|glandular_pattern_tumor_type	reproductive_system_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0003906	ovarian yolk sac tumor, hepatoid pattern	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	oncology|obstetrics_and_gynecology	ovarian_tumor|adrenal_gland_disease|cancer	reproductive_system_disorder|liver_disorder	false	true	false	true	high
MONDO:0003907	ovarian yolk sac tumor, polyvesicular vitelline pattern	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0003908	clivus meningioma	nervous_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	neurology|oncology	neuro|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003909	Bartholin gland adenomyoma	integumentary_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|obstetrics_and_gynecology	inflammatory_disease|adeno|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0003910	mixed cell uveal melanoma	disorder_of_development_or_morphogenesis|disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|disorder_of_visual_system	ophthalmology|oncology	cancer|adrenal_gland_disease	skin_disorder|eye_disorder	false	true	false	false	high
MONDO:0003911	ciliary body mixed cell melanoma	disorder_of_development_or_morphogenesis|disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|disorder_of_visual_system	dermatology|ophthalmology|oncology	neoplasm|cancer|adrenal_gland_disease	skin_disorder|eye_disorder	false	true	false	false	high
MONDO:0003912	malignant ciliary body melanoma	disorder_of_development_or_morphogenesis|disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|disorder_of_visual_system	dermatology|oncology	cancer|malignant_ciliatory_body_melanoma	skin_disorder|eye_disorder	false	true	false	false	very_high
MONDO:0003913	choroid mixed cell melanoma	disorder_of_development_or_morphogenesis|disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|disorder_of_visual_system	ophthalmology|oncology	adrenal_gland_disease|cancer	blood_bone_marrow_disorder|eye_disorder	false	true	false	false	high
MONDO:0003915	cortical thymoma	immune_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	neurology|pulmonology|oncology	adrenal_gland_disease|cancer	immune_disorder|brain_disorder|muscle_disorder|throat_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0003916	overnutrition	nutritional_disorder	other	nutritional_disorder	pediatrics|general_medicine|endocrinology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0003917	heart lymphoma	cancer_or_benign_tumor|cardiovascular_disorder|hematologic_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hematologic_disorder|cardiovascular_disorder|cancer_or_benign_tumor	hematology|cardiology|oncology	cardiovascular_disorder|cancer	heart_lymphatic_disorder	true	true	false	true	high
MONDO:0003918	angiomatous meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neuro|cancer	brain_disorder|vascular_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0003921	posterior foramen magnum meningioma	nervous_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|connective_tissue_disorder	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0003922	ovarian clear cell malignant adenofibroma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	ovarian_disorder|female_reproductive_system_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003923	ethmoid sinus Schneiderian papilloma	otorhinolaryngologic_disease|respiratory_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|nervous_system_disorder|respiratory_system_disorder|connective_tissue_disorder	otolaryngology|oncology	inflammatory_disease|allergy|cancer	nose_disorder|throat_disorder	false	false	false	false	medium
MONDO:0003924	adrenal cortex adenoma	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|oncology	adrenal_gland_disease|cancer	endocrine_disorder|adrenal_disease	false	true	false	true	medium
MONDO:0003925	ethmoid sinus inverted papilloma	otorhinolaryngologic_disease|respiratory_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|nervous_system_disorder|respiratory_system_disorder|connective_tissue_disorder	otolaryngology|oncology	inflammatory_disease|autoimmune_diseases|cancer	nose_disorder|throat_disorder	false	true	false	true	low
MONDO:0003926	neurilemmoma of the pleura	respiratory_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|respiratory_system_disorder	oncology|neurology	neurological_disorder|cancer	lung_disorder|brain_disorder	false	false	false	false	medium
MONDO:0003927	posterior uveal melanoma	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_orbital_region|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system	ophthalmology|oncology	cancer	skin_disorder|eye_disorder	false	true	false	true	high
MONDO:0003928	uterine corpus myxoid leiomyosarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|post_infectious_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|other___corrected_answer_without__other____cancer|cancer	muscle_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003929	vestibular micropapillomatosis	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	otolaryngology|genetics_and_genomics|neurology	neurodegenerative_disease	ear_disorder|eye_disorder	false	false	false	false	low
MONDO:0003930	non-invasive bladder urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	bladder_disease|urothelial_carcinoma|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	low
MONDO:0003931	childhood optic tract astrocytoma	psychiatric_disorder|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor|psychiatric_disorder	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	pediatric|ophthalmology|oncology|neurology	cancer|neurodegenerative_disease	eye_disorder|brain_disorder	false	true	false	true	high
MONDO:0003932	childhood optic nerve glioma	psychiatric_disorder|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor|psychiatric_disorder	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	pediatric|ophthalmology|oncology|neurology	cancer|neurodegenerative_disease	eye_disorder|brain_disorder	false	true	false	true	high
MONDO:0003933	chest wall bone cancer	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	orthopaedic|oncology|cardiothoracic	cancer	bone_disorder|bone_marrow_disorder	false	true	false	true	high
MONDO:0003934	breast apocrine carcinoma	integumentary_system_disorder|cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer	skin_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0003935	oncocytic breast carcinoma	integumentary_system_disorder|cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|all_categories_related_to_the_disease_category__cancer|cancer	reproductive_system_disorder|breast_disorder	false	true	false	false	high
MONDO:0003936	invasive tubular breast carcinoma	integumentary_system_disorder|cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|invasive_tubular_breast_carcinoma	skin_disorder|lymphatic_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0003937	spondylitis	musculoskeletal_system_disorder|inflammatory_disease	other	inflammatory_disease|musculoskeletal_system_disorder	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|spinal_disorder	false	false	false	true	high
MONDO:0003938	bladder colonic type adenocarcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|urinary_tract_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003939	muscle tissue disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology|neurology	inflammatory_disease|muscle_tissue_disorder|autoimmune_diseases|metabolic_disorder	muscle_disorder|muscle_tissue_disorder	false	false	false	false	high
MONDO:0003940	Kummell disease	immune_system_disorder|musculoskeletal_system_disorder	other	immune_system_disorder|musculoskeletal_system_disorder	hematology|rheumatology|oncology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0003941	classic variant of chromophobe renal cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine|oncology	adrenal_gland_disease|cancer	endocrine_disorder|kidney_disorder	false	true	false	false	medium
MONDO:0003942	eosinophilic variant of chromophobe renal cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine|oncology	adrenal_gland_disease|cancer	endocrine_disorder|kidney_disorder	false	true	false	true	medium
MONDO:0003943	central nervous system hibernoma	nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	low
MONDO:0003944	endobronchial leiomyoma	respiratory_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|oncology	tumor|adrenal_gland_disease|cancer	muscle_disorder|lung_disorder	false	false	false	false	medium
MONDO:0003945	bone epithelioid hemangioma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	orthopaedic|hematology|oncology	tumor|bone_disease|cancer	blood_bone_marrow_disorder|bone_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0003946	vaginal villous adenoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0003947	hyper-IgM syndrome	immune_system_disorder|hereditary_disease|hematologic_disorder	other	immune_system_disorder|hereditary_disease|hematologic_disorder	immunology|pediatric|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0003948	cerebral hemangioma	nervous_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|cancer_or_benign_tumor	hematology|oncology|neurology	cancer|neurological_condition	brain_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0003950	nipple carcinoma	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	oncology|dermatology	nipple_carcinoma_is_a_type_of_breast_cancer|cancer	skin_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0003951	scrotal hemangioma	cancer_or_benign_tumor|reproductive_system_disorder|cardiovascular_disorder|integumentary_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|integumentary_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|dermatology	inflammatory_disease|cancer	skin_disorder|vascular_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0003952	adult central nervous system choriocarcinoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	inflammatory_disease|autoimmune_diseases|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003953	pediatric CNS choriocarcinoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pediatric|oncology|neurology	pediatric_cns_choriocarcinoma_is_actually_the_disease_itself_so_this_answer_should_be_ignored_and_just_cancer_left|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0003954	angiokeratoma of Fordyce	cancer_or_benign_tumor|cardiovascular_disorder|integumentary_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|integumentary_system_disorder|cancer_or_benign_tumor	dermatology	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0003955	juvenile breast papillomatosis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|genetics_and_genomics|oncology|obstetrics_and_gynecology	autoimmune_diseases|cancer	lymphatic_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0003956	Baastrup syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	pediatric|neurology	autoimmune_diseases|neurodegenerative_disease	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0003957	adult pineoblastoma	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|oncology|neurology	adrenal_gland_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003958	childhood central nervous system immature teratoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pediatric|oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0003959	breast large cell neuroendocrine carcinoma	endocrine_system_disorder|cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|neuroendocrine_carcinoma	endocrine_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003960	pulmonary large cell neuroendocrine carcinoma	cancer_or_benign_tumor|respiratory_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|respiratory_system_disorder	oncology|pulmonology	neuroendocrine_carcinoma_is_actually_a_type_of_cancer_therefore_it_should_be_categorized_as_just_cancer|cancer|adrenal_gland_disease	endocrine_disorder|neuroendocrine_carcinoma|lung_disorder	false	true	false	false	high
MONDO:0003962	Froelich syndrome	nervous_system_disorder|syndromic_disease	other	nervous_system_disorder|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	immune_disorder|kidney_disorder|endocrine_disorder|blood_bone_marrow_disorder|liver_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0003963	diffuse infiltrative lymphocytosis syndrome	syndromic_disease	other	syndromic_disease	hematology|immunology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0003964	myositis ossificans	musculoskeletal_system_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|inflammatory_disease	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	bone_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0003965	Capgras syndrome	nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|syndromic_disease	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	psychiatric_disorder|brain_disorder|mental_health_disorder	false	false	false	false	medium
MONDO:0003966	testicular monophasic choriocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|urology	cancer|adrenal_gland_disease	blood_bone_marrow_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0003967	synchronous multifocal osteogenic sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|orthopaedic	cancer	bone_disorder|spinal_disorder|joint_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0003968	asynchronous multifocal osteogenic sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|orthopaedic	cancer|sarcoma	bone_disorder|joint_disorder|muscle_disorder	false	true	false	false	high
MONDO:0003969	amphetamine abuse	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	cardiovascular_disorder|neurodegenerative_disease|mental_health_disorder	nose_disorder|brain_disorder|muscle_disorder|vascular_disorder	false	false	false	false	high
MONDO:0003970	gastric fundus carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	gastrointestinal_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0003971	gastric pylorus carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	neoplastic_disease|gastrointestinal_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0003972	gastric body carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	gastrointestinal_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0003973	tubular variant testicular seminoma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|urology	cancer|testicular_seminoma	reproductive_system_disorder	false	true	false	true	medium
MONDO:0003975	Littre gland carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|gastroenterology|urology	cancer|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0003976	malignant type AB thymoma	cancer_or_benign_tumor|endocrine_system_disorder|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|endocrine_system_disorder	oncology|allergy_and_immunology|hematology|cardiothoracic	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|thoracic_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0003978	colon small cell neuroendocrine carcinoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|oncology	cancer|neuroendocrine_carcinoma	endocrine_disorder|lower_gastrointestinal_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0003979	intrahepatic bile duct cystadenoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	hepatology|gastroenterology	liver_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0003980	schwannoma of jugular foramen	musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|nervous_system_disorder|musculoskeletal_system_disorder	oncology|neurology|otolaryngology	tumor|cancer	spinal_disorder|brain_disorder|throat_disorder	false	true	false	false	high
MONDO:0003982	bilateral breast carcinoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	bilateral_breast_carcinoma__is_actually_just_carcinoma|cancer	lymphatic_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0003983	synchronous bilateral breast carcinoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|inflammatory_disease|adrenal_gland_disease	lymphatic_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0003984	internal auditory canal lipoma	nervous_system_disorder|musculoskeletal_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|auditory_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|nervous_system_disorder|auditory_system_disorder|otorhinolaryngologic_disease|musculoskeletal_system_disorder	neurology|otolaryngology	neurological_disease|cancer	bone_disorder|ear_disorder	false	false	false	false	medium
MONDO:0003985	chest wall lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|hematology|cardiothoracic	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|lung_disorder|chest_wall_lymphoma_does_not_fit_perfectly_to_lymphatic_disorder_as_it_is_specifically_chest_wall_related__hence_the_best_fitting_categories_are___lymphatic_disorder	false	true	false	false	high
MONDO:0003987	lung lymphoma	cancer_or_benign_tumor|respiratory_system_disorder|hematologic_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor|hematologic_disorder	oncology|pulmonology|hematology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|lung_disorder	false	false	false	true	high
MONDO:0003988	sternum lymphoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder	oncology|hematology	cancer|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|bone_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0003989	polyembryoma of the ovary	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|obstetrics_and_gynecology	gynecological_disorder|adnexal_mass|cancer	reproductive_system_disorder	false	true	false	false	high
MONDO:0003990	malignant breast myoepithelioma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease|inflammatory_disease	skin_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003991	villoglandular endometrial endometrioid adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	endometrial_adenocarcinoma|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0003992	childhood botryoid rhabdomyosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric	cancer	childhood_disorder|muscle_disorder	false	true	false	true	very_high
MONDO:0003993	childhood vagina botryoid rhabdomyosarcoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|pediatric	cancer|adrenal_gland_disease|neurodegenerative_disease|inflammatory_disease	muscle_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0003994	botryoid-type embryonal rhabdomyosarcoma of the vagina	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|pediatric	cancer|adrenal_gland_disease	muscle_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0003995	vulvar childhood botryoid-type embryonal rhabdomyosarcoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|pediatric	childhood_disease|cancer|adrenal_gland_disease	skin_disorder|muscle_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0003996	basal ganglia disorder	nervous_system_disorder	other	nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0003997	colon Kaposi sarcoma	cancer_or_benign_tumor|infectious_disease|digestive_system_disorder|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder|infectious_disease	digestive_system_disorder|cancer_or_benign_tumor|infectious_disease|cardiovascular_disorder|post_infectious_disorder	oncology|gastroenterology|hematology|dermatology	anemia|autoimmune_diseases|cancer|inflammatory_disease	skin_disorder|lower_gastrointestinal_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0003999	juvenile pilocytic astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|pediatric|neurology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	true	medium
MONDO:0004000	childhood pilocytic astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology|pediatric	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0004001	compartment syndrome	syndromic_disease	other	syndromic_disease	neurology|renal_medicine|orthopaedic|rheumatology	inflammatory_disease|soft_tissue_injury	muscle_disorder|urinary_tract_disorder|spinal_disorder|vascular_disorder|joint_disorder	false	false	false	false	high
MONDO:0004004	motor nerve neuritis	inflammatory_disease|nervous_system_disorder	other	nervous_system_disorder|inflammatory_disease	neurology|orthopaedic|pediatric	inflammatory_disease|autoimmune_diseases	muscle_disorder|neural_disorder	true	false	false	false	high
MONDO:0004005	rete ovarii adenoma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|obstetrics_and_gynecology|genetics_and_genomics	adrenal_gland_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0004006	rete ovarii cystadenofibroma	connective_tissue_disorder|reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|endocrine_system_disorder	oncology|obstetrics_and_gynecology	ovarian_cancer|cancer|gynecologic_disorder	reproductive_system_disorder	false	false	false	false	low
MONDO:0004007	breast intraductal proliferative lesion	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	reproductive_system_disorder|breast_disorder	false	false	false	false	medium
MONDO:0004008	flat ductal epithelial atypia	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|breast_disease|pathology	autoimmune_diseases|adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	medium
MONDO:0004009	kidney pelvis sarcomatoid transitional cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology|renal_medicine	transitional_cell_carcinoma|kidney_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	very_high
MONDO:0004010	infiltrating renal pelvis/ureter urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	urothelial_carcinoma|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0004012	adult botryoid rhabdomyosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric	adrenal_gland_disease|cancer	reproductive_system_disorder|muscle_disorder	false	true	false	false	high
MONDO:0004013	adult vagina botryoid embryonal rhabdomyosarcoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|genetics_and_genomics|pediatric	adrenal_gland_disease|cancer	reproductive_system_disorder|muscle_disorder	false	true	false	false	high
MONDO:0004014	ethmoid sinus ectopic meningioma	connective_tissue_disorder|musculoskeletal_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	otorhinolaryngologic_disease|respiratory_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	neurology|otolaryngology	neuro|cancer	nose_disorder|brain_disorder	false	false	false	false	high
MONDO:0004015	pineal region teratoma	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|pediatric	adrenal_gland_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0004016	pineal region mature teratoma	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	neurology|oncology	adrenal_gland_disease|cancer	spinal_disorder|brain_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0004017	pineal region immature teratoma	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	neurology|oncology|pediatric	neurological_disease_disorder|cancer	brain_disorder|endoctrine_disorder	false	true	false	false	high
MONDO:0004019	oxyphilic endometrial endometrioid adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	endometrial_adenocarcinoma|cancer	upper_gastrointestinal_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004020	mediastinal gray zone lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|pulmonology|hematology	lymphoma|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0004021	mediastinal malignant lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|pulmonology|hematology	malignant_lymphoma|cancer	lymphatic_disorder|lung_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0004022	parasagittal meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neuro_oncology|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0004024	spinal cord neuroblastoma	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	neurology|oncology|pediatric	neuroblastoma|cancer	spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0004026	skin tag	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology	autoimmune_diseases|inflammatory_disease|skin_tag	skin_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0004028	small intestinal fibrosarcoma	connective_tissue_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|digestive_system_disorder	oncology|gastroenterology|pediatric|surgical_oncology_was_in_the_original_list_but_removed_as_it_is_not_provided	sarcoma|small_intestine_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004030	ureter transitional cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology|renal_medicine	ureteral_cancer|cancer|transitional_cell_carcinoma	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0004032	ovarian seromucinous carcinoma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder|ovarian_cancer	false	true	false	false	high
MONDO:0004034	eye lymphoma	nervous_system_disorder|cancer_or_benign_tumor|hematologic_disorder|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_orbital_region|nervous_system_disorder|cancer_or_benign_tumor|hematologic_disorder|disorder_of_visual_system	oncology|ophthalmology|hematology	cancer|autoimmune_diseases	lymphatic_disorder|eye_disorder	false	true	false	true	medium
MONDO:0004035	glomangiomatosis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pathology|genetics_and_genomics	adrenal_gland_disease|cancer	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0004037	retinal edema	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_orbital_region|nervous_system_disorder|disorder_of_visual_system	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease	eye_disorder|retinal_edema	false	false	false	true	high
MONDO:0004038	dental enamel hypoplasia	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	oral_surgery_is_not_listed__so_orthopaedic|genetics_and_genomics|pediatric|otolaryngology	metabolic_disorder|dental_anomalies	teeth_disorder|dental_enamel_hypoplasia_is_likely_a_more_specific_category_name_so_teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0004039	papillary extrahepatic bile duct adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology|hepatology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|biliary_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0004040	urinary bladder inverted papilloma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology|renal_medicine	urinary_bladder_cancer|cancer	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0004041	urothelial papilloma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	urological_diseases|neoplastic_diseases|cancer	urinary_tract_disorder|kidney_disorder	false	false	false	true	low
MONDO:0004042	urethra inverted papilloma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	neoplastic_disease|cancer	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0004043	ureter inverted papilloma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine	urological_disorder|urinary_system_disorder|cancer	urinary_tract_disorder|kidney_disorder	false	false	false	false	low
MONDO:0004044	ureter urothelial papilloma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology|renal_medicine	urinary_system_disorder|urologic_malignancy|cancer|urological_cancer|urogenital_tumor	urinary_tract_disorder|kidney_disorder	false	false	false	false	low
MONDO:0004045	pediatric intraocular retinoblastoma	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_orbital_region|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system	oncology|pediatric|ophthalmology	cancer	eye_disorder	false	true	false	true	high
MONDO:0004046	childhood brain meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology|pediatric	neurological_cancer|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0004047	sphenoidal sinus neoplasm	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	respiratory_system_disorder|musculoskeletal_system_disorder|otorhinolaryngologic_disease|connective_tissue_disorder|cancer_or_benign_tumor	neurology|oncology|otolaryngology	cancer	nose_disorder|brain_disorder	false	true	false	false	high
MONDO:0004048	immature gastric teratoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology|pediatric	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004049	combat disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	acute_disease|psychiatric_disorder|nervous_system_disorder	neurology|pediatric|psychiatry	combat_disorder|mental_health_disorder	mental_disorder|combat_disorder|brain_disorder	false	false	false	false	high
MONDO:0004050	telangiectatic osteogenic sarcoma	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	oncology|orthopaedic	sarcoma|cancer	bone_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0004051	aleukemic monocytic leukemia cutis	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|immune_system_disorder|acute_disease|connective_tissue_disorder|cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	inflammatory_disease|anemia|cancer	skin_disorder|immune_disorder|blood_bone_marrow_disorder	true	true	false	false	high
MONDO:0004052	rectal cloacogenic carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	rectal_disease|carcinogenic_carcinoma|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004053	bartholin gland squamous cell carcinoma	reproductive_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor	oncology|urology|obstetrics_and_gynecology	inflammatory_disease|cancer	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0004054	acute canaliculitis	disorder_of_visual_system	other	disorder_of_orbital_region|acute_disease|disorder_of_visual_system	dermatology|otolaryngology	autoimmune_diseases|allergic_reactions|inflammatory_disease	othogonal|ear_disorder	true	false	false	true	medium
MONDO:0004055	acute inflammation of lacrimal passage	disorder_of_visual_system	other	disorder_of_orbital_region|acute_disease|disorder_of_visual_system	ophthalmology|otolaryngology	autoimmune_diseases|inflammatory_disease	eye_disorder|nasal_disorder	true	false	false	false	low
MONDO:0004056	bladder papillary urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	urothelial_carcinoma|adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	medium
MONDO:0004057	micropapillary variant infiltrating bladder urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|urotheleial_carcinoma|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	very_high
MONDO:0004058	pancreatic cholera	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	gastroenterology|endocrinology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0004059	dentin sensitivity	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	neurology|dentistry|oral_pathology	oral_health_disorder|dentin_sensitivity_can_be_classified_as_an_inflammatory_disease	teeth_disorder	false	false	false	true	low
MONDO:0004060	peripheral epithelioid sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|oncology|hematology|genetics_and_genomics	cancer|adrenal_gland_disease	skin_disorder|soft_tissue_disorder|bone_disorder	false	true	false	false	very_high
MONDO:0004062	intermediate cell type uveal melanoma	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region|nervous_system_disorder|disorder_of_development_or_morphogenesis	ophthalmology|oncology	cancer|adrenal_gland_disease	eye_disorder|skin_disorder	false	true	false	false	high
MONDO:0004063	intermediate cell type iris melanoma	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region|nervous_system_disorder|disorder_of_development_or_morphogenesis	ophthalmology|oncology	cancer___becomes___cancer|cancer|adrenal_gland_disease	eye_disorder|skin_disorder	false	true	false	true	high
MONDO:0004064	iris melanoma	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_visual_system|disorder_of_orbital_region|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis	dermatology|ophthalmology|oncology	cancer|adrenal_gland_disease	eye_disorder|skin_disorder	false	true	false	true	high
MONDO:0004065	intermediate cell type choroid melanoma	disorder_of_visual_system|nervous_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor|cardiovascular_disorder	disorder_of_visual_system|cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_orbital_region|nervous_system_disorder|disorder_of_development_or_morphogenesis	ophthalmology|oncology	cancer|adrenal_gland_disease	eye_disorder	false	true	false	true	medium
MONDO:0004066	intermediate cell type ciliary body melanoma	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_visual_system|disorder_of_orbital_region|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis	dermatology|oncology	melanoma|cancer|adrenal_gland_disease	eye_disorder|skin_disorder	false	true	false	false	high
MONDO:0004067	gallbladder mucinous adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	hepatology|gastroenterology|oncology	cancer|adrenal_gland_disease	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004069	inborn mitochondrial metabolism disorder	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	metabolic_disease	mitochondrial_disease|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0004071	childhood cerebral astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|pediatric	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0004074	ovarian mucinous cystadenofibroma	endocrine_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder|connective_tissue_disorder	oncology|obstetrics_and_gynecology	ovarian_cancer|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0004075	infiltrating lipoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	dermatology|oncology	inflammatory_disease|cancer	skin_disorder|muscle_disorder	false	false	false	false	low
MONDO:0004076	tendon sheath lipoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	dermatology|orthopaedic	inflammatory_disease|cancer	skin_disorder|muscle_disorder|joint_disorder	false	false	false	false	low
MONDO:0004077	lumbosacral lipoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	neurology|orthopaedic|oncology	tumor____corrected_version_of_the_answer___cancer|tumor|cancer	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0004078	mucinous intrahepatic cholangiocarcinoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	hepatology|oncology	intrahepatic_cholangiocarcinoma|cancer	liver_disorder|biliary_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004079	lung mucous gland adenoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|oncology	gland_disease|adrenal_gland_disease|cancer	lung_disorder	false	false	false	false	low
MONDO:0004080	glottis squamous cell carcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer	thoracic_disorder|respiratory_disorder|throat_disorder	false	true	false	true	high
MONDO:0004081	extrahepatic bile duct clear cell adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	hepatology|oncology|gastroenterology	cancer|adrenal_gland_disease	biliary_disorder|liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004082	childhood immature teratoma of ovary	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|obstetrics_and_gynecology|pediatric	pediatric_cancer|ovarian_cancer|cancer	reproductive_system_disorder|ovarian_disorder	false	true	false	true	high
MONDO:0004083	Borst-Jadassohn intraepidermal carcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	autoimmune_diseases|cancer	skin_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0004085	choroid epithelioid cell melanoma	disorder_of_visual_system|nervous_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region|nervous_system_disorder|disorder_of_development_or_morphogenesis	oncology|ophthalmology	eye_disease|melanoma|cancer	eye_disorder	false	true	false	false	high
MONDO:0004086	ciliary body epithelioid cell melanoma	disorder_of_visual_system|nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region|nervous_system_disorder|disorder_of_development_or_morphogenesis	oncology|ophthalmology	autoimmune_diseases|cancer	skin_disorder|eye_disorder	false	true	false	false	high
MONDO:0004087	basaloid large cell lung carcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|oncology	lung_carcinoma|cancer	lung_disorder	false	true	false	false	very_high
MONDO:0004088	cervical basaloid carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	reproductive_system_disorder|throat_disorder	false	true	false	false	very_high
MONDO:0004089	basaloid carcinoma of the penis	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|post_infectious_disorder	urology|oncology	cancer	reproductive_system_disorder|skin_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004090	vulvar basaloid squamous cell carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	dermatology|oncology|obstetrics_and_gynecology	cardiovascular_disorder|autoimmune_diseases|adrenal_gland_disease|inflammatory_disease|cancer	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0004091	skin basaloid carcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	skin_cancer|tumor|cancer	skin_disorder	false	true	false	true	medium
MONDO:0004092	thymic basaloid carcinoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor|endocrine_system_disorder	pulmonology|cardiology|oncology|cardiothoracic	thyroid_cancer|cancer	immune_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0004093	esophageal basaloid carcinoma	digestive_system_disorder|upper_digestive_tract_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|upper_digestive_tract_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004094	multiple skull base meningioma	musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0004095	B-cell neoplasm	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	autoimmune_diseases|cancer	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004096	spinal cord dermoid cyst	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	orthopaedic|neurology	neurological_disease|cancer	skin_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0004098	malignant melanocytic peripheral nerve sheath tumor of mediastinum	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	dermatology|oncology|cardiothoracic|neurology	neurodegenerative_disease|cancer	nerve_disorder|skin_disorder|muscle_disorder|lung_disorder	false	true	false	false	high
MONDO:0004099	adult cystic teratoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics|pediatric	cancer|adrenal_gland_disease	reproductive_system_disorder|muscle_disorder	false	true	false	false	medium
MONDO:0004100	lung mixed small cell and squamous cell carcinoma	respiratory_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|respiratory_system_disorder	oncology|pulmonology	squamous_cell_lung_cancer|small_cell_lung_cancer|cancer|lung_carcinoma	lung_disorder|lower_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0004101	multicentric papillary thyroid carcinoma	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	adrenal_gland_disease|thyroid_carcinoma|autoimmune_diseases|cancer	endocrine_disorder|thyroid_carcinoma	false	true	false	false	high
MONDO:0004102	columnar cell variant thyroid gland papillary carcinoma	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	thyroid_gland_disease|cancer|papillary_carcinoma	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0004103	tall cell variant thyroid gland papillary carcinoma	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	thyroid_gland_disease|cancer|papillary_carcinoma	endocrine_disorder|upper_gastrointestinal_disorder|lung_disorder	false	true	false	false	high
MONDO:0004104	splenic manifestation of hairy cell leukemia	cancer_or_benign_tumor|immune_system_disorder|digestive_system_disorder|hematologic_disorder	cancer_or_benign_tumor	acute_disease|cancer_or_benign_tumor|digestive_system_disorder|immune_system_disorder|hematologic_disorder	oncology|hematology|hematatology	inflammatory_disease|anemia|autoimmune_diseases|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	medium
MONDO:0004105	childhood epithelioid sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics|pediatric|allergy_and_immunology	cancer	skin_disorder|lymphatic_disorder|bone_disorder	false	true	false	false	high
MONDO:0004106	testicular yolk sac tumor, macrocystic pattern	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology|genetics_and_genomics|pediatric	cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	true	high
MONDO:0004107	splenic manifestation of leukemia	immune_system_disorder|digestive_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	digestive_system_disorder|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	anemia|autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	true	true	false	true	high
MONDO:0004108	diaphragma sellae meningioma	musculoskeletal_system_disorder|connective_tissue_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0004109	epiglottis neoplasm	respiratory_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease	oncology|otolaryngology	cancer|adrenal_gland_disease	throat_disorder|lung_disorder|immune_disorder	false	true	false	false	high
MONDO:0004110	refractory hairy cell leukemia	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	acute_disease|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	anemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0004111	refractory hematologic cancer	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	hematologic_cancer|autoimmune_diseases|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0004112	radiation cystitis	urinary_system_disorder|inflammatory_disease	other	inflammatory_disease|urinary_system_disorder	urology|oncology	autoimmune_diseases|cancer|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	true	high
MONDO:0004114	urinary bladder small cell neuroendocrine carcinoma	urinary_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	neuroendocrine_carcinoma|urologic_cancer|cancer	endocrine_disorder|urinary_tract_disorder|kidney_disorder	false	true	false	false	very_high
MONDO:0004116	esophageal small cell neuroendocrine carcinoma	digestive_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	oncology|gastroenterology	neuroendocrine_carcinoma|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0004117	ampulla of vater small cell neuroendocrine carcinoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology|pediatric	neuroendocrine_carcinoma|cancer	neuroendocrine_disorder|lower_gastrointestinal_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0004118	cystitis cystica	inflammatory_disease|urinary_system_disorder	other	inflammatory_disease|urinary_system_disorder	urology|renal_medicine	autoimmune_diseases|metabolic_disorder|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	low
MONDO:0004120	Bartholin gland small cell carcinoma	reproductive_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	integumentary_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|obstetrics_and_gynecology|oncology	autoimmune_diseases|cancer|adrenal_gland_disease|inflammatory_disease	lymphatic_disorder|lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004122	thymus small cell carcinoma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|endocrine_system_disorder|cancer_or_benign_tumor	immunology|oncology|cardiothoracic	cancer|adrenal_gland_disease	lymphatic_disorder|lung_disorder|immune_disorder	false	true	false	false	very_high
MONDO:0004124	prostate stromal sarcoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	cancer|adrenal_gland_disease	muscle_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004125	rectum leiomyoma	musculoskeletal_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|gastroenterology	gastrointestinal_disease|neoplasm|cancer	muscle_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0004126	thyroiditis	inflammatory_disease|endocrine_system_disorder	endocrine_system_disorder	inflammatory_disease|endocrine_system_disorder	endocrinology|rheumatology	autoimmune_diseases|inflammatory_disease	endocrine_disorder|immune_disorder	false	false	false	true	medium
MONDO:0004127	lung occult adenocarcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|pulmonology	lung_cancer|cancer|adenocarcinoma	lung_disorder|lung_disorde	false	true	false	false	high
MONDO:0004128	lung occult large cell carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|pulmonology	lung_cancer|carcinoma|cancer	lung_disorder	false	true	false	false	very_high
MONDO:0004129	cloacogenic carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	urology|oncology|pulmonology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004130	anus basaloid carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004131	anal verrucous carcinoma	digestive_system_disorder|reproductive_system_disorder|infectious_disease|cancer_or_benign_tumor	infectious_disease|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|infectious_disease|reproductive_system_disorder	oncology|dermatology	cancer	skin_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0004132	anal canal squamous cell carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer	skin_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0004133	pituitary gland mixed eosinophil-basophil adenoma	musculoskeletal_system_disorder|connective_tissue_disorder|nervous_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|endocrine_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder	neurology|endocrinology	adrenal_gland_disease|cancer	endocrine_disorder|brain_disorder	false	true	false	false	medium
MONDO:0004134	benign dermal neurilemmoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	neurology|oncology|dermatology	neurodegenerative_disease|cancer	skin_disorder	false	false	false	true	low
MONDO:0004135	subacute lymphocytic thyroiditis	inflammatory_disease|endocrine_system_disorder	endocrine_system_disorder	inflammatory_disease|acute_disease|endocrine_system_disorder	endocrinology|rheumatology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|endocrine_disorder|immune_disorder	false	false	false	true	medium
MONDO:0004136	ovarian endometrioid cystadenoma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	endometrioid_tumor|cancer|ovarian_cancer|gynecologic_cancer|reproductive_system_cancer	reproductive_system_disorder|ovarian_disorder	false	false	false	false	low
MONDO:0004139	normocytic anemia	hematologic_disorder	anemia	hematologic_disorder	hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0004140	intermediate malignant teratoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pathology|oncology|pediatric	cancer|adrenal_gland_disease	blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0004141	melanomatosis	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	oncology|dermatology	cancer|adrenal_gland_disease	skin_disorder|lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	high
MONDO:0004142	lung combined large cell neuroendocrine carcinoma	respiratory_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	respiratory_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	neuroendocrinology|oncology|pulmonology	neuroendocrine_carcinoma|lung_cancer|cancer	neuroendocrine_disorder|breast_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0004143	psammomatous meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurooncology_disorder|cancer	spinal_disorder|brain_disorder	false	true	false	false	medium
MONDO:0004144	fibrous meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neuro|cancer	spinal_disorder|brain_disorder	false	true	false	false	medium
MONDO:0004145	meningothelial meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	medium
MONDO:0004146	transitional meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0004147	noninvasive malignant thymoma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|pulmonology	invasive_malignant_thymoma|cancer|adrenal_gland_disease	lymphatic_disorder|lung_disorder	false	true	false	false	medium
MONDO:0004148	gallbladder papillary neoplasm with an associated invasive carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|inflammatory_disease	upper_gastrointestinal_disorder|liver_disorder	false	true	false	true	very_high
MONDO:0004149	gallbladder pleomorphic giant cell adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	hepatology|oncology|gastroenterology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0004150	breast giant fibroadenoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	female_reproductive_system_disorder|benign_tumor|cancer	breast_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0004151	spinal meninges cancer	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	spinal_meninges_cancer|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0004152	chronic lymphocytic leukemia/small lymphocytic lymphoma with immunoglobulin heavy chain variable-region gene somatic hypermutation	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	acute_disease|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	low
MONDO:0004153	childhood central nervous system embryonal carcinoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric|neurology	cancer	spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0004155	adult central nervous system embryonal carcinoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	central_nervous_system_cancer|embryonal_carcinoma|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0004156	pancreatic mucinous cystadenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cystadenocarcinoma|pancreatic_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004158	pancreatic mucinous-cystic neoplasm with an associated invasive carcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	adrenal_gland_disease|pancreatic_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0004159	pancreatic non-invasive mucinous cystadenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|oncology|gastroenterology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0004160	female stress incontinence	urinary_system_disorder	other	urinary_system_disorder	obstetrics_and_gynecology|urology	inflammatory_disease|neurodegenerative_disease	urinary_tract_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0004161	uterine corpus apoplectic leiomyoma	connective_tissue_disorder|musculoskeletal_system_disorder|hereditary_disease|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder|musculoskeletal_system_disorder	obstetrics_and_gynecology|oncology	cancer	muscle_disorder|vascular_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0004162	uterine corpus cellular leiomyoma	connective_tissue_disorder|musculoskeletal_system_disorder|hereditary_disease|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder|musculoskeletal_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|autoimmune_diseases|cancer	uterus_is_part_of_the_reproductive_system_but_more_specific_to_this_condition_would_be_a_category_related_to_female_genital_organs_so__reproductive_system_disorder|muscle_disorder|female_genital_organ_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0004163	bladder urachal urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	bladder_urothelial_carcinoma|urothelial_carcinoma|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0004164	lymphoepithelioma-like acinar prostate adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	adrenal_gland_disease|autoimmune_diseases|prostate_adenocarcinoma|cancer	lymphatic_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0004165	selective IgD deficiency disease	immune_system_disorder|hereditary_disease|hematologic_disorder	other	hereditary_disease|immune_system_disorder|hematologic_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0004166	hereditary fallopian tube carcinoma	hereditary_disease|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology|genetics_and_genomics	hereditary_cancer|cancer	hereditary_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004168	cribriform variant testicular seminoma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	adrenal_gland_disease|cancer	lymphatic_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004169	premenstrual tension	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|neurology	mental_health_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0004170	nodular episcleritis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder	false	false	false	true	low
MONDO:0004172	uterine corpus adenocarcinofibroma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer	uterine_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0004173	adenocarcinoma of skene gland origin	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004174	secretory uterine corpus endometrioid adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|corpus_endometrial_cancer|endometrial_cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004175	mucin-rich endometrial endometrioid adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004176	childhood extraosseous osteosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|orthopaedic|pediatric	cancer|childhood_disease|bone_cancer	spinal_disorder|bone_disorder	false	true	false	false	very_high
MONDO:0004177	benign urethral neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer	urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0004178	testicular yolk sac tumor, endodermal sinus pattern	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|genetics_and_genomics|oncology|pediatric	cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	true	high
MONDO:0004180	benign urinary system neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer|benign_neoplasm	urinary_tract_disorder|kidney_disorder	false	false	false	false	low
MONDO:0004181	breast adenomyoepithelial adenosis	breast_disorder	other	breast_disorder	obstetrics_and_gynecology|oncology	cancer|breast_cancer|adenomyoepithelioma	breast_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0004182	stage IVb bladder cancer	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer|adrenal_gland_disease	lymphatic_disorder|urinary_tract_disorder	false	true	false	false	very_high
MONDO:0004183	axonal neuropathy	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0004184	urethral disorder	urinary_system_disorder	other	urinary_system_disorder	urethral_disorder|urology|renal_medicine	inflammatory_disease|autoimmune_diseases|urethral_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0004185	ovarian serous cystadenofibroma	connective_tissue_disorder|reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	ovarian_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0004186	cranial nodular fasciitis	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|integumentary_system_disorder|inflammatory_disease	cancer_or_benign_tumor	integumentary_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|inflammatory_disease|musculoskeletal_system_disorder	dermatology|neurology	inflammatory_disease|autoimmune_diseases	muscle_disorder|skin_disorder	false	false	false	true	low
MONDO:0004187	nodular fasciitis	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|integumentary_system_disorder|inflammatory_disease	cancer_or_benign_tumor	integumentary_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|inflammatory_disease|musculoskeletal_system_disorder	orthopaedic|dermatology	inflammatory_disease|autoimmune_diseases	muscle_disorder|skin_disorder	false	false	false	false	low
MONDO:0004188	iris spindle cell melanoma	nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_orbital_region|nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	oncology|dermatology	cancer|adrenal_gland_disease	eye_disorder|skin_disorder	false	true	false	false	high
MONDO:0004189	esophageal tuberculosis	digestive_system_disorder|upper_digestive_tract_disorder|infectious_disease	infectious_disease	digestive_system_disorder|infectious_disease|upper_digestive_tract_disorder	gastroenterology|pulmonology	cancer|inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lung_disorder	true	false	false	true	medium
MONDO:0004190	nephrogenic adenoma of urinary bladder	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine	neurogenic_adenoma_of_urinary_bladder____cancer	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0004191	nephrogenic adenoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine	cancer|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0004192	urethra cancer	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer|urinary_system_disorders	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0004193	pediatric ovarian dysgerminoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	pediatric|oncology	cancer|pediatric_disease	reproductive_system_disorder	false	true	false	true	high
MONDO:0004194	ovarian stromal hyperthecosis	endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|endocrinology|oncology|gastroenterology|hematology|hepatology	cancer|autoimmune_diseases|inflammatory_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0004195	thymic dysplasia	immune_system_disorder|endocrine_system_disorder|hematologic_disorder	endocrine_system_disorder	immune_system_disorder|hematologic_disorder|endocrine_system_disorder	pediatrics|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder_lymphatic_disorder	false	false	false	false	high
MONDO:0004196	rectal sarcomatoid carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004197	male urethral cancer	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer|adrenal_gland_disease	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0004198	testicular yolk sac tumor, solid pattern	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	pediatric|urology|oncology	cancer|solid_tumor|germ_cell_tumor	lymphatic_disorder|blood_bone_marrow_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0004199	vulvar keratinizing squamous cell carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer|inflammatory_disease	skin_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0004200	superficial urinary bladder carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer|urinary_bladder_disease	urinary_tract_disorder|kidney_disorder	false	true	false	true	medium
MONDO:0004201	pituitary hypoplasia	endocrine_system_disorder|nervous_system_disorder|reproductive_system_disorder	endocrine_system_disorder	nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder	endocrinology|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0004202	adrenal medulla carcinoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology|genetics_and_genomics	adrenal_gland_disease|cancer	blood_bone_marrow_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0004203	female urethral cancer	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology|urology	adrenal_gland_disease|cancer|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0004204	squamous cell skin papilloma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	skin_papilloomas_are_a_type_of_cancer_so_i_removed_that_category_from_the_list_and_the_best_fit_is___cancer|cancer	skin_disorder	false	false	false	false	medium
MONDO:0004205	lymphohistiocytoid mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|hematology|pulmonology	cancer|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	true	false	false	high
MONDO:0004206	pulmonary vein leiomyosarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|cardiovascular_disorder	oncology|cardiothoracic|pulmonology	cancer	vascular_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0004207	pulmonary artery leiomyosarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|cardiovascular_disorder	oncology|cardiothoracic|pulmonology	cardiovascular_disorder|cancer	vascular_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0004208	superior vena cava leiomyosarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	musculoskeletal_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|cardiovascular_disorder	oncology|cardiothoracic|hematology	cancer|cardiovascular_disorder	muscle_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0004209	cerebral primitive neuroectodermal tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0004210	colonic L-cell glucagon-like peptide producing tumor	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology	cancer|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0004211	L-cell glucagon-like peptide-producing neuroendocrine tumor	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	neurology|oncology|endocrinology	neuroendocrine_tumor|cancer	upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0004212	vulvar keratoacanthoma-like carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer|inflammatory_disease|autoimmune_diseases	skin_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0004213	vulvar non-keratinizing squamous cell carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	dermatology|obstetrics_and_gynecology|oncology	cancer|inflammatory_disease|autoimmune_diseases	skin_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0004214	ovarian endometrioid cystadenofibroma	cancer_or_benign_tumor|connective_tissue_disorder|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	connective_tissue_disorder|reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	gynecological_cancer|cancer	reproductive_system_disorder|ovarian_disorder	false	false	false	false	low
MONDO:0004215	cutaneous anthrax	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology|microbiology|infectious_diseases	cutaneous_inflammatory_disease|inflammatory_disease|autoimmune_diseases	skin_disorder|lung_disorder	true	false	false	true	medium
MONDO:0004216	pineal region germinoma	cancer_or_benign_tumor|endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|pediatric	tumor|neurological_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0004217	childhood brain germinoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|pediatric	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0004218	childhood germ cell brain tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|pediatric	cancer|childhood|brain_tumor	reproductive_system_disorder|brain_disorder	false	true	false	true	high
MONDO:0004219	polyvesicular vitelline pattern testicular yolk sac tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|pediatric	adrenal_gland_disease|cancer	reproductive_system_disorder|kidney_disorder	false	true	false	true	high
MONDO:0004220	endometrial endometrioid adenocarcinoma with spindled epithelial cells	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer|inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004221	uterine corpus perivascular epithelioid cell tumor	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|autoimmune_diseases	reproductive_system_disorder|vascular_disorder	false	true	false	false	medium
MONDO:0004222	ovarian clear cell cystadenocarcinoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004223	polyp of middle ear	cancer_or_benign_tumor|otorhinolaryngologic_disease|auditory_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|auditory_system_disorder	otolaryngology|pediatric	cancer|inflammatory_disease|autoimmune_diseases	throat_disorder|upper_gastrointestinal_disorder|ear_disorder	false	false	false	false	low
MONDO:0004224	chronic metabolic polyneuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology|endocrinology	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|muscle_disorder	false	false	true	false	high
MONDO:0004225	monoclonal gammopathy of uncertain significance	hematologic_disorder	other	hematologic_disorder	oncology|hematology	anemia|cancer|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0004226	diffuse intraductal papillomatosis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|oncology|pathology|gastroenterology	cancer|adenoma	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0004227	epididymal adenomatoid tumor	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology|urology	cancer	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	none
MONDO:0004229	acantholytic variant squamous cell breast carcinoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|squamous_cell_breast_carcinoma|cancer|autoimmune_diseases	reproductive_system_disorder|skin_disorder	false	true	false	false	very_high
MONDO:0004230	adenomatoid tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	neurology|oncology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|kidney_disorder	false	false	false	false	low
MONDO:0004231	spindle cell variant squamous cell breast carcinoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	breast_carcinoma|cancer	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0004232	large cell keratinizing variant squamous cell breast carcinoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	dermatology|obstetrics_and_gynecology|oncology	breast_carcinoma|squamous_cell_carcinoma|cancer	reproductive_system_disorder|skin_disorder	false	true	false	false	very_high
MONDO:0004233	childhood pleomorphic rhabdomyosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics|pediatric	adrenal_gland_disease|cancer	childhood_disorder|muscle_disorder	false	true	false	true	very_high
MONDO:0004234	chronic lymphoproliferative disorder of NK-cells	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|autoimmune_diseases	immune_disorder_lymphatic_disorder	false	true	false	false	medium
MONDO:0004235	diverticulitis	digestive_system_disorder|inflammatory_disease	other	digestive_system_disorder|inflammatory_disease	gastroenterology|hepatology	gastrointestinal_disorder|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0004236	duodenal somatostatinoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology|gastroenterology	endocrine_disorder|cancer	upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0004237	large cell carcinoma with rhabdoid phenotype	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	neurology|oncology|hematology|pediatric	adrenal_gland_disease|cancer	lung_disorder	false	true	false	false	very_high
MONDO:0004238	petrous apex meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|otolaryngology	neurological_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0004239	cervical keratinizing squamous cell carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|dermatology|oncology	cancer|squamous_cell_carcinoma	skin_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0004240	posterior urethra cancer	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer|adrenal_gland_disease	urinary_tract_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0004241	Osgood-Schlatter disease	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	pediatric|orthopaedic	musculoskeletal_disorder___corrected_answer_again___inflammatory_disease|inflammatory_disease|musculoskeletal_disorder|musculoskeletal_disorder___corrected_answer__inflammatory_disease	joint_disorder|bone_disorder	false	false	false	true	low
MONDO:0004242	active peptic ulcer disease	digestive_system_disorder	other	ulcer_disease|digestive_system_disorder	gastroenterology|hepatology|cardiology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0004243	vulvar proximal-type epithelioid sarcoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	sarcoma|cancer	skin_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004244	proximal-type epithelioid sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|oncology|orthopaedic	inflammatory_disease|cancer|adrenal_gland_disease	muscle_disorder|soft_tissue_disorder	false	true	false	false	very_high
MONDO:0004245	ependymal tumor of brain	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neuro|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0004247	peptic ulcer disease	digestive_system_disorder	other	ulcer_disease|digestive_system_disorder	gastroenterology|internal_medicine|general_medicine	metabolic_disorder|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0004248	pediatric infratentorial ependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|pediatric|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0004249	pediatric supratentorial ependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|pediatric|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0004250	extrahepatic bile duct papillary adenoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	gastroenterology|oncology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|biliary_disorder|liver_disorder	false	false	false	false	low
MONDO:0004251	small intestine neoplasm	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	gastrointestinal_disease|cancer|neoplasm	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0004252	small intestinal L-cell glucagon-like peptide producing tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	gastroenterology|oncology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0004253	intraductal breast papillomatosis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	inflammatory_disease|autoimmune_diseases|cancer	breast_disorder|skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0004254	focal intraductal papillomatosis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pathology_is_incorrect__since_the_category_list_does_not_have_this_label__i_ll_choose_oncology|obstetrics_and_gynecology|oncology|dermatology	benign_tumor|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	low
MONDO:0004255	Wolffian adnexal tumor	musculoskeletal_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	urology|obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0004256	lumbar spinal canal and spinal cord meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder	false	true	false	true	high
MONDO:0004257	childhood central nervous system mixed germ cell tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pediatric|oncology	autoimmune_diseases|neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0004258	female orgasmic disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|obstetrics_and_gynecology	mental_health_disorder|psychological_condition	muscle_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0004259	endocervical carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancerous_condition|cancer|endocrine_disorder	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0004260	peptic ulcer perforation	digestive_system_disorder	other	ulcer_disease|digestive_system_disorder	general_surgery|hepatology|gastroenterology	inflammatory_disease|gastrointestinal_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0004261	periductal breast myoepitheliosis	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology|dermatology	inflammatory_disease|autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	false	false	false	false	low
MONDO:0004262	breast myoepitheliosis	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	autoimmune_diseases|cancer	immune_disorder_lymphatic_disorder	false	false	false	false	low
MONDO:0004263	pediatric infratentorial ependymoblastoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pediatric|oncology|neurology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0004264	acute gonococcal endometritis	inflammatory_disease|reproductive_system_disorder	other	reproductive_system_disorder|inflammatory_disease|acute_disease	urology|obstetrics_and_gynecology	endometritis|inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0004265	acute endometritis	inflammatory_disease|reproductive_system_disorder	other	reproductive_system_disorder|inflammatory_disease|acute_disease	obstetrics_and_gynecology|gynecology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0004266	anal gland adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	urology|oncology	cancer|adrenal_gland_disease	lymphatic_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004267	squamous papillomatosis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|dermatology	infectious_disease|skin_disease|cancer	skin_disorder|reproductive_system_disorder	true	false	false	false	low
MONDO:0004269	breast cystic hypersecretory carcinoma	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	inflammatory_disease|autoimmune_diseases|cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0004270	breast ductal adenoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder	false	false	false	false	low
MONDO:0004271	pregnancy adenoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	cancer|neoplasm|adrenal_gland_disease	female_reproductive_system_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0004272	urinary bladder tuberculosis	urinary_system_disorder|infectious_disease	infectious_disease	infectious_disease|urinary_system_disorder	urology|renal_medicine	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder|subtype	true	false	false	true	medium
MONDO:0004273	breast apocrine adenoma	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0004274	mixed epithelial/mesenchymal metaplastic breast carcinoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	mixed_epithelial_mesenchymal_metaplastic_breast_carcinoma_does_not_fit_into_other_categories_so_this_is_the_first_choice|cancer	upper_gastrointestinal_disorder|breast_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004275	osteosarcoma arising in bone Paget disease	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	genetics_and_genomics|oncology|orthopaedic	autoimmune_diseases|cancer	blood_bone_marrow_disorder|bone_disorder	false	true	false	true	very_high
MONDO:0004276	ceruminoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	otolaryngology|dermatology	cancer|adrenal_gland_disease	teeth_disorder|ear_disorder	false	true	false	false	low
MONDO:0004277	gonorrhea	reproductive_system_disorder|infectious_disease	infectious_disease	infectious_disease|reproductive_system_disorder	urology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0004278	infiltrating bladder urothelial carcinoma sarcomatoid variant	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	urologic_disease|cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	true	false	false	very_high
MONDO:0004279	glossopharyngeal motor neuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|throat_disorder	false	false	false	false	medium
MONDO:0004280	asymmetric motor neuropathy	nervous_system_disorder|inflammatory_disease	other	inflammatory_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0004281	vulvar eccrine porocarcinoma	reproductive_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|skin_disorder	false	true	false	false	medium
MONDO:0004283	vulvar clear cell hidradenocarcinoma	reproductive_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	obstetrics_and_gynecology|dermatology|oncology	hidradenocarcinoma|cancer	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0004285	pancreatic intraductal papillary-mucinous carcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology	cancer|pancreatic	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004286	pancreatic intraductal papillary-mucinous neoplasm	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004287	pancreatic foamy gland adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology	autoimmune_diseases|inflammatory_disease|cancer	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004288	scirrhous breast carcinoma	breast_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0004289	glottis verrucous carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|oncology|otolaryngology	autoimmune_diseases|inflammatory_disease|cancer	throat_disorder|skin_disorder	false	true	false	true	medium
MONDO:0004290	subglottis verrucous carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	inflammatory_disease|cancer	throat_disorder|skin_disorder	false	true	false	false	high
MONDO:0004291	subglottis squamous cell carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|throat_disorder	false	true	false	true	high
MONDO:0004292	supraglottis verrucous carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	autoimmune_diseases|inflammatory_disease|cancer	upper_gastrointestinal_disorder|throat_disorder	false	true	false	true	medium
MONDO:0004293	supraglottis squamous cell carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|throat_disorder	false	true	false	true	high
MONDO:0004294	gestational ovarian choriocarcinoma	reproductive_system_disorder|obstetric_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|obstetric_disorder|cancer_or_benign_tumor|endocrine_system_disorder	obstetrics_and_gynecology|oncology	autoimmune_diseases|inflammatory_disease|cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	true	high
MONDO:0004295	asbestos-related lung carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|oncology	autoimmune_diseases|inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|lung_disorder	false	true	false	true	very_high
MONDO:0004296	cervical lymphoepithelioma-like carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	lymphoma_like_carcinoma|cancer	lymphatic_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004297	lymphoepithelioma-like thymic carcinoma	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|endocrine_system_disorder|hematologic_disorder	hematology|pulmonology|oncology	lymphoma|cancer	lymphatic_disorder|immune_disorder	false	true	false	false	high
MONDO:0004298	stomach disorder	digestive_system_disorder	other	digestive_system_disorder	gastroenterology	metabolic_disorder|inflammatory_disease|gastrointestinal____corrected_response_to_fit_the_original_request_____metabilic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0004299	infiltrating bladder lymphoepithelioma-like carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0004301	fibrosarcomatous osteosarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	oncology|orthopaedic	cancer	joint_disorder|muscle_disorder|upper_gastrointestinal_disorder|bone_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0004302	chief cell adenoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrinology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0004303	parathyroid gland clear cell adenoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	renal_medicine|endocrinology|oncology	metabolic_disorder|cancer	endocrine_disorder|thyroid_disorder	false	false	false	false	high
MONDO:0004304	mixed cell type adenoma of parathyroid	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrinology|oncology|otolaryngology	metabolic_disorder|cancer|endocrine_disorder	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0004305	parathyroid oncocytic adenoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrinology|genetics_and_genomics|oncology	metabolic_disorder|cancer|parathyroid_disease|endocrine_disorder|adrenal_gland_disease	endocrine_disorder|parathyroid_disorder	false	true	false	false	medium
MONDO:0004306	childhood intracortical osteosarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	pediatric|oncology|orthopaedic	skeletal_disorder|childhood_disease|osteosarcoma|cancer	joint_disorder|bone_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0004307	sarcomatosis of the meninges	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	inflammatory_disease|neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0004308	meningeal sarcoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer	brain_disorder_spinal_disorder	false	true	false	false	high
MONDO:0004309	sarcomatosis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|oncology|orthopaedic	cancer|adrenal_gland_disease	muscle_disorder|bone_disorder	false	true	false	false	very_high
MONDO:0004310	adult embryonal tumor with multilayered rosettes, c19mc-altered	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|genetics_and_genomics|oncology	neurodegenerative_disease|cancer	brain_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0004311	carcinoma of Cowper glands	cancer_or_benign_tumor|urinary_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder|reproductive_system_disorder	urology|oncology	cancer|adrenal_gland_disease	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004312	suprasellar meningioma	cancer_or_benign_tumor|nervous_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|nervous_system_disorder	neurology|oncology	neuro|cancer	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0004313	gasserian ganglion meningioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neuro___note__the_category_is_chosen_based_on_the_fact_that_a_gasserian_ganglion_meningioma_is_a_type_of_tumor__specifically_a_benign_brain_tumor__which_falls_under_cancer__additionally__it_affects_the_nervous_system__which_may_also_categorize_it_as_neuro|cancer	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0004314	malignant cutaneous granular cell skin tumor	integumentary_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|nervous_system_disorder	dermatology|oncology	cancer|skin_cancer	skin_disorder	false	true	false	false	medium
MONDO:0004315	cholangiolocellular carcinoma	cancer_or_benign_tumor|digestive_system_disorder|connective_tissue_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|connective_tissue_disorder|endocrine_system_disorder|digestive_system_disorder	oncology|hepatology|gastroenterology	cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004316	acantholytic squamous cell skin carcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	autoimmune_diseases|cancer	skin_disorder	false	true	false	false	high
MONDO:0004317	multiple spinal canal and spinal cord meningioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0004318	pulmonary type ovarian small cell carcinoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology|pulmonology	cancer|adrenal_gland_disease	lung_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0004319	hypercalcemic type ovarian small cell carcinoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	metabolic_disorder|autoimmune_diseases|inflammatory_disease|cancer|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0004320	adult infiltrating astrocytic neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurodegenerative_disease|inflammatory_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0004321	endometrial mixed adenocarcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	endometrial_disease|adenocarcinoma|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004322	non-gestational ovarian choriocarcinoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	blood_bone_marrow_disorder|immune_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0004323	muscular atrophy	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|neurology	muscular_dysfunction|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0004324	testicular fibroma	connective_tissue_disorder|endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder|endocrine_system_disorder	oncology|urology	tumor|cancer	muscle_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0004325	testicular thecoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	oncology|urology	cancer|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	true	false	false	low
MONDO:0004326	sphenoid sinus inverted papilloma	otorhinolaryngologic_disease|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|nervous_system_disorder|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|nervous_system_disorder	oncology|otolaryngology	inflammatory_disease|cancer	eye_disorder|nose_disorder|ear_disorder|throat_disorder	false	false	false	true	medium
MONDO:0004327	sphenoid sinus Schneiderian papilloma	otorhinolaryngologic_disease|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|nervous_system_disorder|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|nervous_system_disorder	oncology|otolaryngology	inflammatory_disease|cancer	nose_disorder|throat_disorder	false	true	false	false	high
MONDO:0004328	maxillary sinus adenocarcinoma	otorhinolaryngologic_disease|musculoskeletal_system_disorder|digestive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|nervous_system_disorder|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|digestive_system_disorder|respiratory_system_disorder|mouth_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|nervous_system_disorder	oncology|otolaryngology	autoimmune_diseases|inflammatory_disease|cancer|adrenal_gland_disease	nose_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004329	pancreatic intraductal papillary-mucinous neoplasm with high grade dysplasia	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004330	leptomeningeal sarcoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0004331	bladder urachal adenocarcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	urologic_cancer|urinary_system_disease|bladder|adenocarcinoma|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0004332	lung hilum cancer	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	cardiothoracic|oncology|pulmonology	lung_cancer|tumor|neoplasm|cancer	lymphatic_disorder|lung_disorder|lung_hilum_cancer_may_also_be_classified_as_lung_disorder_or_lymphatic_disorder	false	true	false	false	very_high
MONDO:0004333	pancreatic ACTH-producing neuroendocrine tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	endocrinology|oncology	neuroendocrine_tumor|cancer	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004334	non-functional pancreatic neuroendocrine tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|gastroenterology	cancer|neuroendocrine_tumor_category	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0004335	digestive system disorder		other		hepatology|gastroenterology	digestive_system_disorder|inflammatory_disease|metabolic_disorder	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0004336	rectal signet ring cell adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology|urinary_tract	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004337	perianal skin Paget disease	digestive_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	autoimmune_diseases|inflammatory_disease|cancer	lower_gastrointestinal_disorder|skin_disorder	false	true	false	false	high
MONDO:0004338	retinal cell cancer	disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|oncology	retina_disease_disorder|cancer	eye_disorder	false	true	false	false	high
MONDO:0004339	tuberculum sellae meningioma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	oncology|neurology	neurological_disorders|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0004340	mixed ductal-endocrine carcinoma of pancreas	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology	pancreatic_cancer|endocrine_cancer|cancer	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004341	colloid carcinoma of the pancreas	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology	pancreatic_disease|cancer|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0004343	pancreatic acinar cell cystadenocarcinoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004344	childhood malignant hemangiopericytoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	pediatric|oncology|hematology	cancer	brain_disorder|vascular_disorder	false	true	false	false	high
MONDO:0004345	childhood malignant schwannoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|oncology|neurology	childhood_malignant_schwannoma_is_actually_the_disease_name__it_should_be_categorized_as_cancer|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0004346	signet ring cell intrahepatic cholangiocarcinoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|hepatology|gastroenterology	intrahepatic_cholangiocarcinoma|cancer	liver_disorder|upper_gastrointestinal_disorder|biliary_disorder	false	true	false	false	very_high
MONDO:0004348	retinal telangiectasia	disorder_of_visual_system|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|retinal_telangiectasia|cardiovascular_disorder	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0004349	retina lymphoma	hematologic_disorder|disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hematologic_disorder	ophthalmology|oncology|hematology	autoimmune_diseases|inflammatory_disease|cancer	eye_disorder|lymphatic_disorder	true	true	false	true	high
MONDO:0004350	pediatric extraocular retinoblastoma	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	pediatric|ophthalmology|oncology	cancer	eye_disorder	false	true	false	true	very_high
MONDO:0004351	intraocular lymphoma	hematologic_disorder|disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|oncology|hematology	autoimmune_diseases|inflammatory_disease|cancer	eye_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004352	adult brain ependymoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neurology	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0004353	extrahepatic biliary papillomatosis	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	genetics_and_genomics|gastroenterology|pediatrics	autoimmune_diseases|inflammatory_disease|cancer	liver_disorder|biliary_disorder	false	false	false	false	medium
MONDO:0004354	neonatal leukemia	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	pediatric|oncology|hematology	cancer	blood_bone_marrow_disorder|immune_disorder	false	true	false	false	very_high
MONDO:0004355	childhood leukemia	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	pediatric|oncology|hematology	childhood_leukemia|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0004356	childhood multilocular cystic kidney neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	pediatric|oncology|urology	kidney_neoplasm|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0004357	carcinoma of supraglottis	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease|allergy|cancer	thoracic_disorder|lung_disorder|throat_disorder	false	true	false	true	high
MONDO:0004358	subglottis carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology|otolaryngology	autoimmune_diseases|inflammatory_disease|cancer	lung_disorder|throat_disorder	false	true	false	true	high
MONDO:0004359	delusional disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|psychiatry_disorder	false	false	false	true	medium
MONDO:0004360	breast extraskeletal osteosarcoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	orthopaedic|oncology	adrenal_gland_disease|cancer	skeletal_disorder|bone_disorder	false	true	false	false	high
MONDO:0004361	adult spinal cord ependymoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurological_cancer|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0004363	adult spinal cord glioblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0004364	choroid necrotic melanoma	disorder_of_visual_system|disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|nervous_system_disorder	ophthalmology|oncology	adrenal_gland_disease|neurodegenerative_disease|cancer	eye_disorder	false	true	false	false	high
MONDO:0004365	necrotic uveal melanoma	disorder_of_visual_system|disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|nervous_system_disorder	ophthalmology|oncology	adrenal_gland_disease|cancer	eye_disorder|skin_disorder	false	true	false	false	very_high
MONDO:0004366	mixed astrocytoma-ependymoma-oligodendroglioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0004367	petroclival meningioma	musculoskeletal_system_disorder|connective_tissue_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder|nervous_system_disorder	oncology|neurology	neurological_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0004368	sphenoorbital meningioma	musculoskeletal_system_disorder|connective_tissue_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder|nervous_system_disorder	ophthalmology|oncology|otolaryngology|neurology	neurodegenerative_disease|inflammatory_disease|cancer	eye_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0004369	renal infectious disease	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	autoimmune_diseases|inflammatory_disease|renal_infectious_disease	urinary_tract_disorder|kidney_disorder	true	false	false	true	high
MONDO:0004370	sphenocavernous meningioma	cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder	neurology|oncology	neuro_cancer|cancer	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0004371	spinal multifocal clear cell meningioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	meningioma|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0004372	chronic toxic polyneuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology	inflammatory_disease|neurodegenerative_disease	nerve_disorder|muscle_disorder	false	false	false	false	high
MONDO:0004373	adult papillary meningioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0004374	adult extraskeletal osteosarcoma	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	orthopaedic|oncology	cancer	bone_disorder|joint_disorder	false	true	false	false	high
MONDO:0004375	end stage renal failure	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	metabolic_disorder|renal_failure	urinary_tract_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0004376	infiltrating nipple syringomatous adenoma	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	obstetrics_and_gynecology|dermatology|oncology	benign_tumor|cancer	skin_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0004377	pancreatic non-functioning delta cell tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrinology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|endocrine_disorder|liver_disorder	false	true	false	false	medium
MONDO:0004378	pediatric cerebral ependymoblastoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|neurology|oncology	neurological_cancer|cancer	spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0004379	female breast carcinoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	autoimmune_diseases|cancer	lung_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0004380	dendritic cell sarcoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology	inflammatory_disease|autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0004381	pancreatic intraductal papillary-mucinous neoplasm with low grade dysplasia	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	pancreatic_cancer_disease___corrected_list___cancer|pancreatic_cancer_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	low
MONDO:0004382	laryngeal disorder	respiratory_system_disorder	other	respiratory_system_disorder	otolaryngology|pulmonology	neurodegenerative_disease|laryngeal_disorder_is_not_a_category__so_it_seems_i_should_say_that_the_answer_is_empty	lung_disorder|respiratory_system_disorder|laryngeal_disorder____throat_disorder	false	false	false	false	high
MONDO:0004383	adult central nervous system germinoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neuro|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0004384	maxillary sinus inverted papilloma	respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|musculoskeletal_system_disorder|respiratory_system_disorder|mouth_disorder|cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder	otolaryngology|oncology	cancer	upper_gastrointestinal_disorder|nose_disorder|teeth_disorder	false	true	false	true	medium
MONDO:0004385	adult xanthogranuloma	immune_system_disorder	other	immune_system_disorder	immunology|allergy_and_immunology|pulmonology|dermatology	inflammatory_disease|autoimmune_diseases|cancer	lung_disorder|immune_disorder|skin_disorder	false	false	false	true	low
MONDO:0004386	uterine corpus atypical polypoid adenomyoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	adenomyosis|tumor|polyp|adenoma|gynecological_cancer|neoplasm|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0004387	luteoma of pregnancy	obstetric_disorder|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|obstetric_disorder|reproductive_system_disorder	obstetrics_and_gynecology|endocrinology|oncology	gynecologic_cancer|cancer	endocrine_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0004389	mite infestation	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	pediatrics|pulmonology|dermatology	inflammatory_disease|corrected_answer___allergy|autoimmune_diseases|anemia|allergy	skin_disorder	true	false	false	true	low
MONDO:0004390	ocular hypotension	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	inflammatory_disease|metabolic_disorder|adrenal_gland_disease	eye_disorder|ocular_disorder	false	false	false	true	medium
MONDO:0004392	intracranial extraskeletal myxoid chondrosarcoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	orthopaedic|neurology|oncology	neurological_disease|sarcoma|soft_tissue_sarcoma|cancer	spinal_disorder|bone_disorder|brain_disorder	false	true	false	false	high
MONDO:0004393	mixed astrocytoma-ependymoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	brain_cancer|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0004394	maxillary sinus squamous cell carcinoma	respiratory_system_disorder|otorhinolaryngologic_disease|nervous_system_disorder|digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|musculoskeletal_system_disorder|mouth_disorder|digestive_system_disorder|respiratory_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|connective_tissue_disorder	otolaryngology|oncology	inflammatory_disease|autoimmune_diseases|cancer	upper_gastrointestinal_disorder|nose_disorder|teeth_disorder	false	true	false	false	high
MONDO:0004396	cervical spinal canal and spinal cord meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurological_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0004397	benign mediastinal psammomatous neurilemmoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neuroendocrine_tumor|cancer	lung_disorder|other____note__i_assumed__mediasinal__refers_to_the_mediastinum_which_is_part_of_the_lung_system	false	false	false	false	low
MONDO:0004398	mediastinal schwannoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	cardiothoracic|neurology|oncology	neuroendocrine_disease|cancer	lung_disorder|spinal_disorder	false	true	false	false	low
MONDO:0004400	malignant type A thymoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	hematologic_disorder|endocrine_system_disorder|cancer_or_benign_tumor|immune_system_disorder	pulmonology|oncology|cardiothoracic	adrenal_gland_disease|cancer	immune_disorder|lung_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0004401	testis refractory cancer	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	adrenal_gland_disease|cancer	male_reproductive_system_disorder|urogenital_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0004402	testicular yolk sac tumor, glandular-alveolar pattern	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	pediatric|urology|oncology	glandular_alveolar_pattern_is_a_specific_histological_feature_of_certain_cancers|cancer	reproductive_system_disorder|yolk_sac_tumor	false	true	false	true	high
MONDO:0004403	childhood precursor T-lymphoblastic lymphoma/leukemia	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	pediatric|hematology|oncology	leukemialymphoma|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0004404	refractory precursor T-lymphoblastic lymphoma/leukemia	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	leukemia|cancer|lymphoma	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0004405	Barrett adenocarcinoma	upper_digestive_tract_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|upper_digestive_tract_disorder	hepatology|gastroenterology|oncology	adrenal_gland_disease|allergy|autoimmune_diseases|anemia|inflammatory_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004406	adult central nervous system mixed germ cell tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	allergy|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0004407	stroma-dominant and stroma-poor composite ganglioneuroblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pediatric|genetics_and_genomics|oncology	cancer	muscle_disorder	false	false	false	false	high
MONDO:0004408	schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pediatric|oncology	cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0004409	nipple duct carcinoma	breast_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	nipple_duct_carcinoma_is_a_type_of_breast_cancer|cancer	reproductive_system_disorder|breast_disorder	false	true	false	false	high
MONDO:0004410	sarcomatoid penile squamous cell carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	skin_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0004411	duodenal gastrin-producing neuroendocrine tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	neuroendocrine_tumor|cancer	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004412	malignant spiradenoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	adrenal_gland_disease|cancer	skin_disorder	false	true	false	false	high
MONDO:0004413	cervical non-keratinizing squamous cell carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	skin_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004414	tamoxifen-related endometrial lesion	reproductive_system_disorder	other	reproductive_system_disorder	oncology|obstetrics_and_gynecology	endometrial_lesion_is_more_specific_than_a_category_in_the_list_so_it_is_excluded|cancer	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0004415	lipid-cell variant infiltrating bladder urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	urothelial_carcinoma|bladder_disease|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0004416	plasmacytoid variant infiltrating bladder urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	hematology|oncology|urology	malignancy|squamous_cell_carcinoma|urinary_system_cancer|cancerous_condition|bladder_cancer|tumor|urothelial_carcinoma|urologic_neoplasm|neoplastic_disease|cancer|adenocarcinoma|urological_malignancy|carcinoma	urinary_tract_disorder|immune_disorder	false	true	false	false	high
MONDO:0004417	nested variant infiltrating bladder urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	cancer|nested_variant_infiltrating_bladder_urothelial_carcinoma	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0004418	microcystic variant infiltrating bladder urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	urothelial_carcinoma|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0004419	lymphoma-like variant infiltrating bladder urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	hematology|oncology|urology	autoimmune_diseases|cancer	lymphatic_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0004420	breast malignant eccrine spiradenoma	breast_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|breast_disorder	oncology|dermatology|obstetrics_and_gynecology	eccrine_spiradenoma|malignant_tumor|rare_cancer|breast_malignant_eccrine_spiradenoma|adrenal_gland_disease|skin_disease|cancer|neoplasm	skin_disorder	false	true	false	false	high
MONDO:0004421	sclerosing breast papilloma	breast_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|breast_disorder	oncology|obstetrics_and_gynecology	autoimmune_diseases|adrenal_gland_disease|cancer	skin_disorder|reproductive_system_disorder	false	false	false	true	low
MONDO:0004422	cerebral falx meningioma	nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neuro|cancer	spinal_disorder|brain_disorder	false	true	false	false	medium
MONDO:0004423	central nervous system extraskeletal osteosarcoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|orthopaedic|neurology	neurodegenerative_disease|cancer	bone_disorder|spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0004425	hyperthyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|thyroid_disorder	false	false	false	true	medium
MONDO:0004426	frontal convexity meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neurooncology	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0004427	supraglottis neoplasm	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology	cancer|neoplasm	throat_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004428	alveoli adenoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology	adrenal_gland_disease|cancer	bone_disorder|muscle_disorder|lung_disorder	false	false	false	false	low
MONDO:0004429	skin meningioma	integumentary_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	oncology|dermatology	cancer	skin_disorder|brain_disorder	false	false	false	false	medium
MONDO:0004430	penis mixed squamous cell carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	autoimmune_diseases|adrenal_gland_disease|cancer	skin_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0004431	hemarthrosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	hematology|rheumatology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	true	high
MONDO:0004432	mature pericardial teratoma	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	oncology|cardiothoracic	cardiovascular_disorder|cancer	muscle_disorder|vessel_disorder|heart_disorder	false	true	false	false	low
MONDO:0004433	papillary carcinoma of the penis	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	skin_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0004435	liver fibrosarcoma	endocrine_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder|connective_tissue_disorder	oncology|hepatology	liver_disease|tumor|cancer	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004436	ovarian myxoid liposarcoma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hereditary_disease	cancer_or_benign_tumor|endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	oncology|obstetrics_and_gynecology	cancer	muscle_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004438	sporadic breast cancer	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|breast_cancer_is_typically_categorized_under_oncology_which_includes_sporadic_breast_cancer_as_well_as_genetics_and_genomics_due_to_genetic_predispositions_of_the_disease	sporadic_breast_cancer|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004439	periocular meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology|ophthalmology	neurological_cancer|cancer	eye_disorder|brain_disorder	false	true	false	true	high
MONDO:0004440	pineal region meningioma	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	tumors|pineal_region|brain_cancer|tumor|meningioma|cancer|neurooncology	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0004441	childhood ovarian embryonal carcinoma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|pediatric|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder|vaccine_related	false	true	false	true	high
MONDO:0004442	testis polyembryoma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|urology|pediatric	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	false	high
MONDO:0004443	chest wall parachordoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pulmonology|cardiothoracic|pediatrics	paraneoplastic_disease|cancer	bone_disorder|muscle_disorder|lung_disorder	false	true	false	false	high
MONDO:0004444	bladder tubulo-cystic clear cell adenocarcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology|renal_medicine	renal_disease|adrenal_gland_disease|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0004445	bladder papillary clear cell adenocarcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	adrenal_gland_disease|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0004446	olfactory groove meningioma	nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	oncology|otolaryngology|neurology	neurological_cancer|cancer	nose_disorder|brain_disorder	false	false	false	false	medium
MONDO:0004447	pituitary stalk meningioma	reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|connective_tissue_disorder	oncology|neurology	neuro|cancer	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0004448	frontal sinus inverted papilloma	nervous_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder|connective_tissue_disorder	oncology|otolaryngology	inflammatory_disease|autoimmune_diseases|cancer	nose_disorder|upper_gastrointestinal_disorder|lung_disorder	false	false	false	true	medium
MONDO:0004449	intraductal breast myoepitheliosis	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|pathology	inflammatory_disease|autoimmune_diseases|cancer	skin_disorder|reproductive_system_disorder|breast_disorder	false	false	false	false	low
MONDO:0004450	carotid artery occlusion	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|cardiology	cardiovascular_disorder|inflammatory_disease	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0004451	sarcomatous intrahepatic cholangiocarcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|hepatology	adrenal_gland_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004452	childhood central nervous system germinoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|pediatric	childhood|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0004453	testicular yolk sac tumor, myxomatous pattern	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0004454	cellular congenital mesoblastic nephroma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	genetics_and_genomics|oncology|urology|renal_medicine	anemia|cancer	blood_bone_marrow_disorder|kidney_disorder	false	true	false	false	high
MONDO:0004455	classic congenital mesoblastic nephroma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	genetics_and_genomics|oncology|urology|pediatric	anemia|cancer	blood_bone_marrow_disorder|kidney_disorder	false	true	false	true	medium
MONDO:0004456	cocaine abuse	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0004457	maxillary sinus Schneiderian papilloma	nervous_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|respiratory_system_disorder|nervous_system_disorder|otorhinolaryngologic_disease|connective_tissue_disorder	oncology|otolaryngology	inflammatory_disease|cancer	nose_disorder|throat_disorder	false	true	false	false	medium
MONDO:0004458	bladder mixed adenocarcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	bladder|other___corrected_answer__cancer|adrenal_gland_disease|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0004459	bladder hepatoid adenocarcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	adrenal_gland_disease|cancer	liver_disorder|upper_gastrointestinal_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0004460	thyroid gland fetal adenoma	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrinology|oncology|obstetrics_and_gynecology	metabolic_disorder|cancer	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0004461	vaginal tubulovillous adenoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	adenoma|tumor|adenocarcinoma|gynecologic_disorder|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0004462	extrahepatic bile duct cystadenoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0004463	cellular phase chronic idiopathic myelofibrosis	cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder|hematologic_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor|anemia	cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder|idiopathic_disease|hematologic_disorder|connective_tissue_disorder	oncology|hematology	autoimmune_diseases|inflammatory_disease|anemia|cancer	immune_disorder|blood_bone_marrow_disorder|lung_disorder	false	true	false	true	high
MONDO:0004464	nephrogenic adenoma of the urethra	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine	neurodegenerative_disease|cancer	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0004465	periampullary adenocarcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004466	neuronitis	nervous_system_disorder|inflammatory_disease	other	inflammatory_disease|nervous_system_disorder	neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder|muscle_disorder|neuronal_disorders_often_overlap_with_spinal_disorders_and_can_affect_muscles	true	false	false	false	medium
MONDO:0004467	mature gastric teratoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|pediatric|general_surgery|gastroenterology	teratoma|gastrointestinal_disease|rare_disorder|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	low
MONDO:0004468	anal canal Paget disease	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|urology	autoimmune_diseases|inflammatory_disease|cancer	skin_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0004469	pseudovascular skin squamous cell carcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	squamous_cell_carcinoma|skin_cancer|cancer	skin_disorder|vascular_disorder	false	true	false	false	high
MONDO:0004471	bacterial arthritis	inflammatory_disease|infectious_disease|musculoskeletal_system_disorder	infectious_disease	inflammatory_disease|musculoskeletal_system_disorder|infectious_disease	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|joint_disorder	true	false	false	true	high
MONDO:0004472	breast columnar cell mucinous carcinoma	breast_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	oncology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease|cancer	breast|reproductive_system_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0004473	epiglottis cancer	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease|digestive_system_disorder	oncology|otolaryngology	inflammatory_disease|cancer	thorat_disorder|lung_disorder	false	true	false	true	high
MONDO:0004474	gallbladder lymphoma	cancer_or_benign_tumor|digestive_system_disorder|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|hematologic_disorder	oncology|hematology|gastroenterology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004475	thymus clear cell carcinoma	endocrine_system_disorder|cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|immune_system_disorder|endocrine_system_disorder|hematologic_disorder	oncology|hematology|pulmonology	autoimmune_diseases|adrenal_gland_disease|cancer	immune_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0004477	adrenal gland ganglioneuroblastoma	nervous_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|endocrine_system_disorder|nervous_system_disorder	oncology|pediatric	adrenal_gland_disease|cancer	endocrine_disorder	false	true	false	false	high
MONDO:0004478	pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	acute_disease|cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	oncology|hematology	lymphoma|autoimmune_diseases|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0004479	malignant childhood germ cell neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric	neurodegenerative_disease|adrenal_gland_disease|cancer	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004481	pancreatic intraductal papillary-mucinous neoplasm with an associated invasive carcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004482	fibroosseous pseudotumor of the digits	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	bone_disorder|skin_disorder|joint_disorder	false	false	false	false	low
MONDO:0004483	thyroid gland oncocytic adenoma	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|oncology	thyroid_gland_disease|adrenal_gland_disease|cancer	endocrine_disorder	false	true	false	true	low
MONDO:0004484	gallbladder melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|digestive_system_disorder	oncology|hepatology|gastroenterology	adrenal_gland_disease|cancer	liver_disorder|biliary_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004485	interstitial myocarditis	cardiovascular_disorder|inflammatory_disease|musculoskeletal_system_disorder	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder|musculoskeletal_system_disorder	pediatrics|pulmonology|hepatology|cardiology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|muscle_disorder|heart_disorder|lung_disorder	true	false	false	false	high
MONDO:0004486	endocervical type cervical adenomyoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|genetics_and_genomics	adenomyoma_is_a_benign_tumor_that_can_become_malignant|cancer	muscle_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0004487	endometrial type cervical adenomyoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|gastroenterology	adeno|inflammatory_disease|gynecologic_disorder|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0004488	cervical atypical polypoid adenomyoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adnomyoma|gland_disease|cancer	reproductive_system_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0004489	fallopian tube gestational choriocarcinoma	reproductive_system_disorder|obstetric_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|obstetric_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	inflammatory_disease|cancer	ovarian_cancer|reproductive_system_disorder	false	true	false	true	high
MONDO:0004491	uterine corpus choriocarcinoma	reproductive_system_disorder|obstetric_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|obstetric_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|glandular_cancer|uterine_gland_disease	blood_bone_marrow_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0004492	mediastinitis	inflammatory_disease	other	inflammatory_disease	pulmonology|otolaryngology|cardiothoracic	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder|upper_gastrointestinal_disorder|lung_disorder	true	false	false	true	high
MONDO:0004493	testicular yolk sac tumor, papillary pattern	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|pediatric|urology	cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	true	high
MONDO:0004494	testicular yolk sac tumor, hepatoid pattern	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|pediatric|urology	cancer|adrenal_gland_disease	reproductive_system_disorder|liver_disorder	false	true	false	true	high
MONDO:0004495	myotonic cataract	nervous_system_disorder|disorder_of_visual_system|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_visual_system|disorder_of_orbital_region|musculoskeletal_system_disorder|nervous_system_disorder|syndromic_disease|hereditary_disease	neurology|ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0004496	myocarditis	cardiovascular_disorder|inflammatory_disease|musculoskeletal_system_disorder	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder|musculoskeletal_system_disorder	pulmonology|cardiothoracic|cardiology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	true	false	false	true	medium
MONDO:0004497	tertiary syphilis	reproductive_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease	neurology|psychiatry	inflammatory_disease|neurodegenerative_disease	immune_disorder|spinal_disorder|skin_disorder|vascular_disorder|lymphatic_disorder|brain_disorder	true	false	false	true	very_high
MONDO:0004498	sacral spinal canal and spinal cord meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neurological_disease|spinal_cord_disease	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0004499	lung hilum carcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology	cancer|respiratory_disorder|lung_carcinoma	lymphatic_disorder|lung_disorder	false	true	false	false	high
MONDO:0004500	lung superior sulcus carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|neurology|pulmonology	tumor|cancer|lung_carcinoma|thoracic_tumors	upper_gastrointestinal_disorder|lung_disorder|spinal_disorder	false	true	false	false	high
MONDO:0004501	fallopian tube cystadenofibroma	reproductive_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	oncology|obstetrics_and_gynecology|urology	reproductive_system_disease|gynecologic_cancer|cancer	reproductive_system_disorder	false	false	false	false	low
MONDO:0004502	parapharyngeal meningioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology|neurology	neurological_disease|cancer	brain_disorder|throat_disorder|spinal_disorder	false	false	false	false	high
MONDO:0004503	upper clivus meningioma	cancer_or_benign_tumor|nervous_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	oncology|otolaryngology|neurology	neuro|cancer	brain_disorder|upper_gastrointestinal_disorder|spinal_disorder	false	false	false	false	high
MONDO:0004504	penile urethral cancer	reproductive_system_disorder|urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0004505	central breast papilloma	cancer_or_benign_tumor|integumentary_system_disorder|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	oncology|obstetrics_and_gynecology	benign_tumor|breast_disorder|cancer	reproductive_system_disorder|skin_disorder	false	false	false	false	low
MONDO:0004506	microscopic breast papilloma	cancer_or_benign_tumor|integumentary_system_disorder|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	oncology|obstetrics_and_gynecology	cancer|skin_disease	reproductive_system_disorder|skin_disorder	false	false	false	false	low
MONDO:0004507	atypical breast papilloma	cancer_or_benign_tumor|integumentary_system_disorder|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder|breast_disorder	false	true	false	true	low
MONDO:0004508	periapical periodontitis	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease	periodontology|oral_and_maxillofacial	autoimmune_diseases|inflammatory_disease	teeth_disorder|bone_disorder	true	false	false	true	high
MONDO:0004509	intrahepatic biliary papillomatosis	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	hepatology|gastroenterology	metabolic_disorder|inflammatory_disease|cancer	biliary_disorder|liver_disorder	false	false	false	false	medium
MONDO:0004510	inflammatory liposarcoma	cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	oncology|hematology	inflammatory_disease|cancer	skin_disorder|soft_tissue_disorder	false	true	false	false	high
MONDO:0004511	lower clivus meningioma	musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	nervous_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	oncology|neurology	neuro|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0004512	meningeal melanomatosis	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	autoimmune_diseases|inflammatory_disease|cancer	brain_disorder|immune_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0004513	adult pleomorphic rhabdomyosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics|hematatology	cancer	bone_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0004514	chronic rhinitis	respiratory_system_disorder|otorhinolaryngologic_disease|inflammatory_disease	other	otorhinolaryngologic_disease|respiratory_system_disorder|inflammatory_disease	otolaryngology|allergy_and_immunology|pulmonology	inflammatory_disease|allergy	nose_disorder|lung_disorder	false	false	false	true	medium
MONDO:0004516	bulbomembranous urethral cancer	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	adrenal_gland_disease|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0004517	ureter tuberculosis	urinary_system_disorder|infectious_disease	infectious_disease	infectious_disease|urinary_system_disorder	renal_medicine|urology	autoimmune_diseases|inflammatory_disease|cancer	urinary_tract_disorder|kidney_disorder	true	false	false	true	high
MONDO:0004518	anterior urethra cancer	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	genitourinary_disorder|cancer|urological_disease	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0004519	synovial angioma	musculoskeletal_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	rheumatology|orthopaedic	inflammatory_disease|cancer	vascular_disorder|joint_disorder	false	false	false	false	medium
MONDO:0004520	intratubular embryonal carcinoma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|pediatric|genetics_and_genomics	adrenal_gland_disease|cancer	kidney_disorder|reproductive_system_disorder	false	true	false	true	low
MONDO:0004521	adult epithelioid sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics|pathology	autoimmune_diseases|cancer	lymphatic_disorder|muscle_disorder	false	true	false	false	high
MONDO:0004522	infectious peritonitis	inflammatory_disease|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	liver_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0004523	clear cell squamous cell skin carcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology|urology	skin_carcinoma|cancer	skin_disorder	false	true	false	false	medium
MONDO:0004524	thyroid gland atypical follicular adenoma	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	thyroid_gland_disease|cancer	thyroid_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0004525	scabies	integumentary_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	integumentary_system_disorder|inflammatory_disease|infectious_disease	pediatrics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0004526	mixed endometrial stromal and smooth muscle tumor	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	muscle_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0004528	lymph node palisaded myofibroblastoma	hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder|connective_tissue_disorder	oncology|oncologic_surgery|pathology|dermatology|surgery	lymphoma|cancer	lymphatic_disorder|immune_disorder	false	false	false	false	low
MONDO:0004529	non-ossifying fibromyxoid tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatrics|orthopaedic	bone_disease|tumor|cancer	blood_bone_marrow_disorder|bone_disorder	false	true	false	false	medium
MONDO:0004530	early invasive cervical adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	autoimmune_diseases|inflammatory_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0004531	sclerosing adenosis of breast	breast_disorder	other	breast_disorder	obstetrics_and_gynecology|oncology	autoimmune_diseases|inflammatory_disease|cancer	reproductive_system_disorder|skin_disorder|breast_disorder	false	false	false	false	low
MONDO:0004532	auditory system cancer	auditory_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|auditory_system_disorder	otolaryngology|oncology	neoplastic_disease|neurological_disease|cancer	ear_disorder|throat_disorder	false	true	false	false	high
MONDO:0004533	perineural angioma	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	neurology|dermatology|oncology	neurodegenerative_disease|cancer	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0004534	microglandular adenosis of breast	breast_disorder	other	breast_disorder	pediatric|obstetrics_and_gynecology|dermatology|psychiatry|oncology	autoimmune_diseases|inflammatory_disease|cancer	reproductive_system_disorder|breast_disorder	false	false	false	false	low
MONDO:0004535	childhood choriocarcinoma of the ovary	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	pediatric|obstetrics_and_gynecology|oncology	other____note__childhood_choriocarcinoma_of_the_ovary_is_a_rare_form_of_ovarian_cancer_in_children__but_since_it_s_specifically_mentioned_as_such__it_falls_under_the_category__other__which_includes_rare_or_specific_conditions_not_covered_by_more_general_categories|cancer	lymphatic_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0004537	intestinal variant cervical mucinous adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004538	endocervical type cervical mucinous adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004539	aortic malignant tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiothoracic|cardiology|oncology	cardiovascular_disorder|cancer	heart_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0004540	epithelioid malignant peripheral nerve sheath tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer	muscle_disorder|nerve_disorder	false	true	false	false	high
MONDO:0004541	pseudoglandular variant testicular seminoma	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	cancer|adrenal_gland_disease	testicular_seminoma|reproductive_system_disorder	false	true	false	true	high
MONDO:0004542	cervical adenosquamous carcinoma, glassy cell variant	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer|allergy|adrenal_gland_disease|autoimmune_diseases	reproductive_system_disorder|throat_disorder	false	true	false	false	very_high
MONDO:0004543	enteric pattern testicular yolk sac tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	gastroenterology|oncology|pediatric	cancer|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004544	chordoid meningioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurological_cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0004545	adult malignant schwannoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0004546	lumbar plexus neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	true	false	false	high
MONDO:0004547	reticular pattern testicular yolk sac tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|hematology|oncology|pediatric|genetics_and_genomics	cancer	blood_bone_marrow_disorder|reproductive_system_disorder|lymphatic_disorder	true	true	false	true	high
MONDO:0004548	adult type testicular granulosa cell tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0004549	cork-handlers' disease	respiratory_system_disorder|inflammatory_disease|infectious_disease|immune_system_disorder	infectious_disease	immune_system_disorder|inflammatory_disease|infectious_disease|respiratory_system_disorder|occupational_disorder	occupational_health__note__i_assume_this_is_the_intended_category|dermatology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	liver_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0004550	malignant cornea melanoma	disorder_of_visual_system|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region	oncology|ophthalmology	cancer|adrenal_gland_disease	skin_disorder|eye_disorder	false	true	false	true	high
MONDO:0004551	Meckel diverticulitis	digestive_system_disorder|inflammatory_disease	other	digestive_system_disorder|inflammatory_disease	gastroenterology|general_surgery|pediatric	cancer|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0004552	microinvasive cervical squamous cell carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer|autoimmune_diseases|adrenal_gland_disease	reproductive_system_disorder|throat_disorder	false	true	false	true	low
MONDO:0004554	childhood kidney angiomyolipoma	urinary_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine|pediatric	cancer|metabolic_disorder|adrenal_gland_disease	kidney_disorder|vascular_disorder|urinary_tract_disorder	false	true	false	true	medium
MONDO:0004555	kidney angiomyolipoma	urinary_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine	cancer|adrenal_gland_disease|kidney	kidney_disorder|vascular_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0004556	carcinoma arising in nasal papillomatosis	respiratory_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|nervous_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|oncology	cancer|inflammatory_disease|allergy|autoimmune_diseases	upper_gastrointestinal_disorder|nose_disorder	false	true	false	true	high
MONDO:0004557	congenital fibrosarcoma	cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	oncology|pediatric|genetics_and_genomics	cancer|congenital_fibrosarcoma_is_actually_a_type_of_cancer	soft_tissue_disorder|bone_disorder	false	true	false	false	medium
MONDO:0004558	thyroid gland macrofollicular adenoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|oncology	cancer|thyroid_gland_disease	thyroid_disorder_is_not_in_the_list__so_i_m_looking_at_the_closest_match__endocrine_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0004559	malignant glandular tumor of peripheral nerve sheath	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	spinal_disorder|muscle_disorder|nerve_disorder	false	true	false	false	high
MONDO:0004560	follicular infundibulum tumor	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	cancer|adrenal_gland_disease	skin_disorder|reproductive_system_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0004561	retinal melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_orbital_region|disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system	oncology|ophthalmology	cancer|eye_disease|neoplasm|tumors	eye_disorder	false	true	false	true	high
MONDO:0004562	breast apocrine carcinoma in situ	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|dermatology	cancer|inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	skin_disorder|reproductive_system_disorder	false	true	false	false	low
MONDO:0004563	physiological polycythemia	hematologic_disorder|immune_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|immune_system_disorder|hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0004564	thyroid malformation	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|adrenal_gland_disease	thyroid_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0004565	intestinal obstruction	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|general_surgery	inflammatory_disease|gastrointestinal_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0004566	postgastrectomy syndrome	digestive_system_disorder	other	digestive_system_disorder	endocrinology|gastroenterology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0004567	ileus	digestive_system_disorder	other	digestive_system_disorder	emergency_medicine|gastroenterology|general_surgery	inflammatory_disease|metabolic_disorder|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0004568	paralytic ileus	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0004569	brachial plexus neuropathy from injury	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	true	high
MONDO:0004570	intestinal volvulus	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|surgery|pediatric	inflammatory_disease|gastrointestinal_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0004571	intestinal impaction	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|pediatric	inflammatory_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0004572	cyclothymic disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	mental_health_disorder|autoimmune_diseases	brain_disorder|mood_disorder_is_incorrect_as_cyclothymic_disorder_is_a_subcategory_of_bipolar_disorder_which_is_an_endocrine_disorder__endocrine_disorder	false	false	false	false	medium
MONDO:0004573	ariboflavinosis	hereditary_disease|nutritional_disorder	other	nutritional_disorder|hereditary_disease	endocrinology|gastroenterology|hepatology|neurology|dermatology	anemia|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0004574	pyridoxine deficiency anemia	nutritional_disorder	other	nutritional_disorder	endocrinology|hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0004575	choline deficiency disease	nutritional_disorder	other	nutritional_disorder	gastroenterology|hepatology|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0004577	corneal ulcer	inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease|ulcer_disease	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder	true	false	false	true	medium
MONDO:0004578	flat retinoschisis	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	pediatric|ophthalmology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|ocular_disorder	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0004579	retinoschisis	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|genetics_and_genomics	congenital_anomaly|ocular_disease|eye_disorder|neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0004580	retinal degeneration	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	skin_disorder|eye_disorder	false	false	false	true	medium
MONDO:0004582	rheumatic myocarditis	cardiovascular_disorder|inflammatory_disease|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|inflammatory_disease|cardiovascular_disorder	cardiology|cardiothoracic|rheumatology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	immune_disorder|heart_disorder|joint_disorder	true	false	false	true	high
MONDO:0004583	transient retinal arterial occlusion	cardiovascular_disorder|nervous_system_disorder|disorder_of_visual_system	cardiovascular_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cardiovascular_disorder	cardiology|ophthalmology	inflammatory_disease|cardiovascular_disorder|neurodegenerative_disease	eye_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0004584	maple bark strippers' lung	respiratory_system_disorder|immune_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	immune_system_disorder|inflammatory_disease|infectious_disease|respiratory_system_disorder|occupational_disorder	pulmonology|occupational_disease	inflammatory_disease|respiratory_disease|autoimmune_diseases	lung_disorder|lower_gastrointestinal_disorder	true	false	false	false	high
MONDO:0004585	polyhydramnios	obstetric_disorder	other	obstetric_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0004586	rheumatoid lung disease	respiratory_system_disorder|immune_system_disorder	autoimmune_disease	immune_system_disorder|respiratory_system_disorder	pulmonology|rheumatology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder|joint_disorder	false	false	false	true	high
MONDO:0004588	night blindness	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|nervous_system_disorder	neurology|ophthalmology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	true	low
MONDO:0004591	impetigo herpetiformis	obstetric_disorder|integumentary_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|obstetric_disorder|integumentary_system_disorder	pediatrics|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0004592	impetigo	integumentary_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|integumentary_system_disorder	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0004593	Bartholin duct cyst	reproductive_system_disorder|integumentary_system_disorder	other	integumentary_system_disorder|reproductive_system_disorder	urology|obstetrics_and_gynecology	cancer|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder	false	false	false	true	low
MONDO:0004594	puerperal pulmonary embolism	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|obstetrics_and_gynecology|pulmonology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	lung_disorder|vascular_disorder	false	false	false	true	high
MONDO:0004596	cor pulmonale	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|pulmonology|cardiothoracic	cardiovascular_disorder	lung_disorder|heart_disorder	false	false	false	true	high
MONDO:0004597	pulmonary embolism and infarction	respiratory_system_disorder	other	respiratory_system_disorder	cardiology|hematology|pulmonology	cardiovascular_disorder|pulmonary__embolism_and_infarction	lung_disorder|vascular_disorder	false	false	false	true	high
MONDO:0004598	acute cor pulmonale	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|acute_disease	cardiology|pulmonology	cardiovascular_disorder|acute_cor_pulmonale	lung_disorder|heart_disorder	false	false	false	true	high
MONDO:0004599	barbiturate abuse	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	liver_disorder|brain_disorder	false	false	false	false	high
MONDO:0004600	monocytic leukemia	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	leukemia|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004601	ulcer of lower limbs	integumentary_system_disorder	other	integumentary_system_disorder	orthopaedic|hematology|renal_medicine	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0004603	collagenopathy	connective_tissue_disorder	other	connective_tissue_disorder	dermatology|rheumatology	connective_tissue_disease|inflammatory_disease|metabolic_disorder	vascular_disorder|joint_disorder|muscle_disorder|skin_disorder	false	false	false	false	high
MONDO:0004604	Hodgkin's lymphoma, lymphocytic-histiocytic predominance	cancer_or_benign_tumor|hereditary_disease|hematologic_disorder	cancer_or_benign_tumor	post_infectious_disorder|cancer_or_benign_tumor|hereditary_disease|hematologic_disorder	oncology|hematology	autoimmune_diseases|cancer|lymphoma	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0004605	chronic ulcer of skin	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|skin_disorder	false	false	false	true	medium
MONDO:0004607	vallecula cancer	cancer_or_benign_tumor|respiratory_system_disorder|digestive_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder	oncology|gastroenterology|hepatology	cancer	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004608	oropharynx cancer	cancer_or_benign_tumor|respiratory_system_disorder|digestive_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder	otolaryngology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|thorat_disorder	false	true	false	true	very_high
MONDO:0004609	herpes simplex infectious disease	infectious_disease	infectious_disease	infectious_disease	dermatology|neurology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	true	false	false	false	medium
MONDO:0004611	soft palate cancer	respiratory_system_disorder|cancer_or_benign_tumor|digestive_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	otolaryngology|oncology	cancer	throat_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0004612	malignant histiocytosis	immune_system_disorder	other	immune_system_disorder	oncology|hematology	cancer|malignant_histiocytosis	lung_disorder|blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0004613	acute intestinal ischemia	digestive_system_disorder|cardiovascular_disorder	cardiovascular_disorder	digestive_system_disorder|cardiovascular_disorder|acute_disease	cardiology|gastroenterology|hematology|renal_medicine	cardiovascular_disorder|inflammatory_disease	lower_gastrointestinal_disorder|vascular_disorder	false	false	false	true	high
MONDO:0004614	chronic monocytic leukemia	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	leukemia|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0004615	upper gum cancer	cancer_or_benign_tumor|digestive_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|musculoskeletal_system_disorder|mouth_disorder|cancer_or_benign_tumor	otolaryngology|oncology	upper_gum_cancer|cancer	upper_gastrointestinal_disorder|teeth_disorder	false	true	false	true	high
MONDO:0004616	herpetic whitlow	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology|pediatric|infectious_disease	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0004617	recurrent hypersomnia	other	other	sleep_disorder	endocrinology|neurology	metabolic_disorder|mental_health_disorder	endocrine_disorder|brain_disorder	false	false	false	false	high
MONDO:0004618	diplegia of upper limb	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|pediatric|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0004619	measles	infectious_disease	infectious_disease	infectious_disease	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0004620	Hodgkin's lymphoma, lymphocytic depletion	cancer_or_benign_tumor|hereditary_disease|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|post_infectious_disorder|cancer_or_benign_tumor|hereditary_disease	oncology|hematology	autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004621	upper lip cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor	otolaryngology|oncology	cancer|upper_lip_cancer	subtype|upper_gastrointestinal_disorder|skin_disorder	false	true	false	true	medium
MONDO:0004622	chronic intestinal vascular insufficiency	digestive_system_disorder|cardiovascular_disorder	cardiovascular_disorder	digestive_system_disorder|cardiovascular_disorder	cardiology|vascular_insufficiency_is_often_related_to_endocrinology_and_renal_medicine|gastroenterology|hematology	cardiovascular_disorder|inflammatory_disease	lower_gastrointestinal_disorder|vascular_disorder	false	false	false	false	high
MONDO:0004624	uvula cancer	cancer_or_benign_tumor|respiratory_system_disorder|digestive_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder	otolaryngology|oncology	adrenal_gland_disease|cancer	throat_disorder|throttle_disorder	false	true	false	true	high
MONDO:0004625	phlebitis	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	vascular_disease|cardiology|hematology	cardiovascular_disorder|inflammatory_disease	lower_gastrointestinal_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0004627	duodenitis	digestive_system_disorder|inflammatory_disease	other	digestive_system_disorder|inflammatory_disease	gastroenterology|hepatology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	low
MONDO:0004628	gastroduodenitis	digestive_system_disorder|inflammatory_disease	other	digestive_system_disorder|inflammatory_disease|ulcer_disease	gastroduodenditis|gastroenterology|hepatology	inflammatory_disease|gastrointestinal_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	low
MONDO:0004629	subacute delirium	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|acute_disease	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0004630	substance-induced psychosis	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|substance_related_disorders	brain_disorder|substance_use_disorder	false	false	false	true	high
MONDO:0004631	tongue cancer	cancer_or_benign_tumor|digestive_system_disorder|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor	otolaryngology|oncology	adrenal_gland_disease|cancer	throat_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0004633	Hodgkin's lymphoma, mixed cellularity	cancer_or_benign_tumor|hereditary_disease|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|post_infectious_disorder|cancer_or_benign_tumor|hereditary_disease	hematology|oncology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004634	vein disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|vascular|cardiology	vein_disorder_could_also_fit_under_metabolic_disorder|cardiovascular_disorder|inflammatory_disease	vascular_disorder|lymphatic_disorder	false	false	false	true	medium
MONDO:0004635	postcricoid region cancer	cancer_or_benign_tumor|respiratory_system_disorder|digestive_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	otolaryngology|oncology	cancer	throat_disorder_upper_gastrointestinal_disorder_lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0004636	lip carcinoma in situ	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|inflammatory_disease	skin_disorder|upper_gastrointestinal_disorder	false	true	false	true	low
MONDO:0004637	aryepiglottic fold cancer	cancer_or_benign_tumor|respiratory_system_disorder|digestive_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	otolaryngology|oncology	autoimmune_diseases|cancer	throat_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004638	lymphosarcoma	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	hematology|oncology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004639	perinatal necrotizing enterocolitis	digestive_system_disorder|hereditary_disease	other	digestive_system_disorder|hereditary_disease	pediatric|gastroenterology	inflammatory_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0004640	alcoholic gastritis	digestive_system_disorder|inflammatory_disease	other	inflammatory_disease|digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0004641	skin carcinoma in situ	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	cancer|skin_carcinoma_in_situ_would_likely_also_fit_into_the_subcategory_of_cancer	skin_disorder	false	true	false	true	medium
MONDO:0004642	tonsillar pillar cancer	musculoskeletal_system_disorder|respiratory_system_disorder|digestive_system_disorder|immune_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease|immune_system_disorder	otolaryngology|oncology	autoimmune_diseases|adrenal_gland_disease|cancer|inflammatory_disease	throat_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004643	myeloid leukemia	musculoskeletal_system_disorder|immune_system_disorder|hematologic_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|immune_system_disorder	oncology|hematology	anemia|autoimmune_diseases|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0004644	subacute monocytic leukemia	cancer_or_benign_tumor|musculoskeletal_system_disorder|immune_system_disorder|hematologic_disorder|connective_tissue_disorder	cancer_or_benign_tumor	hematologic_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|immune_system_disorder|acute_disease	oncology|hematology	autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0004645	cheek mucosa cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor	otolaryngology|oncology	cancer|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0004646	decubitus ulcer	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	cardiovascular_disorder|metabolic_disorder	skin_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0004647	in situ carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|surgery|pathology	adrenal_gland_disease|cancer|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0004648	vascular dementia	psychiatric_disorder|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder|psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|cardiovascular_disorder	cardiology|neurology	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0004649	anaerobic pneumonia	respiratory_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	inflammatory_disease|respiratory_system_disorder|infectious_disease	pulmonology	autoimmune_diseases|inflammatory_disease	lung_disorder	true	false	false	true	high
MONDO:0004650	malignant carotid body paraganglioma	endocrine_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|cardiovascular_disorder	endocrine_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|nervous_system_disorder|cardiovascular_disorder|endocrine_system_disorder|cancer_or_benign_tumor|hereditary_disease	oncology|otolaryngology|neurology	neurodegenerative_disease|cancer	lung_disorder|vascular_disorder|brain_disorder|ear_disorder	false	true	false	false	very_high
MONDO:0004651	smallpox	infectious_disease	infectious_disease	infectious_disease	dermatology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	very_high
MONDO:0004652	bacterial pneumonia	infectious_disease|respiratory_system_disorder|inflammatory_disease	infectious_disease	inflammatory_disease|respiratory_system_disorder|infectious_disease	pediatric|pulmonology	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0004653	atypical chronic myeloid leukemia, BCR-ABL1 negative	musculoskeletal_system_disorder|cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder|connective_tissue_disorder	cancer_or_benign_tumor	hematologic_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|immune_system_disorder	genetics_and_genomics|oncology|hematology	anemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0004656	rubella	infectious_disease	infectious_disease	infectious_disease	pediatric|genetics_and_genomics|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|immune_disorder|eye_disorder|skin_disorder	true	false	false	true	medium
MONDO:0004657	disseminated chorioretinitis	disorder_of_visual_system|inflammatory_disease	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease	immune_disorder|eye_disorder	true	false	false	true	high
MONDO:0004658	breast carcinoma in situ	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|obstetrics_and_gynecology	autoimmune_diseases|cancer|adrenal_gland_disease|inflammatory_disease	reproductive_system_disorder|breast_disorder	false	true	false	true	low
MONDO:0004659	eye carcinoma in situ	cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|oncology	cancer|adrenal_gland_disease|eye_disease	eye_carcinoma_in_situ|eye_disorder	false	true	false	true	low
MONDO:0004660	lung carcinoma in situ	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology|cardiothoracic	cancer	lung_disorder|lung_carcinoma_in_situ_is_also_related_to_upper_gastrointestinal_disorder_but_the_first_category_is_a_better_fit	false	true	false	true	low
MONDO:0004661	trachea carcinoma in situ	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology|pulmonology	autoimmune_diseases|cancer|adrenal_gland_disease|inflammatory_disease|allergy	lung_disorder|throat_disorder	false	true	false	false	low
MONDO:0004662	heterophyiasis	infectious_disease	infectious_disease	infectious_disease	dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	liver_disorder	true	false	false	false	medium
MONDO:0004663	colon carcinoma in situ	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	autoimmune_diseases|cancer|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	low
MONDO:0004664	helminthiasis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease	liver_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0004665	nodular sclerosis classical Hodgkin lymphoma	cancer_or_benign_tumor|hereditary_disease|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|post_infectious_disorder|cancer_or_benign_tumor|hereditary_disease	oncology|hematology	autoimmune_diseases|lymphoma|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0004666	metagonimiasis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|hepatology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|liver_disorder	true	false	false	true	medium
MONDO:0004667	sublingual gland cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	adrenal_gland_disease|cancer	throat_disorder|upper_gastrointestinal_disorder|head_and_neck_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0004668	fascioliasis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|hepatology	autoimmune_diseases|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0004669	salivary gland cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	autoimmune_diseases|adrenal_gland_disease|cancer|inflammatory_disease	oral_disorder|throat_disorder|upper_gastrointestinal_disorder|upper_gastrointestinal_disorder___corrected_list_without_redundancy__throat_disorder	false	true	false	false	high
MONDO:0004670	lupus erythematosus	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	connective_tissue_disorder|immune_system_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder__skin_disorder	false	false	false	true	high
MONDO:0004671	penis carcinoma in situ	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	dermatology|oncology|urology	cancer|urological_disease	reproductive_system_disorder|skin_disorder	false	true	false	true	medium
MONDO:0004672	fasciolopsiasis	infectious_disease	infectious_disease	infectious_disease	veterinary|gastroenterology|hepatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0004673	lower lip cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer|lower_lip_cancer_is_a_type_of_cancer	lower_gastrointestinal_disorder|skin_disorder	false	true	false	true	high
MONDO:0004674	chorioretinitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	true	false	false	true	high
MONDO:0004675	mitochondrial encephalomyopathy	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|musculoskeletal_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|musculoskeletal_system_disorder|metabolic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|mitochondrial_encephalomyopathy_is_a_subset_of_these_categories_so_it_should_be_included_in_the_answer	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0004677	tinea nigra	integumentary_system_disorder|infectious_disease	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|fungal_infection	true	false	false	true	low
MONDO:0004678	dermatophytosis	integumentary_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|integumentary_system_disorder|inflammatory_disease	dermatology	allergy|inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0004679	leukoplakia of vagina	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|dermatology|obstetrics_and_gynecology	inflammatory_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder|skin_disorder	false	false	false	false	low
MONDO:0004680	primary thrombocytopenia	immune_system_disorder|hematologic_disorder	autoimmune_disease	immune_system_disorder|hematologic_disorder	primary_thromboembolic_disease|hematology	metabolic_disorder|anemia|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0004681	learning disability	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	pediatric|neurology|psychiatry	neurodegenerative_disease_mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0004682	retromolar area cancer	connective_tissue_disorder|digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|digestive_system_disorder	ophthalmology|oncology	adrenal_gland_disease|cancer	throat_disorder|eye_disorder	false	true	false	false	high
MONDO:0004684	plantar fibromatosis	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	rheumatology|orthopaedic	inflammatory_disease|musculoskeletal_disorder	joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0004685	Waldeyer's ring cancer	immune_system_disorder|respiratory_system_disorder|digestive_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease|digestive_system_disorder	otolaryngology|oncology	adrenal_gland_disease|cancer	throat_disorder|ear_disorder	false	true	false	false	high
MONDO:0004686	lattice corneal dystrophy	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	true	medium
MONDO:0004687	severe nonproliferative diabetic retinopathy	cardiovascular_disorder|metabolic_disease|disorder_of_visual_system|nervous_system_disorder	metabolic_disease|cardiovascular_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cardiovascular_disorder|metabolic_disease	ophthalmology|endocrinology	diabetic_retinopathy_is_related_to_but_not_exactly_the_same_as_the_condition_specified_in_the_prompt|metabolic_disorder	endocrine_disorder|eye_disorder	false	false	true	true	high
MONDO:0004689	inborn metal metabolism disorder	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|inborn_metabolism_disorder	endocrine_disorder|liver_disorder	false	false	false	true	high
MONDO:0004690	tonsillar fossa cancer	immune_system_disorder|respiratory_system_disorder|digestive_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder|digestive_system_disorder	otolaryngology|oncology	inflammatory_disease|cancer	lymphatic_disorder|throat_disorder	false	true	false	true	high
MONDO:0004691	autosomal dominant polycystic kidney disease	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	pediatric|genetics_and_genomics|renal_medicine	kidney_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0004693	squamous carcinoma in situ	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|dermatology	cancer	reproductive_system_disorder|skin_disorder	false	true	false	true	medium
MONDO:0004694	hepatopulmonary syndrome	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	pulmonology|hepatology|gastroenterology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	lung_disorder|liver_disorder	false	false	false	false	high
MONDO:0004695	liver lymphoma	endocrine_system_disorder|digestive_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|hematologic_disorder|digestive_system_disorder	hepatology|hematology|oncology	autoimmune_diseases|cancer	lymphatic_disorder|liver_disorder	false	true	false	true	high
MONDO:0004696	larynx carcinoma in situ	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|oncology	cancer_in_situ|cancer	thoracic_disorder|throat_disorder	false	true	false	true	low
MONDO:0004697	esophageal leukoplakia	upper_digestive_tract_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|upper_digestive_tract_disorder|digestive_system_disorder	pulmonology|oncology|gastroenterology	inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0004698	intestine carcinoma in situ	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	intestine_carcinoma_in_situ|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	low
MONDO:0004699	gastrointestinal lymphoma	digestive_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|digestive_system_disorder	hepatology|hematology|oncology|gastroenterology	gastrointestinal_disease|cancer|lymphoma	immune_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004700	parotid gland cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|throat_disorder	false	true	false	false	high
MONDO:0004701	uterine polyp	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology	reproductive_system_disorder|cancer|gynecological_condition	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0004702	uterine cervix leukoplakia	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	autoimmune_diseases|cancer|inflammatory_disease	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0004703	bladder carcinoma in situ	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	adrenal_gland_disease|autoimmune_diseases|cancer|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	true	false	true	medium
MONDO:0004705	liver solitary fibrous tumor	digestive_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology|hepatology	liver_cancer|autoimmune_diseases|cancer|inflammatory_disease	liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0004706	discoid lupus erythematosus of eyelid	disorder_of_visual_system|inflammatory_disease	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	dermatology|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder|immune_disorder	false	false	false	true	low
MONDO:0004707	anal canal carcinoma in situ	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	low
MONDO:0004708	esophagus carcinoma in situ	digestive_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	cancer_or_benign_tumor	upper_digestive_tract_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0004709	occipital lobe neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0004710	uterus carcinoma in situ	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0004712	herpes simplex dermatitis	inflammatory_disease|infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease|inflammatory_disease	dermatology|neurology	autoimmune_diseases|allergy|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0004713	lower gum cancer	digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|lower_gum_cancer	teeth_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0004714	atrophic muscular disease	nervous_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder	rheumatology|neurology	neurodegenerative_disease|atrophic_muscular_diseases_are_generally_classified_under_this_category	muscle_disorder|bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0004715	liver carcinoma in situ	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology|hepatology	cancer|liver_carcinoma_situation_is_not_in_the_list__so_i_assume_you_meant_cancer	liver_carcinoma_in_situ_is_more_specific_than_a_general_liver_disorder__however_it_is_classified_under_liver_disorder_so_this_should_be_the_primary_category__liver_disorder|liver_disorder	false	true	false	false	medium
MONDO:0004716	stomach carcinoma in situ	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	adrenal_gland_disease|cancer|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	low
MONDO:0004717	peliosis hepatis	digestive_system_disorder|cardiovascular_disorder|endocrine_system_disorder	cardiovascular_disorder|endocrine_system_disorder	cardiovascular_disorder|digestive_system_disorder|endocrine_system_disorder	gastroenterology|hepatology	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|liver_disorder	true	false	false	false	medium
MONDO:0004718	xeroderma of eyelid	inflammatory_disease|disorder_of_visual_system	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	dermatology|ophthalmology	autoimmune_diseases|cancer	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0004719	hard palate cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer|throat_cancer|head_and_neck_cancer	teeth_disorder|throat_disorder	false	true	false	true	high
MONDO:0004720	variola minor infection	infectious_disease	infectious_disease	infectious_disease	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0004723	liver leiomyoma	endocrine_system_disorder|digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|digestive_system_disorder	hepatology|oncology	tumor|cancer	liver_disorder	false	false	false	false	low
MONDO:0004724	submandibular gland cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor|digestive_system_disorder	otolaryngology|oncology	gland_disease|cancer	throat_disorder|upper_gastrointestinal_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004725	rectum carcinoma in situ	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	inflammatory_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0004726	liver inflammatory myofibroblastic tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	hepatology|oncology|gastroenterology	inflammatory_disease|cancer	muscle_disorder|liver_disorder	false	false	false	false	medium
MONDO:0004727	vestibule of mouth cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor|digestive_system_disorder	otolaryngology|oncology	inflammatory_disease|cancer	throat_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004728	diabetic macular edema	metabolic_disease|disorder_of_visual_system|cardiovascular_disorder|nervous_system_disorder	metabolic_disease|cardiovascular_disorder	disorder_of_visual_system|disorder_of_orbital_region|cardiovascular_disorder|nervous_system_disorder|metabolic_disease	ophthalmology|endocrinology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0004729	dyskinesia of esophagus	upper_digestive_tract_disorder|digestive_system_disorder	other	upper_digestive_tract_disorder|digestive_system_disorder	neurology|gastroenterology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	throat_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0004730	speech disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	otolaryngology|pediatric|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|throat_disorder|ear_disorder	false	false	false	false	medium
MONDO:0004731	central sleep apnea syndrome	syndromic_disease|respiratory_system_disorder	other	syndromic_disease|sleep_disorder|respiratory_system_disorder	neurology|pulmonology	neurodegenerative_disease_cardiovascular_disorder	brain_disorder|lung_disorder	false	false	false	true	high
MONDO:0004732	kidney carcinoma in situ	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	renal_medicine|urology|oncology	kidney_disease|urological_disorder|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	medium
MONDO:0004733	pyriform sinus cancer	digestive_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|respiratory_system_disorder|digestive_system_disorder	otolaryngology|oncology	adrenal_gland_disease|cancer	throat_disorder|nose_disorder	false	true	false	false	high
MONDO:0004736	inborn disorder of amino acid metabolism	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	inborn_disorder_of_amino_acid_metabolism_is_also_closely_related_to_this_category____metabolic_disorder|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0004737	homocystinuria	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|hematology|pediatric	metabolic_disorder|neurodegenerative_disease	vascular_disorder|kidney_disorder	false	false	false	true	high
MONDO:0004739	urea cycle disorder	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|renal_medicine|hepatology	metabolic_disorder|adrenal_gland_disease	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0004741	tyrosinemia	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hematology|pediatric|hepatology|genetics_and_genomics	metabolic_disorder|anemia	kidney_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	true	high
MONDO:0004742	primary cerebellar degeneration	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	neurology	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0004743	hyperhomocysteinemia	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hematology|cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	vascular_disorder|kidney_disorder	false	false	false	true	high
MONDO:0004744	borderline glaucoma	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0004745	priapism	reproductive_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|reproductive_system_disorder	neurology|urology	metabolic_disorder|adrenal_gland_disease|inflammatory_disease	vascular_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0004746	myopathy of extraocular muscle	musculoskeletal_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|musculoskeletal_system_disorder	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0004747	cleft lip	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	otolaryngology|pediatric	metabolic_disorder|inflammatory_disease	nose_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0004748	lip disorder	other	other	mouth_disorder	otolaryngology|dermatology|pediatric|oral_pathology_is_removed_and_replaced_by_genetics_and_genomics	lip_disorder|metabolic_disorder	lip_disorder|liver_disorder	false	false	false	true	medium
MONDO:0004749	myocardium cancer	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiology|cardiothoracic|oncology	cardiovascular_disorder|cancer	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0004750	language disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|throat_disorder	false	false	false	false	medium
MONDO:0004751	disease of orbital part of eye adnexa	other	other	disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|cancer	orbital_part_of_eye_adnexa|eye_disorder	true	false	false	false	medium
MONDO:0004752	neurofibroma of the heart	cardiovascular_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|nervous_system_disorder	pediatric|cardiology|oncology|genetics_and_genomics	cardiovascular_disorder|cancer	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0004753	mechanical strabismus	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology	cardiovascular_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0004754	rectal prolapse	digestive_system_disorder	other	digestive_system_disorder	urology|gastroenterology|general_surgery	gastrointestinal_disorder|metabolic_disorder|inflammatory_disease|anemia|autoimmune_diseases|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0004755	monieziasis	infectious_disease	infectious_disease	infectious_disease	dermatology|infectious_diseases|tropical_medicine_is_not_in_the_list__so_i_ll_remove_it|tropical_medicine___corrected_answer__dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	skin_disorder|fungal_infection_disorder	true	false	false	true	low
MONDO:0004756	nasal cavity neoplasm	respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|oncology	disease|neoplasm|cancer	throat_disorder|nose_disorder	false	true	false	false	high
MONDO:0004757	chronic ethmoidal sinusitis	respiratory_system_disorder|inflammatory_disease|musculoskeletal_system_disorder|otorhinolaryngologic_disease	other	inflammatory_disease|otorhinolaryngologic_disease|respiratory_system_disorder|musculoskeletal_system_disorder	otolaryngology|other___corrected_to___otolaryngology	inflammatory_disease|autoimmune_diseases	nose_disorder|sinus_disorder	true	false	false	true	medium
MONDO:0004758	scotoma	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	cardiovascular_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0004759	zoophilia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|psychology	neurodegenerative_disease|mental_health_disorder	mental_health_disorder|reproductive_system_disorder|neurological_disorder	false	false	false	false	none
MONDO:0004760	urethral false passage	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	urological_disorder|anatomic_anomaly|inflammatory_disease|congenital_abnormality	urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0004762	Taylor syndrome	reproductive_system_disorder	other	reproductive_system_disorder	dermatology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|skin_disorder|endocrine_disorder|bone_disorder	false	false	false	false	medium
MONDO:0004763	carotid artery dissection	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|cardiology	cardiovascular_disorder|inflammatory_disease	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0004764	fibular collateral ligament bursitis	connective_tissue_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|rheumatology	inflammatory_disease	joint_disorder|muscle_disorder|bone_disorder	false	false	false	true	medium
MONDO:0004765	intrinsic asthma	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases|allergy	lung_disorder|immune_disorder	false	false	false	false	high
MONDO:0004766	status asthmaticus	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases|allergy	lung_disorder|immune_disorder|respiratory_system_disorder_is_actually_listed_as_lung_disorder_which_is_a_subset_of_the_broader_category_immune_disorder	false	false	false	true	high
MONDO:0004767	vesiculitis	reproductive_system_disorder|endocrine_system_disorder|inflammatory_disease	endocrine_system_disorder	inflammatory_disease|endocrine_system_disorder|reproductive_system_disorder	dermatology|rheumatology|urology	inflammatory_disease|autoimmune_diseases	joint_disorder|urinary_tract_disorder|immune_disorder	true	false	false	false	medium
MONDO:0004768	keratoconjunctivitis	disorder_of_visual_system|inflammatory_disease	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	eye_disorder|keratoconjunctivitis	true	false	false	true	medium
MONDO:0004769	orbital pseudotumor	other	other	disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|cancer	eye_disorder|orbital_pseudotumor_is_also_related_to_the_eye	false	false	false	true	medium
MONDO:0004770	exophthalmos	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0004772	glaucomatocyclitic crisis	inflammatory_disease|disorder_of_visual_system	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	true	medium
MONDO:0004773	iridocyclitis	inflammatory_disease|disorder_of_visual_system	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|urology	inflammatory_disease|autoimmune_diseases	kidney_disorder|eye_disorder|immune_disorder	true	false	false	true	medium
MONDO:0004774	gonococcal iridocyclitis	inflammatory_disease|infectious_disease|disorder_of_visual_system|reproductive_system_disorder	infectious_disease	inflammatory_disease|reproductive_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|infectious_disease	ophthalmology|urology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|eye_disorder	true	false	false	true	high
MONDO:0004775	lens-induced iridocyclitis	inflammatory_disease|disorder_of_visual_system	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|urology	inflammatory_disease|autoimmune_diseases	eye_disorder	true	false	false	true	high
MONDO:0004777	acute laryngitis	respiratory_system_disorder|inflammatory_disease	other	inflammatory_disease|respiratory_system_disorder|acute_disease	otolaryngology|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|thorat_disorder	true	false	false	true	low
MONDO:0004778	epididymo-orchitis	endocrine_system_disorder|inflammatory_disease|infectious_disease|reproductive_system_disorder	endocrine_system_disorder|infectious_disease	inflammatory_disease|endocrine_system_disorder|reproductive_system_disorder|infectious_disease	obstetrics_and_gynecology|urology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0004779	epididymitis	inflammatory_disease|infectious_disease|reproductive_system_disorder	infectious_disease	inflammatory_disease|reproductive_system_disorder|infectious_disease	obstetrics_and_gynecology|urology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0004780	strictly posterior acute myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|acute_disease	cardiology|cardiothoracic	cardiovascular_disorder|adrenal_gland_disease	heart_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0004781	acute myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|acute_disease	cardiology|cardiothoracic|pulmonology	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0004782	diabetes insipidus	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|endocrinology	metabolic_disorder|autoimmune_diseases	kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0004784	allergic asthma	respiratory_system_disorder|immune_system_disorder	other	immune_system_disorder|respiratory_system_disorder	pediatric|pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|allergy	lung_disorder|immune_disorder	false	false	false	true	high
MONDO:0004785	blepharitis	inflammatory_disease|disorder_of_visual_system	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	true	false	false	true	low
MONDO:0004786	chronic cholangitis	endocrine_system_disorder|digestive_system_disorder|inflammatory_disease	endocrine_system_disorder	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0004787	cervical mullerian papilloma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	malignant_tumor_disease|cancer	reproductive_system_disorder|cervical_mullerian_papilloma_matches_the_category	false	false	false	false	low
MONDO:0004788	cervix squamous papilloma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0004789	cholangitis	endocrine_system_disorder|digestive_system_disorder|inflammatory_disease	endocrine_system_disorder	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0004790	fatty liver disease	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	metabolic_disorder|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	true	true	medium
MONDO:0004792	cancer of isthmus of fallopian tube	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	metabolic_disorder|cardiovascular_disorder|anemia|neurodegenerative_disease|adrenal_gland_disease|mental_health_disorder|inflammatory_disease|autoimmune_diseases|allergy|cancer	reproductive_system_disorder|subtype|lymphatic_disorder	false	true	false	true	high
MONDO:0004794	exposure keratitis	inflammatory_disease|disorder_of_visual_system	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	false	false	false	true	high
MONDO:0004795	otitis externa	inflammatory_disease|infectious_disease|otorhinolaryngologic_disease|auditory_system_disorder	infectious_disease	inflammatory_disease|post_infectious_disorder|infectious_disease|otorhinolaryngologic_disease|auditory_system_disorder	pediatric|ent_specialists_often_treat_otitis_externa_in_adults_and_children__while_pediatric_specialists_may_also_be_involved_in_the_care_of_young_patients|otolaryngology	inflammatory_disease|autoimmune_diseases	throat_disorder|ear_disorder	true	false	false	true	low
MONDO:0004796	infectious meningitis	inflammatory_disease|infectious_disease|nervous_system_disorder	infectious_disease	inflammatory_disease|infectious_disease|nervous_system_disorder	pediatric|neurology	inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder|spinal_disorder	true	false	false	true	high
MONDO:0004797	mononeuritis of lower limb	inflammatory_disease|nervous_system_disorder	other	inflammatory_disease|nervous_system_disorder	neurology|orthopaedic	inflammatory_disease|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0004799	ulcerative blepharitis	inflammatory_disease|disorder_of_visual_system	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	true	false	false	true	medium
MONDO:0004800	chronic dacryoadenitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	ophthalmology|otolaryngology	autoimmune_diseases|inflammatory_disease	eye_disorder|nose_disorder	false	false	false	true	medium
MONDO:0004801	unilateral hypoactive labyrinth	otorhinolaryngologic_disease|auditory_system_disorder	other	otorhinolaryngologic_disease|auditory_system_disorder	otolaryngology|neurology	mental_health_disorder|neurodegenerative_disease	ear_disorder|brain_disorder	true	false	false	false	low
MONDO:0004802	pulmonary eosinophilia	hematologic_disorder|syndromic_disease|cardiovascular_disorder|immune_system_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|cardiovascular_disorder|syndromic_disease	pulmonology|allergy_and_immunology	allergy|autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0004803	disseminated eosinophilic collagen disease	hematologic_disorder|syndromic_disease|cardiovascular_disorder|connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|cardiovascular_disorder|syndromic_disease|connective_tissue_disorder	hematology|rheumatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0004804	dacryoadenitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease	eye_disorder|throat_disorder	true	false	false	true	low
MONDO:0004805	leukocyte disorder	hematologic_disorder|immune_system_disorder	other	hematologic_disorder|immune_system_disorder	hematology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0004806	chronic eosinophilic pneumonia	infectious_disease|respiratory_system_disorder|inflammatory_disease	infectious_disease	infectious_disease|inflammatory_disease|respiratory_system_disorder	pulmonology|allergy_and_immunology	autoimmune_diseases|allergy|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	true	high
MONDO:0004808	benign mammary dysplasia	breast_disorder|integumentary_system_disorder	other	breast_disorder|integumentary_system_disorder	obstetrics_and_gynecology|oncology	benign_mammary_dysplasia_is_related_to_cancer_but_it_s_usually_a_precursor_to_breast_cancer_so_more_fitting_would_be_the_category_cancer_but_for_this_question_specifically_since_it_s_benign____cancer|cancer	breast_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0004810	acute ethmoiditis	musculoskeletal_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder|inflammatory_disease	other	otorhinolaryngologic_disease|musculoskeletal_system_disorder|acute_disease|inflammatory_disease|respiratory_system_disorder	infectious_diseases|otolaryngology	autoimmune_diseases|inflammatory_disease	nose_disorder|ear_disorder	true	false	false	true	medium
MONDO:0004811	simple chronic conjunctivitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	true	low
MONDO:0004812	acute dacryoadenitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|acute_disease|inflammatory_disease	pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease	nasal_disorder|eye_disorder	true	false	false	true	medium
MONDO:0004813	tuberculous pneumothorax	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiothoracic	cancer|inflammatory_disease	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0004815	osteosclerotic plasma cell myeloma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	anemia|autoimmune_diseases|cancer	bone_disorder|blood_bone_marrow_disorder|lymphatic_disorder|muscle_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0004816	refractory plasma cell neoplasm	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0004817	non-secretory plasma cell myeloma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematatology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	false	high
MONDO:0004819	indolent plasma cell myeloma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	anemia|autoimmune_diseases|cancer	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	medium
MONDO:0004820	peripheral nerve schwannoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurological_cancer	muskle_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0004821	nasopharyngeal disorder	otorhinolaryngologic_disease|respiratory_system_disorder	other	otorhinolaryngologic_disease|respiratory_system_disorder	otolaryngology	autoimmune_diseases|cancer|neurodegenerative_disease|inflammatory_disease	nose_disorder|throat_disorder	true	true	false	false	high
MONDO:0004822	bronchiectasis	hereditary_disease|respiratory_system_disorder	other	hereditary_disease|respiratory_system_disorder	pulmonology|cardiothoracic	inflammatory_disease|respiratory_disease____note__i_have_corrected_the_response_to_reflect_that_bronchiectasis_is_primarily_a_respiratory_disease__although_it_can_also_be_classified_as_an_inflammatory_disease	lung_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0004824	neonatal candidiasis	infectious_disease	infectious_disease	infectious_disease	obstetrics_and_gynecology|dermatology|allergy_and_immunology|pediatric	autoimmune_diseases|inflammatory_disease	skin_disorder|liver_disorder|immune_disorder	true	false	false	true	medium
MONDO:0004826	urethral calculus	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	metabolic_disorder|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0004827	esophagus squamous cell papilloma	cancer_or_benign_tumor|digestive_system_disorder|upper_digestive_tract_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	oncology|gastroenterology	cancer|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0004828	lower urinary tract calculus	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	metabolic_disorder|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0004829	Krukenberg carcinoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|pathology|gastroenterology	cancer|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004830	fasciitis	musculoskeletal_system_disorder|connective_tissue_disorder|inflammatory_disease	other	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	vascular_disorder|muscle_disorder|joint_disorder	true	false	false	false	medium
MONDO:0004831	proliferative fasciitis	musculoskeletal_system_disorder|connective_tissue_disorder|inflammatory_disease	other	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|rheumatology	autoimmune_diseases|cancer|inflammatory_disease	muscle_disorder|joint_disorder	true	false	false	false	high
MONDO:0004832	esophagus leiomyoma	musculoskeletal_system_disorder|digestive_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	cancer_or_benign_tumor	digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	oncology|gastroenterology	cancer|gastrointestinal_disease|tumor	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0004833	plantar fasciitis	musculoskeletal_system_disorder|connective_tissue_disorder|inflammatory_disease	other	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|joint_disorder	false	false	false	true	medium
MONDO:0004834	ischemic fasciitis	musculoskeletal_system_disorder|connective_tissue_disorder|inflammatory_disease	other	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	pulmonology|orthopaedic|vascular_medicine|cardiothoracic	cardiovascular_disorder|inflammatory_disease	vascular_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0004835	necrotizing fasciitis	musculoskeletal_system_disorder|connective_tissue_disorder|inflammatory_disease	other	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|dermatology|emergency_medicine___corrected_list__dermatology|surgical_specialties	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0004836	intravascular fasciitis	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|integumentary_system_disorder|inflammatory_disease	cancer_or_benign_tumor	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|integumentary_system_disorder	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	vascular_disorder|muscle_disorder	true	false	false	false	medium
MONDO:0004837	neurofibroma of the esophagus	digestive_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	cancer_or_benign_tumor	digestive_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	oncology|gastroenterology|genetics_and_genomics|neurology	cancer|neurofibromatosis	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0004838	orthostatic proteinuria	urinary_system_disorder	other	urinary_system_disorder	nephrology|renal_medicine	autoimmune_diseases|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	low
MONDO:0004840	non-congenital cyst of kidney	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	urological_disorder|renal_disease	kidney_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0004841	kidney hypertrophy	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	metabolic_disorder|kidney_hypertrophy_can_also_be_related_to_autoimmune_diseases_but_the_primary_association_is_metabolic_disorder	kidney_disorder|urinary_tract_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0004842	stomatitis	inflammatory_disease	other	mouth_disorder|inflammatory_disease	dermatology|otolaryngology|pediatric	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|skin_disorder|throat_disorder|immune_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0004843	pathologic nystagmus	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|otolaryngology|neurology	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0004844	oral mucosa leukoplakia	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer	teeth_disorder|oral_mucosa_leukoplakia_is_likely_a_synonym_for_this_category	false	false	false	true	medium
MONDO:0004845	aphthous stomatitis	inflammatory_disease	other	mouth_disorder|inflammatory_disease	dermatology|pediatrics|otolaryngology	autoimmune_diseases|inflammatory_disease	teeth_disorder|throat_disorder|oral_disorder	false	false	false	false	low
MONDO:0004846	placental abruption	reproductive_system_disorder|obstetric_disorder	other	reproductive_system_disorder|obstetric_disorder	obstetrics_and_gynecology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	vascular_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0004847	senile cataract	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	true	medium
MONDO:0004848	ulcerative stomatitis	inflammatory_disease	other	mouth_disorder|inflammatory_disease	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0004849	pulmonary emphysema	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiothoracic	respiratory_disease|cardiovascular_disorder|inflammatory_disease	vascular_disorder|lung_disorder|lower_respiratory_disease	false	false	false	false	high
MONDO:0004851	toxic myocarditis	cardiovascular_disorder|inflammatory_disease|musculoskeletal_system_disorder	cardiovascular_disorder	acute_disease|musculoskeletal_system_disorder|inflammatory_disease|cardiovascular_disorder	cardiology|pulmonology|cardiothoracic	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0004852	gonococcal keratitis	inflammatory_disease|reproductive_system_disorder|infectious_disease|disorder_of_visual_system|integumentary_system_disorder	infectious_disease	reproductive_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|infectious_disease|integumentary_system_disorder|inflammatory_disease	urology|dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0004853	gonococcal endophthalmia	inflammatory_disease|reproductive_system_disorder|infectious_disease|disorder_of_visual_system	infectious_disease	reproductive_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|infectious_disease|inflammatory_disease	pediatric|ophthalmology	inflammatory_disease|eye_disease|autoimmune_diseases	eye_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0004854	ophthalmia neonatorum	inflammatory_disease|reproductive_system_disorder|infectious_disease|disorder_of_visual_system	infectious_disease	reproductive_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|infectious_disease|inflammatory_disease	pediatric|ophthalmology	inflammatory_disease|autoimmune_diseases	nose_disorder|eye_disorder	true	false	false	true	medium
MONDO:0004855	tenosynovitis	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	other	connective_tissue_disorder|musculoskeletal_system_disorder|inflammatory_disease	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	muscle_disorder|skin_disorder|joint_disorder	false	false	false	true	medium
MONDO:0004856	rosacea conjunctivitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	nose_disorder|eye_disorder|skin_disorder	false	false	false	true	medium
MONDO:0004857	tendinitis	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	other	connective_tissue_disorder|musculoskeletal_system_disorder|inflammatory_disease	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	muscle_disorder|joint_disorder	false	false	false	true	medium
MONDO:0004858	occlusion of gallbladder	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0004859	hydrops of gallbladder	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|metabolic_disorder	biliary_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0004860	vitreous disorder	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder|vitreous_disorder	false	false	false	false	medium
MONDO:0004861	ophthalmia nodosa	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	immunology|pediatrics|dermatology|ophthalmology|allergology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder	true	false	false	false	medium
MONDO:0004862	vitreous abscess	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	disorder_of_visual_system|infectious_disease|disorder_of_orbital_region|inflammatory_disease	ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	true	false	false	true	high
MONDO:0004863	purulent endophthalmitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	disorder_of_visual_system|infectious_disease|disorder_of_orbital_region|inflammatory_disease	ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder	true	false	false	true	high
MONDO:0004864	acute allergic mucoid otitis media	inflammatory_disease|otorhinolaryngologic_disease|auditory_system_disorder	other	auditory_system_disorder|otorhinolaryngologic_disease|acute_disease|inflammatory_disease	pediatric|otolaryngology	inflammatory_disease|allergy|autoimmune_diseases	ear_disorder|throat_disorder|immune_disorder	false	false	false	false	medium
MONDO:0004865	blue drum syndrome	inflammatory_disease|otorhinolaryngologic_disease|auditory_system_disorder	other	otorhinolaryngologic_disease|acute_disease|inflammatory_disease|auditory_system_disorder	pulmonology|pediatric|otolaryngology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	biliary_disorder|liver_disorder	false	false	false	false	medium
MONDO:0004866	eustachian tube disorder	otorhinolaryngologic_disease|auditory_system_disorder	other	otorhinolaryngologic_disease|auditory_system_disorder	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	false	false	false	true	medium
MONDO:0004867	upper respiratory tract disorder	respiratory_system_disorder	other	respiratory_system_disorder	otolaryngology|pulmonary	inflammatory_disease|allergy|upper_respiratory_tract_disorder|autoimmune_diseases	lung_disorder|throat_disorder	true	false	false	true	medium
MONDO:0004868	biliary tract disorder	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	biliary_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0004869	pelvic varices	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	obstetrics_and_gynecology|hepatology|hematology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	liver_disorder|vascular_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0004871	perianal hematoma	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	gastroenterology|dermatology|hematology|general_surgery	inflammatory_disease|cancer	vascular_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0004872	hemorrhoid	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	gastroenterology|hematology	inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0004873	internal hemorrhoid	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	gastroenterology|urology|hematology	inflammatory_disease|metabolic_disorder|cancer	lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0004874	ganglion or cyst of synovium/tendon/bursa	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|muscle_disorder	false	false	false	false	low
MONDO:0004875	xanthogranulomatous cholecystitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|inflammatory_disease	gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases	biliary_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0004876	myocardial stunning	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|pulmonology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0004877	transient neonatal thrombocytopenia	hematologic_disorder	other	hematologic_disorder	pediatric|hematology	metabolic_disorder|anemia|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0004878	female breast upper-outer quadrant cancer	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	female_breast_cancer|breast_cancer|cancer|upper_outer_quadrant_cancer	reproductive_system_disorder|subtype|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0004879	senile atrophy of choroid	cardiovascular_disorder|nervous_system_disorder|disorder_of_visual_system	cardiovascular_disorder|neurodegenerative_disease	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cardiovascular_disorder	neurology|ophthalmology	neurodegenerative_disease|senile_atrophy_of_choroid_does_not_fit_well_into_this_category_because_it_is_more_specific_to_the_eye_choroid__however__neurodegenerative_diseases_can_involve_the_eye	eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0004880	bowel dysfunction	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0004881	myositis fibrosa	inflammatory_disease|musculoskeletal_system_disorder	other	inflammatory_disease|musculoskeletal_system_disorder	renal_medicine|rheumatology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder|muscle_disorder	false	false	false	false	high
MONDO:0004882	angioid streaks of choroid	cardiovascular_disorder|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	cardiovascular_disorder|neurodegenerative_disease	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cardiovascular_disorder|hereditary_disease	hematology|genetics_and_genomics|ophthalmology	metabolic_disorder|autoimmune_diseases	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0004883	hereditary choroidal atrophy	cardiovascular_disorder|nervous_system_disorder|disorder_of_visual_system	cardiovascular_disorder|neurodegenerative_disease	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cardiovascular_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder|hereditary|vascular_disorder	false	false	false	false	medium
MONDO:0004884	eye degenerative disorder	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	eye_degenerative_disorder_is_a_subset_of_this_category|neurodegenerative_disease	eye_degenerative_disorder|eye_disorder	false	false	false	true	high
MONDO:0004885	choroidal sclerosis	cardiovascular_disorder|nervous_system_disorder|disorder_of_visual_system	cardiovascular_disorder|neurodegenerative_disease	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cardiovascular_disorder	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0004886	diffuse secondary choroid atrophy	cardiovascular_disorder|nervous_system_disorder|disorder_of_visual_system	cardiovascular_disorder|neurodegenerative_disease	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cardiovascular_disorder	neurology|ophthalmology	inflammatory_disease|metabolic_disorder|cancer	eye_disorder|vascular_disorder	false	false	false	false	low
MONDO:0004888	partial circumpapillary choroid dystrophy	cardiovascular_disorder|nervous_system_disorder|disorder_of_visual_system	cardiovascular_disorder|neurodegenerative_disease	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cardiovascular_disorder	genetics_and_genomics|ophthalmology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0004889	total central choroidal atrophy	cardiovascular_disorder|nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder|cardiovascular_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|nervous_system_disorder|cardiovascular_disorder|hereditary_disease	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0004890	partial central choroid dystrophy	cardiovascular_disorder|hereditary_disease|disorder_of_visual_system	cardiovascular_disorder	disorder_of_visual_system|disorder_of_orbital_region|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|ophthalmology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0004891	hyperopia	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	medium
MONDO:0004892	refractive error	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	true	medium
MONDO:0004893	hypertropia	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0004894	cyclotropia	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0004895	accommodative esotropia	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0004896	esotropia	nervous_system_disorder	other	nervous_system_disorder	otolaryngology|neurology	autoimmune_diseases|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	true	medium
MONDO:0004897	hypotropia	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology	metabolic_disorder|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	true	medium
MONDO:0004898	total circumpapillary dystrophy of choroid	nervous_system_disorder|cardiovascular_disorder|disorder_of_visual_system	neurodegenerative_disease|cardiovascular_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cardiovascular_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0004899	monofixation syndrome	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0004900	peripheral vertigo	auditory_system_disorder|otorhinolaryngologic_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder|otorhinolaryngologic_disease	otolaryngology|neurology	peripheral_nervous_system_disease|neurodegenerative_disease	brain_disorder|ear_disorder	false	false	false	true	medium
MONDO:0004901	lingual-facial-buccal dyskinesia	nervous_system_disorder	other	nervous_system_disorder	otolaryngology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0004902	interstitial keratitis	inflammatory_disease|disorder_of_visual_system|connective_tissue_disorder	other	inflammatory_disease|connective_tissue_disorder|disorder_of_visual_system|disorder_of_orbital_region	pulmonology|dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder|eye_disorder	true	false	false	true	medium
MONDO:0004903	deep keratitis	inflammatory_disease|disorder_of_visual_system	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	true	false	false	true	high
MONDO:0004904	toxic maculopathy	disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease	eye_disorder|liver_disorder	false	false	false	false	high
MONDO:0004905	intestinal disaccharidase deficiency	digestive_system_disorder|metabolic_disease	metabolic_disease	metabolic_disease|digestive_system_disorder	pediatric|genetics_and_genomics|gastroenterology	gastrointestinal_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	true	true	medium
MONDO:0004907	alopecia	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology|endocrinology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0004909	urethral gland abscess	urinary_system_disorder	other	urinary_system_disorder	urology	inflammatory_disease|autoimmune_diseases	kidney_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0004910	mitral valve prolapse	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0004911	cardiovascular syphilis	reproductive_system_disorder|infectious_disease	infectious_disease	infectious_disease|reproductive_system_disorder	cardiothoracic|cardiology	inflammatory_disease|cardiovascular_disorder|cardiovascular_sypilis_is_most_likely_a_misspelling_of_cardiovascular_syphilis_so_this_should_be_treated_as_an_error_in_the_input_data__but_assuming_it_refers_to_a_disease_of_the_cardiovascular_system__cardiovascular_disorder	vascular_disorder|heart_disorder	true	false	false	true	high
MONDO:0004913	alternating esotropia	nervous_system_disorder	other	nervous_system_disorder	neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0004914	celiac artery stenosis from compression by median arcuate ligament of diaphragm	syndromic_disease|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|hereditary_disease|cardiovascular_disorder	cardiothoracic|renal_medicine|pulmonology|cardiology|general_terms_would_suggest__pulmonary____however_given_the_median_arcuate_ligament_of_diaphragm_is_mentioned__this_should_be_categorized_under_cardiothoracic|hematology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	vascular_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0004917	internal hordeolum	integumentary_system_disorder|inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|integumentary_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	otolaryngology|dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	true	false	false	true	medium
MONDO:0004918	central corneal ulcer	inflammatory_disease|disorder_of_visual_system	other	inflammatory_disease|ulcer_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	throat_disorder|eye_disorder	true	false	false	true	high
MONDO:0004919	infected hydrocele	reproductive_system_disorder	other	reproductive_system_disorder	general_surgery|urology	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder|urinary_tract_disorder	true	false	false	true	high
MONDO:0004920	hydrocele	reproductive_system_disorder	other	reproductive_system_disorder	urology|genitourinary	inflammatory_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0004922	developmental coordination disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|developmental_coordination_disorder_falls_under_the_category_of_neurodevelopmental_disorders_which_can_be_closely_related_to_neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0004923	chronic inflammation of lacrimal passage	inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	otolaryngology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|nose_disorder	true	false	false	false	medium
MONDO:0004924	chronic canaliculitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	infectious_disease|disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	otolaryngology|dermatology	inflammatory_disease|autoimmune_diseases	ear_disorder|skin_disorder	true	false	false	true	low
MONDO:0004925	chronic dacryocystitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	otolaryngology|pediatric|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|nose_disorder	true	false	false	true	medium
MONDO:0004926	dacryocystitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	urology|otolaryngology	inflammatory_disease|autoimmune_diseases	nasal_disorder|eye_disorder	true	false	false	true	medium
MONDO:0004927	dacryocystocele	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	urology|obstetrics_and_gynecology|otolaryngology|pediatric|ophthalmology	inflammatory_disease|autoimmune_diseases	nasal_disorder|eye_disorder	false	false	false	false	low
MONDO:0004928	lymph node disorder	immune_system_disorder	other	immune_system_disorder	lymph_node_disorder_is_closely_related_to_the_immune_system__which_would_also_make_allergy_and_immunology_a_fitting_category|hematology	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0004929	constant exophthalmos	other	other	disorder_of_orbital_region	neurology|ophthalmology	inflammatory_disease|adrenal_gland_disease|autoimmune_diseases|metabolic_disorder	brain_disorder|endocrine_disorder|eye_disorder	false	false	false	true	high
MONDO:0004930	steroid-induced glaucoma	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	endocrinology|ophthalmology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	endocrine_disorder|eye_disorder	false	false	false	true	medium
MONDO:0004931	residual stage corticosteroid-induced glaucoma	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|endocrinology|ophthalmology	metabolic_disorder|inflammatory_disease	endocrine_disorder|eye_disorder	false	false	false	false	high
MONDO:0004932	null-cell leukemia	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|acute_disease|cancer_or_benign_tumor	oncology|hematology	cancer|leukemia	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0004933	hypoplastic left heart syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|cardiovascular|cardiology	congenital_heart_defect|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0004934	periostitis	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	other	musculoskeletal_system_disorder|connective_tissue_disorder|inflammatory_disease	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	bone_disorder|upper_gastrointestinal_disorder|joint_disorder	true	false	false	true	medium
MONDO:0004936	uterine inversion	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|pediatric|obgyn	obstetric_complication|gynecological_condition	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0004937	hypervitaminosis D	nutritional_disorder	other	nutritional_disorder	pediatric|endocrinology	inorganic_disorder|metabolic_disorder	endocrine_disorder|liver_disorder	false	false	false	false	low
MONDO:0004938	substance dependence	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder	brain_disorder	false	false	false	true	high
MONDO:0004939	hallucinogen dependence	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	addiction|mental_health_disorder	brain_disorder	false	false	false	false	medium
MONDO:0004940	acute female pelvic peritonitis	inflammatory_disease|reproductive_system_disorder	other	acute_disease|reproductive_system_disorder|inflammatory_disease	pediatric|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	true	false	false	false	high
MONDO:0004941	eosinophilia-myalgia syndrome	syndromic_disease|immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cardiovascular_disorder	cardiovascular_disorder	hematologic_disorder|syndromic_disease|musculoskeletal_system_disorder|cardiovascular_disorder|immune_system_disorder	hematology|rheumatology|allergy_and_immunology|pulmonology	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|muscle_disorder	false	false	false	false	high
MONDO:0004942	orbit lymphoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|disorder_of_orbital_region|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|cancer|lymphoma	immune_disorder|eye_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004943	orbit sarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|disorder_of_orbital_region|cancer_or_benign_tumor	ophthalmology|oncology|orthopaedic	orbital_sarcoma_is_a_type_of_cancer|cancer	eye_disorder|bone_disorder	false	true	false	false	medium
MONDO:0004944	neurosyphilis	infectious_disease|reproductive_system_disorder	infectious_disease	infectious_disease|reproductive_system_disorder	pediatric|neurology|psychiatry|oncology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder|brain_disorder	true	false	false	true	very_high
MONDO:0004946	hypoglycemia	metabolic_disease	metabolic_disease	metabolic_disease	pediatrics|endocrinology	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	blood_bone_marrow_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0004947	B-cell acute lymphoblastic leukemia	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|acute_disease|immune_system_disorder|cancer_or_benign_tumor	hematology|pediatric|oncology	inflammatory_disease|autoimmune_diseases|cancer|anemia	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004948	B-cell chronic lymphocytic leukemia	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|acute_disease|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004949	neoplasm of mature B-cells	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004950	gastric carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	gastrointestinal_disease|digestive_system_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0004952	Hodgkins lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|post_infectious_disorder|cancer_or_benign_tumor	hematology|oncology	inflammatory_disease|autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004953	invasive ductal breast carcinoma	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|integumentary_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|pediatric|oncology	inflammatory_disease|cancer	reproductive_system_disorder|breast_disorder	false	true	false	true	high
MONDO:0004956	metastatic prostate carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|urinary_tract_disorder	false	true	false	true	very_high
MONDO:0004957	mucinous adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	gynecology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0004958	oral cavity squamous cell carcinoma	otorhinolaryngologic_disease|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|otorhinolaryngologic_disease|digestive_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology	oral_cavity_squamous_cell_carcinoma_also_somewhat_fits_into_the_category_of_disease_so__cancer|cancer	throat_disorder|teeth_disorder	false	true	false	true	high
MONDO:0004959	plasma cell neoplasm	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0004960	monoclonal gammopathy	hematologic_disorder	other	hematologic_disorder	oncology|hematology	autoimmune_diseases|anemia|cancer	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0004961	stage I endometrioid carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0004962	stage II endometrioid carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	inflammatory_disease|anemia|autoimmune_diseases|cancer|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0004963	T-cell acute lymphoblastic leukemia	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|acute_disease|immune_system_disorder|cancer_or_benign_tumor	pediatric|immunology|oncology|hematology	autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0004964	peripheral T-cell lymphoma, not otherwise specified	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0004965	acinar cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonology|oncology	cancer|adrenal_gland_disease	lung_disorder|liver_disorder	false	true	false	false	high
MONDO:0004966	gastritis	inflammatory_disease|digestive_system_disorder	other	inflammatory_disease|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0004967	acute lymphoblastic leukemia	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|acute_disease|cancer_or_benign_tumor	pediatric|hematolgy|oncology|hematology	autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0004969	acute quadriplegic myopathy	musculoskeletal_system_disorder	other	acute_disease|musculoskeletal_system_disorder	pediatric|neurology	neurodegenerative_disease|myopathy	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0004970	adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|cardiothoracic|pulmonology|oncology|gastroenterology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lung_disorder|lower_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0004971	adenoid cystic carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	otolaryngology|oncology	adrenal_gland_disease|cancer	ear_disorder|throat_disorder|nose_disorder	false	true	false	false	high
MONDO:0004972	adenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|oncology|gastroenterology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0004973	adenosquamous lung carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|oncology	cancer|carcinoma|lung_cancer	lung_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0004974	adrenal gland pheochromocytoma	disorder_of_development_or_morphogenesis|nervous_system_disorder|endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	oncology|endocrinology	cancer|adrenal_gland_disease	vascular_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0004975	Alzheimer disease	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology|psychiatry	mental_health_disorder|neurodegenerative_disease|cardiovascular_disorder	brain_disorder	false	false	false	false	very_high
MONDO:0004976	amyotrophic lateral sclerosis	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0004977	angioimmunoblastic T-cell lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	inflammatory_disease|autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0004979	asthma	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases|allergy	immune_disorder|lung_disorder|respiratory_disorder	false	false	false	true	medium
MONDO:0004980	atopic eczema	inflammatory_disease|immune_system_disorder|integumentary_system_disorder	other	immune_system_disorder|integumentary_system_disorder|inflammatory_disease	allergy_and_immunology|dermatology|pediatric	inflammatory_disease|autoimmune_diseases|allergy	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0004981	atrial fibrillation	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology|pulmonology	autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0004982	pancreatitis	endocrine_system_disorder|inflammatory_disease|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|inflammatory_disease	endocrinology|gastroenterology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0004983	spermatogenic failure	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|endocrinology	anemia|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0004984	basal-like breast carcinoma	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	obstetrics_and_gynecology|genetics_and_genomics|oncology	cancer|adrenal_gland_disease	immune_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0004985	bipolar disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|mental_health_disorder	false	false	false	true	high
MONDO:0004986	urinary bladder carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0004987	urinary bladder neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer|neoplasm	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0004988	breast adenocarcinoma	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	obstetrics_and_gynecology|oncology	autoimmune_diseases|cancer	reproductive_system_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0004989	breast carcinoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	autoimmune_diseases|cancer	lymphatic_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0004990	breast tumor luminal A or B	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	autoimmune_diseases|cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0004991	minimally invasive lung adenocarcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	cardiothoracic|pulmonology|oncology	adenocarcinoma|cancer|lung_cancer	lung_disorder	false	true	false	true	medium
MONDO:0004992	cancer	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|oncology|hematology	cancer	lymphatic_disorder|vascular_disorder|bone_disorder	false	true	false	true	very_high
MONDO:0004993	carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology	cancer|adrenal_gland_disease	lung_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0004994	cardiomyopathy	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder	cardiothoracic|cardiology	cardiomyopathy_is_often_categorized_under_this_broader_category_as_well|cardiovascular_disorder	muscle_disorder|heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0004995	cardiovascular disorder				cardiothoracic|cardiology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0004996	childhood acute myeloid leukemia	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|acute_disease|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	oncology|pediatric|hematology	cancer|anemia	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0004997	chondroblastoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|genetics_and_genomics|oncology	cancer|bone_disease	bone_disorder|joint_disorder	false	true	false	true	medium
MONDO:0005001	chronic gastritis	digestive_system_disorder|inflammatory_disease	other	digestive_system_disorder|inflammatory_disease	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005002	chronic obstructive pulmonary disease	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiology	cardiovascular_disorder|inflammatory_disease	vascular_disorder|lung_disorder	false	false	false	false	high
MONDO:0005003	chronic pancreatitis	digestive_system_disorder|endocrine_system_disorder|inflammatory_disease	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|inflammatory_disease	gastroenterology|endocrinology	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0005004	clear cell adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	renal_medicine|oncology|urology	cancer|adrenal_gland_disease	kidney_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0005005	clear cell renal carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	renal_medicine|oncology|urology	cancer|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0005006	clear cell sarcoma of kidney	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	cancer|kidney_disease|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	true	false	false	very_high
MONDO:0005007	colon mucinous adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0005008	colorectal adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|adenocarcinoma	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0005009	congestive heart failure	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder|inflammatory_disease	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005010	coronary artery disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|cardiothoracic|cardiology	cardiovascular_disorder|coronary_artery_disorder_is_actually_the_same_thing_so_you_should_just_have_cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005011	Crohn disease	immune_system_disorder|digestive_system_disorder|hereditary_disease	other	digestive_system_disorder|immune_system_disorder|hereditary_disease	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder	false	false	false	false	high
MONDO:0005012	cutaneous melanoma	disorder_of_development_or_morphogenesis|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology|oncology	cancer|skin_cancer	lymphatic_disorder|skin_disorder	false	true	false	true	high
MONDO:0005013	dedifferentiated chondrosarcoma	musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder	oncology|orthopaedic	cancer	bone_disorder|spinal_disorder|joint_disorder	false	true	false	false	very_high
MONDO:0005015	diabetes mellitus	metabolic_disease|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	metabolic_disease|digestive_system_disorder|endocrine_system_disorder	renal_medicine|endocrinology	autoimmune_diseases|metabolic_disorder|cardiovascular_disorder	endocrine_disorder|kidney_disorder|urinary_tract_disorder	false	false	true	true	high
MONDO:0005016	diabetic kidney disease	metabolic_disease|urinary_system_disorder	metabolic_disease	metabolic_disease|urinary_system_disorder	renal_medicine|endocrinology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	endocrine_disorder|kidney_disorder|urinary_tract_disorder	false	false	true	true	very_high
MONDO:0005017	diffuse gastric adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	digestive_system_disease|cancer|adenocarcinoma|gastrointestinal_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0005019	diffuse scleroderma	immune_system_disorder|connective_tissue_disorder|integumentary_system_disorder	autoimmune_disease	immune_system_disorder|integumentary_system_disorder|connective_tissue_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|muscle_disorder|joint_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0005020	intestinal disorder	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	false	medium
MONDO:0005021	dilated cardiomyopathy	cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder	pulmonology|cardiothoracic|cardiology	cardiovascular_disorder|dilated_cardiomyopathy_is_also_a_type_of_metabolic_disorder	vascular_disorder|muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0005023	ductal breast carcinoma in situ	cancer_or_benign_tumor|integumentary_system_disorder|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|breast_disorder	oncology|obstetrics_and_gynecology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|cancer|allergy|anemia|cardiovascular_disorder|mental_health_disorder|adrenal_gland_disease	reproductive_system_disorder|breast_disorder	false	true	false	true	medium
MONDO:0005025	endocarditis	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	renal_medicine|pulmonology|cardiology|cardiothoracic|rheumatology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder	true	false	false	true	high
MONDO:0005026	endometrioid adenocarcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	other___corrected_answer_without__other____cancer|cancer|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0005027	epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0005028	esophageal adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder|upper_digestive_tract_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|upper_digestive_tract_disorder	oncology|gastroenterology	inflammatory_disease|allergy___note__the_inclusion_of__adrenal_gland_disease__is_not_as_clear_cut__but_given_the_context__it_s_possible_that_some_esophageal_adenocarcinomas_might_be_associated_with_pge2_and_other_factors_related_to_adrenal_glands|autoimmune_diseases|cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0005029	essential thrombocythemia	cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|immune_system_disorder|hematologic_disorder	hematology|genetics_and_genomics|oncology	blood_disorder|cancer|anemia	vascular_disorder|blood_bone_marrow_disorder	false	true	false	true	medium
MONDO:0005030	fetal growth restriction	reproductive_system_disorder|obstetric_disorder	other	reproductive_system_disorder|obstetric_disorder	obstetrics_and_gynecology|pediatric	fetal_growth_restriction_is_often_associated_with_placental_insufficiency_which_can_be_caused_by_maternal_metabolic_disorders_such_as_hypertension_and_diabetes|metabolic_disorder	vascular_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0005031	fibromatosis	cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	genetics_and_genomics|rheumatology	inflammatory_disease|autoimmune_diseases|cancer	bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0005032	follicular thyroid adenoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	metabolic_disorder|cancer	endocrine_disorder	false	false	false	true	low
MONDO:0005033	ganglioneuroma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurological_disease|cancer	nerve_disorder|spinal_disorder|muscle_disorder	false	true	false	true	low
MONDO:0005034	thyroid gland follicular carcinoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	cancer|thyroid_gland_disease	endocrine_disorder|thyroid_gland_disorder	false	true	false	true	medium
MONDO:0005035	ganglioneuroblastoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology|pediatric	neuroblastoma|cancer	brain_disorder|nervous_system_disorder	false	true	false	true	very_high
MONDO:0005036	gastric adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	gastrointestinal_cancer|cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0005037	gastric intestinal type adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	adenocarcinoma|gastrointestinal_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0005039	reproductive system disorder		other		reproductive_system_disorder_is_already_the_name_of_a_category_in_the_list__so_it_will_be_included_as_well__obstetrics_and_gynecology|obstetrics_and_gynecology|urology	reproductive_system_disorder|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0005040	germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|pediatric	cancer|adrenal_gland_disease	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0005041	glaucoma	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|cardiovascular_disorder	eye_disorder	false	false	false	true	medium
MONDO:0005043	hyperplasia	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|genetics_and_genomics|oncology|endocrinology	inflammatory_disease|metabolic_disorder|cancer	upper_gastrointestinal_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0005044	hypertensive disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|cardiology	metabolic_disorder|cardiovascular_disorder	endocrine_disorder|vascular_disorder|kidney_disorder	false	false	false	true	high
MONDO:0005045	hypertrophic cardiomyopathy	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder	cardiology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	true	high
MONDO:0005046	immune system disorder		other		rheumatology|allergy_and_immunology|immunology	inflammatory_disease|immune_system_disorder|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0005047	infertility disorder	reproductive_system_disorder	other	reproductive_system_disorder	urology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	infertility_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0005048	pancreatic insulin-producing neuroendocrine tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	cancer|neuroendocrine_tumor	upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0005050	invasive ductal and lobular carcinoma	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|integumentary_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|invasive_ductal_and_lobular_carcinoma_fits_into_the_category_of_cancer_which_is_a_broad_medical_term_for_diseases_caused_by_abnormal_cell_growth__however__if_you_want_to_be_more_specific_it_also_falls_under_the_subcategory__invasive_ductal_and_lobular_carcinoma	upper_gastrointestinal_disorder|breast_disorder_is_not_in_the_list_so__upper_gastrointestinal_disorder|lymphatic_disorder|lung_disorder	false	true	false	true	high
MONDO:0005051	invasive lobular breast carcinoma	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|integumentary_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|invasive_lobular_breast_carcinoma	lymphatic_disorder|breast_disorder	false	true	false	true	medium
MONDO:0005052	irritable bowel syndrome	syndromic_disease|digestive_system_disorder	other	syndromic_disease|digestive_system_disorder	gastroenterology|neurology|pediatric	inflammatory_disease|metabolic_disorder|mental_health_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0005053	ischemic disease	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|pulmonology|cardiology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005055	Kaposi's sarcoma	cardiovascular_disorder|infectious_disease|cancer_or_benign_tumor	infectious_disease|cardiovascular_disorder|cancer_or_benign_tumor	post_infectious_disorder|cardiovascular_disorder|infectious_disease|cancer_or_benign_tumor	dermatology|hematology|oncology	inflammatory_disease|autoimmune_diseases|cancer|anemia	lymphatic_disorder|skin_disorder	false	true	false	true	high
MONDO:0005056	keratinizing squamous cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|oncology	cancer|keratinizing_squamous_cell_carcinoma_is_actually_a_type_of_cancer__but_it_more_specifically_falls_under_the_category_of_skin_cancer	skin_disorder|eye_disorder	false	true	false	true	high
MONDO:0005057	large cell neuroendocrine carcinoma	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neuroendocrine_carcinoma	endocrine_disorder|brain_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0005058	leiomyosarcoma	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	post_infectious_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	hematology|surgical__assuming_surgical_is_implied_for_leiomysarcoma|oncology	cancer|adrenal_gland_disease	vascular_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0005059	leukemia	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|cancer|anemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0005060	liposarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	oncology|orthopaedic|surgery	cancer|adrenal_gland_disease	bone_disorder|muscle_disorder	false	true	false	false	high
MONDO:0005061	lung adenocarcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|pulmonology	cancer|lung_adenocarcinoma_is_a_subset_of_cancer	lower_gastrointestinal_disorder|lung_disorder	false	true	false	true	high
MONDO:0005062	lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0005063	medullary breast carcinoma	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|integumentary_system_disorder|cancer_or_benign_tumor	other____oncology|oncology|breast_cancer	autoimmune_diseases|anemia|cancer|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder|blood_bone_marrow_disorder	false	true	false	true	medium
MONDO:0005065	mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pulmonology|cardiothoracic	inflammatory_disease|autoimmune_diseases|cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|respiratory_lung_disorders_are_often_associated_with_mesothelioma__however_in_this_category_list_i_have_been_requested_to_choose_from_the_available_categories|lung_disorder	false	true	false	false	very_high
MONDO:0005066	metabolic disease				metabolism|endocrinology	metabolic_disorder|metabolic_disease|cardiovascular_disorder	endocrine_disorder|metabolic_disease_is_not_in_the_list__hence_ignore_it__so_use_endocrine_disorder	false	false	true	true	high
MONDO:0005067	monophasic synovial sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	rheumatology|oncology|orthopaedic	inflammatory_disease|autoimmune_diseases|cancer	bone_disorder|joint_disorder	false	true	false	false	high
MONDO:0005068	myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|pulmonology|cardiology|cardiothoracic	inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005070	neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|oncology	cancer|neoplasm	bone_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0005071	nervous system disorder		other		neurology	nervous_system_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0005072	neuroblastoma	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric	cancer|adrenal_gland_disease	spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0005073	melanocytic nevus	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|integumentary_system_disorder|cancer_or_benign_tumor	dermatology|genetics_and_genomics|oncology	neurocutaneous_disorder|cancer	skin_disorder	false	false	false	false	low
MONDO:0005074	papillary cystadenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	lung_disorder|kidney_disorder|liver_disorder	false	true	false	false	high
MONDO:0005075	thyroid gland papillary carcinoma	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|oncology|endocrinology|cardiothoracic	autoimmune_diseases|cancer|thyroid_gland_disease|adrenal_gland_disease	thyroid_disorder|endocrine_disorder|lymphatic_disorder|other____corrected_to___endocrine_disorder	false	true	false	true	medium
MONDO:0005076	periodontitis	musculoskeletal_system_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|inflammatory_disease	hematology|oral_pathology	inflammatory_disease|autoimmune_diseases	bone_disorder|teeth_disorder	true	false	false	true	medium
MONDO:0005077	pertussis	respiratory_system_disorder|infectious_disease	infectious_disease	respiratory_system_disorder|infectious_disease	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	lung_disorder|upper_gastrointestinal_disorder|throat_disorder	true	false	false	true	medium
MONDO:0005078	phyllodes tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|oncology|surgical_oncology_is_not_in_the_list_so_i_will_replace_it_with_cardiothoracic	cancer|adrenal_gland_disease	liver_disorder|breast_disorder	false	true	false	false	medium
MONDO:0005079	polyp	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|gastroenterology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0005080	portal hypertension	digestive_system_disorder|cardiovascular_disorder|endocrine_system_disorder	endocrine_system_disorder|cardiovascular_disorder	cardiovascular_disorder|digestive_system_disorder|endocrine_system_disorder	pulmonology|cardiology|hepatology|gastroenterology	inflammatory_disease|cardiovascular_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0005081	preeclampsia	cardiovascular_disorder|obstetric_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|obstetric_disorder|hereditary_disease	renal_medicine|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	vascular_disorder|kidney_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0005082	prostate adenocarcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0005083	psoriasis	inflammatory_disease|integumentary_system_disorder|immune_system_disorder|hereditary_disease	other	immune_system_disorder|integumentary_system_disorder|inflammatory_disease|hereditary_disease	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	high
MONDO:0005084	mental disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	mental_health_disorder|mental_disorder	brain_disorder|mental_disorder	false	false	false	true	very_high
MONDO:0005085	pterygium	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cancer_or_benign_tumor	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	true	high
MONDO:0005086	renal cell carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	renal_cell_carcinoma|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0005087	respiratory system disorder		other		respiratory_system_disorder_is_related_to_the_lungs_and_breathing__so_this_category_fits_best|pulmonology|cardiothoracic|since_the_disease_affects_the_respiratory_system__which_is_closely_associated_with_the_thoracic_cavity	inflammatory_disease|allergy|autoimmune_diseases|respiratory_system_disorder	respiratory_system_disorder|lung_disorder|throat_disorder	true	false	false	false	high
MONDO:0005089	sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|orthopaedic|hematology	adrenal_gland_disease|cancer	bone_disorder|muscle_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0005090	schizophrenia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|psychological_disorder	false	false	false	false	very_high
MONDO:0005091	severe acute respiratory syndrome	infectious_disease|respiratory_system_disorder	infectious_disease	infectious_disease|acute_disease|respiratory_system_disorder	respiratory_syndrome|pulmonology	respiratory|inflammatory_disease	lung_disorder|respiratory_syndrome_is_not_in_the_list_but_it_fits_under_lung_disorder_so_i_will_choose_that_one_instead|immune_disorder	true	false	false	false	high
MONDO:0005092	signet ring cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0005093	skin disorder	integumentary_system_disorder	other	integumentary_system_disorder	skin_disorder|dermatology	skin_disorder|autoimmune_diseases	skin_disorder	false	false	false	true	medium
MONDO:0005094	hemangiopericytoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology	tumor_cancer|cancer	brain_disorder|vascular_disorder	false	true	false	false	medium
MONDO:0005095	spondyloarthropathy	immune_system_disorder|musculoskeletal_system_disorder	other	immune_system_disorder|musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|spinal_disorder	false	false	false	true	high
MONDO:0005096	squamous cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|oncology	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases|cancer	skin_disorder|lung_disorder	false	true	false	true	high
MONDO:0005097	squamous cell lung carcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|cardiothoracic|oncology	lung_cancer|cancer	lung_disorder	false	true	false	true	high
MONDO:0005098	stroke disorder	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|cardiology	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0005099	subarachnoid hemorrhage	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|hematology	inflammatory_disease|cardiovascular_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|vascular_disorder	false	false	false	false	high
MONDO:0005100	systemic sclerosis	connective_tissue_disorder|integumentary_system_disorder|immune_system_disorder	autoimmune_disease	integumentary_system_disorder|connective_tissue_disorder|immune_system_disorder	rheumatology|dermatology|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0005101	ulcerative colitis	digestive_system_disorder|hereditary_disease|inflammatory_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease|digestive_system_disorder|inflammatory_disease	hepatology|gastroenterology|rheumatology|hematology	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0005102	undifferentiated (embryonal) sarcoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|pediatric|genetics_and_genomics	cancer|adrenal_gland_disease	soft_tissue_disorder|bone_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0005103	well-differentiated liposarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	oncology|orthopaedic|dermatology	cancer	bone_disorder|muscle_disorder	false	true	false	true	medium
MONDO:0005104	sarcoma G1	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric	cancer|adrenal_gland_disease	muscle_disorder	false	true	false	true	low
MONDO:0005105	melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	oncology|dermatology	cancer|adrenal_gland_disease	skin_disorder	false	true	false	true	high
MONDO:0005106	lipoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|dermatology	cancer	bone_disorder|muscle_disorder|joint_disorder|skin_disorder	false	false	false	false	low
MONDO:0005108	viral infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|infectious_disease	autoimmune_diseases|viral_infectious_disease____inflammatory_disease|other___becomes___inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|viral_infectious_disease_can_be_categorized_under_immune_disorder_or__lymphatic_disorder	true	false	false	true	high
MONDO:0005109	HIV infectious disease	reproductive_system_disorder|infectious_disease	infectious_disease	infectious_disease|reproductive_system_disorder	immunology|allergy_and_immunology|infectious_disease	infectious_disease|inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0005110	idiopathic cardiomyopathy	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|idiopathic_disease	cardiology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0005111	Epstein-Barr virus infection	infectious_disease	infectious_disease	infectious_disease	immunology|pediatric	inflammatory_disease|autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	true	false	false	false	medium
MONDO:0005112	malignant pleural mesothelioma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology|cardiothoracic	autoimmune_diseases|cancer	lung_disorder	false	true	false	false	very_high
MONDO:0005113	bacterial infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|infectious_disease	inflammatory_disease|autoimmune_diseases|bacterial_infectious_disease	immune_disorder|vascular_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005114	pneumococcal infection	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0005115	temporal lobe epilepsy	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0005116	Whipple disease	digestive_system_disorder|infectious_disease	infectious_disease	digestive_system_disorder|infectious_disease	gastroenterology|immunology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005117	Aeromonas hydrophila infectious disease	infectious_disease	infectious_disease	infectious_disease	hepatology|gastroenterology|pediatric|renal_medicine	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005118	human granulocytic ehrlichiosis	hematologic_disorder|infectious_disease|immune_system_disorder	infectious_disease	immune_system_disorder|hematologic_disorder|infectious_disease	infectious_diseases|hematology	inflammatory_disease|autoimmune_diseases|anemia	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0005119	anthrax infection	infectious_disease	infectious_disease	infectious_disease	hematology|allergy_and_immunology|pediatric|pulmonology|renal_medicine	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	true	false	false	true	very_high
MONDO:0005121	Enterococcus faecalis infection	infectious_disease	infectious_disease	infectious_disease	gastroenterology|urology|renal_medicine	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005122	Pectobacterium carotovorum infection	infectious_disease	infectious_disease	infectious_disease	microbiology|plant_pathology|pediatric	inflammatory_disease|bacterial_infection|plant_disease_is_not_in_the_list___plant_disease_does_not_exist_in_the_list_so_we_have____inflammatory_disease|bacterial_infection_does_not_exist_in_the_list_either__so_it_s_just_____inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	false	low
MONDO:0005124	leprosy	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|allergy_and_immunology|dermatology|pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0005125	borderline leprosy	infectious_disease	infectious_disease	infectious_disease	immunology|hematology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0005126	tuberculoid leprosy	infectious_disease	infectious_disease	infectious_disease	immunology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0005127	lepromatous leprosy	infectious_disease	infectious_disease	infectious_disease	neurology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0005129	cataract	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0005130	celiac disease	hereditary_disease|immune_system_disorder|digestive_system_disorder	autoimmune_disease	hereditary_disease|digestive_system_disorder|immune_system_disorder	pediatric|gastroenterology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder_upper_gastrointestinal_disorder_immune_disorder	false	false	false	false	high
MONDO:0005131	cervical carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	autoimmune_diseases|cancer|inflammatory_disease	reproductive_system_disorder|lymphatic_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0005132	cytomegalovirus infection	infectious_disease	infectious_disease	infectious_disease	pediatric|genetics_and_genomics|neurology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	immune_disorder|eye_disorder	true	false	false	true	high
MONDO:0005133	endometriosis	reproductive_system_disorder	other	reproductive_system_disorder	endocrinology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	joint_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0005135	parasitic infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|gastroenterology|parasitology_is_not_in_the_list_so_hematology	parasitic_infectious_disease|autoimmune_diseases|inflammatory_disease	liver_disorder|vascular_disorder|lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	high
MONDO:0005136	malaria	hematologic_disorder|infectious_disease	infectious_disease	hematologic_disorder|infectious_disease	pediatric|hematology	inflammatory_disease|anemia	blood_bone_marrow_disorder|immune_disorder	true	false	false	true	high
MONDO:0005137	nutritional disorder		other		gastroenterology|endocrinology	nutritional_disorder|metabolic_disorder|anemia	endocrine_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0005138	lung carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|oncology|cardiothoracic	cancer|lung_carcinoma	lung_disorder|lung_carcinomas_category_is_sometimes_more_specifically_classified_as_a_type_of_lung_carcinoma_but_the_primary_category_is_lung_disorder	false	true	false	true	very_high
MONDO:0005139	morbid obesity	nutritional_disorder	other	nutritional_disorder	cardiology|pulmonology|endocrinology	metabolic_disorder|cardiovascular_disorder	endocrine_disorder|upper_gastrointestinal_disorder	false	false	false	true	very_high
MONDO:0005140	ovarian carcinoma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|ovarian_carcinoma_is_actually_a_type_of_cancer_that_originates_in_the_ovaries_so_it_would_be_more_accurately_categorized_as_a_cancer__which_can_fall_under_the_category_of_reproductive_system_disorder_but_is_typically_categorized_separately_so_i_will_leave_it_out_and_rely_on_the_given_list_to_determine_the_best_fit__which_is___reproductive_system_disorder	false	true	false	true	very_high
MONDO:0005141	Pseudomonas infection	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	autoimmune_diseases|cancer|inflammatory_disease	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0005142	Pseudomonas aeruginosa CF5 infection	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology|infection_control_is_not_in_the_list_but_based_on_the_categories_i_can_infer_that_pulmonology_would_be_a_primary_fit_for_pseudomonas_aeruginosa_cf5_infection	autoimmune_diseases|inflammatory_disease	lung_disorder|urinary_tract_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005143	Pseudomonas aeruginosa PA14 infection	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|microbiology|pulmonology	bacterial_infection|inflammatory_disease	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0005144	familial amyotrophic lateral sclerosis	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0005145	sporadic amyotrophic lateral sclerosis	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	genetics_and_genomics|neurology	autoimmune_diseases___corrected_to__neurodegenerative_disease|neurodegenerative_disease|inflammatory_disease___corrected_again__neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0005146	post-traumatic stress disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|autoimmune_diseases|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0005147	type 1 diabetes mellitus	metabolic_disease|immune_system_disorder|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|diabetes_mellitus|autoimmune_disease|metabolic_disease	metabolic_disease|digestive_system_disorder|endocrine_system_disorder|immune_system_disorder	endocrinology|pediatric	autoimmune_diseases|metabolic_disorder	endocrine_disorder|immune_disorder	false	false	true	false	high
MONDO:0005148	type 2 diabetes mellitus	metabolic_disease|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|diabetes_mellitus|metabolic_disease	metabolic_disease|digestive_system_disorder|endocrine_system_disorder	endocrinology|pediatric|cardiology|renal_medicine	metabolic_disorder|cardiovascular_disorder	endocrine_disorder|kidney_disorder	false	false	true	true	high
MONDO:0005149	pulmonary hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|pulmonology	cardiovascular_disorder|inflammatory_disease	lung_disorder|vascular_disorder	false	false	false	true	high
MONDO:0005150	age-related macular degeneration	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	disorder_of_orbital_region|nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0005151	endocrine system disorder				endocrine_system_disorder|endocrinology	endocrine_system_disorder|metabolic_disorder|autoimmune_diseases|inflammatory_disease	endocrine_disorder|immune_disorder	false	false	false	false	high
MONDO:0005152	hypopituitarism	endocrine_system_disorder|reproductive_system_disorder|nervous_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	pediatric|endocrinology	metabolic_disorder|endocrine_disease	endocrine_disorder|brain_disorder	false	false	false	true	medium
MONDO:0005153	cervical adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0005154	liver disorder	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	gastroenterology|hepatology	liver_disorder_is_a_subset_of_this_category__but_since_it_s_more_specific_the_category_takes_precedence|metabolic_disorder|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0005155	cirrhosis of liver	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	gastroenterology|hepatology	metabolic_disorder|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0005156	encephalomyelitis	inflammatory_disease|nervous_system_disorder	other	nervous_system_disorder|inflammatory_disease	pediatrics|allergy_and_immunology|neurology	autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder|immune_disorder	true	false	false	false	high
MONDO:0005157	lymphoid neoplasm	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0005159	prostate carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	other_is_removed|cancer|adrenal_gland_disease	reproductive_system_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0005160	aortic aneurysm	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0005161	human papilloma virus infection	infectious_disease	infectious_disease	infectious_disease	dermatology|obstetrics_and_gynecology	cancer|inflammatory_disease	reproductive_system_disorder|skin_disorder	true	false	false	true	high
MONDO:0005164	fibrosarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	orthopaedic|hematology|oncology	cancer	spinal_disorder|bone_disorder|vascular_disorder|muscle_disorder|joint_disorder	false	true	false	false	high
MONDO:0005165	benign neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology	benign_neoplasm|cancer	liver_disorder|bone_disorder|kidney_disorder	false	false	false	false	low
MONDO:0005166	osteoma	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	orthopaedic|otolaryngology	bone|skeletal_system_disease	bone_disorder	false	false	false	true	low
MONDO:0005167	fibroma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	orthopaedic|neurology|otolaryngology|oncology	neurodegenerative_disease|cancer	spinal_disorder|bone_disorder	false	false	false	false	low
MONDO:0005168	neoplasm of immature B and T cells	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology|pediatric	neoplasm|cancer	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0005169	neoplasm of mature T-cells or NK-cells	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	autoimmune_diseases|cancer	immune_disorder_lymphatic_disorder	false	true	false	false	high
MONDO:0005170	myeloid neoplasm	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	myeloid_neoplasm_is_a_type_of_cancer|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0005172	skeletal system disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	skeletal_system_disorder|autoimmune_diseases|inflammatory_disease	bone_disorder|skeletal_system_disorder|joint_disorder	false	false	false	false	medium
MONDO:0005173	actinic keratosis	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer|skin_disease	skin_disorder	false	false	false	true	low
MONDO:0005174	acute hypotension	cardiovascular_disorder	cardiovascular_disorder	acute_disease|cardiovascular_disorder	hematology|renal_medicine|cardiology	cardiovascular_disorder|adrenal_gland_disease	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0005175	aggressive insulitis	digestive_system_disorder|endocrine_system_disorder|immune_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|immune_system_disorder	endocrinology|immunology|rheumatology|renal_medicine|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	endocrine_disorder|immune_disorder	true	false	false	false	high
MONDO:0005176	benign insulitis	digestive_system_disorder|endocrine_system_disorder|immune_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|immune_system_disorder	endocrinology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder_endocrine_disorder	false	false	false	false	low
MONDO:0005177	serous cystadenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|liver_disorder	false	false	false	false	medium
MONDO:0005178	osteoarthritis	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease	rheumatology|orthopaedic	autoimmune_diseases|metabolic_disorder|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0005179	ovarian adenoma benign	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	benign_cancer|cancer|adrenal_gland_disease	ovarian_adenoma_benign|reproductive_system_disorder	false	false	false	false	low
MONDO:0005180	Parkinson disease	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|cardiovascular_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0005181	progressive external ophthalmoplegia	hereditary_disease|mitochondrial_disease|metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|mitochondrial_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0005182	serous cystadenofibroma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0005183	ovarian cystadenoma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|ovarian_cystadenoma_is_a_type_of_benign__non_cancerous__tumor__but_it_s_often_classified_under_this_category_due_to_its_origin_and_characteristics	reproductive_system_disorder|ovarian_cystadenoma_is_more_closely_related_to_reproductive_system_but_also_has_some_connection_to_gi_system_due_to_its_origin_in_the_ovary_near_the_intestines__hence_it_also_belongs_to_lower_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0005184	pancreatic ductal adenocarcinoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|gastroenterology	autoimmune_diseases|cancer|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0005185	chronic childhood arthritis	inflammatory_disease|connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder	autoimmune_disease	connective_tissue_disorder|musculoskeletal_system_disorder|inflammatory_disease|immune_system_disorder	rheumatology|pediatric	autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	true	high
MONDO:0005186	cocaine dependence	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0005187	human herpesvirus 8 infection	infectious_disease	infectious_disease	infectious_disease	dermatology|hematology|oncology|renal_medicine|hepatology	cancer|inflammatory_disease	immune_disorder_lymphatic_disorder_skin_disorder	true	false	false	true	high
MONDO:0005188	iatrogenic Kaposi's sarcoma	infectious_disease|iatrogenic_disease|cardiovascular_disorder|cancer_or_benign_tumor	infectious_disease|cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|post_infectious_disorder|infectious_disease|cardiovascular_disorder|iatrogenic_disease	dermatology|oncology	iatrogenic_condition_is_a_subset_of_the_category__iatrogenic__but_since_that_wasn_t_listed__i_ve_used_the_closest_related_category_which_is__cancer|cancer	skin_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0005189	internal carotid artery stenosis	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	neurology|cardiology	cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0005191	metastatic melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	dermatology|oncology	autoimmune_diseases|cancer|adrenal_gland_disease|mental_health_disorder|inflammatory_disease	skin_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0005192	exocrine pancreatic carcinoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0005193	prostate intraepithelial neoplasia	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	prostate_intraepithelial_neoplasia|cancer	reproductive_system_disorder|urinary_tract_disorder	false	true	false	false	medium
MONDO:0005194	Rotavirus infection	infectious_disease	infectious_disease	infectious_disease	gastroenterology|pediatric	allergy|autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005195	septic peritonitis	inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|inflammatory_disease	emergency_medicine|gastroenterology|general_surgery	autoimmune_diseases|inflammatory_disease	liver_disorder|lower_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0005197	thymus neoplasm	hematologic_disorder|endocrine_system_disorder|immune_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|hematologic_disorder|immune_system_disorder	hematology|allergy_and_immunology|oncology|pediatric	autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	false	true	false	false	medium
MONDO:0005198	vulvar intraepithelial neoplasia	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	dermatology|obstetrics_and_gynecology|oncology	autoimmune_diseases|cancer|adrenal_gland_disease|inflammatory_disease	reproductive_system_disorder|skin_disorder	false	true	false	true	low
MONDO:0005200	viral dilated cardiomyopathy	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|post_infectious_disorder|cardiovascular_disorder	cardiology|cardiothoracic	inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder|muscle_disorder	true	false	false	true	high
MONDO:0005201	restrictive cardiomyopathy	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder	cardiology|pulmonology|cardiothoracic	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0005202	atopic IgE-mediated allergic disorder	immune_system_disorder	other	immune_system_disorder	pediatric|allergy_and_immunology	allergy|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0005204	primary antiphospholipid syndrome	immune_system_disorder|syndromic_disease	autoimmune_disease	immune_system_disorder|syndromic_disease	rheumatology|hematology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	vascular_disorder|immune_disorder	false	false	false	false	high
MONDO:0005206	renal carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine|oncology	cancer|renal_carcinoma	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0005207	choriocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	eye_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0005208	amelanotic skin melanoma	disorder_of_development_or_morphogenesis|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|disorder_of_development_or_morphogenesis	oncology|dermatology	cancer|adrenal_gland_disease	skin_disorder|lymphatic_disorder|immune_disorder	false	true	false	false	high
MONDO:0005210	uterine corpus sarcoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	blood_bone_marrow_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0005211	ovarian serous adenocarcinoma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	ovarian_disorder|reproductive_system_disorder|gynecological_cancer	false	true	false	false	high
MONDO:0005212	rhabdomyosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	cancer|sarcoma|tumor|malignancy|oncology	kidney_disorder|muscle_disorder	false	true	false	true	very_high
MONDO:0005213	uterine carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|uterine_carcinoma_falls_under_the_category_of_cancer_specifically_related_to_the_uterus_therefore_is_more_specific_than_general_cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0005214	vulva sarcoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer	skin_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0005215	vulvar carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology|dermatology	cancer|autoimmune_diseases|adrenal_gland_disease	skin_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0005216	hypopharyngeal carcinoma	respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder|digestive_system_disorder	otolaryngology|oncology	cancer	throat_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0005217	familial cardiomyopathy	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiology|genetics_and_genomics|cardiothoracic	cardiovascular_disorder|familial_cardiomyopathy_is_often_categorized_as_a_type_of_metabolic_disorder_but_more_specifically_it_fits_under_cardiovascular_category_as_well	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0005219	breast fibrocystic disease	breast_disorder	other	breast_disorder	endocrinology|obstetrics_and_gynecology|dermatology|oncology	inflammatory_disease|autoimmune_diseases	joint_disorder|skin_disorder|reproductive_system_disorder|muscle_disorder	false	false	false	false	low
MONDO:0005220	collecting duct carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology|renal_medicine	cancer|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0005221	renal pelvis urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	cancer|renal_pelvis_urothelial_carcinoma_is_a_type_of_cancer_so_it_fits_well_in_this_category__but_since_the_question_asks_for_best_fitting_categories_i_will_include_urologic_cancers_which_is_not_on_the_list_however__urinary_system__or__bladder_cancer__could_be_added_to_the_original_list_to_get_more_accurate_results	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0005223	acute myeloid leukemia with minimal differentiation	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder|acute_disease|connective_tissue_disorder|hematologic_disorder	hematology|oncology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0005224	acute myeloblastic leukemia without maturation	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder|acute_disease|connective_tissue_disorder|hematologic_disorder	hematology|oncology	leukemia|cancer|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder|muscle_disorder	false	true	false	true	very_high
MONDO:0005227	abscess	infectious_disease	infectious_disease	infectious_disease	general_surgery|dermatology|infectious_diseases	inflammatory_disease|autoimmune_diseases	liver_disorder|joint_disorder|skin_disorder	true	false	false	true	medium
MONDO:0005229	bacterial infectious disease with sepsis	infectious_disease	infectious_disease	infectious_disease	hematology|pediatric|pulmonology|infectious_diseases	inflammatory_disease|bacterial_infectious_disease	immune_disorder|bacterial_infectious_disease_with_sepsis	true	false	false	true	very_high
MONDO:0005230	cellulitis	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	infectious_disease|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0005231	hepatitis C virus infection	endocrine_system_disorder|inflammatory_disease|digestive_system_disorder|infectious_disease	infectious_disease|endocrine_system_disorder	digestive_system_disorder|inflammatory_disease|endocrine_system_disorder|infectious_disease	gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases	immune_disorder|liver_disorder	true	false	false	true	high
MONDO:0005232	large cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonology|oncology	cancer	lung_disorder	false	true	false	false	high
MONDO:0005233	non-small cell lung carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|oncology	cancer|inflammatory_disease|cardiovascular_disorder|adrenal_gland_disease	vascular_disorder|lower_gastrointestinal_disorder|lung_disorder	false	true	false	true	very_high
MONDO:0005235	smoldering plasma cell myeloma	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	hematology|oncology	cancer|autoimmune_diseases|anemia	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	low
MONDO:0005236	xanthoma	metabolic_disease	metabolic_disease	metabolic_disease	other___note__xanthoma_is_a_skin_condition_characterized_by_the_deposition_of_yellowish_lipid_material_in_various_parts_of_the_body__making_dermatology_the_primary_category__however__considering_its_relation_to_lipids_and_potential_associations_with_systemic_conditions___other__could_also_be_considered_as_it_may_not_exclusively_fit_into_dermatology_but_has_connections_to_other_medical_specialties|dermatology	metabolic_disorder|inflammatory_disease	liver_disorder|skin_disorder	false	false	false	true	low
MONDO:0005238	round cell liposarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	hematology|orthopaedic|rheumatology|pediatric|neurology|oncology	cancer|adrenal_gland_disease	blood_bone_marrow_disorder|lymphatic_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0005240	kidney disorder	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	metabolic_disorder|inflammatory_disease|autoimmune_diseases|kidney_disorder_is_not_in_the_list_so__metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0005242	empyema	infectious_disease	infectious_disease	infectious_disease	cardiothoracic|pulmonology	cancer|inflammatory_disease|autoimmune_diseases	lung_disorder	true	false	false	true	high
MONDO:0005244	peripheral neuropathy	nervous_system_disorder	other	nervous_system_disorder	hematology|cardiology|neurology|renal_medicine	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0005246	osteomyelitis	musculoskeletal_system_disorder|immune_system_disorder|hematologic_disorder	other	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder|immune_disorder	true	false	false	true	high
MONDO:0005247	bacterial urinary tract infection	urinary_system_disorder|infectious_disease	infectious_disease	urinary_system_disorder|infectious_disease	urology|renal_medicine	bacterial_infection|inflammatory_disease	kidney_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0005249	pneumonia	respiratory_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	inflammatory_disease|respiratory_system_disorder|infectious_disease	cardiothoracic|pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0005250	placental villitis	reproductive_system_disorder|inflammatory_disease|obstetric_disorder	other	inflammatory_disease|obstetric_disorder|reproductive_system_disorder	pediatric|obstetrics_and_gynecology|hematology	inflammatory_disease|autoimmune_diseases	immune_disorder|reproductive_system_disorder	true	false	false	false	low
MONDO:0005252	heart failure	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology|pulmonology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0005253	high output heart failure	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology|pulmonology	metabolic_disorder|inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005254	symptomatic heart failure	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology|pulmonology	symptomatic_heart_failure|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005255	mild heart failure	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology|pulmonology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0005256	moderate heart failure	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|pulmonology	inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005257	advanced heart failure	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology|pulmonology	advanced_cardiovascular_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0005258	autism spectrum disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0005260	autism	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry|genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0005262	central nervous system cyst	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	neurological_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0005264	transient ischemic attack	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|cardiology	cardiovascular_disorder|transient_ischemic_attack_is_often_related_to_cardiovascular_system_issues	vascular_disorder|brain_disorder	false	false	false	true	low
MONDO:0005265	inflammatory bowel disease	immune_system_disorder|hereditary_disease|digestive_system_disorder	other	hereditary_disease|digestive_system_disorder|immune_system_disorder	rheumatology|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0005266	diabetic retinopathy	metabolic_disease|cardiovascular_disorder|disorder_of_visual_system|nervous_system_disorder	metabolic_disease|cardiovascular_disorder	disorder_of_visual_system|cardiovascular_disorder|metabolic_disease|nervous_system_disorder|disorder_of_orbital_region	endocrinology|ophthalmology	inflammatory_disease|metabolic_disorder	endocrine_disorder|eye_disorder	false	false	true	true	high
MONDO:0005267	heart disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiovascular	heart_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005269	carotid artery disorder	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|cardiology|hematology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005271	allergic disease	immune_system_disorder	other	immune_system_disorder	allergy_and_immunology|pediatric	inflammatory_disease|allergy|autoimmune_diseases	skin_disorder|lymphatic_disorder|immune_disorder	false	false	false	true	medium
MONDO:0005272	myelodysplastic syndrome with single lineage dysplasia	cancer_or_benign_tumor|hematologic_disorder|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|hematologic_disorder|cancer_or_benign_tumor	oncology|hematology|genetics_and_genomics	anemia|cancer	blood_bone_marrow_disorder	false	true	false	false	medium
MONDO:0005275	lung disorder	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiology|cardiothoracic	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|lung_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0005276	dental caries	musculoskeletal_system_disorder	other	mouth_disorder|musculoskeletal_system_disorder	general|public_health|pediatric	inflammatory_disease|metabolic_disorder	teeth_disorder	true	false	false	true	medium
MONDO:0005277	migraine disorder	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|psychiatry	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	brain_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0005278	serous adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|gynecology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0005279	pulmonary embolism	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiology|hematology	cancer|cardiovascular_disorder	vascular_disorder|lung_disorder	false	false	false	true	high
MONDO:0005280	prostatitis	reproductive_system_disorder|inflammatory_disease	other	inflammatory_disease|reproductive_system_disorder	andrology|urology	inflammatory_disease|cancer|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0005281	gallbladder disorder	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder|biliary_disorder	false	false	false	true	medium
MONDO:0005282	cutaneous lupus erythematosus	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	connective_tissue_disorder|immune_system_disorder	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0005283	retinal disorder	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder	false	false	false	true	high
MONDO:0005284	chronic progressive multiple sclerosis	immune_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	autoimmune_disease|neurodegenerative_disease	nervous_system_disorder|immune_system_disorder|disorder_of_development_or_morphogenesis	neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0005286	palatal neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer|neoplasm	throat_disorder|teeth_disorder	false	true	false	false	high
MONDO:0005287	developmental disability	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	developmental_disability_is_not_present_in_the_list_so_i_will_leave_it_out|neurodegenerative_disease|mental_health_disorder	brain_disorder|developmental_disability_is_often_categorized_under_a_broader_umbrella_category__brain_disorder_but_more_specifically__developmental_disability_can_be_classified_under_neurological_disorders_which_also_overlap_with__brain_disorder_so_i_will_return_the_most_appropriate_one_which_is__brain_disorder	false	false	false	false	high
MONDO:0005288	intestinal polyp	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|intestinal_polyp	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0005289	paranasal sinus neoplasm	respiratory_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|otolaryngology	inflammatory_disease|cancer|autoimmune_diseases	throat_disorder|nose_disorder	false	true	false	false	high
MONDO:0005291	brain aneurysm	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|cardiovascular	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0005292	colitis	immune_system_disorder|inflammatory_disease|hereditary_disease|digestive_system_disorder	other	hereditary_disease|inflammatory_disease|digestive_system_disorder|immune_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005293	flatfoot	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	pediatric|orthopaedic	inflammatory_disease|musculoskeletal_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0005294	peripheral vascular disease	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|vascular____i_corrected_the_answer_to_reflect_that_peripheral_vascular_disease_is_closely_related_to_cardiology	inflammatory_disease|cardiovascular_disorder	muscle_disorder|vascular_disorder	false	false	false	true	high
MONDO:0005295	intermittent vascular claudication	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiology|hematology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0005296	sleep apnea syndrome	respiratory_system_disorder	other	sleep_disorder|respiratory_system_disorder	pulmonology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	lung_disorder|respiratory_system_disorder	false	false	false	true	high
MONDO:0005297	urethritis	inflammatory_disease|infectious_disease|urinary_system_disorder	infectious_disease	inflammatory_disease|urinary_system_disorder|infectious_disease	urethritis|urology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder	true	false	false	true	medium
MONDO:0005298	osteoporosis	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|rheumatology	inflammatory_disease|metabolic_disorder	bone_disorder|spinal_disorder|joint_disorder	false	false	false	true	high
MONDO:0005299	brain ischemia	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|cardiology	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0005300	chronic kidney disease	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine|nephrology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0005301	multiple sclerosis	immune_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease|autoimmune_disease	immune_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|immune_disorder|spinal_disorder	false	false	false	true	high
MONDO:0005302	attention deficit hyperactivity disorder, inattentive type	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	metabolic_disorder|mental_health_disorder|neurodegenerative_disease_is_incorrect____mental_health_disorder	mental_health_disorder|brain_disorder|nervous_system_disorder|neurological_disorder	false	false	false	true	medium
MONDO:0005303	drug dependence	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	addiction|mental_health_disorder	spinal_disorder|vascular_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0005304	biliary tract neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|hepatology|gastroenterology	cancer|biliary_tract_neoplasm	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0005306	ankylosing spondylitis	inflammatory_disease|immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	autoimmune_disease	connective_tissue_disorder|immune_system_disorder|inflammatory_disease|musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	spinal_disorder|bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0005308	ciliopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|pulmonology	inflammatory_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	lung_disorder|respiratory_disorder	false	false	false	false	high
MONDO:0005310	atrial flutter	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0005311	atherosclerosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|hematology|cardiology|pulmonology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005312	pouchitis	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|liver_disorder	true	false	false	true	medium
MONDO:0005313	necrotizing enterocolitis	hereditary_disease|digestive_system_disorder	other	hereditary_disease|digestive_system_disorder	gastroenterology|pediatric	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0005314	relapsing-remitting multiple sclerosis	disorder_of_development_or_morphogenesis|nervous_system_disorder|immune_system_disorder	neurodegenerative_disease|autoimmune_disease	immune_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|psychiatry	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	immune_disorder|brain_disorder	false	false	false	true	high
MONDO:0005316	bacterial vaginosis	reproductive_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	inflammatory_disease|reproductive_system_disorder|infectious_disease	obstetrics_and_gynecology	inflammatory_disease	reproductive_system_disorder|urinary_tract_disorder	true	false	false	true	low
MONDO:0005318	canker sore	inflammatory_disease	other	mouth_disorder|inflammatory_disease	dermatology|otolaryngology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|throat_disorder	false	false	false	true	low
MONDO:0005321	Fuchs' endothelial dystrophy	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	inflammatory_disease|autoimmune_diseases	kidney_disorder|eye_disorder	false	false	false	true	high
MONDO:0005323	bacterial sexually transmitted disease	reproductive_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease	obstetrics_and_gynecology|urology	infectious_disease|autoimmune_diseases	skin_disorder|immune_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0005324	seasonal allergic rhinitis	inflammatory_disease|immune_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder	other	immune_system_disorder|otorhinolaryngologic_disease|inflammatory_disease|respiratory_system_disorder	otolaryngology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|allergy	upper_gastrointestinal_disorder|immune_disorder|lung_disorder|nose_disorder	false	false	false	true	medium
MONDO:0005326	sunburn	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	inflammatory_disease|skin_condition	skin_disorder|eye_disorder	false	false	false	true	low
MONDO:0005328	eye disorder	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology	inflammatory_disease|autoimmune_diseases|eye_disorder	eye_disorder	false	false	false	true	high
MONDO:0005333	hyperthyroxinemia	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	genetics_and_genomics|endocrinology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	endocrinology_disorders|thyroid_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0005334	hereditary nephritis	hereditary_disease|inflammatory_disease|urinary_system_disorder	other	hereditary_disease|inflammatory_disease|urinary_system_disorder	genetics_and_genomics|pediatric|renal_medicine	inflammatory_disease|autoimmune_diseases	immune_disorder|kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0005335	colorectal neoplasm	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	allergy|inflammatory_disease|anemia|metabolic_disorder|cancer|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0005336	myopathy	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	neurology|orthopaedic	myopathy|neurodegenerative_disease	muscle_disorder|myopathy	false	false	false	false	medium
MONDO:0005338	open-angle glaucoma	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	eye_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0005339	androgenetic alopecia	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|endocrinology	inflammatory_disease|metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0005340	alopecia areata	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0005341	skin basal cell carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	cancer|skin_disease	cutaneous_disorder|skin_disorder	false	true	false	true	low
MONDO:0005342	IgA glomerulonephritis	hereditary_disease|inflammatory_disease|urinary_system_disorder	other	hereditary_disease|inflammatory_disease|urinary_system_disorder	hematology|immunology|allergy_and_immunology|renal_medicine	inflammatory_disease|autoimmune_diseases	immune_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0005344	hepatitis B virus infection	endocrine_system_disorder|inflammatory_disease|infectious_disease|digestive_system_disorder	infectious_disease|endocrine_system_disorder	endocrine_system_disorder|inflammatory_disease|digestive_system_disorder|infectious_disease	gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases	immune_disorder|liver_disorder	true	false	false	true	high
MONDO:0005345	hypospadias	disorder_of_development_or_morphogenesis|hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis	urology|pediatric	pediatric_surgical_condition|congenital_anomaly|reproductive_system_disorder	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0005346	gallstones	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|biliary_disorder|liver_disorder	false	false	false	true	medium
MONDO:0005347	hypertriglyceridemia	metabolic_disease	metabolic_disease	metabolic_disease	hepatology|endocrinology|cardiology	metabolic_disorder|adrenal_gland_disease|cardiovascular_disorder	liver_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0005348	keloid	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|plastic_surgery_is_not_listed_so_none	inflammatory_disease|autoimmune_diseases	muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0005349	otosclerosis	hereditary_disease|auditory_system_disorder|otorhinolaryngologic_disease	other	auditory_system_disorder|otorhinolaryngologic_disease|hereditary_disease	genetics_and_genomics|otolaryngology	inflammatory_disease|autoimmune_diseases	bone_disorder|ear_disorder	false	false	false	true	medium
MONDO:0005350	abdominal aortic aneurysm	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	general_surgery|cardiology	inflammatory_disease|cancer|cardiovascular_disorder	upper_gastrointestinal_disorder|vascular_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0005351	anorexia nervosa	psychiatric_disorder|nutritional_disorder	psychiatric_disorder	psychiatric_disorder|nutritional_disorder	psychiatry|pediatric	metabolic_disorder|mental_health_disorder	psychological_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0005352	conduct disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|pediatric	conduct_disorder|mental_health_disorder	mental_health_disorder|brain_disorder	false	false	false	true	high
MONDO:0005354	chronic hepatitis C virus infection	inflammatory_disease|endocrine_system_disorder|infectious_disease|digestive_system_disorder	infectious_disease|endocrine_system_disorder	inflammatory_disease|endocrine_system_disorder|infectious_disease|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|immune_disorder|lower_gastrointestinal_disorder|liver_disorder	true	false	false	true	high
MONDO:0005355	coronary restenosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|hematology|cardiology|pulmonology|cardiothoracic	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005356	coronary vasospasm	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiovascular	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005357	Creutzfeldt Jacob disease	nervous_system_disorder|infectious_disease	infectious_disease	infectious_disease|nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0005358	Dengue hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|hepatology|hematology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder	true	false	false	true	high
MONDO:0005359	drug-induced liver injury	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0005361	eosinophilic esophagitis	inflammatory_disease|digestive_system_disorder|upper_digestive_tract_disorder	other	upper_digestive_tract_disorder|inflammatory_disease|digestive_system_disorder	gastroenterology|pediatric	inflammatory_disease|autoimmune_diseases|allergy	upper_gastrointestinal_disorder|immune_disorder	false	false	false	true	medium
MONDO:0005362	erectile dysfunction	reproductive_system_disorder	other	reproductive_system_disorder	neurology|urology	mental_health_disorder|cardiovascular_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0005363	inherited focal segmental glomerulosclerosis	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	renal_medicine|genetics_and_genomics	metabolic_disorder|genetic_disorder|kidney_disease	vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0005364	Graves disease	inflammatory_disease|endocrine_system_disorder|immune_system_disorder	autoimmune_disease|endocrine_system_disorder	immune_system_disorder|inflammatory_disease|endocrine_system_disorder	endocrinology|allergy_and_immunology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|immune_disorder	false	false	false	true	medium
MONDO:0005365	hearing loss disorder	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	neurology|otolaryngology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	ear_disorder	false	false	false	false	medium
MONDO:0005366	chronic hepatitis B virus infection	inflammatory_disease|endocrine_system_disorder|infectious_disease|digestive_system_disorder	infectious_disease|endocrine_system_disorder	inflammatory_disease|endocrine_system_disorder|infectious_disease|digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder|liver_disorder	true	false	false	true	high
MONDO:0005367	heroin dependence	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	addiction|mental_health_disorder	brain_disorder	false	false	false	true	very_high
MONDO:0005369	carcinoid tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|pulmonology|oncology	cancer|adrenal_gland_disease	endocrine_disorder|lung_disorder	false	true	false	true	medium
MONDO:0005371	mood disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	autoimmune_diseases|mental_health_disorder	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0005372	male infertility	reproductive_system_disorder	other	reproductive_system_disorder	genetics_and_genomics|endocrinology|urology|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|male_infertility	false	false	false	true	medium
MONDO:0005373	meningococcal infection	infectious_disease	infectious_disease	infectious_disease	neurology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|throat_disorder|brain_disorder	true	false	false	true	high
MONDO:0005374	bone marrow neoplasm	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	hematology|oncology	anemia|cancer|bone_marrow_neoplasm_is_a_subset_of_this_category	bone_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0005375	nasopharyngeal neoplasm	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder	otolaryngology|oncology	cancer	throat_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0005376	membranous glomerulonephritis	inflammatory_disease|urinary_system_disorder	other	inflammatory_disease|urinary_system_disorder	renal_medicine|hematology|nephrology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	immune_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0005377	nephrotic syndrome	syndromic_disease|urinary_system_disorder	other	syndromic_disease|urinary_system_disorder	renal_medicine|pediatric|nephrology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0005379	neurotic disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurotic_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0005380	osteonecrosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	metabolic_disorder|osteonecrosis	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0005381	bone disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	metabolic_disorder|bone_disorder	bone_disorder|joint_disorder|spinal_disorder|muscle_disorder	false	false	false	true	high
MONDO:0005382	bone Paget disease	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	rheumatology|orthopaedic	inflammatory_disease|metabolic_disorder	bone_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0005383	panic disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	autoimmune_diseases|mental_health_disorder	mental_health_disorder|brain_disorder	false	false	false	true	high
MONDO:0005384	focal epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	neurological_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0005385	vascular disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|vascular_disorders	vascular_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0005386	peripheral arterial disease	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|vascular	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005387	primary ovarian failure	reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0005388	primary biliary cholangitis	premature_aging_syndrome|endocrine_system_disorder|digestive_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|digestive_system_disorder|premature_aging_syndrome	gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases	biliary_disorder|liver_disorder	false	false	false	true	high
MONDO:0005391	restless legs syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|sleep_disorders	neurodegenerative_disease|inflammatory_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0005392	scoliosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0005393	gout	metabolic_disease	metabolic_disease	metabolic_disease	rheumatology|renal_medicine	metabolic_disorder|inflammatory_disease	kidney_disorder|joint_disorder	false	false	false	true	high
MONDO:0005394	brain infarction	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	vascular_is_implied_but_not_listed|neurology|cardiology	neurodegenerative_disease|cardiovascular_disorder|inflammatory_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0005395	movement disorder	nervous_system_disorder	other	nervous_system_disorder	neurology	movement_disorder|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0005396	thoracic aortic aneurysm	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiothoracic|cardiology|renal_medicine	aort|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005397	goiter	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	thyroid|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|thyroid_disorder	false	false	false	true	medium
MONDO:0005398	upper aerodigestive tract neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	otolaryngology|oncology|gastroenterology	cancer|upper_aerodigestive_neoplasm	throat_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0005399	venous thromboembolism	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	thoracic|cardiology|hematology	cardiovascular_disorder|inflammatory_disease	vascular_disorder	false	false	false	true	high
MONDO:0005401	colonic neoplasm	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	colonic_neoplasm|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0005402	lymphoid leukemia	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|autoimmune_diseases|lymphoid_leukemia_is_more_specifically_related_to_a_cancer_and_an_autoimmune_disease__so_the_most_fitting_category_is__cancer	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0005404	myalgic encephalomeyelitis/chronic fatigue syndrome	musculoskeletal_system_disorder|immune_system_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	other	musculoskeletal_system_disorder|syndromic_disease|nervous_system_disorder|immune_system_disorder|hereditary_disease	neurology|rheumatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder_muscle_disorder_brain_disorder_spinal_disorder	false	false	false	false	very_high
MONDO:0005405	childhood onset asthma	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|pulmonology	allergy|inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	false	false	false	true	high
MONDO:0005406	gestational diabetes	metabolic_disease|endocrine_system_disorder|obstetric_disorder|digestive_system_disorder	endocrine_system_disorder|metabolic_disease|diabetes_mellitus	metabolic_disease|obstetric_disorder|endocrine_system_disorder|digestive_system_disorder	obstetrics_and_gynecology|endocrinology	metabolic_disorder|gestational_diabetes	reproductive_system_disorder|endocrine_disorder	false	false	true	true	medium
MONDO:0005407	childhood eosinophilic esophagitis	inflammatory_disease|upper_digestive_tract_disorder|digestive_system_disorder	other	upper_digestive_tract_disorder|inflammatory_disease|digestive_system_disorder	gastroenterology|pediatric|allergy_and_immunology	allergy|inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder_immune_disorder_lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0005408	diabetes mellitus type 2 associated cataract	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	endocrinology|ophthalmology	metabolic_disorder|cardiovascular_disorder	endocrine_disorder|eye_disorder	false	false	true	true	high
MONDO:0005411	gallbladder cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	metabolic_disorder|inflammatory_disease|autoimmune_diseases|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0005412	duodenal ulcer	digestive_system_disorder	other	digestive_system_disorder|ulcer_disease	gastrointestinal|gastroenterology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005413	cystic fibrosis associated meconium ileus	perinatal_disease|digestive_system_disorder	other	perinatal_disease|digestive_system_disorder	genetics_and_genomics|pediatric|gastroenterology	metabolic_disorder|inflammatory_disease	lung_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0005414	treatment-refractory schizophrenia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	mental_health_disorder|treatment_refractory_schizophrenia_is_often_associated_with_severe_mental_illness	mental_health_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0005416	osteoarthritis, knee	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0005417	wet macular degeneration	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	neurology|ophthalmology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0005418	non-compaction cardiomyopathy	cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder	genetics_and_genomics|pulmonology|cardiology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0005419	methamphetamine dependence	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0005420	hypothyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology	metabolic_disorder|autoimmune_diseases	thyroid_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0005424	elephantiasis	immune_system_disorder	other	immune_system_disorder	dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|skin_disorder	true	false	false	true	high
MONDO:0005425	podoconiosis	immune_system_disorder	other	immune_system_disorder	pulmonology|dermatology|orthopaedic	metabolic_disorder|inflammatory_disease	joint_disorder|skin_disorder	false	false	false	true	high
MONDO:0005426	MRI defined brain infarct	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	neurology|cardiology	cardiovascular_disorder|inflammatory_disease|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	true	medium
MONDO:0005429	prion disease	nervous_system_disorder|infectious_disease	infectious_disease	infectious_disease|nervous_system_disorder	neurology|genetics_and_genomics	prion_disease_is_closely_related_to_mad_cow_disease_which_falls_under_this_category|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0005430	early onset hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|renal_medicine	metabolic_disorder|cardiovascular_disorder	vascular_disorder|endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0005432	alcohol and nicotine codependence	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder|addictive_disorder	liver_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0005433	alcohol withdrawal	psychiatric_disorder|syndromic_disease	psychiatric_disorder	psychiatric_disorder|syndromic_disease	neurology|psychiatry	metabolic_disorder|mental_health_disorder	liver_disorder|brain_disorder	false	false	false	true	high
MONDO:0005434	skin sensitivity to sun	inflammatory_disease|integumentary_system_disorder	other	inflammatory_disease|integumentary_system_disorder|radiation_induced_disorder	allergy_and_immunology|dermatology	allergy|inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0005435	anti-neutrophil antibody associated vasculitis	immune_system_disorder	autoimmune_disease	immune_system_disorder	rheumatology|hematology	autoimmune_diseases|inflammatory_disease	immune_disorder_vascular_disorder	false	false	false	true	high
MONDO:0005436	postoperative ventricular dysfunction	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|pulmonology|cardiothoracic|cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0005437	testicular dysgenesis syndrome	reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder	urology|genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0005438	metastatic malignant neoplasm in the lymph nodes	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|metastatic_malignant_neoplasm_in_the_lymph_nodes	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0005439	familial hypercholesterolemia	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0005440	embryonal carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	liver_disorder|kidney_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0005441	otitis media	otorhinolaryngologic_disease|auditory_system_disorder|inflammatory_disease	other	inflammatory_disease|auditory_system_disorder|otorhinolaryngologic_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	true	false	false	true	medium
MONDO:0005445	visceral leishmaniasis	infectious_disease|hereditary_disease	infectious_disease	infectious_disease|hereditary_disease	gastroenterology|hematology|pediatric	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder|lymphatic_disorder	true	false	false	true	very_high
MONDO:0005446	cutaneous leishmaniasis	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0005447	testicular cancer	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	lymphatic_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0005448	hepatitis C induced liver cirrhosis	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|post_infectious_disorder	hepatology|gastroenterology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	liver_disorder|liver_cirrhosis	true	false	false	true	high
MONDO:0005449	conduction system disorder	cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder	pulmonology|cardiothoracic|cardiology	cardiovascular_disorder|conduction_system_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0005451	eating disorder	psychiatric_disorder|nutritional_disorder	psychiatric_disorder	psychiatric_disorder|nutritional_disorder	psychiatry|pediatric	mental_health_disorder|eating_disorders	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	very_high
MONDO:0005452	bulimia nervosa	psychiatric_disorder|nutritional_disorder	psychiatric_disorder	psychiatric_disorder|nutritional_disorder	psychiatry|neurology	mental_health_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0005453	congenital heart disease	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|cardiology	cardiovascular_disorder|congenital_heart_disease_is_more_accurately_described_by_the_single_category__cardiovascular_disorder	congenital_heart_disease|heart_disorder	false	false	false	true	high
MONDO:0005454	lung neuroendocrine neoplasm	respiratory_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|oncology	adrenal_gland_disease|cancer	lung_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0005459	human African trypanosomiasis	infectious_disease	infectious_disease	infectious_disease	parasitology|hematology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0005460	swine influenza	respiratory_system_disorder|infectious_disease	infectious_disease	respiratory_system_disorder|infectious_disease	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	true	false	false	true	medium
MONDO:0005461	endometrium adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0005462	primitive neuroectodermal tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0005463	aortic valve calcification	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder|metabolic_disorder|inflammatory_disease	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0005464	rhegmatogenous retinal detachment	nervous_system_disorder|hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0005465	methamphetamine-induced psychosis	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	psychosis|brain_disorder	false	false	false	true	high
MONDO:0005466	hypersomnia	other	other	sleep_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	brain_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0005467	occupation-related stress disorder	other	other	occupational_disorder	psychiatry|neurology	occupational_health_disorder|mental_health_disorder	brain_disorder	false	false	false	true	high
MONDO:0005468	hypotensive disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0005469	orthostatic hypotension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|neurology	cardiovascular_disorder|autoimmune_diseases	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0005470	postprandial hypotension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|cardiology	cardiovascular_disorder|metabolic_disorder	upper_gastrointestinal_disorder|vascular_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0005471	neurally mediated hypotension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	neurology|renal_medicine|hematology|cardiology	neurodegenerative_disease|autoimmune_diseases	vascular_disorder|brain_disorder	false	false	false	false	medium
MONDO:0005473	temporomandibular joint disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	neurology|orthopaedic|rheumatology	joint_disease|inflammatory_disease	muscle_disorder|joint_disorder|bone_disorder	false	false	false	true	medium
MONDO:0005475	migraine with aura	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|otolaryngology|genetics_and_genomics|pediatric|cardiology|psychiatry	neurodegenerative_disease|mental_health_disorder|autoimmune_diseases|inflammatory_disease	vascular_disorder|brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0005476	atrioventricular node disorder	cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder	cardiothoracic|cardiology	cardiovascular_disorder|atrioventricular_node_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0005477	ventricular tachycardia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder|autoimmune_diseases	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0005478	torsades de pointes	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|pulmonology|cardiothoracic|pediatrics|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0005479	atrial tachycardia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiothoracic|cardiology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0005480	contact dermatitis	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease	allergy_and_immunology|dermatology	allergy|autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0005481	contact dermatitis due to nickel	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease	allergy_and_immunology|dermatology	allergy|autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0005483	chemotherapy-induced alopecia	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|oncology	cancer|autoimmune_diseases|inflammatory_disease	hair_loss|skin_disorder	false	false	false	true	high
MONDO:0005484	colorectal adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	colorectal_adenoma_is_also_classified_under_adenoma_which_is_a_type_of_cancer_but_in_the_provided_list_we_can_consider_it_as_one_disease_so_best_fit_is_just_cancer|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0005485	psychotic disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	mental_health_disorder|psychotic_disorder	psychotic_disorder|brain_disorder	false	false	false	true	high
MONDO:0005486	tooth agenesis	hereditary_disease|musculoskeletal_system_disorder	other	mouth_disorder|hereditary_disease|musculoskeletal_system_disorder	otolaryngology|orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases	teeth_disorder|bone_disorder	false	false	false	false	high
MONDO:0005487	schizoaffective disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|immune_disorder	false	false	false	true	high
MONDO:0005488	adolescent idiopathic scoliosis	musculoskeletal_system_disorder	other	idiopathic_disease|musculoskeletal_system_disorder	orthopaedic|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0005489	dyslexia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	medium
MONDO:0005490	large artery stroke	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	cardiology|neurology	neurodegenerative_disease|cardiovascular_disorder	vascular_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0005491	Chagas cardiomyopathy	cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|post_infectious_disorder|musculoskeletal_system_disorder	pulmonology|cardiology|pediatric	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	true	false	false	true	high
MONDO:0005492	urticaria	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease	allergy_and_immunology|dermatology	inflammatory_disease|allergy|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0005493	carbon monoxide-induced delayed encephalopathy	poisoning|nervous_system_disorder	other	poisoning|nervous_system_disorder	pulmonology|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	lung_disorder|brain_disorder	false	false	false	false	high
MONDO:0005494	triple-negative breast carcinoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology|pediatric	adrenal_gland_disease|cancer	lymphatic_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0005495	adrenal gland disorder	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology	inflammatory_disease|metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	adrenal_gland_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0005496	bile duct carcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	hepatology|gastroenterology|oncology	cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	true	very_high
MONDO:0005497	bone development disease	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric|rheumatology	metabolic_disorder|developmental_disorder|bone_development_disease_is_not_in_the_list__however_an_alternative__skeletal_disease_is_not_present_but_a_fitting_option_from_the_list_could_be_metabolic_disorder	teeth_disorder|spinal_disorder|bone_disorder	false	false	false	true	high
MONDO:0005498	botulism	infectious_disease	infectious_disease	infectious_disease	pediatric|neurology	neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|brain_disorder	true	false	false	true	high
MONDO:0005499	brain glioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0005500	congenital disorder of glycosylation type I	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder	liver_disorder	false	false	true	false	high
MONDO:0005501	congenital disorder of glycosylation type II	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric	metabolic_disorder|congenital_disease	liver_disorder	false	false	true	false	high
MONDO:0005502	dengue disease	infectious_disease	infectious_disease	infectious_disease	pediatric|hematology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|vascular_disorder|liver_disorder	true	false	false	true	high
MONDO:0005503	developmental disorder of mental health	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	pediatric|psychiatry	mental_health_disorder|developmental_disorder	brain_disorder|mental_health_disorder	false	false	false	false	high
MONDO:0005504	diphtheria	infectious_disease	infectious_disease	infectious_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|throat_disorder	true	false	false	true	medium
MONDO:0005505	dysembryoplastic neuroepithelial tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neuroepithelial_tumor|cancer	spinal_disorder|brain_disorder	false	false	false	true	low
MONDO:0005506	eccrine sweat gland cancer	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	inflammatory_disease|cancer|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder|skin_disorder	false	true	false	false	medium
MONDO:0005507	gingival cancer	digestive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder|musculoskeletal_system_disorder	oncology|oral_medicine	inflammatory_disease|cancer	oral_disorder|teeth_disorder	false	true	false	true	high
MONDO:0005508	hereditary multiple osteochondromas	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease|connective_tissue_disorder|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|genetic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0005509	histiocytoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|hematology	cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	low
MONDO:0005510	hydronephrosis	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	corrected_list____urinary_system_disorder_is_missing_from_the_original_category_list__so_i_changed_it_to_renal_disorder_which_is_a_more_general_term_that_fits_the_description_of_hydronephrosis__i_removed__other__since_there_are_multiple_categories_that_fit|metabolic_disorder|renal_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0005511	janus kinase-3 deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|oncology|immunology|pediatric|hematology	inflammatory_disease|metabolic_disorder	muscle_disorder|immune_disorder|blood_bone_marrow_disorder|joint_disorder	false	false	false	true	very_high
MONDO:0005512	malignant peritoneal mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonary|hepatology|oncology	cancer|malignant_peritoneal_mesothelioma_is_a_specific_type_of_cancer	lung_disorder|lower_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0005514	nanophthalmia	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	pediatric|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0005515	oral cavity cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	otolaryngology|oncology	inflammatory_disease|cancer|autoimmune_diseases	throat_disorder|teeth_disorder	false	true	false	true	high
MONDO:0005516	osteochondrodysplasia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|genetic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0005517	pharynx cancer	respiratory_system_disorder|digestive_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder	otolaryngology|oncology	adrenal_gland_disease|cancer	throat_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0005518	pseudohermaphroditism	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	urology|pediatric|endocrinology	inflammatory_disease|adrenal_gland_disease|genetic_disorder_is_replaced_by_a_single_category_for_this_example___adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0005519	renal pelvis carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology|renal_medicine	adrenal_gland_disease|cancer|renal_carcinoma	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0005520	rickets	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	pediatric|endocrinology	inflammatory_disease|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0005522	small intestine carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	gastrointestinal_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0005523	steroid inherited metabolic disorder	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder	false	false	false	false	high
MONDO:0005524	sweat gland carcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology_dermatology	adrenal_gland_disease|cancer|autoimmune_diseases	skin_disorder	false	true	false	false	medium
MONDO:0005525	T-cell leukemia	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology	cancer|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0005526	tetanus	infectious_disease|nervous_system_disorder	infectious_disease	infectious_disease|nervous_system_disorder	otolaryngology|neurology	inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder	true	false	false	true	high
MONDO:0005527	toxic encephalopathy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0005528	inborn vitamin metabolic disorder	metabolic_disease|nutritional_disorder|hereditary_disease	metabolic_disease	hereditary_disease|nutritional_disorder|metabolic_disease	genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|inborn_vitamin_metabolic_disorder	endocrine_disorder|liver_disorder	false	false	false	true	high
MONDO:0005530	opiate dependence	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	mental_disorder_is_not_listed_but_closest_match_is_brain_disorder|brain_disorder	false	false	false	true	high
MONDO:0005531	morphine dependence	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0005532	Crohn's colitis	digestive_system_disorder|immune_system_disorder|hereditary_disease	other	hereditary_disease|digestive_system_disorder|immune_system_disorder	pediatrics|gastroenterology	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0005533	distal colitis	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	other	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	gastroenterology|gastrointestinal	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005534	ileocolitis	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	other	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	gastroenterology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005535	oral Crohn disease	digestive_system_disorder|immune_system_disorder|hereditary_disease	other	mouth_disorder|digestive_system_disorder|immune_system_disorder|hereditary_disease	gastroenterology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|upper_gastrointestinal_disorder|teeth_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0005536	pancolitis	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	other	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	gastroenterology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|upper_gastrointestinal_disorder|joint_disorder	false	false	false	true	very_high
MONDO:0005537	perianal Crohn disease	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	other	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	gastroenterology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0005538	proctitis	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	other	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	gastroenterology|hepatology	inflammatory_disease|cancer|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005539	small bowel Crohn disease	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	other	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	gastroenterology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0005541	spondylolysis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0005542	acute coronary syndrome	cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	syndromic_disease|acute_disease|cardiovascular_disorder	cardiothoracic|pulmonology|cardiology	inflammatory_disease|metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0005543	autoimmune hepatitis type 1	digestive_system_disorder|inflammatory_disease|immune_system_disorder|endocrine_system_disorder	endocrine_system_disorder|autoimmune_disease	endocrine_system_disorder|digestive_system_disorder|inflammatory_disease|immune_system_disorder	hepatology|immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|liver_disorder	false	false	false	true	high
MONDO:0005544	hippocampal sclerosis of aging	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0005545	staphylococcus aureus infection	infectious_disease	infectious_disease	infectious_disease	general|pediatric|cardiothoracic|pulmonology|dermatology|renal_medicine	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0005546	fibromyalgia	syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder|idiopathic_disease	rheumatology|neurology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0005549	renal cell adenocarcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology|renal_medicine	renal_cell_adenocarcinoma|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0005550	infectious disease				pediatric|allergy_and_immunology	inflammatory_disease|infectious_disease|autoimmune_diseases	immune_disorder|infectious_disease_is_not_in_the_list_but_a_category_it_fits_into_is_immune_disorder	true	false	false	true	high
MONDO:0005551	eye allergy	disorder_of_visual_system|immune_system_disorder	other	disorder_of_orbital_region|disorder_of_visual_system|immune_system_disorder	ophthalmology|allergy_and_immunology	allergy|autoimmune_diseases	immune_disorder|eye_disorder|nose_disorder	false	false	false	true	medium
MONDO:0005552	ocular vascular disorder	disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	disorder_of_orbital_region|disorder_of_visual_system|cardiovascular_disorder	ophthalmology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|eye_disorder	false	false	false	true	medium
MONDO:0005554	rheumatic disorder	connective_tissue_disorder	other	connective_tissue_disorder	rheumatic_disorder|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder|muscle_disorder	false	false	false	true	high
MONDO:0005555	cycloplegia	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0005556	lupus nephritis	inflammatory_disease|urinary_system_disorder	other	urinary_system_disorder|inflammatory_disease	rheumatology|renal_medicine	inflammatory_disease|autoimmune_diseases	immune_disorder|urinary_tract_disorder|kidney_disorder	false	false	false	true	high
MONDO:0005557	calcium metabolic disease	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|orthopaedic|renal_medicine|endocrinology	metabolic_disorder|adrenal_gland_disease	bone_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0005558	ovarian disorder	reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder	oncology|obstetrics_and_gynecology	inflammatory_disease|cancer|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0005559	neurodegenerative disease	nervous_system_disorder		nervous_system_disorder	neurodegenerative_disease|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0005560	brain disorder	nervous_system_disorder	other	nervous_system_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0005561	aortic disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|pulmonology|cardiology	cardiovascular_disorder|aortic_disorder	heart_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0005563	nut midline carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	otolaryngology|oncology|pulmonology	adrenal_gland_disease|cancer	lymphatic_disorder	false	true	false	false	very_high
MONDO:0005564	embryonal neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|oncology|pediatric	cancer|embryonal_neoplasm	brain_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0005565	blastoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric	adrenal_gland_disease|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0005566	neonatal abstinence syndrome	syndromic_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|syndromic_disease	obstetrics_and_gynecology|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|withdrawal_syndrome	false	false	false	true	high
MONDO:0005567	substance withdrawal syndrome	syndromic_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|syndromic_disease	psychiatry|neurology	mental_health_disorder|substance_withdrawal_syndrome_is_also_related_to_substance_abuse_which_is_a_mental_health_issue	brain_disorder|substance_withdrawal_syndrome	false	false	false	true	high
MONDO:0005568	cholesterol embolism	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|pulmonology|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0005570	hematologic disorder		other		hematologic_disorder|hematology	autoimmune_diseases|inflammatory_disease|anemia	hematologic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0005571	polycythemia	musculoskeletal_system_disorder|hematologic_disorder|immune_system_disorder	other	hematologic_disorder|immune_system_disorder|musculoskeletal_system_disorder	oncology|hematology	metabolic_disorder|cancer	blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0005572	polycythemia due to hypoxia	musculoskeletal_system_disorder|hematologic_disorder|immune_system_disorder	other	hematologic_disorder|immune_system_disorder|musculoskeletal_system_disorder	cardiology|pulmonology|hematology	metabolic_disorder|anemia	lung_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0005574	tauopathy	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0005575	colorectal cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder|cancer|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0005576	cryoglobulinemia	immune_system_disorder	autoimmune_disease	immune_system_disorder	rheumatology|renal_medicine|hematology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0005578	arthritic joint disease	musculoskeletal_system_disorder|inflammatory_disease	other	inflammatory_disease|musculoskeletal_system_disorder	rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease	joint_disorder|muscle_disorder|bone_disorder	false	false	false	true	high
MONDO:0005579	idiopathic generalized epilepsy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|psychiatry|neurology	autoimmune_diseases|neurodegenerative_disease|mental_health_disorder|inflammatory_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0005580	esophageal squamous cell carcinoma	upper_digestive_tract_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|upper_digestive_tract_disorder|cancer_or_benign_tumor	pulmonology|gastroenterology|oncology	autoimmune_diseases|cancer|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0005582	binge eating disorder	psychiatric_disorder|nutritional_disorder	psychiatric_disorder	psychiatric_disorder|nutritional_disorder	endocrinology|pediatric|psychiatry|gastroenterology	mental_health_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0005584	congenital left-sided heart lesions	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|cardiology	cardiovascular_disorder|congenital_heart_disease	heart_disorder|congenital_disorder	false	false	false	false	very_high
MONDO:0005585	chemotherapy-induced hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|oncology|hematology	cardiovascular_disorder|cancer	vascular_disorder|kidney_disorder	false	false	false	true	high
MONDO:0005586	head and neck neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology	cancer	head_neck_disorder|throat_disorder	false	true	false	true	high
MONDO:0005588	chemotherapy-induced oral mucositis	inflammatory_disease	other	inflammatory_disease|mouth_disorder	allergy_and_immunology|oncology|gastroenterology|hematology	autoimmune_diseases|cancer|inflammatory_disease	throat_disorder|skin_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0005589	thiopurine immunosuppressant-induced pancreatitis	endocrine_system_disorder|digestive_system_disorder|inflammatory_disease	endocrine_system_disorder	digestive_system_disorder|inflammatory_disease|endocrine_system_disorder	endocrinology|oncology|gastroenterology	autoimmune_diseases|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0005590	breast ductal adenocarcinoma	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	autoimmune_diseases|adrenal_gland_disease|cancer|inflammatory_disease	lymphatic_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0005591	pit and fissure surface dental caries	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	general_practice|oral_medicine|gastroenterology	oral_condition|metabolic_disorder	teeth_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0005592	smooth surface dental caries	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	general_practice|pediatric|other__removed|oral_surgery	metabolic_disorder|inflammatory_disease	teeth_disorder	false	false	false	true	low
MONDO:0005593	chronic periodontitis	musculoskeletal_system_disorder|inflammatory_disease	other	inflammatory_disease|musculoskeletal_system_disorder	oral_medicine|hematology	autoimmune_diseases|inflammatory_disease	teeth_disorder|bone_disorder	true	false	false	true	medium
MONDO:0005594	severe cutaneous adverse reaction	integumentary_system_disorder	other	integumentary_system_disorder	allergy_and_immunology|dermatology	autoimmune_diseases|allergy|inflammatory_disease	skin_disorder|severe_adverse_reaction	true	false	false	true	very_high
MONDO:0005595	laryngeal squamous cell carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	laryngeal_squamous_cell_carcinoma|cancer	throat_disorder|upper_gastrointestinal_disorder|lung_disorder	false	true	false	true	high
MONDO:0005596	cystadenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0005597	cystic renal cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	renal_cell_carcinoma|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0005598	dopaminergic neuroblastoma	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	pediatric|oncology|neurology	cancer|neuroblastoma	brain_disorder	false	true	false	false	very_high
MONDO:0005599	malignant epithelioid mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonology|oncology	malignant_epithelioid_mesothelioma_does_not_fit_well_in_autoimmune_diseases_or_inflammatory_disease_categories|cancer	thoracic_cavity_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0005601	ovarian mucinous adenocarcinoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|ovarian_cancer|mucinous_adenocarcinoma|adenocarcinoma	reproductive_system_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0005602	ovarian teratoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	ovarian|cancer|adrenal_gland_disease	reproductive_system_disorder|ovarian_disorder	false	true	false	true	medium
MONDO:0005605	transitional cell papilloma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|urology	cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	low
MONDO:0005606	tubular adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pathology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0005607	chronic bronchitis	inflammatory_disease|respiratory_system_disorder	other	respiratory_system_disorder|inflammatory_disease	pulmonology|cardiothoracic	autoimmune_diseases___inflammatory_disease|autoimmune_diseases|inflammatory_disease|respiratory_disease__not_listed_but_implied_____incorrect_response__inflammatory_disease	lower_gastrointestinal_disorder|lung_disorder	false	false	false	false	high
MONDO:0005608	varicella zoster infection	infectious_disease	infectious_disease	infectious_disease	pediatrics|dermatology|neurology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0005609	herpes zoster	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease|post_infectious_disorder	dermatology|neurology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|nerve_disorder	true	false	false	true	high
MONDO:0005610	Kashin-Beck disease	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0005611	bladder transitional cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0005613	mesonephric adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	kidney_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0005614	pancreatic adenosquamous carcinoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0005615	plasmacytoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	anemia|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0005616	pulmonary mucoepidermoid carcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|cardiothoracic|oncology	cancer	lung_disorder|lower_respiratory_disorder|lung_cancer	false	true	false	false	high
MONDO:0005617	undifferentiated carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology	adrenal_gland_disease|cancer	lung_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0005618	anxiety disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	mental_health_disorder	brain_disorder|mental_health_disorder	false	false	false	true	high
MONDO:0005619	typhoid fever	infectious_disease	infectious_disease	infectious_disease	hematology|pediatric|hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0005620	cerebral amyloid angiopathy	nervous_system_disorder|hereditary_disease|metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|metabolic_disease	nervous_system_disorder|cardiovascular_disorder|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0005621	vascular brain injury	nervous_system_disorder|cardiovascular_disorder|injury	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	neurology|cardiology|hematatology	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0005623	autoimmune thyroid disease	inflammatory_disease|immune_system_disorder|endocrine_system_disorder	autoimmune_disease|endocrine_system_disorder	immune_system_disorder|endocrine_system_disorder|inflammatory_disease	endocrinology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0005624	atrophic thyroiditis	inflammatory_disease|immune_system_disorder|endocrine_system_disorder	autoimmune_disease|endocrine_system_disorder	immune_system_disorder|endocrine_system_disorder|inflammatory_disease	endocrinology	inflammatory_disease|autoimmune_diseases	immune_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0005625	cerebral malaria	nervous_system_disorder|hematologic_disorder|infectious_disease	infectious_disease	nervous_system_disorder|infectious_disease|hematologic_disorder	neurology|hematology|pediatric	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder|vascular_disorder	true	false	false	true	very_high
MONDO:0005626	epithelial neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|gastroenterology|dermatology	epithelial_neoplasm|cancer	epithelial_neoplasm_is_related_to_the_lining_of_organs_including_the_liver|liver_disorder	false	true	false	false	high
MONDO:0005627	head and neck cancer	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	otolaryngology|oncology	adrenal_gland_disease|cancer	throat_disorder|head_and_neck_cancer_is_not_a_direct_match_in_the_list_so_it_has_been_replaced_with___throat_disorder|ear_disorder	false	true	false	true	very_high
MONDO:0005628	male breast carcinoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	breast_cancer|urology|oncology	adrenal_gland_disease|cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0005629	Acanthamoeba keratitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	disorder_of_visual_system|disorder_of_orbital_region|infectious_disease|inflammatory_disease	ophthalmology	inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder	true	false	false	true	high
MONDO:0005631	actinomycosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|dermatology	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|joint_disorder|lung_disorder	true	false	false	true	medium
MONDO:0005632	acute chest syndrome	syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|acute_disease|syndromic_disease	pulmonology|cardiothoracic	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	lung_disorder|heart_disorder	true	false	false	true	high
MONDO:0005634	acute hemorrhagic conjunctivitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	disorder_of_visual_system|disorder_of_orbital_region|acute_disease|infectious_disease|inflammatory_disease	hematology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	true	false	false	true	low
MONDO:0005635	adenomyoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|neurology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	muscle_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0005636	adenosarcoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	hematology|oncology|genetics_and_genomics	adrenal_gland_disease|cancer	lymphatic_disorder|muscle_disorder|blood_bone_marrow_disorder|bone_disorder	false	true	false	false	medium
MONDO:0005638	agnosia	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0005639	AIDS related complex	reproductive_system_disorder|infectious_disease	infectious_disease	infectious_disease|reproductive_system_disorder	hematology|pulmonology|hepatology|oncology|immunology	mental_health_disorder|cancer|inflammatory_disease|autoimmune_diseases	immune_disorder_lymphatic_disorder	true	false	false	true	high
MONDO:0005640	akinetic mutism	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0005642	atopic conjunctivitis	inflammatory_disease|disorder_of_visual_system|immune_system_disorder	other	disorder_of_visual_system|immune_system_disorder|disorder_of_orbital_region|inflammatory_disease	ophthalmology|allergy_and_immunology	allergy|inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|eye_disorder	false	false	false	true	medium
MONDO:0005643	Alphavirus infectious disease	infectious_disease	infectious_disease	infectious_disease	hematology|pediatric|infectious_disease	inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder	true	false	false	true	high
MONDO:0005644	amebiasis	infectious_disease	infectious_disease	infectious_disease	hepatology|gastroenterology	inflammatory_disease|gastrointestinal_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005645	ancylostomiasis	infectious_disease	infectious_disease	infectious_disease	dermatology|hematology	inflammatory_disease|autoimmune_diseases	skin_disorder|lower_gastrointestinal_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0005647	anogenital human papillomavirus infection	infectious_disease|reproductive_system_disorder	infectious_disease	infectious_disease|reproductive_system_disorder	dermatology|obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer|inflammatory_disease	skin_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0005648	aortic valve insufficiency	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0005649	appendicitis	inflammatory_disease|digestive_system_disorder	other	inflammatory_disease|digestive_system_disorder	pediatric|gastroenterology	inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0005650	Arenaviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|infectious_disease	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0005651	arenavirus hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	hematology|pediatric|pulmonology|infectious_diseases	viral_infection|inflammatory_disease|hemorrhagic_fever	vascular_disorder|liver_disorder	true	false	false	false	high
MONDO:0005652	Arterivirus infectious disease	infectious_disease	infectious_disease	infectious_disease	cardiology|pulmonology|renal_medicine	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	immune_disorder|vascular_disorder	true	false	false	true	low
MONDO:0005654	ascariasis	infectious_disease	infectious_disease	infectious_disease	pediatric|gastroenterology	inflammatory_disease|parasitic_disease|gastrointestinal_disorder	lower_gastrointestinal_disorder|gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005655	ascaridiasis	infectious_disease	infectious_disease	infectious_disease	pediatric|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	low
MONDO:0005656	Ascaridida infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|hepatology|gastroenterology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|parasitic_infection|intestinal_disorder	true	false	false	true	low
MONDO:0005657	aspergillosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|allergy_and_immunology	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0005658	Astroviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	hepatology|gastroenterology|pediatrics	inflammatory_disease|autoimmune_diseases|infectious_disease_does_not_exist_in_the_list__so_i_will_choose__autoimmune_diseases	liver_disorder|kidney_disorder	true	false	false	true	low
MONDO:0005659	atrophic rhinitis	inflammatory_disease|otorhinolaryngologic_disease|respiratory_system_disorder	other	otorhinolaryngologic_disease|inflammatory_disease|respiratory_system_disorder	otolaryngology|pulmonology	allergy|inflammatory_disease	lung_disorder|nose_disorder	true	false	false	false	low
MONDO:0005660	Avulavirus infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|hematology|pulmonology|hepatology|neurology	inflammatory_disease|autoimmune_diseases	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	low
MONDO:0005661	babesiosis	infectious_disease	infectious_disease	infectious_disease	parasitology|hematology	inflammatory_disease|autoimmune_diseases|anemia	liver_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0005662	balantidiasis	digestive_system_disorder|infectious_disease	infectious_disease	digestive_system_disorder|infectious_disease	hepatology|gastroenterology	gastrointestinal_disease|inflammatory_disease	lower_gastrointestinal_disorder|intestinal_disorder	true	false	false	true	medium
MONDO:0005663	Barre-Lieou syndrome	syndromic_disease|nervous_system_disorder	other	nervous_system_disorder|syndromic_disease	genetics_and_genomics|pediatrics|neurology	neurodegenerative_disease|metabolic_disorder	joint_disorder|spinal_disorder|blood_bone_marrow_disorder|bone_disorder	false	false	false	false	medium
MONDO:0005664	bartonellosis	infectious_disease	infectious_disease	infectious_disease	pediatric|infectious_diseases|tropical_medicine	inflammatory_disease|neurodegenerative_disease	liver_disorder	true	false	false	true	medium
MONDO:0005665	Bell's palsy	nervous_system_disorder	other	nervous_system_disorder	otolaryngology|neurology	inflammatory_disease|neurological_disease|autoimmune_diseases	brain_disorder|muscle_disorder|ear_disorder	false	false	false	true	medium
MONDO:0005667	biliary dyskinesia	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0005668	bird fancier's lung	inflammatory_disease|immune_system_disorder|respiratory_system_disorder	other	occupational_disorder|immune_system_disorder|inflammatory_disease|respiratory_system_disorder	pulmonology|allergy_and_immunology	respiratory_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	false	false	false	true	high
MONDO:0005669	black piedra	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	pediatric|dermatology	inflammatory_disease|autoimmune_diseases|anemia	skin_disorder	true	false	false	true	low
MONDO:0005670	blackwater fever	hematologic_disorder|infectious_disease	infectious_disease	infectious_disease|hematologic_disorder	hematology|hepatology|renal_medicine	inflammatory_disease|autoimmune_diseases	liver_disorder|kidney_disorder	true	false	false	true	high
MONDO:0005671	Blastocystis infectious disease	digestive_system_disorder|infectious_disease	infectious_disease	digestive_system_disorder|infectious_disease	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder	true	false	false	false	medium
MONDO:0005672	blastomycosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|dermatology	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|lung_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0005673	blind loop syndrome	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology|renal_medicine	gastrointestinal_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0005674	bone giant cell tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	orthopaedic|oncology	bone_tumor|cancer|soft_tissue_tumor	spinal_disorder|blood_bone_marrow_disorder|bone_disorder	false	true	false	true	medium
MONDO:0005677	Rickettsia conorii infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0005680	Brill-Zinsser disease	infectious_disease	infectious_disease	infectious_disease	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder_skin_disorder	true	false	false	true	medium
MONDO:0005682	bronchopneumonia	respiratory_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|inflammatory_disease|respiratory_system_disorder	pediatric|pulmonology	cardiovascular_disorder|inflammatory_disease	lung_disorder|lower_respiratory_infection	true	false	false	true	high
MONDO:0005683	brucellosis	infectious_disease	infectious_disease	infectious_disease	rheumatology|hematology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	true	medium
MONDO:0005684	bulbar polio	inflammatory_disease|infectious_disease|nervous_system_disorder	neurodegenerative_disease|infectious_disease	nervous_system_disorder|acute_disease|infectious_disease|inflammatory_disease	pediatric|otolaryngology|neurology	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	true	false	false	false	very_high
MONDO:0005687	Caliciviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	hepatology|gastroenterology|pediatrics	inflammatory_disease|autoimmune_diseases	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005688	campylobacteriosis	inflammatory_disease|digestive_system_disorder|infectious_disease	infectious_disease	digestive_system_disorder|infectious_disease|inflammatory_disease	gastroenterology|pediatrics	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005689	cannabis dependence	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	medium
MONDO:0005690	Caplan syndrome	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|pulmonology|allergy_and_immunology	allergy|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0005691	cardiovirus infectious disease	infectious_disease	infectious_disease	infectious_disease	cardiology|pediatric|infectious_disease	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	heart_disorder|vascular_disorder	true	false	false	false	medium
MONDO:0005692	cat-scratch disease	inflammatory_disease|infectious_disease|immune_system_disorder	infectious_disease	immune_system_disorder|infectious_disease|inflammatory_disease	pediatrics|dermatology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0005693	cauda equina syndrome	syndromic_disease|nervous_system_disorder	other	nervous_system_disorder|syndromic_disease	oncology|neurology|orthopaedic	cancer|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0005694	cecal neoplasm	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0005695	central nervous system AIDS arteritis	inflammatory_disease|reproductive_system_disorder|infectious_disease|nervous_system_disorder|cardiovascular_disorder	infectious_disease|cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|infectious_disease|inflammatory_disease|reproductive_system_disorder	rheumatology|allergy_and_immunology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|immune_disorder|vascular_disorder	true	false	false	false	very_high
MONDO:0005696	central nervous system tuberculosis	infectious_disease|nervous_system_disorder	infectious_disease	nervous_system_disorder|infectious_disease	pulmonology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder	true	false	false	true	very_high
MONDO:0005697	cerebral toxoplasmosis	infectious_disease	infectious_disease	infectious_disease	pediatric|neurology	cancer|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	lymphatic_disorder|brain_disorder	true	false	false	true	high
MONDO:0005698	cervical incompetence	reproductive_system_disorder	other	reproductive_system_disorder	pediatric|obstetrics_and_gynecology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0005699	cervicofacial actinomycosis	infectious_disease	infectious_disease	infectious_disease	otolaryngology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|nose_disorder|throat_disorder	true	false	false	true	medium
MONDO:0005700	chickenpox	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0005701	chlamydia trachomatis infectious disease	infectious_disease|reproductive_system_disorder	infectious_disease	reproductive_system_disorder|infectious_disease	pediatrics|urology|obstetrics_and_gynecology	inflammatory_disease|infectious_disease	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0005704	Ciliophora infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	cancer|inflammatory_disease|autoimmune_diseases	lung_disorder|respiratory_infection	true	false	false	false	medium
MONDO:0005705	clonorchiasis	infectious_disease	infectious_disease	infectious_disease	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder	true	false	false	true	medium
MONDO:0005706	coccidioidomycosis	infectious_disease	infectious_disease	infectious_disease	dermatology|pulmonology	inflammatory_disease|autoimmune_diseases	skin_disorder|lung_disorder|immune_disorder	true	false	false	true	medium
MONDO:0005707	coccidiosis	infectious_disease	infectious_disease	infectious_disease	pediatric|gastroenterology|pulmonology	inflammatory_disease|autoimmune_diseases	liver_disorder|lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	medium
MONDO:0005708	Colorado tick fever	inflammatory_disease|nervous_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|nervous_system_disorder|acute_disease	pediatrics|dermatology|infectious_diseases	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0005709	common cold	inflammatory_disease|otorhinolaryngologic_disease|respiratory_system_disorder	other	inflammatory_disease|otorhinolaryngologic_disease|respiratory_system_disorder	pediatric|pulmonology	inflammatory_disease|allergy	upper_gastrointestinal_disorder|lung_disorder|throat_disorder|nose_disorder	true	false	false	false	low
MONDO:0005710	composite lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	cancer|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder	true	true	false	false	high
MONDO:0005711	congenital diaphragmatic hernia	respiratory_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|respiratory_system_disorder	pediatric|cardiothoracic|general_surgery	congenital_abnormality|cardiovascular_disorder	upper_gastrointestinal_disorder|joint_disorder|muscle_disorder|abdominal_wall_disorder	false	false	false	false	high
MONDO:0005712	congenital nystagmus	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	ophthalmology|pediatric|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0005714	congenital syphilis	disorder_of_development_or_morphogenesis|infectious_disease|reproductive_system_disorder	infectious_disease	disorder_of_development_or_morphogenesis|reproductive_system_disorder|infectious_disease	pediatric|obstetrics_and_gynecology	inflammatory_disease____corrected_to_match_the_original_request____neurodegenerative_disease|inflammatory_disease|congenital_anomaly|neurodegenerative_disease	skin_disorder|lymphatic_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0005715	congenital toxoplasmosis	nervous_system_disorder|disorder_of_development_or_morphogenesis|infectious_disease	infectious_disease	disorder_of_development_or_morphogenesis|infectious_disease|nervous_system_disorder	pediatric|genetics_and_genomics|obstetrics_and_gynecology	inflammatory_disease|neurodegenerative_disease	brain_disorder|eye_disorder|immune_disorder	true	false	false	true	high
MONDO:0005716	contagious pleuropneumonia	inflammatory_disease|respiratory_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|respiratory_system_disorder	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0005717	contagious pustular dermatitis	infectious_disease	infectious_disease	infectious_disease	dermatology|infectious_diseases|immunology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0005718	Coronaviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|infectious_disease|pulmonary|pulmonology	inflammatory_disease|autoimmune_diseases|infectious_disease	lung_disorder|immune_disorder|vascular_disorder	true	false	false	true	high
MONDO:0005719	Coronavinae infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0005720	cowpox	infectious_disease	infectious_disease	infectious_disease	dermatology|allergy_and_immunology	cancer|inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0005721	coxsackievirus infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|infectious_disease|rheumatology	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder|kidney_disorder	true	false	false	false	medium
MONDO:0005722	croup	inflammatory_disease|respiratory_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|acute_disease|respiratory_system_disorder	pediatric|otolaryngology|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|throat_disorder	true	false	false	true	medium
MONDO:0005723	Cryptococcal meningitis	inflammatory_disease|nervous_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|nervous_system_disorder	infectious_diseases|immunology|neurology	inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder	true	false	false	true	high
MONDO:0005724	cryptococcosis	infectious_disease	infectious_disease	infectious_disease	immunology|pulmonology|neurology	inflammatory_disease|autoimmune_diseases	skin_disorder|lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0005725	cyclosporiasis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|gastrointestinal_disorder	true	false	false	true	low
MONDO:0005728	diaphragm disorder	respiratory_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|respiratory_system_disorder	obstetrics_and_gynecology|pulmonology	autoimmune_diseases|neurodegenerative_disease	upper_gastrointestinal_disorder|muscle_disorder|respiratory_disorder	false	false	false	false	medium
MONDO:0005729	dicrocoeliasis	infectious_disease	infectious_disease	infectious_disease	hepatology|hematology|gastroenterology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	liver_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0005731	dipetalonemiasis	infectious_disease	infectious_disease	infectious_disease	hematogenetics|pediatrics|genetics_and_genomics|hematology	metabolic_disorder|anemia	joint_disorder|blood_bone_marrow_disorder	true	false	false	false	medium
MONDO:0005736	eastern equine encephalitis	inflammatory_disease|nervous_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|nervous_system_disorder|acute_disease	pediatric|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder|vascular_disorder	true	false	false	false	very_high
MONDO:0005737	Ebola hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	hepatology|hematology|pulmonology|neurology	inflammatory_disease|autoimmune_diseases|anemia	immune_disorder|vascular_disorder	true	false	false	true	very_high
MONDO:0005738	echinococcosis	infectious_disease	infectious_disease	infectious_disease	hepatology|hematology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|lung_disorder|kidney_disorder|vascular_disorder	true	false	false	true	high
MONDO:0005739	echinostomiasis	infectious_disease	infectious_disease	infectious_disease	urology|hepatology|gastroenterology|pulmonology	inflammatory_disease|autoimmune_diseases	liver_disorder|gastrointestinal_disorder	true	false	false	false	medium
MONDO:0005740	Echovirus infectious disease	infectious_disease	infectious_disease	infectious_disease	infectious_disease|pediatric|infectious_diseases|other____but_this_list_contains_the_word__infectious_disease__which_is_not_in_the_provided_category_list__assuming_it_was_a_typo_and_meant_to_be_just_one_of_the_categories_____pediatrics	inflammatory_disease|autoimmune_diseases	liver_disorder|kidney_disorder	true	false	false	true	medium
MONDO:0005742	emphysematous cholecystitis	endocrine_system_disorder|digestive_system_disorder|urinary_system_disorder|inflammatory_disease	endocrine_system_disorder	inflammatory_disease|urinary_system_disorder|digestive_system_disorder|endocrine_system_disorder	gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005743	encephalitozoonosis	infectious_disease	infectious_disease	infectious_disease	internal_medicine|parasitology|pulmonology|infectious_diseases|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	immune_disorder|brain_disorder	true	false	false	true	medium
MONDO:0005744	yolk sac tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	tumor|cancer	reproductive_system_disorder|liver_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0005745	Enoplea infectious disease	infectious_disease	infectious_disease	infectious_disease	gastroenterology|renal_medicine|hematology|infectious_disease|hepatology|immunology|pulmonology|pediatrics	inflammatory_disease|autoimmune_diseases	kidney_disorder|urinary_tract_disorder	true	false	false	false	medium
MONDO:0005746	enterobiasis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|pediatrics	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	low
MONDO:0005747	enterovirus infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|neurology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|liver_disorder	true	false	false	true	medium
MONDO:0005749	eosinophilic pneumonia	inflammatory_disease|respiratory_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|respiratory_system_disorder|infectious_disease	pediatric|pulmonology	inflammatory_disease|allergy|autoimmune_diseases	immune_disorder|lung_disorder	false	false	false	true	high
MONDO:0005751	epidemic pleurodynia	infectious_disease	infectious_disease	infectious_disease	rheumatology|pulmonology	inflammatory_disease|autoimmune_diseases	joint_disorder|lung_disorder	true	false	false	true	medium
MONDO:0005752	epidural abscess	cancer_or_benign_tumor|nervous_system_disorder|infectious_disease	cancer_or_benign_tumor|infectious_disease	infectious_disease|nervous_system_disorder|cancer_or_benign_tumor	infectious_diseases|neurology	inflammatory_disease|cancer|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	true	false	false	true	very_high
MONDO:0005753	epiglottitis	inflammatory_disease|otorhinolaryngologic_disease|respiratory_system_disorder	other	inflammatory_disease|respiratory_system_disorder|otorhinolaryngologic_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	throat_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005754	epilepsy with generalized tonic-clonic seizures	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|psychiatry|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0005756	ethmoid sinusitis	inflammatory_disease|otorhinolaryngologic_disease|musculoskeletal_system_disorder|respiratory_system_disorder	other	inflammatory_disease|respiratory_system_disorder|musculoskeletal_system_disorder|otorhinolaryngologic_disease	otolaryngology	inflammatory_disease|autoimmune_diseases	nose_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005757	eumycotic mycetoma	inflammatory_disease|integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|inflammatory_disease|infectious_disease	dermatology|infectious_diseases|mycology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005758	eunuchism	endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	endocrinology|urology	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0005759	fascioloidiasis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|hematology|hepatology|pulmonology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	true	false	false	false	medium
MONDO:0005761	filarial elephantiasis	immune_system_disorder|inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	inflammatory_disease|immune_system_disorder|infectious_disease|disorder_of_visual_system|disorder_of_orbital_region	dermatology|pediatrics	metabolic_disorder|inflammatory_disease	lymphatic_disorder|lower_gastrointestinal_disorder|skin_disorder	true	false	false	true	high
MONDO:0005762	Filoviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	hematology|infectious_disease|pulmonology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	vascular_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0005763	Flaviviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	virology|hepatology|pulmonology|neurology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	vascular_disorder|liver_disorder	true	false	false	true	high
MONDO:0005764	follicular dendritic cell sarcoma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|post_infectious_disorder|immune_system_disorder|hematologic_disorder	hematology|oncology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	medium
MONDO:0005766	fungal lung infectious disease	respiratory_system_disorder|infectious_disease	infectious_disease	respiratory_system_disorder|infectious_disease	infectious_disease|pulmonology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|infectious_disease	immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0005767	gas gangrene	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	general_surgery|emergency_medicine|infectious_diseases	autoimmune_diseases|inflammatory_disease	vascular_disorder|muscle_disorder|skin_disorder	true	false	false	true	very_high
MONDO:0005768	gastrointestinal tuberculosis	digestive_system_disorder|infectious_disease	infectious_disease	infectious_disease|digestive_system_disorder	pulmonology|gastroenterology	autoimmune_diseases|inflammatory_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005769	geniculate herpes zoster	inflammatory_disease|integumentary_system_disorder|nervous_system_disorder|otorhinolaryngologic_disease|infectious_disease	infectious_disease	inflammatory_disease|post_infectious_disorder|integumentary_system_disorder|infectious_disease|otorhinolaryngologic_disease|nervous_system_disorder	dermatology|neurology	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|eye_disorder	true	false	false	true	high
MONDO:0005770	genital herpes	reproductive_system_disorder|infectious_disease	infectious_disease	infectious_disease|reproductive_system_disorder	urology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|skin_disorder	true	false	false	false	medium
MONDO:0005771	geographic tongue	inflammatory_disease	other	inflammatory_disease|mouth_disorder	dermatology|psychiatry	autoimmune_diseases|inflammatory_disease	mucous_membrane_disorder|skin_disorder	false	false	false	false	low
MONDO:0005772	geotrichosis	infectious_disease	infectious_disease	infectious_disease	dermatology|occupational_health	autoimmune_diseases|inflammatory_disease	skin_disorder	true	false	false	true	low
MONDO:0005773	Gerstmann syndrome	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0005774	glanders	infectious_disease	infectious_disease	infectious_disease	pediatric|otolaryngology	autoimmune_diseases|glandular_disease	immune_disorder_lymphatic_disorder	true	false	false	true	medium
MONDO:0005775	G6PD deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	medium
MONDO:0005776	gnathomiasis	infectious_disease	infectious_disease	infectious_disease	pediatric|neurology|otolaryngology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	teeth_disorder|oral_disorder	true	false	false	false	medium
MONDO:0005777	granuloma inguinale	reproductive_system_disorder|infectious_disease	infectious_disease	infectious_disease|reproductive_system_disorder	dermatology|urology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder|reproductive_system_disorder|skin_disorder	true	false	false	false	medium
MONDO:0005778	haemonchiasis	infectious_disease	infectious_disease	infectious_disease	hematology|parasitology	autoimmune_diseases|anemia|metabolic_disorder|inflammatory_disease|allergic_reaction	immune_disorder|lower_gastrointestinal_disorder|lung_disorder	true	false	false	true	medium
MONDO:0005779	hand, foot and mouth disease	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder|skin_disorder	true	false	false	false	medium
MONDO:0005780	hantavirus infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	vascular_disorder|immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0005783	hemopericardium	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic|hematology	inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0005784	hantavirus hemorrhagic fever with renal syndrome	infectious_disease|urinary_system_disorder	infectious_disease	infectious_disease|urinary_system_disorder	hematology|pulmonology|renal_medicine	anemia|metabolic_disorder|inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	kidney_disorder|vascular_disorder|immune_disorder	true	false	false	true	medium
MONDO:0005785	henipavirus infectious disease	infectious_disease	infectious_disease	infectious_disease	virology|infectious_diseases|neurology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	false	high
MONDO:0005786	Hepadnaviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	hepatology|gastroenterology	hepadnaviridae_infectious_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	kidney_disorder|vascular_disorder|liver_disorder	true	false	false	true	medium
MONDO:0005787	hepatic tuberculosis	digestive_system_disorder|infectious_disease|inflammatory_disease|endocrine_system_disorder	endocrine_system_disorder|infectious_disease	infectious_disease|digestive_system_disorder|inflammatory_disease|endocrine_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	biliary_disorder|liver_disorder	true	false	false	true	high
MONDO:0005788	hepatitis E virus infection	digestive_system_disorder|infectious_disease|inflammatory_disease|endocrine_system_disorder	endocrine_system_disorder|infectious_disease	infectious_disease|digestive_system_disorder|inflammatory_disease|endocrine_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	true	false	false	false	medium
MONDO:0005789	hepatitis D virus infection	digestive_system_disorder|infectious_disease|inflammatory_disease|endocrine_system_disorder	endocrine_system_disorder|infectious_disease	post_infectious_disorder|infectious_disease|digestive_system_disorder|inflammatory_disease|endocrine_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	immune_disorder|liver_disorder	true	false	false	false	medium
MONDO:0005790	hepatitis A virus infection	digestive_system_disorder|infectious_disease|inflammatory_disease|endocrine_system_disorder	endocrine_system_disorder|infectious_disease	infectious_disease|digestive_system_disorder|endocrine_system_disorder|inflammatory_disease	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder	true	false	false	true	medium
MONDO:0005791	herpangina	infectious_disease	infectious_disease	infectious_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	thorat_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0005792	herpes simplex virus gingivostomatitis	infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|mouth_disorder|inflammatory_disease	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder|oral_disorder___note__i_corrected_the_original_disease_name_to_herpes_simplex_virus_gingivostomatitis__which_is_more_accurately_referred_to_as_herpes_simplex_virus__hsv__gingivostomatitis_or_simply_oral_herpes	true	false	false	true	medium
MONDO:0005794	Herpesviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	dermatology|infectious_disease_is_not_listed_so_this_will_be_ignored	inflammatory_disease|infectious_disease|autoimmune_diseases	skin_disorder|lymphatic_disorder|immune_disorder	true	false	false	false	medium
MONDO:0005796	HIV enteropathy	immune_system_disorder	other	post_infectious_disorder|immune_system_disorder	pediatric|hepatology|immunology|gastroenterology	inflammatory_disease|gastrointestinal_disease____corrected_list_to_match_the_original_category_list___autoimmune_diseases|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder	true	false	false	false	high
MONDO:0005797	HIV wasting syndrome	immune_system_disorder|reproductive_system_disorder|infectious_disease	infectious_disease	post_infectious_disorder|immune_system_disorder|infectious_disease|reproductive_system_disorder	renal_medicine|endocrinology|immunology|pulmonology|gastroenterology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005798	HIV-associated nephropathy	urinary_system_disorder|immune_system_disorder|hereditary_disease	other	post_infectious_disorder|immune_system_disorder|urinary_system_disorder|hereditary_disease	allergy_and_immunology|renal_medicine|hematology	inflammatory_disease|autoimmune_diseases	kidney_disorder|immune_disorder|urinary_tract_disorder	true	false	false	true	high
MONDO:0005799	hookworm infectious disease	infectious_disease	infectious_disease	infectious_disease	dermatology|pediatric|hepatology|hematology|gastroenterology	inflammatory_disease|parasitic_disease	skin_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005800	hordeolum	integumentary_system_disorder|disorder_of_visual_system|inflammatory_disease|infectious_disease	infectious_disease	integumentary_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|infectious_disease|inflammatory_disease	dermatology|infectious_diseases	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	true	false	false	true	low
MONDO:0005801	human T-lymphotropic virus 1 infectious disease	infectious_disease	infectious_disease	infectious_disease	hematology|pediatrics|allergy_and_immunology|immunology	infectious_disease|inflammatory_disease|autoimmune_diseases	immune_disorder_lymphatic_disorder	true	false	false	false	very_high
MONDO:0005802	hymenolepiasis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|allergy_and_immunology|pediatric	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0005803	hyperinsulinemic hypoglycemia	hereditary_disease|endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease	hereditary_disease|metabolic_disease|endocrine_system_disorder	pediatric|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder	false	false	true	true	high
MONDO:0005804	hyperprolactinemia	reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder	reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|endocrinology	metabolic_disorder|endocrine_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0005805	hypodermyiasis	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	pediatrics|dermatology	inflammatory_disease|autoimmune_diseases	lice_disorder|skin_disorder	true	false	false	false	medium
MONDO:0005806	hypopharynx cancer	respiratory_system_disorder|otorhinolaryngologic_disease|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|otolaryngology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|throat_disorder	false	true	false	true	very_high
MONDO:0005807	idiopathic CD4-positive T-lymphocytopenia	hematologic_disorder|hereditary_disease|immune_system_disorder	other	hereditary_disease|idiopathic_disease|immune_system_disorder|hematologic_disorder	hematology|immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0005808	inclusion conjunctivitis	reproductive_system_disorder|inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	reproductive_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|infectious_disease|inflammatory_disease	pediatric|ophthalmology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	true	false	false	true	low
MONDO:0005810	infectious mononucleosis	infectious_disease	infectious_disease	infectious_disease	hematology|oncology|pediatric	autoimmune_diseases|infectious_disease	immune_disorder_lymphatic_disorder	true	false	false	false	medium
MONDO:0005812	influenza	respiratory_system_disorder|infectious_disease	infectious_disease	infectious_disease|respiratory_system_disorder	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lung_disorder	true	false	false	true	medium
MONDO:0005813	interdigitating dendritic cell sarcoma	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	oncology|hematoloogy|dermatology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	false	very_high
MONDO:0005814	intestinal cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	intestinal_cancer|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0005815	pancreatic neuroendocrine neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|gastroenterology	cancer|tumor|endocrine_disorder	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0005817	Kluver-Bucy syndrome	psychiatric_disorder|nervous_system_disorder|syndromic_disease|inflammatory_disease|infectious_disease	infectious_disease|psychiatric_disorder	infectious_disease|syndromic_disease|nervous_system_disorder|psychiatric_disorder|acute_disease|inflammatory_disease	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0005819	laryngeal tuberculosis	respiratory_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|respiratory_system_disorder|inflammatory_disease	pulmonology|otolaryngology	inflammatory_disease|cancer|autoimmune_diseases	lung_disorder|throat_disorder|immune_disorder	true	false	false	true	medium
MONDO:0005820	Lassa fever	infectious_disease	infectious_disease	infectious_disease	pediatric|infectious_diseases	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	true	high
MONDO:0005821	late congenital syphilis	reproductive_system_disorder|disorder_of_development_or_morphogenesis|infectious_disease	infectious_disease	infectious_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis	pediatric|obstetrics_and_gynecology|neurology	inflammatory_disease|neurodegenerative_disease|mental_health_disorder|autoimmune_diseases	eye_disorder|joint_disorder|skin_disorder|brain_disorder	true	false	false	true	high
MONDO:0005822	latent syphilis	reproductive_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease	dermatology|neurology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0005823	legionellosis	infectious_disease	infectious_disease	infectious_disease	pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	medium
MONDO:0005824	Legionnaires' disease	respiratory_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|respiratory_system_disorder|inflammatory_disease	pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lung_disorder|lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	high
MONDO:0005825	leptospirosis	infectious_disease	infectious_disease	infectious_disease	renal_medicine|neurology|hematology	inflammatory_disease|autoimmune_diseases	kidney_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0005826	lipid pneumonia	respiratory_system_disorder|inflammatory_disease	other	respiratory_system_disorder|inflammatory_disease	cardiothoracic|pulmonology|cardiology	cardiovascular_disorder|metabolic_disorder|inflammatory_disease	lung_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0005827	lipoatrophic diabetes	endocrine_system_disorder|digestive_system_disorder|metabolic_disease	endocrine_system_disorder|diabetes_mellitus|metabolic_disease	metabolic_disease|digestive_system_disorder|endocrine_system_disorder	pediatric|endocrinology	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	endocrine_disorder|muscle_disorder	false	false	true	true	high
MONDO:0005828	listeriosis	infectious_disease	infectious_disease	infectious_disease	pediatric|allergy_and_immunology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	high
MONDO:0005830	lumpy skin disease	infectious_disease	infectious_disease	infectious_disease	dermatology|genetics_and_genomics	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0005831	lymph node tuberculosis	immune_system_disorder|infectious_disease	infectious_disease	infectious_disease|immune_system_disorder	pulmonology|allergy_and_immunology	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder|lung_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0005832	lymphangitis	cardiovascular_disorder|immune_system_disorder|inflammatory_disease	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease|immune_system_disorder	hematology|rheumatology|pediatric|dermatology	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0005833	lymphatic system disorder	immune_system_disorder	other	immune_system_disorder	hematology|lymphatic_system_disorder_is_a_subset_of_hematology	lymphatic_system_disorder|autoimmune_diseases	immune_disorder_lymphatic_disorder	false	false	false	false	medium
MONDO:0005834	lymphogranuloma venereum	reproductive_system_disorder|immune_system_disorder|infectious_disease	infectious_disease	infectious_disease|immune_system_disorder|reproductive_system_disorder	dermatology|urology	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder|skin_disorder	true	false	false	true	medium
MONDO:0005835	Lynch syndrome	hereditary_disease|syndromic_disease|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|digestive_system_disorder|hereditary_disease	oncology|genetics_and_genomics	adrenal_gland_disease|inflammatory_disease|cancer	reproductive_system_disorder|lymphatic_disorder	false	false	false	true	very_high
MONDO:0005836	male reproductive organ cancer	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	male_reproductive_organ_cancer|cancer	male_reproductive_organ_cancer|reproductive_system_disorder	false	true	false	true	high
MONDO:0005837	mandibular cancer	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|mouth_disorder|digestive_system_disorder	oncology|otolaryngology	cancer	throat_disorder|teeth_disorder	false	true	false	true	high
MONDO:0005838	mansonelliasis	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	liver_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0005841	maxillary neoplasm	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|mouth_disorder	oncology|otolaryngology	cancer|maxillary_neoplasm	teeth_disorder|bone_disorder	false	true	false	false	high
MONDO:0005842	maxillary sinusitis	respiratory_system_disorder|musculoskeletal_system_disorder|otorhinolaryngologic_disease|inflammatory_disease	other	respiratory_system_disorder|otorhinolaryngologic_disease|musculoskeletal_system_disorder|mouth_disorder|inflammatory_disease	pulmonology|otolaryngology	allergy|inflammatory_disease|autoimmune_diseases	nose_disorder|teeth_disorder	true	false	false	true	medium
MONDO:0005843	mediastinal cancer	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|cardiothoracic|pulmonology	adrenal_gland_disease|cancer	lung_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0005844	chalazion	integumentary_system_disorder|inflammatory_disease|infectious_disease|disorder_of_visual_system	infectious_disease	disorder_of_visual_system|disorder_of_orbital_region|infectious_disease|inflammatory_disease|integumentary_system_disorder	dermatology|ophthalmology	allergy|inflammatory_disease|cancer	eye_disorder|skin_disorder	false	false	false	true	low
MONDO:0005845	meningoencephalitis	nervous_system_disorder|inflammatory_disease	other	inflammatory_disease|nervous_system_disorder|acute_disease	pediatric|neurology	inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder	true	false	false	true	high
MONDO:0005846	microsporidiosis	infectious_disease	infectious_disease	infectious_disease	infectious_diseases_____corrected_to_remove_the_category__infectious_diseases__which_is_not_in_the_provided_list______gastoenterology|pediatric|gastroenterology	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005847	middle lobe syndrome	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology|neurology|otolaryngology	neurodegenerative_disease|inflammatory_disease	brain_disorder|liver_disorder	false	false	false	false	medium
MONDO:0005848	miliary tuberculosis	infectious_disease	infectious_disease	infectious_disease	cardiothoracic|pulmonology|cardiology|otolaryngology	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder|lung_disorder	true	false	false	true	very_high
MONDO:0005850	milker's nodule	infectious_disease	infectious_disease	infectious_disease	infectious_disease|dermatology	skin_condition|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	low
MONDO:0005851	Miller Fisher syndrome	nervous_system_disorder|immune_system_disorder|syndromic_disease	autoimmune_disease	syndromic_disease|nervous_system_disorder|immune_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|eye_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0005852	mitral valve stenosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder|inflammatory_disease	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0005853	malignant mixed neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|hematology|genetics_and_genomics	malignant_mixed_neoplasm|cancer	lymphatic_disorder|bone_disorder	false	true	false	true	high
MONDO:0005854	mixed connective tissue disease	connective_tissue_disorder|immune_system_disorder	autoimmune_disease	connective_tissue_disorder|immune_system_disorder	rheumatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder	false	false	false	true	high
MONDO:0005855	molluscum contagiosum	infectious_disease	infectious_disease	infectious_disease	pediatric|dermatology	viral_disease|inflammatory_disease|skin_infection	immune_disorder|lower_gastrointestinal_disorder|skin_disorder	true	false	false	true	low
MONDO:0005856	Mononegavirales infectious disease	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0005857	morbillivirus infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0005858	mucinous cystadenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|gynecology|pathology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0005859	mucocutaneous leishmaniasis	infectious_disease	infectious_disease	infectious_disease	hematology|hepatology|dermatology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|skin_disorder	true	false	false	true	medium
MONDO:0005861	multidrug-resistant tuberculosis	infectious_disease	infectious_disease	infectious_disease	pulmonology	infectious_disease|autoimmune_diseases	immune_disorder|lung_disorder|lower_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0005864	muscle cancer	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|hematoloy	cancer|autoimmune_diseases	muscle_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0005865	mushroom workers' lung	respiratory_system_disorder|immune_system_disorder|inflammatory_disease	other	respiratory_system_disorder|inflammatory_disease|occupational_disorder|immune_system_disorder	occupational_disease|pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0005866	Mycobacterium avium complex disease	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005867	Mycoplasma pneumoniae pneumonia	respiratory_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|respiratory_system_disorder|inflammatory_disease	pulmonology|pediatrics	inflammatory_disease|autoimmune_diseases	lung_disorder|respiratory_disorder	true	false	false	true	medium
MONDO:0005868	myelophthisic anemia	hematologic_disorder	anemia	hematologic_disorder	oncology|hematology|genetics_and_genomics	metabolic_disorder|anemia	immune_disorder|vascular_disorder|blood_bone_marrow_disorder|lymphatic_disorder|bone_disorder	false	false	false	false	high
MONDO:0005870	necatoriasis	infectious_disease	infectious_disease	infectious_disease	hematology|pediatric|gastroenterology	anemia|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005871	Nematoda infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005872	nervous system cancer	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	nervous_system_cancer|cancer	spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0005873	neuroaspergillosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|allergy	lung_disorder|brain_disorder	true	false	false	true	very_high
MONDO:0005874	neuroschistosomiasis	nervous_system_disorder|infectious_disease	infectious_disease	nervous_system_disorder|infectious_disease	neurology	inflammatory_disease|neurodegenerative_disease	lymphatic_disorder|liver_disorder|lung_disorder|spinal_disorder|brain_disorder	true	false	false	true	high
MONDO:0005875	Newcastle disease	infectious_disease	infectious_disease	infectious_disease	veterinary|pediatric	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	true	high
MONDO:0005876	Nidovirales infectious disease	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatrics|infectious_disease_is_often_studied_in_a_subfield_of_medicine_called__infectious_diseases__which_can_be_associated_with_the_category__pulmonology__however_another_related_category_is_also_relevant_here__pediatrics	inflammatory_disease|autoimmune_diseases|infectious_disease_was_not_in_the_list_but_nidovirales_is_a_type_of_virus_so_the_closest_match_would_be___inflammatory_disease	respiratory_disorder|liver_disorder|kidney_disorder|immune_disorder	true	false	false	false	high
MONDO:0005878	ocular onchocerciasis	infectious_disease|disorder_of_visual_system	infectious_disease	disorder_of_visual_system|disorder_of_orbital_region|infectious_disease	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	ocular_disorder|eye_disorder	true	false	false	true	very_high
MONDO:0005879	ocular toxoplasmosis	infectious_disease|disorder_of_visual_system	infectious_disease	disorder_of_visual_system|disorder_of_orbital_region|infectious_disease	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases	brain_disorder|eye_disorder	true	false	false	true	high
MONDO:0005880	oesophagostomiasis	infectious_disease	infectious_disease	infectious_disease	pulmonology|gastroenterology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0005881	oligohydramnios	reproductive_system_disorder|obstetric_disorder	other	reproductive_system_disorder|obstetric_disorder	genetics_and_genomics|obstetrics_and_gynecology|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|kidney_disorder	false	false	false	false	high
MONDO:0005883	ophthalmic herpes zoster	nervous_system_disorder|integumentary_system_disorder|infectious_disease	infectious_disease	post_infectious_disorder|nervous_system_disorder|integumentary_system_disorder|infectious_disease	dermatology|neurology|ophthalmology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder|eye_disorder	true	false	false	true	high
MONDO:0005884	opisthorchiasis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder	true	false	false	true	medium
MONDO:0005885	optic neuritis	nervous_system_disorder|inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease|nervous_system_disorder	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	true	medium
MONDO:0005886	oral candidiasis	infectious_disease	infectious_disease	mouth_disorder|infectious_disease	pediatric	inflammatory_disease|autoimmune_diseases	teeth_disorder|skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0005887	oral tuberculosis	digestive_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	mouth_disorder|digestive_system_disorder|inflammatory_disease|infectious_disease	pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|cancer	teeth_disorder|oral_tuberculosis_fits_into_this_category_and_so_does_not_need_to_be_included_separately	true	false	false	true	medium
MONDO:0005888	ornithosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|anemia	lymphatic_disorder|blood_bone_marrow_disorder|bone_disorder	true	false	false	true	medium
MONDO:0005890	osteitis fibrosa	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	inflammatory_disease|metabolic_disorder|adrenal_gland_disease	bone_disorder	false	false	false	true	high
MONDO:0005891	ostertagiasis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|pediatric	inflammatory_disease|anemia	liver_disorder|lower_gastrointestinal_disorder	true	false	false	false	medium
MONDO:0005892	otitis media with effusion	auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	other	otorhinolaryngologic_disease|inflammatory_disease|auditory_system_disorder	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	false	false	false	true	medium
MONDO:0005893	pancreatic endocrine carcinoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	gastroenterology|oncology|endocrinology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	false	very_high
MONDO:0005894	paracoccidioidomycosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|dermatology	inflammatory_disease|autoimmune_diseases|cancer	skin_disorder|lung_disorder	true	false	false	true	high
MONDO:0005895	paragonimiasis	infectious_disease	infectious_disease	infectious_disease	pulmonology|gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lung_disorder	true	false	false	true	medium
MONDO:0005896	Paramyxoviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0005898	paronychia	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005899	parotid disorder	other	other	mouth_disorder	otolaryngology|general_surgery	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|ear_disorder|throat_disorder	false	false	false	false	medium
MONDO:0005900	parotitis	inflammatory_disease	other	mouth_disorder|inflammatory_disease	otolaryngology|pediatrics	inflammatory_disease|autoimmune_diseases	teeth_disorder|throat_disorder	true	false	false	true	medium
MONDO:0005901	pasteurellosis	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	respiratory_disorder_is_not_present_so__lung_disorder|immune_disorder	true	false	false	true	medium
MONDO:0005903	pericardial tuberculosis	cardiovascular_disorder|inflammatory_disease|infectious_disease	infectious_disease|cardiovascular_disorder	infectious_disease|inflammatory_disease|cardiovascular_disorder	cardiology|cardiothoracic|pulmonology	cardiovascular_disorder|inflammatory_disease	lung_disorder|heart_disorder_lung_disorder___or___heart_disorder|subtype	true	false	false	true	high
MONDO:0005904	pericarditis	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	cardiology|cardiothoracic	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	heart_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0005905	periodic limb movement disorder	other	other	sleep_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0005906	peritonsillar abscess	otorhinolaryngologic_disease|immune_system_disorder|respiratory_system_disorder|infectious_disease	infectious_disease	immune_system_disorder|infectious_disease|respiratory_system_disorder|otorhinolaryngologic_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	thorat_disorder	true	false	false	true	medium
MONDO:0005907	persian gulf syndrome	syndromic_disease	other	syndromic_disease	psychiatry|pulmonology|neurology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|immune_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0005909	pestivirus infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|veterinary_science_is_not_in_the_list_but_it_would_be_relevant_here_as_well|hepatology	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder	true	false	false	true	medium
MONDO:0005910	phagocyte bactericidal dysfunction	hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder	hematology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	true	false	false	false	high
MONDO:0005911	pharyngoconjunctival fever	infectious_disease	infectious_disease	infectious_disease	otolaryngology|pediatrics	inflammatory_disease|autoimmune_diseases	throat_disorder|eye_disorder	true	false	false	true	low
MONDO:0005912	phencyclidine abuse	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0005913	phlebotomus fever	infectious_disease	infectious_disease	infectious_disease	hematology|infectious_diseases	inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder	true	false	false	false	medium
MONDO:0005914	Picornaviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	autoimmune_diseases|inflammatory_disease	liver_disorder|immune_disorder|respiratory_disorder	true	false	false	true	medium
MONDO:0005915	pityriasis versicolor	inflammatory_disease|integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease|inflammatory_disease	dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0005916	placenta accreta	obstetric_disorder|reproductive_system_disorder	other	obstetric_disorder|reproductive_system_disorder	pediatric|obstetrics_and_gynecology	gynecological_complications|obstetric_complications	vascular_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0005917	placenta disorder	obstetric_disorder|reproductive_system_disorder	other	obstetric_disorder|reproductive_system_disorder	pediatric|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	vessel_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0005918	placenta praevia	obstetric_disorder|reproductive_system_disorder	other	obstetric_disorder|reproductive_system_disorder	obstetrics_and_gynecology	anemia|metabolic_disorder	vascular_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0005919	placental insufficiency	obstetric_disorder|reproductive_system_disorder	other	reproductive_system_disorder|obstetric_disorder	cardiology|obstetrics_and_gynecology|hematologynot_renal_medicine|pulmonology	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	vascular_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0005920	Plasmodium falciparum malaria	hematologic_disorder|infectious_disease	infectious_disease	hematologic_disorder|infectious_disease	hematology|pediatric|infectious_disease	inflammatory_disease|anemia	immune_disorder|vascular_disorder|blood_bone_marrow_disorder	true	false	false	true	very_high
MONDO:0005921	Plasmodium vivax malaria	hematologic_disorder|infectious_disease	infectious_disease	hematologic_disorder|infectious_disease	parasitology|hematology	infectious_disease|anemia	immune_disorder|vascular_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0005922	pleural tuberculosis	inflammatory_disease|infectious_disease|respiratory_system_disorder	infectious_disease	respiratory_system_disorder|inflammatory_disease|infectious_disease	immunology|pulmonology|allergy_and_immunology|cardiothoracic	inflammatory_disease|autoimmune_diseases|cancer	immune_disorder|lung_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005923	Pneumocystis infectious disease	infectious_disease	infectious_disease	infectious_disease	pulmonology|allergy_and_immunology|pediatric	inflammatory_disease|autoimmune_diseases|cancer	immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0005925	pneumonic pasteurellosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0005927	polyomavirus infectious disease	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|pediatric|renal_medicine	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder|kidney_disorder	true	false	false	true	high
MONDO:0005928	post-thrombotic syndrome	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|vascular_is_not_in_the_list_but_it_should_be__cardiology|cardiology	inflammatory_disease|cardiovascular_disorder	vascular_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0005929	postpartum depression	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|obstetrics_and_gynecology|neurology	autoimmune_diseases|mental_health_disorder	reproductive_system_disorder|brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0005932	pseudorabies	infectious_disease	infectious_disease	infectious_disease	virology|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	immune_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0005933	pulmonary blastoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|pulmonary	cancer|adrenal_gland_disease	vascular_disorder|bone_disorder|lung_disorder	false	true	false	false	high
MONDO:0005936	recurrent pneumonia	inflammatory_disease|infectious_disease|respiratory_system_disorder	infectious_disease	infectious_disease|respiratory_system_disorder|inflammatory_disease	pediatrics|pulmonology	autoimmune_diseases|inflammatory_disease	immune_disorder|lung_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005937	REM sleep behavior disorder	other	other	sleep_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0005938	renal tuberculosis	urinary_system_disorder|infectious_disease	infectious_disease	infectious_disease|urinary_system_disorder	renal_medicine|urology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|kidney_disorder	true	false	false	true	high
MONDO:0005939	Reoviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	oncology|neurology|pulmonology|pediatric	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0005940	respirovirus infectious disease	infectious_disease	infectious_disease	infectious_disease	pulmonology|allergy_and_immunology|pediatric	inflammatory_disease|autoimmune_diseases|respiratory_infectious_disease_is_not_in_the_list_so__autoimmune_diseases	immune_disorder|respiratory_virus_infectious_disease_is_a_more_descriptive_term_but_fits_in_the_lung_category|lung_disorder	true	false	false	false	medium
MONDO:0005941	retroperitoneal cancer	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|urology	inflammatory_disease|cancer	urinary_tract_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0005942	Reye syndrome	syndromic_disease|connective_tissue_disorder|nervous_system_disorder	other	nervous_system_disorder|syndromic_disease|connective_tissue_disorder	hepatology|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|brain_disorder	false	false	false	false	high
MONDO:0005943	Rhabditida infectious disease	infectious_disease	infectious_disease	infectious_disease	neurology|pediatric|infectious_diseases_category_is_not_present_so_i_will_leave_it_out	infectious_disease|autoimmune_diseases|neurodegenerative_disease	immune_disorder|muscle_disorder|lymphatic_disorder|nervous_system_disorder_is_not_in_the_list_so__blood_bone_marrow_disorder	true	false	false	false	medium
MONDO:0005944	Rhabdoviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|veterinary_science|epidemiology|public_health|neurology|microbiology	inflammatory_disease|autoimmune_diseases|inflammatorydisease|infectious_disease_is_not_in_the_list_so__autoimmunediseases	immune_disorder|vascular_disorder	true	false	false	true	high
MONDO:0005945	rhinoscleroma	infectious_disease	infectious_disease	infectious_disease	otolaryngology|dermatology	inflammatory_disease|autoimmune_diseases|cancer	immune_disorder|nose_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0005946	rhinosporidiosis	infectious_disease	infectious_disease	infectious_disease	otolaryngology|dermatology	inflammatory_disease|autoimmune_diseases	respiratory_disorder|nose_disorder	true	false	false	false	medium
MONDO:0005947	rickettsial pneumonia	inflammatory_disease|infectious_disease|respiratory_system_disorder	infectious_disease	respiratory_system_disorder|inflammatory_disease|infectious_disease	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	respiratory_disorder|lung_disorder	true	false	false	true	medium
MONDO:0005949	roseolovirus infectious disease	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric|dermatology	inflammatory_disease|autoimmune_diseases	nose_disorder|upper_gastrointestinal_disorder|skin_disorder	true	false	false	false	low
MONDO:0005950	Salmonella gastroenteritis	digestive_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	digestive_system_disorder|inflammatory_disease|infectious_disease	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease|gastrointestinal_disease__note__i_replaced_the_original_disease_name_with_a_more_accurate_one	lower_gastrointestinal_disorder_upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005952	scarlet fever	infectious_disease	infectious_disease	infectious_disease	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005953	scirrhous adenocarcinoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0005954	screw worm infectious disease	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease	veterinary__not_listed_but_inferred|pediatrics|dermatology	parasitic_disease|zoonotic_disease	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0005956	septicemic plague	hematologic_disorder|infectious_disease	infectious_disease	hematologic_disorder|infectious_disease	hematology|pulmonology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	very_high
MONDO:0005957	setariasis	infectious_disease	infectious_disease	infectious_disease	dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	liver_disorder|skin_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0005959	sick building syndrome	immune_system_disorder|inflammatory_disease|respiratory_system_disorder	other	respiratory_system_disorder|immune_system_disorder|inflammatory_disease	neurology|pulmonology	autoimmune_diseases|inflammatory_disease|allergy|mental_health_disorder	immune_disorder|lung_disorder	false	false	false	true	medium
MONDO:0005960	silicosis	respiratory_system_disorder	other	respiratory_system_disorder	respiratory_issues_often_related_to_occupational_hazards_are_typically_associated_with_this_field|pulmonology	autoimmune_diseases|inflammatory_disease	lung_disorder	false	false	false	false	very_high
MONDO:0005961	sinusitis	musculoskeletal_system_disorder|inflammatory_disease|otorhinolaryngologic_disease|respiratory_system_disorder	other	otorhinolaryngologic_disease|respiratory_system_disorder|musculoskeletal_system_disorder|inflammatory_disease	otolaryngology|pulmonary	allergy|autoimmune_diseases|inflammatory_disease	throat_disorder|nose_disorder	true	false	false	true	medium
MONDO:0005962	skeletal tuberculosis	musculoskeletal_system_disorder|infectious_disease	infectious_disease	musculoskeletal_system_disorder|infectious_disease	rheumatology|orthopaedic|pulmonology	autoimmune_diseases|inflammatory_disease	spinal_disorder|bone_disorder|joint_disorder	true	false	false	true	high
MONDO:0005963	sparganosis	infectious_disease	infectious_disease	infectious_disease	parasitology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder|lymphatic_disorder	true	false	false	false	medium
MONDO:0005964	sphenoid sinusitis	musculoskeletal_system_disorder|inflammatory_disease|otorhinolaryngologic_disease|respiratory_system_disorder	other	otorhinolaryngologic_disease|respiratory_system_disorder|musculoskeletal_system_disorder|inflammatory_disease	neurology|otolaryngology	allergy|autoimmune_diseases|inflammatory_disease	nose_disorder|brain_disorder	true	false	false	true	medium
MONDO:0005965	spinal stenosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	neurology|orthopaedic	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0005966	spleen cancer	digestive_system_disorder|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|hematologic_disorder|immune_system_disorder	oncology|hematology	spleen_cancer|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0005967	splenic tuberculosis	hematologic_disorder|infectious_disease|immune_system_disorder	infectious_disease	hematologic_disorder|immune_system_disorder|infectious_disease	hematology|pulmonology	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|liver_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0005968	sporotrichosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|lung_disorder	true	false	false	true	medium
MONDO:0005969	st. Louis encephalitis	inflammatory_disease|infectious_disease|nervous_system_disorder	infectious_disease	nervous_system_disorder|acute_disease|inflammatory_disease|infectious_disease	neurology|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	true	false	false	false	high
MONDO:0005970	staphylococcal pneumonia	inflammatory_disease|infectious_disease|respiratory_system_disorder	infectious_disease	respiratory_system_disorder|inflammatory_disease|infectious_disease	cardiothoracic|pulmonology|cardiology	autoimmune_diseases|inflammatory_disease	throat_disorder|immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0005971	staphyloenterotoxemia	infectious_disease	infectious_disease	infectious_disease	gastroenterology|infectious_diseases|pediatrics|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005972	streptococcal pneumonia	inflammatory_disease|infectious_disease|respiratory_system_disorder	infectious_disease	respiratory_system_disorder|inflammatory_disease|infectious_disease	pediatric|pulmonology	autoimmune_diseases|inflammatory_disease	immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0005973	Strongylida infectious disease	infectious_disease	infectious_disease	infectious_disease	gastroenterology|hepatology|hematology	infectious_disease|inflammatory_disease	immune_disorder|lung_disorder|lymphatic_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005974	strongyloidiasis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|pediatrics	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0005975	suppurative otitis media	auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	other	auditory_system_disorder|otorhinolaryngologic_disease|inflammatory_disease	pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease	throat_disorder|ear_disorder	true	false	false	true	high
MONDO:0005976	syphilis	reproductive_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease	sexually_transmitted_diseases__not_listed_but_implied__are_often_associated_with_urology_however_the_primary_symptom_of_syphilis_is_skin_related_thus_dermatology_seems_most_appropriate|dermatology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|skin_disorder	true	false	false	true	medium
MONDO:0005977	tabes dorsalis	reproductive_system_disorder|infectious_disease|nervous_system_disorder	infectious_disease	nervous_system_disorder|reproductive_system_disorder|infectious_disease	neurology|orthopaedic	neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder	true	false	false	true	high
MONDO:0005978	theileriasis	infectious_disease	infectious_disease	infectious_disease	immunology|hematology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder	true	false	false	true	medium
MONDO:0005979	thoracic outlet syndrome	cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease	cardiothoracic|orthopaedic|pulmonology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	spinal_disorder|lung_disorder	false	false	false	false	medium
MONDO:0005980	tick infestation	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease	pediatrics|dermatology	allergy|tick_infestation|inflammatory_disease	immune_disorder|skin_disorder|lymphatic_disorder	false	false	false	true	medium
MONDO:0005981	tick paralysis	infectious_disease|integumentary_system_disorder|nervous_system_disorder	infectious_disease	nervous_system_disorder|integumentary_system_disorder|infectious_disease	neurology|pediatric	neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0005982	tinea infection	inflammatory_disease|infectious_disease|integumentary_system_disorder	infectious_disease	inflammatory_disease|integumentary_system_disorder|infectious_disease	dermatology	allergy|autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	low
MONDO:0005983	tinea favosa	inflammatory_disease|infectious_disease|integumentary_system_disorder	infectious_disease	inflammatory_disease|integumentary_system_disorder|infectious_disease	dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0005984	tinea pedis	inflammatory_disease|infectious_disease|integumentary_system_disorder	infectious_disease	inflammatory_disease|integumentary_system_disorder|infectious_disease	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0005985	Togaviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	virology|pediatric|infectious_disease	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	viral_infection|immune_disorder|liver_disorder	true	false	false	true	high
MONDO:0005986	torovirus infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|infectious_disease	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|liver_disorder	true	false	false	false	medium
MONDO:0005987	toxascariasis	infectious_disease	infectious_disease	infectious_disease	parasitology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder|eye_disorder	true	false	false	true	low
MONDO:0005988	toxocariasis	infectious_disease	infectious_disease	infectious_disease	neurology|pediatric	allergy|autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|eye_disorder	true	false	false	true	medium
MONDO:0005989	toxoplasmosis	infectious_disease	infectious_disease	infectious_disease	obstetrics_and_gynecology|neurology|pediatrics	autoimmune_diseases|inflammatory_disease|infectious_disease	immune_disorder|upper_gastrointestinal_disorder|brain_disorder|eye_disorder	true	false	false	true	medium
MONDO:0005990	tracheitis	inflammatory_disease|infectious_disease|respiratory_system_disorder	infectious_disease	respiratory_system_disorder|inflammatory_disease|infectious_disease	pediatric|pulmonology	autoimmune_diseases|inflammatory_disease	throat_disorder|lung_disorder	true	false	false	true	medium
MONDO:0005991	trench fever	infectious_disease	infectious_disease	infectious_disease	hematology|immunology|pediatric|pulmonology|infectious_disease	autoimmune_diseases|inflammatory_disease|anemia	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0005993	Trichomonas vaginitis urogenital infection	reproductive_system_disorder|urinary_system_disorder|infectious_disease	infectious_disease	infectious_disease|reproductive_system_disorder|urinary_system_disorder	obstetrics_and_gynecology|urogenital_infection	urogenital_infection|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder|urogenital_infection	true	false	false	true	medium
MONDO:0005994	trichostrongyloidiasis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|hepatology|pediatrics	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005995	trichostrongylosis	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology|allergy_and_immunology	autoimmune_diseases|allergy|neurodegenerative_disease|inflammatory_disease	throat_disorder|muscle_disorder|joint_disorder	true	false	false	true	low
MONDO:0005996	trichuriasis	infectious_disease	infectious_disease	infectious_disease	pediatric|dermatology	inflammatory_disease|parasitic_disease	skin_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0005997	tricuspid valve stenosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0005998	trombiculiasis	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease	hematology|dermatology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	vascular_disorder|skin_disorder	true	false	false	true	low
MONDO:0005999	tuberculous empyema	respiratory_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	respiratory_system_disorder|inflammatory_disease|infectious_disease	pulmonology|cardiothoracic	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|lung_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0006000	tuberculous peritonitis	inflammatory_disease|digestive_system_disorder|infectious_disease	infectious_disease	digestive_system_disorder|inflammatory_disease|infectious_disease	hepatology|pulmonology|gastroenterology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder|lung_disorder	true	false	false	true	high
MONDO:0006001	urinary schistosomiasis	infectious_disease|urinary_system_disorder	infectious_disease	urinary_system_disorder|infectious_disease	renal_medicine|urology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|kidney_disorder	true	false	false	true	high
MONDO:0006002	urogenital tuberculosis	infectious_disease	infectious_disease	infectious_disease	renal_medicine|urology|urogenital_tuberculosis_can_also_be_related_to_obstetrics_and_gynecology_due_to_its_name_but_that_is_less_clear	autoimmune_diseases|inflammatory_disease	kidney_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0006003	uterine corpus cancer	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	uterine_corpus_cancer|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0006004	vasomotor rhinitis	inflammatory_disease|otorhinolaryngologic_disease|respiratory_system_disorder|immune_system_disorder	other	respiratory_system_disorder|otorhinolaryngologic_disease|immune_system_disorder|inflammatory_disease	pulmonology|otolaryngology	allergy|inflammatory_disease	nose_disorder|vascular_disorder	false	false	false	true	low
MONDO:0006005	Venezuelan equine encephalitis	inflammatory_disease|nervous_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|nervous_system_disorder|infectious_disease	neurology|virology	infectious_disease|neurodegenerative_disease	brain_disorder|immune_disorder	true	false	false	true	medium
MONDO:0006006	verrucous carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|oncology	adrenal_gland_disease|autoimmune_diseases|cancer	skin_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006007	vesicoureteral reflux	urinary_system_disorder	other	urinary_system_disorder	urology|pediatric	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0006008	vestibular neuronitis	inflammatory_disease|nervous_system_disorder|auditory_system_disorder	other	inflammatory_disease|auditory_system_disorder|nervous_system_disorder	neurology|otolaryngology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	ear_disorder|brain_disorder	false	false	false	true	medium
MONDO:0006009	viral encephalitis	inflammatory_disease|nervous_system_disorder|infectious_disease	infectious_disease	acute_disease|inflammatory_disease|nervous_system_disorder|infectious_disease	neurology|pediatric	neurodegenerative_disease|inflammatory_disease	brain_disorder|immune_disorder	true	false	false	true	high
MONDO:0006011	viral hepatitis	inflammatory_disease|digestive_system_disorder|infectious_disease|endocrine_system_disorder	infectious_disease|endocrine_system_disorder	infectious_disease|digestive_system_disorder|inflammatory_disease|endocrine_system_disorder	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	liver_disorder|immune_disorder	true	false	false	true	high
MONDO:0006012	viral pneumonia	inflammatory_disease|infectious_disease|respiratory_system_disorder	infectious_disease	infectious_disease|respiratory_system_disorder|inflammatory_disease	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0006014	vulvovaginal candidiasis	inflammatory_disease|reproductive_system_disorder|integumentary_system_disorder|infectious_disease	infectious_disease	infectious_disease|reproductive_system_disorder|inflammatory_disease|integumentary_system_disorder	dermatology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	skin_disorder|reproductive_system_disorder	true	false	false	true	low
MONDO:0006015	Waterhouse-Friderichsen syndrome	syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	acute_disease|syndromic_disease|endocrine_system_disorder	cardiology|pulmonology|hematology|genetics_and_genomics	adrenal_gland_disease|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	true	false	false	false	very_high
MONDO:0006018	Wissler syndrome	connective_tissue_disorder|syndromic_disease	other	connective_tissue_disorder|syndromic_disease	pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	bone_disorder|skeletal_dysplasia_disorder	false	false	false	false	high
MONDO:0006019	yaws	reproductive_system_disorder|infectious_disease	infectious_disease	infectious_disease|reproductive_system_disorder	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	skin_disorder|joint_disorder	true	false	false	true	medium
MONDO:0006021	Prinzmetal angina	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology|pulmonology	metabolic_disorder|cardiovascular_disorder	heart_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0006022	acidosis disorder	metabolic_disease	metabolic_disease	metabolic_disease	renal_medicine|endocrinology	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0006025	autosomal recessive disease	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	autosomal_recessive_disease_tends_to_also_fit_neurodegenerative_disease_and_adrenal_gland_disease|metabolic_disorder	blood_bone_marrow_disorder|kidney_disorder|liver_disorder	false	false	false	true	medium
MONDO:0006026	urinary bladder disorder	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0006027	breast synovial sarcoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|rheumatology|obstetrics_and_gynecology|orthopaedic	cancer|inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	true	false	false	high
MONDO:0006028	cecum adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006029	cecum carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0006030	chronic cystitis	urinary_system_disorder|inflammatory_disease	other	urinary_system_disorder|inflammatory_disease	renal_medicine|urology	inflammatory_disease|autoimmune_diseases	kidney_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0006031	chronic rhinosinusitis	otorhinolaryngologic_disease|inflammatory_disease|respiratory_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|otorhinolaryngologic_disease|inflammatory_disease|respiratory_system_disorder	allergy_and_immunology|otolaryngology	inflammatory_disease|autoimmune_diseases|allergy	throat_disorder|nose_disorder	false	false	false	true	high
MONDO:0006032	cystitis	urinary_system_disorder|inflammatory_disease	other	urinary_system_disorder|inflammatory_disease	renal_medicine|urology	inflammatory_disease|autoimmune_diseases	kidney_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0006033	diffuse intrinsic pontine glioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0006034	gastric adenosquamous carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0006035	gastric tubular adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	adenocarcinoma|cancer|gastrointestinal_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006036	granulosa cell tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0006037	hydrolethalus syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|obstetrics_and_gynecology	metabolic_disorder|genetic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0006038	indeterminate colitis	hereditary_disease|immune_system_disorder|inflammatory_disease|digestive_system_disorder	other	hereditary_disease|inflammatory_disease|digestive_system_disorder|immune_system_disorder	gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0006039	infectious colitis	hereditary_disease|infectious_disease|immune_system_disorder|inflammatory_disease|digestive_system_disorder	infectious_disease	hereditary_disease|infectious_disease|inflammatory_disease|digestive_system_disorder|immune_system_disorder	pediatric|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	medium
MONDO:0006040	lactic acidosis	metabolic_disease	metabolic_disease	metabolic_disease	cardiology|pulmonology	metabolic_disorder|adrenal_gland_disease	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0006041	lung carcinoid tumor	cancer_or_benign_tumor|endocrine_system_disorder|respiratory_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder	oncology|cardiothoracic|pulmonology	cancer|adrenal_gland_disease	lung_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0006042	meningeal tuberculosis	nervous_system_disorder|infectious_disease|reproductive_system_disorder|inflammatory_disease	infectious_disease	infectious_disease|reproductive_system_disorder|inflammatory_disease|nervous_system_disorder	pediatric|neurology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	subtype|immune_disorder|spinal_disorder|brain_disorder	true	false	false	true	high
MONDO:0006043	metaplastic breast carcinoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|obstetrics_and_gynecology	metastatic_carcinoma|cancer	breast_disorder|reproductive_system_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0006044	nephrosclerosis	urinary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	urinary_system_disorder|cardiovascular_disorder	renal_medicine|nephrology	metabolic_disorder___corrected_answer__cardiovascular_disorder|kidney_disease|metabolic_disorder|cardiovascular_disorder|kidney_disease_disorders	urinary_tract_disorder|vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0006045	ovarian clear cell adenocarcinoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	ovarian|cancer	ovarian_disorder|lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0006046	ovarian serous cystadenocarcinoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder|ovarian	false	true	false	false	high
MONDO:0006047	pancreatic adenocarcinoma	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|pancreatic_adenocarcinoma	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0006049	papillary lung adenocarcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology	cancer|lung_adenocarcinoma	lung_disorder	false	true	false	true	high
MONDO:0006050	pleomorphic breast carcinoma	cancer_or_benign_tumor|integumentary_system_disorder|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|breast_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	true	very_high
MONDO:0006052	pulmonary tuberculosis	infectious_disease|respiratory_system_disorder	infectious_disease	infectious_disease|respiratory_system_disorder	oncology|allergy_and_immunology|cardiothoracic|cardiology|pulmonology|hematol	cancer|inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0006053	renal leiomyoma	cancer_or_benign_tumor|urinary_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine	cancer|adrenal_gland_disease	kidney_disorder|muscle_disorder|renal_leiomyoma_is_likely_related_to_kidney__so_i_ll_remove_the__r__from_renal_leiomyoma_and_treat_it_as_kidney_leiomyoma_for_this_exercise__however__given_its_origin_in_the_kidney_but_being_a_type_of_leiomyoma__smooth_muscle_tumor___the_best_fitting_categories_are_actually_kidney_disorder	false	false	false	false	low
MONDO:0006054	reproductive system neoplasm	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	reproductive_system_neoplasm|cancer	reproductive_system_disorder|reproductive_system_neoplasm	false	true	false	true	high
MONDO:0006055	sex cord-stromal tumor	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0006056	squamous cell breast carcinoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|obstetrics_and_gynecology	squamous_cell_carcinoma|cancer|breast_carcinoma	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0006058	Wilms tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric|urology	renal_disease|cancer|childhood_cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0006059	nasal cavity squamous cell carcinoma	cancer_or_benign_tumor|nervous_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder|nervous_system_disorder	oncology|otolaryngology	cancer|inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	throat_disorder|nose_disorder	false	true	false	false	high
MONDO:0006060	nasopharyngeal squamous cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology	cancer	nose_disorder|throat_disorder	false	true	false	true	high
MONDO:0006061	cervical artery dissection	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	vascular_surgery|neurology|cardiology|cardiothoracic	cardiovascular_disorder|vascular_disorder	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0006065	lactose intolerance adult type	hereditary_disease|metabolic_disease|nutritional_disorder|digestive_system_disorder	metabolic_disease	hereditary_disease|nutritional_disorder|digestive_system_disorder|metabolic_disease	endocrinology|gastroenterology	metabolic_disorder|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0006066	acinar prostate adenocarcinoma, foamy gland variant	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	cancer|adrenal_gland_disease	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0006067	acinar prostate mucinous adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	cancer	urinary_tract_disorder|lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0006068	ACTH-producing pituitary gland adenoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	neurology|endocrinology	neuroendocrine_cancer|adrenal_disorder|cancer|endocrine_disorder|pituitary_gland_disease	endocrine_disorder|brain_disorder	false	true	false	true	high
MONDO:0006069	ACTH-producing pituitary gland carcinoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrinology|oncology	cancer|adrenal_gland_disease	endocrine_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0006071	adenofibroma	reproductive_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|connective_tissue_disorder	oncology|urology|pathology	cancer	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0006073	adenomatoid odontogenic tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder	oncology|orthopaedic	odontogenic_tumor|cancer	teeth_disorder|bone_disorder	false	false	false	false	low
MONDO:0006074	adenosquamous carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|cardiothoracic|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|lung_disorder	false	true	false	false	high
MONDO:0006075	adrenal gland myelolipoma	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology|hematology	cancer|adrenal_gland_disease	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0006076	adrenal gland neuroblastoma	disorder_of_development_or_morphogenesis|endocrine_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|endocrine_system_disorder	oncology|endocrinology|pediatric	cancer|adrenal_gland_disease	endocrine_disorder|neuroblastoma____as_neuroblastoma_is_a_type_of_cancer_that_originates_from_the_adrenal_glands	false	true	false	true	very_high
MONDO:0006077	adrenal medullary hyperplasia	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrinology|pediatric	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0006078	AIDS-related primary central nervous system lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|post_infectious_disorder|hematologic_disorder	oncology|neurology|hematoloy	cancer|inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder|lymphatic_disorder	true	true	false	true	very_high
MONDO:0006079	ameloblastic carcinoma	digestive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	oncology	cancer	upper_gastrointestinal_disorder|teeth_disorder	false	true	false	false	high
MONDO:0006081	anal melanoma	digestive_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|digestive_system_disorder	oncology|dermatology	cancer|adrenal_gland_disease	melanoma|skin_disorder	false	true	false	true	very_high
MONDO:0006082	anal squamous cell carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|dermatology	cancer|inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	reproductive_system_disorder|skin_disorder	false	true	false	true	high
MONDO:0006085	angiolipoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	orthopaedic|renal_medicine|neurology|hematology|oncology	cancer|adrenal_gland_disease	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0006086	angiomyxoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	oncology|dermatology|cardiothoracic	cancer|inflammatory_disease|adrenal_gland_disease	vascular_disorder|muscle_disorder	false	false	false	false	low
MONDO:0006087	appendix adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|surgery|gastroenterology	cancer|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006088	appendix adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	pediatric|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0006090	appendix hyperplastic polyp	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|surgical|gastroenterology	cancer|gastrointestinal_disease|polyp	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0006091	appendix neuroendocrine tumor G1	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|neurology|endocrinology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder	false	true	false	true	low
MONDO:0006092	appendix villous adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	cancer|neoplasm|gastrointestinal_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006093	ascending colon neuroendocrine tumor G1	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	gastroenterology|oncology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006094	Askin tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	dermatology|oncology	cancer|adrenal_gland_disease	skin_disorder	false	true	false	false	high
MONDO:0006095	atypical carcinoid tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	neurology|pulmonology|oncology	other____note__atypical_carcinoid_tumor_is_a_type_of_neuroendocrine_tumor_which_can_be_related_to_the_adrenal_gland__however__it_s_more_specifically_classified_as_a_cancer|cancer|adrenal_gland_disease	endocrine_disorder|lung_disorder	false	true	false	true	high
MONDO:0006096	atypical endometrial hyperplasia	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|gastroenterology|endocrinology	cancer|inflammatory_disease|endocrine_disorder	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0006097	atypical lipomatous tumor	cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	dermatology|oncology	lipomatous_tumor|cancer|adrenal_gland_disease	muscle_disorder|skin_disorder	false	true	false	false	medium
MONDO:0006098	atypical lobular breast hyperplasia	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|breast_disorder	obstetrics_and_gynecology|oncology	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder|anemia|cancer|inflammatory_disease|adrenal_gland_disease|autoimmune_diseases|allergy|mental_health_disorder____only_the_top_9_categories	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0006102	basaloid carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|pathology|oncology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0006103	benign adrenal gland pheochromocytoma	endocrine_system_disorder|hereditary_disease|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|hereditary_disease|disorder_of_development_or_morphogenesis	urology|renal_medicine|endocrinology|oncology	cancer|adrenal_gland_disease	endocrine_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0006104	benign carotid body paraganglioma	endocrine_system_disorder|hereditary_disease|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder|endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|cardiovascular_disorder|endocrine_system_disorder|cancer_or_benign_tumor|hereditary_disease|disorder_of_development_or_morphogenesis	pulmonology|cardiology|neurology	cancer|cardiovascular_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	true	low
MONDO:0006105	benign conjunctival neoplasm	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cancer_or_benign_tumor	ophthalmology|oncology	cancer	eye_disorder|skin_disorder	false	false	false	true	low
MONDO:0006106	benign smooth muscle neoplasm	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	urology|renal_medicine|oncology	cancer|benign_smooth_muscle_neoplasm_does_fit_under_this_category	soft_tissue_disorder|muscle_disorder	false	false	false	false	low
MONDO:0006107	benign thyroid gland neoplasm	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|oncology	cancer	endocrine_disorder	false	false	false	true	low
MONDO:0006108	bile duct adenoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology|hepatology	liver_disease|cancer|gastrointestinal_disease	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0006109	malignant biphasic mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonology|oncology|cardiothoracic	cancer|adrenal_gland_disease	lung_disorder|mesothelioma	false	true	false	false	very_high
MONDO:0006111	bladder flat intraepithelial lesion	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer|autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	true	false	false	medium
MONDO:0006112	bladder inflammatory myofibroblastic tumor	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer|inflammatory_disease	urinary_tract_disorder|muscle_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0006115	blast phase chronic myelogenous leukemia, BCR-ABL1 positive	immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder	oncology|hematology	leukemia|cancer|anemia	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0006116	breast carcinoma by gene expression profile	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology|genetics_and_genomics	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0006117	breast diffuse large B-cell lymphoma	immune_system_disorder|cancer_or_benign_tumor|breast_disorder|hematologic_disorder|integumentary_system_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|integumentary_system_disorder|breast_disorder	oncology|hematology	cancer|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0006118	breast fibrosis	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|breast_disorder	obstetrics_and_gynecology|pulmonology|oncology	cancer|autoimmune_diseases|inflammatory_disease	breast_fibrosis_is_most_likely_related_to_either_reproductive_system_disorder_or_breast_fibrosis_could_be_a_part_of_skin_disorder	false	false	false	false	medium
MONDO:0006119	breast mucosa-associated lymphoid tissue lymphoma	immune_system_disorder|hereditary_disease|cancer_or_benign_tumor|hematologic_disorder|integumentary_system_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|integumentary_system_disorder|hereditary_disease	obstetrics_and_gynecology|oncology|hematology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	false	true	false	true	medium
MONDO:0006120	C-cell hyperplasia	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	urology|renal_medicine|oncology|endocrinology|hematology	cancer|anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0006121	calcifying fibrous tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	orthopaedic|oncology	cancer|adrenal_gland_disease	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	low
MONDO:0006122	calcifying nested epithelial stromal tumor of the liver	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|oncology|hepatology	cancer	liver_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0006123	cardiac rhabdomyoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder|musculoskeletal_system_disorder	pediatric|cardiology	cardiovascular_disorder|cardiac	vasculardisorder|heart_disorder|muscledisorder	false	false	false	false	low
MONDO:0006126	cecum neuroendocrine tumor G1	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|oncology|endocrinology	cancer|neuroendocrine_tumor	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	low
MONDO:0006128	central nervous system anaplastic large cell lymphoma	immune_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|hematologic_disorder	cancer_or_benign_tumor	post_infectious_disorder|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|nervous_system_disorder	oncology|hematology|neurology	cancer|lymphoma	lymphatic_disorder|spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0006130	central nervous system neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	central_nervous_system_neoplasm_is_an_oxymoron_in_this_case_so_i_ll_replace_it_with_the_more_general_category_cancer|cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0006131	cerebellar liponeurocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	medium
MONDO:0006132	cervical adenoid basal carcinoma	cancer_or_benign_tumor|reproductive_system_disorder|integumentary_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	throat_disorder|reproductive_system_disorder	false	true	false	false	low
MONDO:0006133	cervical adenoid cystic carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|otolaryngology|oncology	adrenal_gland_disease|cancer	throat_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0006134	cervical adenosquamous carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	throat_disorder|upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0006135	cervical clear cell adenocarcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|female_reproductive_system_disorder	false	true	false	false	high
MONDO:0006137	cervical intraepithelial neoplasia grade 2/3	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006138	cervical large cell neuroendocrine carcinoma	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	obstetrics_and_gynecology|oncology	cancer|neuroendocrine_carcinoma	neuroendocrine_carcinoma_is_primarily_associated_with_endocrine_disorders__however__it_also_has_associations_to_lung_disorder__due_to_its_neuroendocrine_origins	false	true	false	false	very_high
MONDO:0006139	cervical metaplasia	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology	cancer|metabolic_disorder|inflammatory_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0006140	cervical mucinous adenocarcinoma, minimal deviation variant	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer|allergy|autoimmune_diseases|other___corrected_to_remove__allergy___as_cervical_mucinous_adenocarcinoma_is_a_type_of_cancer_and_not_an_allergic_reaction__but_it_should_be_removed_from_the_list_as_it_was_given___cancer|inflammatory_disease	reproductive_system_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0006141	cervical villoglandular adenocarcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer|adenocarcinoma	reproductive_system_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006142	cervical small cell carcinoma	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	lung_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0006143	cervical squamous cell carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer|autoimmune_diseases	lung_disorder|throat_disorder|reproductive_system_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0006144	cervical Wilms tumor	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	pediatric|urology|obstetrics_and_gynecology|oncology	cancer	kidney_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0006145	chondroid chordoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|oncology|genetics_and_genomics|hematology	cancer|chordoma	spinal_disorder|bone_disorder	false	true	false	false	high
MONDO:0006146	chondroid hamartoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|orthopaedic|genetics_and_genomics	adrenal_gland_disease|cancer|anemia|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0006149	clear cell papillary cystadenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|renal_medicine	adrenal_gland_disease|cancer	liver_disorder|kidney_disorder	false	false	false	true	low
MONDO:0006150	colon Burkitt lymphoma	digestive_system_disorder|immune_system_disorder|hereditary_disease|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|digestive_system_disorder|post_infectious_disorder|hereditary_disease	pediatric|oncology|gastroenterology|hematology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0006151	colon dysplasia	digestive_system_disorder	other	digestive_system_disorder	oncology|gastroenterology	cancer|colorectal_disease|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0006152	colon inflammatory polyp	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	pediatric|oncology|gastroenterology	cancer|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0006153	colon juvenile polyp	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	pediatric|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0006154	colon mucosa-associated lymphoid tissue lymphoma	digestive_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|digestive_system_disorder	oncology|gastroenterology|hematology	cancer|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder_lymphatic_disorder_immune_disorder	false	true	false	true	medium
MONDO:0006155	colon neuroendocrine tumor G1	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|gastroenterology	cancer|neuroendocrine_tumor	endocrine_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	low
MONDO:0006156	colon sessile serrated adenoma/polyp	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|polyp|adenoma	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0006157	colorectal adenosquamous carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease|other____corrected_to__cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006158	colorectal diffuse large B-cell lymphoma	digestive_system_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|digestive_system_disorder	oncology|gastroenterology|hematology	autoimmune_diseases|cancer|inflammatory_disease	lower_gastrointestinal_disorder_lymphatic_disorder	false	true	false	true	high
MONDO:0006159	colorectal gastrointestinal stromal tumor	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|gastrointestinal_tumor	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0006160	colorectal hamartoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	hereditary_condition|cancer|gastrointestinal_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0006161	colorectal juvenile polyp	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	pediatric|gastroenterology	cancer|colorectal_disease|polyp|intestinal_polyp|gastrointestinal_disease|tumor	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0006162	colorectal neuroendocrine tumor G1	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrinology|oncology|gastroenterology	cancer|neuroendocrine_tumor	lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006163	colorectal serrated adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006164	colorectal sessile serrated adenoma/polyp	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|polyp|adenoma|gastrointestinal_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006165	colorectal squamous cell carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006166	columnar cell hyperplasia of the breast	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	autoimmune_diseases|cancer|inflammatory_disease	skin_disorder|breast_disorder	false	false	false	false	low
MONDO:0006167	combined lung carcinoma	endocrine_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|respiratory_system_disorder	oncology|cardiothoracic|pulmonology	cancer	lung_carcinoma|lung_disorder	false	true	false	false	very_high
MONDO:0006169	complex endometrial hyperplasia	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|endocrinology	endocrine_disorder|gynecological_disorder|metabolic_disorder	endocrine_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0006170	conjunctival disorder	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|conjunctival_disorder	false	false	false	true	medium
MONDO:0006172	conjunctival nevus	disorder_of_development_or_morphogenesis|nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	dermatology|ophthalmology	neurocutaneous_syndrome|eye_disease|nevus|skin_cancer	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0006173	conjunctival squamous cell carcinoma	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	oncology|ophthalmology	cancer|inflammatory_disease	skin_disorder|eye_disorder	false	true	false	true	medium
MONDO:0006174	cortisol-producing adrenal cortex adenoma	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrinology|oncology	cancer|adrenal_gland_disease|metabolic_disorder	endocrine_disorder	false	true	false	true	high
MONDO:0006176	cribriform carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	otolaryngology|oncology|neurology	cancer|adrenal_gland_disease	brain_disorder|nose_disorder	false	true	false	false	high
MONDO:0006178	dedifferentiated solitary fibrous tumor	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	pathology|oncology|surgeries	cancer	soft_tissue_disorder|lung_disorder|bone_disorder|vascular_disorder	false	false	false	false	high
MONDO:0006179	desmoplastic ameloblastoma	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|musculoskeletal_system_disorder	oral_surgery|orthopaedic|oncology	cancer	teeth_disorder|bone_disorder	false	true	false	false	medium
MONDO:0006180	digestive system adenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hepatology|oncology|gastroenterology	cancer|digestive_system_adenoma_is_already_in_the_list_so_it_was_not_added_as_a_separate_entry	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0006181	digestive system carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	hepatology|oncology|gastroenterology	digestive_system_carcinoma|cancer	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0006182	digestive system mixed adenoneuroendocrine carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|neuroendocrine_diseases_is_not_in_the_list_so_use__cancer|adrenal_gland_disease	endocrine_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006183	disseminated peritoneal leiomyomatosis	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	obstetrics_and_gynecology|oncology	autoimmune_diseases|cancer|inflammatory_disease	reproductive_system_disorder|muscle_disorder	false	false	false	false	low
MONDO:0006184	ductal breast carcinoma in situ and lobular carcinoma in situ	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|breast_disorder	false	true	false	true	medium
MONDO:0006186	duodenal adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006187	duodenal villous adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006188	EBV-positive T-cell lymphoproliferative disorder of childhood	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	pediatric|oncology|hematology	autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	true	true	false	false	very_high
MONDO:0006189	eccrine porocarcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer|adrenal_gland_disease	skin_disorder|liver_disorder	false	true	false	false	high
MONDO:0006190	endolymphatic sac tumor	auditory_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|auditory_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology	tumor|cancer|adrenal_gland_disease|neurodegenerative_disease	lymphatic_disorder|ear_disorder	false	true	false	true	high
MONDO:0006191	endometrial clear cell adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease|gynecologic_cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006192	endometrial endometrioid adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|endometrial_adenocarcinoma	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0006193	endometrial hyperplasia without atypia	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology	cancer|endometrial_hyperplasia_is_a_pre_cancerous_condition__however_it_is_often_categorized_as_cancer_because_it_has_the_potential_to_become_malignant_if_left_untreated	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0006195	endometrial polyp	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	gynecology|obstetrics_and_gynecology	cancer|inflammatory_disease	reproductive_system_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0006196	endometrial serous adenocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0006197	endometrial small cell carcinoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0006198	endometrial squamous cell carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease|endometrial_cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006199	endometrial undifferentiated carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0006200	epithelioid cell uveal melanoma	cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_development_or_morphogenesis|nervous_system_disorder	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region|nervous_system_disorder|disorder_of_development_or_morphogenesis	ophthalmology|oncology	adrenal_gland_disease|cancer|uveal_melanoma_category__assuming_this_is_a_category_for_the_given_disease	eye_disorder|skin_disorder	false	true	false	false	very_high
MONDO:0006201	ethmoid sinus adenoid cystic carcinoma	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder|nervous_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder|connective_tissue_disorder	oncology|otolaryngology	inflammatory_disease|cancer|autoimmune_diseases	throat_disorder|nose_disorder	false	true	false	true	high
MONDO:0006202	extrahepatic bile duct adenosquamous carcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|biliary_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0006203	extrahepatic bile duct squamous cell carcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|hepatology|gastroenterology	adrenal_gland_disease|cancer|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0006206	fallopian tube carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	inflammatory_disease|cancer|autoimmune_diseases	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0006207	fallopian tube carcinosarcoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	gland_disease|cancer	upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0006208	fallopian tube serous adenocarcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	inflammatory_disease|adrenal_gland_disease|cancer|autoimmune_diseases	gynecological_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0006209	fibroblastic neoplasm	cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	oncology|hematology|genetics_and_genomics|obstetrics_and_gynecology|pediatric	fibroblastic_neoplasm|cancer	blood_bone_marrow_disorder|muscle_disorder	false	true	false	false	medium
MONDO:0006210	fibrolamellar hepatocellular carcinoma	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|hepatology|gastroenterology	liver_cancer|hepatic_cancer|malignant_tumor|tumor|cancer	liver_disorder	false	true	false	false	high
MONDO:0006211	fibrous hamartoma of infancy	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics|pediatric	adrenal_gland_disease|cancer	liver_disorder|muscle_disorder|gastrointestinal_disorder	false	false	false	false	low
MONDO:0006212	flat urothelial hyperplasia	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|renal_medicine	urotheilial_hyperplasia_can_be_classified_as_a_type_of_cancer__specifically_a_non_cancerous__benign__growth_in_the_bladder_lining|cancer	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0006213	floor of mouth mucoepidermoid carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	oncology|otolaryngology	adrenal_gland_disease|cancer	mouth_disorder|teeth_disorder	false	true	false	true	high
MONDO:0006214	follicular variant thyroid gland papillary carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	endocrinology|oncology	adrenal_gland_disease|cancer|thyroid_gland_disease	thyroid_gland_papillary_carcinoma|endocrine_disorder	false	true	false	true	medium
MONDO:0006215	gallbladder adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|hepatology|gastroenterology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0006216	gallbladder adenoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology|hpatology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	low
MONDO:0006217	gallbladder adenosquamous carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|hepatology|gastroenterology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0006218	gallbladder biliary intraepithelial neoplasia	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|hepatology|gastroenterology	inflammatory_disease|biliary_intraepithelial_neoplasia|cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	medium
MONDO:0006219	gallbladder small cell neuroendocrine carcinoma	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer|neuroendocrine_carcinoma	endocrine_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0006220	gallbladder squamous cell carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|biliary_disorder|liver_disorder	false	true	false	false	high
MONDO:0006221	gastric adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	adenoma|gastrointestinal_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006222	gastric choriocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0006223	gastric diffuse large B-cell lymphoma	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	oncology|hematology|gastroenterology	inflammatory_disease|allergic_disease|cancer|autoimmune_diseases	upper_gastrointestinal_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0006224	gastric hamartomatous polyp	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|genetics_and_genomics|gastroenterology	gastrointestinal_disease|benign_tumor|cancer|polyp	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0006225	gastric mantle cell lymphoma	digestive_system_disorder|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|digestive_system_disorder	oncology|hematology|gastroenterology	inflammatory_disease|cancer|autoimmune_diseases	upper_gastrointestinal_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0006226	gastric mucosa-associated lymphoid tissue lymphoma	digestive_system_disorder|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|digestive_system_disorder	oncology|hematology|gastroenterology	cancer|autoimmune_diseases	upper_gastrointestinal_disorder|immune_disorder|lymphatic_disorder	true	true	false	true	medium
MONDO:0006227	gastric neuroendocrine tumor G1	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|gastroenterology|endocrinology	gastrointestinal_cancer|cancer|neuroendocrine_tumor	endocrine_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006228	gastric papillary adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006229	gastric small cell neuroendocrine carcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|gastroenterology	gastrointestinal_disease|cancer|neuroendocrine_carcinoma	endocrine_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0006230	gastric squamous cell carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	gastrointestinal_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0006231	gastrointestinal hamartoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|genetics_and_genomics|gastroenterology|pediatric	gastrointestinal_disease|neoplastic_disorder|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0006232	giant cell tumor of soft tissue	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|orthopaedic	cancer|soft_tissue_tumor	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0006233	gonadal teratoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric|obstetrics_and_gynecology	gynecologic_cancer|tumor|cancer	reproductive_system_disorder	false	true	false	true	medium
MONDO:0006234	grade III prostatic intraepithelial neoplasia	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	cancer	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0006235	granular cell tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|dermatology	neoplastic_disease|cancer	skin_disorder|muscle_disorder	false	true	false	false	low
MONDO:0006237	granulocytic sarcoma	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder|acute_disease|immune_system_disorder|connective_tissue_disorder	oncology|hematology	cancer	blood_bone_marrow_disorder|skin_disorder|vascular_disorder|muscle_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0006238	growth hormone-producing pituitary gland adenoma	cancer_or_benign_tumor|reproductive_system_disorder|nervous_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	musculoskeletal_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder|connective_tissue_disorder	endocrinology|neurology	pituitary_disorder|endocrine_disease|cancer	endocrine_disorder|brain_disorder	false	true	false	true	high
MONDO:0006239	head and neck paraganglioma	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|nervous_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	oncology|otolaryngology|neurology	cancer	spinal_disorder|brain_disorder|throat_disorder	false	false	false	true	high
MONDO:0006241	hepatic granuloma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	immune_disorder|liver_disorder	false	false	false	false	low
MONDO:0006243	hepatoid adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|hepatology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0006244	HER2 positive breast carcinoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|cancer	lymphatic_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0006245	hidradenocarcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	inflammatory_disease|cancer|skin_cancer	skin_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0006246	high grade surface osteosarcoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|oncology	adrenal_gland_disease|cancer	spinal_disorder|joint_disorder|bone_disorder	false	true	false	false	very_high
MONDO:0006247	histiocytic and dendritic cell neoplasm	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	histiocytic_and_dendritic_cell_neoplasm|cancer	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	false	high
MONDO:0006248	hydatidiform mole	obstetric_disorder|reproductive_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|obstetric_disorder|hereditary_disease	oncology|obstetrics_and_gynecology	cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0006249	hyperplastic polyp	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|gastroenterology	gastrointestinal_disease|cancer|polyp_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0006250	ileal neuroendocrine tumor G1	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer|neuroendocrine_tumor	endocrine_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006254	intestinal type adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|gastroenterology	intestinal_type_adenocarcinoma|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006255	intimal sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cardiothoracic|oncology|hematology|general_surgery	adrenal_gland_disease|cancer|cardiovascular_disorder	vascular_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0006256	invasive breast carcinoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|obstetrics_and_gynecology	invasive_breast_carcinoma_is_a_type_of_cancer__specifically_a_carcinoma|cancer	lymphatic_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0006257	jejunal neuroendocrine tumor G1	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|gastroenterology	neuroendocrine_tumor_g1|cancer	endocrine_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006258	juvenile polyp	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|otolaryngology|pediatric	inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0006260	kidney medullary carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology|renal_medicine	kidney_disease|adrenal_gland_disease|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	false	very_high
MONDO:0006262	lacrimal gland adenoid cystic carcinoma	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region|nervous_system_disorder	oncology|otolaryngology|ophthalmology	adenoid_cystic_carcinoma_is_a_type_of_cancer_that_affects_the_lacrimal_gland_therefore_it_fits_into_this_category|cancer	eye_disorder	false	true	false	false	high
MONDO:0006264	laryngeal adenoid cystic carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology	cancer	upper_gastrointestinal_disorder|throat_disorder	false	true	false	false	medium
MONDO:0006265	laryngeal small cell carcinoma	otorhinolaryngologic_disease|respiratory_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|respiratory_system_disorder|endocrine_system_disorder|otorhinolaryngologic_disease	oncology|pulmonology|otolaryngology	adrenal_gland_disease|cancer	throat_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0006266	Leydig cell tumor	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	endocrinology|oncology|urology	adrenal_gland_disease|cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	true	low
MONDO:0006267	liver cavernous hemangioma	cancer_or_benign_tumor|hematologic_disorder|cardiovascular_disorder|endocrine_system_disorder|digestive_system_disorder	cardiovascular_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder|hematologic_disorder|endocrine_system_disorder|digestive_system_disorder	oncology|hepatology|hematology	liver_disease|tumor|cancer	vascular_disorder|liver_disorder	false	false	false	false	low
MONDO:0006268	liver diffuse large B-cell lymphoma	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|hematologic_disorder|endocrine_system_disorder|immune_system_disorder|digestive_system_disorder	oncology|hepatology|hematology	autoimmune_diseases|cancer	liver_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0006270	lobular breast carcinoma in situ	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	oncology|obstetrics_and_gynecology	inflammatory_disease|cancer	breast_disorder|lymphatic_disorder|reproductive_system_disorder	false	true	false	true	low
MONDO:0006271	low grade central osteosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|orthopaedic	anemia|cancer	spinal_disorder|bone_disorder	false	true	false	true	medium
MONDO:0006272	low grade fibromyxoid sarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	oncology|hematology|orthopaedic	sarcoma|cancer	muscle_disorder|bone_disorder	false	true	false	false	medium
MONDO:0006273	low grade fibromyxoid sarcoma with giant collagen rosettes	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	oncology|genetics_and_genomics|orthopaedic	adrenal_gland_disease|cancer	muscle_disorder|bone_disorder	false	true	false	false	medium
MONDO:0006274	low grade vulvar intraepithelial neoplasia	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|dermatology|obstetrics_and_gynecology	intraepithelial_neoplasia|cancer	skin_disorder|reproductive_system_disorder	false	true	false	true	low
MONDO:0006275	lung giant cell carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology	adenocarcinoma|carcinoma|lung_cancer|cancer	lung_disorder|immune_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0006276	lung inflammatory myofibroblastic tumor	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology	inflammatory_disease|cancer	lung_disorder|muscle_disorder	false	false	false	false	high
MONDO:0006277	lung lymphangioleiomyomatosis	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|cardiothoracic	rare_disease|lymphatic_disorder|cancer	lung_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0006278	lung papilloma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology	inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|lung_disorder	false	false	false	true	medium
MONDO:0006279	lung sarcomatoid carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology	adrenal_gland_disease|cancer	lung_disorder	false	true	false	false	very_high
MONDO:0006280	lung sclerosing hemangioma	cancer_or_benign_tumor|respiratory_system_disorder|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	respiratory_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	pulmonology|hematology|oncology	cardiovascular_disorder|cancer|inflammatory_disease|lymphoma|tumor	vascular_disorder|lung_disorder	false	false	false	false	low
MONDO:0006281	lung signet ring cell carcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|cardiothoracic|oncology	lung|cancer	lymphatic_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0006282	lymphangiosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology	adrenal_gland_disease|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0006283	lymphoepithelioma-like lung carcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|cardiothoracic|oncology	cancer|lymphoma	lymphatic_disorder|lung_disorder	false	true	false	false	high
MONDO:0006284	major salivary gland carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|mouth_disorder	otolaryngology|oncology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|throat_disorder|ear_disorder	false	true	false	false	medium
MONDO:0006285	major salivary gland carcinoma ex pleomorphic adenoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|mouth_disorder	otolaryngology|oncology	adrenal_gland_disease|cancer|autoimmune_diseases	teeth_disorder|throat_disorder	false	true	false	false	high
MONDO:0006286	major salivary gland mucoepidermoid carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|mouth_disorder	otolaryngology|oncology	cancer	upper_gastrointestinal_disorder|throat_disorder|ear_disorder	false	true	false	false	medium
MONDO:0006287	malignancy in giant cell tumor of bone	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	hematology|orthopaedic|oncology	cancer|malignancy	upper_gastrointestinal_disorder|bone_disorder	false	true	false	false	high
MONDO:0006288	malignant adrenal gland pheochromocytoma	endocrine_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|hereditary_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	urology|endocrinology|oncology	adrenal_gland_disease|cancer|malignancy	endocrine_disorder|vascular_disorder	false	true	false	true	very_high
MONDO:0006290	malignant germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0006291	malignant jugulotympanic paraganglioma	connective_tissue_disorder|endocrine_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor|connective_tissue_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	otolaryngology|oncology	adrenal_gland_disease|cancer	throat_disorder|ear_disorder	false	true	false	false	very_high
MONDO:0006292	malignant mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonology|oncology	adrenal_gland_disease|cancer	lymphatic_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0006294	pleural cancer	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|cardiothoracic|oncology	autoimmune_diseases|cancer|inflammatory_disease	lung_disorder	false	true	false	false	very_high
MONDO:0006295	malignant urinary system neoplasm	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer|neoplasm|malignancy	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0006297	maxillary sinus adenoid cystic carcinoma	connective_tissue_disorder|cancer_or_benign_tumor|digestive_system_disorder|nervous_system_disorder|musculoskeletal_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor|digestive_system_disorder|connective_tissue_disorder|mouth_disorder|nervous_system_disorder|musculoskeletal_system_disorder|otorhinolaryngologic_disease	otolaryngology|oncology	adrenal_gland_disease|cancer|maxillary_sinus_adenoid_cystic_carcinoma_is_a_rare_cancer_of_the_paranasal_sinuses	upper_gastrointestinal_disorder|throat_disorder|nose_disorder	false	true	false	false	high
MONDO:0006298	mediastinal malignant germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|cardiothoracic|oncology	cancer	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0006300	medullomyoblastoma with myogenic differentiation	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric	adrenal_gland_disease|cancer	blood_bone_marrow_disorder|brain_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0006301	metanephric adenoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|pediatric|renal_medicine	adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	low
MONDO:0006302	micropapillary serous carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	neurodegenerative_disease|adrenal_gland_disease|cancer	eye_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0006303	middle ear squamous cell carcinoma	otorhinolaryngologic_disease|auditory_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	auditory_system_disorder|nervous_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	oncology|otolaryngology	allergy|inflammatory_disease|autoimmune_diseases|cancer	ear_disorder|throat_disorder	false	true	false	false	high
MONDO:0006304	minor salivary gland adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	oncology|otolaryngology|genetics_and_genomics	adrenal_gland_disease|cancer	ear_disorder|upper_gastrointestinal_disorder|throat_disorder	false	true	false	false	medium
MONDO:0006306	mixed lobular and ductal breast carcinoma	integumentary_system_disorder|cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	oncology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|cancer	breast_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0006307	mixed somatotroph-lactotroph pituitary gland adenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	endocrinology|neurology	cancer|endocrine_disorder	brain_disorder|vascular_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0006309	mucinous gastric adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	inflammatory_disease|cancer|autoimmune_diseases|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006311	myelodysplastic/myeloproliferative neoplasm	cancer_or_benign_tumor|musculoskeletal_system_disorder|immune_system_disorder|hematologic_disorder|connective_tissue_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder	oncology|hematology	anemia|myelodysplastic_neoplasm|cancer|myeloproliferative_neoplasm	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0006312	myofibroma	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	oncology|hematology|genetics_and_genomics|orthopaedic	cancer	joint_disorder|muscle_disorder	false	false	false	false	low
MONDO:0006313	nabothian cyst	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|dermatology	dermatological_condition|female_reproductive_system_disorder	breast_disorder|liver_disorder	false	false	false	false	none
MONDO:0006314	nasal cavity polyp	cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|respiratory_system_disorder	allergy_and_immunology|otolaryngology	allergy|inflammatory_disease	nose_disorder|throat_disorder	false	false	false	true	medium
MONDO:0006316	neuroblastic tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric	cancer|adrenal_gland_disease	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0006317	neurothekeoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	low
MONDO:0006320	non-cutaneous melanoma	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	oncology|hematology|dermatology	adrenal_gland_disease|cancer	lymphatic_disorder|skin_disorder	true	true	false	true	high
MONDO:0006321	non-functioning adrenal cortex adenoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	adrenal_gland_disease|cancer	adrenal_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0006322	non-neoplastic bile duct disorder	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0006323	non-seminomatous lesion	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|urology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0006324	normal breast-like subtype of breast carcinoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|cancer	breast_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0006325	ocular melanoma	disorder_of_development_or_morphogenesis|disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|oncology	adrenal_gland_disease|cancer	eye_disorder|skin_disorder	false	true	false	true	high
MONDO:0006326	ocular melanoma with extraocular extension	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|disorder_of_visual_system|nervous_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|oncology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease|cancer	eye_disorder|skin_disorder	false	true	false	true	very_high
MONDO:0006327	ocular sebaceous carcinoma	integumentary_system_disorder|disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	oncology|dermatology	inflammatory_disease|autoimmune_diseases|cancer	eye_disorder|skin_disorder	false	true	false	false	high
MONDO:0006328	odontogenic cyst	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	otolaryngology|pediatric	neurodegenerative_disease|inflammatory_disease	teeth_disorder|bone_disorder	false	false	false	true	low
MONDO:0006329	olfactory neuroblastoma	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|nose_disorder	false	true	false	false	high
MONDO:0006330	ossifying fibromyxoid tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|oncology|orthopaedic	bone_disease|tumor|cancer	teeth_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0006335	ovarian endometrioid adenocarcinoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	autoimmune_diseases|adrenal_gland_disease_is_not_a_valid_category_for_ovarian_disease_so_that_is_removed|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0006336	ovarian endometrioid adenocarcinoma with squamous differentiation	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0006337	ovarian endometriosis	endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	endocrinology|obstetrics_and_gynecology	cancer|inflammatory_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0006339	ovarian microcystic stromal tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder|endocrine_disorder	false	true	false	false	low
MONDO:0006340	ovarian serous adenofibroma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	endocrine_system_disorder|cancer_or_benign_tumor	connective_tissue_disorder|reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|ovarian_serous_adenofibroma_is_actually_a_type_of_cancer__so_it_should_just_be_categorized_as_cancer	reproductive_system_disorder|ovarian_tumor	false	false	false	false	low
MONDO:0006343	ovarian transitional cell carcinoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0006344	ovarian yolk sac tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|inflammatory_disease|autoimmune_diseases	reproductive_system_disorder	false	true	false	true	high
MONDO:0006345	palmar fibromatosis	cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	dermatology|rheumatology	metabolic_disorder|autoimmune_diseases	skin_disorder|joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0006346	pancreatic acinar cell carcinoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	pancreatic_disease|cancer	upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	false	very_high
MONDO:0006347	pancreatic large cell neuroendocrine carcinoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrinology|oncology|gastroenterology	cancer|neuroendocrine_carcinoma_subtype	upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	false	very_high
MONDO:0006348	pancreatic small cell neuroendocrine carcinoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrinology|oncology|gastroenterology	neuroendocrine_carcinoma|cancer	lower_gastrointestinal_disorder|endocrine_disorder	false	true	false	false	very_high
MONDO:0006349	papillary cystic neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	biliary_disorder|liver_disorder	false	true	false	true	low
MONDO:0006350	papillary transitional cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|oncology|pulmonology	adrenal_gland_disease|transitional_cell_carcinoma|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	medium
MONDO:0006351	parachordoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|hematology	adrenal_gland_disease|cancer	blood_bone_marrow_disorder|spinal_disorder|joint_disorder|bone_disorder	false	true	false	false	medium
MONDO:0006352	paranasal sinus adenoid cystic carcinoma	connective_tissue_disorder|respiratory_system_disorder|otorhinolaryngologic_disease|musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|oncology	cancer	throat_disorder|nose_disorder	false	true	false	true	very_high
MONDO:0006353	paranasal sinus Schneiderian papilloma	connective_tissue_disorder|respiratory_system_disorder|otorhinolaryngologic_disease|musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology|oncology	cancer|inflammatory_disease	throat_disorder|nose_disorder	false	true	false	false	medium
MONDO:0006354	parathyroid hyperplasia	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|genetics_and_genomics|renal_medicine	autoimmune_diseases|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	false	medium
MONDO:0006355	parotid gland acinic cell carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	otolaryngology|oncology	adrenal_gland_disease|cancer	head_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0006356	parotid gland adenoid cystic carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	otolaryngology|oncology	autoimmune_diseases|cancer	ear_disorder|throat_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006357	parotid gland carcinoma ex pleomorphic adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	otolaryngology|oncology	adrenal_gland_disease|cancer	ear_disorder|throat_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0006358	parotid gland squamous cell carcinoma	digestive_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	otolaryngology|oncology	adrenal_gland_disease|cancer	ear_disorder|throat_disorder	false	true	false	false	high
MONDO:0006359	neoplasm with perivascular epithelioid cell differentiation	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|hematology|neurology	neoplasm|cancer	liver_disorder|vascular_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0006360	penile carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0006362	peritoneal mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|hematology|pulmonology|gastroenterology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0006363	peritoneal multicystic mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hepatology|genetics_and_genomics|oncology|hematology|gastroenterology	mesothelioma|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|lung_disorder	false	true	false	false	medium
MONDO:0006364	peritoneal well differentiated papillary mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pulmonology	mesothelioma|cancer	lung_disorder	false	true	false	true	medium
MONDO:0006365	Peutz-Jeghers polyp	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	pediatrics|genetics_and_genomics|gastroenterology	cardiovascular_disorder|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0006366	Peutz-Jeghers polyp of the stomach	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	pediatric|genetics_and_genomics|genetic_disorders|gastroenterology	gastrointestinal_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0006367	pharyngeal adenoid cystic carcinoma	digestive_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|digestive_system_disorder|respiratory_system_disorder	otolaryngology|oncology	adrenal_gland_disease|cancer	throat_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006368	phosphaturic mesenchymal tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	adrenal_gland_disease|cancer	bone_disorder|muscle_disorder	false	true	false	false	high
MONDO:0006369	pineal parenchymal tumor of intermediate differentiation	endocrine_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurological_disorder|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0006372	pituicytoma	endocrine_system_disorder|reproductive_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	endocrine_system_disorder|cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|endocrine_disorder	false	true	false	false	low
MONDO:0006373	pituitary gland adenoma	endocrine_system_disorder|reproductive_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	endocrine_system_disorder|cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrinology|neurology	cancer|inflammatory_disease|neurodegenerative_disease	brain_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0006374	placental choriocarcinoma	reproductive_system_disorder|cancer_or_benign_tumor|obstetric_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|obstetric_disorder|reproductive_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder|vascular_disorder	false	true	false	true	very_high
MONDO:0006375	placental hemangioma	reproductive_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor|obstetric_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|obstetric_disorder|cardiovascular_disorder|reproductive_system_disorder	obstetrics_and_gynecology|hematology	adrenal_gland_disease|cancer	reproductive_system_disorder|vascular_disorder	false	false	false	false	low
MONDO:0006377	pleural biphasic mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pulmonology|cardiothoracic	cancer|inflammatory_disease	pleural_biphasic_mesothelioma_is_more_specifically_a_lung_issue_so_this_category_fits_best|lung_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0006378	pleural epithelioid mesothelioma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology|cardiothoracic	autoimmune_diseases|cancer|inflammatory_disease	pleural_disorder_is_implied_to_be_an_existing_category_in_this_list_but_it_is_not_present|lung_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0006380	pleural sarcomatoid mesothelioma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology|cardiothoracic	autoimmune_diseases|cancer|inflammatory_disease	lung_disorder|vascular_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0006381	plexiform ameloblastoma	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|mouth_disorder	genetics_and_genomics|oncology|neurology|pediatric	adrenal_gland_disease|cancer	bone_disorder|teeth_disorder	false	true	false	false	high
MONDO:0006382	poorly differentiated thyroid gland carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|endocrinology	adrenal_gland_disease|autoimmune_diseases|cancer	endocrine_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0006383	primary cutaneous diffuse large B-cell lymphoma, Leg type	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	oncology|hematology|dermatology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|skin_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0006385	primary intraosseous squamous cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|dermatology|orthopaedic	intraosseous_squamous_cell_carcinoma|cancer	skin_disorder|bone_disorder	false	true	false	false	high
MONDO:0006386	primary peritoneal serous adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0006387	primary pulmonary diffuse large B-cell lymphoma	hematologic_disorder|respiratory_system_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|respiratory_system_disorder|immune_system_disorder	oncology|hematology|pulmonology	lymphoma|cancer	lung_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0006388	prolactin-producing pituitary gland carcinoma	endocrine_system_disorder|reproductive_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder|connective_tissue_disorder	oncology|endocrinology	endocrine_disorder|pituitary_gland_disease|cancer	brain_disorder|pituitary_gland_carcinoma|endocrine_disorder	false	true	false	false	very_high
MONDO:0006389	prostate rhabdomyosarcoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology|pediatric	adrenal_gland_disease|cancer	reproductive_system_disorder|muscle_disorder	false	true	false	false	high
MONDO:0006390	prostate small cell carcinoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	urology|oncology	adrenal_gland_disease|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0006391	pyloric gland adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0006392	rectal hyperplastic polyp	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	gastrointestinal_disease|neoplasm|polyp|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0006393	rectal traditional serrated adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	urology|oncology|gastrointestinal|gastroenterology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0006394	rectal tubular adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	urology|oncology|gastroenterology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0006395	rectal tubulovillous adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006396	rectal villous adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	gastrointestinal_disease|neoplasm|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006397	renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusions	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	genetics_and_genomics|urology|oncology	adrenal_gland_disease|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0006398	retroperitoneal inflammatory myofibroblastic tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology	cancer|inflammatory_disease	lymphatic_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0006400	salivary gland acinic cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology	adrenal_gland_disease|cancer	teeth_disorder|endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0006401	salivary gland adenosquamous carcinoma	digestive_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	oncology|otolaryngology	head_and_neck_cancer|gland_disease|cancer	teeth_disorder|upper_gastrointestinal_disorder|throat_disorder	false	true	false	false	very_high
MONDO:0006402	salivary gland basal cell adenocarcinoma	digestive_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|integumentary_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	oncology|otolaryngology	autoimmune_diseases|neoplasms|endocrine_disorder|adenocarcinoma____corrected_list_removing_non_provided_categories_____cancer|adrenal_gland_disease|cancer|inflammatory_disease|salivary_gland_disease	skin_disorder|teeth_disorder	false	true	false	false	medium
MONDO:0006403	salivary gland carcinoma ex pleomorphic adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer	upper_gastrointestinal_disorder|throat_disorder	false	true	false	true	medium
MONDO:0006404	salivary gland large cell carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|throat_disorder	false	true	false	false	very_high
MONDO:0006405	salivary gland small cell carcinoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	adrenal_gland_disease|cancer	lung_disorder|throat_disorder	false	true	false	false	very_high
MONDO:0006406	sarcomatoid carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonology|orthopaedic|oncology	adrenal_gland_disease|cancer	sarcomatoid_carcinoma|muscle_disorder	false	true	false	false	very_high
MONDO:0006407	sarcomatoid mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonology|cardiothoracic|oncology	adrenal_gland_disease|cancer	pleural_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0006408	sex hormone-producing adrenal cortex adenoma	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|oncology	adrenal_gland_disease|metabolic_disorder|cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0006409	signet ring cell gastric adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0006410	simple endometrial hyperplasia	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|endocrinology	endometrial|metabolic_disorder|cancer|inflammatory_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0006411	sinonasal undifferentiated carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology	adrenal_gland_disease|neurodegenerative_disease|cancer	lung_disorder|upper_gastrointestinal_disorder|nose_disorder	false	true	false	false	very_high
MONDO:0006412	sinus histiocytosis with massive lymphadenopathy	immune_system_disorder	other	immune_system_disorder	hematology|oncology|otolaryngology	autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0006414	skin sarcoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	autoimmune_diseases|cancer|inflammatory_disease	skin_disorder|muscle_disorder	false	true	false	true	medium
MONDO:0006416	small intestinal Burkitt lymphoma	immune_system_disorder|digestive_system_disorder|hereditary_disease|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|hereditary_disease|digestive_system_disorder|post_infectious_disorder|cancer_or_benign_tumor	hematologypediatric|oncology	lymphoma|other_is_incorrect___replace_that_with___cancer|cancer|autoimmune_diseases	lymphatic_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0006417	small intestinal diffuse large B-cell lymphoma	immune_system_disorder|digestive_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|digestive_system_disorder|cancer_or_benign_tumor	hematology|oncology	cancer|autoimmune_diseases	lymphatic_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0006418	small intestinal enteropathy-associated T-cell lymphoma	immune_system_disorder|digestive_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|digestive_system_disorder|cancer_or_benign_tumor	hematology|oncology|gastroenterology|pediatric	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder_lymphatic_disorder_lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006419	small intestinal intraepithelial neoplasia	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	intraepithelial_neoplasia_is_a_precursor_to_cancer|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0006420	small intestinal mucosa-associated lymphoid tissue lymphoma	immune_system_disorder|digestive_system_disorder|hereditary_disease|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|digestive_system_disorder|hereditary_disease|cancer_or_benign_tumor	hematology|oncology|gastroenterology	autoimmune_diseases|cancer	lymphatic_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006421	small intestinal tubular adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	gastrointestinal_disease|cancer|benign_tumor	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0006422	small intestinal tubulovillous adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	gastrointestinal_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006423	soft tissue chondroma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	oncology|orthopaedic	soft_tissue_tumor|cancer	muscle_disorder|joint_disorder	false	false	false	false	low
MONDO:0006424	soft tissue neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|oncology|orthopaedic	soft_tissue_neoplasm|cancer	soft_tissue_neoplasm|muscle_disorder	false	true	false	true	high
MONDO:0006426	spinal cord primitive neuroectodermal tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	anomaly|neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0006427	spindle cell melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	oncology|dermatology	adrenal_gland_disease|cancer	skin_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0006428	splenic diffuse large B-cell lymphoma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0006429	splenic hodgkin lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|post_infectious_disorder|cancer_or_benign_tumor	hematology|oncology	lymphoma|autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0006430	splenic mantle cell lymphoma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0006432	stromal predominant kidney Wilms tumor	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology|pediatric	kidney_disease|pediatric_cancer|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0006435	submandibular gland adenocarcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor	otolaryngology|oncology	adrenal_gland_disease|autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006436	submandibular gland adenoid cystic carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor	otolaryngology|oncology	adrenal_gland_disease|cancer	lymphatic_disorder|teeth_disorder|throat_disorder	false	true	false	true	high
MONDO:0006438	synovial chondromatosis	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	rheumatology|orthopaedic	cancer|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0006442	tendon sheath fibroma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	rheumatology|orthopaedic	inflammatory_disease|benign_tumor____however__since_the_provided_category_list_does_not_have__soft_tissue_disease__or__benign_tumor___i_will_revise_my_answer_to_match_the_given_categories____inflammatory_disease|soft_tissue_disease|cancer	muscle_disorder|joint_disorder	false	false	false	false	low
MONDO:0006444	teratoma with malignant transformation	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|oncology|pediatric	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	true	very_high
MONDO:0006446	testicular embryonal carcinoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	testicular_disorder|reproductive_system_disorder|genitourinary_disorder	false	true	false	true	high
MONDO:0006447	testicular non-seminomatous germ cell tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	germ_cell_cancer|disease|tumor|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0006450	therapy-related myeloid neoplasm	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|immune_system_disorder|connective_tissue_disorder|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	anemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0006451	thymic carcinoma	endocrine_system_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	pulmonology|thoracic|oncology	autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	false	true	false	false	very_high
MONDO:0006452	thymic sarcomatoid carcinoma	endocrine_system_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	pulmonology|oncology|cardiothoracic|pediatric	adrenal_gland_disease|autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	false	true	false	false	very_high
MONDO:0006455	thymic undifferentiated carcinoma	endocrine_system_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	immunology|oncology	adrenal_gland_disease|autoimmune_diseases|cancer	immune_disorder_lymphatic_disorder_bone_disorder	false	true	false	false	high
MONDO:0006456	thymoma	endocrine_system_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0006458	thymoma type B3	endocrine_system_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	immunology|hematology|oncology|allergy_and_immunology	autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0006459	thymoma type B1	endocrine_system_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	immunology|hematology|oncology	autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	false	true	false	false	medium
MONDO:0006460	thyroglossal duct cyst	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|otolaryngology	cancer|inflammatory_disease|thyroglossal_duct_cyst	endocrine_disorder|throat_disorder	false	false	false	false	low
MONDO:0006462	thyroid gland diffuse large B-cell lymphoma	immune_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder|hematologic_disorder	endocrine_system_disorder|cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|endocrine_system_disorder	endocrinology|oncology|hematology	cancer|autoimmune_diseases	lymphatic_disorder|immune_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0006463	thyroid gland mucoepidermoid carcinoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrinology|oncology	cancer|thyroid_gland_disease	thyroid_gland|endocrine_disorder	false	true	false	false	medium
MONDO:0006464	thyroid gland mucosa-associated lymphoid tissue lymphoma	immune_system_disorder|hereditary_disease|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|hereditary_disease|cancer_or_benign_tumor|immune_system_disorder	endocrinology|oncology|hematology	cancer|autoimmune_diseases	lymphatic_disorder|immune_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0006466	thyroid gland spindle cell tumor with thymus-like differentiation	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrinology|oncology	autoimmune_diseases|cancer	immune_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0006467	thyroid gland squamous cell carcinoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrinology|oncology	autoimmune_diseases|cancer	endocrine_disorder|skin_disorder	false	true	false	false	high
MONDO:0006468	thyroid gland undifferentiated (anaplastic) carcinoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrinology|oncology	adrenal_gland_disease|other_is_incorrect_as_per_instructions_so_removing_it___cancer|cancer	endocrine_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0006469	tibial adamantinoma	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|oncology	bone_cancer|malignant_tumor|cancer	teeth_disorder|bone_disorder	false	true	false	false	high
MONDO:0006470	tonsillar squamous cell carcinoma	immune_system_disorder|cancer_or_benign_tumor|digestive_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|digestive_system_disorder|cancer_or_benign_tumor|immune_system_disorder|otorhinolaryngologic_disease	otolaryngology|oncology	cancer|adrenal_gland_disease	lymphatic_disorder|throat_disorder	false	true	false	true	high
MONDO:0006471	tracheal adenoid cystic carcinoma	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology|pulmonology	cancer|adrenal_gland_disease	lung_disorder|throat_disorder	false	true	false	false	high
MONDO:0006474	transitional cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|renal_medicine|oncology	cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0006476	undifferentiated gallbladder carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	hepatology|gastroenterology|oncology	cancer|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0006477	undifferentiated ovarian carcinoma	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	ovarian_carcinoma|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0006478	undifferentiated pancreatic carcinoma	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|oncology	cancer|adrenal_gland_disease|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0006479	undifferentiated pancreatic carcinoma with osteoclast-like giant cells	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|oncology	cancer|autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|bone_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0006480	undifferentiated pleomorphic sarcoma, inflammatory variant	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	genetics_and_genomics|oncology|hematology	cancer|inflammatory_disease	muscle_disorder	false	true	false	false	high
MONDO:0006481	ureter carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer|adrenal_gland_disease|other____cancer_is_more_specific___cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0006482	ureter small cell carcinoma	cancer_or_benign_tumor|endocrine_system_disorder|urinary_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder|endocrine_system_disorder	urology|oncology	cancer|urinary_system_disorder|urological_disease	urinary_tract_disorder|kidney_disorder	false	true	false	false	very_high
MONDO:0006483	urothelial dysplasia	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	uronal_medicine|urology|oncology	cancer|urothelial_dysplasia_is_also_a_precursor_to_cancer	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0006484	usual ductal breast hyperplasia	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	cancer|autoimmune_diseases|adrenal_gland_disease|inflammatory_disease	breast_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0006485	uterine carcinosarcoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	uterus_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0006486	uveal melanoma	cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_development_or_morphogenesis|nervous_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|disorder_of_visual_system|disorder_of_orbital_region|cancer_or_benign_tumor|nervous_system_disorder	ophthalmology|oncology	cancer|adrenal_gland_disease	eye_disorder|skin_disorder	false	true	false	false	high
MONDO:0006487	vaginal adenoid cystic carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006488	vaginal carcinosarcoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	cancer_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0006489	vaginal melanoma	cancer_or_benign_tumor|reproductive_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology|dermatology	cancer|adrenal_gland_disease	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0006490	vaginal squamous cell carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0006491	vulvar lichen sclerosus	inflammatory_disease|hereditary_disease|reproductive_system_disorder|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|reproductive_system_disorder|inflammatory_disease	obstetrics_and_gynecology|dermatology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|skin_disorder	false	false	false	true	medium
MONDO:0006493	Warthin tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	pathology|otolaryngology|oncology	cancer|adrenal_gland_disease	lymphatic_disorder|head_and_neck_disorder	false	false	false	true	low
MONDO:0006496	palsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0006497	cerebral palsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0006498	adenomatous colon polyp	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer|neoplastic_disease|gastrointestinal_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0006499	hamartoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|genetics_and_genomics|gastroenterology|oncology	cancer|neurodegenerative_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0006500	hemangioma	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	hematology|dermatology	cardiovascular_disorder|tumor|cancer	skin_disorder|vascular_disorder	false	false	false	true	low
MONDO:0006502	acute respiratory distress syndrome	syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|syndromic_disease|acute_disease	pulmonology|cardiothoracic|cardiology	autoimmune_diseases|inflammatory_disease	lung_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0006504	acquired metabolic disease	metabolic_disease	metabolic_disease	metabolic_disease	hepatology|renal_medicine|genetics_and_genomics|endocrinology	acquired_metabolic_disease|metabolic_disorder	liver_disorder|endocrine_disorder|metabolic_disease_is_categorized_as_endocrine_disorder_and_more_specifically_acquired_metabolic_disease_would_be_liver_disorder	false	false	false	false	high
MONDO:0006505	basal ganglia cerebrovascular disorder	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|cardiology	neurodegenerative_disease|cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0006506	congenital nonspherocytic hemolytic anemia	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	pediatric|hematology|genetics_and_genomics	anemia|metabolic_disorder	congenital_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0006507	hereditary hemochromatosis	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|hematology|genetics_and_genomics|gastroenterology	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0006509	papillary carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonology|gynecology|oncology	autoimmune_diseases|adrenal_gland_disease|anemia|allergy|neurodegenerative_disease|inflammatory_disease|mental_health_disorder|metabolic_disorder|cardiovascular_disorder|cancer	lung_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0006510	renal tubular transport disease	urinary_system_disorder	other	urinary_system_disorder	pediatric|renal_medicine|genetics_and_genomics	renal_tubular_transport_diseases_often_overlap_with_other_diseases_such_as_metabolic_disorders_because_they_involve_a_defect_in_the_transport_of_molecules_across_renal_tubular_cells_but_can_be_considered_under_this_category|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0006512	estrogen-receptor positive breast cancer	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0006513	estrogen-receptor negative breast cancer	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0006515	acute pancreatitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|inflammatory_disease|acute_disease	hepatology|gastroenterology	inflammatory_disease|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0006517	childhood malignant neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	childhood_malignant_neoplasm|cancer	childhood_malignant_neoplasm|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0006518	sporadic Creutzfeld Jacob disease	infectious_disease|nervous_system_disorder	infectious_disease	infectious_disease|nervous_system_disorder	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|lymphatic_disorder	true	false	false	false	very_high
MONDO:0006519	rectal cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	autoimmune_diseases|inflammatory_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0006520	Achenbach syndrome	syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|syndromic_disease	pulmonology|psychiatry|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	liver_disorder|vascular_disorder	false	false	false	false	low
MONDO:0006521	acneiform dermatitis	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	low
MONDO:0006522	acquired keratosis	integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0006523	acrodermatitis	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0006524	acrodermatitis chronica atrophicans	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease	pediatric|dermatology	autoimmune_diseases|anemia|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0006525	allergic contact dermatitis	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	other	inflammatory_disease|immune_system_disorder|integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|allergy|inflammatory_disease	immune_disorder_skin_disorder	false	false	false	true	medium
MONDO:0006526	allergic urticaria	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	other	inflammatory_disease|immune_system_disorder|integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|allergy|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	low
MONDO:0006527	anhidrosis	integumentary_system_disorder	other	integumentary_system_disorder	neurology|endocrinology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	endocrine_disorder|skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0006528	bacterial exanthem	integumentary_system_disorder|infectious_disease	infectious_disease	infectious_disease|integumentary_system_disorder	pediatric|dermatology	autoimmune_diseases|inflammatory_disease|bacterial_exanthem_is_not_in_the_category_list_therefore__autoimmunediseases	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0006530	cholesteatoma	integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|otolaryngology	cancer|inflammatory_disease	teeth_disorder|ear_disorder	false	false	false	false	medium
MONDO:0006531	cholesteatoma of attic	integumentary_system_disorder|auditory_system_disorder|otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|auditory_system_disorder|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	pediatric|otolaryngology	cancer|inflammatory_disease	ear_disorder|throat_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0006532	cholesteatoma of external ear	integumentary_system_disorder|auditory_system_disorder|otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|auditory_system_disorder|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	pediatric|otolaryngology	cancer|inflammatory_disease	external_ear_disorder|ear_disorder	false	false	false	true	medium
MONDO:0006533	cholesteatoma of middle ear	integumentary_system_disorder|auditory_system_disorder|otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|auditory_system_disorder|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	pediatric|otolaryngology	ear_nose_throat_disease|middle_ear_disorder|inflammatory_disease	ear_disorder|bone_disorder	false	false	false	false	high
MONDO:0006534	cholinergic urticaria	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|allergy	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0006536	congenital generalized lipodystrophy	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	pediatric|dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	muscle_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0006537	conjunctival pigmentation	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	dermatology|ophthalmology	cancer|autoimmune_diseases|anemia|inflammatory_disease|metabolic_disorder	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0006539	diffuse lipomatosis	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	dermatology|genetics_and_genomics	adrenal_gland_disease|inflammatory_disease|metabolic_disorder	muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0006540	dyshidrosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	autoimmune_diseases|allergic_disease|inflammatory_disease	lower_gastrointestinal_disorder|skin_disorder	false	false	false	true	medium
MONDO:0006541	epidermolysis bullosa	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0006543	epidermolysis bullosa dystrophica	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	muscle_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0006544	erythema infectiosum	integumentary_system_disorder|infectious_disease	infectious_disease	infectious_disease|integumentary_system_disorder	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder|skin_disorder	true	false	false	true	low
MONDO:0006545	erythema multiforme	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0006546	erythematosquamous dermatosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0006547	exanthem	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatrics	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	false	medium
MONDO:0006548	facial dermatosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder	false	false	false	false	medium
MONDO:0006549	fibroepithelial polyp of the anus	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0006550	fibroepithelial polyp of urethra	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	autoimmune_diseases|cancer|adrenal_gland_disease	urinary_tract_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0006551	alopecia mucinosa	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	hair_disorder_is_not_listed__but_the_closest_match_would_be_skin_disorder__since_it_s_related_to_scalp|immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0006552	folliculitis	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease	dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0006553	Fox-Fordyce disease	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder_lymphatic_disorder	false	false	false	false	low
MONDO:0006554	granuloma annulare	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	joint_disorder|immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0006555	granulomatous dermatitis	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0006556	hand dermatosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	liver_disorder|skin_disorder	false	false	false	true	medium
MONDO:0006557	hemangioma of subcutaneous tissue	integumentary_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	dermatology|hematology	cancer|other____i_removed__neurodegenerative_disease__from_the_list_because_it_is_highly_unlikely_that_a_subcutaneous_hemangioma_would_fit_under_this_category	vascular_disorder|skin_disorder	false	false	false	true	low
MONDO:0006558	pemphigoid gestationis	integumentary_system_disorder|inflammatory_disease|immune_system_disorder|obstetric_disorder	autoimmune_disease	obstetric_disorder|integumentary_system_disorder|inflammatory_disease|immune_system_disorder	dermatology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0006559	hidradenitis suppurativa	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease	dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0006561	eyelid hypopigmentation	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	dermatology|ophthalmology	autoimmune_diseases|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0006563	inverted follicular keratosis	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	dermatology|oncology	autoimmune_diseases|cancer|skin_condition|inflammatory_disease	skin_disorder	false	false	false	true	low
MONDO:0006564	irritant dermatitis	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease	dermatology	autoimmune_diseases|allergy|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0006565	juvenile dermatitis herpetiformis	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	autoimmune_disease	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	pediatric|dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder_skin_disorder	true	false	false	false	medium
MONDO:0006566	keratosis	integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	true	low
MONDO:0006567	kernicterus due to isoimmunization	metabolic_disease|hematologic_disorder|nervous_system_disorder|hereditary_disease	anemia|metabolic_disease	hematologic_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	pediatric|hematology|obstetrics_and_gynecology	autoimmune_diseases|anemia|metabolic_disorder	liver_disorder|immune_disorder	false	false	false	true	high
MONDO:0006569	leg dermatosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	autoimmune_diseases|dermatitis	skin_disorder|leg_dermatosis	false	false	false	false	medium
MONDO:0006570	lichen disease	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|allergy|inflammatory_disease	liver_disorder|skin_disorder	true	false	false	true	low
MONDO:0006571	lichen nitidus	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0006572	lichen planus	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0006573	lipodystrophy	metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|metabolic_disease	dermatology|endocrinology	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	endocrine_disorder|skin_disorder	false	false	true	false	high
MONDO:0006574	lipomatosis	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	dermatology|orthopaedic	autoimmune_diseases|cancer|metabolic_disorder|inflammatory_disease	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0006576	Ludwig's angina	integumentary_system_disorder|infectious_disease	infectious_disease	infectious_disease|integumentary_system_disorder|mouth_disorder	pulmonology|cardiothoracic	autoimmune_diseases|inflammatory_disease	throat_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0006577	maxillary sinus cholesteatoma	integumentary_system_disorder|musculoskeletal_system_disorder|respiratory_system_disorder|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	musculoskeletal_system_disorder|integumentary_system_disorder|mouth_disorder|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease|respiratory_system_disorder	pediatric|otolaryngology	cancer|inflammatory_disease	nose_disorder|teeth_disorder|ear_disorder	false	false	false	false	medium
MONDO:0006578	mediastinal lipomatosis	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	pulmonology|cardiothoracic	cancer|lipid_dysregulation_disorder	lung_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0006579	melanoacanthoma	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|oncology	cancer	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0006580	miliaria	integumentary_system_disorder|syndromic_disease	other	integumentary_system_disorder|syndromic_disease	pediatric|dermatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	liver_disorder|skin_disorder	false	false	false	true	low
MONDO:0006581	miliaria rubra	integumentary_system_disorder|syndromic_disease	other	integumentary_system_disorder|syndromic_disease	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0006582	mongolian spot	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|dermatology	autoimmune_diseases|skin_condition|congenital_disorder	eye_disorder|skin_disorder	false	false	false	false	none
MONDO:0006583	necrobiosis lipoidica	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|rheumatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	joint_disorder|lower_gastrointestinal_disorder|muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0006585	neurodermatitis	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder	dermatology|neurology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0006586	neurotic excoriation	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	mental_disorder|brain_disorder|neurotic_disorder|skin_disorder	false	false	false	true	medium
MONDO:0006589	occupational dermatitis	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease|occupational_disorder	dermatology|occupational_health	autoimmune_diseases|allergy|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	high
MONDO:0006590	palmoplantar keratosis	disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	skin_disorder	false	false	false	false	medium
MONDO:0006591	panniculitis	inflammatory_disease|connective_tissue_disorder|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease|connective_tissue_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0006592	parapsoriasis	inflammatory_disease|immune_system_disorder|hereditary_disease|integumentary_system_disorder	other	immune_system_disorder|integumentary_system_disorder|inflammatory_disease|hereditary_disease	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0006593	pelvic lipomatosis	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|urology	cancer|inflammatory_disease|metabolic_disorder	reproductive_system_disorder|lymphatic_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0006594	pemphigus	inflammatory_disease|immune_system_disorder|integumentary_system_disorder	autoimmune_disease	immune_system_disorder|integumentary_system_disorder|inflammatory_disease	dermatology|allergy_and_immunology|immunology	autoimmune_diseases|inflammatory_disease	immune_disorder_skin_disorder	false	false	false	true	high
MONDO:0006595	perinatal jaundice due to hepatocellular damage	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|pediatric|hepatology	hepatocellular_damage_is_related_to_liver_function_which_can_also_be_categorized_as_a_type_of_metabolic_disorder|metabolic_disorder	hepatic_disorder|liver_disorder	false	false	false	true	high
MONDO:0006596	photoallergic dermatitis	inflammatory_disease|immune_system_disorder|integumentary_system_disorder	other	immune_system_disorder|integumentary_system_disorder|inflammatory_disease|radiation_induced_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|allergy	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0006597	photosensitivity disease	inflammatory_disease|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease|radiation_induced_disorder	dermatology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	medium
MONDO:0006598	phototoxic dermatitis	inflammatory_disease|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease|radiation_induced_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|allergy	eye_disorder|skin_disorder	false	false	false	true	medium
MONDO:0006599	physical urticaria	inflammatory_disease|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease	dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|allergy	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0006601	pityriasis rosea	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0006602	porokeratosis	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	skin_disorder|liver_disorder	false	false	false	true	medium
MONDO:0006603	reactive cutaneous fibrous lesion	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0006604	rosacea	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|nose_disorder	false	false	false	true	medium
MONDO:0006605	scalp dermatosis	integumentary_system_disorder	other	integumentary_system_disorder	allergy_and_immunology|pediatric|dermatology	dermatological_condition|inflammatory_disease|autoimmune_diseases	skin_disorder|scalp_dermatosis_is_not_in_the_list__immune_disorder	false	false	false	true	medium
MONDO:0006606	scleredema adultorum	integumentary_system_disorder	other	integumentary_system_disorder	cardiology|neurology|dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0006607	sebaceous gland disorder	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0006608	seborrheic dermatitis	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0006609	seborrheic infantile dermatitis	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	low
MONDO:0006610	skin atrophy	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	vascular_disorder|skin_disorder|muscle_disorder|bone_disorder	false	false	false	false	low
MONDO:0006611	skin sarcoidosis	syndromic_disease|connective_tissue_disorder|integumentary_system_disorder	other	connective_tissue_disorder|integumentary_system_disorder|syndromic_disease	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0006612	steroid lipomatosis	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	dermatology|endocrinology	metabolic_disorder|adrenal_gland_disease|inflammatory_disease|cancer	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0006613	stromal corneal pigmentation	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|dermatology	adrenal_gland_disease|cancer|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0006614	subcorneal pustular dermatosis	immune_system_disorder|inflammatory_disease|integumentary_system_disorder	autoimmune_disease	inflammatory_disease|integumentary_system_disorder|immune_system_disorder	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0006615	sweat gland disorder	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|sweat_gland_disorder	false	false	false	true	medium
MONDO:0006616	toxicodendron dermatitis	immune_system_disorder|inflammatory_disease|integumentary_system_disorder	other	inflammatory_disease|integumentary_system_disorder|immune_system_disorder	allergy_and_immunology|dermatology	allergy|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0006617	vesiculobullous skin disease	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0006618	vibratory urticaria	inflammatory_disease|integumentary_system_disorder	other	inflammatory_disease|integumentary_system_disorder	allergy_and_immunology|dermatology	allergy|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0006619	viral exanthem	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	false	medium
MONDO:0006620	vulva fibroepithelial polyp	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	inflammatory_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0006621	vulvar inverted follicular keratosis	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|hereditary_disease|reproductive_system_disorder|integumentary_system_disorder	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder|reproductive_system_disorder	dermatology|obstetrics_and_gynecology	inflammatory_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder|skin_disorder	false	false	false	false	low
MONDO:0006622	vulvar seborrheic keratosis	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|hereditary_disease|reproductive_system_disorder|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder|reproductive_system_disorder|hereditary_disease	dermatology|obstetrics_and_gynecology	inflammatory_disease|cancer|autoimmune_diseases	reproductive_system_disorder|skin_disorder	false	false	false	true	low
MONDO:0006624	overactive bladder	urinary_system_disorder	other	urinary_system_disorder	neurology|renal_medicine|urology	metabolic_disorder|inflammatory_disease|urinary_incontinence	kidney_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0006625	altitude sickness	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|neurology	metabolic_disorder|inflammatory_disease|cardiovascular_disorder	lung_disorder	false	false	false	true	medium
MONDO:0006626	diabetic neuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology|endocrinology	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|vascular_disorder	false	false	true	false	high
MONDO:0006629	osteoarthritis, hip	inflammatory_disease|musculoskeletal_system_disorder	other	inflammatory_disease|musculoskeletal_system_disorder	orthopaedic|rheumatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	true	high
MONDO:0006630	osteoarthritis, spine	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease	orthopaedic|rheumatology	osteoarthritic_disease|musculoskeletal_disorder|spine_condition|inflammatory_disease	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0006631	osteoarthritis, toe	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	true	medium
MONDO:0006632	osteoarthritis, hand	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	true	medium
MONDO:0006633	acalculous cholecystitis	endocrine_system_disorder|urinary_system_disorder|digestive_system_disorder|inflammatory_disease	endocrine_system_disorder	urinary_system_disorder|inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0006634	pituitary gland acidophil adenoma	connective_tissue_disorder|reproductive_system_disorder|musculoskeletal_system_disorder|endocrine_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	endocrinology|neurology	neurodegenerative_disease|cancer	brain_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0006635	Acinetobacter infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|lung_disorder	true	false	false	true	high
MONDO:0006636	Actinobacillus infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric	autoimmune_diseases|infectious_disease	vascular_disorder|immune_disorder	true	false	false	true	medium
MONDO:0006637	acute kidney tubular necrosis	urinary_system_disorder	other	acute_disease|urinary_system_disorder	nephrology|renal_medicine	kidney_disease_is_not_present__so_it_defaults_to_anemia|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0006638	acute retinal necrosis syndrome	inflammatory_disease|nervous_system_disorder|disorder_of_visual_system	other	acute_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|inflammatory_disease	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease	vascular_disorder|eye_disorder	true	false	false	true	high
MONDO:0006639	adrenal cortex carcinoma	urinary_system_disorder|cardiovascular_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder|endocrine_system_disorder	endocrine_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor|urinary_system_disorder	endocrinology|oncology	adrenal_gland_disease|cancer	endocrine_disorder|vascular_disorder	false	true	false	false	high
MONDO:0006640	adrenal gland hyperfunction	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|adrenal_gland_hyperfunction_is_closely_related_to_the_endocrine_system	adrenal_gland_disease|autoimmune_diseases|metabolic_disorder	adrenal_gland_disease|endocrine_disorder	false	false	false	true	high
MONDO:0006641	afferent loop syndrome	digestive_system_disorder	other	digestive_system_disorder	pulmonology|neurology|psychiatry	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0006642	alcohol withdrawal delirium	syndromic_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder	neurology|psychiatry	metabolic_disorder|mental_health_disorder	brain_disorder|mental_disorder	false	false	false	true	very_high
MONDO:0006643	alcoholic cardiomyopathy	cardiovascular_disorder|musculoskeletal_system_disorder|psychiatric_disorder	cardiovascular_disorder|psychiatric_disorder	cardiovascular_disorder|psychiatric_disorder|musculoskeletal_system_disorder	cardiothoracic|cardiovascular|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006644	alcoholic liver cirrhosis	digestive_system_disorder|endocrine_system_disorder|psychiatric_disorder	psychiatric_disorder|endocrine_system_disorder	endocrine_system_disorder|psychiatric_disorder|digestive_system_disorder	hepatology|gastroenterology	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0006645	alcoholic polyneuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	true	high
MONDO:0006646	angioleiomyoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	muscle_disorder|vascular_disorder	false	false	false	false	low
MONDO:0006647	anterior cerebral artery infarction	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|cardiology	neurodegenerative_disease|cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0006648	anterior compartment of tibia syndrome	syndromic_disease|musculoskeletal_system_disorder	other	syndromic_disease|musculoskeletal_system_disorder	rheumatology|orthopaedic	musculoskeletal_disorder|inflammatory_disease	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0006649	anterior ischemic optic neuropathy	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder	neurology|ophthalmology	autoimmune_diseases|cardiovascular_disorder	vascular_disorder|eye_disorder	false	false	false	false	high
MONDO:0006650	anterior spinal artery syndrome	syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease	neurology|orthopaedic	neurological_disorder|cardiovascular_disorder|inflammatory_disease	spinal_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0006651	anterior uveitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|immune_disorder	true	false	false	true	medium
MONDO:0006652	anterolateral myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	adrenal_gland_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006653	anthracosilicosis	respiratory_system_disorder	other	respiratory_system_disorder	occupational_health|rheumatology|pulmonary_medicine	autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder|lung_disorder	false	false	false	false	high
MONDO:0006654	anthracosis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiothoracic	autoimmune_diseases|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|liver_disorder|lung_disorder	false	false	false	false	high
MONDO:0006655	aortic valve prolapse	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0006656	aortitis	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	rheumatology|hematology|cardiology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	heart_disorder|vascular_disorder	true	false	false	true	high
MONDO:0006658	arteriolosclerosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiothoracic|renal_medicine|rheumatology|cardiology	metabolic_disorder|cardiovascular_disorder|inflammatory_disease	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0006659	arteriosclerosis obliterans	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiothoracic|renal_medicine|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006660	arthus reaction	immune_system_disorder	autoimmune_disease	immune_system_disorder	immunology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder	false	false	false	false	low
MONDO:0006662	aseptic meningitis	inflammatory_disease|nervous_system_disorder	other	nervous_system_disorder|inflammatory_disease	neurology|pediatric	autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder|immune_disorder	true	false	false	true	medium
MONDO:0006663	perinatal asphyxia	respiratory_system_disorder	other	respiratory_system_disorder	obstetrics_and_gynecology|neonatology|pediatric	metabolic_disorder|cardiovascular_disorder|perinatal_asphyxia	heart_disorder|brain_disorder|lung_disorder	false	false	false	false	high
MONDO:0006664	atrial septal defect	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiothoracic|pediatrics|cardiology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0006665	chronic atrophic gastritis	digestive_system_disorder|inflammatory_disease	other	digestive_system_disorder|inflammatory_disease	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0006666	atrophy of thyroid	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|thyroid_disorder	false	false	false	false	low
MONDO:0006668	bacterial conjunctivitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	disorder_of_visual_system|disorder_of_orbital_region|infectious_disease|inflammatory_disease	pediatric|ophthalmology	autoimmune_diseases|inflammatory_disease	immune_disorder|eye_disorder	true	false	false	true	low
MONDO:0006669	bacterial endocarditis	cardiovascular_disorder|inflammatory_disease|infectious_disease	infectious_disease|cardiovascular_disorder	cardiovascular_disorder|infectious_disease|inflammatory_disease	pulmonology|hematology|cardiology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	heart_disorder|immune_disorder|vascular_disorder	true	false	false	true	high
MONDO:0006670	bacterial meningitis	inflammatory_disease|nervous_system_disorder|infectious_disease	infectious_disease	infectious_disease|nervous_system_disorder|inflammatory_disease	neurology|pediatric	inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder|immune_disorder	true	false	false	true	high
MONDO:0006671	Bacteroides infectious disease	infectious_disease	infectious_disease	infectious_disease	gastroenterology|infectious_disease	inflammatory_disease|infectious_disease	lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	medium
MONDO:0006672	balanitis	reproductive_system_disorder|inflammatory_disease	other	reproductive_system_disorder|inflammatory_disease	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder_lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0006673	pituitary gland basophil adenoma	cancer_or_benign_tumor|immune_system_disorder|reproductive_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|endocrine_system_disorder|nervous_system_disorder|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|nervous_system_disorder|hematologic_disorder|connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	endocrinology|neurology	neuroendocrine_disease|endocrine_disorder|cancer	brain_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0006676	beriberi	nutritional_disorder	other	nutritional_disorder	endocrinology|neurology|gastroenterology|cardiology	cardiovascular_disorder|metabolic_disorder	muscle_disorder|vascular_disorder|nervous_system_disorder	false	false	false	true	medium
MONDO:0006677	bile reflux	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0006678	bladder calculus	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	inflammatory_disease|metabolic_disorder|cancer	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0006679	bladder neck obstruction	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	urinary_system_disease|prostate_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0006680	blue nevus	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	oncology|dermatology	cancer|skin_condition	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0006681	Borrelia infectious disease	infectious_disease	infectious_disease	infectious_disease	hematolgy|dermatology|infectious_diseases|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0006682	brachial plexus neuritis	inflammatory_disease|nervous_system_disorder	other	nervous_system_disorder|inflammatory_disease	neurology|orthopaedic	inflammatory_disease|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0006683	brachial plexus neuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology|orthopaedic	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0006684	brain edema	nervous_system_disorder	other	nervous_system_disorder	neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0006685	brain hypoxia - ischemia	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|cardiothoracic|cardiology	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0006686	brain stem infarction	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|cardiology|hematology	neurological_disorder|cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0006687	burning mouth syndrome	syndromic_disease	other	syndromic_disease|mouth_disorder	dermatology|neurology	inflammatory_disease|autoimmune_diseases	skin_disorder|oral_disorder	false	false	false	false	high
MONDO:0006688	byssinosis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|allergy_and_immunology	autoimmune_diseases|allergy	respiratory_system_disorder|lung_disorder	false	false	false	false	medium
MONDO:0006690	carotid artery thrombosis	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|cardiology|hematology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0006692	central pontine myelinolysis	nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0006693	cerebral arterial disease	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|cardiology	cerebral_arterial_disease_falls_under_cardiovascular_category_rather_than_being_a_disorder_of_the_adrenal_gland_or_other_option|cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006694	cerebral atherosclerosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	neurology|cardiology	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006696	cervix erosion	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0006698	cholecystolithiasis	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|cardiovascular_disorder|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	medium
MONDO:0006699	choledocholithiasis	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	medium
MONDO:0006700	choroid cancer	cancer_or_benign_tumor|cardiovascular_disorder|nervous_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor|cardiovascular_disorder	disorder_of_orbital_region|cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder|cardiovascular_disorder	ophthalmology|oncology	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases|cancer	veterinary_disorder|eye_disorder|neoplasm_disorder	false	true	false	false	high
MONDO:0006701	chromophobe adenoma	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|nervous_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|reproductive_system_disorder|nervous_system_disorder	urology|endocrinology	adrenal_gland_disease|cancer	endocrine_disorder	false	true	false	true	medium
MONDO:0006702	chronic inflammatory demyelinating polyradiculoneuropathy	inflammatory_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease	disorder_of_development_or_morphogenesis|inflammatory_disease|nervous_system_disorder	neurology|rheumatology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|immune_disorder|spinal_disorder	false	false	false	true	high
MONDO:0006704	CNS demyelinating autoimmune disease	immune_system_disorder	autoimmune_disease	immune_system_disorder	genetics_and_genomics|immunology|neurology|rheumatology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	immune_disorder|brain_disorder	false	false	false	true	high
MONDO:0006705	Bacteroidaceae infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|bacteroidaceae_infectious_disease	immune_disorder|lower_gastrointestinal_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0006706	Bifidobacteriales infectious disease	infectious_disease	infectious_disease	infectious_disease	gastroenterology|obstetrics_and_gynecology|pediatrics	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0006708	Desulfovibrionaceae infectious disease	infectious_disease	infectious_disease	infectious_disease	hematology|gastroenterology|hepatology|pulmonology|infectious_disease	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder|vascular_disorder|liver_disorder	true	false	false	false	medium
MONDO:0006709	common bile duct neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases|cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	true	very_high
MONDO:0006710	complex partial epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0006711	constrictive pericarditis	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	cardiothoracic|cardiology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006712	corneal edema	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	corneal_edema_is_an_eye_problem|eye_disorder	false	false	false	true	medium
MONDO:0006713	corneal neovascularization	inflammatory_disease|disorder_of_visual_system	other	disorder_of_orbital_region|inflammatory_disease|disorder_of_visual_system	ophthalmology	autoimmune_diseases|inflammatory_disease	vascular_disorder|eye_disorder	false	false	false	false	medium
MONDO:0006714	coronary aneurysm	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0006715	coronary stenosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiothoracic|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006716	coronary thrombosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|cardiology	cardiovascular_disorder|inflammatory_disease	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006717	cutaneous fibrous histiocytoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer	skin_disorder	false	false	false	false	low
MONDO:0006718	cutaneous syphilis	reproductive_system_disorder|integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease|reproductive_system_disorder	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0006720	cystic, mucinous, and serous neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|gastroenterology|pathology	adrenal_gland_disease|cancer|other____note__there_is_no_clear_category_that_specifically_matches__cystic__mucinous__and_serous_neoplasm__so_the_best_fit_was_selected_based_on_the_provided_options	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	medium
MONDO:0006721	de Quervain disease	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|joint_disorder	false	false	false	true	medium
MONDO:0006722	dental fluorosis	musculoskeletal_system_disorder	other	mouth_disorder|musculoskeletal_system_disorder	pediatric|general_practice	dental_fluorosis_is_often_caused_by_excessive_fluoride_exposure_in_early_childhood|metabolic_disorder	teeth_disorder	false	false	false	false	medium
MONDO:0006723	denture stomatitis	inflammatory_disease	other	mouth_disorder|inflammatory_disease	pediatric|dermatology|otolaryngology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|teeth_disorder	true	false	false	true	low
MONDO:0006726	diaphragmatic eventration	respiratory_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|respiratory_system_disorder	obstetrics_and_gynecology|pulmonology|pediatric|cardiothoracic	inflammatory_disease|abdominal_wall_anomaly|congenital_abnormality	muscle_disorder|abdominal_disorder|lung_disorder	false	false	false	false	medium
MONDO:0006727	diastolic heart failure	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiothoracic|cardiology	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006729	discrete subaortic stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	pulmonology|cardiothoracic|cardiology	cardiovascular_disorder|adrenal_gland_disease	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0006730	drug psychosis	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	mental_health_disorder	brain_disorder	false	false	false	true	high
MONDO:0006731	drug-induced akathisia	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0006732	drug-induced dyskinesia	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0006733	dry eye syndrome	disorder_of_visual_system|inflammatory_disease|syndromic_disease	other	syndromic_disease|inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|otolaryngology	autoimmune_diseases|inflammatory_disease	eye_disorder|nose_disorder	false	false	false	true	medium
MONDO:0006734	benign duodenal neoplasm	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0006735	duodenogastric reflux	upper_digestive_tract_disorder|hereditary_disease|digestive_system_disorder	other	hereditary_disease|upper_digestive_tract_disorder|digestive_system_disorder	gastroenterology|hepatology|pulmonology	inflammatory_disease|gastro_intestinal_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0006736	dysplasia of cervix	reproductive_system_disorder	other	reproductive_system_disorder	oncology|obstetrics_and_gynecology	inflammatory_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0006737	dystocia	obstetric_disorder	other	obstetric_disorder	obstetrics_and_gynecology	adrenal_gland_disease|metabolic_disorder	reproductive_system_disorder|joint_disorder|blood_bone_marrow_disorder|muscle_disorder	false	false	false	false	high
MONDO:0006738	eccrine acrospiroma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology	autoimmune_diseases|adrenal_gland_disease	skin_disorder	false	true	false	false	low
MONDO:0006739	Ehrlich tumor carcinoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|hematology	adrenal_gland_disease|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0006740	empty sella syndrome	reproductive_system_disorder|endocrine_system_disorder|syndromic_disease|nervous_system_disorder	endocrine_system_disorder	syndromic_disease|nervous_system_disorder|endocrine_system_disorder|reproductive_system_disorder	neurology|neurosurgery	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0006741	encephalomalacia	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	true	false	false	false	high
MONDO:0006742	endemic goiter	endocrine_system_disorder|nutritional_disorder	endocrine_system_disorder	endocrine_system_disorder|nutritional_disorder	endocrinology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	endocrine_disorder|thyroid_disorder	false	false	false	true	medium
MONDO:0006743	endocrine tuberculosis	endocrine_system_disorder|infectious_disease	endocrine_system_disorder|infectious_disease	endocrine_system_disorder|infectious_disease	endocrinology|pulmonology	autoimmune_diseases|inflammatory_disease	endocrine_disorder|lung_disorder	true	false	false	true	medium
MONDO:0006744	endolymphatic hydrops	otorhinolaryngologic_disease|psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder|otorhinolaryngologic_disease	otolaryngology|genetics_and_genomics|pediatric	neurodegenerative_disease|inflammatory_disease	ear_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0006745	endometrioid stromal sarcoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder|muscle_disorder	false	true	false	true	high
MONDO:0006746	endomyocardial fibrosis	cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder	cardiothoracic|cardiology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0006749	mixed epithelioid and spindle cell melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	oncology|dermatology	adrenal_gland_disease|cancer	skin_disorder	false	true	false	true	high
MONDO:0006751	Erysipelothrix infectious disease	infectious_disease	infectious_disease	infectious_disease	infectious_disease|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0006752	Erysipelothrix rhusiopathiae infectious disease	infectious_disease	infectious_disease	infectious_disease	infectious_disease|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|lymphatic_disorder	true	false	false	true	low
MONDO:0006753	Escherichia coli meningitis	inflammatory_disease|infectious_disease|nervous_system_disorder	infectious_disease	nervous_system_disorder|inflammatory_disease|infectious_disease	neurology|pediatric	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0006754	esophageal diverticulosis	upper_digestive_tract_disorder|digestive_system_disorder	other	upper_digestive_tract_disorder|digestive_system_disorder	gastroenterology|pulmonology|cardiothoracic	gastrointestinal_disorder|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0006755	euthyroid sick syndrome	endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder	endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder	false	false	false	false	medium
MONDO:0006757	extrahepatic cholestasis	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0006758	female genital tuberculosis	reproductive_system_disorder	other	reproductive_system_disorder	allergy_and_immunology|pulmonology|obstetrics_and_gynecology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0006759	femoral neuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology|orthopaedic	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0006760	fetal erythroblastosis	hematologic_disorder	anemia	hematologic_disorder	hematology|pediatric|obstetrics_and_gynecology	metabolic_disorder|anemia	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0006761	fibromuscular dysplasia	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	renal_medicine|cardiology|orthopaedic|rheumatology	cardiovascular_disorder|renal_disease__not_in_list_but_related	kidney_disorder|vascular_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0006763	frozen shoulder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	neurology|orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	joint_disorder|spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0006764	fungal meningitis	inflammatory_disease|infectious_disease|nervous_system_disorder	infectious_disease	nervous_system_disorder|inflammatory_disease|infectious_disease	neurology|pediatric	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	true	false	false	true	high
MONDO:0006765	Fusobacterium infectious disease	infectious_disease	infectious_disease	infectious_disease	gastroenterology|hepatology|pulmonology	autoimmune_diseases|gastrointestinal_disease|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0006766	gait apraxia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|orthopaedic	neurodegenerative_disease|adrenal_gland_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0006767	gastric antral vascular ectasia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|gastroenterology	cardiovascular_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|vascular_disorder	false	false	false	false	high
MONDO:0006769	gastroparesis	digestive_system_disorder	other	digestive_system_disorder	neurology|gastroenterology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0006770	giant cell reparative granuloma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	pediatric|pulmonology|gastroenterology	autoimmune_diseases|inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0006771	glossitis	inflammatory_disease	other	inflammatory_disease|mouth_disorder	dermatology|otolaryngology	autoimmune_diseases|inflammatory_disease	teeth_disorder|throat_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0006773	gonadal tissue neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	urology|obstetrics_and_gynecology|oncology	gonadal_tissue_neoplasm_is_a_redundant_duplicate_category_and_can_be_removed_adrenal_gland_disease__cancer|cancer	reproductive_system_disorder|gonadal_tissue_neoplasm	false	true	false	false	high
MONDO:0006774	habitual spontaneous abortion	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics|gastroenterology|hematology	anemia|autoimmune_diseases|metabolic_disorder|inflammatory_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0006777	hairy tongue	other	other	mouth_disorder	dermatology|otolaryngology	autoimmune_diseases|inflammatory_disease	throat_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0006778	halo nevus	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|integumentary_system_disorder	pediatric|dermatology	autoimmune_diseases|neurodegenerative_disease	skin_disorder	false	false	false	false	low
MONDO:0006779	heart aneurysm	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0006781	Helicobacter pylori infectious disease	infectious_disease	infectious_disease	infectious_disease	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0006782	hemometra	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|hematology	anemia|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|lower_gastrointestinal_disorder	true	false	false	false	medium
MONDO:0006783	hemopneumothorax	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology|hematology	inflammatory_disease|cancer	lung_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006784	hemorrhagic disease of newborn	nutritional_disorder|hematologic_disorder	other	nutritional_disorder|hematologic_disorder	pediatric|obstetrics_and_gynecology|hematology	anemia|metabolic_disorder|inflammatory_disease	liver_disorder|vascular_disorder	true	false	false	true	high
MONDO:0006786	hepatic vein thrombosis	digestive_system_disorder|cardiovascular_disorder|endocrine_system_disorder	endocrine_system_disorder|cardiovascular_disorder	cardiovascular_disorder|digestive_system_disorder|endocrine_system_disorder	hepatology|gastroenterology|hematology	cardiovascular_disorder|metabolic_disorder	liver_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006787	hidrocystoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	pediatric|dermatology	neurocutaneous_syndromes_is_not_in_the_list_so__adrenal_gland_disease|inflammatory_disease|cancer|neurodegenerative_disease	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0006789	hyperamylasemia	hematologic_disorder	other	hematologic_disorder	hepatology|renal_medicine|gastroenterology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	liver_disorder|kidney_disorder	false	false	false	false	low
MONDO:0006790	hypercementosis	musculoskeletal_system_disorder	other	mouth_disorder|musculoskeletal_system_disorder	endocrinology|neurology|dermatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|liver_disorder	false	false	false	false	low
MONDO:0006791	hyperemesis gravidarum	obstetric_disorder	other	obstetric_disorder	obstetrics_and_gynecology|gastroenterology	metabolic_disorder|mental_health_disorder	upper_gastrointestinal_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0006792	hyperglobulinemic purpura	integumentary_system_disorder|hematologic_disorder	other	integumentary_system_disorder|hematologic_disorder	allergy_and_immunology|hematology	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0006793	hyperpituitarism	reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder	reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder	endocrinology|pediatrics	endocrine_disorder|metabolic_disorder	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0006794	hypersensitivity vasculitis	inflammatory_disease|immune_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|immune_system_disorder|inflammatory_disease	allergy_and_immunology|rheumatology|dermatology	allergy|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0006795	hypersplenism	immune_system_disorder|hematologic_disorder	other	hematologic_disorder|immune_system_disorder	hematology	autoimmune_diseases|metabolic_disorder|anemia	lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0006796	hypertensive encephalopathy	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	cardiology|neurology|renal_medicine	metabolic_disorder|cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006797	hypertensive retinopathy	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	cardiology|renal_medicine|ophthalmology	metabolic_disorder|cardiovascular_disorder	eye_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0006798	hypervitaminosis A	nutritional_disorder	other	nutritional_disorder	pediatric|endocrinology	metabolic_disorder|inflammatory_disease	endocrine_disorder|liver_disorder	false	false	false	true	medium
MONDO:0006799	hypothalamic neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|endocrine_disorder	false	true	false	false	very_high
MONDO:0006800	ideomotor apraxia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0006801	ileal neoplasm	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	neoplasm|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006802	inappropriate ADH syndrome	syndromic_disease|nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|syndromic_disease|endocrine_system_disorder	neurology|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0006803	inferior myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0006804	inflammatory breast carcinoma	breast_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0006805	intermediate coronary syndrome	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiothoracic|cardiology	inflammatory_disease|cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0006806	intermediate uveitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	rheumatology|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|immune_disorder	true	false	false	true	medium
MONDO:0006807	intestinal perforation	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|general_surgery	inflammatory_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0006808	intracranial arterial disease	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	neurology|cardiothoracic|cardiology	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	true	high
MONDO:0006809	intracranial embolism	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	neurology|hematology|cardiology	inflammatory_disease|cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0006810	intracranial hypertension	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006811	intracranial hypotension	nervous_system_disorder	other	nervous_system_disorder	neurology|headache	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0006812	intracranial vasospasm	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology	cardiovascular_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006813	intradermal nevus	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	dermatology	anemia|autoimmune_diseases|allergy|cancer|neurodegenerative_disease|inflammatory_disease	skin_disorder	false	false	false	false	low
MONDO:0006814	iritis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	true	medium
MONDO:0006815	jejunal cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer_type|gastrointestinal_cancer|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006816	arthropathy	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0006817	juxtacortical osteosarcoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|oncology	cancer|adrenal_gland_disease	bone_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0006820	kidney cortex necrosis	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	autoimmune_diseases|kidney_cortex_necrosis____metabolic_disorder|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0006821	kidney papillary necrosis	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	metabolic_disorder|kidney_disease|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	true	high
MONDO:0006823	Klinefelter syndrome	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|chromosomal_disorder	endocrine_system_disorder	reproductive_system_disorder|chromosomal_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|genetics_and_genomics|pediatric	metabolic_disorder|genetic_condition	chromosome_disorder|endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0006824	Krebs 2 carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonology|cardiothoracic|oncology	cancer|adrenal_gland_disease	blood_bone_marrow_disorder|lung_disorder	false	true	false	false	high
MONDO:0006825	kuru	nervous_system_disorder|infectious_disease	infectious_disease|neurodegenerative_disease	infectious_disease|nervous_system_disorder	neurology|infectious_diseases	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	true	false	false	false	high
MONDO:0006826	kwashiorkor	nutritional_disorder	other	nutritional_disorder	gastroenterology|pediatric	anemia|metabolic_disorder	liver_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0006827	lateral medullary syndrome	nervous_system_disorder|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|nervous_system_disorder	neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0006828	nasal cavity and paranasal sinus lethal midline granuloma	otorhinolaryngologic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor	otolaryngology|oncology	autoimmune_diseases|cancer|inflammatory_disease	nose_disorder|immune_disorder|lymphatic_disorder	true	true	false	true	very_high
MONDO:0006829	leukemoid reaction	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	pediatrics|hematology|oncology	autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0006830	leukoplakia of penis	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	dermatology|urology	inflammatory_disease|cancer	reproductive_system_disorder|skin_disorder	false	false	false	false	medium
MONDO:0006831	leukostasis	hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder	hematology|oncology|pulmonology	inflammatory_disease|autoimmune_diseases|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	very_high
MONDO:0006833	lingual goiter	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|otolaryngology|pulmonology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	endocrine_disorder|throat_disorder	false	false	false	true	medium
MONDO:0006834	lip cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|mouth_disorder	dermatology|oncology	autoimmune_diseases|cancer	oral_disorder|skin_disorder	false	true	false	true	medium
MONDO:0006835	lipoid nephrosis	inflammatory_disease|urinary_system_disorder	other	urinary_system_disorder|inflammatory_disease	renal_medicine|nephrology	inflammatory_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0006836	Listeria meningitis	nervous_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	inflammatory_disease|nervous_system_disorder|infectious_disease	pediatric|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0006837	low tension glaucoma	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	true	medium
MONDO:0006838	lupus vulgaris	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0006839	Lutembacher syndrome	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	developmental_disorder|genetic_disorder|chromosomal_abnormality|cardiovascular_disorder|congenital_heart_disease	heart_disorder|brain_disorder	false	false	false	false	high
MONDO:0006840	lymphangiectasis	cardiovascular_disorder|immune_system_disorder	cardiovascular_disorder	immune_system_disorder|cardiovascular_disorder	cardiology|hematology|oncology	inflammatory_disease|autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0006841	lymphangioendothelioma	cardiovascular_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	immune_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	hematology|oncology|pediatric	lymphatic_disorder|cancer	lymphatic_disorder|vascular_disorder	false	true	false	false	high
MONDO:0006842	lymphangiomyoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|oncology|pediatric	cancer|adrenal_gland_disease	lymphatic_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0006843	macular holes	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0006844	magnesium deficiency	nutritional_disorder	other	nutritional_disorder	neurology|cardiology|endocrinology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|bone_disorder	false	false	false	true	medium
MONDO:0006845	male genital tuberculosis	reproductive_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease	urology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0006846	malignant hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|cardiology	cardiovascular_disorder|autoimmune_diseases|metabolic_disorder	vascular_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0006847	malignant lymphatic vessel tumor	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	inflammatory_disease|autoimmune_diseases|cancer|adrenal_gland_disease	immune_disorder|lymphatic_disorder|vascular_disorder	false	true	false	false	high
MONDO:0006848	marasmus	nutritional_disorder	other	nutritional_disorder	endocrinology|pediatric	anemia|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0006849	mastitis	inflammatory_disease|breast_disorder	other	breast_disorder|inflammatory_disease	obstetrics_and_gynecology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0006850	maxillary sinus neoplasm	otorhinolaryngologic_disease|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|mouth_disorder|connective_tissue_disorder	otolaryngology|oncology	neoplasm|cancer	nose_disorder|maxillary_sinus_is_also_related_to_nose_disorder|upper_gastrointestinal_disorder|maxillary_sinuses_are_part_of_the_upper_gastrointestinal_system|throat_disorder	false	true	false	false	high
MONDO:0006851	meconium aspiration syndrome	syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|syndromic_disease	pediatric|pulmonology	inflammatory_disease|metabolic_disorder|respiratory	lower_gastrointestinal_disorder_lung_disorder	false	false	false	true	high
MONDO:0006853	mesenchymal chondrosarcoma	hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|connective_tissue_disorder	orthopaedic|oncology	cancer	muscle_disorder|bone_disorder	false	true	false	false	very_high
MONDO:0006854	mesenchymoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	orthopaedic|oncology	tumor|cancer	muscle_disorder|bone_disorder	false	true	false	false	medium
MONDO:0006855	mesenteric vascular occlusion	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|gastroenterology|hematology	inflammatory_disease|cardiovascular_disorder	lower_gastrointestinal_disorder|vascular_disorder	false	false	false	false	high
MONDO:0006856	mesothelial neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cardiothoracic|gastroenterology|oncology|hematology	adrenal_gland_disease|autoimmune_diseases|cancer	liver_disorder|lung_disorder	false	true	false	false	high
MONDO:0006857	middle cerebral artery infarction	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	cardiology|neurology	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006858	mouth disorder	other	other		dentistry|otolaryngology|oral__maxillofacial_surgery	inflammatory_disease|oral_disease|metabolic_disorder	teeth_disorder|upper_gastrointestinal_disorder|mouth_disorder_is_not_in_the_list_so_it_s_removed	true	false	false	true	medium
MONDO:0006859	mucinous cystadenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	gastroenterology|oncology	adrenal_gland_disease|inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0006861	myeloid sarcoma	immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder|acute_disease	oncology|hematology	cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0006862	myofascial pain syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic|neurology	inflammatory_disease|mental_health_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0006863	myxosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pathology	adrenal_gland_disease|cancer	soft_tissue_disorder|bone_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0006864	necrotizing sialometaplasia	other	other	mouth_disorder	dermatology|gastroenterology|otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|cancer	teeth_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0006865	necrotizing ulcerative gingivitis	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease|mouth_disorder	dentistry|oral_pathology|pediatric	inflammatory_disease|autoimmune_diseases|cancer	teeth_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0006866	neonatal myasthenia gravis	immune_system_disorder|nervous_system_disorder	autoimmune_disease	immune_system_disorder|nervous_system_disorder	pediatrics|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|immune_disorder	false	false	false	true	medium
MONDO:0006868	neurogenic bowel	digestive_system_disorder	other	digestive_system_disorder	neurogenic_is_a_subset_of_this_category|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0006869	nodular goiter	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	thyroid_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0006871	non-gestational choriocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	blood_bone_marrow_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0006873	nutritional deficiency disease	nutritional_disorder	other	nutritional_disorder	nutritional_deficiency_disease_is_more_directly_related_to_gastroenterology_than_endocrinology_but_both_categories_fit|gastroenterology|endocrinology	anemia|nutritional_deficiency_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0006874	obstructive jaundice	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	gastroenterology_hepatology	inflammatory_disease|metabolic_disorder|cancer	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0006875	ocular hypertension	cardiovascular_disorder|disorder_of_visual_system	cardiovascular_disorder	cardiovascular_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|cardiovascular_disorder|metabolic_disorder	eye_disorder|vital_sign_abnormality	false	false	false	true	medium
MONDO:0006876	ocular tuberculosis	infectious_disease|disorder_of_visual_system	infectious_disease	disorder_of_visual_system|disorder_of_orbital_region|infectious_disease	pulmonology|renal_medicine|rheumatology|ophthalmology|hematology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0006877	oophoritis	inflammatory_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|inflammatory_disease	urology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	liver_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0006878	Moraxellaceae infectious disease	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	respiratory_infection|lung_disorder	true	false	false	false	medium
MONDO:0006879	optic papillitis	inflammatory_disease|disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease|nervous_system_disorder	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	eye_disorder|brain_disorder	true	false	false	true	high
MONDO:0006880	oral leukoedema	other	other	mouth_disorder	oncology|hematology|pediatric	cancer|autoimmune_diseases	teeth_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0006881	orbital cellulitis	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|disorder_of_orbital_region|acute_disease|infectious_disease	otolaryngology|ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	eye_disorder|ear_disorder|orbital_cellulitis_is_closely_related_to_the_orbit_of_the_eye__but_can_be_caused_by_an_infection_in_the_teeth_or_jaw_which_are_located_in_close_proximity_to_the_eye__therefore____eye_disorder|throat_disorder	true	false	false	true	high
MONDO:0006882	orchitis	inflammatory_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|inflammatory_disease	urology|pediatric	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0006883	malignant superior sulcus neoplasm	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	cardiothoracic|oncology|neurology	cancer|malignant_superior_sulcus_neoplasm_is_a_subset_of_cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0006884	panophthalmitis	inflammatory_disease|infectious_disease|disorder_of_visual_system	infectious_disease	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease|infectious_disease	ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder|lymphatic_disorder	true	false	false	false	very_high
MONDO:0006886	thyroid gland papillary and follicular carcinoma	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrinology|oncology	cancer|autoimmune_diseases|thyroid_gland_disease	endocrine_disorder	false	true	false	true	low
MONDO:0006887	parametritis	inflammatory_disease|reproductive_system_disorder|musculoskeletal_system_disorder	other	reproductive_system_disorder|inflammatory_disease|musculoskeletal_system_disorder	obstetrics_and_gynecology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	true	false	false	false	medium
MONDO:0006888	paraneoplastic polyneuropathy	nervous_system_disorder|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|nervous_system_disorder	oncology|neurology	cancer|autoimmune_diseases	muscle_disorder|immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0006889	paraphimosis	reproductive_system_disorder	other	reproductive_system_disorder	urology|pediatric	inflammatory_disease|autoimmune_diseases	skin_disorder|reproductive_system_disorder|joint_disorder	false	false	false	true	medium
MONDO:0006890	parathyroid gland adenoma	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	cancer|metabolic_disorder	parathyroid_gland_adenoma|endocrine_disorder	false	false	false	true	medium
MONDO:0006891	partial motor epilepsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	epilepsy|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0006892	partial sensory epilepsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0006893	Pasteurella hemorrhagic septicemia	infectious_disease	infectious_disease	infectious_disease	hematology|veterinary_medicine	inflammatory_disease|autoimmune_diseases|septicemia	blood_bone_marrow_disorder|immune_disorder|respiratory_disorder	true	false	false	true	low
MONDO:0006894	patellofemoral pain syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|musculoskeletal_disorder	muscle_disorder|joint_disorder	false	false	false	true	medium
MONDO:0006895	penile neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0006896	peptic esophagitis	inflammatory_disease|digestive_system_disorder|upper_digestive_tract_disorder	other	ulcer_disease|digestive_system_disorder|upper_digestive_tract_disorder|inflammatory_disease	cardiology|gastroenterology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0006897	periapical granuloma	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease	radiology|general_pathology___note__the_best_fitting_categories_for_periapical_granuloma_would_be_related_to_the_diagnosis_of_a_jaw_related_condition__specifically_involving_the_periapical_region__the_area_surrounding_the_root_tip_of_a_tooth|oral_pathology|maxillofacial_surgery	cancer|inflammatory_disease	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0006898	periarthritis	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	muscle_disorder|bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0006899	pericoronitis	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease|mouth_disorder	pulmonology|cardiology|rheumatology	inflammatory_disease|autoimmune_diseases	throat_disorder|heart_disorder	true	false	false	true	medium
MONDO:0006900	perinephritis	inflammatory_disease|urinary_system_disorder	other	inflammatory_disease|urinary_system_disorder	renal_medicine|urology	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder	true	false	false	true	medium
MONDO:0006901	peritoneal neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|gastroenterology|oncology	peritoneal_neoplasm|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0006903	peroneal nerve paralysis	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0006904	phimosis	reproductive_system_disorder	other	reproductive_system_disorder	urology|pediatric	inflammatory_disease|neurological_disease|autoimmune_diseases	skin_disorder|urinary_tract_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0006905	pigmented spindle cell nevus	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology	skin_cancer|melanoma|melanocytic_nevus|neurocutaneous_disease|neurofibromatosis|benign_neoplasm|congenital_nevus	skin_disorder|muscle_disorder	false	false	false	false	low
MONDO:0006907	pilar sheath acanthoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|ophthalmology|pediatric	anatomo_epithelial_disorders|cancer	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0006908	pituitary apoplexy	reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder	endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder|reproductive_system_disorder	endocrinology|neurology	pituitary_gland_disease|neurodegenerative_disease	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0006909	pituitary dwarfism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	genetics_and_genomics|endocrinology|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	bone_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0006912	pneumatosis cystoides intestinalis	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|pulmonology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|lung_disorder	false	false	false	false	medium
MONDO:0006913	pneumococcal meningitis	inflammatory_disease|nervous_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|nervous_system_disorder|infectious_disease	pediatric|neurology	inflammatory_disease|autoimmune_diseases	spinal_disorder|immune_disorder|brain_disorder|lung_disorder	true	false	false	true	very_high
MONDO:0006915	polyradiculoneuropathy	nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis	rheumatology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	polyradiculoneuropathy_is_also_associated_with_the_nervous_system|muscle_disorder|nervous_system_disorder	true	false	false	false	high
MONDO:0006916	postcholecystectomy syndrome	digestive_system_disorder|urinary_system_disorder	other	digestive_system_disorder|urinary_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0006917	posterior cerebral artery infarction	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	cardiology|neurology	inflammatory_disease|cardiovascular_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0006918	posterior uveitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_orbital_region|inflammatory_disease|disorder_of_visual_system	ophthalmology|rheumatology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder	true	false	false	true	high
MONDO:0006919	potassium deficiency	nutritional_disorder	other	nutritional_disorder	cardiology|endocrinology|renal_medicine	cardiovascular_disorder|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0006920	prediabetes syndrome	metabolic_disease	metabolic_disease	metabolic_disease	endocrinology	prediabetes_syndrome|metabolic_disorder	endocrine_disorder	false	false	true	true	medium
MONDO:0006921	Actinomycetales infectious disease	infectious_disease	infectious_disease	infectious_disease	infectious_disease|pediatric	inflammatory_disease|autoimmune_diseases|infectious_disease|cancer	immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0006922	Anaplasmataceae infectious disease	infectious_disease	infectious_disease	infectious_disease	hematology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|infectious_disease	immune_disorder|vascular_disorder	true	false	false	true	low
MONDO:0006923	Bacillaceae infectious disease	infectious_disease	infectious_disease	infectious_disease	infectious_disease|pulmonology	inflammatory_disease|autoimmune_diseases|allergy|infectious_disease	immune_disorder|liver_disorder	true	false	false	true	medium
MONDO:0006924	Bartonellaceae infectious disease	infectious_disease	infectious_disease	infectious_disease	hematology|rheumatology	inflammatory_disease|autoimmune_diseases|infectious_disease	immune_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0006925	Fusobacteriaceae infectious disease	infectious_disease	infectious_disease	infectious_disease	obstetrics_and_gynecology|gastroenterology|pediatrics	inflammatory_disease|infectious_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0006926	haemophilus infectious disease	infectious_disease	infectious_disease	infectious_disease	hematology|infectious_diseases	inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0006927	Rickettsiaceae infectious disease	infectious_disease	infectious_disease	infectious_disease	hematology|allergy_and_immunology|infectious_disease|genetics_and_genomics|pulmonology|dermatology|pediatric	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0006929	Proteus infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|urology	inflammatory_disease|autoimmune_diseases	immune_disorder|urinary_tract_disorder|kidney_disorder	true	false	false	true	medium
MONDO:0006930	pseudobulbar palsy	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0006931	pulmonary coin lesion	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology	cancer|inflammatory_disease|autoimmune_diseases	lower_respiratory_disorder|lung_disorder	false	false	false	false	medium
MONDO:0006932	pulmonary edema	respiratory_system_disorder	other	respiratory_system_disorder|acute_disease	cardiothoracic|pulmonology	inflammatory_disease|cardiovascular_disorder	heart_disorder|lung_disorder	false	false	false	true	high
MONDO:0006933	pulmonary plasma cell granuloma	respiratory_system_disorder	other	respiratory_system_disorder	immunology|allergy_and_immunology|pulmonology	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	false	false	false	false	medium
MONDO:0006935	pulmonary subvalvular stenosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic|pulmonology	pulmonary_disease|cardiovascular_disorder	heart_disorder|lung_disorder	false	false	false	true	high
MONDO:0006936	pulmonary valve stenosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|pulmonology|pediatric	autoimmune_diseases|cardiovascular_disorder	heart_disorder|lung_disorder	false	false	false	true	medium
MONDO:0006937	pulpitis	inflammatory_disease|musculoskeletal_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|musculoskeletal_system_disorder|mouth_disorder|infectious_disease	cardiology|pulmonology|neurology	inflammatory_disease|cardiovascular_disorder	teeth_disorder|pulpitis	true	false	false	true	medium
MONDO:0006938	pyelitis	inflammatory_disease|urinary_system_disorder	other	inflammatory_disease|urinary_system_disorder	renal_medicine|urology	inflammatory_disease|urinary_infection_disorder|kidney_disorder	urinary_tract_disorder|kidney_disorder	true	false	false	true	medium
MONDO:0006939	pyelonephritis	reproductive_system_disorder|inflammatory_disease|infectious_disease|urinary_system_disorder	infectious_disease	inflammatory_disease|urinary_system_disorder|infectious_disease|reproductive_system_disorder	renal_medicine|urology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder	true	false	false	true	high
MONDO:0006940	radial nerve lesion	nervous_system_disorder|inflammatory_disease	other	inflammatory_disease|nervous_system_disorder	orthopaedic|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder|nerve_disorder	false	false	false	true	medium
MONDO:0006941	rat-bite fever	infectious_disease	infectious_disease	infectious_disease	pediatric_dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0006944	renal aminoaciduria	urinary_system_disorder	other	urinary_system_disorder	pediatric|renal_medicine|genetics_and_genomics	metabolic_disorder|renal_aminoaciduria_fits_the_description_of_a_metabolic_disorder_where_an_excess_of_certain_amino_acids_is_excreted_in_the_urine	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0006945	renal artery obstruction	urinary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|urinary_system_disorder	urology|renal_medicine	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	kidney_disorder|vascular_disorder	false	false	false	false	high
MONDO:0006946	renal osteodystrophy	musculoskeletal_system_disorder|urinary_system_disorder|endocrine_system_disorder	endocrine_system_disorder	musculoskeletal_system_disorder|endocrine_system_disorder|urinary_system_disorder	urology|renal_medicine|kidney|nephrology	metabolic_disorder|renal_gland_disease	kidney_disorder|renal_osteodystrophy_is_most_commonly_associated_with_kidney_disorder_so_i_will_exclude_bone_disorder|bone_disorder	false	false	false	true	high
MONDO:0006947	renovascular hypertension	urinary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|urinary_system_disorder	renal_medicine|cardiology	cardiovascular_disorder|metabolic_disorder	kidney_disorder|vascular_disorder	false	false	false	true	high
MONDO:0006948	retinal artery occlusion	nervous_system_disorder|disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	disorder_of_visual_system|disorder_of_orbital_region|cardiovascular_disorder|nervous_system_disorder	ophthalmology|neurology	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|eye_disorder	false	false	false	false	medium
MONDO:0006949	retinal drusen	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0006950	retinal vasculitis	inflammatory_disease|nervous_system_disorder|disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region|cardiovascular_disorder|nervous_system_disorder	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease	vascular_disorder|eye_disorder	true	false	false	true	medium
MONDO:0006951	retinal vein occlusion	nervous_system_disorder|disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	disorder_of_visual_system|disorder_of_orbital_region|cardiovascular_disorder|nervous_system_disorder	ophthalmology|neurology	cardiovascular_disorder|inflammatory_disease	vascular_disorder|eye_disorder	false	false	false	true	medium
MONDO:0006952	retinopathy of prematurity	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	disorder_of_visual_system|disorder_of_orbital_region|cardiovascular_disorder|hereditary_disease|nervous_system_disorder	pediatric|ophthalmology|neonatology_is_incorrect_since_it_was_not_in_the_provided_list___corrected_answer__pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	spinal_disorder|eye_disorder	false	false	false	true	high
MONDO:0006953	Rh isoimmunization	hematologic_disorder	other	hematologic_disorder	pediatric|obstetrics_and_gynecology|hematology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0006955	rheumatic heart disease	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	cardiology|rheumatology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	joint_disorder|heart_disorder	false	false	false	true	high
MONDO:0006956	Rickettsiosis	infectious_disease	infectious_disease	infectious_disease	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0006957	root caries	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	pediatric|general_practice|oral_health|oral_health___revised__pediatric	inflammatory_disease|metabolic_disorder	lower_gastrointestinal_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0006960	sciatic neuropathy	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0006961	scrapie	nervous_system_disorder|infectious_disease	infectious_disease	nervous_system_disorder|infectious_disease	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0006962	sebaceous adenocarcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer|adrenal_gland_disease	skin_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0006963	sebaceous gland neoplasm	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	neoplasm|gland_disease|cancer|skin_disease	skin_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0006964	secondary hyperparathyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	renal_medicine|endocrinology	adrenal_gland_disease|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0006965	secondary hypertrophic osteoarthropathy	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0006966	secondary Parkinson disease	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	psychiatry|genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0006968	shoulder impingement syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	overuse_injury|musculoskeletal_disorder|inflammatory_disease	joint_disorder|spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0006969	sialadenitis	inflammatory_disease|immune_system_disorder	other	immune_system_disorder|mouth_disorder|inflammatory_disease	oral_pathology_is_not_listed_but_is_associated_so_otolaryngology_is_correct_also|otolaryngology|dermatology	autoimmune_diseases|inflammatory_disease	oral_disorder|salivary_gland_disorder|teeth_disorder	true	false	false	true	medium
MONDO:0006970	sialolithiasis	other	other	mouth_disorder	urology|otolaryngology|renal_medicine	inflammatory_disease|metabolic_disorder	oral_disorder|lower_gastrointestinal_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0006971	sigmoid neoplasm	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0006972	silo filler disease	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|occupational_health	autoimmune_diseases|inflammatory_disease|metabolic_disorder	lung_disorder|liver_disorder	true	false	false	false	high
MONDO:0006973	skin appendage carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	skin_cancer|cancer|appendage_carcinoma|carcinomas	skin_appendage_carcinoma_is_actually_a_type_of_cancer_so_the_best_fitting_category_would_be_a_subset_of_that_which_is_skin_disorder_and_more_specifically_lower_gastrointestinal_disorder_is_not_a_good_fit_but_its_closest_relation_in_this_list_would_be__upper_gastrointestinal_disorder|skin_disorder	false	true	false	false	medium
MONDO:0006974	small cell sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology|cardiothoracic	cancer|adrenal_gland_disease	lung_disorder|bone_disorder	false	true	false	false	high
MONDO:0006975	smooth muscle tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer|smooth_muscle_tumor_is_a_type_of_cancer_that_arises_from_the_smooth_muscle_cells_in_various_parts_of_the_body__it_can_occur_in_the_uterus__leiomyosarcoma___digestive_tract__and_other_organs	muscle_disorder|smooth_muscle_tumor_does_not_match_so	false	true	false	false	medium
MONDO:0006976	somatostatinoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|oncology	cancer|metabolic_disorder	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0006977	spermatocele	reproductive_system_disorder	other	reproductive_system_disorder	urology	urological_disorder|genitourinary_disorder	urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0006978	splenic infarction	immune_system_disorder|cardiovascular_disorder|hematologic_disorder	cardiovascular_disorder	hematologic_disorder|immune_system_disorder|cardiovascular_disorder	cardiology|hematology	cardiovascular_disorder|inflammatory_disease	immune_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0006980	struma ovarii	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|ovarian_cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0006981	subacute bacterial endocarditis	inflammatory_disease|infectious_disease|cardiovascular_disorder	infectious_disease|cardiovascular_disorder	inflammatory_disease|acute_disease|cardiovascular_disorder|infectious_disease	cardiology|hematology|cardiothoracic	cardiovascular_disorder|inflammatory_disease	blood_bone_marrow_disorder|heart_disorder	true	false	false	true	medium
MONDO:0006982	subacute thyroiditis	inflammatory_disease|endocrine_system_disorder	endocrine_system_disorder	inflammatory_disease|acute_disease|endocrine_system_disorder	endocrinology	autoimmune_diseases|inflammatory_disease	endocrine_disorder|immune_disorder	false	false	false	true	medium
MONDO:0006983	subclavian steal syndrome	syndromic_disease|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|nervous_system_disorder	pulmonology|cardiology|cardiovascular_medicine	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0006984	subdural empyema	nervous_system_disorder|infectious_disease	infectious_disease	nervous_system_disorder|infectious_disease	neurosurgery|neurology	neurological_disease|inflammatory_disease|infectious_disease	brain_disorder|spinal_disorder	true	false	false	true	high
MONDO:0006986	substernal goiter	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	cardiothoracic|pulmonology|endocrinology	autoimmune_diseases|endocrine_disorder	endocrine_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0006987	subvalvular aortic stenosis	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0006988	sulfhemoglobinemia	hematologic_disorder	other	hematologic_disorder	pediatric|genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|genetic_disorder_____i_corrected_to_use_the_provided_category_list	false	false	false	false	medium
MONDO:0006989	suppurative periapical periodontitis	musculoskeletal_system_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|inflammatory_disease	pediatric|orthopaedic|general_medicine|oral_surgery	autoimmune_diseases|inflammatory_disease	teeth_disorder|bone_disorder	true	false	false	true	high
MONDO:0006990	suppurative uveitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|immune_disorder	true	false	false	true	high
MONDO:0006992	syphilitic aortitis	infectious_disease|reproductive_system_disorder	infectious_disease	reproductive_system_disorder|infectious_disease	cardiology|rheumatology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	vascular_disorder|heart_disorder	true	false	false	true	high
MONDO:0006993	systolic heart failure	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|pulmonology|cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0006994	tarsal tunnel syndrome	syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder	orthopaedic|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0006995	tethered spinal cord syndrome	syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder	pediatric|obstetrics_and_gynecology|orthopaedic|neurology	neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0006996	thyroid crisis	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	pediatric|medicine|endocrinology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	true	very_high
MONDO:0006997	tibial neuropathy	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0006998	tonsil cancer	immune_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|digestive_system_disorder|respiratory_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|digestive_system_disorder|respiratory_system_disorder|immune_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology	cancer|adrenal_gland_disease	throat_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0006999	tooth disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	dentistry|otolaryngology	oral_condition|metabolic_disorder	teeth_disorder|bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0007000	Treponema infectious disease	infectious_disease|reproductive_system_disorder	infectious_disease	reproductive_system_disorder|infectious_disease	dermatology|infectiology	infectious_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0007001	tricuspid valve prolapse	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pulmonology|cardiology|cardiothoracic	cardiac|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0007002	trochlear nerve disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|ophthalmology|otolaryngology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007004	type III hypersensitivity disease	immune_system_disorder	autoimmune_disease	immune_system_disorder	allergy_and_immunology|rheumatology	inflammatory_disease|allergy|autoimmune_diseases	joint_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0007005	ulcerative proctosigmoiditis	immune_system_disorder|digestive_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0007006	ulnar neuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology|orthopaedic	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0007007	Ureaplasma urethritis	inflammatory_disease|infectious_disease|urinary_system_disorder	infectious_disease	urinary_system_disorder|infectious_disease|inflammatory_disease	urology|renal_medicine	inflammatory_disease|autoimmune_diseases	kidney_disorder|reproductive_system_disorder	true	false	false	true	low
MONDO:0007008	uremia	urinary_system_disorder	other	urinary_system_disorder	hematology|renal_medicine	metabolic_disorder|inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0007009	ureterolithiasis	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	metabolic_disorder|kidney_disease_is_not_in_the_list_so|cardiovascular_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0007011	uveoparotid fever	syndromic_disease|connective_tissue_disorder	other	syndromic_disease|connective_tissue_disorder	allergy_and_immunology|ophthalmology|rheumatology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder	true	false	false	false	medium
MONDO:0007012	variant Creutzfeldt-Jakob disease	infectious_disease|nervous_system_disorder	infectious_disease	infectious_disease|nervous_system_disorder	neurology|genetics_and_genomics	mental_health_disorder|adrenal_gland_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0007013	vasculogenic impotence	reproductive_system_disorder	other	reproductive_system_disorder	urology|neurology	cardiovascular_disorder|neurodegenerative_disease	muscle_disorder|vascular_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0007014	vibrio infectious disease	infectious_disease	infectious_disease	infectious_disease	hematology|pediatric|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0007015	viral meningitis	inflammatory_disease|infectious_disease|nervous_system_disorder	infectious_disease	infectious_disease|inflammatory_disease|nervous_system_disorder	neurology|pediatric	inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder|immune_disorder	true	false	false	false	medium
MONDO:0007016	vitamin A deficiency	nutritional_disorder	other	nutritional_disorder	pediatrics|dermatology|ophthalmology|gastroenterology	metabolic_disorder|anemia	eye_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0007017	vitreous detachment	disorder_of_visual_system|nervous_system_disorder|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	false	low
MONDO:0007018	vulvitis	inflammatory_disease|reproductive_system_disorder	other	reproductive_system_disorder|inflammatory_disease	dermatology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	skin_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0007019	vulvovaginitis	inflammatory_disease|reproductive_system_disorder	other	reproductive_system_disorder|inflammatory_disease	urology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	low
MONDO:0007020	Wernicke encephalopathy	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	brain_disorder|liver_disorder	false	false	false	true	high
MONDO:0007022	xanthogranulomatous pyelonephritis	inflammatory_disease|infectious_disease|reproductive_system_disorder|urinary_system_disorder	infectious_disease	urinary_system_disorder|reproductive_system_disorder|infectious_disease|inflammatory_disease	urology|renal_medicine	inflammatory_disease|autoimmune_diseases	immune_disorder|urinary_tract_disorder|kidney_disorder	true	false	false	true	high
MONDO:0007023	Yersinia infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	medium
MONDO:0007024	Yersinia pseudotuberculosis infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|infectious_diseases	infectious_disease|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	true	medium
MONDO:0007025	chancre	infectious_disease|reproductive_system_disorder	infectious_disease	infectious_disease|reproductive_system_disorder	dermatology	cancer|inflammatory_disease|autoimmune_diseases	skin_disorder|lower_gastrointestinal_disorder|lymphatic_disorder|immune_disorder	true	false	false	true	low
MONDO:0007027	metabolic dysfunction-associated steatohepatitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|inflammatory_disease|digestive_system_disorder	hepatology|gastroenterology	metabolic_disorder|metabolic_dysfunction_associated_steatohepatitis_is_actually_part_of_this_category_but_i_assume_you_want_the_general_one_so___metabolic_disorder|inflammatory_disease	endocrine_disorder|liver_disorder	false	false	true	true	high
MONDO:0007028	rotator cuff syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology|neurology	musculoskeletal_disorder|inflammatory_disease	muscle_disorder|joint_disorder	false	false	false	true	medium
MONDO:0007029	branchio-oto-renal syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	urology|pediatric|genetics_and_genomics	renal_disease|inflammatory_disease|autoimmune_diseases	ear_disorder|kidney_disorder	false	false	false	false	high
MONDO:0007030	autosomal dominant Aarskog syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|neurodegenerative_disease	joint_disorder|urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0007031	familial abdominal aortic aneurysm	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	cardiology|genetics_and_genomics|cardiovascular___generally_accepted_spelling	cardiovascular_disorder|genetic_disorder	lower_gastrointestinal_disorder|vascular_disorder	false	false	false	true	high
MONDO:0007032	prune belly syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|urinary_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|urinary_system_disorder|hereditary_disease|syndromic_disease	urology|renal_medicine|pediatric|genetics_and_genomics	metabolic_disorder|renal_dysfunction	kidney_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0007033	abducens nerve palsy	nervous_system_disorder	other	nervous_system_disorder	neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007034	Adams-Oliver syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	neurology|pediatric|genetics_and_genomics	anemia|metabolic_disorder|neurodegenerative_disease	muscle_disorder|heart_disorder|joint_disorder|skeletal_disorder|vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0007035	acanthosis nigricans	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease	dermatology|endocrinology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	skin_disorder|endocrine_disorder	false	false	true	false	medium
MONDO:0007036	Achard syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|endocrinology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|endocrine_disorder|vascular_disorder	false	false	true	false	medium
MONDO:0007037	achondroplasia	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disease	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007038	Achoo syndrome	hereditary_disease	other	hereditary_disease	pulmonology|allergy_and_immunology|otolaryngology	autoimmune_diseases|allergy	immune_disorder|upper_gastrointestinal_disorder|nose_disorder	false	false	false	true	medium
MONDO:0007039	NF2-related schwannomatosis	cancer_or_benign_tumor|nervous_system_disorder|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007040	Sakati-Nyhan syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	developmental_disorders|genetics_and_genomics|pediatrics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder|joint_disorder|skin_disorder|brain_disorder	false	false	false	false	high
MONDO:0007041	Apert syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|skeletal_dysplasia	teeth_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0007042	Saethre-Chotzen syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	endocrinology|genetics_and_genomics|pediatrics|dermatology	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	bone_disorder|ear_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007043	Pfeiffer syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	pediatric|pulmonology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	hearing_loss_disorder|lower_gastrointestinal_disorder|lung_disorder|skeletal_dysplasia_disorder|throat_disorder|ear_disorder|kidney_disorder	false	false	false	false	high
MONDO:0007044	Acrodysostosis 1 with or without hormone resistance	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	endocrinology|genetics_and_genomics|orthopaedic	metabolic_disorder|anemia	endocrine_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007045	acrofacial dysostosis, Catania type	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic|dermatology	autoimmune_diseases|metabolic_disorder	teeth_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007046	hereditary papulotranslucent acrokeratoderma	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics|dermatology	genetic_condition|metabolic_disorder	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0007047	punctate palmoplantar keratoderma type III	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0007048	acrokeratosis verruciformis	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0007049	acroleukopathy, symmetric	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder|brain_disorder	false	false	false	false	none
MONDO:0007050	acromegaloid changes, cutis verticis gyrata, and corneal leukoma	hereditary_disease	other	hereditary_disease	ophthalmology|endocrinology|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder|endocrine_disorder|skin_disorder	false	false	false	true	medium
MONDO:0007051	acromegaloid facial appearance syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	endocrinology|genetics_and_genomics	metabolic_disorder|genetic_disorder|endocrine_disorder	growth_disorder|endocrine_disorder|bone_disorder|facial_disorder	false	false	false	false	medium
MONDO:0007052	growth hormone secreting pituitary adenoma 1	endocrine_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder|connective_tissue_disorder|reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrinology|neurology	adenoma|pituitary_disease|neuroendocrine_disorders	endocrine_disorder|brain_disorder	false	false	false	true	medium
MONDO:0007054	acromial dimples	hereditary_disease	other	hereditary_disease	orthopaedic|dermatology	metabolic_disorder|neurodegenerative_disease	bone_disorder|skin_disorder	false	false	false	false	low
MONDO:0007055	Acromicric dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	endocrinology|genetics_and_genomics|orthopaedic	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007056	acroosteolysis	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|skin_disorder	false	false	false	false	low
MONDO:0007057	acroosteolysis dominant type	syndromic_disease|connective_tissue_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|connective_tissue_disorder|syndromic_disease	genetics_and_genomics|orthopaedic	metabolic_disorder|neurodegenerative_disease	muscle_disorder|bone_disorder|spinal_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0007058	Acropectorovertebral dysplasia	disorder_of_development_or_morphogenesis|respiratory_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	respiratory_system_disorder|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0007059	acrorenal syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	endocrinology|genetics_and_genomics|renal_medicine	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|bone_disorder|kidney_disorder	false	false	false	false	high
MONDO:0007060	spermatogenic failure 6	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	anemia|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0007062	adactylia, unilateral	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|orthopaedic	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	joint_disorder|ear_disorder	false	false	false	false	medium
MONDO:0007064	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency	immune_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|immune_system_disorder|metabolic_disease	pediatric|genetics_and_genomics|allergy_and_immunology	autoimmune_diseases|cancer|inflammatory_disease|metabolic_disorder	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0007066	adenosine triphosphatase deficiency, anemia due to	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0007067	pyruvate kinase hyperactivity	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hematatology|endocrinology|genetics_and_genomics	metabolic_disorder	muscle_disorder|metabolic_disorder|liver_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0007068	adenylosuccinate lyase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|neurology	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|enzyme_disorder|liver_disorder	false	false	false	false	high
MONDO:0007070	adiposis dolorosa	integumentary_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	dermatology|endocrinology	metabolic_disorder|inflammatory_disease	muscle_disorder|skin_disorder	false	false	false	true	high
MONDO:0007071	adrenocortical hypofunction, chronic primary congenital	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	pediatric|endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	congenital_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0007072	ADULT syndrome	integumentary_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|integumentary_system_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|adult_onset_disorders	false	false	false	true	high
MONDO:0007073	Hypoglossia-hypodactyly syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	teeth_disorder|lower_gastrointestinal_disorder|joint_disorder|throat_disorder	false	false	false	false	high
MONDO:0007074	ainhum	integumentary_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|connective_tissue_disorder|integumentary_system_disorder	general_surgery|pediatric|orthopaedic	inflammatory_disease|metabolic_disorder	lower_gastrointestinal_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0007075	alacrima, congenital, autosomal dominant	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	urinary_tract_disorder|eye_disorder|ear_disorder|nose_disorder	false	false	false	false	medium
MONDO:0007077	Tietz syndrome	integumentary_system_disorder|disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|integumentary_system_disorder	genetics_and_genomics|neurology	autoimmune_diseases|adrenal_gland_disease|inflammatory_disease	immune_disorder|liver_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0007078	pseudohypoparathyroidism type 1A	metabolic_disease|disorder_of_development_or_morphogenesis|urinary_system_disorder|musculoskeletal_system_disorder|hereditary_disease|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder	urinary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|metabolic_disease|endocrine_system_disorder	endocrinology|genetics_and_genomics	metabolic_disorder|genetic_disease	endocrine_disorder|bone_disorder	false	false	false	false	high
MONDO:0007079	alcohol dependence	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	very_high
MONDO:0007080	glucocorticoid-remediable aldosteronism	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	cardiology|endocrinology|renal_medicine	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0007082	alopecia areata 1	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	low
MONDO:0007083	autosomal dominant palmoplantar keratoderma and congenital alopecia	syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|integumentary_system_disorder	dermatology|pediatric|genetics_and_genomics	congenital_disease|metabolic_disorder|skin_condition|genetic_disorder|neurodegenerative_disease	congenital_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007084	familial focal alopecia	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	hair_disorder|skin_disorder	false	false	false	false	low
MONDO:0007085	alopecia-epilepsy-pyorrhea-intellectual disability syndrome	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease|integumentary_system_disorder	genetics_and_genomics|neurology|dermatology	intellectual_disability|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	intellectual_disability_suggests__joint_disorder__although_not_a_direct_match__is_incorrect___immune_disorder|skin_disorder|brain_disorder	false	false	false	false	high
MONDO:0007086	autosomal dominant Alport syndrome	syndromic_disease|urinary_system_disorder|hereditary_disease|inflammatory_disease	other	urinary_system_disorder|hereditary_disease|inflammatory_disease|syndromic_disease	renal_medicine|genetics_and_genomics	metabolic_disorder|anemia|autoimmune_diseases	kidney_disorder|eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0007087	alternating hemiplegia of childhood 1	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007088	Alzheimer disease type 1	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	lymphatic_disorder|vessel|muscle_disorder|immune_disorder|blood_bone_marrow_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0007089	Alzheimer disease 2	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	very_high
MONDO:0007090	amastia, bilateral, with ureteral triplication and dysmorphism	hereditary_disease	other	hereditary_disease	urology|pediatric|genetics_and_genomics	developmental_disorder|metabolic_disorder|anatomic_anomaly|genetic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0007091	amelia and terminal transverse hemimelia	hereditary_disease	other	hereditary_disease	pediatric|orthopaedic	metabolic_disorder|amniotic_band_syndrome|congenital_abnormality	muscle_disorder|limb_disorder|bone_disorder	false	false	false	true	high
MONDO:0007092	amelogenesis imperfecta type 1B	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	genetics_and_genomics|pediatrics|dermatology	metabolic_disorder|anemia|inflammatory_disease	teeth_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0007093	hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	pediatric|genetics_and_genomics|dentistry	metabolic_disorder|anemia|inflammatory_disease|autoimmune_diseases	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007094	amelogenesis imperfecta type 1A	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	pediatric|rheumatology|genetics_and_genomics|hematology|dermatology	metabolic_disorder|anemia|genetic_disorder	teeth_disorder|bone_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0007095	ameloonychohypohidrotic syndrome	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease|integumentary_system_disorder	pediatric|genetics_and_genomics|dermatology	metabolic_disorder|anemia|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	immune_disorder|teeth_disorder|bone_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0007096	amenorrhea-galactorrhea syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|endocrinology|obstetrics_and_gynecology	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0007097	Finnish type amyloidosis	metabolic_disease|syndromic_disease|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease|syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder|vascular_disorder	false	false	false	true	high
MONDO:0007098	ACys amyloidosis	metabolic_disease|nervous_system_disorder|cardiovascular_disorder|hereditary_disease	metabolic_disease|cardiovascular_disorder	nervous_system_disorder|hereditary_disease|cardiovascular_disorder|metabolic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	immune_disorder|liver_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0007099	familial visceral amyloidosis	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|gastroenterology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0007100	familial amyloid neuropathy	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0007101	familial primary localized cutaneous amyloidosis	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases	cutaneous_amyloidosis|skin_disorder	false	false	false	false	medium
MONDO:0007102	amyotrophic dystonic paraplegia	hereditary_disease	other	hereditary_disease	neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007103	amyotrophic lateral sclerosis type 1	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0007104	amyotrophic lateral sclerosis-parkinsonism-dementia complex	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease|cancer|inflammatory_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0007105	frontotemporal dementia and/or amyotrophic lateral sclerosis 1	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0007106	anal sphincter dysplasia	hereditary_disease	other	hereditary_disease	obstetrics_and_gynecology|pediatric|urology|gastroenterology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0007107	anal sphincter myopathy, internal	hereditary_disease	other	hereditary_disease	urology|neurology	neurodegenerative_disease|inflammatory_disease	muscle_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0007108	anal canal carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|anemia|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0007109	congenital dyserythropoietic anemia type 3	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	pediatric|genetics_and_genomics|hematology	anemia|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0007110	Diamond-Blackfan anemia 1	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	autoimmune_diseases|anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0007111	aneurysm, intracranial berry type 1	hereditary_disease|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|hereditary_disease	general_surgery|neurology|vascular_surgery|cardiology	neurodegenerative_disease|cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0007112	interventricular septum aneurysm	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic	congenital_heart_defect|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0007113	Angelman syndrome	hereditary_disease|nervous_system_disorder|syndromic_disease	other	nervous_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007114	Angel-shaped phalango-epiphyseal dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	genetic_dysplasia|developmental_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007115	angioma serpiginosum, autosomal dominant	integumentary_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	genetics_and_genomics|dermatology|pediatrics	neurodegenerative_disease	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0007116	hereditary neurocutaneous angioma	cancer_or_benign_tumor|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|dermatology	neurocutaneous_syndrome|genetic_disorder	vascular_disorder|skin_disorder	false	false	false	false	high
MONDO:0007118	isolated anhidrosis with normal sweat glands	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	neurology|endocrinology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0007119	isolated aniridia	disorder_of_visual_system|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder|aniridia_is_a_genetic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0007120	aniridia-absent patella syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|orthopaedic|ophthalmology|pediatric	developmental_disorder|genetic_disorder|metabolic_disorder	eye_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007121	aniridia, microcornea, and spontaneously Reabsorbed cataract	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology	genetic_disorder|metabolic_disorder	eye_disorder	false	false	false	false	low
MONDO:0007122	anisocoria	hereditary_disease	other	hereditary_disease	neurology|ophthalmology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|allergy	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0007123	ankyloblepharon filiforme adnatum-cleft palate syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|otolaryngology|pediatric	adrenal_gland_disease|metabolic_disorder	eye_disorder|cleft_palate_syndrome_is_not_explicitly_listed_so_exclude_that_part|joint_disorder	false	false	false	false	high
MONDO:0007124	ankyloblepharon-ectodermal defects-cleft lip/palate syndrome	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|orthopaedic|ophthalmology|otolaryngology|pediatric	autoimmune_diseases|neurodegenerative_disease|anemia|inflammatory_disease|metabolic_disorder	eye_disorder|cleft_palate_syndrome_category_not_in_list|joint_disorder	false	false	false	false	medium
MONDO:0007125	ankyloglossia	hereditary_disease	other	hereditary_disease|mouth_disorder	otolaryngology|pediatric	autoimmune_diseases|inflammatory_disease	throat_disorder|joint_disorder	false	false	false	true	low
MONDO:0007127	diffuse idiopathic skeletal hyperostosis	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|idiopathic_disease|hereditary_disease	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007128	annular erythema	hereditary_disease	other	hereditary_disease	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0007129	tooth agenesis, selective, 1	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|mouth_disorder	genetics_and_genomics|otolaryngology|pediatric	autoimmune_diseases|anemia_____corrected_to_exclude_duplicate___metabolic_disorder|anemia|metabolic_disorder	teeth_disorder	false	false	false	false	medium
MONDO:0007130	congenital total pulmonary venous return anomaly	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	congenital_anomalie__none_of_the_provided_options_exactly_match__congenital_anomalie|cardiology|pediatric	congenital_anomaly|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0007131	anonychia with flexural pigmentation	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|dermatology|pediatric	anemia|metabolic_disorder|autoimmune_diseases	skin_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007132	anonychia-ectrodactyly	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases	muscle_disorder|bone_disorder|skin_disorder|joint_disorder	false	false	false	true	medium
MONDO:0007133	anonychia-onychodystrophy with brachydactyly type b and ectrodactyly	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	genetic_condition|metabolic_disorder|ectodermal_dysplasia	bone_disorder|skin_disorder|joint_disorder	false	false	false	false	high
MONDO:0007134	Cooks syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	hepatology|gastroenterology|pediatrics	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0007135	nonsyndromic congenital nail disorder 6	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric	neurodegenerative_disease|metabolic_disorder	nail_disorder|skin_disorder	false	false	false	false	low
MONDO:0007136	hereditary anorectal anomalies	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|genetic_disorders|gastroenterology|genetics_and_genomics___becomes|genetics|pediatrics|genomics|pediatric	anorectal_anomalies|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0007137	isolated congenital anosmia	otorhinolaryngologic_disease|hereditary_disease	other	otorhinolaryngologic_disease|hereditary_disease	neurology|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	brain_disorder|nose_disorder	false	false	false	false	low
MONDO:0007138	anterior segment dysgenesis 1	hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007142	Townes-Brocks syndrome	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric	cardiovascular_disorder|metabolic_disorder	heart_disorder|spinal_disorder|congenital_heart_disorders|blood_bone_marrow_disorder|joint_disorder	false	false	false	false	high
MONDO:0007143	aortic arch anomaly-facial dysmorphism-intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|cardiology|pediatric	intellectual_disability|cardiovascular_disorder	facial_dysmorphism|heart_disorder|vascular_disorder|intellectual_disability	false	false	false	false	high
MONDO:0007144	aortic arch interruption, facial palsy, and retinal coloboma	hereditary_disease	other	hereditary_disease	neonatology|cardiology|ophthalmology|pediatric	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder|eye_disorder	false	false	false	false	high
MONDO:0007145	aplasia cutis congenita	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology|hematology|pediatric	neurodegenerative_disease|anemia	skin_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0007147	obstructive sleep apnea syndrome	syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|syndromic_disease|sleep_disorder	cardiothoracic|pulmonology	cardiovascular_disorder|metabolic_disorder	respiratory_system_disorder|lung_disorder	false	false	false	true	medium
MONDO:0007150	arcus senilis	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	dermatology|ophthalmology	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	none
MONDO:0007151	arms, malformation of	hereditary_disease	other	hereditary_disease	oncology|pediatric	neurodegenerative_disease|cancer	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0007152	arrhythmogenic right ventricular dysplasia 1	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiology|cardiothoracic|pediatric|genetics_and_genomics	cardiovascular_disorder|arrhythmogenic_right_ventricular_dysplasia	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007153	arteries, anomalies of	hereditary_disease	other	hereditary_disease	vascular_surgery|renal_medicine|hematology|cardiology|cardiothoracic|pulmonology	arteries__anomalies_of_fits_under_this_category_as_it_deals_with_issues_related_to_the_arteries|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0007154	arteriovenous malformations of the brain	hereditary_disease|cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|hereditary_disease	neurology	neurological_disorders|cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0007155	arteritis, familial granulomatous, with juvenile polyarthritis	hereditary_disease	other	hereditary_disease	rheumatology|pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder|joint_disorder	false	false	false	false	high
MONDO:0007156	arthritis, sacroiliac	hereditary_disease	other	hereditary_disease	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	spinal_disorder|bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0007157	arthrogryposis, distal, type 1A	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	neurology|orthopaedic|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	muscle_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007158	arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	neurology|orthopaedic|ophthalmology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	muscle_disorder|eye_disorder|joint_disorder	false	false	false	false	high
MONDO:0007159	arthrogryposis-like hand anomaly-sensorineural deafness syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	ear_disorder|muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0007160	Stickler syndrome type 1	syndromic_disease|connective_tissue_disorder|disorder_of_visual_system|hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	connective_tissue_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder|syndromic_disease	neurology|orthopaedic|rheumatology|ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder|joint_disorder	false	false	false	false	high
MONDO:0007161	spermatogenic failure 2	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|endocrinology	anemia|metabolic_disorder	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0007162	asymmetric short stature syndrome	hereditary_disease	other	hereditary_disease	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	growth_disorder|bone_disorder|endocrine_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007163	episodic ataxia type 2	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0007164	spastic ataxia 1	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0007165	spastic ataxia 7	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0007166	ataxia with fasciculations	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007167	atelosteogenesis type I	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	developmental_genetics|pediatric|endocrinology|genetics_and_genomics	anemia|metabolic_disorder|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0007168	atelosteogenesis type III	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|skeletal_system_disorder|joint_disorder	false	false	false	false	high
MONDO:0007170	atresia of external auditory canal and conductive deafness	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	pediatric|otolaryngology	conductive_deafness_is_not_a_direct_fit_in_this_list_but_the_condition_may_involve_an_inflammatory_component______atresia_of_external_auditory_canal_and_conductive_deafness_is_more_closely_related_to_conductive_deafness_which_could_be_linked_to__inflammatory_disease|inflammatory_disease	conductive_deafness|ear_disorder	false	false	false	false	medium
MONDO:0007171	atrial standstill 1	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiothoracic|pulmonology|cardiology	cardiovascular_disorder|atrial_standstill	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0007172	atrial septal defect 1	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	pediatrics|cardiology	cardiovascular_disorder|heart_disease|congenital_heart_disease	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0007173	atrial septal defect 7	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	pediatric|cardiothoracic|pulmonology|cardiology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0007174	Lown-Ganong-Levine syndrome	syndromic_disease	other	syndromic_disease	neurology|renal_medicine|genetics_and_genomics|cardiology	adrenal_gland_disease|metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0007175	PR interval, variation in	hereditary_disease	other	hereditary_disease	cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0007176	helicoid peripapillary chorioretinal degeneration	hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|vision_related_disorder	false	false	false	false	high
MONDO:0007177	auriculoosteodysplasia	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatrics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	bone_disorder|ear_disorder	false	false	false	false	medium
MONDO:0007178	aurocephalosyndactyly	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0007179	autoimmune disease	immune_system_disorder		immune_system_disorder	rheumatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|autoimmune_disease	false	false	false	true	high
MONDO:0007180	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics|orthopaedic|ophthalmology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|eye_disorder|muscle_disorder|skeletal_disorder	false	false	false	false	very_high
MONDO:0007181	axial osteomalacia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	endocrinology|rheumatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007182	Machado-Joseph disease	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|psychiatric_disorder|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007183	azotemia, familial	hereditary_disease	other	hereditary_disease	renal_medicine|hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	high
MONDO:0007184	alopecia, androgenetic, 1	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	endocrinology|dermatology	metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0007185	Banki syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	endocrinology|pediatric	adrenal_gland_disease|metabolic_disorder	kidney_disorder|endocrine_disorder|ear_disorder	false	false	false	false	low
MONDO:0007186	gastroesophageal reflux disease	hereditary_disease|upper_digestive_tract_disorder|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease|upper_digestive_tract_disorder	cardiothoracic|pulmonology|gastroenterology|cardiology|hepatology	autoimmune_diseases|inflammatory_disease|gastrointestinal_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0007187	nevoid basal cell carcinoma syndrome	syndromic_disease|hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|hereditary_disease|syndromic_disease|nervous_system_disorder	dermatology|genetics_and_genomics|oncology	hereditary_cancer_syndrome|neurocutaneous_syndrome|inheritable_cancer|genetic_disorder|family_cancer_predisposition_syndrome___corrected_to_fit_the_format___cancer|cancer	skin_disorder|bone_disorder|muscle_disorder	false	true	false	true	medium
MONDO:0007188	primary basilar invagination	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	neurology|pediatric|otolaryngology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007190	leukemia, chronic lymphocytic, susceptibility to, 2	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	hematology|oncology	allergy|autoimmune_diseases|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0007191	Behcet disease	syndromic_disease|integumentary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder|integumentary_system_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|joint_disorder|eye_disorder|vascular_disorder	false	false	false	false	high
MONDO:0007192	beta-amino acids, renal transport of	hereditary_disease	other	hereditary_disease	renal_medicine|genetics_and_genomics	renal_transport|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0007193	primary biliary cholangitis 1	hereditary_disease|digestive_system_disorder|endocrine_system_disorder|premature_aging_syndrome	endocrine_system_disorder	digestive_system_disorder|hereditary_disease|premature_aging_syndrome|endocrine_system_disorder	gastroenterology|hepatology	autoimmune_diseases|inflammatory_disease	liver_disorder|biliary_disorder	false	false	false	true	high
MONDO:0007194	familial bicuspid aortic valve	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	pediatric|cardiovascular___corrected_to_remove__cardiovascular__as_it_is_a_broader_category_than_the_others____cardiology|genetics_and_genomics|cardiology	cardiovascular_disorder|familial_cardiovascular_disorders	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0007195	bifid nose, autosomal dominant	otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|otolaryngology	metabolic_disorder|neurodegenerative_disease	bone_disorder|nose_disorder	false	false	false	false	low
MONDO:0007197	bladder diverticulum	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	renal_medicine|urology	urinary_system_disorder|inflammatory_disease|cancer	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0007198	Ascher syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	liver_disorder|vascular_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0007199	blepharochalasis, superior	hereditary_disease	other	hereditary_disease	dermatology|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	low
MONDO:0007200	blepharonasofacial malformation syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	dermatology|pediatric|genetics_and_genomics|ophthalmology	metabolic_disorder|genetic_syndrome	eye_disorder	false	false	false	false	high
MONDO:0007201	blepharophimosis, ptosis, and epicanthus inversus syndrome	reproductive_system_disorder|disorder_of_visual_system|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	disorder_of_visual_system|disorder_of_orbital_region|reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|ophthalmology	metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0007202	blepharoptosis-myopia-ectopia lentis syndrome	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007203	blue rubber bleb nevus	integumentary_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|integumentary_system_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease	pediatrics|dermatology|genetics_and_genomics	metabolic_disorder|vascular_disorder	skin_disorder|vascular_disorder	false	false	false	false	high
MONDO:0007204	Cole-Carpenter syndrome 1	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatrics|dermatology|endocrinology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	skin_disorder|eye_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007205	diaphyseal medullary stenosis-bone malignancy syndrome	musculoskeletal_system_disorder|metabolic_disease|cancer_or_benign_tumor|hereditary_disease|connective_tissue_disorder	metabolic_disease|cancer_or_benign_tumor	metabolic_disease|cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder|hereditary_disease	oncology|orthopaedic|hematology	bone_malignancy|cancer	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0007206	bone pain, periodic	hereditary_disease	other	hereditary_disease	orthopaedic|rheumatology|neurology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|blood_bone_marrow_disorder|spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007207	Böök syndrome	integumentary_system_disorder|hereditary_disease|syndromic_disease	other	integumentary_system_disorder|syndromic_disease|hereditary_disease	pediatrics|neurology|genetics_and_genomics	mental_health_disorder|inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0007208	Boomerang dysplasia	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0007209	Weismann-Netter syndrome	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	cardiology|pulmonology|allergy_and_immunology|hematology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0007210	Brachmann-de Lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|brain_disorder|developmental_delay	false	false	false	false	very_high
MONDO:0007211	brachydactyly-arterial hypertension syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiology|renal_medicine|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0007212	brachydactyly-long thumb syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics	inflammatory_disease|congenital_anomaly|genetic_disorder|autoimmune_disease|developmental_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0007213	Ballard syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	ear_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007214	brachydactyly-preaxial hallux varus syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	genetic_disorder|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0007215	brachydactyly type A1	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0007216	brachydactyly type A2	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics	neurodegenerative_disease|developmental_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0007217	brachydactyly type A3	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics	genetic_disorder|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007218	brachydactyly type A4	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics	genetic_disorder|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0007219	Osebold-Remondini syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007220	brachydactyly type B1	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0007221	brachydactyly type C	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics	neurodegenerative_disease|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0007222	brachydactyly type D	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disorder|genetic_disorder____corrected_to_match_the_format_requested___metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0007223	brachydactyly type E1	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics	metabolic_disorder|birth_defect|genetic_disease|hand_anomaly	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0007224	brachydactyly, type E, with atrial septal defect, type 2	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|cardiology	congenital_heart_defect|cardiovascular_disorder|genetic_disorder	heart_disorder|joint_disorder	false	false	false	false	low
MONDO:0007225	fibular aplasia-ectrodactyly syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|anemia	joint_disorder|upper_gastrointestinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0007226	brachydactyly-nystagmus-cerebellar ataxia syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|cerebellar_ataxia_syndrome	cerebellar_ataxia_syndrome_seems_to_be_a_better_match_than_just_brain_disorder_so___brain_disorder|brain_disorder|joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007227	Sillence syndrome	syndromic_disease	other	syndromic_disease	pulmonology|neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0007228	brachymesomelia-renal syndrome	hereditary_disease	other	hereditary_disease	pediatric|renal_medicine|genetics_and_genomics	metabolic_disorder|renal_syndrome	renal_syndrome|kidney_disorder	false	false	false	false	medium
MONDO:0007229	Brachymetatarsus 4	hereditary_disease	other	hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|skeletal_abnormality|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007230	Brachymorphism-onychodysplasia-dysphalangism syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatrics|genetics_and_genomics	metabolic_disorder|genetic_disorder_was_removed_from_list__not_in_original_list__but_the_closest_match_was_a_genetic_disorder__therefore__metabolic_disorder_is_the_correct_answer|neurodegenerative_disease	joint_disorder|bone_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007231	brachytelephalangy-dysmorphism-Kallmann syndrome	reproductive_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder|hereditary_disease|syndromic_disease	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|developmental_disorder	endocrine_disorder|bone_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0007232	autosomal dominant brachyolmia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|connective_tissue_disease	joint_disorder|upper_gastrointestinal_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0007233	second branchial cleft anomaly	otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease|hereditary_disease	pediatric|otolaryngology	developmental_disorder|cardiovascular_disorder|congenital_anomaly	throat_disorder|ear_disorder	false	false	false	false	medium
MONDO:0007234	branchial myoclonus with spastic paraparesis and cerebellar ataxia	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007235	branchiooculofacial syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	face_disorder|ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0007236	branchiootorenal syndrome 1	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|urology|genetics_and_genomics	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	ear_disorder|kidney_disorder	false	false	false	false	high
MONDO:0007237	familial juvenile hypertrophy of the breast	hereditary_disease|breast_disorder	other	breast_disorder|hereditary_disease	pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|cancer	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0007238	amastia	hereditary_disease|breast_disorder	other	breast_disorder|hereditary_disease	cardiovascular|cardiology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	liver_disorder|biliary_disorder	false	false	false	false	low
MONDO:0007239	epidermolytic ichthyosis	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0007240	progressive familial heart block, type 1A	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics|cardiology	neurodegenerative_disease|cardiovascular_disorder	heart_disorder|muscle_disorder|vascular_disorder	false	false	false	false	high
MONDO:0007241	bundle branch block, familial isolated complete right	hereditary_disease	other	hereditary_disease	genetics_and_genomics|cardiology	adrenal_gland_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0007242	butyrylesterase 1	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hepatology|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0007243	Burkitt lymphoma	immune_system_disorder|hematologic_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	post_infectious_disorder|cancer_or_benign_tumor|hereditary_disease|immune_system_disorder|hematologic_disorder	hematology|oncology	lymphoma|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0007244	Caffey disease	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	true	medium
MONDO:0007245	cafe au lait spots, multiple	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0007246	calcific aortic disease with immunologic abnormalities, familial	hereditary_disease	other	hereditary_disease	immunology|genetics_and_genomics|cardiology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	heart_disorder|immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0007247	basal ganglia calcification, idiopathic, childhood-onset	immune_system_disorder|connective_tissue_disorder|hereditary_disease|syndromic_disease|nervous_system_disorder	neurodegenerative_disease	idiopathic_disease|connective_tissue_disorder|nervous_system_disorder|immune_system_disorder|hereditary_disease|syndromic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007248	hereditary painful callosities	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	dermatology|rheumatology|genetics_and_genomics	metabolic_disorder|inflammatory_disease	joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007249	camptobrachydactyly	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disease	musculoskeletal_disorder|joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0007250	camptodactyly of fingers	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0007251	campomelic dysplasia	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|skeletal_rare_disease|developmental_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0007252	Gordon syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0007253	cancer, familial, with in vitro Radioresistance	hereditary_disease	other	hereditary_disease	hematology|oncology|genetics_and_genomics	familial|cancer	lymphatic_disorder|blood_bone_marrow_disorder|lung_disorder	false	true	false	false	high
MONDO:0007254	breast cancer	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	autoimmune_diseases|cancer	lymphatic_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0007256	hepatocellular carcinoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology|hepatology	liver_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0007257	candidiasis, familial, 1	integumentary_system_disorder|immune_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease|immune_system_disorder	pediatric|dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0007258	canine teeth, absence of upper permanent	hereditary_disease	other	hereditary_disease	pediatric|orthopaedic	metabolic_disorder|congenital_anomaly|dental_abnormality	teeth_disorder|bone_disorder	false	false	false	true	low
MONDO:0007259	craniofaciofrontodigital syndrome	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|teeth_disorder|bone_disorder	false	false	false	false	high
MONDO:0007260	Car factor deficiency	hereditary_disease	other	hereditary_disease	immunology|pediatric|hematology	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0007261	Carabelli anomaly of maxillary molar teeth	hereditary_disease	other	hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	developmental_anomaly|dental_abnormality	bone_disorder|teeth_disorder	false	false	false	false	low
MONDO:0007263	cardiac rhythm disease	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiothoracic|cardiology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0007265	cardiofaciocutaneous syndrome 1	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|cardiovascular_disorder|integumentary_system_disorder|hereditary_disease	pediatric|dermatology|genetics_and_genomics|cardiology	autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0007266	hypertrophic cardiomyopathy 2	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiothoracic|cardiology	hypertrophic_cardiomyopathy|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	true	high
MONDO:0007267	hypertrophic cardiomyopathy 3	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	pediatric|cardiothoracic|genetics_and_genomics|cardiology	hypertrophic_cardiomyopathy|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	true	high
MONDO:0007268	hypertrophic cardiomyopathy 4	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiothoracic|cardiology	adrenal_gland_disease|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0007269	dilated cardiomyopathy 1A	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiothoracic|cardiology	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	true	high
MONDO:0007270	cardiomyopathy, familial restrictive, 1	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	pulmonology|cardiology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0007271	familial cutaneous collagenoma	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|dermatology|oncology|genetics_and_genomics	skin_disease|genetic_disorder|cancer	skin_disorder|vascular_disorder|hereditary_disorder	false	false	false	false	low
MONDO:0007272	hereditary hypercarotenemia and vitamin A deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|dermatology|genetics_and_genomics	anemia|metabolic_disorder	liver_disorder|eye_disorder	false	false	false	false	low
MONDO:0007273	pheochromocytoma/paraganglioma syndrome 4	disorder_of_development_or_morphogenesis|hereditary_disease|cancer_or_benign_tumor|endocrine_system_disorder|nervous_system_disorder|syndromic_disease	endocrine_system_disorder|cancer_or_benign_tumor	syndromic_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor|hereditary_disease	oncology|otolaryngology|neurology	neurodegenerative_disease|adrenal_gland_disease|cancer	brain_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0007274	carpal displacement	hereditary_disease	other	hereditary_disease	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0007275	carpal tunnel syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	orthopaedic|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	joint_disorder|spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0007276	cat-eye syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	pediatric|ophthalmology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|anemia|cancer|metabolic_disorder	ear_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007277	cataract-aberrant oral frenula-growth delay syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|ophthalmology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	growth_delay_syndrome|eye_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0007278	cataract 32 multiple types	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0007279	cataract 7	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0007280	cataract 8 multiple types	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0007281	cataract 4 multiple types	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0007282	cataract 29	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0007283	cataract 42	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|cardiovascular_disorder|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0007284	cataract 20 multiple types	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0007285	cataract 1 multiple types	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0007286	cataract 30	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0007287	cataract 41	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0007288	cataract 6 multiple types	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0007289	cataract 13 with adult I phenotype	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0007290	cataract 5 multiple types	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	medium
MONDO:0007293	leukocyte adhesion deficiency 1	immune_system_disorder|hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease|immune_system_disorder	immunology|hematology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0007294	central core myopathy	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007295	self-limited epilepsy with centrotemporal spikes	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0007296	spinocerebellar ataxia type 31	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0007297	ADan amyloidosis	hereditary_disease|nervous_system_disorder|metabolic_disease|cardiovascular_disorder	neurodegenerative_disease|metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0007298	spinocerebellar ataxia type 29	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology	neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0007300	cerebral sarcoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neurological_cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0007301	cerebrocostomandibular syndrome	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	otolaryngology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder|brain_disorder|teeth_disorder|throat_disorder	false	false	false	false	high
MONDO:0007302	cervical hypertrichosis with underlying kyphoscoliosis	hereditary_disease	other	hereditary_disease	neurology|obstetrics_and_gynecology|orthopaedic	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007303	cervical rib disease	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	cardiothoracic|orthopaedic	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	spinal_disorder|muscle_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007304	cervical vertebral Bridge	hereditary_disease	other	hereditary_disease	neurology|orthopaedic	neurodegenerative_disease|cervical_vertebral_bridge_is_a_condition_where_the_cervical_vertebrae_fuse_together	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0007305	cervical vertebral dysplasia	hereditary_disease	other	hereditary_disease	neurology|orthopaedic	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007306	Klippel-Feil syndrome 1, autosomal dominant	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	autoimmune_diseases|neurodegenerative_disease|skeletal_disorder|metabolic_disorder|genetic_disease|inflammatory_disease	ear_disorder|bone_disorder|joint_disorder|throat_disorder	false	false	false	false	medium
MONDO:0007307	Charcot-Marie-Tooth disease type 1B	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|orthopaedic	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|muscle_disorder|nerve_disorder_is_not_in_the_list_so	false	false	false	false	medium
MONDO:0007308	Charcot-Marie-Tooth disease type 2A1	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007309	Charcot-Marie-Tooth disease type 1A	nervous_system_disorder|chromosomal_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|chromosomal_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	muscle_disorder|nervous_system_disorder	false	false	false	false	medium
MONDO:0007310	Charcot-Marie-Tooth disease, Guadalajara neuronal type	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscledisorder	false	false	false	false	medium
MONDO:0007311	Charcot-Marie-Tooth disease type 1E	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	muscle_disorder|nerve_disorder	false	false	false	false	medium
MONDO:0007312	Charcot-Marie-Tooth disease with ptosis and parkinsonism	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0007313	cheilitis glandularis	integumentary_system_disorder	other	integumentary_system_disorder	otolaryngology|dermatology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007314	chemodectoma, intraabdominal, with cutaneous angiolipomas	hereditary_disease	other	hereditary_disease	oncology|neurology|dermatology	cancer|adrenal_gland_disease	vascular_disorder|upper_gastrointestinal_disorder|skin_disorder	false	true	false	false	high
MONDO:0007315	cherubism	connective_tissue_disorder|cancer_or_benign_tumor|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	otolaryngology|genetics_and_genomics|pediatric	metabolic_disorder|adrenal_gland_disease	bone_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0007316	Chiari malformation type I	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0007318	Alagille syndrome	disorder_of_visual_system|digestive_system_disorder|cardiovascular_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder|syndromic_disease|digestive_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	hepatology|gastroenterology|genetics_and_genomics|pediatric	genetic_disorder|metabolic_disorder	biliary_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0007319	chondrocalcinosis 2	connective_tissue_disorder|inflammatory_disease|metabolic_disease|hereditary_disease|musculoskeletal_system_disorder	metabolic_disease	hereditary_disease|inflammatory_disease|musculoskeletal_system_disorder|metabolic_disease|connective_tissue_disorder	rheumatology|orthopaedic	metabolic_disorder|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0007320	chondrocalcinosis due to apatite crystal deposition	musculoskeletal_system_disorder|inflammatory_disease|metabolic_disease	metabolic_disease	metabolic_disease|inflammatory_disease|musculoskeletal_system_disorder	rheumatology|orthopaedic	metabolic_disorder|autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0007321	autosomal dominant chondrodysplasia punctata	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|dermatology|orthopaedic	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007322	chondrodysplasia punctata, tibial-metacarpal type	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	bone_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0007323	Chondronectin	hereditary_disease	other	hereditary_disease	rheumatology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007325	choreoathetosis, familial inverted	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0007327	chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase	syndromic_disease	other	syndromic_disease	hepatology|pediatrics|cardiology|genetics_and_genomics|endocrinology	genetic_disorder|lipid_disorder|metabolic_disorder	lymphatic_disorder|liver_disorder	false	false	false	true	high
MONDO:0007328	choroidal osteoma, bilateral	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	bone_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007329	cirrhosis, familial	digestive_system_disorder|endocrine_system_disorder|premature_aging_syndrome|hereditary_disease	endocrine_system_disorder	hereditary_disease|premature_aging_syndrome|endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology|genetics_and_genomics	metabolic_disorder|liver_disease	familial|liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0007330	congenital pseudoarthrosis of clavicle	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	musculoskeletal_disorder|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007332	split-hand/foot malformation with long bone deficiency 1	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	bone_diseases|metabolic_disorder|genetic_disorders	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007333	van der Woude syndrome 1	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007334	autosomal dominant popliteal pterygium syndrome	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	genetics_and_genomics|orthopaedic	inherited_syndrome|hereditary_condition|metabolic_disorder|autosomal_dominant_disease	muscle_disorder|joint_disorder|eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0007335	orofacial cleft 1	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	otolaryngology|pediatric	congenital_disorder|neurodevelopmental_disease|birth_defect	nose_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0007336	isolated cleft palate	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	otolaryngology|pediatric	developmental_disorder|metabolic_disorder|congenital_abnormality	throat_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0007337	cleft palate-lateral synechia syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	otolaryngology|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	throat_disorder|nose_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0007338	cleft soft palate	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	otolaryngology|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	throat_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0007339	blepharocheilodontic syndrome	disorder_of_visual_system|integumentary_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|disorder_of_visual_system|disorder_of_orbital_region|integumentary_system_disorder	genetics_and_genomics|ophthalmology|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	teeth_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007340	cleidocranial dysplasia 1	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	skeletal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007341	cleidorhizomelic syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	muscle_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007342	clubfoot	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric	congenital_condition|birth_defect|musculoskeletal_disease	bone_disorder|joint_disorder	false	false	false	true	low
MONDO:0007343	isolated congenital digital clubbing	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	pulmonology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	vascular_disorder|lung_disorder|joint_disorder	false	false	false	false	low
MONDO:0007344	cluster headache, familial	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|nervous_system_disorder|cardiovascular_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	vascular_disorder|brain_disorder	false	false	false	true	high
MONDO:0007345	aorta coarctation	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiology|cardiothoracic|pediatric	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0007346	cochleosaccular degeneration-cataract syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|ophthalmology|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0007349	familial cold autoinflammatory syndrome 1	connective_tissue_disorder|immune_system_disorder|syndromic_disease|hereditary_disease	other	connective_tissue_disorder|hereditary_disease|immune_system_disorder|syndromic_disease	rheumatology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease	joint_disorder|immune_disorder	false	false	false	true	high
MONDO:0007350	coloboma, ocular, autosomal dominant	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	false	low
MONDO:0007351	coloboma of macula	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007352	renal coloboma syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|urology|genetics_and_genomics|renal_medicine	metabolic_disorder|autoimmune_diseases|inflammatory_disease|renal_coloboma_syndrome	kidney_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0007353	coloboma of macula-brachydactyly type B syndrome	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|joint_disorder	false	false	false	false	high
MONDO:0007354	coloboma of optic nerve	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|pediatric|genetics_and_genomics|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0007355	uveal coloboma-cleft lip and palate-intellectual disability	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	ophthalmology|pediatric|genetics_and_genomics|neurology	intellectual_disability|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	eye_disorder|intellectual_disability_is_not_in_the_list_but_brain_disorder_is_a_related_category_so_also_include_it___brain_disorder	false	false	false	false	high
MONDO:0007356	Lynch syndrome 1	hereditary_disease|syndromic_disease|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|digestive_system_disorder|cancer_or_benign_tumor	oncology|genetics_and_genomics	hereditary_condition|cancer|genetic_disorder	reproductive_system_disorder	false	false	false	true	high
MONDO:0007357	colonic varices without portal hypertension	hereditary_disease	other	hereditary_disease	hematology|hepatology|gastroenterology	cancer|inflammatory_disease	lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	low
MONDO:0007358	comedones, familial Dyskeratotic	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	cancer|familial_dyskeratotic_is_a_rare_genetic_disorder_characterized_by_the_presence_of_comedones__blackheads__among_other_symptoms__it_is_classified_as_a_type_of_skin_cancer	other___corrected_answer__skin_disorder|skin_disorder	false	false	false	false	low
MONDO:0007359	commissural lip pits	hereditary_disease	other	hereditary_disease	otolaryngology|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	teeth_disorder|skin_disorder	false	false	false	false	low
MONDO:0007360	branchiootic syndrome 2	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	throat_disorder|ear_disorder	false	false	false	false	medium
MONDO:0007361	C1 inhibitor deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	hematology|rheumatology|allergy_and_immunology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0007362	cone-rod dystrophy 2	hereditary_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease|disorder_of_visual_system	metabolic_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007363	congenital contractural arachnodactyly	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|connective_tissue_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|connective_tissue_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	genetic_disorder|congenital_abnormality|neurodegenerative_disease|musculoskeletal_disorder	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007364	arthrogryposis, distal, type 2E	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology|orthopaedic	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007365	seizures, benign familial neonatal, 1	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder	false	false	false	true	low
MONDO:0007366	seizures, benign familial neonatal, 2	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	medium
MONDO:0007367	febrile seizures, familial, 1	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder	false	false	false	true	low
MONDO:0007368	familial benign copper deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	metabolic_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	false	low
MONDO:0007369	hereditary coproporphyria	hereditary_disease|endocrine_system_disorder|integumentary_system_disorder|metabolic_disease|digestive_system_disorder	endocrine_system_disorder|metabolic_disease	hereditary_disease|metabolic_disease|endocrine_system_disorder|integumentary_system_disorder|digestive_system_disorder	hematology|pediatric|genetics_and_genomics|hepatology	metabolic_disorder|hereditary_disease	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0007370	coracoclavicular joint, anomalous	hereditary_disease	other	hereditary_disease	rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007371	cornea guttata with anterior polar cataracts	hereditary_disease	other	hereditary_disease	ophthalmology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0007372	cornea plana 1, autosomal dominant	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|autosomal_dominant_disorders	eye_disorder|spinal_disorder	false	false	false	false	low
MONDO:0007373	corneal degeneration, ribbonlike, with deafness	hereditary_disease	other	hereditary_disease	ophthalmology|otolaryngology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0007374	Schnyder corneal dystrophy	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|skin_disorder	false	false	false	true	medium
MONDO:0007375	epithelial basement membrane dystrophy	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|dermatology	autoimmune_diseases|epidermolysis_bullosa_acquisita_related_disease_is_a_subcategory_of_autoimmune_diseases__epithelial_basement_membrane_dystrophy_shares_some_similarities_with_it_in_terms_of_autoantibody_presence_and_immune_system_dysfunction_which_makes_it_closely_related_to_autoimmune_diseases_category	eye_disorder|joint_disorder|skin_disorder	false	false	false	true	medium
MONDO:0007376	fleck corneal dystrophy	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	low
MONDO:0007377	granular corneal dystrophy type I	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	high
MONDO:0007378	posterior polymorphous corneal dystrophy 1	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007379	Meesmann corneal dystrophy	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	eye_disorder|muscle_disorder|skin_disorder	false	false	false	false	low
MONDO:0007380	lattice corneal dystrophy type I	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0007381	epithelial recurrent erosion dystrophy	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	dermatology	cancer|autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	medium
MONDO:0007382	Ramos-Arroyo syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|renal_medicine	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0007383	Stern-Lubinsky-Durrie syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|hereditary_disease|syndromic_disease|integumentary_system_disorder	pediatric|genetics_and_genomics|endocrinology|neurology	metabolic_disorder|autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	bone_disorder|liver_disorder|immune_disorder	false	false	false	false	medium
MONDO:0007384	congenital trigeminal anesthesia	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	nerve_disorder|brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0007385	idiopathic spontaneous coronary artery dissection	cardiovascular_disorder	cardiovascular_disorder	idiopathic_disease|cardiovascular_disorder	cardiothoracic|cardiology|genetics_and_genomics|pulmonology|renal_medicine|hematology	inflammatory_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0007387	Cornelia de Lange syndrome 1	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	joint_disorder|muscle_disorder|brain_disorder|skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0007388	congenitally short costocoracoid ligament	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|genetics_and_genomics|orthopaedic	musculoskeletal_disease|cardiovascular_disorder	bone_disorder|spinal_disorder	false	false	false	false	low
MONDO:0007389	spondylocostal dysostosis 5	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic	genetic_disorder|metabolic_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007390	coumarin resistance	hereditary_disease	other	hereditary_disease	hematology|genetics_and_genomics|hepatology	metabolic_disorder|allergy|autoimmune_diseases|inflammatory_disease	liver_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0007391	coxa vara	hereditary_disease	other	hereditary_disease	orthopaedic|oncology|pediatric	metabolic_disorder|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007392	coxoauricular syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|cardiothoracic|genetics_and_genomics|rheumatology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	ear_disorder|joint_disorder	false	false	false	false	low
MONDO:0007393	cranioacrofacial syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	teeth_disorder|bone_disorder|skull_disorder|ear_disorder|joint_disorder|face_disorder	false	false	false	false	high
MONDO:0007395	craniofacial-deafness-hand syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder|anemia|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	teeth_disorder|ear_disorder|craniofacial_disorder	false	false	false	false	medium
MONDO:0007396	dysostosis, Stanescu type	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|dysostosis__stancescu_type_is_a_congenital_disorder_affecting_bone_development	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0007397	craniometaphyseal dysplasia, autosomal dominant	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	teeth_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007398	craniorhiny	hereditary_disease	other	hereditary_disease	otolaryngology|neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder|skull_disorder|cranial_disorder	false	false	false	false	none
MONDO:0007399	TWIST1-related craniosynostosis	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	skull_abnormality|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0007400	Jackson-Weiss syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|brain_disorder|blood_bone_marrow_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0007401	craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	hydrocephalus_syndrome|metabolic_disorder|neurodegenerative_disease	brain_disorder|joint_disorder|craniosynostosis|hydrocephalus|spinal_disorder	false	false	false	false	very_high
MONDO:0007402	creatine phosphokinase, elevated serum	hereditary_disease	other	hereditary_disease	cardiology|hematology|renal_medicine	cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	false	low
MONDO:0007403	inherited Creutzfeldt-Jakob disease	hereditary_disease|infectious_disease|nervous_system_disorder	infectious_disease|neurodegenerative_disease	infectious_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	inherited|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0007404	Cri-du-chat syndrome	syndromic_disease|chromosomal_disorder	other	chromosomal_disorder|syndromic_disease	genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0007405	Crouzon syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|facial_disorder|skull_disorder	false	false	false	false	high
MONDO:0007406	cryofibrinogenemia, familial primary	hereditary_disease|immune_system_disorder	autoimmune_disease	immune_system_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|autoimmune_diseases|metabolic_disorder	immune_disorder|vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0007407	Cryoglobulinemic vasculitis	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	hematology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|vascular_disorder	false	false	false	true	high
MONDO:0007408	cryptotia, familial	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	skin_disorder|eye_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0007409	cryptomicrotia-brachydactyly-excess fingertip arch syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	congenital_abnormality|metabolic_disorder	joint_disorder|limb_abnormality|bone_disorder	false	false	false	false	medium
MONDO:0007410	isolated cryptophthalmia	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology	adrenal_gland_disease|inflammatory_disease|metabolic_disorder	eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0007411	cutis laxa, autosomal dominant 1	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics_dermatology	metabolic_disorder|cutis_laxa_autosomal_dominant	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007412	Beare-Stevenson cutis gyrata syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0007413	Cyprus facial-neuromusculoskeletal syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007414	Gorham-Stout disease	syndromic_disease|connective_tissue_disorder|immune_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder|cardiovascular_disorder|syndromic_disease	pediatrics|genetics_and_genomics|orthopaedic|rheumatology|dermatology	inflammatory_disease|metabolic_disorder	joint_disorder|vascular_disorder|bone_disorder	false	false	false	false	high
MONDO:0007415	mitochondrial complex III deficiency nuclear type 1	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	neurology|pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_disease	false	false	false	true	high
MONDO:0007416	Balkan nephropathy	urinary_system_disorder|hereditary_disease|inflammatory_disease	other	hereditary_disease|urinary_system_disorder|inflammatory_disease	nephrology|renal_medicine	autoimmune_diseases|inflammatory_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0007417	Darier disease	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder	liver_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007418	Darwinian tubercle of pinna	hereditary_disease	other	hereditary_disease	pediatric|otolaryngology|pulmonology	autoimmune_diseases|cancer|inflammatory_disease	lung_disorder|ear_disorder	false	false	false	false	low
MONDO:0007420	autosomal dominant deafness - onychodystrophy syndrome	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|syndromic_disease|integumentary_system_disorder	pediatric|genetics_and_genomics|otolaryngology	metabolic_disorder|neurodegenerative_disease	onychodystrophy_is_a_nail_disorder_but_that_aspect_of_the_name_suggests_skin_disorder_as_well___ear_disorder|skin_disorder|ear_disorder	false	false	false	true	medium
MONDO:0007421	deafness-ear malformation-facial palsy syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|otolaryngology|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	ear_malformation|ear_disorder|facial_palsy_syndrome	false	false	false	false	high
MONDO:0007422	keratoderma hereditarium mutilans	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0007423	deafness, mid-tone neural	hereditary_disease	other	hereditary_disease	otolaryngology|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|ear_disorder	false	false	false	true	medium
MONDO:0007424	autosomal dominant nonsyndromic hearing loss 1	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	pediatric|genetics_and_genomics|otolaryngology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	ear_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0007425	deafness, sensorineural, with peripheral neuropathy and arterial disease	hereditary_disease	other	hereditary_disease	otolaryngology|neurology|cardiology	cardiovascular_disorder|inflammatory_disease|neurodegenerative_disease	vascular_disorder|muscle_disorder|ear_disorder	false	false	false	false	high
MONDO:0007426	deafness, unilateral	hereditary_disease	other	hereditary_disease	otolaryngology|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	unspecified_specialty___note__the_provided_categorization_is_based_on_the_assumption_that_deafness__unilateral_refers_to_a_condition_affecting_one_ear_s_ability_to_hear|ear_disorder	false	false	false	false	low
MONDO:0007427	deafness with anhidrotic ectodermal dysplasia	hereditary_disease	other	hereditary_disease	otorhinolaryngology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	skin_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0007428	deafness-craniofacial syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|otolaryngology	craniofacial_syndrome_is_not_listed_so_cannot_be_identified|neurodegenerative_disease	craniofacial_syndrome|ear_disorder	false	false	false	false	medium
MONDO:0007429	optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|mitochondrial_disease	neurodegenerative_disease	hereditary_disease|mitochondrial_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	genetics_and_genomics|ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder|eye_disorder|spinal_disorder	true	false	false	false	high
MONDO:0007430	dens evaginatus	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic	anemia|autoimmune_diseases|inflammatory_disease|metabolic_disorder	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007431	dens in dente and palatal invaginations	hereditary_disease	other	hereditary_disease	pediatric|oral_surgery	autoimmune_diseases|inflammatory_disease|metabolic_disorder	teeth_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007432	cerebral arteriopathy with subcortical infarcts and leukoencephalopathy	syndromic_disease|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|syndromic_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0007433	dementia/parkinsonism with non-Alzheimer amyloid plaques	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0007434	primary failure of tooth eruption	hereditary_disease	other	hereditary_disease	pediatric|orthopaedic	autoimmune_diseases|metabolic_disorder	teeth_disorder|bone_disorder	false	false	false	true	medium
MONDO:0007435	dentatorubral-pallidoluysian atrophy	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology	adrenal_gland_disease|mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0007436	dentin dysplasia type I	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	pediatric|genetics_and_genomics	genetic_disease|developmental_disorder_____corrected_list_to_directly_answer_the_request_without_additional_text_____metabolic_disorder|developmental_disorder|metabolic_disorder	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007437	dentin dysplasia type II	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	pediatric|genetics_and_genomics	metabolic_disorder|dentin_dysplasia_type_ii_does_not_fit_into_this_category_so_i_removed_it_and_the_other_categories_also_do_not_fit_well__however___dentin_dysplasia_type_ii_is_a_known_consequence_of_some_metabolic_disorders_such_as_hypophosphatasia_therefore_i_will_put_only_that_one	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007438	dentin dysplasia-sclerotic bones syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	skeletal_system_disease|genetic_disorder|bone_disorder|metabolic_disorder	teeth_disorder|bone_disorder	false	false	false	false	high
MONDO:0007439	deoxyribose-5-phosphate aldolase deficiency	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|hematology|metabolism_related|hepatology|neurology	neurodegenerative_disease|metabolic_disorder	liver_disorder|metabolic_disorder	false	false	false	false	medium
MONDO:0007440	major affective disorder 1	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|major_affective_disorder	brain_disorder	false	false	false	true	high
MONDO:0007441	dentinogenesis imperfecta type 2	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	pediatric|genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	teeth_disorder|eye_disorder	false	false	false	false	high
MONDO:0007442	dentinogenesis imperfecta type 3	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	genetics_and_genomics|pediatrics|orthopaedic|dermatology	metabolic_disorder|genetic_disorder	teeth_disorder|skin_disorder	false	false	false	false	high
MONDO:0007443	congenital unilateral hypoplasia of depressor anguli oris	chromosomal_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|immune_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|chromosomal_disorder|immune_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|otolaryngology	congenital_abnormality|congenital_ailment___corrected_list___cardiovascular_disorder|cardiovascular_disorder	teeth_disorder|vascular_disorder|lower_gastrointestinal_disorder|mouth_disorder	false	false	false	false	low
MONDO:0007444	dermal Ridges, patternless	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|dermal_anomalies	skin_disorder	false	false	false	false	low
MONDO:0007445	dermatopathia pigmentosa reticularis	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|dermatology	autoimmune_diseases|dermatological_disease	joint_disorder|immune_disorder|muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007446	dermatosis papulosa nigra	hereditary_disease|integumentary_system_disorder|inflammatory_disease	other	hereditary_disease|integumentary_system_disorder|inflammatory_disease	dermatology|dermatological	autoimmune_diseases|dermatological_disease|skin_condition___corrected_to__inflammatory_disease	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0007447	autosomal dominant vibratory urticaria	hereditary_disease|integumentary_system_disorder|inflammatory_disease	other	hereditary_disease|integumentary_system_disorder|inflammatory_disease	genetics_and_genomics|dermatology	autoimmune_diseases|allergic_disorders|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007448	familial dermatographia	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|hereditary_condition	false	false	false	false	medium
MONDO:0007449	dermo-odonto dysplasia	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|dermatology	autoimmune_diseases|dermo_odonto_dysplasia_is_a_rare_genetic_disorder_that_affects_the_development_of_teeth_and_skin__metabolic_disorder|inflammatory_disease	teeth_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007450	neurohypophyseal diabetes insipidus	endocrine_system_disorder|urinary_system_disorder|hereditary_disease|nervous_system_disorder|reproductive_system_disorder	endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder|urinary_system_disorder	endocrinology|neurology	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|brain_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0007451	diabetes insipidus, nephrogenic, autosomal	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	genetics_and_genomics|endocrinology|renal_medicine	autosomal|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0007452	maturity-onset diabetes of the young type 1	endocrine_system_disorder|hereditary_disease|metabolic_disease|digestive_system_disorder	diabetes_mellitus|endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|digestive_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology|pediatrics	autoimmune_diseases|metabolic_disorder	endocrine_disorder	false	false	true	false	high
MONDO:0007453	maturity-onset diabetes of the young type 2	endocrine_system_disorder|hereditary_disease|metabolic_disease|digestive_system_disorder	diabetes_mellitus|endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|digestive_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	endocrine_disorder	false	false	true	true	low
MONDO:0007456	diarrhea, glucose-stimulated secretory, with common variable immunodeficiency	hereditary_disease	other	hereditary_disease	immunology|gastroenterology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0007457	diastema, dental medial	hereditary_disease	other	hereditary_disease	pediatric|general_surgery|orthopaedic|dentistry	autoimmune_diseases|metabolic_disorder|inflammatory_disease	teeth_disorder|dental_medial	false	false	false	false	low
MONDO:0007458	digitotalar dysmorphism; ulnar drift, hereditary	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	skeletal_disorder___note__the_original_request_specified_that__ulnar_drift__hereditary__should_be_categorized_as_part_of_the_disease_digitotalar_dysmorphism__which_it_is_a_symptom_of__as_such__i_have_also_included__skeletal_disorder__in_the_response__although_this_category_was_not_provided_in_the_original_list|joint_disorder	false	false	false	false	medium
MONDO:0007459	dilution, pigmentary	hereditary_disease	other	hereditary_disease	pigmentation|dermatology	autoimmune_diseases|dilution|pigmentary	liver_disorder|skin_disorder	false	false	false	false	low
MONDO:0007460	discrimination, Two-point, reduction 1N	hereditary_disease	other	hereditary_disease	immunology|allergy_and_immunology|genetics_and_genomics____note__based_on_the_provided_categories__it_appears_that_discrimination__two_point__reduction_1n_is_related_to_immunology_and_genetics_genomics	metabolic_disorder|neurodegenerative_disease	digestive_system_disorder_____corrected_response_to_remove_incorrect_entry_____lower_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	none
MONDO:0007461	short stature-valvular heart disease-characteristic facies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder|valvular_heart_disease	endocrine_disorder|heart_disorder|bone_disorder	true	false	false	false	high
MONDO:0007463	distal osteosclerosis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0007465	distichiasis with congenital anomalies of the heart and peripheral vasculature	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|cardiology	cardiovascular_disorder|congenital_anomalies_of_the_heart_and_peripheral_vasculature	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0007466	DNA, satellite, 3	hereditary_disease	other	hereditary_disease	genetics_and_genomics|oncology	satellite|autoimmune_diseases|dna|cancer|neurodegenerative_disease	immune_disorder|vascular_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0007467	DNA, low-repetitive sequences of	hereditary_disease	other	hereditary_disease	genetics_and_genomics|genetic_and_genomic	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|skin_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0007469	double nail for fifth toe	hereditary_disease	other	hereditary_disease	orthopaedic|dermatology	autoimmune_diseases|inflammatory_disease|anemia	toe_disorder|bone_disorder|nail_disorder|lower_extremity_disorder	false	false	false	false	low
MONDO:0007470	calvarial doughnut lesions-bone fragility syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic|rheumatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0007471	Doyne honeycomb retinal dystrophy	hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|ophthalmology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0007472	basal laminar drusen	hereditary_disease|nervous_system_disorder|psychiatric_disorder|cardiovascular_disorder|disorder_of_visual_system	psychiatric_disorder|cardiovascular_disorder	nervous_system_disorder|hereditary_disease|cardiovascular_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0007473	Duane retraction syndrome	hereditary_disease|syndromic_disease|nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|syndromic_disease	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007474	duodenal ulcer due to antral G-cell hyperfunction	hereditary_disease	other	hereditary_disease	endocrinology|gastroenterology	inflammatory_disease|metabolic_disorder	endocrine_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0007475	duodenal ulcer, hyperpepsinogenemic 1	hereditary_disease	other	hereditary_disease	gastroenterology|hepatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0007476	familial Dupuytren contracture	connective_tissue_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|integumentary_system_disorder	genetics_and_genomics|orthopaedic	metabolic_disorder|inflammatory_disease	joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007477	3-M syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|brain_disorder|liver_disorder|heart_disorder|eye_disorder|bone_disorder|vascular_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0007478	autosomal dominant Kenny-Caffey syndrome	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	joint_disorder|brain_disorder|muscle_disorder|eye_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0007479	dwarfism, Levi type	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007480	dwarfism with stiff joints and ocular abnormalities	hereditary_disease	other	hereditary_disease	genetics_and_genomics|rheumatology|pediatric|endocrinology|orthopaedic|ophthalmology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	bone_disorder|joint_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007481	Leri-Weill dyschondrosteosis	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|rheumatology|pediatric|orthopaedic	inflammatory_disease|metabolic_disorder|autoimmune_diseases	bone_disorder|upper_gastrointestinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007482	dyschondrosteosis-nephritis syndrome	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|rheumatology|pediatric|renal_medicine	inflammatory_disease|autoimmune_diseases	bone_disorder|immune_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0007483	dyschromatosis symmetrica hereditaria	syndromic_disease|hereditary_disease|integumentary_system_disorder|connective_tissue_disorder	other	hereditary_disease|integumentary_system_disorder|syndromic_disease|connective_tissue_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0007485	dyskeratosis congenita, autosomal dominant 1	syndromic_disease|cancer_or_benign_tumor|hereditary_disease|premature_aging_syndrome|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|premature_aging_syndrome|hereditary_disease|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|pediatric|dermatology	metabolic_disorder|neurodegenerative_disease	bone_disorder|skin_disorder	false	false	false	false	high
MONDO:0007486	hereditary benign intraepithelial dyskeratosis	syndromic_disease|disorder_of_visual_system	other	syndromic_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|dermatology	genetic_disorder|cancer|anatomic_abnormality	skin_disorder	false	false	false	false	low
MONDO:0007488	Lewy body dementia	metabolic_disease|nervous_system_disorder|hereditary_disease|psychiatric_disorder	metabolic_disease|neurodegenerative_disease|psychiatric_disorder	metabolic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurology|psychiatry	inflammatory_disease|neurodegenerative_disease|mental_health_disorder	lung_disorder|brain_disorder	false	false	false	false	high
MONDO:0007489	dysplasia epiphysealis hemimelica	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|genetic_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007490	carpotarsal osteochondromatosis	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007491	dystelephalangy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric|orthopaedic	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0007492	early-onset generalized limb-onset dystonia	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007493	torsion dystonia 4	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007495	dystonia 5	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007496	dystonia 12	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|psychiatry	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007497	ear antitragus, tag at base of	hereditary_disease	other	hereditary_disease	otolaryngology|pediatrics	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	false	false	false	false	low
MONDO:0007498	ear exostoses	hereditary_disease	other	hereditary_disease	otolaryngology|orthopaedic	allergy|inflammatory_disease	bone_disorder|ear_disorder	false	false	false	false	medium
MONDO:0007499	ear folding	hereditary_disease	other	hereditary_disease	otolaryngology|pediatric	neurodegenerative_disease|autoimmune_diseases	ear_disorder	false	false	false	false	low
MONDO:0007500	ear malformation	hereditary_disease	other	hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	congenital_disorder|developmental_disorder|neurodegenerative_disease	ear_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007501	preauricular fistulae, congenital	hereditary_disease	other	hereditary_disease	pediatric|otolaryngology	congenital_disease|inflammatory_disease	ear_disorder	false	false	false	true	low
MONDO:0007502	ear pits, posterior helical	hereditary_disease	other	hereditary_disease	pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	ear_disorder	false	false	false	false	low
MONDO:0007503	ear without helix	otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	ear_disorder|throat_disorder	false	false	false	false	low
MONDO:0007504	thickened earlobes-conductive deafness syndrome	hereditary_disease	other	hereditary_disease	otolaryngology|neurology	autoimmune_diseases|metabolic_disorder	ear_disorder|conductive_deafness_syndrome	false	false	false	false	medium
MONDO:0007507	absence of fingerprints-congenital milia syndrome	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	congenital_disorder|metabolic_disorder	skin_disorder|congenital_disorder	false	false	false	false	low
MONDO:0007508	Rapp-Hodgkin syndrome	integumentary_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|integumentary_system_disorder	oncology|hematology	autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0007509	ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	hair_nail_disorder____note__i_assume__hair_nail_disorder__is_a_type_of_skin_disorder__if_it_s_a_separate_category__please_provide_more_information|skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007510	Clouston syndrome	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	pediatric|psychiatry|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0007511	ectodermal dysplasia, trichoodontoonychial type	integumentary_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|integumentary_system_disorder	pediatric|dermatology|genetics_and_genomics	adrenal_gland_disease|genetic_disorder	teeth_disorder|skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0007512	ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feet	hereditary_disease	other	hereditary_disease	pediatric|dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	kidney_disorder|joint_disorder|teeth_disorder|skin_disorder|eye_disorder|vascular_disorder|bone_disorder|blood_bone_marrow_disorder|heart_disorder|ear_disorder	false	false	false	false	medium
MONDO:0007513	ectodermal dysplasia with adrenal cyst	hereditary_disease	other	hereditary_disease	endocrinology|dermatology|genetics_and_genomics|pediatrics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	teeth_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007514	ectopia lentis 1, isolated, autosomal dominant	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	pediatric|ophthalmology|genetics_and_genomics|neurology	autosomal_dominant_disorder_____corrected_to_remove_the__isolated__part_as_it_is_not_a_category|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	true	medium
MONDO:0007515	ectopia pupillae	hereditary_disease	other	hereditary_disease	ophthalmology|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007516	ectrodactyly and ectodermal dysplasia without cleft lip/palate	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics|pediatrics	genetic_disorder|metabolic_disorder	ectodermal_dysplasia|teeth_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007517	ectrodactyly-cleft palate syndrome	hereditary_disease	other	hereditary_disease	ophthalmology|orthopaedic|genetics_and_genomics|otolaryngology|pediatrics|neurology	syndrome|congenital_disorder|neurodegenerative_disease	joint_disorder|teeth_disorder	false	false	false	false	high
MONDO:0007518	edema, familial idiopathic, prepubertal	hereditary_disease	other	idiopathic_disease|hereditary_disease	pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	lymphatic_disorder|skin_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0007519	Edinburgh malformation syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|joint_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0007520	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1	disorder_of_development_or_morphogenesis|disorder_of_visual_system|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	disorder_of_visual_system|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|dermatology|genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	teeth_disorder|skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007522	Ehlers-Danlos syndrome, classic type	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|dermatology|genetics_and_genomics	autoimmune_diseases|cardiovascular_disorder|metabolic_disorder	joint_disorder|skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0007523	Ehlers-Danlos syndrome, hypermobility type	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|dermatology|genetics_and_genomics	autoimmune_diseases|cardiovascular_disorder|metabolic_disorder|inflammatory_disease	joint_disorder|skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0007524	autosomal dominant Ehlers-Danlos syndrome, vascular type	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|dermatology|genetics_and_genomics|cardiology|hematology	cardiovascular_disorder|metabolic_disorder	joint_disorder|muscle_disorder|skin_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0007525	Ehlers-Danlos syndrome, arthrochalasia type	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|orthopaedic|genetics_and_genomics	autoimmune_diseases|cardiovascular_disorder|metabolic_disorder|inflammatory_disease	joint_disorder|muscle_disorder|vascular_disorder	false	false	false	false	high
MONDO:0007526	Ehlers-Danlos syndrome, spondylodysplastic type	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease	metabolic_disease	syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|orthopaedic|genetics_and_genomics	musculoskeletal_disease|genetic_disorders|metabolic_disorder|inflammatory_disease|connective_tissue_disease	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0007527	Ehlers-Danlos syndrome, periodontitis type	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	joint_disorder|skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0007528	Ehlers-Danlos syndrome, autosomal dominant, type unspecified	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|dermatology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	joint_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0007529	elastosis perforans serpiginosa	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	adrenal_gland_disease|autoimmune_diseases|cancer	skin_disorder	false	false	false	false	low
MONDO:0007530	electroencephalographic peculiarity: 14 and 6 per sec. positive spike phenomenon	hereditary_disease	other	hereditary_disease	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|electroencephalographic_parity	false	false	false	the_electroencephalographic_findings_you_mention__such_as__14_and_6_per_sec__positive_spike_phenomenon___suggest_the_presence_of_specific_abnormal_brain_activity_often_associated_with_certain_types_of_epilepsy_or_other_neurological_conditions____for_conditions_such_as_epilepsy__there_are_indeed_efficacious_treatments_that_can_help_manage_seizures__including_antiepileptic_medications__dietary_therapies__like_the_ketogenic_diet___and_in_some_cases__surgical_intervention____thus__if_the_condition_is_related_to_epilepsy__we_can_assert_that_true__efficacious_treatments_exist	high
MONDO:0007531	electroencephalographic peculiarity: fronto-precentral beta wave groups	hereditary_disease	other	hereditary_disease	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	none
MONDO:0007533	elliptocytosis 2	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	anemia|autoimmune_diseases|metabolic_disorder	kidney_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0007534	Beckwith-Wiedemann syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cancer_or_benign_tumor|cardiovascular_disorder|syndromic_disease	cancer_or_benign_tumor|cardiovascular_disorder	syndromic_disease|musculoskeletal_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	genetics_and_genomics|pediatric	metabolic_disorder	kidney_disorder|reproductive_system_disorder|liver_disorder	false	false	false	false	high
MONDO:0007535	emphysema, hereditary pulmonary	respiratory_system_disorder|hereditary_disease	other	respiratory_system_disorder|hereditary_disease	pulmonology|genetics_and_genomics	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|hereditary|lung_disorder	false	false	false	true	high
MONDO:0007536	congenital lobar emphysema	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	congenital_condition|genetic_disorder|respiratory_disease	chest_disorder|lung_disorder|respiratory_disorder	false	false	false	false	high
MONDO:0007537	lateral meningocele syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	pediatric|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007538	amelogenesis imperfecta, type 3A	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|mouth_disorder|hereditary_disease	genetics_and_genomics|pediatrics	anemia|metabolic_disorder	teeth_disorder|bone_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0007539	encephalopathy, recurrent, of childhood	hereditary_disease|nervous_system_disorder|syndromic_disease	other	syndromic_disease|hereditary_disease|nervous_system_disorder	pediatric|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007540	multiple endocrine neoplasia type 1	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor|endocrine_system_disorder	syndromic_disease|cancer_or_benign_tumor|hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder	genetics_and_genomics|endocrinology|oncology	metabolic_disorder|cancer	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0007542	Camurati-Engelmann disease	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007544	eosinophilia, familial	hereditary_disease	other	hereditary_disease	genetics_and_genomics|immunology|pediatric|hematology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|allergy	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0007545	Eosinophilopenia	hereditary_disease	other	hereditary_disease	immunology|pediatric|hematology	metabolic_disorder|anemia|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0007546	myeloproliferative disorder, chronic, with eosinophilia	musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|immune_system_disorder|hereditary_disease|connective_tissue_disorder|hematologic_disorder	hematology|oncology	anemia|autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0007547	epidermoid cysts	hereditary_disease	other	hereditary_disease	dermatology|general_surgery	inflammatory_disease|cancer	skin_disorder|reproductive_system_disorder	false	false	false	true	low
MONDO:0007548	transient bullous dermolysis of the newborn	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|pediatric	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0007549	generalized dominant dystrophic epidermolysis bullosa	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0007550	epidermolysis bullosa simplex 1A, generalized severe	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0007551	epidermolysis bullosa simplex 1C, localized	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0007552	pretibial dystrophic epidermolysis bullosa	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007553	epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0007554	epidermolysis bullosa simplex 1B, generalized intermediate	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0007555	epidermolysis bullosa simplex 5A, Ogna type	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric	metabolic_disorder|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0007556	epidermolysis bullosa simplex 2F, with mottled pigmentation	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0007557	epidermolysis bullosa with congenital localized absence of skin and deformity of nails	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology|pediatric	genetic_disorder|inflammatory_disease|congenital_abnormality|skin_condition|nail_condition	skin_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007558	self-limited childhood occipital epilepsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	epilepsy_is_not_in_the_list_but__its_subcategory_would_be__autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	medium
MONDO:0007559	photoparoxysmal response 1	hereditary_disease|nervous_system_disorder	other	radiation_induced_disorder|hereditary_disease|nervous_system_disorder	dermatology|ophthalmology|neurology|allergy_and_immunology|pulmonology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007560	reading seizures	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	mental_health_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0007561	multiple epiphyseal dysplasia type 1	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007562	multiple epiphyseal dysplasia, Beighton type	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|connective_tissue_disorder|hereditary_disease|syndromic_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|connective_tissue_disorder|syndromic_disease	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|genetic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007564	pilomatrixoma	hereditary_disease|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder	dermatology|oncology	cancer	skin_disorder	false	false	false	true	low
MONDO:0007565	familial cylindromatosis	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	genetics_and_genomics|dermatology	genetic_disorders|cancer|familial_diseases	skin_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0007566	multiple self-healing squamous epithelioma	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	dermatology|oncology	autoimmune_diseases|cancer	skin_disorder	false	false	false	false	medium
MONDO:0007568	aortic aneurysm, familial thoracic 4	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	pulmonology|genetics_and_genomics|cardiothoracic|cardiology|hematology	cardiovascular_disorder|familial_diseases	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0007569	erythema nodosum, familial	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0007570	erythema palmare hereditarium	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|hereditary_disorder	false	false	false	false	none
MONDO:0007571	primary erythermalgia	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	neurology|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0007572	primary familial polycythemia due to EPO receptor mutation	musculoskeletal_system_disorder|hereditary_disease|hematologic_disorder|immune_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|immune_system_disorder|hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	endocrine_disorder|blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0007573	erythroleukemia, familial, susceptibility to	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	hematology|genetics_and_genomics	anemia|cancer	immune_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0007574	spinocerebellar ataxia type 34	psychiatric_disorder|hereditary_disease|nervous_system_disorder|integumentary_system_disorder	psychiatric_disorder|neurodegenerative_disease	integumentary_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics	cardiovascular_disorder|inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007576	esophageal cancer	cancer_or_benign_tumor|upper_digestive_tract_disorder|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	pulmonology|gastroenterology|oncology	autoimmune_diseases|cancer	lower_gastrointestinal_disorder_upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0007577	esophageal ring, lower	hereditary_disease	other	hereditary_disease	pulmonology|gastroenterology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|throat_disorder	false	false	false	false	low
MONDO:0007581	exchondrosis of pinna, posterior	hereditary_disease	other	hereditary_disease	orthopaedic|otolaryngology	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease|cancer	bone_disorder|joint_disorder|ear_disorder	false	false	false	false	low
MONDO:0007584	exostoses-anetodermia-brachydactyly type E syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology|orthopaedic	autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|skin_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007585	exostoses, multiple, type 1	syndromic_disease|connective_tissue_disorder|musculoskeletal_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder	orthopaedic|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|cancer	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007586	exostoses, multiple, type 2	syndromic_disease|connective_tissue_disorder|musculoskeletal_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder	orthopaedic|oncology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	bone_bone_marrow_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007587	external auditory canal atresia-vertical talus-hypertelorism syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|otorhinolaryngologic_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	orthopaedic|pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder|joint_disorder|ear_disorder	false	false	false	false	high
MONDO:0007588	extrasystoles-short stature-hyperpigmentation-microcephaly syndrome	disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|skin_disorder|skeletal_disorder	false	false	false	false	high
MONDO:0007589	exudative vitreoretinopathy 1	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|cardiovascular_disorder|nervous_system_disorder	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0007590	hemifacial hypertrophy	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	dermatology|pediatric|neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007592	familial recurrent peripheral facial palsy	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	brain_disorder|nerve_disorder_is_incorrect_so_replace_that_with_ear_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007593	facial spasm	hereditary_disease	other	hereditary_disease	otolaryngology|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	low
MONDO:0007594	factor 5 excess with spontaneous thrombosis	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	cardiology|thrombosis_is_more_specific_to_one_category_but_it_can_also_be_related_to_the_above_categories|hematology|genetics_and_genomics	cardiovascular_disorder|inflammatory_disease	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0007595	factor VII and Factor VIII, combined deficiency of	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|inflammatory_disease|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	true	false	false	true	high
MONDO:0007597	factor VIII and Factor IX, combined deficiency of	hereditary_disease	other	hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0007598	factors VIII, IX and XI, combined deficiency of	hereditary_disease	other	hereditary_disease	hematology|genetics_and_genomics	anemia|inflammatory_disease|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder|vascular_disorder	true	false	false	true	high
MONDO:0007599	factor 9 and Factor XI, combined deficiency of	hereditary_disease	other	hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0007600	primary Fanconi syndrome	hereditary_disease|urinary_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|urinary_system_disorder	nephrology|genetics_and_genomics|pediatric	inflammatory_disease|adrenal_gland_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0007601	familial Mediterranean fever, autosomal dominant	hereditary_disease|connective_tissue_disorder|immune_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|connective_tissue_disorder|immune_system_disorder	genetics_and_genomics|pediatric|rheumatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|immune_disorder|liver_disorder|lymphatic_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0007603	Felty syndrome	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder|syndromic_disease	autoimmune_disease	immune_system_disorder|syndromic_disease|musculoskeletal_system_disorder|connective_tissue_disorder|inflammatory_disease	pulmonology|allergy_and_immunology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|liver_disorder|lung_disorder	false	false	false	false	high
MONDO:0007604	femoral-facial syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0007605	fibrinolytic defect	hereditary_disease	other	hereditary_disease	hematology|cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0007606	fibrodysplasia ossificans progressiva	hereditary_disease|musculoskeletal_system_disorder|integumentary_system_disorder	other	musculoskeletal_system_disorder|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|rheumatology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0007608	desmoid tumor	hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|hereditary_disease	oncology|dermatology|orthopaedic	adrenal_gland_disease|cancer	muscle_disorder|skin_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0007609	fibromatosis, gingival, 1	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	mouth_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|dermatology|rheumatology	inflammatory_disease|cancer|anemia|autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007610	gingival fibromatosis-hypertrichosis syndrome	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	teeth_disorder|skin_disorder	false	false	false	false	high
MONDO:0007612	gingival fibromatosis-progressive deafness syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|otolaryngology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	teeth_disorder|ear_disorder	false	false	false	false	high
MONDO:0007614	congenital fibrosis of extraocular muscles	hereditary_disease|musculoskeletal_system_disorder|disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|disorder_of_orbital_region|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007615	laurin-Sandrow syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|dermatology|pediatric|neurology	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0007616	fibula, recurrent dislocation of head of	hereditary_disease	other	hereditary_disease	orthopaedic|bone_and_joint	inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007617	Coffin-Siris syndrome 1	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	skin_disorder|lower_gastrointestinal_disorder|bone_disorder|eye_disorder|joint_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0007618	Eng-Strom syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|ophthalmology	autoimmune_diseases|neurodegenerative_disease	vascular_disorder|eye_disorder|vitreoretinal_disorder	false	false	false	false	medium
MONDO:0007619	isolated congenital adermatoglyphia	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology|pediatric	metabolic_disorder|genetic_disorder	skin_disorder|immune_disorder|reproductive_system_disorder	false	false	false	true	low
MONDO:0007620	fish eye disease	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|ophthalmology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|eye_disorder	false	false	false	true	medium
MONDO:0007621	Floating-Harbor syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder|musculoskeletal_disorder|bone_disorder|eye_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007623	flushing of ears and somnolence	hereditary_disease	other	hereditary_disease	endocrinology|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder_endocrine_disorder	false	false	false	false	low
MONDO:0007624	Flynn-Aird syndrome	hereditary_disease|premature_aging_syndrome	other	premature_aging_syndrome|hereditary_disease	genetics_and_genomics|pulmonology|allergy_and_immunology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0007625	focal epithelial hyperplasia of the oral mucosa	hereditary_disease	other	hereditary_disease	dermatology|pediatric|otolaryngology	epithelial_hyperplasia|inflammatory_disease|cancer|oral_mucosa_disease	teeth_disorder|oral_mucosa_disorder	false	false	false	true	low
MONDO:0007626	familial congenital palsy of trochlear nerve	hereditary_disease|disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0007627	focal facial dermal dysplasia type I	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|bone_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007628	foveal hypoplasia 1	hereditary_disease|cancer_or_benign_tumor|disorder_of_visual_system|urinary_system_disorder|nervous_system_disorder	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region|nervous_system_disorder|urinary_system_disorder|hereditary_disease	genetics_and_genomics|ophthalmology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0007629	fragile site 10Q23	hereditary_disease	other	hereditary_disease	oncology|genetics_and_genomics|pediatric	cancer|neurodegenerative_disease	blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0007630	North Carolina macular dystrophy	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0007631	chromosome 16p12.1 deletion syndrome, 520kb	hereditary_disease|chromosomal_disorder|syndromic_disease	other	syndromic_disease|chromosomal_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|joint_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007633	Friedreich ataxia, so-called, with optic atrophy and sensorineural deafness	hereditary_disease	other	hereditary_disease	genetics_and_genomics|otolaryngology|neurology|ophthalmology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	ear_disorder|eye_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007634	intellectual disability, FRA12A type	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder|genetic_disorder_is_not_listed_but_could_be_inferred_as_fra12a_type_suggests_a_genetic_basis_of_the_intellectual_disability	false	false	false	false	high
MONDO:0007635	Frasier syndrome	hereditary_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|cardiovascular_disorder	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0007636	frontorhiny	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	psychiatry|otolaryngology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	nose_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007637	corneal dystrophy, Fuchs endothelial, 1	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|ophthalmology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0007638	fucosidase regulator	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder	false	false	false	false	high
MONDO:0007639	fundus albipunctatus	hereditary_disease|disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|ophthalmology	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	low
MONDO:0007640	Sorsby fundus dystrophy	hereditary_disease|disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0007642	isolated agenesis of gallbladder	digestive_system_disorder	other	digestive_system_disorder	hepatology|genetics_and_genomics|gastroenterology	inflammatory_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	low
MONDO:0007643	gamma-A-globulin, defect in assembly of	hereditary_disease	other	hereditary_disease	rheumatology|genetics_and_genomics|hematology|allergy_and_immunology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	true	false	false	true	none
MONDO:0007644	IgAD1	hematologic_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hematologic_disorder|hereditary_disease	hepatology|obstetrics_and_gynecology|endocrinology|pediatric	metabolic_disorder|autoimmune_diseases	endocrine_disorder|liver_disorder	false	false	false	false	medium
MONDO:0007646	Gamstorp-Wohlfart syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|obstetrics_and_gynecology|endocrinology|pediatric|neurology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	bone_disorder|joint_disorder|immune_disorder	false	false	false	false	high
MONDO:0007647	gastric volvulus, intrathoracic	hereditary_disease	other	hereditary_disease	pulmonology|gastroenterology|cardiothoracic	abdominal_condition|digestive_system_disorder|gastrointestinal_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0007648	hereditary diffuse gastric adenocarcinoma	hereditary_disease|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|hereditary_disease	oncology|genetics_and_genomics|gastroenterology	cancer|gastrointestinal_disease|genetic_disorder|hereditary_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0007650	MALT lymphoma	hereditary_disease|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|hereditary_disease	oncology|hematology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0007651	gastrocutaneous syndrome	integumentary_system_disorder	other	integumentary_system_disorder	gastroenterology|dermatology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0007652	gastric mucosal hypertrophy	hereditary_disease|digestive_system_disorder|inflammatory_disease	other	inflammatory_disease|digestive_system_disorder|hereditary_disease	gastroenterology|endocrinology	inflammatory_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0007653	genochondromatosis	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|rheumatology	inflammatory_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0007654	genu valgum, st. Helena familial	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007655	fissured tongue	other	other	mouth_disorder	dermatology|oral_pathology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|skin_disorder	false	false	false	false	low
MONDO:0007656	Gerstmann-Straussler-Scheinker syndrome	hereditary_disease|infectious_disease|nervous_system_disorder	infectious_disease	infectious_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0007657	giant neutrophil leukocytes	hereditary_disease	other	hereditary_disease	oncology|hematology|gastroenterology	inflammatory_disease|autoimmune_diseases|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	low
MONDO:0007660	familial ossifying fibroma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease	oncology|genetics_and_genomics|orthopaedic	cancer|familial_tumor_syndromes	bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0007661	Tourette syndrome	syndromic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|syndromic_disease|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007662	anterior segment dysgenesis 4	disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007663	glaucoma with elevated episcleral venous pressure	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	neurology|ophthalmology	inflammatory_disease|cardiovascular_disorder	vascular_disorder|eye_disorder	false	false	false	true	high
MONDO:0007664	glaucoma 1, open angle, A	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|eye_disorder	false	false	false	true	medium
MONDO:0007666	glaucoma-sleep apnea syndrome	disorder_of_visual_system|syndromic_disease	other	disorder_of_visual_system|disorder_of_orbital_region|syndromic_disease	pulmonology|neurology|ophthalmology	sleep_apnea_syndrome_is_not_a_clear_match_for_the_categories_but_it_can_be_associated_with_cardiovascular_disorder__therefore__metabolic_disorder|metabolic_disorder|cardiovascular_disorder	vascular_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007667	subependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurooncology|cancer	brain_disorder|spinal_disorder	false	true	false	false	low
MONDO:0007668	globulin anomaly involving beta (2A)-globulin	hereditary_disease	other	hereditary_disease	hematology|immunology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|adrenal_gland_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0007669	renal cysts and diabetes syndrome	endocrine_system_disorder|digestive_system_disorder|metabolic_disease|hereditary_disease|syndromic_disease	diabetes_mellitus|endocrine_system_disorder|metabolic_disease	metabolic_disease|digestive_system_disorder|endocrine_system_disorder|hereditary_disease|syndromic_disease	pediatric|renal_medicine|genetics_and_genomics|endocrinology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	kidney_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0007670	hypotrichosis-lymphedema-telangiectasia syndrome (grouping)	syndromic_disease|immune_system_disorder	other	immune_system_disorder|syndromic_disease	pediatric|dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	lymphatic_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007671	fibronectin glomerulopathy	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	renal_medicine|nephrology	autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0007672	glomuvenous malformation	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	hematology|genetics_and_genomics	neurodegenerative_disease|cardiovascular_disorder	vascular_disorder|skin_disorder|vessel_disorder	false	false	false	false	medium
MONDO:0007673	Glucoglycinuria	hereditary_disease	other	hereditary_disease	renal_medicine|endocrinology	genetic_disease|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0007674	glucose-6-phosphate dehydrogenase-like	hereditary_disease	other	hereditary_disease	pediatrics|hematology|renal_medicine|genetics_and_genomics|endocrinology	anemia|metabolic_disorder	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0007675	glutamic acid decarboxylase, brain, membrane form	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|psychiatry	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	brain_disorder|brain	false	false	false	false	high
MONDO:0007676	glutathione transferase activity toward trans-stilbene oxide	hereditary_disease	other	hereditary_disease	hepatology|oncology|genetics_and_genomics	cancer|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	low
MONDO:0007677	hyperglycinuria	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	renal_medicine|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0007679	GMS syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007680	multinodular goiter-cystic kidney-polydactyly syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	renal_medicine|genetics_and_genomics|endocrinology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	kidney_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0007681	goiter, multinodular 1, with or without Sertoli-Leydig cell tumors	hereditary_disease|syndromic_disease|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|hereditary_disease|syndromic_disease	oncology|endocrinology	cancer|autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0007682	granddad syndrome	hereditary_disease	other	hereditary_disease	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007683	Grant syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|endocrinology	autoimmune_diseases|adrenal_gland_disease|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0007685	granulosis rubra nasi	hereditary_disease	other	hereditary_disease	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0007686	gray platelet syndrome	hereditary_disease|syndromic_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease|syndromic_disease	hematology|pediatric|genetics_and_genomics	anemia|metabolic_disorder	vascular_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0007687	graying of hair, precocious	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics|endocrinology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	endocrine_disorder|vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0007688	Myhre syndrome	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|psychiatric_disorder	pediatric|genetics_and_genomics|endocrinology	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007689	guanylate kinase 3	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|urology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	kidney_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	none
MONDO:0007690	aromatase excess syndrome	reproductive_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|reproductive_system_disorder|hereditary_disease	pediatric|obstetrics_and_gynecology|endocrinology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0007691	Guillain-Barre syndrome, familial	syndromic_disease|immune_system_disorder|nervous_system_disorder|hereditary_disease	autoimmune_disease	nervous_system_disorder|hereditary_disease|immune_system_disorder|syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|immune_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007693	hypertrichosis cubiti-short stature syndrome	syndromic_disease|integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|orthopaedic|endocrinology	growth_disorder|genetic_disorder|metabolic_disorder|endocrine_disease	bone_disorder|endocrine_disorder|skin_disorder|joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007694	hairy nose tip	hereditary_disease	other	hereditary_disease	dermatology|otolaryngology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	nose_disorder|skin_disorder	false	false	false	false	low
MONDO:0007695	hairy palms and soles	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	congenital_disorder|skin_disorder	false	false	false	false	none
MONDO:0007696	Emery-Nelson syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	hematology|pediatric|genetics_and_genomics	neurodegenerative_disease|anemia|metabolic_disorder	blood_bone_marrow_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007697	hand clasping pattern	hereditary_disease	other	hereditary_disease	pediatrics|neurology|psychiatry	neurodegenerative_disease|autoimmune_diseases|mental_health_disorder	joint_disorder|muscle_disorder	false	false	false	false	none
MONDO:0007698	hand-foot-genital syndrome	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|reproductive_system_disorder|joint_disorder	false	false	false	false	high
MONDO:0007699	Hashimoto thyroiditis	endocrine_system_disorder|immune_system_disorder|inflammatory_disease|hereditary_disease	autoimmune_disease|endocrine_system_disorder	inflammatory_disease|endocrine_system_disorder|hereditary_disease|immune_system_disorder	allergy_and_immunology|rheumatology|endocrinology	autoimmune_diseases|inflammatory_disease	endocrine_disorder|immune_disorder	false	false	false	false	medium
MONDO:0007700	hawkinsinuria	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|renal_medicine	metabolic_disorder|adrenal_gland_disease	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0007701	progressive familial heart block type II	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	pediatric|genetics_and_genomics|cardiology|neurology	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0007702	heart-hand syndrome type 3	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder	heart|vascular_disorder	false	false	false	false	medium
MONDO:0007705	Heinz body anemia	hematologic_disorder	anemia	hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	medium
MONDO:0007706	cavernous hemangiomas of face-supraumbilical midline raphe syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|oncology|dermatology|neurology	congenital_lesion|vascular_anomaly|benign_tumor|birthmark|cancer|genetic_disorder|cutaneous_condition|skin_disorder	vascular_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007707	hemangiomas of small intestine	cancer_or_benign_tumor|digestive_system_disorder|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|cardiovascular_disorder	oncology|hematology|gastroenterology	cancer|inflammatory_disease	vascular_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0007708	Kasabach-Merritt syndrome	hereditary_disease	other	hereditary_disease	oncology|hematology|dermatology	cancer|autoimmune_diseases|inflammatory_disease	vascular_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0007709	hematuria, benign familial, 1	hereditary_disease	other	hereditary_disease	hematology|urology|renal_medicine	cancer|anemia|metabolic_disorder|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0007710	facial hemiatrophy	nervous_system_disorder|syndromic_disease	other	nervous_system_disorder|syndromic_disease	hematology|dermatology	autoimmune_diseases|inflammatory_disease	vascular_disorder|skin_disorder	false	false	false	false	high
MONDO:0007711	Bencze syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	kidney_disorder|urinary_tract_disorder|liver_disorder	false	false	false	false	medium
MONDO:0007712	oculoauriculovertebral spectrum with radial defects	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	spinal_disorder|bone_disorder|eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0007713	clonic hemifacial spasm	nervous_system_disorder	other	nervous_system_disorder	hematology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007715	hemolytic poikilocytic anemia due to reduced ankyrin binding sites	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0007716	alpha thalassemia-intellectual disability syndrome type 1	chromosomal_disorder|hematologic_disorder|syndromic_disease	other	syndromic_disease|hematologic_disorder|chromosomal_disorder	genetics_and_genomics|hematology	neurodegenerative_disease|anemia	brain_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0007717	hemoglobin--variants for which the chain carrying the mutation 1S unknown or uncertain	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	kidney_disorder|vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	none
MONDO:0007718	hepatic adenomas, familial	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor|hereditary_disease	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	hepatology|genetics_and_genomics	cancer|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0007719	diaphragmatic hernia 1	musculoskeletal_system_disorder|hereditary_disease|respiratory_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|respiratory_system_disorder	cardiothoracic|general_surgery|urology	cardiovascular_disorder|inflammatory_disease|surgical_condition	abdominal_disorder|upper_gastrointestinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007720	hernia, double inguinal	hereditary_disease	other	hereditary_disease	pediatric|urology	adrenal_gland_disease|inflammatory_disease	reproductive_system_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0007721	hiatus hernia	digestive_system_disorder	other	digestive_system_disorder	cardiothoracic|surgical|gastroenterology	cardiovascular_disorder|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0007722	heterochromia iridis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|autoimmune_diseases|anemia	eye_disorder	false	false	false	false	low
MONDO:0007724	hirsutism-skeletal dysplasia-intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|endocrinology|dermatology	genetic_disease|developmental_disorder|endocrine_disease|metabolic_disorder	spinal_disorder|reproductive_system_disorder|endocrine_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007725	hereditary progressive mucinous histiocytosis	immune_system_disorder	other	immune_system_disorder	genetics_and_genomics|oncology|pediatrics	hereditary___note__i_corrected_the_formatting_to_meet_your_requirements|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	low
MONDO:0007726	hip dysplasia, Beukes type	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|rheumatology|genetics_and_genomics|orthopaedic	genetic_disorder|orthopedic_condition|joint_disease|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0007727	TNF receptor 1-associated periodic fever syndrome	hereditary_disease|syndromic_disease|connective_tissue_disorder|immune_system_disorder	other	hereditary_disease|immune_system_disorder|syndromic_disease|connective_tissue_disorder	rheumatology|genetics_and_genomics|pediatrics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder	false	false	false	false	high
MONDO:0007728	acne inversa, familial, 1	hereditary_disease|inflammatory_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|inflammatory_disease	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	liver_disorder|skin_disorder|immune_disorder	false	false	false	true	high
MONDO:0007729	developmental dysplasia of the hip 1	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|orthopaedic	neurodegenerative_disease|developmental_disease|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0007730	histiocytic dermatoarthritis	hereditary_disease	other	hereditary_disease	rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|joint_disorder|immune_disorder	false	false	false	false	high
MONDO:0007732	Holt-Oram syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease|syndromic_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|genetics_and_genomics|cardiology	developmental_disorder|cardiovascular_disorder|congenital_disorder	ear_disorder|heart_disorder	false	false	false	false	medium
MONDO:0007733	holoprosencephaly 3	endocrine_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	endocrine_system_disorder	nervous_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder	pediatric|genetics_and_genomics|neurology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0007734	holoprosencephaly 4	endocrine_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	endocrine_system_disorder	nervous_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder	genetics_and_genomics|neurology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|lung_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0007735	congenital Horner syndrome	nervous_system_disorder	other	nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0007737	humeroradial synostosis	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	autoimmune_diseases|metabolic_disorder|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007738	spondyloepiphyseal dysplasia with congenital joint dislocations	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|rheumatology|genetics_and_genomics|orthopaedic	autoimmune_diseases|metabolic_disorder|inflammatory_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0007739	Huntington disease	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0007740	Wagner disease	nervous_system_disorder|hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease	cardiothoracic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	vascular_disorder|eye_disorder|liver_disorder	false	false	false	true	high
MONDO:0007741	congenital hydronephrosis	urinary_system_disorder	other	urinary_system_disorder	pediatric|urology	congenital_anomaly|metabolic_disorder|urological_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0007742	5-hydroxytryptamine oxygenase regulator	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0007743	attention deficit-hyperactivity disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	pediatric|neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0007744	cholesterol-ester transfer protein deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|cardiology|endocrinology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|liver_disorder	false	false	false	true	medium
MONDO:0007745	Gilbert syndrome	hereditary_disease|metabolic_disease|syndromic_disease	metabolic_disease	hereditary_disease|metabolic_disease|syndromic_disease	hepatology|genetics_and_genomics|hematology	anemia|metabolic_disorder	liver_disorder	false	false	false	false	low
MONDO:0007746	orthostatic hypotensive disorder, Streeten type	hereditary_disease	other	hereditary_disease	pediatric|cardiology|neurology	cardiovascular_disorder|adrenal_gland_disease	vascular_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0007747	isolated hyperchlorhidrosis	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|otolaryngology|ophthalmology	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	skin_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0007748	hypercalciuria, absorptive, 2	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	gastroenterology|renal_medicine	metabolic_disorder|absorptive|adrenal_gland_disease	kidney_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0007750	hypercholesterolemia, familial, 1	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|rheumatology|cardiology|hematology|renal_medicine|endocrinology	cardiovascular_disorder|metabolic_disorder	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0007751	hypercholesterolemia, autosomal dominant, type B	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|cardiology|endocrinology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0007752	hyperheparinemia	hereditary_disease	other	hereditary_disease	oncology|cardiology|hematology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|liver_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0007753	Frey syndrome	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	otolaryngology|neurology	autoimmune_diseases|inflammatory_disease	nose_disorder|throat_disorder	false	false	false	false	medium
MONDO:0007754	hyperhidrosis palmaris ET plantaris	hereditary_disease	other	hereditary_disease	dermatology|neurology	autoimmune_diseases|inflammatory_disease	skin_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0007755	hyperimmunoglobulin G1(A1) syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|immunology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0007756	hyperkeratosis lenticularis perstans	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder_liver_disorder	false	false	false	false	low
MONDO:0007757	hyperkeratosis-hyperpigmentation syndrome	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	liver_disorder|skin_disorder	false	false	false	false	low
MONDO:0007758	epidermolytic palmoplantar keratoderma, 1	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0007759	hyperlipidemia, familial combined, LPL related	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|cardiology|endocrinology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0007760	hyperlipoproteinemia, type II, and deafness	hereditary_disease	other	hereditary_disease	genetics_and_genomics|otolaryngology|endocrinology	autoimmune_diseases|metabolic_disorder	ear_disorder|liver_disorder	false	false	false	false	medium
MONDO:0007762	hyperlipoproteinemia type V	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology|pediatric	cardiovascular_disorder|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0007763	nonpapillary renal cell carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	renal_cell_carcinoma|cancer	kidney_disorder|urinary_tract_disorder|renal_disorder	false	true	false	true	high
MONDO:0007764	autosomal dominant osteosclerosis, Worth type	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0007765	hyperostosis cranialis interna	hereditary_disease	other	hereditary_disease	rheumatology|neurology|orthopaedic	autoimmune_diseases|metabolic_disorder|inflammatory_disease	spinal_disorder|bone_disorder|skull_bone_disorder	false	false	false	false	low
MONDO:0007766	Morgagni-Stewart-Morel syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|genetics_and_genomics|cardiology|pediatrics|dermatology|neurology|renal_medicine|orthopaedic	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	bone_disorder|joint_disorder|musculoskeletal_disorder_is_not_listed_so__bone_disorder	false	false	false	false	low
MONDO:0007767	hyperparathyroidism 1	endocrine_system_disorder|cancer_or_benign_tumor|hereditary_disease|musculoskeletal_system_disorder|connective_tissue_disorder|syndromic_disease	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|musculoskeletal_system_disorder|cancer_or_benign_tumor|syndromic_disease|connective_tissue_disorder|endocrine_system_disorder	renal_medicine|endocrinology	endocrine_disease|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0007768	hyperparathyroidism 2 with jaw tumors	endocrine_system_disorder|cancer_or_benign_tumor|hereditary_disease|musculoskeletal_system_disorder|connective_tissue_disorder|syndromic_disease	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|musculoskeletal_system_disorder|cancer_or_benign_tumor|syndromic_disease|connective_tissue_disorder|endocrine_system_disorder	oncology|otolaryngology|endocrinology	metabolic_disorder|cancer	teeth_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0007769	hyperpigmentation of eyelid	hereditary_disease	other	hereditary_disease	dermatology|ophthalmology	autoimmune_diseases|metabolic_disorder|pigmentation_disorder|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0007770	hyperpigmentation of Fuldauer and Kuijpers	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0007771	hyperpigmentation with or without hypopigmentation, familial progressive	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	neurodegenerative_disease|metabolic_disorder	skin_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0007772	pseudohypoaldosteronism type 2A	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	genetics_and_genomics|renal_medicine|endocrinology|pediatric	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0007773	hyperproglucagonemia	hereditary_disease	other	hereditary_disease	endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder	false	false	true	false	high
MONDO:0007774	hyperreflexia	hereditary_disease	other	hereditary_disease	neurology|psychiatry	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007775	hypersecretion of adrenal androgens, familial	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatrics|endocrinology	metabolic_disorder|autoimmune_diseases|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0007776	hypersensitivity pneumonitis, familial	immune_system_disorder|respiratory_system_disorder|hereditary_disease|inflammatory_disease	other	hereditary_disease|immune_system_disorder|respiratory_system_disorder|inflammatory_disease	genetics_and_genomics|pulmonology|allergy_and_immunology	allergy|autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	true	high
MONDO:0007777	hypotaurinemic retinal degeneration and cardiomyopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|cardiology|ophthalmology	cardiovascular_disorder|metabolic_disorder	kidney_disorder|eye_disorder|heart_disorder	false	false	false	false	medium
MONDO:0007781	essential hypertension, genetic	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	genetics_and_genomics|cardiology|renal_medicine	cardiovascular_disorder|metabolic_disorder	kidney_disorder|vascular_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0007782	hyperthermia, cutaneous, with headaches and nausea	hereditary_disease	other	hereditary_disease	general_medicine|emergency_medicine|pediatrics|internal_medicine|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	vascular_disorder|skin_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0007784	selective pituitary resistance to thyroid hormone	endocrine_system_disorder|hereditary_disease|metabolic_disease	endocrine_system_disorder|metabolic_disease	hereditary_disease|metabolic_disease|endocrine_system_disorder	genetics_and_genomics|pediatrics|neurology|endocrinology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	brain_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0007785	hyperthyroxinemia, dystransthyretinemic	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	endocrinology	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0007787	Ambras type hypertrichosis universalis congenita	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	hereditary_disease|syndromic_disease|integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	skin_disorder|immune_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0007788	hypertriglyceridemia 1	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|cardiology|endocrinology	cardiovascular_disorder|metabolic_disorder	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0007789	hypertrophia musculorum vera	hereditary_disease	other	hereditary_disease	genetics_and_genomics|endocrinology|pediatric	autoimmune_diseases|metabolic_disorder	muscle_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0007790	Charcot-Marie-Tooth disease type 3	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007791	familial hypocalciuric hypercalcemia 1	musculoskeletal_system_disorder|respiratory_system_disorder|hereditary_disease|endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease	hereditary_disease|metabolic_disease|endocrine_system_disorder|respiratory_system_disorder|musculoskeletal_system_disorder	genetics_and_genomics|renal_medicine|endocrinology	familial_hypercalciuric_hypocalcemia|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0007792	familial hypocalciuric hypercalcemia 2	respiratory_system_disorder|hereditary_disease|endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease	hereditary_disease|metabolic_disease|endocrine_system_disorder|respiratory_system_disorder	genetics_and_genomics|renal_medicine|endocrinology	familial_hypercalcemic_syndrome|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0007793	hypochondroplasia	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	skeletal_disease|genetic_disorder|metabolic_disorder	bone_disorder|muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	low
MONDO:0007794	hypogonadotropic hypogonadism 7 with or without anosmia	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	pediatric|neurology|endocrinology	metabolic_disorder|endocrine_system_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0007795	mullerian duct anomalies-limb anomalies syndrome	disorder_of_development_or_morphogenesis|reproductive_system_disorder|syndromic_disease	other	syndromic_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|developmental_abnormality	limb_anomalies_syndrome|reproductive_system_disorder	false	false	false	false	medium
MONDO:0007796	hypoparathyroidism, familial isolated 1	hereditary_disease|endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease	hereditary_disease|metabolic_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder	hypoparathyroidism|endocrine_disorder	false	false	false	false	medium
MONDO:0007797	hypoparathyroidism-deafness-renal disease syndrome	hereditary_disease|chromosomal_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|chromosomal_disorder	genetics_and_genomics|renal_medicine|endocrinology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	kidney_disorder|ear_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0007799	hypophosphatemic bone disease	hereditary_disease	other	hereditary_disease	renal_medicine|rheumatology|endocrinology	adrenal_gland_disease|metabolic_disorder	bone_disorder|kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0007800	chromosome 18p deletion syndrome	chromosomal_disorder|syndromic_disease	other	syndromic_disease|chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|immune_disorder	false	false	false	false	high
MONDO:0007802	hypospadias 3, autosomal	disorder_of_development_or_morphogenesis|hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|urology	genetic_disorder|metabolic_disorder	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0007803	multiple system atrophy	hereditary_disease|metabolic_disease|nervous_system_disorder	neurodegenerative_disease|metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	renal_medicine|neurology	neurodegenerative_disease|adrenal_gland_disease	vascular_disorder|spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0007804	Pallister-Hall syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder|musculoskeletal_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|endocrine_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0007805	hypotrichosis 2	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	hair_disorder_is_not_a_category_in_the_list_so__skin_disorder|liver_disorder|skin_disorder	false	false	false	true	low
MONDO:0007807	hypoxanthine guanine phosphoribosyltransferase suppressor	hereditary_disease	other	hereditary_disease	pediatrics|genetics_and_genomics|oncology	genetic_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0007808	ichthyosis hystrix of Curth-Macklin	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0007809	ichthyosis histrix, Lambert type	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0007810	autosomal dominant ichthyosis vulgaris	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder	skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0007811	ichthyosis-cheek-eyebrow syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007812	ichthyosis, lamellar, autosomal dominant	hereditary_disease|integumentary_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	skin_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0007813	superficial epidermolytic ichthyosis	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	skin_disorder	false	false	false	false	medium
MONDO:0007814	immune deficiency, familial variable	hereditary_disease|immune_system_disorder|syndromic_disease|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor|syndromic_disease	allergy_and_immunology|genetics_and_genomics	immune_deficiency|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0007817	IgE responsiveness, atopic	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	allergy_and_immunology|pediatric	autoimmune_diseases|allergy	skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0007818	hyper-IgE recurrent infection syndrome 1, autosomal dominant	hereditary_disease|immune_system_disorder|hematologic_disorder	other	hematologic_disorder|hereditary_disease|immune_system_disorder	pediatrics|allergy_and_immunology|genetics_and_genomics|immunology|medicine	inflammatory_disease|autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	true	false	false	false	high
MONDO:0007819	solitary median maxillary central incisor syndrome	endocrine_system_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	dental|genetics_and_genomics	adrenal_gland_disease|autoimmune_diseases|cancer	teeth_disorder|bone_disorder|jaw_disorder	false	false	false	false	medium
MONDO:0007820	fused mandibular incisors	hereditary_disease	other	hereditary_disease	otolaryngology|orthopaedic|pediatric	inflammatory_disease|autoimmune_diseases	teeth_disorder|bone_disorder	false	false	false	false	low
MONDO:0007824	incisors, lower central, absence of	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|oral_surgery|pediatric	neurodegenerative_disease|autoimmune_diseases	teeth_disorder|lower_central_dental_disorder	false	false	false	false	medium
MONDO:0007825	incisors, rotation of upper central	hereditary_disease	other	hereditary_disease	neurology|orthopaedic|pediatric	neurodegenerative_disease|developmental_disorder	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007826	incisors, shovel-shaped	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|otolaryngology|orthopaedic|pediatric	neurodegenerative_disease|metabolic_disorder	teeth_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0007827	inclusion body myositis	musculoskeletal_system_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|inflammatory_disease	neurology|rheumatology	inflammatory_disease|autoimmune_diseases	muscle_disorder|immune_disorder	false	false	false	false	high
MONDO:0007829	cholestasis, intrahepatic, of pregnancy, 1	hereditary_disease|endocrine_system_disorder|digestive_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease	metabolic_disease|hereditary_disease|digestive_system_disorder|endocrine_system_disorder	hepatology|obstetrics_and_gynecology	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0007830	insensitivity to pain with hyperplastic Myelinopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|blood_bone_marrow_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007831	insect Stings, hypersensitivity to	hereditary_disease	other	hereditary_disease	allergy_and_immunology|dermatology	autoimmune_diseases|allergy	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0007832	interferon antiviral depressor	hereditary_disease	other	hereditary_disease	neurology|immunology|psychiatry|allergy_and_immunology	mental_health_disorder|autoimmune_diseases	liver_disorder|immune_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0007833	iris pigment layer, cleavage of	hereditary_disease	other	hereditary_disease	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	none
MONDO:0007834	islet cell adenomatosis	endocrine_system_disorder|digestive_system_disorder|hereditary_disease	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	endocrine_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0007835	intussusception	digestive_system_disorder|hereditary_disease	other	digestive_system_disorder|hereditary_disease	pediatric|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0007836	IVIC syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|allergy_and_immunology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0007837	Johnson neuroectodermal syndrome	syndromic_disease|integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	lymphatic_disorder|brain_disorder|muscle_disorder|immune_disorder|blood_bone_marrow_disorder|throat_disorder|spinal_disorder|nose_disorder	false	false	false	false	high
MONDO:0007838	Jacobsen syndrome	syndromic_disease|hereditary_disease|chromosomal_disorder|hematologic_disorder	other	hematologic_disorder|hereditary_disease|syndromic_disease|chromosomal_disorder	pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0007839	Aase-Smith syndrome	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0007840	internal carotid artery, spontaneous dissection of	hereditary_disease	other	hereditary_disease	cardiology|neurology|hematology	vessel_disorder|cardiovascular_disorder|arterial_disorder	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0007841	coxopodopatellar syndrome	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007842	joint laxity, familial	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	orthopaedic|rheumatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0007843	Kabuki syndrome 1	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	joint_disorder|skin_disorder|reproductive_system_disorder|eye_disorder	false	false	false	false	high
MONDO:0007844	hypogonadotropic hypogonadism 2 with or without anosmia	syndromic_disease|reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder|syndromic_disease	endocrinology|neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0007845	Kaposi sarcoma, susceptibility to	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	genetics_and_genomics|oncology|dermatology|hematology	anemia|cancer|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder|skin_disorder	true	true	false	true	high
MONDO:0007846	KBG syndrome	syndromic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0007847	keloid formation	hereditary_disease	other	hereditary_disease	plastic_surgery|dermatology	inflammatory_disease|autoimmune_diseases	muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007848	autosomal dominant keratitis	disorder_of_visual_system|inflammatory_disease|hereditary_disease	other	hereditary_disease|inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0007849	keratitis fugax hereditaria	hereditary_disease	other	hereditary_disease	ophthalmology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	low
MONDO:0007850	autosomal dominant keratitis-ichthyosis-hearing loss syndrome	syndromic_disease|integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease|syndromic_disease	otolaryngology|pediatric|genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	skin_disorder|ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0007851	keratoconus 1	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|optometrist	inflammatory_disease|autoimmune_diseases	bone_disorder|muscle_disorder|skin_disorder|spinal_disorder|eye_disorder	false	false	false	true	medium
MONDO:0007852	palmoplantar keratoderma-deafness syndrome	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	otolaryngology|pediatric|neurology|genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	skin_disorder|ear_disorder	false	false	false	false	high
MONDO:0007853	palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome	syndromic_disease|integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	muscle_disorder|skin_disorder	false	false	false	true	medium
MONDO:0007854	keratolytic winter erythema	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007855	keratosis, familial actinic	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	cancer|inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0007856	palmoplantar keratoderma-esophageal carcinoma syndrome	integumentary_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|oncology|dermatology	cancer|autoimmune_diseases	skin_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0007857	keratosis palmaris et plantaris-clinodactyly syndrome	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	orthopaedic|pediatric|genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007858	palmoplantar keratoderma, punctate type 1A	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder	false	false	false	false	medium
MONDO:0007859	palmoplantar keratoderma i, striate, focal, or diffuse	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	rheumatology|genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007860	focal palmoplantar and gingival keratoderma	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	gingival_disorder|skin_disorder|palmoplantar_disorder	false	false	false	true	medium
MONDO:0007861	isolated cloverleaf skull syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	bone_disorder|skull_disorder	false	false	false	false	high
MONDO:0007862	Waardenburg syndrome type 3	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	hearing_loss|ear_disorder	false	false	false	false	medium
MONDO:0007863	Kleine-Levin syndrome	syndromic_disease	other	sleep_disorder|syndromic_disease	psychiatry|neurology	mental_health_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|sleep_disorder	false	false	false	false	medium
MONDO:0007864	angioosteohypertrophic syndrome	syndromic_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	cardiology|pediatric|pulmonology	cardiovascular_disorder|adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0007865	knuckle pads	hereditary_disease	other	hereditary_disease	orthopaedic|rheumatology|dermatology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0007866	Bart-Pumphrey syndrome	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics|pulmonology	adrenal_gland_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0007867	nonsyndromic congenital nail disorder 2	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder	skin_disorder|nail_disorder	false	false	false	false	low
MONDO:0007868	hyperekplexia 1	nervous_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0007869	Kyrle disease	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder|neurodegenerative_disease	joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007870	labia minora, incomplete adhesion of	hereditary_disease	other	hereditary_disease	obstetrics_and_gynecology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|reproductive_system_disorder	false	false	false	true	low
MONDO:0007871	familial congenital nasolacrimal duct obstruction	otorhinolaryngologic_disease|hereditary_disease	other	hereditary_disease|otorhinolaryngologic_disease	otolaryngology|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|congenital_duct_obstruction	nose_disorder|eye_disorder	false	false	false	false	low
MONDO:0007872	LADD syndrome	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	ear_disorder|eye_disorder	false	false	false	true	high
MONDO:0007873	lactic acidosis, chronic adult form	hereditary_disease	other	hereditary_disease	cardiology|endocrinology|gastroenterology|renal_medicine|pulmonology	adrenal_gland_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0007874	trichorhinophalangeal syndrome type II	integumentary_system_disorder|syndromic_disease|musculoskeletal_system_disorder|chromosomal_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease|syndromic_disease|chromosomal_disorder|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0007875	Larsen syndrome	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	endocrinology|orthopaedic|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	bone_disorder|joint_disorder|ear_disorder	false	false	false	false	high
MONDO:0007876	laryngeal abductor paralysis	respiratory_system_disorder|otorhinolaryngologic_disease	other	otorhinolaryngologic_disease|respiratory_system_disorder	otolaryngology|neurology|pulmonology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|throat_disorder	false	false	false	false	medium
MONDO:0007877	laryngeal adductor paralysis	hereditary_disease	other	hereditary_disease	otolaryngology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|throat_disorder	false	false	false	false	high
MONDO:0007878	congenital laryngomalacia	respiratory_system_disorder	other	respiratory_system_disorder	otolaryngology|pediatric	respiratory_disorder|neurodevelopmental_disorder	muscle_disorder|throat_disorder	false	false	false	false	low
MONDO:0007879	larynx atresia	respiratory_system_disorder|otorhinolaryngologic_disease	other	otorhinolaryngologic_disease|respiratory_system_disorder	otolaryngology|pediatric	congenital_disorder|neurodegenerative_disease	throat_disorder	false	false	false	false	high
MONDO:0007880	congenital laryngeal web	syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|syndromic_disease	pediatric|otolaryngology	congenital__disorder|respiratory_disease	lung_disorder|throat_disorder	false	false	false	false	medium
MONDO:0007881	tooth agenesis, selective, 4	integumentary_system_disorder|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|integumentary_system_disorder|hereditary_disease|syndromic_disease|mouth_disorder	pediatric|genetics_and_genomics|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	selective|teeth_disorder	false	false	false	true	medium
MONDO:0007882	lattice degeneration of retina leading to retinal detachment	hereditary_disease	other	hereditary_disease	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0007883	periodic fever, immunodeficiency, and thrombocytopenia syndrome	hereditary_disease	other	hereditary_disease	hematology|pediatric|immunology	immunodeficiency|inflammatory_disease|anemia|thrombocytopenia	liver_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0007884	leg ulcers, familial, of juvenile onset	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	joint_disorder|blood_bone_marrow_disorder|immune_disorder|skin_disorder	false	false	false	true	high
MONDO:0007885	Legg-Calve-Perthes disease	syndromic_disease|connective_tissue_disorder|hereditary_disease|musculoskeletal_system_disorder	other	connective_tissue_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007886	uterine corpus leiomyoma	reproductive_system_disorder|connective_tissue_disorder|hereditary_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|hereditary_disease|reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|obstetrics_and_gynecology	cancer|gynecological_disorder	muscle_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0007887	leiomyoma of vulva and esophagus	urinary_system_disorder|chromosomal_disorder	other	urinary_system_disorder|chromosomal_disorder	oncology|obstetrics_and_gynecology	cancer	muscle_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0007888	hereditary leiomyomatosis and renal cell cancer	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	urology|genetics_and_genomics|oncology	cancer|hereditary_disorder	reproductive_system_disorder|urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0007890	lentiginosis, centrofacial neurodysraphic	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	brain_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007891	familial generalized lentiginosis	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|neurodegenerative_disease	skin_disorder	false	false	false	false	low
MONDO:0007892	Lenz-Majewski hyperostotic dwarfism	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|inflammatory_disease	muscle_disorder|joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0007893	Noonan syndrome with multiple lentigines	syndromic_disease|hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|dermatology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	heart_disorder|skin_disorder	false	false	false	false	high
MONDO:0007894	Leri pleonosteosis	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	neurology|orthopaedic|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007895	platyspondylic dysplasia, Torrance type	syndromic_disease|connective_tissue_disorder|hereditary_disease|musculoskeletal_system_disorder	other	connective_tissue_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0007896	acute monocytic leukemia	immune_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor|acute_disease|musculoskeletal_system_disorder	hematology|oncology	autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0007898	leukocyte nuclear appendages, hereditary prevalence of	hereditary_disease	other	hereditary_disease	hematology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	none
MONDO:0007899	lichen sclerosus et atrophicus	integumentary_system_disorder|inflammatory_disease|hereditary_disease	other	integumentary_system_disorder|hereditary_disease|inflammatory_disease	pediatric|dermatology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007900	nonsyndromic congenital nail disorder 3	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	genetic_disorder|congenital_disease|metabolic_disorder	skin_disorder|nail_disorder	false	false	false	false	medium
MONDO:0007901	levator-medial rectus synkinesis	hereditary_disease	other	hereditary_disease	neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0007902	lichen planus, familial	hereditary_disease|integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|hereditary_disease|inflammatory_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	liver_disorder|skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0007904	median nodule of the upper lip	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|otolaryngology|dermatology	cancer|autoimmune_diseases|inflammatory_disease	skin_disorder|upper_gastrointestinal_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0007905	lip, hamartomatous	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|oncology	adrenal_gland_disease|metabolic_disorder|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0007906	familial partial lipodystrophy, Dunnigan type	hereditary_disease|integumentary_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	endocrinology|genetics_and_genomics|dermatology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|skin_disorder	false	false	true	false	high
MONDO:0007907	lipoma of the conjunctiva	disorder_of_visual_system|nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region|nervous_system_disorder|musculoskeletal_system_disorder	dermatology|ophthalmology	cancer|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0007908	multiple symmetric lipomatosis	hereditary_disease|integumentary_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|integumentary_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|dermatology	lipomatosis|metabolic_disorder	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007909	familial multiple lipomatosis	integumentary_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|integumentary_system_disorder|musculoskeletal_system_disorder	genetics_and_genomics|dermatology	neurofibromatosis_is_not_listed_but_this_disease_has_some_similarities_to_it__however_familial_multiple_lipomatosis_could_be_categorized_as___metabolic_disorder|cancer|inflammatory_disease	skin_disorder|muscle_disorder	false	false	false	false	low
MONDO:0007910	lipoprotein types--Lt system	hereditary_disease	other	hereditary_disease	endocrinology|hepatology|cardiology	cardiovascular_disorder|metabolic_disorder	liver_disorder|lipoprotein_types__lt_system	false	false	false	false	none
MONDO:0007911	lipoprotein, variant of beta	hereditary_disease	other	hereditary_disease	endocrinology|genetics_and_genomics|hematology|cardiology	cardiovascular_disorder|metabolic_disorder	liver_disorder|vascular_disorder	false	false	false	false	none
MONDO:0007912	lithium transport	hereditary_disease	other	hereditary_disease	endocrinology|psychiatry|neurology|renal_medicine	mental_health_disorder|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	false	none
MONDO:0007913	low density lipoprotein, variation in molecular weight of	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology|cardiology	cardiovascular_disorder|metabolic_disorder	liver_disorder|vascular_disorder	false	false	false	true	high
MONDO:0007914	lumbar stenosis, familial	hereditary_disease	other	hereditary_disease	orthopaedic|neurology	neurodegenerative_disease|inflammatory_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007915	systemic lupus erythematosus	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	immune_system_disorder|connective_tissue_disorder	allergy_and_immunology|rheumatology	autoimmune_diseases|inflammatory_disease	joint_disorder|skin_disorder|kidney_disorder|immune_disorder	false	false	false	true	high
MONDO:0007916	primary intestinal lymphangiectasia	digestive_system_disorder	other	digestive_system_disorder	pediatric|gastroenterology|oncology	autoimmune_diseases|cancer|inflammatory_disease	upper_gastrointestinal_disorder|lymphatic_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0007917	lymphedema-cerebral arteriovenous anomaly syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|hematology|neurology	cardiovascular_disorder|neurodegenerative_disease|autoimmune_diseases|anemia|inflammatory_disease	brain_disorder|lymphatic_disorder|vascular_disorder	false	false	false	false	high
MONDO:0007918	microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability	hereditary_disease|cardiovascular_disorder|syndromic_disease|disorder_of_visual_system|immune_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|psychiatric_disorder	cardiovascular_disorder|psychiatric_disorder	psychiatric_disorder|syndromic_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|immune_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|lymphatic_disorder|intellectual_disability|eye_disorder	true	false	false	false	very_high
MONDO:0007919	lymphatic malformation 1	hereditary_disease|cardiovascular_disorder|immune_system_disorder	cardiovascular_disorder	hereditary_disease|immune_system_disorder|cardiovascular_disorder	pediatric|hematology|oncology	cancer|lymphatic_disorder	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0007920	lymphatic malformation 5	hereditary_disease|nervous_system_disorder|cardiovascular_disorder|immune_system_disorder	cardiovascular_disorder	hereditary_disease|nervous_system_disorder|cardiovascular_disorder|immune_system_disorder	hematology|oncology|pediatric	vascular_disorder|lymphatic_disorder|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0007921	yellow nail syndrome	syndromic_disease|immune_system_disorder	other	syndromic_disease|immune_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|inflammatory_disease	liver_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007922	lymphedema-distichiasis syndrome	hereditary_disease|syndromic_disease|cardiovascular_disorder|immune_system_disorder	cardiovascular_disorder	syndromic_disease|hereditary_disease|cardiovascular_disorder|immune_system_disorder	genetics_and_genomics|dermatology|hematology|oncology	autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0007923	macrocephaly, benign familial	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	true	low
MONDO:0007924	Bannayan-Riley-Ruvalcaba syndrome	hereditary_disease|syndromic_disease|cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|cardiovascular_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|cancer|metabolic_disorder	spinal_disorder|vascular_disorder	false	false	false	false	high
MONDO:0007925	myelodysplastic syndrome associated with isolated del(5q)	hematologic_disorder|hereditary_disease|chromosomal_disorder|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor|anemia	cancer_or_benign_tumor|hematologic_disorder|syndromic_disease|chromosomal_disorder|hereditary_disease	genetics_and_genomics|hematology|oncology	cancer|anemia	bone_disorder|blood_bone_marrow_disorder	false	true	false	true	medium
MONDO:0007927	congenital macroglossia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|congenital_disease	endocrine_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007930	Bernard-Soulier syndrome, type A2, autosomal dominant	hematologic_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|hematologic_disorder|hereditary_disease	genetics_and_genomics|pediatrics|hematology|cardiology	neurodegenerative_disease|metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0007931	vitelliform macular dystrophy 2	psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0007932	age related macular degeneration 2	psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0007933	vitelliform macular dystrophy 1	psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0007934	benign concentric annular macular dystrophy	psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0007935	cystoid macular edema	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0007936	macular dystrophy, fenestrated sheen type	psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	eye_disorder	false	false	false	true	medium
MONDO:0007937	renal hypomagnesemia 2	urinary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|urinary_system_disorder|hereditary_disease	nephrology|renal_medicine	metabolic_disorder|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0007938	46,XY sex reversal 4	musculoskeletal_system_disorder|hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder|endocrine_system_disorder	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease|cardiovascular_disorder|reproductive_system_disorder	genetics_and_genomics|endocrinology|urology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0007941	malocclusion due to protuberant upper front teeth	hereditary_disease	other	hereditary_disease	otolaryngology|orthopaedic|pediatric	dental_disease|orthodontic_problem|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder|muscle_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0007942	Mammastatin	hereditary_disease	other	hereditary_disease	neurology|hematology|oncology	autoimmune_diseases|cancer|adrenal_gland_disease	blood_bone_marrow_disorder|breast_disorder	false	false	false	false	medium
MONDO:0007943	Nager acrofacial dysostosis	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|ear_disorder|spinal_disorder|bone_disorder|skin_disorder|muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0007944	Treacher Collins syndrome 1	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|otolaryngology|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder|throat_disorder|facial_disorder|skin_disorder	false	false	false	false	medium
MONDO:0007945	mannose 6-phosphate receptor recognition defect, Lebanese type	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0007946	jaw-winking syndrome	nervous_system_disorder|syndromic_disease|disorder_of_visual_system	other	disorder_of_visual_system|syndromic_disease|nervous_system_disorder	neurology|otolaryngology|ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|mental_health_disorder	spinal_disorder|muscle_disorder|eye_disorder	false	false	false	false	low
MONDO:0007947	Marfan syndrome	musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder|syndromic_disease	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|connective_tissue_disorder	genetics_and_genomics|orthopaedic|cardiology	autoimmune_diseases|metabolic_disorder|cardiovascular_disorder	joint_disorder|vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0007948	marfanoid hypermobility syndrome	hereditary_disease	other	hereditary_disease	rheumatology|genetics_and_genomics|orthopaedic	genetic_disorder|cardiovascular_disorder	joint_disorder|vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0007949	Marshall syndrome	musculoskeletal_system_disorder|hereditary_disease|integumentary_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	disorder_of_development_or_morphogenesis|disorder_of_visual_system|musculoskeletal_system_disorder|syndromic_disease|disorder_of_orbital_region|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|neurology|dermatology|cardiology|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0007950	mastocytosis	hematologic_disorder|hereditary_disease|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|hereditary_disease|immune_system_disorder	immunology|hematology|allergy_and_immunology	allergy|autoimmune_diseases|cancer	blood_bone_marrow_disorder|skin_disorder|immune_disorder	false	false	false	true	high
MONDO:0007951	masticatory muscles, hypertrophy of	hereditary_disease	other	hereditary_disease	neurology|orthopaedic	neuromuscular_disease|musculoskeletal_disease|metabolic_disorder	muscle_disorder|teeth_disorder	true	false	false	false	low
MONDO:0007952	maxillofacial dysostosis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|otolaryngology|orthopaedic|pediatric	inflammatory_disease|autoimmune_diseases|developmental_disorder|metabolic_disorder	spinal_disorder|bone_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0007953	Binder syndrome	respiratory_system_disorder|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease|respiratory_system_disorder	neurology|pediatric	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007955	Meckel diverticulum	hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease	surgery|gastroenterology|pediatric	inflammatory_disease|cancer|cardiovascular_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0007956	Pai syndrome	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|orthopaedic	inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0007957	mediosternal depigmentation line	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|anemia|metabolic_disorder|adrenal_gland_disease	skin_disorder	false	false	false	false	low
MONDO:0007958	familial medullary thyroid carcinoma	hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor|syndromic_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder|cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|syndromic_disease|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology|oncology	familial_medullary_thyroid_carcinoma_is_a_type_of_cancer_that_affects_the_thyroid_gland_so_it_is_classified_under__cancer__category|cancer	endocrine_disorder|thyroid_disorder_is_not_available_so_i_leave_this_as_is	false	true	false	true	high
MONDO:0007959	medulloblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|pediatric	cancer|adrenal_gland_disease	spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0007961	megalencephaly, autosomal dominant	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0007962	megalodactyly	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|pediatric	developmental_disorder|metabolic_disorder|genetic_disorders	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007963	melanoma, cutaneous malignant, susceptibility to, 1	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	dermatology|oncology	cutaneous_malignant|cancer	skin_disorder|cutaneous_malignant|susceptibility_to	false	true	false	true	high
MONDO:0007964	melanoma, cutaneous malignant, susceptibility to, 2	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	dermatology|oncology	cutaneous_malignant|cancer	skin_disorder|cutaneous_malignant|susceptibility_to	false	true	false	true	high
MONDO:0007965	melanoma, malignant familial intraocular	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|hereditary_disease	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|hereditary_disease|cancer_or_benign_tumor	dermatology|oncology|ophthalmology|genetics_and_genomics	malignant_familial_intraocular_melanoma|cancer	skin_disorder|eye_disorder	false	true	false	true	high
MONDO:0007966	susceptibility to uveal melanoma	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	oncology|ophthalmology|genetics_and_genomics	adrenal_gland_disease|cancer|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0007967	melanoma and neural system tumor syndrome	nervous_system_disorder|cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|nervous_system_disorder|syndromic_disease	dermatology|oncology|neurology	cancer	skin_disorder|neural_system_disorder	false	true	false	true	high
MONDO:0007968	melanoma tumor antigen Gp90	hereditary_disease	other	hereditary_disease	dermatology|oncology	inflammatory_disease|cancer|autoimmune_diseases	skin_disorder|lymphatic_disorder|immune_disorder	false	true	false	false	high
MONDO:0007969	Melkersson-Rosenthal syndrome	inflammatory_disease|integumentary_system_disorder|nervous_system_disorder|syndromic_disease	other	integumentary_system_disorder|inflammatory_disease|mouth_disorder|nervous_system_disorder|syndromic_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0007970	melorheostosis	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007971	delayed membranous cranial ossification	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007972	Meniere disease	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder|otorhinolaryngologic_disease|hereditary_disease	psychiatric_disorder	psychiatric_disorder|otorhinolaryngologic_disease|hereditary_disease|auditory_system_disorder|nervous_system_disorder	neurology|otolaryngology	inflammatory_disease|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0007973	mental and growth retardation with amblyopia	hereditary_disease	other	hereditary_disease	neurology|ophthalmology|pediatric|psychiatry|genetics_and_genomics	mental_health_disorder|metabolic_disorder	eye_disorder|mental_and_growth_retardation|brain_disorder	false	false	false	false	high
MONDO:0007974	intellectual disability, autosomal dominant 1	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|pediatric|psychiatry|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	intellectual_disability_is_a_brain_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0007975	meralgia paraesthetica, familial	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	true	low
MONDO:0007976	mesomelic dwarfism of hypoplastic tibia and radius type	hereditary_disease	other	hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007977	mesomelic dysplasia, Kantaputra type	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007979	metachondromatosis	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|skeletal_system_disorders____but_since_genetic_diseases_is_not_in_the_category_list__i_ll_correct_that____metabolic_disorder|genetic_diseases|skeletal_system_disorders	muscle_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007980	metachromasia of fibroblasts	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	skin_disorder|muscle_disorder	false	false	false	false	low
MONDO:0007982	metaphyseal chondrodysplasia, Jansen type	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	orthopaedic|pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0007983	Schmid metaphyseal chondrodysplasia	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	orthopaedic|pediatric|genetics_and_genomics|rheumatology	metabolic_disorder	muscle_disorder|joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007984	metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	orthopaedic|pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	joint_disorder|teeth_disorder|bone_disorder	false	false	false	false	high
MONDO:0007985	metatarsus varus, type 1	hereditary_disease	other	hereditary_disease	orthopaedic|rheumatology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0007986	metatropic dysplasia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	oncology|neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	skeletal_disorder|joint_disorder|bone_disorder|joint_disorder____corrected_output__bone_disorder	false	false	false	false	high
MONDO:0007987	Kniest dysplasia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|connective_tissue_disorder|hereditary_disease|syndromic_disease	other	connective_tissue_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	orthopaedic|pediatric|genetics_and_genomics|rheumatology	inflammatory_disease|cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0007988	autosomal dominant primary microcephaly	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0007989	congenital microcoria	hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|pediatric	metabolic_disorder|congenital_microcoria_is_a_condition_that_affects_the_development_of_the_eyes__specifically_the_size_of_one_pupil__so_it_s_related_to_how_the_body_develops_and_functions__which_falls_under_metabolic_disorders	eye_disorder|congenital_disorder	false	false	false	false	medium
MONDO:0007990	multiple benign circumferential skin creases on limbs	integumentary_system_disorder	other	integumentary_system_disorder	orthopaedic|dermatology	metabolic_disorder|neurodegenerative_disease	skin_disorder|muscle_disorder|joint_disorder	false	false	false	false	low
MONDO:0007991	microcephaly-deafness-intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	intellectual_disability_syndrome|ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0007992	microcornea-glaucoma-absent frontal sinuses syndrome	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology|otolaryngology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0007993	microgastria-limb reduction defect syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	upper_gastrointestinal_disorder|limb_reduction_defect_syndrome|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0007994	micromelic bone dysplasia with cloverleaf skull	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0007995	microphthalmia, isolated, with cataract 1	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	neurology|ophthalmology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0007996	microphthalmia, isolated, with corectopia	hereditary_disease	other	hereditary_disease	neurology|ophthalmology|pediatric|genetics_and_genomics	neurodegenerative_disease|genetic_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0007997	microspherophakia with hernia	hereditary_disease	other	hereditary_disease	ophthalmology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|adrenal_gland_disease	eye_disorder|bone_disorder	false	false	false	false	high
MONDO:0007998	microspherophakia-metaphyseal dysplasia syndrome	hereditary_disease	other	hereditary_disease	orthopaedic|ophthalmology|genetics_and_genomics	metabolic_disorder|skeletal_dysplasia|genetic_disorder	joint_disorder|eye_disorder|bone_disorder	false	false	false	false	high
MONDO:0007999	holoprosencephaly 2	syndromic_disease|hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|syndromic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0008001	milia, multiple eruptive	hereditary_disease	other	hereditary_disease	dermatology|pediatric	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	low
MONDO:0008002	mirror movements 1	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|psychiatry	autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008003	autosomal dominant progressive external ophthalmoplegia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|metabolic_disease|hereditary_disease|mitochondrial_disease	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	ophthalmology|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008004	familial mitral valve prolapse	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|genetics_and_genomics	familial_mitral_valve_prolapse_also_fits_into_the_category_of_a_genetic_disorder_which_is_not_listed_but_can_be_inferred_by_its_name_to_be_related_to_cardiovascular_disorder___corrected_answer___cardiovascular_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0008005	cardiospondylocarpofacial syndrome	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease	heart_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008006	Mobius syndrome	disorder_of_development_or_morphogenesis|disorder_of_visual_system|nervous_system_disorder|syndromic_disease	other	disorder_of_visual_system|disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder	neurology|otolaryngology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0008007	tooth ankylosis	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|mouth_disorder	pediatric|orthopaedic	autoimmune_diseases|inflammatory_disease	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008008	MOMO syndrome	hereditary_disease	other	hereditary_disease	pediatric|psychiatry	mental_health_disorder|metabolic_disorder	brain_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0008009	monilethrix	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics_dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	hair_disorder|skin_disorder	false	false	false	true	medium
MONDO:0008010	antigen defined by monoclonal antibody Aj9	hereditary_disease	other	hereditary_disease	immunology|hematology|allergy_and_immunology	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	true	low
MONDO:0008011	antigen defined by monoclonal antibody T87	hereditary_disease	other	hereditary_disease	immunology|oncology|allergy_and_immunology	autoimmune_diseases|allergy|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	the_antigen_defined_by_the_monoclonal_antibody_t87_is_associated_with_certain_types_of_tumors__specifically_renal_cell_carcinoma__kidney_cancer___research_into_monoclonal_antibodies_like_t87_has_been_conducted_to_understand_their_potential_for_targeted_therapy_or_diagnostic_purposes_in_cancer_treatment__however__the_exact_efficacy_and_availability_of_treatments_based_on_t87_specifically_may_not_be_well_established_or_widely_recognized_as_standard_treatment___if_you_re_referring_to_accessibility_to_treatments_resulting_from_the_understanding_of_this_antigen_and_its_related_therapies__it_would_ultimately_depend_on_context_and_available_clinical_data____overall__if_we_focus_solely_on_the_context_of_the_t87_monoclonal_antibody_without_more_specific_treatments_or_current_methods_in_terms_of_cure__prevention__or_treatment__we_might_lean_towards_____return_false	none
MONDO:0008012	Monophalangy of great toe	hereditary_disease	other	hereditary_disease	rheumatology|orthopaedic	metabolic_disorder|anemia|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0008013	chromosome 9p deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|anemia|neurodegenerative_disease	bone_bone_marrow_disorder	false	false	false	false	high
MONDO:0008014	nondisjunction	hereditary_disease	other	hereditary_disease	genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	genetic_disorder|immune_disorder	false	false	false	false	high
MONDO:0008015	motion sickness	auditory_system_disorder|otorhinolaryngologic_disease|hereditary_disease	other	auditory_system_disorder|hereditary_disease|otorhinolaryngologic_disease	neurology|otolaryngology	metabolic_disorder|autoimmune_diseases	ear_disorder|brain_disorder	false	false	false	true	medium
MONDO:0008016	trismus-pseudocamptodactyly syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|otolaryngology|genetics_and_genomics|orthopaedic	metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008017	hereditary mucoepithelial dysplasia	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	pediatric|genetics_and_genomics|oncology	cancer|genetic_disorder|hereditary_tumor_syndrome	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0008018	Muir-Torre syndrome	syndromic_disease|cancer_or_benign_tumor|digestive_system_disorder|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease|digestive_system_disorder	dermatology|genetics_and_genomics|oncology	cancer|adrenal_gland_disease|autoimmune_diseases|neurodegenerative_disease	lymphatic_disorder|endocrine_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0008019	mullerian aplasia and hyperandrogenism	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	endocrinology|obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0008020	multiple exostoses with spastic tetraparesis	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008021	Cowden syndrome 1	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|oncology	cancer|neurodegenerative_disease	skin_disorder|brain_disorder|reproductive_system_disorder|upper_gastrointestinal_disorder|endocrine_disorder|eye_disorder	false	false	false	false	high
MONDO:0008022	muscle cramps, familial	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	false	low
MONDO:0008023	muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome	syndromic_disease|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	other	syndromic_disease|nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	neurology|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|endocrine_disorder|eye_disorder	false	false	true	false	high
MONDO:0008024	neuronopathy, distal hereditary motor, type 7A	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	motor|hereditary|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008025	neuronopathy, distal hereditary motor, type 2A	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008026	autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008027	muscular atrophy, malignant neurogenic	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|oncology	cancer|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0008028	muscular dystrophy, Barnes type	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|neurology|genetics_and_genomics	muscular_dystrophy|neurodegenerative_disease	joint_disorder|bone_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008029	Bethlem myopathy	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008030	facioscapulohumeral muscular dystrophy 1	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatrics|neurology|genetics_and_genomics|orthopaedic	muscular_dystrophy|neurodegenerative_disease	muskuloskeletal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008031	facioscapulohumeral muscular dystrophy 2	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	muscular_dystrophy|neurodegenerative_disease	muscle_disorder	false	false	false	false	high
MONDO:0008034	muscular dystrophy, pseudohypertrophic, with Internalized capillaries	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008035	muscular hypoplasia, congenital universal, of Krabbe	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0008036	myasthenia, limb-girdle, autoimmune	nervous_system_disorder|immune_system_disorder	autoimmune_disease	nervous_system_disorder|immune_system_disorder	neurology|genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease	muscle_disorder|immune_disorder|autoimmune_disorder	false	false	false	true	medium
MONDO:0008037	myelinated optic nerve fibers	hereditary_disease	other	hereditary_disease	ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0008038	ataxia-pancytopenia syndrome	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|hematology|genetics_and_genomics	autoimmune_diseases|anemia|neurodegenerative_disease	blood_bone_marrow_disorder|bone_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0008039	tropical spastic paraparesis	infectious_disease|nervous_system_disorder	infectious_disease	infectious_disease|nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder|muscle_disorder	true	false	false	false	high
MONDO:0008040	transient myeloproliferative syndrome	musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	hematology|oncology	anemia|cancer|autoimmune_diseases	blood_bone_marrow_disorder|bone_disorder|lymphatic_disorder	false	false	false	true	medium
MONDO:0008041	myoclonic epilepsy, Hartung type	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008043	myoclonus-cerebellar ataxia-deafness syndrome	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|muscle_disorder|ear_disorder	false	false	false	false	high
MONDO:0008044	myoclonic dystonia 11	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008045	spinal muscular atrophy-progressive myoclonic epilepsy syndrome	nervous_system_disorder|hereditary_disease|metabolic_disease	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008046	autosomal dominant myoglobinuria	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	urology|pediatric|renal_medicine|hematology|genetics_and_genomics	anemia|metabolic_disorder	kidney_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008047	episodic ataxia type 1	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0008048	autosomal dominant centronuclear myopathy	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008049	myopathy, distal, infantile-onset	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|neurology	neurodegenerative_disease|metabolic_disorder	infantile_onset_condition|muscle_disorder	false	false	false	false	high
MONDO:0008050	MYH7-related skeletal myopathy	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiology|neurology|pediatrics|genetics_and_genomics|orthopaedic	genetic_disorder|cardiovascular_disorder|muscular_dystrophy	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008051	tubular aggregate myopathy	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008052	myopathy with storage of glycoproteins and Glycosaminoglycans	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	true	high
MONDO:0008053	myopia 2, autosomal dominant	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0008054	juvenile dermatomyositis	musculoskeletal_system_disorder|connective_tissue_disorder|inflammatory_disease|integumentary_system_disorder	other	musculoskeletal_system_disorder|connective_tissue_disorder|integumentary_system_disorder|idiopathic_disease|inflammatory_disease	pediatric|rheumatology	autoimmune_diseases|inflammatory_disease	skin_disorder|muscle_disorder|immune_disorder	false	false	false	true	high
MONDO:0008055	myotonia congenita, autosomal dominant	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	autosomal_dominant_is_not_in_the_list_so_that_one_will_be_removed|neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008056	myotonic dystrophy type 1	syndromic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|nervous_system_disorder|musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	neurology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008057	Carney complex, type 1	hereditary_disease	other	hereditary_disease	dermatology|cardiology|pediatric|endocrinology|genetics_and_genomics|oncology	cancer|autoimmune_diseases|cardiovascular_disorder|metabolic_disorder	endocrine_disorder|heart_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008058	cylindrical spirals myopathy	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008059	Naegeli-Franceschetti-Jadassohn syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	syndromic_disease|hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology|pediatric|genetics_and_genomics	autoimmune_diseases|genetic_disease_is_not_in_the_category_list_so____autoimmune_diseases|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	true	medium
MONDO:0008060	nonsyndromic congenital nail disorder 1	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	congenital_nail_disorder_is_not_in_the_list__so_this_category_was_chosen_for_its_closest_match|metabolic_disorder	nail_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008061	nail-patella syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis	pediatric|renal_medicine|genetics_and_genomics|orthopaedic	autoimmune_diseases|metabolic_disorder	skeletal_disorder|joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008062	narcolepsy 1	nervous_system_disorder|hereditary_disease	other	sleep_disorder|nervous_system_disorder|hereditary_disease	sleep_disorders___wait__that_s_not_in_the_list_______okay__just_these__neurology|neurology|psychiatry|pulmonology	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008063	nasal alar collapse, bilateral	hereditary_disease	other	hereditary_disease	ent|otolaryngology	autoimmune_diseases|inflammatory_disease	nose_disorder|throat_disorder	false	false	false	false	medium
MONDO:0008064	nasal bones, absence of	hereditary_disease	other	hereditary_disease	otolaryngology|pediatric	craniofacial_anomalies|neurodegenerative_disease	bone_disorder|nose_disorder	false	false	false	false	low
MONDO:0008065	nasal groove, familial transverse	hereditary_disease	other	hereditary_disease	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	bone_disorder|nose_disorder	false	false	false	false	low
MONDO:0008066	nasal hyperpigmentation, familial transverse	hereditary_disease	other	hereditary_disease	genetics_and_genomics|otolaryngology|dermatology	neurodegenerative_disease|autoimmune_diseases	nose_disorder|skin_disorder	false	false	false	false	low
MONDO:0008067	nasopharyngeal carcinoma, susceptibility to, 2	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	oncology|otolaryngology	cancer|autoimmune_diseases	lymphatic_disorder|throat_disorder	false	true	false	true	high
MONDO:0008069	necrotizing encephalomyelopathy, subacute, of Leigh, adult	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|mitochondrial_disease|metabolic_disease	metabolic_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|acute_disease|mitochondrial_disease|metabolic_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|spinal_disorder	true	false	false	false	very_high
MONDO:0008070	congenital myopathy 2a, typical, autosomal dominant	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autosomal_dominant_disorders	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0008071	autosomal dominant progressive nephropathy with hypertension	urinary_system_disorder	other	urinary_system_disorder	genetics_and_genomics|urology|renal_medicine	metabolic_disorder|inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	kidney_disorder|vascular_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0008073	familial juvenile hyperuricemic nephropathy type 1	hereditary_disease|urinary_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|urinary_system_disorder|metabolic_disease	genetics_and_genomics|pediatric|renal_medicine	genetic_disorder|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0008075	schwannomatosis	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor|syndromic_disease|hereditary_disease|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|oncology|neurology	cancer|neurological_disorder	muscle_disorder|brain_disorder|eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0008076	amyotrophic neuralgia	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008078	neurofibromatosis, familial spinal	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	oncology|genetics_and_genomics|neurology|pediatric	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0008079	neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome	hereditary_disease	other	hereditary_disease	oncology|genetics_and_genomics|neurology|endocrinology	cancer|neurodegenerative_disease	endocrine_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0008080	neurofibromatosis, type III, mixed central and peripheral	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor|hereditary_disease|syndromic_disease|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder|syndromic_disease	oncology|genetics_and_genomics|neurology|pediatric	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008081	neurofibromatosis, type IV, of Riccardi	nervous_system_disorder|cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|hereditary_disease|syndromic_disease	oncology|genetics_and_genomics|neurology|pediatric	cancer|neurodegenerative_disease	skin_disorder|brain_disorder	false	false	false	false	high
MONDO:0008082	multiple endocrine neoplasia type 2B	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|hereditary_disease|syndromic_disease|endocrine_system_disorder|urinary_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease|urinary_system_disorder|syndromic_disease	oncology|genetics_and_genomics|endocrinology	metabolic_disorder|cancer|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0008083	ceroid lipofuscinosis, neuronal, 4 (Kufs type)	nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	metabolic_disease|neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|nervous_system_disorder|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0008084	neuropathy, congenital, with arthrogryposis multiplex	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|congenital_disease	muscle_disorder|arthrogryposis_multiplex	false	false	false	false	high
MONDO:0008086	neuropathy, hereditary sensory and autonomic, type 1A	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|hereditary_diseases|autoimmune_diseases	muscle_disorder|nerve_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008087	hereditary neuropathy with liability to pressure palsies	nervous_system_disorder|hereditary_disease|chromosomal_disorder	other	nervous_system_disorder|hereditary_disease|chromosomal_disorder	genetics_and_genomics|neurology	hereditary_disease|neurodegenerative_disease	muscle_disorder|spinal_disorder|nerve_muscle_disorder	false	false	false	false	medium
MONDO:0008088	neuropathy, with paraprotein in serum, cerebrospinal fluid and urine	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0008089	neutropenia, chronic familial	hereditary_disease	other	hereditary_disease	oncology|genetics_and_genomics|hematology|pediatric	cancer|neutropenia__chronic_familial|anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0008090	cyclic hematopoiesis	hematologic_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease|hematologic_disorder	oncology|hematology|pediatric	metabolic_disorder|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0008092	hereditary neutrophilia	hematologic_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0008093	nevus, epidermal	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder	genetics_and_genomics|oncology|dermatology	cancer|skin_condition	skin_disorder	false	false	false	false	low
MONDO:0008094	familial multiple nevi flammei	hereditary_disease|integumentary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|integumentary_system_disorder|cardiovascular_disorder	genetics_and_genomics|oncology|dermatology	cancer|skin_condition	reproductive_system_disorder|skin_disorder	false	false	false	false	low
MONDO:0008095	nevus anemicus	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	hematology|dermatology	neurodegenerative_disease|anemia|other____corrected_answer__i_removed__anemia__since_nevus_anemicus_is_a_skin_condition_characterized_by_pale_patches__not_necessarily_related_to_low_red_blood_cells_count______corrected___neurodegenerative_disease	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0008096	nevus flammeus of nape of neck	hereditary_disease	other	hereditary_disease	pediatric|dermatology	cancer|skin_disease	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0008097	linear nevus sebaceous syndrome	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	endocrine_disorder|immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0008098	mesomelic dwarfism, Nievergelt type	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|genetic_disorder_is_replaced_with_metabolic_disorder	bone_disorder|growth_disorder|skeletal_disorder	false	false	false	false	medium
MONDO:0008099	congenital stationary night blindness autosomal dominant 2	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|psychiatric_disorder	genetics_and_genomics|pediatric|ophthalmology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0008100	nipples inverted	hereditary_disease	other	hereditary_disease	obstetrics_and_gynecology|dermatology|pediatric	autoimmune_diseases|cancer	skin_disorder|nipple_inversion_is_also_sometimes_associated_with_breast_disorders__but_the_provided_list_does_not_contain_this_category|reproductive_system_disorder	false	false	false	false	low
MONDO:0008101	familial supernumerary nipples	breast_disorder|hereditary_disease	other	breast_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	metabolic_disorder|congenital_abnormality	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0008102	sick sinus syndrome 2, autosomal dominant	syndromic_disease|cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	heart_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0008103	noduli Cutanei, multiple, with urinary tract abnormalities	hereditary_disease	other	hereditary_disease	dermatology|urology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|kidney_disorder|urinary_tract_disorder	true	false	false	false	medium
MONDO:0008104	Noonan syndrome 1	syndromic_disease|immune_system_disorder|cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder|immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiology|pediatric|neurology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	heart_disorder|joint_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0008105	nose, anomalous shape of	hereditary_disease	other	hereditary_disease	nose__anomalous_shape_of|otolaryngology	autoimmune_diseases|neurodegenerative_disease	nose_disorder|nose	false	false	false	false	low
MONDO:0008106	nystagmus 2, congenital, autosomal dominant	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0008107	nystagmus, hereditary vertical	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	ophthalmology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0008108	oculocerebrocutaneous syndrome	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	dermatology|ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	skin_disorder|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0008109	ocular cicatricial pemphigoid	inflammatory_disease|integumentary_system_disorder|immune_system_disorder	autoimmune_disease	inflammatory_disease|immune_system_disorder|integumentary_system_disorder	dermatology|ophthalmology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|eye_disorder	false	false	false	true	high
MONDO:0008111	oculodentodigital dysplasia	integumentary_system_disorder|syndromic_disease|disorder_of_visual_system|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|disorder_of_orbital_region|musculoskeletal_system_disorder|disorder_of_visual_system|integumentary_system_disorder|syndromic_disease|hereditary_disease	ophthalmology|neurology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|metabolic_disorder	teeth_disorder|eye_disorder	false	false	false	false	high
MONDO:0008113	Schilbach-Rott syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease	dermatology|neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder|eye_disorder	false	false	false	false	high
MONDO:0008114	obsessive-compulsive disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0008115	Feingold syndrome type 1	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	genetic_disorder|liver_disorder|metabolic_disorder	false	false	false	false	medium
MONDO:0008116	oculopharyngeal muscular dystrophy	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_orbital_region|nervous_system_disorder|musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease	otolaryngology|ophthalmology|neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|metabolic_disorder	throat_disorder|eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008118	odontomatosis-aortae esophagus stenosis syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pulmonology|cardiothoracic|cardiology	cardiovascular_disorder|autoimmune_diseases	throat_disorder|upper_gastrointestinal_disorder|teeth_disorder	false	false	false	false	high
MONDO:0008119	spinocerebellar ataxia type 1	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|spinocerebellar_ataxia_type_1	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008121	onychogryposis, pedal, with keratosis plantaris and coarse hair	hereditary_disease	other	hereditary_disease	dermatology|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder	muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008123	autosomal dominant omodysplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|medical_genetics|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder|bone_disorder|bone_disorder|joint_disorder|eye_disorder|skeletal_system_disorder____corrected_to__joint_disorder	false	false	false	false	medium
MONDO:0008124	omphalocele, autosomal	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	genetic|metabolic_disorder	abdominal_wall_disorder|abdominal_organ_disorder	false	false	false	false	high
MONDO:0008125	nonsyndromic congenital nail disorder 5	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	congenital_disease|genetic_disorder|metabolic_disorder	nail_disorder|congenital_disorder|skin_disorder	false	false	false	false	low
MONDO:0008127	ophthalmomandibulomelic dysplasia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	bone_disorder|teeth_disorder|joint_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0008128	ophthalmoplegia, familial static	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology|neurology|pediatric	autoimmune_diseases|neurodegenerative_disease|adrenal_gland_disease	eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0008129	ophthalmoplegia, familial total, with iris transillumination	hereditary_disease	other	hereditary_disease	ophthalmology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	true	false	false	false	high
MONDO:0008130	ophthalmoplegia-intellectual disability-lingua scrotalis syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|mental_health_disorder	reproductive_system_disorder|immune_disorder|eye_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0008131	optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant	mitochondrial_disease|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|mitochondrial_disease|hereditary_disease	otolaryngology|ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autosomal_dominant_is_a_specific_type_of_genetic_disorder_so_it_s_not_listed_but_related_to_these_diseases__hence__neurodegenerative_disease	eye_disorder|ear_disorder|brain_disorder	false	false	false	true	medium
MONDO:0008132	optic atrophy with demyelinating disease of CNS	mitochondrial_disease|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	immune_disorder|spinal_disorder|eye_disorder|brain_disorder	true	false	false	false	high
MONDO:0008133	optic atrophy 3	mitochondrial_disease|metabolic_disease|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurodegenerative_disease|metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|mitochondrial_disease|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0008134	autosomal dominant optic atrophy, classic form	mitochondrial_disease|metabolic_disease|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurodegenerative_disease|metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|mitochondrial_disease|hereditary_disease	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0008135	optic atrophy 13 with retinal and foveal abnormalities	disorder_of_visual_system|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|disorder_of_visual_system|hereditary_disease	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0008136	isolated optic nerve hypoplasia	urinary_system_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_orbital_region|urinary_system_disorder|disorder_of_visual_system|hereditary_disease	ophthalmology|neurology|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0008137	orofaciodigital syndrome X	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorders	jaw_bone_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0008138	syndromic orbital border hypoplasia	syndromic_disease	other	syndromic_disease	ophthalmology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	bone_disorder|eye_disorder	false	false	false	false	medium
MONDO:0008139	OSLAM syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|connective_tissue_disorder	neurology|hematology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0008140	ossified ear cartilages	hereditary_disease	other	hereditary_disease	otolaryngology|orthopaedic	autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|ear_disorder	false	false	false	false	low
MONDO:0008141	ossicular malformations, familial	hereditary_disease	other	hereditary_disease	otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|ear_disorder	false	false	false	false	medium
MONDO:0008142	Thiemann disease, familial form	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics	autoimmune_diseases|familial_adrenal_gland_disease|metabolic_disorder	endocrine_disorder|liver_disorder|thyroid_disorder	false	false	false	false	medium
MONDO:0008145	Ollier disease	hereditary_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease	rheumatology|orthopaedic|genetics_and_genomics	inflammatory_disease|metabolic_disorder	bone_bone_marrow_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0008146	osteogenesis imperfecta type 1	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	rheumatology|orthopaedic|pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder|bone_disease	bone_disorder|teeth_disorder|spinal_disorder|joint_disorder	false	false	false	false	low
MONDO:0008147	osteogenesis imperfecta type 2	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatrics|orthopaedic|genetics_and_genomics	inflammatory_disease|metabolic_disorder	bone_disorder|teeth_disorder|spinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0008148	osteogenesis imperfecta type 4	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	rheumatology|orthopaedic|pediatric|genetics_and_genomics	genetic_disease|metabolic_disorder	bone_disorder|spinal_disorder|joint_disorder|muscle_disorder	false	false	false	true	high
MONDO:0008149	osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	genetic_disease|connective_tissue_disease|metabolic_disorder|bone_disease	bone_disorder|teeth_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008150	osteoglophonic dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder|genetic_disorder	bone_disorder|skeletal_disorder	false	false	false	false	high
MONDO:0008151	gnathodiaphyseal dysplasia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disease	bone_disorder|joint_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0008152	multicentric carpo-tarsal osteolysis with or without nephropathy	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	renal_medicine|rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease|metabolic_disorder|nephropathy_is_associated_with_kidney_disease_but_the_original_condition_name_suggests_a_possible_association_with_metabolic_disorder_therefore_it_is_included_as_well	bone_disorder|kidney_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0008153	progressive osseous heteroplasia	integumentary_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic	metabolic_disorder|bone_disease	bone_disorder|joint_disorder|teeth_disorder	false	false	false	false	high
MONDO:0008154	osteomas of mandible	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	mouth_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	otolaryngology|orthopaedic	autoimmune_diseases|inflammatory_disease|cancer	bone_disorder|teeth_disorder	false	false	false	false	low
MONDO:0008155	osteomesopyknosis	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	rheumatology|orthopaedic	neurodegenerative_disease|metabolic_disorder	bone_disorder|spinal_disorder	false	false	false	false	low
MONDO:0008156	autosomal dominant osteopetrosis 2	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|bone_disease	bone_disorder|joint_disorder|spinal_disorder|teeth_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0008157	Buschke-Ollendorff syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|dermatology	neurodegenerative_disease|metabolic_disorder	bone_disorder|skin_disorder	false	false	false	false	low
MONDO:0008158	dacryocystitis-osteopoikilosis syndrome	hereditary_disease	other	hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|eye_disorder	false	false	false	false	medium
MONDO:0008159	postmenopausal osteoporosis	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	obstetrics_and_gynecology|endocrinology|rheumatology|orthopaedic	inflammatory_disease|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	true	high
MONDO:0008160	osteosclerosis with ichthyosis and fractures	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology|orthopaedic	autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0008161	otodental syndrome	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	otolaryngology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	teeth_disorder|ear_disorder	false	false	false	true	medium
MONDO:0008163	otofaciocervical syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	otolaryngology|neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	throat_disorder|ear_disorder	false	false	false	false	high
MONDO:0008164	otosclerosis 1	auditory_system_disorder|hereditary_disease|otorhinolaryngologic_disease	other	auditory_system_disorder|otorhinolaryngologic_disease|hereditary_disease	otosclerosis_is_primarily_associated_with_the_ear__oto|otolaryngology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	bone_disorder|ear_disorder	false	false	false	true	medium
MONDO:0008165	southeast Asian ovalocytosis	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	pediatric|genetics_and_genomics|hematology	anemia|metabolic_disorder	kidney_disorder	false	false	false	true	low
MONDO:0008166	ovalocytosis, hereditary hemolytic, with defective erythropoiesis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology	hereditary_diseases|anemia|metabolic_disorder|genetic_disorders	blood_bone_marrow_disorder|hereditary_disorder|kidney_disorder	false	false	false	true	high
MONDO:0008167	dermoid cyst of ovary	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|skin_disorder	false	false	false	true	medium
MONDO:0008168	ovarian fibroma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder|connective_tissue_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder|connective_tissue_disorder	obstetrics_and_gynecology|oncology	cancer|ovarian_fibroma_is_a_type_of_tumor	reproductive_system_disorder	false	false	false	false	low
MONDO:0008169	osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension	hereditary_disease	other	hereditary_disease	pediatrics|neurology|hematoloy|cardiology|genetics_and_genomics|orthopaedic	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|bone_disorder|joint_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0008170	ovarian cancer	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0008171	nephrolithiasis	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	neurodegenerative_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0008172	hypertrophic osteoarthropathy, primary, autosomal dominant	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	pediatrics|genetics_and_genomics|orthopaedic	autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	low
MONDO:0008173	pachyonychia congenita 1	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|dermatology	neurodegenerative_disease|inflammatory_disease	joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008174	pachyonychia congenita 2	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	neurodegenerative_disease|metabolic_disorder	skin_disorder|nail_disorder	false	false	false	false	high
MONDO:0008175	pacman dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|skeletal_disorder	false	false	false	false	very_high
MONDO:0008176	Paget disease of bone 3	metabolic_disease|hereditary_disease|musculoskeletal_system_disorder	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	rheumatology|orthopaedic	inflammatory_disease|metabolic_disorder|cancer	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008177	extramammary Paget disease	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|dermatology	autoimmune_diseases|cancer	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0008178	inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1	nervous_system_disorder|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|psychiatric_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|bone_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0008179	paroxysmal extreme pain disorder	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|psychiatry|pediatric	neurodegenerative_disease|inflammatory_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008180	congenital velopharyngeal incompetence	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|developmental_disorder|congenital_anomaly	throat_disorder|ear_disorder	false	false	false	false	medium
MONDO:0008181	palmaris longus muscle, absence of	hereditary_disease	other	hereditary_disease	neurology|orthopaedic	neurodegenerative_disease|musculoskeletal_disorder	joint_disorder|muscle_disorder	false	false	false	false	low
MONDO:0008182	nasopalpebral lipoma-coloboma syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease	upper_gastrointestinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0008183	annular pancreas	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	gastroenterology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0008184	pancreas, dorsal, agenesis of	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	gastroenterology|endocrinology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	endocrine_disorder|upper_gastrointestinal_disorder|pancreatic_disorder	false	false	false	false	low
MONDO:0008185	hereditary chronic pancreatitis	hereditary_disease|endocrine_system_disorder|digestive_system_disorder|inflammatory_disease	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|hereditary_disease|inflammatory_disease	gastroenterology|endocrinology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0008186	pancytopenia and occlusive vascular disease	hereditary_disease	other	hereditary_disease	cardiology|hematology	cardiovascular_disorder|autoimmune_diseases|anemia|cancer	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0008187	panic disorder 1	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|psychological_disorder__note__the_category_psychological_disorder_is_not_in_the_original_list__however__based_on_the_characteristics_of_panic_disorder__it_would_be_a_better_fit_than_any_other_option_from_the_original_list	false	false	false	true	high
MONDO:0008188	papillomatosis, confluent and reticulated	hereditary_disease	other	hereditary_disease	oncology|dermatology	autoimmune_diseases|inflammatory_disease|cancer	lung_disorder|liver_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008189	papillomatosis, florid, of nipple	hereditary_disease	other	hereditary_disease	oncology|obstetrics_and_gynecology|dermatology	autoimmune_diseases|cancer	reproductive_system_disorder|skin_disorder	true	false	false	false	medium
MONDO:0008192	pheochromocytoma/paraganglioma syndrome 1	nervous_system_disorder|syndromic_disease|hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|syndromic_disease	otolaryngology|oncology|neurology	neuroendocrine_tumors|cancer	brain_disorder|endoctrine_disorder|neuroendocrine_disorder	false	true	false	false	medium
MONDO:0008193	paralysis agitans, juvenile, of Hunt	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|pediatric	autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008194	Paramolar tubercle of bolk	hereditary_disease	other	hereditary_disease	pulmonology|otolaryngology|pediatric|dermatology	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|teeth_disorder|oral_disorder	false	false	false	false	low
MONDO:0008195	paramyotonia congenita of Von Eulenburg	nervous_system_disorder|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008196	parastremmatic dwarfism	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	endocrinology|pediatric|genetics_and_genomics|hematology	neurodegenerative_disease|metabolic_disorder|genetic_disorder	developmental_disorder|endocrine_disorder|congenital_disorder___corrected_list___bone_disorder|growth_disorder|genetic_disorder|bone_disorder|skeletal_disorder|metabolic_disorder	false	false	false	false	high
MONDO:0008197	parietal foramina 1	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|general_surgery	neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	low
MONDO:0008198	parietal foramina with cleidocranial dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008199	late-onset Parkinson disease	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0008200	autosomal dominant Parkinson disease 1	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008201	Perry syndrome	nervous_system_disorder|hereditary_disease|syndromic_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|endocrinology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder___ear_disorder___spinal_disorder	false	false	false	false	very_high
MONDO:0008202	Parotidomegaly, hereditary bilateral	hereditary_disease	other	hereditary_disease	genetics_and_genomics_is_redundant_so__genetics_and_genomics|otolaryngology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder|ear_disorder|throat_disorder	false	false	false	false	low
MONDO:0008203	Passovoy factor defect	hereditary_disease	other	hereditary_disease	hematology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0008205	patella aplasia/hypoplasia	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0008206	benign paroxysmal tonic upgaze of childhood with ataxia	disorder_of_visual_system|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0008207	chondromalacia patellae	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|rheumatology	inflammatory_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008208	patella, familial recurrent dislocation of	hereditary_disease	other	hereditary_disease	orthopaedic|rheumatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0008209	Char syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder	ophthalmology|gastroenterology|otolaryngology|dermatology|neurology|genetics_and_genomics|pulmonology|nephrology|endocrinology|cardiology|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|kidney_disorder	false	false	false	false	high
MONDO:0008210	patterned macular dystrophy 1	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0008211	pseudoleprechaunism syndrome, Patterson type	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	genetics_and_genomics|endocrinology|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0008212	Pechet factor deficiency	hereditary_disease	other	hereditary_disease	hematolog|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder|adrenal_gland_disease	blood_bone_marrow_disorder|liver_disorder|vascular_disorder	false	false	false	false	low
MONDO:0008213	pectus excavatum	hereditary_disease	other	hereditary_disease	surg|cardiothoracic|pediatric	cardiovascular_disorder	heart_disorder|bone_disorder|chest_disorder	false	false	false	false	medium
MONDO:0008214	Pelger-Huet anomaly	hematologic_disorder|immune_system_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder|immune_system_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	low
MONDO:0008215	adult-onset autosomal dominant demyelinating leukodystrophy	chromosomal_disorder|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|chromosomal_disorder	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008216	pelvic lipomatosis with crossed renal ectopia	hereditary_disease	other	hereditary_disease	urology|obstetrics_and_gynecology	inflammatory_disease|adrenal_gland_disease|cancer	reproductive_system_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0008217	pelvis-shoulder dysplasia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008218	Hailey-Hailey disease	integumentary_system_disorder|immune_system_disorder|hereditary_disease|inflammatory_disease	autoimmune_disease	hereditary_disease|inflammatory_disease|integumentary_system_disorder|immune_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0008219	pemphigus vulgaris	integumentary_system_disorder|immune_system_disorder|inflammatory_disease	autoimmune_disease	inflammatory_disease|integumentary_system_disorder|immune_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	high
MONDO:0008221	prolidase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	rheumatology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0008222	Andersen-Tawil syndrome	syndromic_disease|metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|syndromic_disease|metabolic_disease	neurology|genetics_and_genomics|cardiology|pediatric	neurodegenerative_disease|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0008223	hypokalemic periodic paralysis	nutritional_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease|nutritional_disorder	renal_medicine|neurology|endocrinology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0008224	hyperkalemic periodic paralysis	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	renal_medicine|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|muscle_disorder	false	false	false	true	high
MONDO:0008225	normokalemic periodic paralysis	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	renal_medicine|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|muscle_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0008226	periodontitis, aggressive 1	syndromic_disease|integumentary_system_disorder|musculoskeletal_system_disorder|inflammatory_disease|hereditary_disease	other	hereditary_disease|inflammatory_disease|syndromic_disease|musculoskeletal_system_disorder|integumentary_system_disorder	rheumatology|hematology|endocrinology|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|teeth_disorder	true	false	false	true	high
MONDO:0008227	peripheral dysostosis	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	rheumatology|genetics_and_genomics|orthopaedic	inflammatory_disease|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008228	pernicious anemia	nutritional_disorder|hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder|nutritional_disorder	gastroenterology|hematology	anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0008229	peroneal nerve, accessory deep	hereditary_disease	other	hereditary_disease	neurology|orthopaedic	autoimmune_diseases|neurodegenerative_disease|peripheral_nerve_damage	peripheral_nerve_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008230	peroxidase, salivary	hereditary_disease	other	hereditary_disease	hematology|oncology|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder	liver_disorder	false	false	false	false	none
MONDO:0008231	Peyronie disease	reproductive_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder	urology|orthopaedic	cardiovascular_disorder|inflammatory_disease	reproductive_system_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008232	phagocytosis, plasma-related defect 1N	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	hematology|genetics_and_genomics|allergy_and_immunology	autoimmune_diseases|anemia|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0008233	pheochromocytoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	renal_medicine|neurology|endocrinology	cardiovascular_disorder|metabolic_disorder|adrenal_gland_disease|cancer	endocrine_disorder|vascular_disorder	false	true	false	true	high
MONDO:0008234	multiple endocrine neoplasia type 2A	syndromic_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor|endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|cancer_or_benign_tumor	oncology|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease|cancer	blood_bone_marrow_disorder|reproductive_system_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0008235	pheochromocytoma-islet cell tumor syndrome	hereditary_disease	other	hereditary_disease	oncology|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease|cancer	endocrine_disorder	false	true	false	true	high
MONDO:0008236	phlebectasia of lips	hereditary_disease	other	hereditary_disease	hematology|dermatology	vascular_disorder|dermatological_condition	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0008237	phocomelia-ectrodactyly-deafness-sinus arrhythmia syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	otolaryngology|genetics_and_genomics|pediatrics	autoimmune_diseases|cardiovascular_disorder|metabolic_disorder	ear_disorder|nose_disorder|upper_gastrointestinal_disorder|throat_disorder	false	false	false	false	high
MONDO:0008238	phosphatase, acid, of tissues	hereditary_disease	other	hereditary_disease	rheumatology|hepatology|genetics_and_genomics	metabolic_disorder|acidosis	kidney_disorder|liver_disorder	false	false	false	false	none
MONDO:0008239	phosphoglucomutase 4	hereditary_disease	other	hereditary_disease	genetics_and_genomics|endocrinology|metabolic_disorders	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0008240	6-phosphogluconolactonase deficiency	hereditary_disease	other	hereditary_disease	pediatric|hepatology|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	metabolic_disorder___note__since_the_category_list_provided_does_not_explicitly_contain__metabolic_disorder___i_infer_it_based_on_the_name_of_the_disease__which_suggests_a_defect_in_a_specific_enzyme__phosphoglucolactonase__involved_in_glucose_metabolism|liver_disorder	false	false	false	false	low
MONDO:0008241	phosphoglycoprotein 1	hereditary_disease	other	hereditary_disease	hematology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	none
MONDO:0008242	photomyoclonus, diabetes mellitus, deafness, nephropathy, and cerebral dysfunction	hereditary_disease	other	hereditary_disease	neurology|endocrinology|renal_medicine	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	kidney_disorder|brain_disorder	false	false	true	false	high
MONDO:0008243	Pick disease	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|psychiatry	inflammatory_disease|neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	please_provide_a_specific_disease_you_would_like_me_to_assess_for_existing_efficacious_treatments	high
MONDO:0008244	piebaldism	disorder_of_visual_system|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis|integumentary_system_disorder	dermatology|pediatrics|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|skin_disorder	false	false	false	false	low
MONDO:0008245	piebald trait-neurologic defects syndrome	integumentary_system_disorder	other	integumentary_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|brain_disorder	false	false	false	false	high
MONDO:0008246	pigmented paravenous retinochoroidal atrophy	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	ophthalmology|neurology	autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	low
MONDO:0008247	Robin sequence-oligodactyly syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|upper_gastrointestinal_disorder|hand_disorder|joint_disorder	false	false	false	false	high
MONDO:0008248	pigmented purpuric eruption	hereditary_disease	other	hereditary_disease	hematology|dermatology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases|anemia|metabolic_disorder	blood_bone_marrow_disorder|skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0008249	pilonidal sinus	hereditary_disease	other	hereditary_disease	dermatology|surgical_specialties__orthopaedic	inflammatory_disease|cancer	skin_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0008250	isolated growth hormone deficiency type II	hereditary_disease|reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|nervous_system_disorder	pediatric|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|brain_disorder	false	false	false	false	medium
MONDO:0008251	familial pityriasis rubra pilaris	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	pediatric|dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0008252	platelet adenylate cyclase activity	hereditary_disease	other	hereditary_disease	hematology	cardiovascular_disorder|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0008253	platelet aggregation, spontaneous	hereditary_disease	other	hereditary_disease	hematology|cardiology|allergy_and_immunology|pulmonology|renal_medicine|genetics_and_genomics	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0008254	platelet disorder, undefined	hereditary_disease	other	hereditary_disease	hematology|genetics_and_genomics	platelet_disorder_is_actually_related_to_bleeding_issues_but_anemia_can_be_a_result_of_the_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0008255	platelet factor 3 deficiency	hereditary_disease	other	hereditary_disease	hematology|pediatric|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0008256	platelet membrane fluidity	hereditary_disease	other	hereditary_disease	hematology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	vascular_disorder	false	false	false	false	medium
MONDO:0008257	platelet responsiveness to adrenaline, depressed	hereditary_disease	other	hereditary_disease	hematology|cardiology	cardiovascular_disorder|mental_health_disorder|autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0008258	platelet signal processing defect	hereditary_disease	other	hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder|immune_disorder	false	false	false	false	high
MONDO:0008259	familial spontaneous pneumothorax	respiratory_system_disorder|hereditary_disease	other	hereditary_disease|respiratory_system_disorder	pulmonology|genetics_and_genomics	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	lung_disorder|family_history___corrected_answer__lung_disorder	false	false	false	false	medium
MONDO:0008260	Kindler syndrome	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|eye_disorder|immune_disorder|joint_disorder	false	false	false	false	high
MONDO:0008261	hereditary sclerosing poikiloderma, Weary type	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0008262	Poland syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|breast_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|breast_disorder|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|allergy|cardiovascular_disorder|autoimmune_diseases|metabolic_disorder	ear_disorder|bone_disorder|spinal_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008263	polycystic kidney disease 1	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	genetics_and_genomics|renal_medicine|urology	kidney_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0008264	autosomal dominant medullary cystic kidney disease with or without hyperuricemia	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	genetics_and_genomics|renal_medicine	inherited_condition|kidney_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0008265	polycystic liver disease 1	digestive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|digestive_system_disorder|endocrine_system_disorder	hepatology|gastroenterology	liver_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0008266	polydactyly, postaxial, type A1	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0008267	orofaciodigital syndrome V	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	genetic_disorder_is_not_in_the_list_so_i_ll_remove_it____metacategory_removed_from_original_response_neurodegenerative_disease|genetic_disorder____corrected_to_match_format____metabolic_disorder|metabolic_disorder	ear_disorder|bone_disorder|teeth_disorder|spinal_disorder|eye_disorder|lower_gastrointestinal_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0008268	polydactyly-myopia syndrome	syndromic_disease	other	syndromic_disease	ophthalmology|orthopaedic|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	low
MONDO:0008269	polydactyly of a biphalangeal thumb	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	congenital_disorder|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0008270	polydactyly of a triphalangeal thumb	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	skeletal_system_disorder|genetic_disorder|congenital_abnormality	bone_disorder|thumb_is_part_of_a_hand_which_is_classified_as_a_upper_gastrointestinal_disorder_is_not_relevant_here_but_this_condition_affects_the_limb_so_some_may_categorize_it_under_limb_disorder_however_that_is_not_in_the_list_therefore__bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008271	polydactyly of an index finger	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	inflammatory_disease|genetic_disorder|congenital_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0008272	polysyndactyly 4	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	developmental_disorder|skeletal_disorder_becomes__skeletal_disorder|genetic_disease|congenital_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008273	actinic prurigo	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|dermatology	inflammatory_disease|allergy|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	low
MONDO:0008274	polyostotic fibrous dysplasia	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|rheumatology	autoimmune_diseases|bone_disease|metabolic_disorder	blood_bone_marrow_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0008275	familial expansile osteolysis	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|rheumatology	bone_disease|metabolic_disorder	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008276	generalized juvenile polyposis/juvenile polyposis coli	digestive_system_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|digestive_system_disorder|syndromic_disease	pediatric|gastroenterology|oncology|genetics_and_genomics	gastrointestinal_disease|genetic_disorder|inherited_disorder|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0008277	stomach polyp	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	gastrointestinal_disease_is_not_in_the_list_but_i_assume_you_meant_to_choose_from_it_so__cancer|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0008278	juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	pediatrics|gastroenterology|genetics_and_genomics|hematology	cardiovascular_disorder|anemia|cancer	lower_gastrointestinal_disorder|vascular_disorder	false	false	false	false	high
MONDO:0008280	Peutz-Jeghers syndrome	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	pediatrics|gastroenterology|genetics_and_genomics	inflammatory_disease|cardiovascular_disorder|anemia|metabolic_disorder|cancer	lower_gastrointestinal_disorder|vascular_disorder	false	false	false	false	high
MONDO:0008281	polyposis, intestinal, scattered and discrete	cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor	gastroenterology|genetics_and_genomics	polyposis__intestinal|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0008282	polyposis, intestinal, with multiple exostoses	hereditary_disease	other	hereditary_disease	pediatric|polyposis__intestinal__with_multiple_exostoses_is_best_categorized_under_the_following_category__gastroenterology|gastroenterology|oncology|genetics_and_genomics	cancer|inflammatory_disease	bone_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0008283	Cronkhite-Canada syndrome	syndromic_disease|integumentary_system_disorder|cancer_or_benign_tumor|hereditary_disease|digestive_system_disorder	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor|integumentary_system_disorder|digestive_system_disorder	pediatric|pulmonology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0008284	polyposis of gastric fundus without polyposis coli	cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor	gastroenterology|oncology|genetics_and_genomics	cancer|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0008285	polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	hereditary_disease	other	hereditary_disease	hepatology|gastroenterology|oncology	cancer|inflammatory_disease	lower_gastrointestinal_disorder_upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0008286	crossed polysyndactyly	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	skeletal_abnormality|genetic_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008287	Greig cephalopolysyndactyly syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|congenital_condition|genetic_disorder|developmental_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0008288	popliteal cyst	hereditary_disease	other	hereditary_disease	urology|orthopaedic	inflammatory_disease|metabolic_disorder	spinal_disorder|joint_disorder|muscle_disorder	false	false	false	false	low
MONDO:0008289	brain small vessel disease 1 with or without ocular anomalies	nervous_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|nervous_system_disorder|cardiovascular_disorder	neurology|ophthalmology	neurodegenerative_disease|cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0008290	porokeratosis 1, Mibelli type	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology|genetics_and_genomics	metabolic_disorder|skin_disease|genetic_condition	liver_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008291	porokeratosis plantaris palmaris et disseminata	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0008292	punctate palmoplantar keratoderma type 2	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder	false	false	false	false	low
MONDO:0008293	porokeratosis 3, disseminated superficial actinic type	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology|oncology|genetics_and_genomics	cancer|inflammatory_disease|autoimmune_diseases	liver_disorder|skin_disorder	false	false	false	false	low
MONDO:0008294	acute intermittent porphyria	integumentary_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|metabolic_disease	hereditary_disease|endocrine_system_disorder|metabolic_disease|acute_disease|integumentary_system_disorder|digestive_system_disorder	hematology|neurology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	high
MONDO:0008295	sporadic porphyria cutanea tarda	integumentary_system_disorder|metabolic_disease|inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|metabolic_disease	inflammatory_disease|endocrine_system_disorder|metabolic_disease|integumentary_system_disorder|digestive_system_disorder	dermatology|hematology|hepatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|skin_disorder	false	false	false	true	medium
MONDO:0008296	familial porphyria cutanea tarda	integumentary_system_disorder|metabolic_disease|hereditary_disease|inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|metabolic_disease	hereditary_disease|inflammatory_disease|endocrine_system_disorder|metabolic_disease|integumentary_system_disorder|digestive_system_disorder	dermatology|hematology|hepatology|genetics_and_genomics	autoimmune_diseases|anemia|metabolic_disorder	liver_disorder|skin_disorder	false	false	false	true	medium
MONDO:0008297	variegate porphyria	integumentary_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|metabolic_disease	hereditary_disease|endocrine_system_disorder|metabolic_disease|integumentary_system_disorder|digestive_system_disorder	dermatology|hematology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	liver_disorder|skin_disorder	false	false	false	true	high
MONDO:0008298	postaxial tetramelic oligodactyly	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	congenital_disease|metabolic_disorder|developmental_disorder	bone_disorder|limb_abnormality|spinal_disorder|skeletal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008299	posterior column ataxia	hereditary_disease	other	hereditary_disease	neurology|orthopaedic	neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0008300	Prader-Willi syndrome	nervous_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|chromosomal_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|endocrine_system_disorder|chromosomal_disorder|nervous_system_disorder	endocrinology|pediatric|genetics_and_genomics	genetic_disease|neurodevelopmental_disorder|metabolic_disorder	upper_gastrointestinal_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0008301	Guttmacher syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|gastroenterology|pediatrics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0008302	central precocious puberty 1	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrinology|pediatric	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0008303	familial male-limited precocious puberty	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrinology|pediatric	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0008304	premature chromatid separation trait	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	genetic_disease|metabolic_disorder	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0008305	Currarino triad	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|reproductive_system_disorder	other	musculoskeletal_system_disorder|reproductive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|oncology	adrenal_gland_disease|metabolic_disorder|cancer	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008306	ABri amyloidosis	nervous_system_disorder|metabolic_disease|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder|neurodegenerative_disease|metabolic_disease	cardiovascular_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	lymphatic_disorder|brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0008307	presenile dementia, Kraepelin type	hereditary_disease	other	hereditary_disease	psychiatry|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	vascular_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0008308	priapism, familial idiopathic	hereditary_disease	other	idiopathic_disease|hereditary_disease	genetics_and_genomics|urology	adrenal_gland_disease|metabolic_disorder	vascular_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0008309	primary release disorder of platelets	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	cardiology|hematology	autoimmune_diseases|metabolic_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0008310	Hutchinson-Gilford progeria syndrome	premature_aging_syndrome|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	premature_aging_syndrome|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|skin_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0008311	progeria-short stature-pigmented nevi syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|dermatology	genetic_disorder____updated_to_provide_a_more_specific_category__since_progeria_is_a_genetic_disorder|metabolic_disorder	bone_disorder|skin_disorder	false	false	false	false	high
MONDO:0008312	autosomal dominant prognathism	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	endocrinology|pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|neurodegenerative_disease	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008314	pronation-supination of the forearm, impairment of	hereditary_disease	other	hereditary_disease	neurology|orthopaedic	inflammatory_disease|neurodegenerative_disease	joint_disorder|muscle_disorder	false	false	false	false	low
MONDO:0008315	prostate cancer	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0008316	thrombophilia due to protein C deficiency, autosomal dominant	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	cardiovascular_disorder|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0008317	proteolytic capacity of plasma	hereditary_disease	other	hereditary_disease	renal_medicine|hepatology|cardiology|gastroenterology|allergy_and_immunology|hematology	inflammatory_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	none
MONDO:0008318	Proteus syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|dermatology|pediatrics	genetic_disorder|metabolic_disorder	skin_disorder|vascular_disorder	false	false	false	false	high
MONDO:0008319	protoporphyria, erythropoietic, 1	endocrine_system_disorder|digestive_system_disorder|metabolic_disease|hereditary_disease|integumentary_system_disorder	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|hereditary_disease|endocrine_system_disorder|integumentary_system_disorder|metabolic_disease	genetics_and_genomics|dermatology|hematology	anemia|metabolic_disorder	liver_disorder|skin_disorder	false	false	false	true	high
MONDO:0008320	Protrusio acetabuli	hereditary_disease	other	hereditary_disease	osteopathology|orthopaedic	inflammatory_disease|metabolic_disorder	joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008321	pruritus, hereditary localized	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|allergy|metabolic_disorder	liver_disorder|skin_disorder	false	false	false	false	low
MONDO:0008322	pseudoachondroplasia	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic|rheumatology	inflammatory_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0008323	Liddle syndrome	hereditary_disease|syndromic_disease|urinary_system_disorder	other	hereditary_disease|syndromic_disease|urinary_system_disorder	pediatric|genetics_and_genomics|renal_medicine	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	immune_disorder_kidney_disorder	false	false	false	true	high
MONDO:0008324	pseudoarthrogryposis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|orthopaedic	inflammatory_disease|neurodegenerative_disease	joint_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008325	Pseudoatrophoderma colli	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0008327	exfoliation syndrome	hereditary_disease|syndromic_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|syndromic_disease|disorder_of_visual_system	endocrinology|pediatric|genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	skin_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0008328	glaucoma 1, open angle, P	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder|open_angle	false	false	false	true	medium
MONDO:0008329	autosomal dominant pseudohypoaldosteronism type 1	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	endocrinology|genetics_and_genomics|renal_medicine|pediatrics	adrenal_gland_disease|cardiovascular_disorder|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0008330	pseudomonilethrix	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|anemia|neurodegenerative_disease	hair_disorder|skin_disorder	false	false	false	false	high
MONDO:0008332	platelet-type von Willebrand disease	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0008333	pseudoxanthoma elasticum, forme fruste	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0008335	short stature-craniofacial anomalies-genital hypoplasia syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|genetic_disorders	joint_disorder|bone_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0008336	pterygium colli, isolated	hereditary_disease	other	hereditary_disease	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	low
MONDO:0008337	familial pterygium of the conjunctiva	cancer_or_benign_tumor|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder	genetics_and_genomics|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0008338	contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	joint_disorder|spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0008339	antecubital pterygium syndrome	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	joint_disorder|eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008340	ptosis, hereditary congenital, 1	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	pediatric|genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease|hereditary_congenital_conditions	eye_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0008341	ptosis-strabismus-ectopic pupils syndrome	syndromic_disease	other	syndromic_disease	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008342	pubic bone dysplasia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic	skeletal_diseases|metabolic_disorder|genetic_disorders	joint_disorder|bone_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0008343	pulmonary atresia with ventricular septal defect	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|cardiology|cardiothoracic	cardiovascular_disorder	heart_disorder|lung_disorder	false	false	false	false	high
MONDO:0008346	pulmonary hemosiderosis	metabolic_disease|respiratory_system_disorder	metabolic_disease	metabolic_disease|respiratory_system_disorder	pulmonology|hematology	inflammatory_disease|autoimmune_diseases|anemia	blood_bone_marrow_disorder|lung_disorder	false	false	false	false	high
MONDO:0008348	pulmonary nodular lymphoid hyperplasia	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|lung_disorder|immune_disorder	false	false	false	false	medium
MONDO:0008349	pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities	hereditary_disease	other	hereditary_disease	cardiology|cardiothoracic|pediatric	atrial_septal_defect|cardiovascular_disorder	heart_disorder|lung_disorder	false	false	false	true	medium
MONDO:0008350	pulmonic stenosis and deafness	hereditary_disease	other	hereditary_disease	cardiothoracic|otolaryngology|pulmonology	cardiovascular_disorder|congenital_anomaly_disease	ear_disorder|lung_disorder	false	false	false	true	medium
MONDO:0008352	pupillary membrane, persistence of	hereditary_disease	other	hereditary_disease	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0008353	pruritic urticarial papules and plaques of pregnancy	inflammatory_disease|integumentary_system_disorder|obstetric_disorder	other	obstetric_disorder|integumentary_system_disorder|inflammatory_disease	dermatology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|allergy	skin_disorder|immune_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0008354	purpura simplex	hereditary_disease	other	hereditary_disease	dermatology|hematology	inflammatory_disease|autoimmune_diseases|anemia	vascular_disorder|skin_disorder|blood_bone_marrow_disorder	false	false	false	true	low
MONDO:0008355	pyloric stenosis, infantile hypertrophic, 1	digestive_system_disorder|hereditary_disease	other	digestive_system_disorder|hereditary_disease	gastroenterology|pediatric	infantile_hypertrophic_pyloric_stenosis_does_not_fit_well_in_other_categories__but_it_is_often_associated_with_conditions_like_congenital_hypertrohpic_pyloric_stenosis_which_can_be_linked_to_metabolic_disorders_or_more_specifically__genetic_abnormalities|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0008356	radial heads, posterior dislocation of	hereditary_disease	other	hereditary_disease	orthopaedic|neurology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008357	radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease	orthopaedic|pediatric|genetics_and_genomics	autoimmune_diseases|cardiovascular_disorder|metabolic_disorder	skeletal_disorder|joint_disorder|bone_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0008358	radial ray hypoplasia-choanal atresia syndrome	syndromic_disease	other	syndromic_disease	orthopaedic|otolaryngology|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	bone_disorder|throat_disorder	false	false	false	false	high
MONDO:0008359	radio-renal syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	renal_medicine|urology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0008361	radius, aplasia of, with cleft lip/palate	hereditary_disease	other	hereditary_disease	orthopaedic|otolaryngology|pediatric	autoimmune_diseases|anemia|metabolic_disorder	bone_disorder|teeth_disorder	false	false	false	false	high
MONDO:0008362	ragweed sensitivity	hereditary_disease	other	hereditary_disease	pulmonology|dermatology|allergy_and_immunology	autoimmune_diseases|allergy	nose_disorder|immune_disorder|lung_disorder	false	false	false	true	medium
MONDO:0008363	raindrop hypopigmentation	hereditary_disease	other	hereditary_disease	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases|anemia	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0008364	Raynaud disease	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	rheumatology|hematology	inflammatory_disease|autoimmune_diseases	skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0008365	recombinant 8 syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|immunology|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0008366	red cell permeability defect	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0008367	red cell phospholipid defect with hemolysis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	hemolysis|red_cell_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0008368	autosomal dominant distal renal tubular acidosis	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	genetics_and_genomics|renal_medicine|pediatric	autoimmune_diseases|anemia|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0008369	proximal renal tubular acidosis	metabolic_disease|urinary_system_disorder	metabolic_disease	urinary_system_disorder|metabolic_disease	genetics_and_genomics|renal_medicine	kidney_disease|metabolic_disorder	renal_tubular_acidosis|kidney_disorder	false	false	false	true	medium
MONDO:0008371	Dowling-Degos disease	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|integumentary_system_disorder|metabolic_disease	dermatology|gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	low
MONDO:0008372	retinal aplasia	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	anemia|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0008373	retinal arterial tortuosity	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	ophthalmology|neurology	adrenal_gland_disease|cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|eye_disorder	false	false	false	false	medium
MONDO:0008374	retinal cone dystrophy type 1	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0008375	retinal detachment	disorder_of_visual_system|hereditary_disease|nervous_system_disorder	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder	ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	true	high
MONDO:0008376	retinal venous beading	hereditary_disease	other	hereditary_disease	hematology|ophthalmology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	vascular_disorder|eye_disorder	false	false	false	false	medium
MONDO:0008377	retinitis pigmentosa 1	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|metabolic_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_orbital_region|metabolic_disease|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology|neurology	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0008378	retinitis pigmentosa 9	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|metabolic_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_orbital_region|metabolic_disease|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	adrenal_gland_disease|neurodegenerative_disease	lower_gastrointestinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0008379	retinitis pigmentosa 10	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|metabolic_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_orbital_region|metabolic_disease|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	lower_gastrointestinal_disorder|eye_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0008380	retinoblastoma	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder	oncology|pediatric|genetics_and_genomics|ophthalmology	cancer	bone_disorder|eye_disorder	false	true	false	true	high
MONDO:0008381	dominant pericentral pigmentary retinopathy	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|metabolic_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	hereditary_disease|psychiatric_disorder|disorder_of_orbital_region|metabolic_disease|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0008382	retinoschisis, autosomal dominant	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	true	medium
MONDO:0008383	rheumatoid arthritis	musculoskeletal_system_disorder|connective_tissue_disorder|inflammatory_disease|immune_system_disorder	autoimmune_disease	connective_tissue_disorder|immune_system_disorder|inflammatory_disease|musculoskeletal_system_disorder	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|joint_disorder	false	false	false	true	high
MONDO:0008384	rheumatoid nodulosis	musculoskeletal_system_disorder|inflammatory_disease	other	inflammatory_disease|musculoskeletal_system_disorder	rheumatology|dermatology|rheumatoid	autoimmune_diseases|inflammatory_disease	bone_disorder|immune_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008385	rhiny	hereditary_disease	other	hereditary_disease	otolaryngology|pediatrics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	nose_disorder|upper_gastrointestinal_disorder	false	false	false	false	none
MONDO:0008386	Axenfeld-Rieger syndrome type 1	disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease|disorder_of_orbital_region|disorder_of_visual_system|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	teeth_disorder|bone_disorder|spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0008387	ring dermoid of cornea	disorder_of_visual_system|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|disorder_of_orbital_region|disorder_of_visual_system	dermatology|ophthalmology	autoimmune_diseases|allergy|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	low
MONDO:0008388	ringed hair disease	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|general_practitioning__pediatric	anemia|autoimmune_diseases	skin_disorder|hair_disorder	false	false	false	false	none
MONDO:0008389	autosomal dominant Robinow syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease	bone_disorder|eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008390	Rombo syndrome	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	vascular_disorder|spinal_disorder|lower_gastrointestinal_disorder|eye_disorder|skin_disorder|immune_disorder|ear_disorder|joint_disorder|lung_disorder|upper_gastrointestinal_disorder|kidney_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0008391	Robinow-Sorauf syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	skin_disorder|joint_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0008392	Roussy-Levy syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0008393	Rubinstein-Taybi syndrome due to CREBBP mutations	musculoskeletal_system_disorder|hereditary_disease|psychiatric_disorder|syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	psychiatric_disorder	musculoskeletal_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	lymphatic_disorder|bone_disorder|muscle_disorder|skin_disorder|eye_disorder|joint_disorder|brain_disorder|upper_gastrointestinal_disorder|heart_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0008394	Silver-Russell syndrome	hereditary_disease|syndromic_disease|chromosomal_disorder|disorder_of_development_or_morphogenesis	other	chromosomal_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|endocrine_disorder|genetic_disorder	endocrine_disorder|growth_disorder	false	false	false	false	medium
MONDO:0008395	Ruvalcaba syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|vascular_disorder|joint_disorder|brain_disorder|upper_gastrointestinal_disorder|blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0008396	oculodental syndrome, Rutherfurd type	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|teeth_disorder	false	false	false	false	high
MONDO:0008397	aplasia of lacrimal and salivary glands	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	hematology|otolaryngology	inflammatory_disease|autoimmune_diseases	eye_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0008398	salivary substance, Clostridium botulinum type	hereditary_disease	other	hereditary_disease	otolaryngology|neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|upper_gastrointestinal_disorder	true	false	false	false	high
MONDO:0008400	salivary duct calculi	hereditary_disease	other	hereditary_disease	urology|otolaryngology	metabolic_disorder|kidney_disease|urinary_system_disorder	upper_gastrointestinal_disorder|teeth_disorder|oral_disorder	false	false	false	true	medium
MONDO:0008401	pleomorphic adenoma	hereditary_disease|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|hereditary_disease|cancer_or_benign_tumor	oncology|pathology	cancer|adrenal_gland_disease	bone_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0008402	cleft palate-large ears-small head syndrome	hereditary_disease	other	hereditary_disease	otolaryngology|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder|congenital_disorder	head_disorder|bone_disorder|teeth_disorder|ear_disorder	false	false	false	false	high
MONDO:0008403	scalp defects-postaxial polydactyly syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|integumentary_system_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|integumentary_system_disorder	neurology|oncology|obstetrics_and_gynecology|dermatology|pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	skin_disorder	false	false	false	false	medium
MONDO:0008404	scalp-ear-nipple syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	pediatrics|dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|ear_disorder|lymphatic_disorder|immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008407	neurogenic scapuloperoneal syndrome, Kaeser type	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008408	scapuloperoneal spinal muscular atrophy, autosomal dominant	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant_disorder_is_not_in_the_list_but_it_implies_genetic_which_is_close_to_metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008409	congenital myopathy 7A, myosin storage, autosomal dominant	nervous_system_disorder|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008410	Scheuermann disease	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	neurology|pediatric|orthopaedic	skeletal_disease|metabolic_disorder|musculoskeletal_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008411	ulnar-mammary syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008412	intestinal schistosomiasis	infectious_disease|digestive_system_disorder	infectious_disease	infectious_disease|digestive_system_disorder	gastroenterology|hepatology	allergy|autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0008414	schizophrenia 1	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|mind_disorder	false	false	false	false	high
MONDO:0008416	palmoplantar keratoderma-sclerodactyly syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	rheumatology|dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	muscle_disorder|joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008417	sclerocornea, autosomal dominant	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0008418	scleroderma, familial progressive	connective_tissue_disorder|immune_system_disorder|integumentary_system_disorder	autoimmune_disease	immune_system_disorder|integumentary_system_disorder|connective_tissue_disorder	rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	joint_disorder|immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0008420	seborrheic keratosis	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	dermatology	inflammatory_disease|skin_condition	skin_disorder	false	false	false	true	low
MONDO:0008421	flat face-microstomia-ear anomaly syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|otolaryngology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	facial_disorder|ear_disorder	false	false	false	false	high
MONDO:0008422	autosomal dominant sideroblastic anemia	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	blood_disorder|anemia|genetic_disorder	blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0008423	sinus node disease and myopia	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease|syndromic_disease	cardiology|ophthalmology	cardiovascular_disorder|metabolic_disorder	eye_disorder|heart_disorder	false	false	false	for_sinus_node_disease__also_known_as_sick_sinus_syndrome___there_are_treatments_available_that_can_help_manage_the_condition__including_medications_and_the_implantation_of_a_pacemaker_to_regulate_heart_rhythm__therefore__efficacious_treatments_exist_for_sinus_node_disease___for_myopia__nearsightedness___there_are_various_methods_to_manage_and_treat_the_condition__including_corrective_lenses__glasses_and_contact_lenses___refractive_surgery__like_lasik___and_orthokeratology__thus__efficacious_treatments_also_exist_for_myopia___since_both_conditions_have_existing_efficacious_treatments__the_answer_is_true	medium
MONDO:0008424	sella turcica, bridged	hereditary_disease	other	hereditary_disease	endocrinology|neurology	inflammatory_disease|autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008425	omphalocele syndrome, Shprintzen-Goldberg type	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	autoimmune_diseases|cardiovascular_disorder|metabolic_disorder	vascular_disorder|joint_disorder|heart_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008426	Shprintzen-Goldberg syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|connective_tissue_disorder|syndromic_disease|hereditary_disease	other	musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|anemia	lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0008427	sister chromatid exchange, frequency of	hereditary_disease	other	hereditary_disease	oncology|genetics_and_genomics	cancer|genetic_disorder	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0008428	septooptic dysplasia	nervous_system_disorder|syndromic_disease|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	pulmonology|pediatric|cardiothoracic	autoimmune_diseases|metabolic_disorder|inflammatory_disease	heart_disorder|congenital_heart_disorder	false	false	false	false	high
MONDO:0008429	Singleton-Merten dysplasia	connective_tissue_disorder|syndromic_disease|hereditary_disease	other	connective_tissue_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0008430	skeletal dysplasia with delayed epiphyseal and carpal bone ossification	hereditary_disease	other	hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	skeletal_dysplasia|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008433	small cell lung carcinoma	cancer_or_benign_tumor|endocrine_system_disorder|respiratory_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	respiratory_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	pulmonology|oncology	inflammatory_disease|cancer|adrenal_gland_disease|autoimmune_diseases|cardiovascular_disorder	lung_disorder	false	true	false	false	very_high
MONDO:0008434	Smith-Magenis syndrome	psychiatric_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|chromosomal_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|chromosomal_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	teeth_disorder|bone_disorder|face_disorder|muscle_disorder|eye_disorder|joint_disorder|spinal_disorder|reproductive_system_disorder|ear_disorder	false	false	false	false	high
MONDO:0008435	Somatomedin, embryonic	hereditary_disease	other	hereditary_disease	endocrinology|pediatric	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	none
MONDO:0008436	Sneddon syndrome	connective_tissue_disorder|syndromic_disease|hereditary_disease|integumentary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|connective_tissue_disorder|integumentary_system_disorder|hereditary_disease|syndromic_disease	dermatology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0008437	hereditary spastic paraplegia 3A	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0008438	hereditary spastic paraplegia 4	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0008439	spastic paraplegia-epilepsy-intellectual disability syndrome	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008440	spastic paraplegia-nephritis-deafness syndrome	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|syndromic_disease	renal_medicine|neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|ear_disorder|kidney_disorder	true	false	false	false	high
MONDO:0008441	spastic paraplegia with associated extrapyramidal signs	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008442	spastic paraplegia-neuropathy-poikiloderma syndrome	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|syndromic_disease	dermatology|neurology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	muscle_disorder|skin_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008443	spastic paraplegia-precocious puberty syndrome	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|syndromic_disease	endocrinology|pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0008444	spastic paraplegia, optic atrophy, and dementia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	muscle_disorder|eye_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008445	delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0008446	sperm protamine P4	hereditary_disease	other	hereditary_disease	urology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder	false	false	false	false	low
MONDO:0008447	hereditary spherocytosis type 1	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	hereditary_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0008449	spina bifida	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology	congenital_disorder|neurological_disease	bone_disorder|brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0008450	spinal arachnoiditis	nervous_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|nervous_system_disorder|inflammatory_disease	rheumatology|neurology	inflammatory_disease|autoimmune_diseases	muscle_disorder|spinal_disorder|immune_disorder	false	false	false	false	high
MONDO:0008451	neuronopathy, distal hereditary motor, autosomal dominant 1	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|hereditary_condition	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0008452	spinal muscular atrophy, facioscapulohumeral type	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008453	adult-onset proximal spinal muscular atrophy, autosomal dominant	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autosomal_dominant_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008454	spinal intradural arachnoid cysts	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	spinal_surgery|orthopaedic|neurology	neurosurgical_condition|neurological_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0008455	spinal muscular atrophy, segmental	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	true	high
MONDO:0008456	spinocerebellar ataxia with rigidity and peripheral neuropathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008457	spinocerebellar ataxia type 6	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0008458	spinocerebellar ataxia type 2	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|spinal_cord_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008459	spinocerebellar atrophy with pupillary paralysis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008460	splenogonadal fusion-limb defects-micrognathia syndrome	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatrics|genetics_and_genomics	inflammatory_disease|cancer|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|anemia	limb_defect|micrognathia|reproductive_system_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0008461	splenomegaly syndrome with splenic Germinal center hypoplasia and reduced circulating T helper cells	hereditary_disease	other	hereditary_disease	hematology|immunology	inflammatory_disease|autoimmune_diseases|anemia	immune_disorder_lymphatic_disorder	false	false	false	false	high
MONDO:0008462	split lower lip	hereditary_disease	other	hereditary_disease	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|mouth_disorder	false	false	false	false	low
MONDO:0008463	split-hand and split-foot with hypodontia	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	teeth_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008464	split hand-foot malformation 1	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disease	joint_disorder|skin_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008465	Patterson-Stevenson-Fontaine syndrome	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|hearing_disorder|ear_disorder	false	false	false	false	high
MONDO:0008466	Karsch-Neugebauer syndrome	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	skin_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0008467	Czeizel-Losonci syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	lymphatic_disorder|ear_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0008469	spondyloepimetaphyseal dysplasia-hypotrichosis syndrome	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|dermatology|genetics_and_genomics	genetic_disorder|skeletal_system_disease|metabolic_disorder	bone_disorder|skin_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008470	spondyloepiphyseal dysplasia with punctate corneal dystrophy	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|ophthalmology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder|joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008471	spondyloepiphyseal dysplasia congenita	connective_tissue_disorder|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|orthopaedic|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0008472	spondyloepiphyseal dysplasia, MacDermot type	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008473	spondyloepimetaphyseal dysplasia, Maroteaux type	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008474	spondyloepiphyseal dysplasia tarda, autosomal dominant	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|rheumatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008475	spondylolisthesis	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|neurology|rheumatology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008476	spondyloepimetaphyseal dysplasia, Strudwick type	connective_tissue_disorder|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	orthopaedic|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0008477	spondylometaphyseal dysplasia, Kozlowski type	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|orthopaedic|rheumatology|genetics_and_genomics	inflammatory_disease|adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0008478	spondylometaphyseal dysplasia, Schmidt type	connective_tissue_disorder|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease|syndromic_disease	orthopaedic|rheumatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0008479	spondylometaphyseal dysplasia, 'corner fracture' type	connective_tissue_disorder|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease|syndromic_disease	orthopaedic|rheumatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008481	spondylosis, cervical	hereditary_disease	other	hereditary_disease	orthopaedic|neurology|rheumatology	inflammatory_disease|neurodegenerative_disease	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0008482	Sprengel deformity	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|orthopaedic	genetic_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0008483	stuttering, familial persistent, 1	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	throat_disorder|brain_disorder	false	false	false	false	medium
MONDO:0008484	stapes ankylosis with broad thumbs and toes	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|otolaryngology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder|ear_disorder	false	false	false	false	medium
MONDO:0008485	sebocystomatosis	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	skin_disorder	false	false	false	false	low
MONDO:0008486	steatocystoma multiplex-natal teeth syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|dermatology|genetics_and_genomics	skin_disease|metabolic_disorder	teeth_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008487	polycystic ovary syndrome	endocrine_system_disorder|syndromic_disease|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|syndromic_disease	endocrinology|obstetrics_and_gynecology	endocrine_disorders|hormonal_disorder|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	true	false	medium
MONDO:0008488	holoprosencephaly-radial heart renal anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics|congenital_anomalies	cardiovascular_disorder|metabolic_disorder	kidney_disorder|heart_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0008489	sternum, premature obliteration of sutures of	hereditary_disease	other	hereditary_disease	orthopaedic|cardiothoracic	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	bone_disorder|vascular_disorder	false	false	false	false	high
MONDO:0008490	otospondylomegaepiphyseal dysplasia, autosomal dominant	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008491	stiff-person syndrome	nervous_system_disorder|syndromic_disease	other	nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0008492	stiff skin syndrome	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0008493	overhydrated hereditary stomatocytosis	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0008494	cryohydrocytosis	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0008495	platelet storage pool deficiency	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0008496	storm syndrome	hereditary_disease	other	hereditary_disease	pediatric|endocrinology|rheumatology|genetics_and_genomics	inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	liver_disorder|endocrine_disorder|immune_disorder	false	false	false	false	high
MONDO:0008497	Stormorken syndrome	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	pediatric|hematoloy|cardiology|dermatology|neurology|genetics_and_genomics|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0008499	short stature-wormian bones-dextrocardia syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|orthopaedic|cardiology|genetics_and_genomics	cardiovascular_disorder|skeletal_abnormality|metabolic_disorder	bone_disorder|skeletal_disorder|heart_disorder	true	false	false	false	high
MONDO:0008500	striae distensae, familial	hereditary_disease	other	hereditary_disease	pediatric|dermatology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|skin_disorder	false	false	false	false	low
MONDO:0008501	Sturge-Weber syndrome	disorder_of_visual_system|nervous_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	dermatology|neurology|genetics_and_genomics	autoimmune_diseases|neurological_disorder	skin_disorder|vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0008502	sulfhemoglobinemia, congenital	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0008503	Worster-Drought syndrome	nervous_system_disorder	other	nervous_system_disorder	pediatric|neonatology|obstetrics_and_gynecology	metabolic_disorder|adrenal_gland_disease	biliary_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0008504	supravalvular aortic stenosis	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiology|cardiothoracic	cardiovascular_disorder|congenital_heart_defect	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0008505	surface antigen, glycoprotein 75	hereditary_disease	other	hereditary_disease	hematology|hepatology|genetics_and_genomics|immunology	autoimmune_diseases|surface_antigen_is_typically_associated_with_autoimmune_diseases	surface_antigen_related_diseases_can_be_associated_with_liver_disorders|liver_disorder	false	false	false	false	none
MONDO:0008506	symphalangism of toes	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0008507	surface polypeptides, anonymous	hereditary_disease	other	hereditary_disease	dermatology|neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	none
MONDO:0008508	symphalangism, C. S. Lewis type	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	neurology|orthopaedic	adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008509	distal symphalangism	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic	inflammatory_disease|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0008510	symphalangism with multiple anomalies of hands and feet	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0008511	proximal symphalangism	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	rheumatology|orthopaedic	autoimmune_diseases|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008512	syndactyly type 1	disorder_of_development_or_morphogenesis|chromosomal_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|chromosomal_disorder	genetics_and_genomics|orthopaedic	congenital_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	true	low
MONDO:0008513	synpolydactyly type 1	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic	congenital_anomaly|metabolic_disorder|genetic_disorder|developmental_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008514	syndactyly type 3	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_condition	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008515	syndactyly type 4	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0008516	syndactyly type 5	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder_is_the_best_fit_but_it_s_not_in_the_list_so_the_answer_is___metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0008517	syndactyly-polydactyly-ear lobe syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|orthopaedic	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	bone_disorder|ear_disorder|joint_disorder	false	false	false	false	low
MONDO:0008518	calcaneonavicular coalition	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic	inflammatory_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008519	multiple synostoses syndrome 1	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|congenital_dysmorphism	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0008520	brachydactyly-elbow wrist dysplasia syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic	genetic_disorder|neurodegenerative_disease|developmental_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008521	tarsal-carpal coalition syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	inflammatory_disease|genetic_disorder|congenital_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008522	synovial chondromatosis, familial, with dwarfism	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	inflammatory_disease|metabolic_disorder	bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008523	Blau syndrome	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	connective_tissue_disorder|syndromic_disease|hereditary_disease	rheumatology|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder	immune_disorder|vascular_disorder|joint_disorder	false	false	false	true	high
MONDO:0008524	syringomas, multiple	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|cancer|neurodegenerative_disease	nerve_disorder|skin_disorder|brain_disorder	false	false	false	false	low
MONDO:0008525	syringomyelia, isolated	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0008526	talonavicular coalition	hereditary_disease	other	hereditary_disease	orthopaedic|pediatric	musculoskeletal_disorder|genetic_disorder|congenital_disorder|cardiovascular_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008527	tarsal coalition	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|orthopedic|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008528	tear protein, anodal	hereditary_disease	other	hereditary_disease	cardiology|genetics_and_genomics|ophthalmology|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	low
MONDO:0008529	T-cell Subgroups, non-HLA-linked	hereditary_disease	other	hereditary_disease	allergy_and_immunology|hematology___becomes__immunology|hematology|hematology_becomes__immunology|immunology	autoimmune_diseases|inflammatory_disease|t_cell_subgroups_are_often_implicated_in_autoimmune_diseases_and_inflammation	immune_disorder|lymphatic_disorder	false	false	false	false	none
MONDO:0008530	teeth, odd shapes of	hereditary_disease	other	hereditary_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder	teeth_disorder|teeth	false	false	false	false	low
MONDO:0008532	teeth present at birth	hereditary_disease	other	hereditary_disease	otolaryngology|genetics_and_genomics|pediatric	anatomic_anomaly|metabolic_disorder|developmental_disorder	teeth_disorder	false	false	false	true	none
MONDO:0008533	teeth, supernumerary	hereditary_disease	other	hereditary_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	teeth_disorder|supernumerary_tissue_disorder	false	false	false	false	low
MONDO:0008534	generalized essential telangiectasia	integumentary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder	rheumatology|hematology|genetics_and_genomics|renal_medicine|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|skin_disorder|kidney_disorder|vascular_disorder	false	false	false	false	low
MONDO:0008535	telangiectasia, hereditary hemorrhagic, type 1	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	hematology|genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|anemia	skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0008536	temperature-sensitive lethal mutation	hereditary_disease	other	hereditary_disease	genetics_and_genomics	genetic_disorder|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0008537	telecanthus	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	otolaryngology|ophthalmology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	throat_disorder|eye_disorder	false	false	false	false	low
MONDO:0008538	temporal arteritis	inflammatory_disease|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	inflammatory_disease|nervous_system_disorder|cardiovascular_disorder	neurology|rheumatology	inflammatory_disease|autoimmune_diseases	eye_disorder|vascular_disorder|joint_disorder	false	false	false	true	high
MONDO:0008540	extensor tendons of finger anomalies	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	rheumatology|orthopaedic	musculoskeletal_disorder|autoimmune_diseases|inflammatory_disease	muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008541	spermatic cord torsion	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	pediatric|urology	inflammatory_disease|metabolic_disorder|cancer	reproductive_system_disorder|muscle_disorder	false	false	false	true	high
MONDO:0008542	tetralogy of fallot	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiology|cardiothoracic|pediatric	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0008543	tetralogy of fallot and glaucoma	hereditary_disease	other	hereditary_disease	cardiothoracic|ophthalmology	glaucoma|cardiovascular_disorder	heart_disorder|eye_disorder	false	false	false	true	medium
MONDO:0008544	tetramelic monodactyly	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic	birth_defect|genetic_disorder|metabolic_disorder|congenital_disorder|developmental_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0008545	thalassemia, beta+, silent allele	hematologic_disorder|hereditary_disease|endocrine_system_disorder	anemia|endocrine_system_disorder	hematologic_disorder|hereditary_disease|endocrine_system_disorder	hematology|genetics_and_genomics|pediatric	metabolic_disorder|anemia	genetic_disorder|blood_bone_marrow_disorder|beta_disorder	false	false	false	false	medium
MONDO:0008546	thanatophoric dysplasia type 1	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|skeletal_system_disorder	false	false	false	false	high
MONDO:0008547	thanatophoric dysplasia type 2	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|neurodegenerative_disease	musculoskeletal_disorder|bone_disorder|skeletal_disorder	false	false	false	false	very_high
MONDO:0008549	thoracic dysostosis, isolated	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	genetic_disease|developmental_disease|skeletal_abnormality|metabolic_disorder|bone_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008551	thoracolaryngopelvic dysplasia	hereditary_disease|musculoskeletal_system_disorder|respiratory_system_disorder	other	respiratory_system_disorder|musculoskeletal_system_disorder|hereditary_disease	neurology|pediatric|otolaryngology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	throat_disorder|thoracolaryngopelvic_dysplasia|ear_disorder	false	false	false	false	high
MONDO:0008552	platelet-type bleeding disorder 16	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics|platelet_type_bleeding_disorders_fall_under_the_umbrella_of_hematology__and_because_they_have_a_genetic_basis_they_also_fall_into_the_category_of__genetics_and_genomics	inflammatory_disease|anemia|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0008553	platelet-type bleeding disorder 17	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	inflammatory_disease|anemia|cardiovascular_disorder|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0008554	thrombocythemia 1	hereditary_disease|musculoskeletal_system_disorder|hematologic_disorder	other	hematologic_disorder|musculoskeletal_system_disorder|hereditary_disease	hematology|thrombocythemia	anemia|metabolic_disorder|autoimmune_diseases|cancer	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0008555	thrombocytopenia 2	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology	inflammatory_disease|anemia|autoimmune_diseases	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0008556	thrombocytopenia, cyclic	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	inflammatory_disease|anemia|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immunological_disorder	false	false	false	true	medium
MONDO:0008557	Paris-Trousseau thrombocytopenia	chromosomal_disorder|hereditary_disease|hematologic_disorder	other	hematologic_disorder|chromosomal_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0008558	autoimmune thrombocytopenic purpura	hereditary_disease|immune_system_disorder|hematologic_disorder	autoimmune_disease	immune_system_disorder|hematologic_disorder|hereditary_disease	hematology|immunology	inflammatory_disease|anemia|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0008559	thrombophilia due to thrombin defect	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0008560	thrombophilia due to activated protein C resistance	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0008561	thumb deformity	hereditary_disease	other	hereditary_disease	pediatric|orthopaedic	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008562	thumb deformity-alopecia-pigmentation anomaly syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|joint_disorder	true	false	false	false	medium
MONDO:0008563	thumb stiffness-brachydactyly-intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008564	DiGeorge syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|immune_system_disorder|cardiovascular_disorder|chromosomal_disorder	cardiovascular_disorder	immune_system_disorder|cardiovascular_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|chromosomal_disorder	pediatric|pulmonology|genetics_and_genomics|cardiothoracic	cardiovascular_disorder|metabolic_disorder	muscle_disorder|upper_gastrointestinal_disorder|heart_disorder|immune_disorder|bone_disorder	false	false	false	false	high
MONDO:0008565	familial thyroglossal duct cyst	hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|otorhinolaryngologic_disease	pediatric|otolaryngology	cancer|thyroglossal_duct_cyst_is_a_congenital_anomaly_and_a_type_of_cancer	endocrine_disorder_throat_disorder	false	false	false	false	low
MONDO:0008566	thyroid cancer, nonmedullary, 2	hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|hereditary_disease	oncology|endocrinology	thyroid_cancer|cancer	endocrine_disorder|thyroid_disorder	false	true	false	true	medium
MONDO:0008567	thyroid cancer, nonmedullary, 1	hereditary_disease|endocrine_system_disorder|syndromic_disease|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|syndromic_disease|hereditary_disease	oncology|endocrinology	cancer	endocrine_disorder|thyroid_disorder	false	true	false	true	medium
MONDO:0008568	thyroid hormone plasma membrane transport defect	hereditary_disease	other	hereditary_disease	genetics_and_genomics|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|immune_disorder	false	false	false	true	medium
MONDO:0008569	thyroid hormone resistance, generalized, autosomal dominant	hereditary_disease|endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|generalized_endocrine_disorder	false	false	false	false	high
MONDO:0008571	Blount disease, infantile	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|cardiology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	liver_disorder|biliary_disorder	false	false	false	true	medium
MONDO:0008572	tibia, hypoplasia or aplasia of, with polydactyly	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	anemia|metabolic_disorder	blood_bone_marrow_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0008573	tibial torsion, bilateral medial	hereditary_disease	other	hereditary_disease	orthopaedic|pediatric	inflammatory_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008575	nicotine dependence	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	mental_health_disorder|metabolic_disorder	lung_disorder|brain_disorder	false	false	false	true	high
MONDO:0008576	toe, fifth, number of phalanges 1N	hereditary_disease	other	hereditary_disease	orthopaedic|pediatric	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0008577	toe, misshapen	hereditary_disease	other	hereditary_disease	podiatry_is_not_listed_but_a_correct_option_would_be__cardiology|orthopaedic|neurology	neurodegenerative_disease|cardiovascular_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0008578	toe, rotated fifth	hereditary_disease	other	hereditary_disease	general_medicine_is_not_listed_so_none|orthopaedic|pediatric	neurodegenerative_disease|inflammatory_disease	musculoskeletal_system_disorder_is_not_available_so__spinal_disorder|joint_disorder	false	false	false	based_on_your_query_regarding__toe__rotated_fifth___it_seems_like_you_might_be_referring_to_a_condition_such_as_a_bunion_or_a_similar_deformity_involving_the_fifth_toe__pinky_toe___if_that_is_the_case__treatments_for_bunions_or_toe_deformities_can_include_both_non_surgical_and_surgical_options_____non_surgical_treatments___can_include____orthotic_devices___custom_footwear___physical_therapy___pain_relief_medications____surgical_treatments___may_involve_procedures_to_realign_the_toe___considering_the_existence_of_these_treatments__the_answer_is_true__efficacious_treatments_exist_for_managing_conditions_related_to_a_rotated_fifth_toe	medium
MONDO:0008579	toes, relative length of first and second	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0008580	toes, space between first and second	hereditary_disease	other	hereditary_disease	orthopaedic|podiatry|pediatric	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0008581	malposition of teeth with or without hypodontia/oligodontia	hereditary_disease	other	hereditary_disease	orthopaedic|pediatric	metabolic_disorder|developmental_disorder	teeth_disorder|bone_disorder	false	false	false	false	low
MONDO:0008582	tooth and nail syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|syndromic_disease|hereditary_disease	neurology|dermatology|genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	teeth_disorder|nail_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008583	inherited torticollis	hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|inherited_condition	muscle_disorder|spinal_disorder	false	false	false	false	low
MONDO:0008584	torus palatinus and torus mandibularis	hereditary_disease	other	hereditary_disease	oral_surgery|otolaryngology	neurodegenerative_disease	teeth_disorder|bone_disorder	false	false	false	false	low
MONDO:0008585	HELLP syndrome	hereditary_disease|syndromic_disease|cardiovascular_disorder|obstetric_disorder	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|hereditary_disease|obstetric_disorder	hematology|hepatology|obstetrics_and_gynecology	inflammatory_disease|anemia|metabolic_disorder	liver_disorder|vascular_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0008586	esophageal atresia/tracheoesophageal fistula	upper_digestive_tract_disorder|digestive_system_disorder	other	upper_digestive_tract_disorder|digestive_system_disorder	gastroenterology|otolaryngology|pediatric|pulmonology	congenital_disorder|surgical_condition|esophageal_disease|congenital_anomaly|gastrointestinal_condition|birth_defect|pediatric_condition	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0008587	tracheobronchopathia osteochondroplastica	respiratory_system_disorder	other	respiratory_system_disorder	genetics_and_genomics|pediatric|pulmonology	neurodegenerative_disease|metabolic_disorder	joint_disorder|lung_disorder	false	false	false	false	medium
MONDO:0008588	hereditary geniospasm	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|hereditary|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0008589	tremor of intention, ataxia, and lipofuscinosis	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|lipofuscinosis_is_a_hallmark_of_this_disease	muscle_disorder|brain_disorder	true	false	false	true	high
MONDO:0008590	tremor, hereditary essential, 1	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	hereditary_essential_tremor_is_often_associated_with_a_metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008591	tremor-nystagmus-duodenal ulcer syndrome	nervous_system_disorder	other	nervous_system_disorder	gastroenterology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0008592	tricho-dento-osseous syndrome	musculoskeletal_system_disorder|syndromic_disease|integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|dermatology|pediatric	metabolic_disorder|autoimmune_diseases	teeth_disorder|bone_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008593	trichomegaly	hereditary_disease	other	hereditary_disease	dermatology|pediatrics	mental_health_disorder|neurodegenerative_disease	hair_growth_disorder|reproductive_system_disorder|skin_disorder	false	false	false	false	low
MONDO:0008594	familial multiple discoid fibromas	cancer_or_benign_tumor|integumentary_system_disorder|hereditary_disease	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|cancer	joint_disorder|skin_disorder	false	false	false	false	low
MONDO:0008595	trichoepitheliomas, multiple desmoplastic	hereditary_disease	other	hereditary_disease	oncology|dermatology	adrenal_gland_disease|cancer	muscle_disorder|skin_disorder	false	true	false	false	low
MONDO:0008596	trichorhinophalangeal syndrome type I	musculoskeletal_system_disorder|syndromic_disease|integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|dermatology|orthopaedic|pediatric	mental_health_disorder|neurodegenerative_disease|autoimmune_diseases	joint_disorder|bone_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008598	trichodysplasia-xeroderma syndrome	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric	genetic_disorder|neurodegenerative_disease	eye_disorder|immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008599	trigeminal neuralgia	nervous_system_disorder	other	nervous_system_disorder	otolaryngology|neurology	inflammatory_disease|autoimmune_diseases|neurological_disorder	nerve_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008600	trigger thumb	hereditary_disease	other	hereditary_disease	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	musculoskeletal_disorder|joint_disorder	false	false	false	true	medium
MONDO:0008601	triglyceride storage disease, type 1	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|endocrinology|hepatology|pediatrics	metabolic_disorder|cardiovascular_disorder	endocrine_disorder|liver_disorder	false	false	false	true	high
MONDO:0008602	triglyceride storage disease, type 2	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|endocrinology|hepatology|cardiology	metabolic_disorder|cardiovascular_disorder	endocrine_disorder|liver_disorder	false	false	false	true	high
MONDO:0008603	trigonocephaly 1	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|pediatric	congenital_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0008604	triphalangeal thumb with double phalanges	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics	congenital_disease|genetic_disorder|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008605	triphalangeal thumb, Nonopposable	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	musculoskeletal_disorder|congenital_disorder|neurodegenerative_disease	bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008606	Say-field-Coldwell syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	allergy_and_immunology|genetics_and_genomics|pulmonology|neurology|pediatrics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	vascular_disorder|kidney_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0008607	triphalangeal thumbs-brachyectrodactyly syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|congenital_dysmorphism_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008608	Down syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008609	Tristichiasis	hereditary_disease	other	hereditary_disease	neonatology|pediatrics	metabolic_disorder|anemia___note__trichiasis_is_a_condition_where_eyelashes_grow_back_towards_the_eye__but_i_m_assuming_you_meant_to_ask_about_trichiasis_of_the_iris__trichiachisis___which_is_related_to_metabolic_disorders__however__this_disease_is_also_linked_to_other_categories__and_it_s_worth_noting_that_there_are_different_types_of_trichiasis|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	vascular_disorder|eye_disorder	false	false	false	true	medium
MONDO:0008610	blue color blindness	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0008611	humerus trochlea aplasia	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	rheumatology|orthopaedic	anemia|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0008612	tuberous sclerosis 1	syndromic_disease|hereditary_disease|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|syndromic_disease|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|brain_disorder|muscle_disorder|skin_disorder|vascular_disorder|kidney_disorder|lymphatic_disorder|joint_disorder	false	false	false	true	medium
MONDO:0008613	Tuftsin deficiency	hereditary_disease	other	hereditary_disease	allergy_and_immunology|genetics_and_genomics|pediatric	allergy|metabolic_disorder|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0008614	suppressor of tumorigenicity 3	hereditary_disease	other	hereditary_disease	oncology|genetics_and_genomics|pulmonology|hematology	metabolic_disorder|cancer|neurodegenerative_disease|autoimmune_diseases	immune_disorder__lymphatic_disorder	false	false	false	false	high
MONDO:0008615	tune deafness	hereditary_disease	other	hereditary_disease	otolaryngology|neurology	metabolic_disorder|neurodegenerative_disease	throat_disorder|ear_disorder	false	false	false	false	low
MONDO:0008617	inflammatory bowel disease 11	hereditary_disease|immune_system_disorder|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease|immune_system_disorder	rheumatology|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0008618	mesomelic dwarfism, Reinhardt-Pfeiffer type	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|genetic_disorder	skeletal_disorder|bone_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0008619	ulna metaphyseal dysplasia syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|skeletal_dysplasia	muscle_disorder|bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0008620	upper limb mesomelic dysplasia	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008621	uncombable hair syndrome	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	skin_disorder|hair_disorder	false	false	false	false	low
MONDO:0008622	tricho-retino-dento-digital syndrome	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	syndromic_disease|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|ophthalmology|pediatric	metabolic_disorder|neurodegenerative_disease	teeth_disorder|eye_disorder	false	false	false	false	high
MONDO:0008623	Undritz anomaly	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	biliary_disorder|liver_disorder	false	false	false	false	medium
MONDO:0008624	Upington disease	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	psychiatry|neurology	neurodegenerative_disease|adrenal_gland_disease	bone_disorder|liver_disorder	false	false	false	false	medium
MONDO:0008626	ureter, bifid or double	hereditary_disease	other	hereditary_disease	renal_medicine|urology	ureter__bifid_or_double	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0008627	ureter cancer	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0008628	ureterocele	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	renal_medicine|urology	urinary_system_disorder|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0008629	urolithiasis, uric acid, autosomal dominant	hereditary_disease	other	hereditary_disease	genetics_and_genomics|renal_medicine|urology	uric_acid|autosomal_dominant|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0008630	urinary bladder, atony of	hereditary_disease	other	hereditary_disease	renal_medicine|urology	neurodegenerative_disease|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0008632	urticaria, aquagenic	integumentary_system_disorder|hereditary_disease|inflammatory_disease	other	hereditary_disease|integumentary_system_disorder|inflammatory_disease	allergy_and_immunology|dermatology	allergy|inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0008633	Muckle-Wells syndrome	syndromic_disease|hereditary_disease|immune_system_disorder|connective_tissue_disorder	other	connective_tissue_disorder|syndromic_disease|hereditary_disease|immune_system_disorder	genetics_and_genomics|cardiology|renal_medicine	metabolic_disorder|adrenal_gland_disease|inflammatory_disease	vascular_disorder|kidney_disorder	false	false	false	true	high
MONDO:0008634	urticaria, familial localized heat	hereditary_disease|inflammatory_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|inflammatory_disease	allergy_and_immunology|dermatology	allergy|inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	low
MONDO:0008635	uterine anomalies	hereditary_disease	other	hereditary_disease	obstetrics_and_gynecology	metabolic_disorder|cancer|autoimmune_diseases	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0008636	double uterus-hemivagina-renal agenesis syndrome	syndromic_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis	other	syndromic_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|renal_medicine|obstetrics_and_gynecology	genetic_disorder|renal_agenesis|anomaly	reproductive_system_disorder|kidney_disorder	false	false	false	false	high
MONDO:0008637	bifid uvula	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	throat_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0008638	varicose disease	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	dermatology|cardiovascular	inflammatory_disease|cardiovascular_disorder	skin_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0008639	vascular helix of umbilical cord	hereditary_disease	other	hereditary_disease	pediatric|obstetrics_and_gynecology	anemia|inflammatory_disease|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder|immune_disorder	false	false	false	false	none
MONDO:0008640	vasculitis, lymphocytic, nodular	hereditary_disease|cardiovascular_disorder|inflammatory_disease|integumentary_system_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|integumentary_system_disorder|inflammatory_disease	rheumatology|hematology	autoimmune_diseases|inflammatory_disease	vascular_disorder|lymphatic_disorder|immune_disorder	true	false	false	true	medium
MONDO:0008641	retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations	hereditary_disease|syndromic_disease|cardiovascular_disorder|psychiatric_disorder|nervous_system_disorder|connective_tissue_disorder|disorder_of_visual_system	psychiatric_disorder|cardiovascular_disorder	disorder_of_visual_system|cardiovascular_disorder|nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease|disorder_of_orbital_region|connective_tissue_disorder	genetics_and_genomics|ophthalmology|neurology|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0008642	VACTERL/vater association	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	cardiovascular_disorder|congenital_anomaly	limb_disorder|heart_disorder|spinal_disorder|kidney_disorder	false	false	false	false	high
MONDO:0008643	veins, pattern of, on anterior thorax	hereditary_disease	other	hereditary_disease	dermatology|pulmonology|hematology|cardiothoracic	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	vascular_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0008644	velocardiofacial syndrome	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|immune_system_disorder|chromosomal_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|immune_system_disorder|chromosomal_disorder	genetics_and_genomics|cardiology|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	heart_disorder|joint_disorder|vascular_disorder|throat_disorder	false	false	false	false	high
MONDO:0008645	ventricular extrasystoles with syncopal episodes-perodactyly-robin sequence syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|cardiology|pediatric	neurodegenerative_disease|cardiovascular_disorder	bone_disorder|muscle_disorder|ear_disorder|lower_gastrointestinal_disorder|heart_disorder	false	false	false	false	high
MONDO:0008647	hypertrophic cardiomyopathy 1	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0008648	ventricular tachycardia, familial	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	genetics_and_genomics|cardiology	cardiovascular_disorder|familial	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0008649	venular insufficiency, systemic	hereditary_disease	other	hereditary_disease	pulmonology|cardiology|hematology|renal_medicine|cardiothoracic	systemic|cardiovascular_disorder	vascular_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0008650	posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	ophthalmology|orthopaedic|neurology	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0008651	vertebral hypoplasia with lumbar kyphosis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0008652	congenital vertical talus	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|pediatric	metabolic_disorder|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008653	vesicoureteral reflux 1	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	urology|pediatric	urogenital_disorder|inflammatory_disease|congenital_condition	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0008654	spinocerebellar ataxia 27A	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008655	vestibulocochlear dysfunction, progressive	hereditary_disease	other	hereditary_disease	otolaryngology|neurology	neurodegenerative_disease|vestibulocochlear_dysfunction_implies_damage_to_a_specific_nerve_so_is_likely_related_to_the_nervous_system_but_this_category_is_too_broad_so__neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0008659	transcobalamin I deficiency	metabolic_disease|hereditary_disease|nutritional_disorder	metabolic_disease	metabolic_disease|hereditary_disease|nutritional_disorder	genetics_and_genomics|hematologist|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	high
MONDO:0008660	autosomal dominant hypophosphatemic rickets	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|adrenal_gland_disease	bone_disorder|endocrine_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0008661	vitiligo	inflammatory_disease|integumentary_system_disorder|immune_system_disorder	autoimmune_disease	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0008662	autosomal dominant vitreoretinochoroidopathy	hereditary_disease|nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0008663	snowflake vitreoretinal degeneration	hereditary_disease|nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0008665	ptosis-vocal cord paralysis syndrome	syndromic_disease	other	syndromic_disease	otolaryngology|neurology|pulmonology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	throat_disorder|ear_disorder	false	false	false	false	medium
MONDO:0008666	volvulus of midgut	hereditary_disease	other	hereditary_disease	gastroenterology|pediatric	gastrointestinal_disease|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0008667	von Hippel-Lindau disease	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	oncology|genetics_and_genomics|renal_medicine	cancer|cardiovascular_disorder	brain_disorder|vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0008668	von Willebrand disease 1	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0008669	vulvovaginitis, allergic seminal	reproductive_system_disorder|inflammatory_disease|immune_system_disorder	other	reproductive_system_disorder|inflammatory_disease|immune_system_disorder	allergy_and_immunology|obstetrics_and_gynecology	allergy|autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|urinary_tract_disorder|immune_disorder	false	false	false	true	low
MONDO:0008670	Waardenburg syndrome type 1	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	pediatrics|otolaryngology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	ear_disorder|bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0008671	Waardenburg syndrome type 2A	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder|skin_disorder|spinal_disorder|vascular_disorder|hearing_disorder	false	false	false	false	medium
MONDO:0008672	Watson syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|endocrine_disorder|vascular_disorder|immune_disorder	false	false	false	false	medium
MONDO:0008673	acrofacial dysostosis, Weyers type	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|integumentary_system_disorder	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|developmental_disorder|genetic_disorders	bone_disorder|spinal_disorder|joint_disorder|teeth_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0008675	Freeman-Sheldon syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0008676	white sponge nevus 1	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	dermatology|pediatric	neurodegenerative_disease|autoimmune_diseases|cancer|inflammatory_disease	skin_disorder|vascular_disorder	false	false	false	true	low
MONDO:0008678	Williams syndrome	syndromic_disease|nervous_system_disorder|chromosomal_disorder	other	nervous_system_disorder|syndromic_disease|chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0008679	Wilms tumor 1	hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor	oncology|pediatric	adrenal_gland_disease|pediatric_cancer|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0008680	Wilms tumor 2	hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor	urology|pediatric|renal_medicine|oncology	adrenal_gland_disease|cancer	kidney_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0008681	WAGR syndrome	syndromic_disease|hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder|chromosomal_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder|cancer_or_benign_tumor	chromosomal_disorder|hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|oncology	developmental_disorder|genetic_disorder|cancer	kidney_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0008682	Denys-Drash syndrome	syndromic_disease|hereditary_disease|endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	urology|pediatric|genetics_and_genomics|renal_medicine	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder|blood_bone_marrow_disorder|immune_disorder|renal_disorder	false	false	false	false	very_high
MONDO:0008683	Wilms tumor 3	hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor	urology|pediatric|oncology	adrenal_gland_disease|cancer	kidney_disorder|urological_disorder	false	true	false	true	high
MONDO:0008684	Wolf-Hirschhorn syndrome	syndromic_disease|chromosomal_disorder|disorder_of_development_or_morphogenesis	other	chromosomal_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	developmental_disorder|congenital_immune_dysfunction|metabolic_disorder|genetic_disorder	kidney_disorder|eye_disorder|upper_gastrointestinal_disorder|reproductive_system_disorder|bone_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0008685	Wolff-Parkinson-White syndrome	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiology|pediatric|electrophysiology	neurodegenerative_disease|cardiovascular_disorder	ear_disorder|heart_disorder|brain_disorder	false	false	false	true	medium
MONDO:0008686	isolated familial wooly hair disorder	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	hair_disorder|skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0008687	Woronets trait	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	joint_disorder|vascular_disorder	false	false	false	false	none
MONDO:0008688	WT limb-blood syndrome	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	pediatric|genetics_and_genomics|hematology	inflammatory_disease|anemia|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0008689	dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	pediatric|genetics_and_genomics|hematology|renal_medicine	anemia|metabolic_disorder	blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0008690	xeroderma pigmentosum, autosomal dominant, mild	hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	dermatology|pediatric|genetics_and_genomics|oncology	cancer|metabolic_disorder	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008692	abetalipoproteinemia	digestive_system_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder|hematologic_disorder	anemia|neurodegenerative_disease|metabolic_disease	hereditary_disease|hematologic_disorder|nervous_system_disorder|digestive_system_disorder|metabolic_disease	genetics_and_genomics|hematology|renal_medicine	anemia|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0008693	ablepharon macrostomia syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|otolaryngology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0008694	pseudoprogeria syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0008695	chorea-acanthocytosis	hereditary_disease|nervous_system_disorder|psychiatric_disorder|integumentary_system_disorder	neurodegenerative_disease|psychiatric_disorder	integumentary_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0008696	acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome	inflammatory_disease|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease	dermatology|endocrinology|pediatrics	cardiovascular_disorder|metabolic_disorder	endocrine_disorder|muscle_disorder|skin_disorder	false	false	true	false	high
MONDO:0008698	achalasia	digestive_system_disorder|upper_digestive_tract_disorder	other	upper_digestive_tract_disorder|digestive_system_disorder	pulmonology|cardiothoracic|gastroenterology	neurodegenerative_disease|gastrointestinal_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0008699	achalasia microcephaly syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0008700	acheiropody	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|dermatology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|adrenal_gland_disease	bone_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0008701	achondrogenesis type IA	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0008702	achondrogenesis type II	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|connective_tissue_disorder|syndromic_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|connective_tissue_disorder	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder____however__since_the_provided_category_list_does_not_explicitly_include__genetic_disorder___i_will_remove_it_from_the_response____metabolic_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0008703	acromesomelic dysplasia 2A	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008704	short-limb skeletal dysplasia with severe combined immunodeficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	immunology|hematology|orthopaedic|rheumatology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	bone_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0008705	lysosomal acid phosphatase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder|lysosomal_storage_disorder	false	false	false	false	high
MONDO:0008706	Ackerman syndrome	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	endocrinology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|immune_disorder	false	false	false	false	high
MONDO:0008707	acro-renal-mandibular syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	renal_medicine|endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|bone_disorder|joint_disorder|kidney_disorder	false	false	false	false	high
MONDO:0008708	acrocallosal syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008709	acrocephalopolydactyly	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|congenital_disorder	bone_disorder|brain_disorder|joint_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0008710	RAB23-related Carpenter syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	oncology|obstetrics_and_gynecology|neurology|cardiology|pediatric|genetics_and_genomics|pulmonology	metabolic_disorder|neurodegenerative_disease	liver_disorder|bone_disorder|skin_disorder|joint_disorder	false	false	false	false	high
MONDO:0008711	Goodman syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|joint_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0008712	acrocraniofacial dysostosis	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	genetic_diseases|metabolic_disorder	bone_disorder|joint_disorder|teeth_disorder	false	false	false	false	high
MONDO:0008713	acrodermatitis enteropathica	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	dermatology|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease	liver_disorder|skin_disorder|other___corrected_answer__liver_disorder	false	false	false	true	high
MONDO:0008714	acrofacial dysostosis Rodriguez type	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|pediatric|genetics_and_genomics	skeletal_disorder|metabolic_disorder|genetic_condition	bone_disorder|skeletal_disorder|skeletal_disorder____corrected_to____bone_disorder	false	false	false	false	very_high
MONDO:0008715	acrofrontofacionasal dysostosis	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|skeletal_system_dysfunction|genetic_disorder	upper_gastrointestinal_disorder|bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008716	acrogeria	integumentary_system_disorder|premature_aging_syndrome|hereditary_disease	other	premature_aging_syndrome|integumentary_system_disorder|hereditary_disease	neurology|endocrinology|pediatrics|dermatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008717	acromesomelic dysplasia 2C, Hunter-Thompson type	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	bone_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008718	Morvan syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	endocrine_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0008719	acrorenal syndrome, autosomal recessive	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	endocrinology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0008720	congenital isolated adrenocorticotropic hormone deficiency	nervous_system_disorder|reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder|nervous_system_disorder	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0008721	medium chain acyl-CoA dehydrogenase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|hepatology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder	false	false	false	true	high
MONDO:0008722	short chain acyl-CoA dehydrogenase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	metabolism|endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	liver_disorder|endocrine_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0008723	very long chain acyl-CoA dehydrogenase deficiency	metabolic_disease|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	metabolism|cardiology|pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	liver_disorder|muscle_disorder	false	false	false	true	high
MONDO:0008724	adducted thumbs-arthrogryposis syndrome, Christian type	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	joint_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0008725	congenital lipoid adrenal hyperplasia due to STAR deficency	metabolic_disease|reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease|hereditary_disease|reproductive_system_disorder	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	liver_disorder|endocrine_disorder	false	false	false	true	very_high
MONDO:0008726	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	obstetrics_and_gynecology|endocrinology|pediatric|urology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|bone_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0008727	congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency	metabolic_disease|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	metabolic_disease|endocrine_system_disorder	hereditary_disease|metabolic_disease|endocrine_system_disorder|reproductive_system_disorder	pediatric|genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0008728	classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency	metabolic_disease|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	metabolic_disease|endocrine_system_disorder	hereditary_disease|metabolic_disease|endocrine_system_disorder|reproductive_system_disorder	pediatric|genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0008729	congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency	metabolic_disease|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	metabolic_disease|endocrine_system_disorder	hereditary_disease|metabolic_disease|endocrine_system_disorder|reproductive_system_disorder	pediatric|genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder|kidney_disorder	false	false	false	true	high
MONDO:0008730	congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency	metabolic_disease|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	metabolic_disease|endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|metabolic_disease|reproductive_system_disorder	pediatric|genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0008731	familial adrenal hypoplasia with absent pituitary luteinizing hormone	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder	pediatric|genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0008732	adrenal hypoplasia, cytomegalic type	nervous_system_disorder|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|nervous_system_disorder|reproductive_system_disorder	pediatric|genetics_and_genomics|endocrinology	inflammatory_disease|adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder	false	false	false	false	high
MONDO:0008733	familial glucocorticoid deficiency	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	pediatric|genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0008734	adrenocortical carcinoma, hereditary	endocrine_system_disorder|urinary_system_disorder|hereditary_disease|cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor|endocrine_system_disorder	urinary_system_disorder|cardiovascular_disorder|hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|oncology|endocrinology	adrenal_gland_disease|cancer	endocrine_disorder|reproductive_system_disorder|hereditary	false	true	false	false	high
MONDO:0008735	adrenocortical unresponsiveness to ACTH with postreceptor defect	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder	false	false	false	false	high
MONDO:0008736	peroxisome biogenesis disorder 2B	nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	neurodegenerative_disease|metabolic_disease	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	peroxisome_biosynthesis_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0008737	congenital afibrinogenemia	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|hematology	genetic_disorder|inflammatory_disease|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0008738	aganglionosis, total intestinal	hereditary_disease	other	hereditary_disease	neurology|gastroenterology	neurodegenerative_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0008739	agenesis of cerebral white matter	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0008740	agnathia-otocephaly complex	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|otolaryngology|pediatric	inflammatory_disease|neurodegenerative_disease	teeth_disorder|ear_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0008741	PAGOD syndrome	syndromic_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	endocrine_system_disorder	syndromic_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder	neurology|pediatric	neurodegenerative_disease|mental_health_disorder	spinal_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0008742	autosomal dominant severe congenital neutropenia	hematologic_disorder|hereditary_disease|immune_system_disorder	other	hereditary_disease|hematologic_disorder|immune_system_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0008743	Stimmler syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0008744	alar cartilages hypoplasia-coloboma-telecanthus syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|otolaryngology|pediatric	congenital_disorder|eye_disorder|metabolic_disorder|developmental_disorder	eye_disorder|joint_disorder|skull_disorder	false	false	false	false	low
MONDO:0008745	oculocutaneous albinism type 1A	metabolic_disease|integumentary_system_disorder|hereditary_disease|disorder_of_visual_system	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system	genetics_and_genomics|ophthalmology|dermatology|pediatric	genetic_disorder|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0008746	oculocutaneous albinism type 2	metabolic_disease|integumentary_system_disorder|hereditary_disease	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|ophthalmology|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0008747	oculocutaneous albinism type 3	metabolic_disease|integumentary_system_disorder|hereditary_disease	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics_dermatology_ophthalmology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0008748	Hermansky-Pudlak syndrome 1	syndromic_disease|respiratory_system_disorder|metabolic_disease|hematologic_disorder|integumentary_system_disorder|hereditary_disease	metabolic_disease	integumentary_system_disorder|syndromic_disease|hematologic_disorder|hereditary_disease|respiratory_system_disorder|metabolic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|anemia|metabolic_disorder	skin_disorder|immune_disorder|eye_disorder|joint_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0008749	pseudohypoparathyroidism type 2	metabolic_disease|endocrine_system_disorder|urinary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease|endocrine_system_disorder	urinary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|metabolic_disease	genetics_and_genomics|endocrinology|pediatric	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	endocrine_disorder|thyroid_disorder	false	false	false	false	medium
MONDO:0008750	microcephaly-albinism-digital anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder|joint_disorder|brain_disorder|skin_disorder	false	false	false	false	high
MONDO:0008751	corticosterone methyloxidase type 1 deficiency	metabolic_disease|endocrine_system_disorder|hereditary_disease	metabolic_disease|endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|metabolic_disease	genetics_and_genomics|endocrinology	adrenal_gland_disease|inflammatory_disease|metabolic_disorder	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0008752	Alexander disease	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0008753	alkaptonuria	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|renal_medicine	neurodegenerative_disease|metabolic_disorder	joint_disorder|kidney_disorder	false	false	false	false	high
MONDO:0008754	alopecia - contractures - dwarfism - intellectual disability syndrome	syndromic_disease|integumentary_system_disorder|hereditary_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|neurology|dermatology|psychiatry|endocrinology|pediatric	neurodegenerative_disease|metabolic_disorder|neurodegenerative_disease___corrected_answer___metabolic_disorder|genetic_disease	endocrine_disorder|muscle_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0008755	Moynahan syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatrics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0008756	alopecia - intellectual disability syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|skin_disorder	false	false	false	false	high
MONDO:0008757	alopecia universalis congenita	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology|pediatric	congenital_condition|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0008758	mitochondrial DNA depletion syndrome 4a	syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|nervous_system_disorder	neurodegenerative_disease|metabolic_disease	syndromic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|nervous_system_disorder	genetics_and_genomics|pediatrics	neurodegenerative_disease|anemia|metabolic_disorder	mitochondrial_dna_depletion_syndrome_4a_is_related_to_mitochondrial_disorders__therefore__the_best_fitting_categories_are___muscle_disorder_kidney_disorder	false	false	false	false	very_high
MONDO:0008759	oxoglutaricaciduria	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|nervous_system_disorder	genetics_and_genomics|metabolic_disorders_is_not_in_the_list_so_hematoloogy_is_the_best_match_for_oxoglutaricaciduria_since_it_deals_with_inherited_blood_disorders|pediatric	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	bone_disorder|metabolic_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0008760	beta-ketothiolase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology|pediatric	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|liver_disorder	false	false	false	true	high
MONDO:0008762	autosomal recessive Alport syndrome	syndromic_disease|urinary_system_disorder|hereditary_disease|inflammatory_disease	other	urinary_system_disorder|syndromic_disease|hereditary_disease|inflammatory_disease	genetics_and_genomics|renal_medicine	anemia|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0008763	Alstrom syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	eye_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0008764	Leber congenital amaurosis 1	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_orbital_region	genetics_and_genomics|neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	true	high
MONDO:0008765	Leber congenital amaurosis 2	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_orbital_region	genetics_and_genomics|ophthalmology|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	true	high
MONDO:0008766	amaurosis-hypertrichosis syndrome	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_orbital_region	genetics_and_genomics|ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	endocrine_disorder|eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0008767	neuronal ceroid lipofuscinosis 3	metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurodegenerative_disease|psychiatric_disorder|metabolic_disease	psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0008768	ceroid lipofuscinosis, neuronal, 6B (Kufs type)	metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurodegenerative_disease|psychiatric_disorder|metabolic_disease	psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0008769	neuronal ceroid lipofuscinosis 2	metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurodegenerative_disease|psychiatric_disorder|metabolic_disease	psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0008770	amelogenesis imperfecta type 1C	musculoskeletal_system_disorder|hereditary_disease	other	mouth_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	teeth_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0008771	amelogenesis imperfecta type 1G	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	mouth_disorder|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatrics	anemia|metabolic_disorder	teeth_disorder|blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0008772	amelogenesis imperfecta type 2A1	musculoskeletal_system_disorder|hereditary_disease	other	mouth_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|hematology|pediatric	anemia|metabolic_disorder|autoimmune_diseases	skin_disorder|teeth_disorder|vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0008773	amino aciduria with mental deficiency, dwarfism, muscular dystrophy, osteoporosis, and acidosis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|renal_medicine|orthopaedic|neurology|endocrinology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|kidney_disorder|bone_disorder	false	false	false	false	high
MONDO:0008774	2-aminoadipic 2-oxoadipic aciduria	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|renal_medicine|pediatric	metabolic_disorder|adrenal_gland_disease	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0008775	Amobarbital, deficient N-hydroxylation of	hereditary_disease	other	hereditary_disease	neurology|psychiatry	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0008776	amyloidosis of gingiva and conjunctiva, with intellectual disability	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|psychiatry|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|teeth_disorder|eye_disorder	false	false	false	false	high
MONDO:0008777	gelatinous drop-like corneal dystrophy	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology	metabolic_disorder|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	true	high
MONDO:0008778	amyloidosis, cutaneous bullous	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder|muscle_disorder	false	false	false	true	high
MONDO:0008779	arthrogryposis	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|orthopaedic|neurology|rheumatology	neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008780	amyotrophic lateral sclerosis type 2, juvenile	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|juvenile	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008781	juvenile amyotrophic lateral sclerosis with dementia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0008782	amyotrophic lateral sclerosis with polyglucosan bodies	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008783	Tangier disease	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|hepatology|cardiology	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	vascular_disorder|liver_disorder	false	false	false	false	high
MONDO:0008785	sideroblastic anemia 2	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	renal_medicine|hematology|genetics_and_genomics|oncology	sideroblastic_anemia_is_a_subtype_of_myelodysplastic_syndrome_which_is_a_type_of_blood_cancer_so_the_best_fit_category_would_be__cancer__but_specifically_related_to_blood__therefore_also__anemia|anemia|cancer	bone_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0008786	pyridoxine-responsive sideroblastic anemia	hematologic_disorder	anemia	hematologic_disorder	hematology|genetics_and_genomics|pediatric	anemia|metabolic_disorder	pyridoxine_responsive_sideroblastic_anemia_is_often_associated_with_a_blood_disorder|blood_bone_marrow_disorder	false	false	false	true	low
MONDO:0008787	microcytic anemia with liver iron overload	hematologic_disorder|metabolic_disease|hereditary_disease	anemia|metabolic_disease	hereditary_disease|hematologic_disorder|metabolic_disease	hematology|gastroenterology|hepatology	anemia|metabolic_disorder	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0008788	IRIDA syndrome	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics|pediatric	anemia|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	true	true	high
MONDO:0008789	anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics|medicine	anemia|metabolic_disorder|inflammatory_disease|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0008790	anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hepatology|dermatology|genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	medium
MONDO:0008791	anencephaly 1	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|anemia|inflammatory_disease|mental_health_disorder|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0008792	familial angiolipomatosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics|hematology	metabolic_disorder|adrenal_gland_disease	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0008793	angiomatosis, diffuse Corticomeningeal, of Divry and van Bogaert	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|cancer|autoimmune_diseases	brain_disorder|vascular_disorder	true	false	false	false	very_high
MONDO:0008794	anhidrosis, familial generalized, with abnormal or absent sweat glands	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	neurology|dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	skin_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0008795	aniridia-cerebellar ataxia-intellectual disability syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system	other	hereditary_disease|syndromic_disease|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|disorder_of_visual_system	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|intellectual_disability_syndrome	brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0008796	aniridia-renal agenesis-psychomotor retardation syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system	neurology|ophthalmology|pediatric|urology|genetics_and_genomics|renal_medicine	neurodegenerative_disease|mental_health_disorder	brain_disorder|eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:0008797	anodontia	musculoskeletal_system_disorder|hereditary_disease	other	mouth_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|genetic_condition|developmental_disorder	teeth_disorder|bone_disorder	false	false	false	true	high
MONDO:0008798	nonsyndromic congenital nail disorder 4	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	congenital_disorder|metabolic_disorder	skin_disorder|nail_disorder_is_not_present_but_related_to_skin__note__after_analyzing_the_given_disease__i_found_that_nonsyndromic_congenital_nail_disorder_4_is_closely_related_to_skin_disorder_and_a_possible_subcategory_of_it_could_be_considered_as_a_subcategory_of__nail_disorder__which_isn_t_in_the_list	false	false	false	false	medium
MONDO:0008799	anophthalmia/microphthalmia-esophageal atresia syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system	other	hereditary_disease|syndromic_disease|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|disorder_of_visual_system	pediatric|genetics_and_genomics	neurodegenerative_disease|anemia|metabolic_disorder	eye_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0008800	microphthalmia with limb anomalies	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	ophthalmology|genetics_and_genomics|orthopaedic|pediatric	birth_defect|limb_anomaly|congenital_disease|skeletal_dysplasia___corrected_to__metabolic_disorder|metabolic_disorder|genetic_disorder|eye_abnormality|developmental_disorder	limb_anomaly|eye_disorder	false	false	false	false	high
MONDO:0008801	anosmia for isobutyric acid	hereditary_disease	other	hereditary_disease	otolaryngology|neurology	neurodegenerative_disease|metabolic_disorder	nose_disorder|brain_disorder	false	false	false	false	low
MONDO:0008802	antithrombin, familial hemorrhagic diathesis due to	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology|allergy_and_immunology	bleeding_disorder|inherited_condition|cardiovascular_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0008803	Antley-Bixler syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder	eye_disorder|ear_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0008806	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	urology|genetics_and_genomics|pediatric	urogenital_disorder|metabolic_disorder	spinal_disorder|lower_gastrointestinal_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0008808	aplasia cutis congenita-intestinal lymphangiectasia syndrome	digestive_system_disorder|immune_system_disorder|syndromic_disease|integumentary_system_disorder	other	immune_system_disorder|integumentary_system_disorder|digestive_system_disorder|syndromic_disease	obstetrics_and_gynecology|gastroenterology|genetics_and_genomics|hematology|dermatology|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	lymphatic_disorder|lower_gastrointestinal_disorder|skin_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0008809	polyneuropathy-hand defect syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	nerve_disorder_is_not_in_the_list_so__muscle_disorder|muscle_disorder	false	false	false	false	low
MONDO:0008810	familial apolipoprotein C-II deficiency	metabolic_disease|hereditary_disease|syndromic_disease	metabolic_disease	metabolic_disease|hereditary_disease|syndromic_disease	hepatology|genetics_and_genomics|pediatrics	metabolic_disorder|genetic_disorders____wait__genetic_disorders_isn_t_on_the_original_list___so_____metabolic_disorder	liver_disorder|metabolic_disorder	false	false	false	false	medium
MONDO:0008811	XK aprosencephaly	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0008812	AREDYLD syndrome	syndromic_disease|integumentary_system_disorder|hereditary_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	skeletal_system_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0008813	arachnoid cyst	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric	inflammatory_disease|neurological_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0008814	arginase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|renal_medicine|endocrinology|pediatric	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	metabolic_disorder__note__metabolic_disorder_was_not_in_the_original_category_list__the_correct_categorization_is_kidney_disorder|kidney_disorder	false	false	false	false	high
MONDO:0008815	argininosuccinic aciduria	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	metabolic__removed_because_it_is_not_in_the_original_list|genetics_and_genomics|renal_medicine|pediatric	metabolic_disorder|adrenal_gland_disease	metabolic_disorder|bone_disorder|kidney_disorder	false	false	false	true	high
MONDO:0008816	Chiari malformation type II	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurology|pediatric	congenital_anomaly|neurodevelopmental_disorder|neurological_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0008817	arterial calcification, generalized, of infancy, 1	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	pediatric|cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0008818	arterial tortuosity syndrome	connective_tissue_disorder|integumentary_system_disorder|cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|integumentary_system_disorder|cardiovascular_disorder|connective_tissue_disorder|hereditary_disease	renal_medicine|cardiothoracic|hematology|cardiology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	heart_disorder_vascular_disorder	false	false	false	false	medium
MONDO:0008819	arteriosclerosis, severe juvenile	hereditary_disease	other	hereditary_disease	pediatric|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0008821	arthrogryposis, distal, with intellectual disability and characteristic facies	hereditary_disease	other	hereditary_disease	genetics_and_genomics|psychiatry|orthopaedic|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0008822	arthrogryposis, renal dysfunction, and cholestasis 1	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|syndromic_disease|metabolic_disease|hereditary_disease	rheumatology|hepatology|gastroenterology|genetics_and_genomics|neonatology|renal_medicine|orthopaedic|pediatric	metabolic_disorder|inflammatory_disease	liver_disorder|joint_disorder|kidney_disorder	false	false	false	false	high
MONDO:0008823	arthrogryposis multiplex congenita 2, neurogenic type	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0008824	fetal akinesia deformation sequence	disorder_of_development_or_morphogenesis|syndromic_disease|respiratory_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|respiratory_system_disorder|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0008825	arthrogryposis multiplex congenita-whistling face syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	muscle_disorder|throat_disorder|ear_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0008826	arthrogryposis-hyperkeratosis syndrome, lethal form	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0008827	progressive pseudorheumatoid arthropathy of childhood	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder|bone_disorder	false	false	false	false	high
MONDO:0008828	camptodactyly-arthropathy-coxa vara-pericarditis syndrome	hereditary_disease|connective_tissue_disorder	other	connective_tissue_disorder|hereditary_disease	rheumatology|orthopaedic|pediatric|cardiology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0008829	chylous ascites	immune_system_disorder	other	immune_system_disorder	gastroenterology_hepatology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|liver_disorder	false	false	false	false	high
MONDO:0008830	aspartylglucosaminuria	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|renal_medicine|pediatric	genetic_disorder|kidney_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0008831	asphyxiating thoracic dystrophy 1	musculoskeletal_system_disorder|urinary_system_disorder|syndromic_disease|respiratory_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|syndromic_disease|respiratory_system_disorder|urinary_system_disorder|hereditary_disease	pulmonology|pediatric	genetic_disorder|metabolic_disorder|respiratory_disorder	muscle_disorder|throat_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0008832	right atrial isomerism	disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder|hereditary_disease	cardiothoracic|pediatric|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0008833	renal-hepatic-pancreatic dysplasia 1	hereditary_disease	other	hereditary_disease	gastroenterology|hepatology|renal_medicine	pancreatic_disorder|renal_disease|metabolic_disorder|liver_disease	upper_gastrointestinal_disorder|liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0008834	asthma, nasal polyps, and aspirin intolerance	hereditary_disease	other	hereditary_disease	pulmonology|otolaryngology|allergy_and_immunology	allergy|inflammatory_disease|autoimmune_diseases	nose_disorder|immune_disorder|lung_disorder	false	false	false	true	high
MONDO:0008835	asthma, short stature, and elevated IgA	hereditary_disease	other	hereditary_disease	pulmonology|allergy_and_immunology|pediatric	allergy|inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|immune_disorder|lung_disorder	false	false	false	true	medium
MONDO:0008836	ataxia with myoclonic epilepsy and presenile dementia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	true	false	false	false	very_high
MONDO:0008837	ataxia, deafness, and cardiomyopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|cardiology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|heart_disorder|ear_disorder	true	false	false	false	high
MONDO:0008838	ataxia - deafness - intellectual disability syndrome	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|ear_disorder	true	false	false	false	very_high
MONDO:0008839	ataxia-microcephaly-cataract syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0008840	ataxia telangiectasia	hereditary_disease|nervous_system_disorder|endocrine_system_disorder|immune_system_disorder|reproductive_system_disorder	endocrine_system_disorder|neurodegenerative_disease	reproductive_system_disorder|immune_system_disorder|nervous_system_disorder|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	immune_disorder_brain_disorder	false	false	false	false	very_high
MONDO:0008841	ataxia-telangiectasia with generalized skin pigmentation and early death	hereditary_disease|nervous_system_disorder|endocrine_system_disorder|immune_system_disorder|reproductive_system_disorder	endocrine_system_disorder|neurodegenerative_disease	reproductive_system_disorder|immune_system_disorder|nervous_system_disorder|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|dermatology|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|immune_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0008842	ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0008843	atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|renal_medicine|endocrinology|neurology|cardiology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	kidney_disorder|vascular_disorder|endocrine_disorder	false	false	true	false	very_high
MONDO:0008844	Athrombia, essential	hereditary_disease	other	hereditary_disease	thrombosis|hematology	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0008845	atonic-astatic syndrome of Foerster	hereditary_disease	other	hereditary_disease	pediatric|neurology	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder_spinal_disorder	false	false	false	false	medium
MONDO:0008846	atransferrinemia	hereditary_disease|metabolic_disease|hematologic_disorder	metabolic_disease|anemia	hematologic_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0008847	atrichia with papular lesions	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|anemia|autoimmune_diseases	hair_growth_abnormality|skin_disorder	true	false	false	false	medium
MONDO:0008848	atrioventricular dissociation	hereditary_disease	other	hereditary_disease	cardiothoracic|cardiology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0008849	atrophoderma vermiculata	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology	inflammatory_disease|anemia|autoimmune_diseases	lower_gastrointestinal_disorder|skin_disorder	false	false	false	false	low
MONDO:0008850	Cooper-Jabs syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|psychiatry|pediatric|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0008853	Barber-Say syndrome	hereditary_disease|disorder_of_visual_system|integumentary_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|disorder_of_orbital_region|syndromic_disease|integumentary_system_disorder|disorder_of_visual_system|hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases	joint_disorder|immune_disorder|skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0008854	Bardet-Biedl syndrome 1	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|psychiatry|pediatric|neurology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder|spinal_disorder|kidney_disorder	false	false	false	false	high
MONDO:0008855	MHC class II deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|allergy_and_immunology|rheumatology|immunology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0008857	Beemer-Ertbruggen syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|oncology|dermatology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	liver_disorder|vascular_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0008858	Behr syndrome	hereditary_disease|metabolic_disease|disorder_of_visual_system|nervous_system_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|dermatology|pediatric|cardiology	cardiovascular_disorder|metabolic_disorder|autoimmune_diseases	kidney_disorder|eye_disorder|liver_disorder|vascular_disorder|joint_disorder	false	false	false	false	high
MONDO:0008859	berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification	hereditary_disease	other	hereditary_disease	hepatology|pulmonology|neurology|cardiology	cardiovascular_disorder|cerebral_calcification_is_not_a_clear_match_but_can_be_related_to_cardiovascular_disorder	brain_disorder|liver_disorder|vascular_disorder|lung_disorder	false	false	false	false	high
MONDO:0008860	beta-aminoisobutyric acid, urinary excretion of	hereditary_disease	other	hereditary_disease	renal_medicine|nephrology	adrenal_gland_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	none
MONDO:0008861	3-methylcrotonyl-CoA carboxylase 1 deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	metabolism__this_disease_is_related_to_metabolism|pediatric|genetics_and_genomics|cardiology___genetics_and_genomics_and_pediatric_are_the_best_fitting_categories__metabolism_was_added_for_context_of_the_disease_but_is_not_in_the_provided_category_list	metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008862	3-methylcrotonyl-CoA carboxylase 2 deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|hepatology|cardiology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|metabolic_disorder|muscle_disorder	false	false	false	true	high
MONDO:0008863	sitosterolemia	metabolic_disease|syndromic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|syndromic_disease	hepatology|genetics_and_genomics|endocrinology	adrenal_gland_disease|cardiovascular_disorder|metabolic_disorder	liver_disorder|lipid_storage_disease|genetic_disorder	false	false	false	true	high
MONDO:0008864	Biemond syndrome type 2	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|dermatology|genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	kidney_disorder|liver_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0008865	Bietti crystalline corneoretinal dystrophy	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|psychiatric_disorder|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology	inflammatory_disease|metabolic_disorder	eye_disorder|corneal_disorder	false	false	false	false	high
MONDO:0008866	bifid nose, autosomal recessive	otorhinolaryngologic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|otorhinolaryngologic_disease	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder	muscle_disorder|nose_disorder	false	false	false	false	low
MONDO:0008867	biliary atresia	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	pediatric|hepatology|gastroenterology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0008868	biliary malformation with renal tubular insufficiency	hereditary_disease	other	hereditary_disease	renal_medicine|pediatric|hepatology	inflammatory_disease|metabolic_disorder	kidney_disorder|liver_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0008869	Seckel syndrome 1	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	developmental_disorder|genetic_disease|metabolic_disorder	eye_disorder|joint_disorder|growth_disorder|skeletal_disorder|developmental_delay|ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0008870	bird headed-dwarfism, Montreal type	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	bone_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0008871	microcephalic osteodysplastic primordial dwarfism type I	nervous_system_disorder|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|syndromic_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|endocrinology	genetic_disease|metabolic_disorder	muscle_disorder|bone_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0008872	microcephalic osteodysplastic primordial dwarfism type II	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder	growth_disorder|bone_disorder|brain_disorder	false	false	false	false	high
MONDO:0008873	microcephalic osteodysplastic primordial dwarfism, type 3	nervous_system_disorder|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|syndromic_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disorders___note__the_original_list_of_categories_did_not_have_the_exact_category_name__genetic_disorders___however__given_that_microcephalic_osteodysplastic_primordial_dwarfism__type_3_is_a_rare_genetic_disorder__it_would_be_more_accurately_categorized_under_metabolic_disorder_or_possibly_other_if_available	growth_disorder|skeletal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0008874	Bangstad syndrome	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	neurology|psychiatry	inflammatory_disease|neurodegenerative_disease	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0008875	blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|orthopaedic|genetics_and_genomics|ophthalmology	syndrome|metabolic_disorder|genetic_disorder	eye_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008876	Bloom syndrome	chromosomal_disorder|integumentary_system_disorder|syndromic_disease|hematologic_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hematologic_disorder|chromosomal_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|oncology	metabolic_disorder|cancer	immune_disorder|bone_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0008877	blue diaper syndrome	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|allergy_and_immunology	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|immune_disorder	false	false	false	true	medium
MONDO:0008878	bone dysplasia, lethal Holmgren type	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disorder	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0008879	Bowen-Conradi syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|dermatology|genetics_and_genomics|oncology	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder|skin_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0008880	Bowen syndrome of multiple malformations	hereditary_disease	other	hereditary_disease	pediatric|obstetrics_and_gynecology|genetics_and_genomics|oncology	metabolic_disorder|cancer	skin_disorder|spinal_disorder	false	false	false	false	high
MONDO:0008881	kyphomelic dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008882	congenital bowing of long bones	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	skeletal_dysplasia|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008883	brachydactyly, type A2, with microcephaly	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|inflammatory_disease|mental_health_disorder|metabolic_disorder|neurodegenerative_disease	joint_disorder|brain_disorder|bone_disorder	false	false	false	brachydactyly__type_a2__with_microcephaly_is_a_genetic_condition_characterized_by_short_fingers_and_toes__brachydactyly__and_an_abnormally_small_head__microcephaly___as_of_my_last_knowledge_update_in_october_2023__there_are_no_specific_treatments_that_cure_these_conditions_since_they_are_typically_caused_by_genetic_factors__management_generally_focuses_on_supportive_care_and_addressing_any_associated_health_issues___therefore__the_answer_is_false	high
MONDO:0008884	oculoosteocutaneous syndrome	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	dermatology|genetics_and_genomics|rheumatology|ophthalmology	autoimmune_diseases|inflammatory_disease	joint_disorder|eye_disorder|skin_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0008885	Elsahy-Waters syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0008886	Sabinas brittle hair syndrome	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	hair_related_disorder|immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0008887	bronchiectasis with or without elevated sweat chloride 1	respiratory_system_disorder|hereditary_disease	other	hereditary_disease|idiopathic_disease|respiratory_system_disorder	pediatric|pulmonology	inflammatory_disease|metabolic_disorder	lung_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0008888	Williams-Campbell syndrome	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|cardiology|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder|throat_disorder|bone_disorder	false	false	false	false	high
MONDO:0008889	thromboangiitis obliterans	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	cardiology|hematology|pulmonology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	blood_bone_marrow_disorder|vascular_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0008890	progressive bulbar palsy	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0008891	riboflavin transporter deficiency	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatrics|genetics_and_genomics|metabolism|endocrinology	metabolic_disorder|neurodegenerative_disease|anemia	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0008892	progressive familial intrahepatic cholestasis type 1	digestive_system_disorder|metabolic_disease|syndromic_disease|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|endocrine_system_disorder|metabolic_disease|hereditary_disease|syndromic_disease	hepatology|genetics_and_genomics	metabolic_disorder|genetic_disorder	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0008893	C syndrome	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|psychiatry	adrenal_gland_disease|neurodegenerative_disease	liver_disorder	false	false	false	false	high
MONDO:0008894	cataract-hypertrichosis-intellectual disability syndrome	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0008895	hereditary arterial and articular multiple calcification syndrome	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	cardiology|genetics_and_genomics|rheumatology	cardiovascular_disorder|metabolic_disorder	joint_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0008896	campomelia, Cumming type	immune_system_disorder|cardiovascular_disorder|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|immune_system_disorder	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0008898	camptodactyly syndrome, Guadalajara type 1	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008899	camptodactyly syndrome, Guadalajara type 2	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0008900	camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	skeletal_dysplasia|metabolic_disorder	joint_disorder|skeletal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008901	Tel Hashomer camptodactyly syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	developmental_disorder|metabolic_disorder|genetic_disorders	joint_disorder|muscle_disorder|skeletal_disorder	false	false	false	false	medium
MONDO:0008902	camptodactyly-ichthyosis syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|orthopaedic|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008903	lung cancer	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|oncology	lung_cancer|cancer	lung_cancer|lung_disorder	false	true	false	true	very_high
MONDO:0008904	camptomelic syndrome, long-limb type	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|anemia|neurodegenerative_disease|autoimmune_diseases	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0008907	PMM2-congenital disorder of glycosylation	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	congenital_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0008908	MGAT2-congenital disorder of glycosylation	metabolic_disease|hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	metabolic_disease|cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|cardiovascular_disorder	pediatric|genetics_and_genomics	congenital_disorder_of_glycosylation|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	true	high
MONDO:0008909	congenital disorder of glycosylation, type i/IIx	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|congenital_disorder	joint_disorder|kidney_disorder|liver_disorder|muscle_disorder|vascular_disorder	false	false	true	false	high
MONDO:0008910	carboxypeptidase N deficiency	hereditary_disease	other	hereditary_disease	hepatology|genetics_and_genomics|pediatrics|endocrinology	metabolic_disorder|neurodegenerative_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0008911	cardiac lipidosis, familial	hereditary_disease|metabolic_disease|mitochondrial_disease|cardiovascular_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease|cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|cardiovascular_disorder|mitochondrial_disease|musculoskeletal_system_disorder	cardiology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0008912	cardiac septal defects with coarctation of the aorta	hereditary_disease	other	hereditary_disease	pediatric|cardiothoracic|cardiology	cardiac_septal_defects|cardiovascular_disorder|coarctation_of_the_aorta	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0008913	cardiac valvular defect, developmental	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|cardiology|genetics_and_genomics	cardiovascular_disorder|developmental	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0008914	cardioauditory syndrome of Sanchez Cascos	hereditary_disease	other	hereditary_disease	cardiology|otolaryngology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	heart_disorder|ear_disorder	true	false	false	false	low
MONDO:0008915	dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome	hereditary_disease|cardiovascular_disorder|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cardiovascular_disorder	reproductive_system_disorder|endocrine_system_disorder|cardiovascular_disorder|hereditary_disease	cardiology|endocrinology	hypergonadotropic_hypogonadism_syndrome|cardiovascular_disorder|metabolic_disorder	heart_disorder|endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0008916	cardiomyopathy associated with myopathy and sudden death	hereditary_disease	other	hereditary_disease	cardiology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease	heart_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0008917	heart defects-limb shortening syndrome	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|cardiology|genetics_and_genomics	cardiovascular_disorder|congenital_abnormality	heart_disorder|limb_shortening_syndrome_can_be_associated_with_joint_disorder_as_well_but_it_is_more_specific_to_the_heart_so_this_will_be_excluded|bone_disorder	false	false	false	true	high
MONDO:0008918	carnitine-acylcarnitine translocase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|cardiology|hepatology|genetics_and_genomics|metabolism|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0008919	systemic primary carnitine deficiency disease	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|hepatology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0008920	carnitine deficiency, myopathic	hereditary_disease	other	hereditary_disease	cardiology|hepatology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder	false	false	false	true	high
MONDO:0008921	carnosinemia	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0008922	Sengers syndrome	metabolic_disease|hereditary_disease|mitochondrial_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	metabolic_disease|cardiovascular_disorder	disorder_of_development_or_morphogenesis|metabolic_disease|cardiovascular_disorder|mitochondrial_disease|hereditary_disease	pediatric|neurology	neurodegenerative_disease|mental_health_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0008923	autosomal recessive palmoplantar keratoderma and congenital alopecia	syndromic_disease|hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|integumentary_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|dermatology	metabolic_disorder|genetic_disorder	congenital_disorder|muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0008924	congenital cataract-ichthyosis syndrome	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0008925	cataract 46 juvenile-onset	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	pediatric|ophthalmology	autoimmune_diseases|adrenal_gland_disease|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	juvenile_onset_disorder|eye_disorder	false	false	false	true	high
MONDO:0008926	COFS syndrome	syndromic_disease|metabolic_disease|hereditary_disease|disorder_of_visual_system	metabolic_disease	syndromic_disease|disorder_of_visual_system|metabolic_disease|hereditary_disease|disorder_of_orbital_region	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0008927	colobomatous optic disc-macular atrophy-chorioretinopathy syndrome	syndromic_disease|hereditary_disease|disorder_of_visual_system	other	syndromic_disease|disorder_of_visual_system|hereditary_disease	genetics_and_genomics|ophthalmology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0008928	cataract-ataxia-deafness syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|otolaryngology|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0008931	Cenani-Lenz syndactyly syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008932	premature centromere division	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	inflammatory_disease|cancer|autoimmune_diseases	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0008933	cephalin lipidosis	hereditary_disease	other	hereditary_disease	hepatology|genetics_and_genomics|neurology	cardiovascular_disorder|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0008934	cerebellar ataxia-ectodermal dysplasia syndrome	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0008935	cerebellar ataxia-hypogonadism syndrome	hereditary_disease|nervous_system_disorder|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|neurodegenerative_disease	reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|neurology|endocrinology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder|brain_disorder	false	false	false	false	high
MONDO:0008936	cerebellar ataxia and neurosensory deafness	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder|ear_disorder	true	false	false	false	high
MONDO:0008937	cerebellar ataxia, benign, with thermoanalgesia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	true	false	false	true	medium
MONDO:0008938	early-onset cerebellar ataxia with retained tendon reflexes	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0008939	isolated cerebellar hypoplasia/agenesis	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0008941	hepatic fibrosis-renal cysts-intellectual disability syndrome	syndromic_disease	other	syndromic_disease	pediatric|hepatology|genetics_and_genomics|renal_medicine|neurology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder	true	false	false	false	high
MONDO:0008943	autosomal recessive spinocerebellar ataxia 2	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0008944	Joubert syndrome 1	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0008945	myoclonic cerebellar dyssynergia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0008946	cerebral angiopathy, dysphoric	hereditary_disease	other	hereditary_disease	neurology|psychiatry	inflammatory_disease|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0008947	bilateral striopallidodentate calcinosis	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	hepatology|gastroenterology|neurology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0008948	cerebrotendinous xanthomatosis	disorder_of_visual_system|hereditary_disease|syndromic_disease|metabolic_disease|nervous_system_disorder|integumentary_system_disorder|psychiatric_disorder	metabolic_disease|psychiatric_disorder|neurodegenerative_disease	integumentary_system_disorder|disorder_of_visual_system|syndromic_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|skin_disorder|brain_disorder	false	false	false	true	high
MONDO:0008949	cerebral malformation, seizures, hypertrichosis, and overlapping fingers	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|skin_disorder|brain_disorder	false	false	false	false	high
MONDO:0008950	cerebral sclerosis similar to Pelizaeus-Merzbacher disease	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0008951	cerebrocortical degeneration of infancy	hereditary_disease	other	hereditary_disease	pediatric|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	true	false	false	false	high
MONDO:0008953	peroxisome biogenesis disorder 1A (Zellweger)	hereditary_disease|syndromic_disease|metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder|metabolic_disease|hereditary_disease	pediatric|hepatology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0008954	peroxisome biogenesis disorder 2A (Zellweger)	hereditary_disease|syndromic_disease|metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder|metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|peroxisome_biogenesis_disorder_2a__zellweger__is_a_rare_genetic_disorder_affecting_the_metabolism_of_lipids_in_the_liver	false	false	false	false	very_high
MONDO:0008955	cerebrooculofacioskeletal syndrome 1	disorder_of_visual_system|hereditary_disease|syndromic_disease|metabolic_disease	metabolic_disease	disorder_of_visual_system|syndromic_disease|metabolic_disease|disorder_of_orbital_region|hereditary_disease	pediatric|genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0008957	cervical vertebrae, agenesis of	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|neurology	inflammatory_disease|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008958	Klippel-Feil syndrome 2, autosomal recessive	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|ear_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008959	CHAND syndrome	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	endocrine_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0008960	Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	intellectual_disability_syndrome|muscle_disorder|hearing_disorder|nerve_disorder	false	false	false	false	high
MONDO:0008961	Charcot-Marie-Tooth disease type 4A	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008962	Griscelli syndrome type 1	hereditary_disease|syndromic_disease|metabolic_disease|nervous_system_disorder|integumentary_system_disorder	metabolic_disease	syndromic_disease|nervous_system_disorder|metabolic_disease|hereditary_disease|integumentary_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	bone_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0008963	Chediak-Higashi syndrome	hereditary_disease|syndromic_disease|metabolic_disease|nervous_system_disorder|immune_system_disorder|integumentary_system_disorder|hematologic_disorder	metabolic_disease|neurodegenerative_disease	syndromic_disease|hematologic_disorder|nervous_system_disorder|immune_system_disorder|metabolic_disease|hereditary_disease|integumentary_system_disorder	pediatric|genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	eye_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0008964	congenital secretory chloride diarrhea 1	hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease	pediatric|gastroenterology	congenital_secretory_chloride_diarrhea_is_often_associated_with_mutations_in_the_slc26a3_gene_which_codes_for_a_transport_protein_involved_in_salt_absorption_in_the_intestine|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0008965	CHARGE syndrome	hereditary_disease|syndromic_disease|endocrine_system_disorder|reproductive_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder|endocrine_system_disorder	reproductive_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder|endocrine_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	congenital_anomaly|neurodevelopmental_disorder|genetic_disorder	heart_disorder|ear_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0008966	Aagenaes syndrome	digestive_system_disorder|syndromic_disease|endocrine_system_disorder|immune_system_disorder	endocrine_system_disorder	syndromic_disease|immune_system_disorder|digestive_system_disorder|endocrine_system_disorder	genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	liver_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0008967	congenital bile acid synthesis defect 4	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|hepatology|genetics_and_genomics|gastroenterology	metabolic_disorder|congenital_disease|inherited_condition	liver_disorder|upper_gastrointestinal_disorder|biliary_disorder	false	false	false	true	high
MONDO:0008968	cholestasis with gallstone, ataxia, and visual disturbance	hereditary_disease	other	hereditary_disease	hepatology|gastroenterology|ophthalmology|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	liver_disorder|upper_gastrointestinal_disorder|biliary_disorder	false	false	false	false	high
MONDO:0008969	cholesterol pneumonia	hereditary_disease	other	hereditary_disease	cardiology|pulmonology	inflammatory_disease|cardiovascular_disorder|metabolic_disorder	lung_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0008970	chondrodysplasia Blomstrand type	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|anemia	bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0008971	chondrodysplasia calcificans Metaphysealis	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|rheumatology|orthopaedic	inflammatory_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0008972	rhizomelic chondrodysplasia punctata type 1	disorder_of_visual_system|hereditary_disease|syndromic_disease|metabolic_disease|nervous_system_disorder|musculoskeletal_system_disorder	metabolic_disease|neurodegenerative_disease	musculoskeletal_system_disorder|disorder_of_visual_system|syndromic_disease|nervous_system_disorder|metabolic_disease|disorder_of_orbital_region|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic|dermatology	metabolic_disorder|neurodegenerative_disease	liver_disorder|skin_disorder|bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0008973	chondrodysplasia punctata, Toriello type	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic|dermatology	metabolic_disorder|neurodegenerative_disease	skin_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0008974	Greenberg dysplasia	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	metabolic_disease	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	bone_disorder|skeletal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0008975	otospondylomegaepiphyseal dysplasia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	skeletal_abnormality___corrected_list_removing_unnecessary_categories___neurodegenerative_disease|skeletal_abnormality|neurodegenerative_disease|genetic_disorder	spinal_disorder|bone_disorder|ear_disorder|joint_disorder	false	false	false	false	high
MONDO:0008976	chondroitin-6-sulfaturia, defective cellular immunity, nephrotic syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|rheumatology|renal_medicine|immunology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|joint_disorder|immune_disorder	false	false	false	false	high
MONDO:0008977	chondrosarcoma	hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|hereditary_disease	orthopaedic|oncology	cancer	spinal_disorder|bone_disorder|joint_disorder	false	true	false	false	high
MONDO:0008978	chordoma	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	orthopaedic|oncology	tumor_disease|bone_disorder|cancer	spinal_disorder|bone_disorder	false	true	false	true	high
MONDO:0008979	chorea, benign familial	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0008980	ataxia-hypogonadism-choroidal dystrophy syndrome	hereditary_disease|nervous_system_disorder|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics|neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|reproductive_system_disorder|brain_disorder	false	false	false	false	high
MONDO:0008981	infantile choroidocerebral calcification syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	eye_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0008982	central areolar choroidal dystrophy	disorder_of_visual_system|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	disorder_of_visual_system|cardiovascular_disorder|hereditary_disease|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0008983	chromosomal instability with tissue-specific radiosensitivity	hereditary_disease	other	hereditary_disease	genetics_and_genomics|oncology	cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0008984	ciliary discoordination due to random ciliary orientation	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	syndromic_disease|respiratory_system_disorder|hereditary_disease	pulmonology|neurology	ciliary_disorder|neurodegenerative_disease	eye_disorder|nose_disorder	false	false	false	false	medium
MONDO:0008985	ciliary dyskinesia with transposition of ciliary microtubules	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	syndromic_disease|respiratory_system_disorder|hereditary_disease	genetics_and_genomics|pulmonology|pediatric	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0008986	circumvallate placenta syndrome	hereditary_disease	other	hereditary_disease	obstetrics_and_gynecology|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|reproductive_system_disorder|vascular_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0008988	citrullinemia type I	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0008989	citrulline transport defect	hereditary_disease	other	hereditary_disease	genetics_and_genomics|renal_medicine|pediatric	metabolic_disorder|inherited_disorder|genetic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0008990	cleft larynx, posterior	upper_digestive_tract_disorder|respiratory_system_disorder|digestive_system_disorder	other	digestive_system_disorder|upper_digestive_tract_disorder|respiratory_system_disorder	pulmonology|otolaryngology|pediatric	autoimmune_diseases|inflammatory_disease|cancer	lung_disorder|throat_disorder	false	false	false	false	medium
MONDO:0008991	Verloove Vanhorick-Brubakk syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|cardiology|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	liver_disorder|biliary_disorder	false	false	false	false	very_high
MONDO:0008992	Juberg-Hayward syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	skeletal_system_disorder___note__juberg_hayward_syndrome_is_a_genetic_disorder_characterized_by_abnormalities_of_the_bones__skeletal_system__and_brain|bone_disorder	false	false	false	false	high
MONDO:0008993	cleft palate-stapes fixation-oligodontia syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	otolaryngology|pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	teeth_disorder|bone_disorder|ear_disorder	false	false	false	false	high
MONDO:0008994	cleidocranial dysplasia, recessive form	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|inflammatory_disease	skeletal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0008995	Yunis-Varon syndrome	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|hematologist	autoimmune_diseases|neurodegenerative_disease	bone_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0008998	Cockayne syndrome type 3	hereditary_disease|premature_aging_syndrome|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|premature_aging_syndrome|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0008999	Cohen syndrome	hereditary_disease|immune_system_disorder|syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hematologic_disorder|psychiatric_disorder	psychiatric_disorder	hematologic_disorder|immune_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	lower_gastrointestinal_disorder|lymphatic_disorder|joint_disorder|upper_gastrointestinal_disorder|skin_disorder|brain_disorder|muscle_disorder|urinary_tract_disorder|eye_disorder	false	false	false	false	high
MONDO:0009000	familial reactive perforating collagenosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|rheumatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	joint_disorder|skin_disorder	false	false	false	false	low
MONDO:0009001	macular coloboma-cleft palate-hallux valgus syndrome	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	orthopaedic|ophthalmology|genetics_and_genomics	congenital_disorder|metabolic_disorder|genetic_disorder	teeth_disorder|joint_disorder|eye_disorder	false	false	false	false	high
MONDO:0009002	coloboma, ocular, autosomal recessive	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	pediatric|ophthalmology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	ocular_disorder|eye_disorder	false	false	false	false	low
MONDO:0009003	achromatopsia 2	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0009005	complement component C1r/C1s deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	allergy_and_immunology|immunology_is_missing_from_the_list_but_would_be_a_better_fit_than_allergy_and_immunology_if_it_were_included__so_this_answer_will_use_that_instead|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0009006	complement component 2 deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	renal_medicine|allergy_and_immunology|rheumatology|genetics_and_genomics|hematology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder|kidney_disorder	false	false	false	true	high
MONDO:0009007	Jalili syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|skeletal_system_disorder|genetic_disorder	false	false	false	false	high
MONDO:0009008	heart defect - tongue hamartoma - polysyndactyly syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|cardiology|genetics_and_genomics	congenital_abnormality|cardiovascular_disorder	joint_disorder|throat_disorder|heart_disorder	false	false	false	false	high
MONDO:0009009	hypoplasminogenemia	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|autoimmune_diseases|metabolic_disorder	immune_disorder|vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0009010	aortic arch interruption	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|cardiology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0009012	multiple pterygium-malignant hyperthermia syndrome	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009013	convulsive disorder, familial, with prenatal or early onset	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0009014	cornea plana 2	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	ophthalmology|pediatrics	inflammatory_disease|autoimmune_diseases	eye_disorder|corneal_disorder	false	false	false	false	medium
MONDO:0009015	corneal dystrophy-perceptive deafness syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	eye_disorder|ear_disorder	false	false	false	false	medium
MONDO:0009016	band keratopathy	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0009017	corneal degeneration, band-shaped spheroid	hereditary_disease	other	hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0009018	central cloudy dystrophy of François	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder|spinal_disorder	false	false	false	false	low
MONDO:0009019	congenital hereditary endothelial dystrophy of cornea	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	pediatric|ophthalmology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0009020	macular corneal dystrophy	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	ophthalmology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|corneal_disorder	false	false	false	false	high
MONDO:0009021	Toriello-Carey syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|joint_disorder|skin_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0009022	corpus callosum, agenesis of	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0009024	cortical blindness-intellectual disability-polydactyly syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|disorder_of_visual_system	other	disorder_of_development_or_morphogenesis|disorder_of_visual_system|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0009025	apparent mineralocorticoid excess	endocrine_system_disorder|metabolic_disease|syndromic_disease|hereditary_disease	endocrine_system_disorder|metabolic_disease	metabolic_disease|endocrine_system_disorder|hereditary_disease|syndromic_disease	endocrinology|renal_medicine	adrenal_gland_disease|autoimmune_diseases|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0009026	Costello syndrome	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	pulmonology|cardiology|dermatology|pediatrics|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	upper_gastrointestinal_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0009027	cramps, familial adolescent	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0009028	Crane-Heise syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009029	cranial nerves, congenital paresis of	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0009030	cranial nerves, recurrent paresis of	hereditary_disease	other	hereditary_disease	neurology|otolaryngology	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0009031	craniodiaphyseal dysplasia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder|spinal_disorder|teeth_disorder	false	false	false	false	high
MONDO:0009032	cranioectodermal dysplasia	integumentary_system_disorder|disorder_of_development_or_morphogenesis|respiratory_system_disorder|syndromic_disease|hereditary_disease|urinary_system_disorder|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|urinary_system_disorder|musculoskeletal_system_disorder|respiratory_system_disorder|integumentary_system_disorder|hereditary_disease|syndromic_disease	pediatric|dermatology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|skin_disorder|bone_disorder|eye_disorder|ear_disorder|teeth_disorder	false	false	false	false	high
MONDO:0009033	temtamy syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009034	craniofacial dyssynostosis	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	bone_disorder|teeth_disorder	false	false	false	false	high
MONDO:0009035	craniometaphyseal dysplasia, autosomal recessive	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder|spinal_disorder|teeth_disorder	false	false	false	false	high
MONDO:0009036	cardiocranial syndrome, Pfeiffer type	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	pediatric|cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	brain_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0009037	craniosynostosis with anomalies of the cranial base and digits	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|spinal_disorder|teeth_disorder	false	false	false	false	high
MONDO:0009038	craniosynostosis-fibular aplasia syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	orthopaedic|pediatric|genetics_and_genomics	other___note__this_disease_is_a_rare_genetic_syndrome_that_affects_the_development_of_the_bones_and_joints__particularly_in_the_skull_and_lower_limbs__it_falls_under_the_category_of_metabolic_disorders_due_to_its_association_with_abnormalities_in_the_development_and_growth_of_the_bones__which_are_influenced_by_various_metabolic_processes|metabolic_disorder	bone_disorder|craniosynostosis	false	false	false	false	medium
MONDO:0009039	Baller-Gerold syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder|immune_disorder	false	false	false	false	medium
MONDO:0009040	craniosynostosis-intellectual disability syndrome of 51N and Gettig	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	bone_disorder|brain_disorder	false	false	false	false	high
MONDO:0009041	craniosynostosis-intellectual disability-clefting syndrome	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	bone_disorder|brain_disorder|clefting_syndrome_is_more_closely_related_to_throat_disorder	false	false	false	false	high
MONDO:0009042	craniotelencephalic dysplasia	nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0009043	generalized resistance to thyroid hormone	endocrine_system_disorder|metabolic_disease|hereditary_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease|hereditary_disease	endocrinology|genetics_and_genomics	thyroid_hormone_is_associated_with_the_adrenal_gland__but_this_disease_is_broader_than_an_adrenal_gland_disease|autoimmune_diseases|metabolic_disorder	thyroid_hormone_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0009044	Crigler-Najjar syndrome	metabolic_disease|hereditary_disease|syndromic_disease	metabolic_disease	syndromic_disease|metabolic_disease|hereditary_disease	hepatology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0009045	cataract-nephropathy-encephalopathy syndrome	syndromic_disease	other	syndromic_disease	renal_medicine|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|kidney_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009046	Fraser syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|disorder_of_visual_system	other	disorder_of_orbital_region|syndromic_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|teeth_disorder|throat_disorder|ear_disorder	false	false	false	false	high
MONDO:0009047	cryptorchidism	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	pediatric|urology	endocrine_disease|metabolic_disorder|congenital_anomaly	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0009048	curved nail of fourth toe	hereditary_disease	other	hereditary_disease	orthopaedic|dermatology	anemia|autoimmune_diseases|metabolic_disorder	bone_disorder|nail_disorder	false	false	false	false	low
MONDO:0009049	Cushing syndrome due to macronodular adrenal hyperplasia	endocrine_system_disorder|hereditary_disease|syndromic_disease	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|hereditary_disease	endocrinology	inflammatory_disease|adrenal_gland_disease|metabolic_disorder	adrenal_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0009050	Cushing disease due to pituitary adenoma	connective_tissue_disorder|reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	syndromic_disease|musculoskeletal_system_disorder|reproductive_system_disorder|connective_tissue_disorder|endocrine_system_disorder|nervous_system_disorder|hereditary_disease|cancer_or_benign_tumor	endocrinology|pulmonology|neurology	endocrine_disease|pituitary_adenoma|metabolic_disorder	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0009051	cutaneous photosensitivity-lethal colitis syndrome	digestive_system_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|digestive_system_disorder|hereditary_disease	dermatology|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|skin_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0009052	cutis laxa, autosomal recessive, type 1A	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	pediatric|dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009053	ALDH18A1-related de Barsy syndrome	premature_aging_syndrome|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|integumentary_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|integumentary_system_disorder|metabolic_disease|hereditary_disease|premature_aging_syndrome	hepatology|neurology|obstetrics_and_gynecology|genetics_and_genomics|pediatrics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	liver_disorder|metabolic_disorder___note__i_added_metabolic_disorder_which_is_a_more_accurate_category_for_this_disease	false	false	false	false	high
MONDO:0009054	autosomal recessive cutis laxa type 2, classic type	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	pediatric|dermatology|genetics_and_genomics	metabolic_disorder|autosomal_recessive_disease	skin_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009055	cutis marmorata telangiectatica congenita	cardiovascular_disorder|integumentary_system_disorder	cardiovascular_disorder	cardiovascular_disorder|integumentary_system_disorder	dermatology|genetics_and_genomics|pediatrics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0009056	cutis verticis gyrata and intellectual disability	hereditary_disease	other	hereditary_disease	dermatology|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	skin_disorder|brain_disorder	false	false	false	false	high
MONDO:0009057	cyanosis and hepatic disease	hereditary_disease	other	hereditary_disease	hepatology|pulmonology|cardiology	anemia|hepatic_disease|metabolic_disorder|cardiovascular_disorder	liver_disorder|heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0009058	cystathioninuria	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	renal_medicine|genetics_and_genomics	metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0009059	cysteine Peptiduria	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	genetic_disorder|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0009060	cystic disease of lung	hereditary_disease	other	hereditary_disease	pulmonology|cardiothoracic	inflammatory_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|lung_disorder	false	false	false	false	high
MONDO:0009061	cystic fibrosis	respiratory_system_disorder|hereditary_disease	other	respiratory_system_disorder|hereditary_disease	pediatric|pulmonology|genetics_and_genomics	inflammatory_disease|metabolic_disorder	liver_disorder|lung_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0009062	cystic fibrosis-gastritis-megaloblastic anemia syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	hematology|pediatric|gastroenterology|genetics_and_genomics	anemia|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0009063	ventriculomegaly-cystic kidney disease	hereditary_disease	other	hereditary_disease	pediatric|renal_medicine|urology	kidney_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0009064	ocular cystinosis	metabolic_disease|hereditary_disease|disorder_of_visual_system	metabolic_disease	disorder_of_orbital_region|disorder_of_visual_system|metabolic_disease|hereditary_disease	urology|ophthalmology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|kidney_disorder	false	false	false	true	low
MONDO:0009066	juvenile nephropathic cystinosis	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|urology|genetics_and_genomics	kidney_disease_is_not_present_in_the_list_but_it_is_related_to_kidney_disease_so_it_s_closest_match|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0009067	cystinuria	hereditary_disease|metabolic_disease|syndromic_disease|urinary_system_disorder	metabolic_disease	urinary_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease	pediatric|renal_medicine|urology|genetics_and_genomics	genetic_disorder|genetic_disorder___corrected_response____metabolic_disorder|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0009069	congenital lactic acidosis, Saguenay-Lac-Saint-Jean type	disorder_of_development_or_morphogenesis|nervous_system_disorder|metabolic_disease|hereditary_disease|mitochondrial_disease	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	congenital_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009070	D-glyceric aciduria	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	renal_medicine|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0009071	hereditary renal hypouricemia	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	pediatric|renal_medicine|genetics_and_genomics	hereditary_renal_hypouricemia_is_a_type_of_inborn_error_of_metabolism_that_affects_the_kidneys__ability_to_reabsorb_urate|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0009072	Dandy-Walker syndrome	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009073	Ritscher-Schinzel syndrome 1	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	bone_disorder|eye_disorder|kidney_disorder|joint_disorder	false	false	false	false	high
MONDO:0009074	facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009075	Dandy-Walker malformation-postaxial polydactyly syndrome	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0009076	autosomal recessive nonsyndromic hearing loss 1A	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	high
MONDO:0009077	deafness, congenital, and familial myoclonic epilepsy	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|familial_disease	muscle_disorder|ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0009079	DOORS syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	psychiatry|neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	upper_gastrointestinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0009080	split hand-foot malformation 1 with sensorineural hearing loss	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|genetic_disorder	bone_disorder|ear_disorder	false	false	false	false	high
MONDO:0009081	deafness, congenital, with total albinism	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	eye_disorder|skin_disorder|ear_disorder	false	false	false	false	high
MONDO:0009082	high myopia-sensorineural deafness syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	ophthalmology|genetics_and_genomics|otolaryngology	neurodegenerative_disease|sensorineural_deafness_syndrome	eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0009083	conductive deafness-malformed external ear syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	ear_disorder|external_ear_disorder	false	false	false	false	medium
MONDO:0009084	conductive deafness-ptosis-skeletal anomalies syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	skeletal_anomalies_syndrome_is_likely_a_made_up_name_so_its_category_is_unclear_but_it_could_fit_here_as_well|metabolic_disorder	skeletal_anomalies|ear_disorder	false	false	false	true	high
MONDO:0009085	deafness-vitiligo-achalasia syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|otolaryngology	inflammatory_disease|autoimmune_diseases	skin_disorder|throat_disorder|ear_disorder	false	false	false	false	medium
MONDO:0009086	deafness-small bowel diverticulosis-neuropathy syndrome	hereditary_disease	other	hereditary_disease	gastroenterology|neurology|otolaryngology	neurodegenerative_disease|autoimmune_diseases	lower_gastrointestinal_disorder|ear_disorder|neuropathy_is_associated_with_other_but_it_is_a_symptom_of_this_syndrome_so_not_included	false	false	false	false	high
MONDO:0009087	deafness, neural, congenital moderate	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology|otolaryngology	congenital|neural	ear_disorder|neural	false	false	false	false	medium
MONDO:0009088	deafness, neural, with atypical atopic dermatitis	hereditary_disease	other	hereditary_disease	dermatology|neurology|otolaryngology	allergy|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	skin_disorder|ear_disorder|neural	false	false	false	false	high
MONDO:0009089	deafness-oligodontia syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	teeth_disorder|ear_disorder	false	false	false	false	medium
MONDO:0009090	hearing loss, sensorineural, autosomal-mitochondrial type	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|otolaryngology|neurology	neurodegenerative_disease|autosomal_mitochondrial_type_is_not_in_the_list__but_sensorineural_hearing_loss_is_often_associated_with_metabolic_disorder|metabolic_disorder	ear_disorder|sensorineural	false	false	false	false	high
MONDO:0009091	non-acquired combined pituitary hormone deficiency with spine abnormalities	nervous_system_disorder|reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|nervous_system_disorder	orthopaedic|endocrinology|pediatric|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases|metabolic_disorder	spinal_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0009092	polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	kidney_disorder|brain_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0009093	dermatoleukodystrophy	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|dermatology|pediatrics|neurology	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0009094	dermochondrocorneal dystrophy	syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|syndromic_disease	genetics_and_genomics|ophthalmology|dermatology	inflammatory_disease|metabolic_disorder	joint_disorder|eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0009095	dermatoosteolysis, Kirghizian type	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder	bone_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0009097	persistent hyperplastic primary vitreous, autosomal recessive	nervous_system_disorder|hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0009098	dextrocardia with unusual facies and microphthalmia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|cardiology	anemia|cardiovascular_disorder|metabolic_disorder	heart_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0009099	nephrogenic diabetes insipidus-intracranial calcification syndrome	hereditary_disease|urinary_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|urinary_system_disorder	renal_medicine|genetics_and_genomics|endocrinology|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0009101	Wolfram syndrome 1	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	endocrine_disorder|brain_disorder	false	false	true	false	high
MONDO:0009102	diaminopentanuria	hereditary_disease	other	hereditary_disease	renal_medicine|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0009103	diaphragmatic hernia 2	hereditary_disease|respiratory_system_disorder|musculoskeletal_system_disorder	other	respiratory_system_disorder|hereditary_disease|musculoskeletal_system_disorder	urology|general_surgery|cardiothoracic	abdominal_disorder|inflammatory_disease	muscle_disorder|upper_gastrointestinal_disorder|abdominal_disorder	false	false	false	false	high
MONDO:0009104	Donnai-Barrow syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	ear_disorder|joint_disorder|brain_disorder|spinal_disorder|skeletal_deformity_disorder|hearing_loss_disorder	false	false	false	false	very_high
MONDO:0009105	trichohepatoenteric syndrome	syndromic_disease|hereditary_disease|digestive_system_disorder|immune_system_disorder|connective_tissue_disorder	other	hereditary_disease|digestive_system_disorder|syndromic_disease|immune_system_disorder|connective_tissue_disorder	gastroenterology|pediatric|hepatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|liver_disorder	true	false	false	false	very_high
MONDO:0009106	diastematomyelia	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|pediatric	inflammatory_disease___corrected_to_fit_the_format__neurodegenerative_disease|neurodegenerative_disease|inflammatory_disease|skeletal_system_disease	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009107	diastrophic dysplasia	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009108	hyperdibasic aminoaciduria type 1	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	renal_medicine|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0009109	lysinuric protein intolerance	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|renal_medicine|genetics_and_genomics	inherited_disorder|metabolic_disorder	kidney_disorder|renal_disorder	false	false	false	false	high
MONDO:0009110	dicarboxylic aminoaciduria	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|hematology|renal_medicine|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder	false	false	false	true	high
MONDO:0009111	dihydropyrimidinuria	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|renal_medicine|genetics_and_genomics	metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	true	high
MONDO:0009112	rhizomelic chondrodysplasia punctata type 2	metabolic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_visual_system	metabolic_disease	metabolic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|skin_disorder	false	false	false	false	high
MONDO:0009113	hemolytic anemia due to diphosphoglycerate mutase deficiency	metabolic_disease|hereditary_disease|hematologic_disorder	metabolic_disease|anemia	hereditary_disease|hematologic_disorder|metabolic_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0009114	congenital sucrase-isomaltase deficiency	metabolic_disease|digestive_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|digestive_system_disorder|metabolic_disease	pediatric|genetics_and_genomics|gastroenterology	metabolic_disorder|genetic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0009115	congenital lactase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|gastroenterology	metabolic_disorder|congenital_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0009118	disseminated sclerosis with narcolepsy	hereditary_disease	other	hereditary_disease	neurology|psychiatry	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|immune_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009119	diverticulosis, small-intestinal	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0009120	diverticulosis of bowel, hernia, and retinal detachment	digestive_system_disorder|syndromic_disease	other	digestive_system_disorder|syndromic_disease	general_surgery|ophthalmology|gastroenterology	cancer|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0009121	von Voss-Cherstvoy syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	biliary_disorder|vascular_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0009122	Dohle bodies and leukemia	hereditary_disease	other	hereditary_disease	oncology|hematology	leukemia|autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder	true	true	false	true	high
MONDO:0009123	orthostatic hypotension 1	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|cardiology|renal_medicine	neurodegenerative_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0009124	Dubowitz syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0009126	duodenal atresia	digestive_system_disorder|disorder_of_development_or_morphogenesis	other	digestive_system_disorder|disorder_of_development_or_morphogenesis	pediatric|gastroenterology	birth_defect|abdominal_surgery|gastrointestinal_disorder|developmental_abnormality|congenital_anomaly	lower_gastrointestinal_disorder_upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0009127	dwarfism, low-birth-weight type, with unresponsiveness to growth hormone	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	bone_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0009128	dwarfism, intellectual disability, and eye abnormality	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|eye_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0009129	dwarfism, proportionate, with hip dislocation	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	hip_dislocation|metabolic_disorder|dwarfism|with|proportionate|adrenal_gland_disease|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	true	medium
MONDO:0009130	Dyggve-Melchior-Clausen disease	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatrics|neurology	neurodegenerative_disease|metabolic_disorder	joint_disorder|muscle_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0009131	Riley-Day syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|allergy_and_immunology|immunology	metabolic_disorder|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0009132	dysautonomia-like disorder	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0009133	cerebellar ataxia, intellectual disability, and dysequilibrium	hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|neurology	intellectual_disability|neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	true	false	false	false	high
MONDO:0009134	congenital dyserythropoietic anemia type 2	hereditary_disease|metabolic_disease|hematologic_disorder	anemia|metabolic_disease	hereditary_disease|hematologic_disorder|metabolic_disease	pediatric|hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0009135	anemia, congenital dyserythropoietic, type 1a	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	pediatric|hematology|genetics_and_genomics	metabolic_disorder|anemia	congenital_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0009136	dyskeratosis congenita, autosomal recessive 1	hereditary_disease|syndromic_disease|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	hereditary_disease|integumentary_system_disorder|cancer_or_benign_tumor|syndromic_disease	pediatric|hematology|genetics_and_genomics|dermatology	neurodegenerative_disease|metabolic_disorder	skin_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0009137	dysmyelination with jaundice	hereditary_disease	other	hereditary_disease	hepatology|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	liver_disorder|brain_disorder	false	false	false	false	high
MONDO:0009138	dysosteosclerosis	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic	metabolic_disorder|autoimmune_diseases	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0009139	dyssegmental dysplasia, Rolland-Desbuquois type	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	joint_disorder|vascular_disorder|bone_disorder	false	false	false	false	high
MONDO:0009140	Silverman-Handmaker type dyssegmental dysplasia	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0009141	torsion dystonia 2	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0009142	dystonia with Ringbinden	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0009143	Meier-Gorlin syndrome 1	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	joint_disorder|skeletal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0009144	Ebstein anomaly	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics|cardiology	cardiovascular_disorder|anemia	heart_disorder|cardiac_disorder	false	false	false	false	high
MONDO:0009145	Schöpf-Schulz-Passarge syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|integumentary_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0009146	ectodermal dysplasia-sensorineural deafness syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|psychiatry|otolaryngology|neurology	neurodegenerative_disease|allergy|inflammatory_disease|metabolic_disorder|autoimmune_diseases	teeth_disorder|skin_disorder|ear_disorder	false	false	false	false	high
MONDO:0009147	ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|integumentary_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|dermatology	neurodegenerative_disease|metabolic_disorder	teeth_disorder|skin_disorder|ear_disorder	false	false	false	false	medium
MONDO:0009148	Rosselli-Gulienetti syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|integumentary_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0009149	ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	neurology|pediatric|genetics_and_genomics|psychiatry	neurodegenerative_disease|mental_health_disorder	teeth_disorder|eye_disorder|joint_disorder|skin_disorder|blood_bone_marrow_disorder|brain_disorder|spinal_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0009150	hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome	hereditary_disease|endocrine_system_disorder|syndromic_disease|integumentary_system_disorder	endocrine_system_disorder	hereditary_disease|integumentary_system_disorder|endocrine_system_disorder|syndromic_disease	neurology|pediatric|genetics_and_genomics|endocrinology|dermatology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder|endocrine_disorder|skin_disorder	false	false	false	false	high
MONDO:0009151	cleft lip/palate-ectodermal dysplasia syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|integumentary_system_disorder|musculoskeletal_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|otolaryngology	metabolic_disorder|genetic_disorder	teeth_disorder|mouth_disorder	false	false	false	true	high
MONDO:0009152	ectopia lentis 2, isolated, autosomal recessive	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disease	eye_disorder	false	false	false	false	medium
MONDO:0009153	ectopia lentis et pupillae	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|eye_disorder	eye_disorder	false	false	false	false	medium
MONDO:0009154	hypothyroidism, congenital, nongoitrous, 5	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|congenital	false	false	false	true	medium
MONDO:0009155	EEM syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|integumentary_system_disorder|disorder_of_visual_system|psychiatric_disorder|musculoskeletal_system_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_orbital_region|integumentary_system_disorder|nervous_system_disorder|disorder_of_visual_system|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|endocrinology|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder|liver_disorder	false	false	false	false	medium
MONDO:0009156	ectrodactyly-polydactyly syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|psychiatry|orthopaedic|neurology	neurodegenerative_disease|developmental_disorder|genetic_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	low
MONDO:0009157	split hand-foot malformation 6	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	skeletal_dysplasia|metabolic_disorder	bone_disorder|joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0009158	Ehlers-Danlos syndrome, fibronectinemic type	hereditary_disease|disorder_of_development_or_morphogenesis|hematologic_disorder|syndromic_disease	other	hematologic_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|rheumatology|dermatology	inflammatory_disease|metabolic_disorder|cardiovascular_disorder|autoimmune_diseases	joint_disorder|vascular_disorder|skin_disorder	false	false	false	false	high
MONDO:0009159	Ehlers-Danlos syndrome, cardiac valvular type	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|rheumatology|cardiology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0009161	Ehlers-Danlos syndrome, dermatosparaxis type	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|rheumatology|dermatology	inflammatory_disease|metabolic_disorder|cardiovascular_disorder|autoimmune_diseases	joint_disorder|skin_disorder|vascular_disorder	false	false	false	false	high
MONDO:0009162	Ellis-van Creveld syndrome	hereditary_disease|urinary_system_disorder|cardiovascular_disorder|respiratory_system_disorder|syndromic_disease|integumentary_system_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|integumentary_system_disorder|respiratory_system_disorder|urinary_system_disorder|syndromic_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|eye_disorder|dental_disorder	false	false	false	false	high
MONDO:0009163	encephalomalacia, multilocular	hereditary_disease	other	hereditary_disease	pediatric|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009164	encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts	hereditary_disease	other	hereditary_disease	ophthalmology|genetics_and_genomics|cardiology|neurology	neurodegenerative_disease|cardiovascular_disorder	eye_disorder|muscle_disorder|heart_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009165	Aicardi-Goutieres syndrome 1	hereditary_disease|connective_tissue_disorder|nervous_system_disorder|immune_system_disorder|syndromic_disease	neurodegenerative_disease	immune_system_disorder|connective_tissue_disorder|nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|pediatrics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	immune_disorder|brain_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0009166	pontocerebellar hypoplasia type 4	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0009167	Bonnemann-Meinecke-Reich syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0009168	Fowler syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	joint_disorder|skeletal_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0009169	endocardial fibroelastosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiothoracic|cardiology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0009170	endocardial fibroelastosis and coarctation of abdominal aorta	hereditary_disease	other	hereditary_disease	pediatric|cardiothoracic|cardiovascular|cardiology	cardiovascular_disorder|coarctation_of_abdominal_aorta_category_is_not_clear_but_might_fit_this_category_as_well	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0009171	endothelial dystrophy, congenital hereditary, with nail hypoplasia	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|dermatology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|skin_disorder	false	false	false	false	medium
MONDO:0009172	enterocolitis	hereditary_disease	other	hereditary_disease	gastroenterology|pediatrics	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0009173	congenital enteropathy due to enteropeptidase deficiency	hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|gastroenterology	metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0009174	protein-losing enteropathy	hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease	gastroenterology|pediatrics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0009175	eosinophilic fasciitis	inflammatory_disease|connective_tissue_disorder|musculoskeletal_system_disorder	other	inflammatory_disease|connective_tissue_disorder|idiopathic_disease|musculoskeletal_system_disorder	pulmonology|rheumatology|dermatology|neurology	inflammatory_disease|autoimmune_diseases	muscle_disorder|immunne_disorder	false	false	false	true	high
MONDO:0009176	epidermodysplasia verruciformis	hereditary_disease|immune_system_disorder|integumentary_system_disorder	other	immune_system_disorder|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	false	high
MONDO:0009177	late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology|neurology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	intellectual_disability|skin_disorder	false	false	false	false	high
MONDO:0009178	epidermolysis bullosa dystrophica Neurotrophica	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|skin_disorder	false	false	false	false	high
MONDO:0009179	recessive dystrophic epidermolysis bullosa	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology|pediatric	epidermolysis_bullosa_is_a_rare_skin_disorder__metabolic_disorder|inflammatory_disease|anemia|autoimmune_diseases	muscle_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0009180	junctional epidermolysis bullosa, non-Herlitz type	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	high
MONDO:0009181	epidermolysis bullosa simplex 5B, with muscular dystrophy	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder|nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|dermatology|neurology	neurodegenerative_disease|metabolic_disorder|muscular_dystrophy	muscle_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0009182	junctional epidermolysis bullosa Herlitz type	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology|pediatric	inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0009183	junctional epidermolysis bullosa with pyloric atresia	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|gastroenterology|dermatology|pediatric	metabolic_disorder|adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0009184	epidermolysis bullosa with diaphragmatic hernia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases	muscle_disorder|immune_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0009185	amelocerebrohypohidrotic syndrome	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology|endocrinology|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder|throat_disorder|upper_gastrointestinal_disorder|joint_disorder|heart_disorder|immune_disorder|ear_disorder|skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0009186	epilepsy, photogenic, with spastic diplegia and intellectual disability	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009187	celiac disease-epilepsy-cerebral calcification syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|gastroenterology|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0009188	epilepsy-telangiectasia syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|skin_disorder	false	false	false	false	high
MONDO:0009189	multiple epiphyseal dysplasia type 4	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	genetic_disorder|metabolic_disorder|developmental_disorder|musculoskeletal_disorder	joint_disorder|bone_disorder|skeletal_disorder	false	false	false	false	medium
MONDO:0009190	epiphyseal dysplasia of femoral head, myopia, and deafness	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder|ear_disorder|bone_disorder	false	false	false	false	medium
MONDO:0009191	Lowry-Wood syndrome	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0009192	Wolcott-Rallison syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|endocrinology|pediatric	rare_disease|metabolic_disorder|endocrine_disease	endocrine_disorder|kidney_disorder	false	false	true	false	very_high
MONDO:0009193	epithelial squamous dysplasia, keratinizing desquamative, of urinary tract	hereditary_disease	other	hereditary_disease	oncology|urology|dermatology	inflammatory_disease|autoimmune_diseases|cancer	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0009194	immunodeficiency 32B	infectious_disease|hereditary_disease	infectious_disease	infectious_disease|post_infectious_disorder|hereditary_disease	immunology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	true	false	false	true	high
MONDO:0009195	erythema of acral regions	hereditary_disease	other	hereditary_disease	dermatology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|skin_disorder	false	false	false	false	medium
MONDO:0009196	ermine phenotype	syndromic_disease	other	syndromic_disease	genetics_and_genomics|dermatology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0009197	transient erythroblastopenia of childhood	hematologic_disorder	anemia	hematologic_disorder	hematology|pediatric	metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	true	low
MONDO:0009198	congenital lethal erythroderma	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric	inflammatory_disease|anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0009199	ethanolaminosis	hereditary_disease	other	hereditary_disease	hepatology|gastroenterology	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0009200	eyebrow duplication-syndactyly syndrome	syndromic_disease	other	syndromic_disease	dermatology|genetics_and_genomics|pediatric	inherited_disorder|metabolic_disorder|genetic_condition|congenital_abnormality	eye_disorder|joint_disorder|skin_disorder	false	false	false	false	low
MONDO:0009201	facial abnormalities, kyphoscoliosis, and intellectual disability	hereditary_disease	other	hereditary_disease	pediatrics|psychiatry|orthopaedic|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	facial_abnormality|spinal_disorder|intellectual_disability	false	false	false	true	high
MONDO:0009202	Thakker-Donnai syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0009203	focal facial dermal dysplasia type III	syndromic_disease|integumentary_system_disorder|hereditary_disease	other	syndromic_disease|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0009204	lethal faciocardiomelic dysplasia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	cardiology|pediatric|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	bone_disorder|heart_disorder|facial_disorder	false	false	false	false	very_high
MONDO:0009205	faciocardiorenal syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	cardiology|pediatric|genetics_and_genomics|renal_medicine	cardiovascular_disorder|metabolic_disorder|autoimmune_diseases	heart_disorder|liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0009206	factor V and factor VIII, combined deficiency of, type 1	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0009207	factor V and factor VIII, combined deficiency of, with normal protein C and protein C inhibitor	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0009208	faciothoracogenital syndrome	hereditary_disease	other	hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics|pediatric	genetic_disorder|metabolic_disorder	throat_disorder|eye_disorder|ear_disorder|joint_disorder|liver_disorder	false	false	false	false	high
MONDO:0009209	autosomal recessive faciodigitogenital syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|genetic_condition	reproductive_system_disorder|immune_disorder|bone_disorder|muscle_disorder|eye_disorder|ear_disorder|lymphatic_disorder|spinal_disorder|joint_disorder|liver_disorder|lower_gastrointestinal_disorder|vascular_disorder|skin_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0009210	congenital factor V deficiency	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	hematology|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease	immune_disorder|vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0009211	congenital factor VII deficiency	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0009212	congenital factor X deficiency	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	hematology|pediatric|genetics_and_genomics	anemia|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0009213	Fanconi anemia complementation group C	musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|immune_system_disorder|hematologic_disorder	anemia|metabolic_disease	hereditary_disease|hematologic_disorder|immune_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0009214	Fanconi anemia complementation group D2	hematologic_disorder|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|immune_system_disorder	anemia|metabolic_disease	hereditary_disease|hematologic_disorder|immune_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatrics|hematology|genetics_and_genomics	anemia|metabolic_disorder|genetic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0009215	Fanconi anemia complementation group A	hematologic_disorder|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|immune_system_disorder	anemia|metabolic_disease	hereditary_disease|hematologic_disorder|immune_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0009216	glycogen storage disease due to GLUT2 deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|hepatology|pediatric|genetics_and_genomics	metabolic_disorder|glycogen_storage_disease	endocrine_disorder|liver_disorder	false	false	true	false	high
MONDO:0009217	Fanconi-like syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	oncology|pediatric|genetics_and_genomics|hematatology	neurodegenerative_disease|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder|kidney_disorder	false	false	false	true	high
MONDO:0009218	Farber lipogranulomatosis	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	dermatology|oncology|pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|cancer	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0009219	fascial dystrophy, congenital	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0009220	visceral steatosis, congenital	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	gastroenterology|hepatology|pediatric|genetics_and_genomics	metabolic_disorder|congenital	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0009221	femur-fibula-ulna complex	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0009222	Gollop-Wolfgang complex	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0009223	hypogonadotropic hypogonadism 23 with or without anosmia	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	pediatrics|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0009224	fetal iodine syndrome	endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	thyroid_disorder_is_not_listed_so__endocrine_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0009225	fever, familial lifelong persistent	hereditary_disease	other	hereditary_disease	allergy_and_immunology|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases	immune_disorder|liver_disorder	false	false	false	false	medium
MONDO:0009226	fibrochondrogenesis 1	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	connective_tissue_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0009227	myofibromatosis, infantile, 1	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hereditary_disease	oncology|pediatric|genetics_and_genomics	cancer	bone_disorder|muscle_disorder	false	false	false	true	high
MONDO:0009228	gingival fibromatosis-facial dysmorphism syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	ophthalmology|dermatology|pediatric|genetics_and_genomics	metabolic_disorder	teeth_disorder|skin_disorder	false	false	false	false	medium
MONDO:0009229	hyaline fibromatosis syndrome	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	rheumatology|genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_condition	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0009230	fibrosclerosis, multifocal	immune_system_disorder|hereditary_disease	autoimmune_disease	hereditary_disease|immune_system_disorder	rheumatology|pulmonology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	liver_disorder|lung_disorder	false	false	false	false	high
MONDO:0009231	acromesomelic dysplasia 2B	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009232	Fuhrmann syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009233	Fibulo-ulnar hypoplasia-renal anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic|renal_medicine	metabolic_disorder|inflammatory_disease|renal_anomalies	bone_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0009234	congenital high-molecular-weight kininogen deficiency	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	pediatric|genetics_and_genomics	metabolic_disorder|congenital_disease	immune_disorder|liver_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0009235	familial benign flecked retina	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	low
MONDO:0009236	Kandori fleck retina	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0009237	focal epithelial hyperplasia	cancer_or_benign_tumor|hereditary_disease|infectious_disease	cancer_or_benign_tumor|infectious_disease	cancer_or_benign_tumor|infectious_disease|hereditary_disease	ophthalmology|dermatology|oncology	inflammatory_disease|cancer|epithelial_hyperplasia	upper_gastrointestinal_disorder|kidney_disorder	false	false	false	true	low
MONDO:0009238	hereditary folate malabsorption	metabolic_disease|hereditary_disease|digestive_system_disorder|hematologic_disorder	anemia|metabolic_disease	digestive_system_disorder|hereditary_disease|hematologic_disorder|metabolic_disease	gastroenterology|genetics_and_genomics	anemia|metabolic_disorder|inherited_condition	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0009239	hypogonadotropic hypogonadism 24 without anosmia	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	pediatrics|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0009240	formiminoglutamic aciduria	metabolic_disease|hereditary_disease|hematologic_disorder	anemia|metabolic_disease	hereditary_disease|hematologic_disorder|metabolic_disease	genetics_and_genomics|pediatric|renal_medicine	metabolic_disorder|hereditary_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0009241	fountain syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|adrenal_gland_disease|inflammatory_disease	endocrine_disorder|eye_disorder	false	false	false	false	high
MONDO:0009242	brittle cornea syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|connective_tissue_disorder|disorder_of_visual_system|hereditary_disease	other	connective_tissue_disorder|disorder_of_visual_system|hereditary_disease|syndromic_disease|disorder_of_orbital_region|disorder_of_development_or_morphogenesis	ophthalmology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	very_high
MONDO:0009243	Fraser-like syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	kidney_disorder|bone_disorder|ear_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009244	Freesia Flowers, inability to smell	hereditary_disease	other	hereditary_disease	otolaryngology|neurology	neurodegenerative_disease|autoimmune_diseases	nose_disorder|brain_disorder	false	false	false	false	low
MONDO:0009246	Friedreich ataxia and congenital glaucoma	hereditary_disease	other	hereditary_disease	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|congenital_condition	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009247	frontofacionasal dysplasia	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	otolaryngology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	nose_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0009248	fructose and galactose intolerance	hereditary_disease	other	hereditary_disease	gastroenterology|endocrinology	metabolic_disorder|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0009249	hereditary fructose intolerance	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	gastroenterology|hepatology|genetics_and_genomics|pediatric	metabolic_disorder|hereditary	kidney_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0009251	fructose-1,6-bisphosphatase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|endocrinology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|glycogen_storage_disorder	false	false	false	false	very_high
MONDO:0009252	essential fructosuria	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|renal_medicine	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	false	none
MONDO:0009253	Fryns syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	genetic_disorders|metabolic_disorder	joint_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0009254	fucosidosis	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	musculoskeletal_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	lymphatic_disorder|immunedisorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0009255	galactokinase deficiency	metabolic_disease|disorder_of_visual_system|hereditary_disease	metabolic_disease	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region|metabolic_disease	pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	endocrine_disorder|liver_disorder	false	false	false	false	low
MONDO:0009256	galactorrhea	disorder_of_development_or_morphogenesis|breast_disorder	other	breast_disorder|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|endocrinology|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	endocrine_disorder|liver_disorder	false	false	false	false	low
MONDO:0009257	galactose epimerase deficiency	metabolic_disease|disorder_of_visual_system|hereditary_disease	metabolic_disease	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region|metabolic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	genetic_disorder|liver_disorder	false	false	false	true	high
MONDO:0009258	classic galactosemia	endocrine_system_disorder|metabolic_disease|disorder_of_visual_system|reproductive_system_disorder|hereditary_disease	metabolic_disease|endocrine_system_disorder	disorder_of_visual_system|hereditary_disease|endocrine_system_disorder|disorder_of_orbital_region|metabolic_disease|reproductive_system_disorder	hepatology|endocrinology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0009259	gamma-glutamylcysteine synthetase deficiency	metabolic_disease|hereditary_disease|hematologic_disorder	anemia|metabolic_disease	hereditary_disease|hematologic_disorder|metabolic_disease	pediatrics|hepatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	metabolic_disorder|liver_disorder	false	false	false	true	medium
MONDO:0009260	GM1 gangliosidosis type 1	syndromic_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_visual_system|hereditary_disease	metabolic_disease	musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease|syndromic_disease|disorder_of_orbital_region|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0009261	GM1 gangliosidosis type 2	musculoskeletal_system_disorder|metabolic_disease|disorder_of_visual_system|hereditary_disease	metabolic_disease	musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0009262	GM1 gangliosidosis type 3	hereditary_disease|metabolic_disease|disorder_of_visual_system|musculoskeletal_system_disorder	metabolic_disease	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|metabolic_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0009263	GAPO syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0009264	gastroschisis	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	surgery|pediatric|gastroenterology	congenital_abnormality|gastrointestinal_disorder|prenatal_condition|surgical_condition	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0009265	Gaucher disease type I	hereditary_disease|metabolic_disease|nervous_system_disorder|cardiovascular_disorder|psychiatric_disorder|disorder_of_visual_system|musculoskeletal_system_disorder	metabolic_disease|psychiatric_disorder|cardiovascular_disorder	disorder_of_orbital_region|hereditary_disease|nervous_system_disorder|disorder_of_visual_system|metabolic_disease|psychiatric_disorder|cardiovascular_disorder|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder|joint_disorder	false	false	false	true	high
MONDO:0009266	Gaucher disease type II	hereditary_disease|metabolic_disease|disorder_of_visual_system	metabolic_disease	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|metabolic_disease	genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder|blood_bone_marrow_disorder|joint_disorder	false	false	false	true	very_high
MONDO:0009267	Gaucher disease type III	hereditary_disease|metabolic_disease|disorder_of_visual_system	metabolic_disease	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|metabolic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	bone_bone_marrow_disorder|liver_disorder|joint_disorder	false	false	false	true	very_high
MONDO:0009268	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome	hereditary_disease|metabolic_disease|disorder_of_visual_system	metabolic_disease	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|metabolic_disease	cardiology|genetics_and_genomics|neurology	metabolic_disorder|cardiovascular_disorder|neurodegenerative_disease	eye_disorder|blood_bone_marrow_disorder|joint_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0009269	geleophysic dysplasia 1	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	genetic_condition|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0009270	genito-palato-cardiac syndrome	disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder	cardiology|urology|pediatric|genetics_and_genomics|genitourinary_medicine_is_incorrect_in_this_list_as_it_does_not_exist__however__the_closest_category_would_be_urology___pediatric	autoimmune_diseases|metabolic_disorder|cardiovascular_disorder	palate_disorder|heart_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0009271	geroderma osteodysplastica	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|integumentary_system_disorder	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatrics|dermatology	metabolic_disorder|genetic_disorder	skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0009272	German syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|immune_system_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|immune_system_disorder	genetics_and_genomics|pediatrics|gastroenterology	metabolic_disorder|genetic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0009273	hydatidiform mole, recurrent, 1	reproductive_system_disorder|hereditary_disease|cancer_or_benign_tumor|obstetric_disorder	cancer_or_benign_tumor	hereditary_disease|reproductive_system_disorder|cancer_or_benign_tumor|obstetric_disorder	genetics_and_genomics|oncology|obstetrics_and_gynecology	cancer|gynecological_disorder	reproductive_system_disorder	false	false	false	true	high
MONDO:0009274	ghosal hematodiaphyseal dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic|hematology	autoimmune_diseases|inflammatory_disease|metabolic_disorder|anemia	blood_bone_marrow_disorder|spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009275	neonatal hemochromatosis	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|hepatology|genetics_and_genomics|hematology	metabolic_disorder|anemia	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0009276	Bernard-Soulier syndrome	hereditary_disease|syndromic_disease|hematologic_disorder	other	syndromic_disease|hereditary_disease|hematologic_disorder	pediatric|genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009277	glaucoma 3A	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	neurology|ophthalmology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	true	high
MONDO:0009279	triple-A syndrome	hereditary_disease|syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	syndromic_disease|hereditary_disease|endocrine_system_disorder	pediatric|pulmonology	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	lung_disorder|lower_gastrointestinal_disorder|triple_a_syndrome_is_primarily_associated_with___liver_disorder	false	false	false	false	very_high
MONDO:0009280	monosodium glutamate sensitivity	hereditary_disease	other	hereditary_disease	gastroenterology|neurology	allergy|inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0009281	glutaryl-CoA dehydrogenase deficiency	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0009282	multiple acyl-CoA dehydrogenase deficiency	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease|cardiovascular_disorder|musculoskeletal_system_disorder	metabolic_disease|cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|cardiovascular_disorder|musculoskeletal_system_disorder|mitochondrial_disease	pediatric|genetics_and_genomics|neurology	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009283	glutaric acidemia type 3	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder_muscle_disorder	false	false	false	false	medium
MONDO:0009284	glutathione synthetase deficiency without 5-oxoprolinuria	hereditary_disease|metabolic_disease|immune_system_disorder|hematologic_disorder	anemia|metabolic_disease	hereditary_disease|hematologic_disorder|immune_system_disorder|metabolic_disease	genetics_and_genomics|biochemistry|pediatrics	enzyme_deficiency|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0009285	gamma-glutamyl transpeptidase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|hepatology|genetics_and_genomics	metabolic_disorder|genetic_disorder|enzyme_disorder	liver_disorder|biliary_disorder	false	false	false	false	medium
MONDO:0009286	gluteal muscles, absence of	hereditary_disease	other	hereditary_disease	pediatric|orthopaedic|neurology	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009287	glycogen storage disease due to glucose-6-phosphatase deficiency type IA	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|pediatric|endocrinology	metabolic_disorder	liver_disorder|endocrine_disorder	false	false	true	false	very_high
MONDO:0009288	glycogen storage disease Ib	hereditary_disease|metabolic_disease|immune_system_disorder|hematologic_disorder	metabolic_disease	hereditary_disease|hematologic_disorder|metabolic_disease|immune_system_disorder	hepatology|genetics_and_genomics	metabolic_disorder|glycogen_storage_diseases	liver_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0009290	glycogen storage disease II	hereditary_disease|metabolic_disease|cardiovascular_disorder|musculoskeletal_system_disorder	metabolic_disease|cardiovascular_disorder	hereditary_disease|metabolic_disease|cardiovascular_disorder|musculoskeletal_system_disorder	hepatology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|cardiovascular_disorder	liver_disorder|muscle_disorder	false	false	true	true	very_high
MONDO:0009291	glycogen storage disease III	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|endocrinology	metabolic_disorder|neurodegenerative_disease	liver_disorder|endocrine_disorder|muscle_disorder	false	false	true	true	high
MONDO:0009292	glycogen storage disease due to glycogen branching enzyme deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics_hepatology	metabolic_disorder	kidney_disorder|liver_disorder|muscle_disorder	false	false	true	false	very_high
MONDO:0009293	glycogen storage disease V	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|pediatric	metabolic_disorder	liver_disorder|muscle_disorder	false	false	true	true	medium
MONDO:0009294	glycogen storage disease VI	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|cardiovascular_disorder|glycogen_storage_diseases	liver_disorder|muscle_disorder	false	false	true	true	low
MONDO:0009295	glycogen storage disease VII	hereditary_disease|metabolic_disease|hematologic_disorder	anemia|metabolic_disease	hereditary_disease|hematologic_disorder|metabolic_disease	hepatology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	true	false	medium
MONDO:0009296	glycoprotein storage disease	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder	false	false	false	true	high
MONDO:0009297	familial renal glucosuria	urinary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	urinary_system_disorder|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|renal_medicine	autoimmune_diseases|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0009298	GOMBO syndrome	hereditary_disease	other	hereditary_disease	pulmonology|hematology|rheumatology|neurology	autoimmune_diseases|neurodegenerative_disease	upper_gastrointestinal_disorder|immune_disorder	false	false	false	false	high
MONDO:0009299	46 XX gonadal dysgenesis	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics	reproductive_system_disorder|endocrine_disorder|metabolic_disorder|genetic_disorder|congenital_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0009300	Perrault syndrome 1	hereditary_disease|metabolic_disease|endocrine_system_disorder|reproductive_system_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder|metabolic_disease	disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder|metabolic_disease|hereditary_disease|mitochondrial_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0009301	46,XY sex reversal 7	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	endocrine_system_disorder|cardiovascular_disorder	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|cardiovascular_disorder	genetics_and_genomics|urology|endocrinology	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0009302	XY type gonadal dysgenesis-associated anomalies syndrome	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder	genetics_and_genomics|obstetrics_and_gynecology|endocrinology	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0009303	anti-glomerular basement membrane disease	immune_system_disorder	autoimmune_disease	immune_system_disorder	renal_medicine|hematology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|kidney_disorder	false	false	false	true	high
MONDO:0009305	granulocytopenia with immunoglobulin abnormality	hereditary_disease	other	hereditary_disease	hematology|immunology|allergy_and_immunology	anemia|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0009306	combined immunodeficiency with skin granulomas	hereditary_disease|integumentary_system_disorder|immune_system_disorder	other	immune_system_disorder|integumentary_system_disorder|hereditary_disease	pediatric|immunology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0009307	granulomatous disease with defect in neutrophil chemotaxis	inflammatory_disease|hereditary_disease|immune_system_disorder|hematologic_disorder	other	immune_system_disorder|inflammatory_disease|hereditary_disease|hematologic_disorder	pulmonology|hematology|rheumatology|immunology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0009308	granulomatous disease, chronic, autosomal recessive, cytochrome b-negative	inflammatory_disease|hereditary_disease|immune_system_disorder|hematologic_disorder	other	immune_system_disorder|inflammatory_disease|hereditary_disease|hematologic_disorder	genetics_and_genomics|genetics|pediatrics|rheumatology|immunology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0009309	granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 1	inflammatory_disease|hereditary_disease|immune_system_disorder|hematologic_disorder	other	immune_system_disorder|inflammatory_disease|hereditary_disease|hematologic_disorder	genetics_and_genomics|pulmonology|rheumatology|immunology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|lung_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0009310	granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2	hereditary_disease|immune_system_disorder|hematologic_disorder|inflammatory_disease	other	hematologic_disorder|inflammatory_disease|hereditary_disease|immune_system_disorder	genetics_and_genomics|rheumatology|pulmonology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|kidney_disorder|immune_disorder	false	false	false	true	high
MONDO:0009311	grouped pigmentation of the retina	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0009312	lipodystrophy due to peptidic growth factors deficiency	hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease	metabolic_disease|integumentary_system_disorder|hereditary_disease	dermatology|endocrinology	hormone_disorder|metabolic_disorder	skin_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0009313	Grubben-de Cock-Borghgraef syndrome	syndromic_disease	other	syndromic_disease	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0009315	congenital factor XII deficiency	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|congenital_factor_xii_deficiency_is_often_associated_with_bleeding_disorders__which_can_be_classified_as_a_specific_type_of_metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0009318	Hallermann-Streiff syndrome	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|immunology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	skin_disorder|blood_bone_marrow_disorder|immune_disorder|lung_disorder	false	false	false	false	high
MONDO:0009319	pantothenate kinase-associated neurodegeneration	hereditary_disease|psychiatric_disorder|metabolic_disease|nervous_system_disorder	neurodegenerative_disease|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009320	Hall-Riggs syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	kidney_disorder|vascular_disorder|endocrine_disorder|bone_disorder	false	false	false	false	high
MONDO:0009321	hallux varus-preaxial polysyndactyly syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	foot_disease|genetic_disorder|limb_abnormality|congenital_condition|deformity|neurodevelopmental_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0009323	Halothane hepatitis	hereditary_disease	other	hereditary_disease	hepatology|gastroenterology	adrenal_gland_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|lung_disorder	false	false	false	false	high
MONDO:0009324	Hartnup disease	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|renal_medicine|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|upper_gastrointestinal_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0009326	congenital heart block	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	pediatric|cardiology	cardiovascular_disorder|congenital_abnormality	congenital_disorder|heart_disorder	false	false	false	false	high
MONDO:0009327	heart, malformation of	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiothoracic|cardiology	cardiovascular_disorder|heart	heart|heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0009328	hemangiomatosis, cutaneous, with associated features	hereditary_disease	other	hereditary_disease	hematology|genetics_and_genomics|dermatology	cardiovascular_disorder|inflammatory_disease|metabolic_disorder|autoimmune_diseases|cancer	skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0009329	pulmonary venoocclusive disease 2	hereditary_disease|cardiovascular_disorder|respiratory_system_disorder	cardiovascular_disorder	cardiovascular_disorder|respiratory_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|pulmonology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0009330	hemangiopericytoma, malignant	cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	hematology|oncology	malignant_tumors|cancer	vascular_disorder|brain_disorder	false	true	false	false	high
MONDO:0009331	isolated hemihyperplasia	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|hematology	adrenal_gland_disease|inflammatory_disease|metabolic_disorder	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0009332	congenital hematological disorder	hematologic_disorder	other	hematologic_disorder	pediatric|hematology|genetics_and_genomics	metabolic_disorder|anemia	congenital_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0009333	mullerian derivatives-lymphangiectasia-polydactyly syndrome	immune_system_disorder|syndromic_disease	other	syndromic_disease|immune_system_disorder	pediatric|genetics_and_genomics|obstetrics_and_gynecology	inflammatory_disease|metabolic_disorder|autoimmune_diseases|cancer	reproductive_system_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0009334	hemolytic anemia with thermal sensitivity of red cells	hematologic_disorder	anemia	hematologic_disorder	hematology|genetics_and_genomics|allergy_and_immunology	anemia|autoimmune_diseases	blood_bone_marrow_disorder|vascular_disorder	true	false	false	true	high
MONDO:0009336	hemosiderosis, pulmonary, with deficiency of gamma-a globulin	metabolic_disease|respiratory_system_disorder	metabolic_disease	metabolic_disease|respiratory_system_disorder	hematology|immunology|pulmonology	metabolic_disorder|anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|lung_disorder	false	false	false	true	high
MONDO:0009337	Hennekam lymphangiectasia-lymphedema syndrome 1	hereditary_disease|immune_system_disorder|cardiovascular_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease|syndromic_disease|immune_system_disorder	pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder	skin_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0009338	hepatic veno-occlusive disease-immunodeficiency syndrome	digestive_system_disorder|hereditary_disease|immune_system_disorder|cardiovascular_disorder|endocrine_system_disorder	endocrine_system_disorder|cardiovascular_disorder	endocrine_system_disorder|cardiovascular_disorder|digestive_system_disorder|hereditary_disease|immune_system_disorder	hepatology|gastroenterology|immunology	inflammatory_disease|autoimmune_diseases	immune_disorder_liver_disorder	true	false	false	true	very_high
MONDO:0009339	congenital bile acid synthesis defect 2	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatrics|genetics_and_genomics|hepatology	inherited_condition|metabolic_disorder|congenital_disease	liver_disorder|biliary_disorder	false	false	false	false	very_high
MONDO:0009340	non-spherocytic hemolytic anemia due to hexokinase deficiency	hereditary_disease|metabolic_disease|hematologic_disorder	anemia|metabolic_disease	metabolic_disease|hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics|pediatric	metabolic_disorder|anemia	lysosomal_disorder|genetic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0009341	Mowat-Wilson syndrome	hereditary_disease|psychiatric_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	psychiatric_disorder	disorder_of_development_or_morphogenesis|psychiatric_disorder|hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|kidney_disorder|brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0009342	Hirschsprung disease-hearing loss-polydactyly syndrome	digestive_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|digestive_system_disorder|syndromic_disease	genetics_and_genomics|otolaryngology|pediatric	polydactyly_syndrome_is_not_a_distinct_category__however_this_condition_is_related_to_metabolic_disorder|metabolic_disorder	joint_disorder|polydactyly_is_associated_with_other_disorders_so_will_be_excluded_from_the_category_list___ear_disorder|ear_disorder	false	false	false	false	high
MONDO:0009343	Hirschsprung disease with ulnar polydactyly, polysyndactyly of big toes, and ventricular septal defect	hereditary_disease	other	hereditary_disease	cardiology|genetics_and_genomics|pediatric	cardiovascular_disorder|metabolic_disorder	lower_gastrointestinal_disorder|heart_disorder|joint_disorder	false	false	false	false	high
MONDO:0009344	Hirschsprung disease-nail hypoplasia-dysmorphism syndrome	digestive_system_disorder|syndromic_disease	other	digestive_system_disorder|syndromic_disease	genetics_and_genomics|pediatric	congenital_disorder|neurodevelopmental_disorder|genetic_disorder|metabolic_disorder	lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0009345	histidinemia	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	none
MONDO:0009346	histidinuria due to a renal tubular defect	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	renal_medicine|urology|genetics_and_genomics|nephrology|pediatric	renal_tubular_defect|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0009347	familial lipochrome histiocytosis	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|cancer	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0009348	classic Hodgkin lymphoma	hereditary_disease|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|hereditary_disease|post_infectious_disorder	hematology|oncology	lymphoma|autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0009349	holoprosencephaly 1	hereditary_disease|endocrine_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0009350	Holzgreve-Wagner-Rehder syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	liver_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0009351	homocarnosinosis	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009352	classic homocystinuria	hereditary_disease|disorder_of_visual_system|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_orbital_region|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|hematology|pediatrics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	kidney_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0009353	homocystinuria due to methylene tetrahydrofolate reductase deficiency	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	renal_medicine|genetics_and_genomics|hematology|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	kidney_disorder|vascular_disorder	false	false	false	true	high
MONDO:0009354	methylcobalamin deficiency type cblE	hereditary_disease|nutritional_disorder|hematologic_disorder|metabolic_disease	metabolic_disease|anemia	nutritional_disorder|hematologic_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|hematology|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|blood_bone_marrow_disorder|nervous_system_disorder_is_not_in_the_list_but_seems_to_fit_so_i_ve_used_a_similar_category_from_the_list___brain_disorder	true	false	false	true	high
MONDO:0009355	Hooft disease	hereditary_disease	other	hereditary_disease	orthopaedic|pediatric	metabolic_disorder	vascular_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0009356	autosomal recessive humeroradial synostosis	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0009357	humeroradial synostosis with craniofacial anomalies	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	cancer|inflammatory_disease|metabolic_disorder|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009358	Hutterite cerebroosteonephrodysplasia syndrome	hereditary_disease	other	hereditary_disease	renal_medicine|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|kidney_disorder|bone_disorder	false	false	false	false	high
MONDO:0009359	multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|kidney_disorder	true	false	false	false	very_high
MONDO:0009360	hydrocephalus, nonsyndromic, autosomal recessive 1	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|autosomal_recessive|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009361	autosomal recessive hydrocephalus due to congenital stenosis of aqueduct of Sylvius	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|urinary_tract_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009362	growth delay-hydrocephaly-lung hypoplasia syndrome	syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|syndromic_disease	genetics_and_genomics|neurology|pediatric	developmental_disorder|syndrome|congenital_disorder|growth_delay|neurodegenerative_disease|birth_defect	brain_disorder|growth_delay|lung_disorder	false	false	false	false	very_high
MONDO:0009363	hydrocephaly-tall stature-joint laxity syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|joint_laxity_syndrome_does_not_appear_to_be_directly_related_to_the_conditions_listed__however__i_will_remove__other__from_the_list_and_provide_the_categories__neurodegenerative_disease	brain_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009364	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1	metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0009365	hydrolethalus syndrome 1	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0009366	normal pressure hydrocephalus	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|pediatric	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0009367	McKusick-Kaufman syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009368	urofacial syndrome type 1	hereditary_disease	other	hereditary_disease	genetics_and_genomics|urology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|urofacial_syndrome_type_1_is_related_to_the_genitourinary_system__so_this_category_seems_most_appropriate|urinary_tract_disorder	false	false	false	false	medium
MONDO:0009369	non-immune hydrops fetalis	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatrics|genetics_and_genomics|allergy_and_immunology	metabolic_disorder|anemia	heart_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0009370	L-2-hydroxyglutaric aciduria	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0009371	3-hydroxyisobutyric aciduria	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	renal_medicine|genetics_and_genomics|pediatric	adrenal_gland_disease|metabolic_disorder	metabolic_disorder|liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0009372	encephalopathy due to hydroxykynureninuria	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0009373	seizures-intellectual disability due to hydroxylysinuria syndrome	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatrics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0009374	hydroxyprolinemia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|metabolic_disorders|pediatric	inherited_disease|metabolic_disorder|genetic_disorder	liver_disorder|kidney_disorder	false	false	false	false	low
MONDO:0009375	hymen, imperforate	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	obstetrics_and_gynecology|gynecology|pediatric	metabolic_disorder|autoimmune_diseases	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	true	low
MONDO:0009376	carbamoyl phosphate synthetase I deficiency disease	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	biochemistry|genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	metabolic_disorder|liver_disorder|enzyme_disorder	false	false	false	true	very_high
MONDO:0009377	hyperammonemia due to N-acetylglutamate synthase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	renal_medicine|genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0009378	hyper-beta-alaninemia	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	medical_genetics_is_not_listed_but_could_be_inferred_as_similar_to_genetics_and_genomics|genetics_and_genomics|pediatric	metabolic_disorder|anemia	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0009379	Rotor syndrome	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|vascular_disorder|brain_disorder	false	false	false	false	low
MONDO:0009380	Dubin-Johnson syndrome	hereditary_disease|metabolic_disease|syndromic_disease	metabolic_disease	metabolic_disease|hereditary_disease|syndromic_disease	hepatology|gastroenterology	inflammatory_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	false	low
MONDO:0009381	hyperbilirubinemia, conjugated, type 3	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|hematology	inflammatory_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0009382	hyperbilirubinemia, shunt, primary	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|hematology|pediatric	inflammatory_disease|metabolic_disorder|anemia	liver_disorder|shunt	false	false	false	false	high
MONDO:0009383	transient familial neonatal hyperbilirubinemia	hereditary_disease|metabolic_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease|hereditary_disease|digestive_system_disorder	hematology|genetics_and_genomics|hepatology|pediatric	neonatal_condition|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	true	low
MONDO:0009384	Leydig cell hypoplasia, type 1	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics|pediatric	endocrine_disease|metabolic_disorder|genetic_condition	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0009385	hyperleucine-Isoleucinemia	hereditary_disease	other	hereditary_disease	endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	metabolic_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0009386	hyperlexia	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0009387	familial lipoprotein lipase deficiency	hereditary_disease|metabolic_disease|syndromic_disease	metabolic_disease	metabolic_disease|hereditary_disease|syndromic_disease	biochemistry|genetics_and_genomics|pediatrics|physiology___corrected_list___genetics_and_genomics|pediatric	metabolic_disorder|familial_lipoprotein_lipase_deficiency_is_often_grouped_under_genetic_metabolic_disorders	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0009388	hyperlysinemia	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|genetics_and_genomics|pediatrics	cardiovascular_disorder|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0009389	hyperlysinemia due to defect in lysine transport into mitochondria	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|genetics_and_genomics|pediatric|metabolism	adrenal_gland_disease|cardiovascular_disorder|metabolic_disorder	endocrine_disorder|muscle_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0009390	hyperlysinuria with hyperammonemia	hereditary_disease	other	hereditary_disease	endocrinology|genetics_and_genomics|pediatrics|nephrology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0009391	hypermetabolism due to defect in mitochondria	hereditary_disease	other	hereditary_disease	endocrinology|genetics_and_genomics|pediatrics	mitochondrial_disease_is_often_associated_with_a_category_of_metabolic_disorder_however_in_this_case_it_is_specifically_due_to_a_defect_in_mitochondria_which_can_be_further_classified_as_a_mitochondrial_disease_category_is_not_listed__but_the_closest_one_is___metabolic_disorder|metabolic_disorder|neurodegenerative_disease	endocrine_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009392	hyperopia, high	hereditary_disease	other	hereditary_disease	neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	medium
MONDO:0009393	ornithine translocase deficiency	hereditary_disease|metabolic_disease|syndromic_disease	metabolic_disease	metabolic_disease|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatrics|metabolic	metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009394	juvenile Paget disease	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	endocrinology|hematology|genetics_and_genomics|pediatric	metabolic_disorder	blood_bone_marrow_disorder|bone_disorder	false	false	false	true	high
MONDO:0009395	hyperostosis corticalis generalisata	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|rheumatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0009396	hyperparathyroidism, neonatal self-limited primary, with hypercalciuria	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|renal_medicine	autoimmune_diseases|hyperparathyroidism_is_a_disorder_of_the_parathyroid_glands_which_can_be_considered_as_a_type_of_metabolic_disorder|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0009397	neonatal severe primary hyperparathyroidism	endocrine_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	hereditary_disease|musculoskeletal_system_disorder|endocrine_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	endocrinology|pediatric|renal_medicine	hormonal_disorders|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0009398	hyperphosphatasia with intellectual disability syndrome 1	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	metabolic_disease	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|metabolic_disease	neurology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|bone_disorder	false	false	false	false	high
MONDO:0009399	hyperphosphatemia, polyuria, and seizures	hereditary_disease	other	hereditary_disease	endocrinology|neurology|renal_medicine	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0009400	hyperprolinemia type 1	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatrics|genetics_and_genomics	amino_acid_imbalance|inherited_disease|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0009401	hyperprolinemia type 2	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	metabolic_disorder|kidney_disorder|genetic_disorder	false	false	false	false	medium
MONDO:0009402	acrofrontofacionasal dysostosis 2	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|otolaryngology|pediatrics|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	other____bone_disorder_is_the_most_prominent_category|upper_gastrointestinal_disorder|skin_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0009403	hypertelorism and tetralogy of fallot	hereditary_disease	other	hereditary_disease	cardiology|pediatric	tetralogy_of_falott|cardiovascular_disorder	heart_disorder|lung_disorder	false	false	false	hypertelorism_is_a_condition_characterized_by_an_increased_distance_between_the_eyes__often_associated_with_various_syndromes__whereas_tetralogy_of_fallot_is_a_congenital_heart_defect_that_involves_four_specific_heart_abnormalities___currently__there_are_no_treatments_that__cure__hypertelorism__however__surgical_options_are_available_to_correct_severe_instances__primarily_for_cosmetic_and_functional_purposes__for_tetralogy_of_fallot__surgical_intervention_is_typically_required_to_correct_the_heart_defects__which_is_effective_and_can_significantly_improve_the_quality_of_life_for_those_affected___given_this_information_____for_hypertelorism__treatments_exist__but_they_are_not_curative_and_are_more_focused_on_correction_____for_tetralogy_of_fallot__efficacious_treatments__surgery__exist_that_are_considered_curative_in_improving_heart_function_and_overall_health___since_efficacious_treatments_exist_for_tetralogy_of_fallot__we_will_return_true___true	medium
MONDO:0009404	hypertelorism, microtia, facial clefting syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	otolaryngology|pediatric	metabolic_disorder|autoimmune_diseases|facial_clefting_syndrome	facial_clefting_syndrome_is_a_condition_that_affects_the_ear_and_face_so_it_also_belongs_to|nose_disorder|microtia_is_a_condition_of_the_outer_ear__specifically_affecting_its_size_or_shape__which_means_it_also_belongs_to_nose_disorder|ear_disorder	false	false	false	false	high
MONDO:0009405	cervical hypertrichosis-peripheral neuropathy syndrome	nervous_system_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|dermatology|obstetrics_and_gynecology	autoimmune_diseases|neurodegenerative_disease	skin_disorder|reproductive_system_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0009406	hypertrichotic osteochondrodysplasia Cantu type	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|dermatology|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease	skin_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0009407	hypertrophic neuropathy and cataract	hereditary_disease	other	hereditary_disease	neurology|ophthalmology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0009408	hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase	hereditary_disease	other	hereditary_disease	renal_medicine|genetics_and_genomics|pediatric|rheumatology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|joint_disorder	false	false	false	true	high
MONDO:0009411	autoimmune polyendocrine syndrome type 1	syndromic_disease|hereditary_disease|endocrine_system_disorder|immune_system_disorder	endocrine_system_disorder|autoimmune_disease	immune_system_disorder|syndromic_disease|endocrine_system_disorder|hereditary_disease	endocrinology|pediatric|rheumatology|allergy_and_immunology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0009412	scurvy	metabolic_disease|nutritional_disorder	metabolic_disease	nutritional_disorder|metabolic_disease	hematology|dermatology	metabolic_disorder|anemia	lower_gastrointestinal_disorder|bone_disorder	false	false	false	true	medium
MONDO:0009413	immunodeficiency, common variable, 2	cancer_or_benign_tumor|syndromic_disease|hereditary_disease|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|syndromic_disease|hematologic_disorder|cancer_or_benign_tumor|hereditary_disease	immunology|allergy_and_immunology	immunodeficiency|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0009414	glycogen storage disorder due to hepatic glycogen synthase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|hepatology|pediatric|genetics_and_genomics	metabolic_disorder	liver_disorder|muscle_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0009415	hypoglycemia, leucine-induced	hereditary_disease	other	hereditary_disease	endocrinology|pediatric	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0009416	hypoinsulinemic hypoglycemia and body hemihypertrophy	hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	endocrinology|pediatric|genetics_and_genomics	body_hemihypertrophy|metabolic_disorder	muscle_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0009417	hypergonadotropic hypogonadism-cataract syndrome	syndromic_disease	other	syndromic_disease	endocrinology|ophthalmology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	reproductive_system_disorder|endocrine_disorder|eye_disorder	false	false	false	false	medium
MONDO:0009418	hypogonadism with low-grade mental deficiency and microcephaly	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0009419	Woodhouse-Sakati syndrome	nervous_system_disorder|hereditary_disease|metabolic_disease|endocrine_system_disorder|reproductive_system_disorder|psychiatric_disorder	endocrine_system_disorder|psychiatric_disorder|metabolic_disease|neurodegenerative_disease	endocrine_system_disorder|psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease|reproductive_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|nerve_conduction_disorder	false	false	false	false	high
MONDO:0009420	primary hypergonadotropic hypogonadism-partial alopecia syndrome	syndromic_disease	other	syndromic_disease	endocrinology|urology|dermatology|genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0009421	hypogonadism, male	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrinology|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0009422	hypohidrosis with abnormal palmar dermal Ridges	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	skin_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0009423	hypokalemic alkalosis, familial, with specific renal tubulopathy	hereditary_disease	other	hereditary_disease	renal_medicine|genetics_and_genomics	renal_tubulopathy|metabolic_disorder	muscle_disorder|kidney_disorder|renal_tubulopathy	false	false	false	true	high
MONDO:0009424	Bartter disease type 2	syndromic_disease|hereditary_disease|urinary_system_disorder	other	syndromic_disease|hereditary_disease|urinary_system_disorder	renal_medicine|genetics_and_genomics|pediatric	kidney_disease|renal_disease|metabolic_disorder|electrolyte_disorder	kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0009425	hypomandibular faciocranial dysostosis	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|otolaryngology|genetics_and_genomics|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	skeletal_disorder|facial_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0009426	hypoparathyroidism-retardation-dysmorphism syndrome	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	endocrinology|genetics_and_genomics|pediatric	endocrine_disease|metabolic_disorder	skeletal_disorder|growth_disorder|endocrine_disorder|developmental_disorder|bone_disorder	false	false	false	false	high
MONDO:0009429	hypophosphatemia, renal, with intracerebral calcifications	hereditary_disease	other	hereditary_disease	neurology|renal_medicine	renal_disease|metabolic_disorder	kidney_disorder|endocrine_disorder|bone_disorder	false	false	false	false	high
MONDO:0009430	hypophosphatemic rickets, autosomal recessive, 1	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	endocrinology|orthopaedic|pediatric|genetics_and_genomics	autosomal_recessive|metabolic_disorder	kidney_disorder|endocrine_disorder|bone_disorder	false	false	false	true	high
MONDO:0009431	hereditary hypophosphatemic rickets with hypercalciuria	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	nephrology|pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|endocrine_disorder|bone_disorder	false	false	false	false	high
MONDO:0009432	hypopituitarism, congenital, with central diabetes insipidus	hereditary_disease	other	hereditary_disease	endocrinology|pediatric	adrenal_gland_disease|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0009433	hypoplastic left heart syndrome 1	syndromic_disease|hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	cardiology|pediatric	congenital_abnormality|heart_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0009434	hypoproteinemia, hypercatabolic	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	endocrinology|hepatology|hematology|pediatric	metabolic_disorder|hypercatabolic___note__the_term__hypercatabolic__itself_indicates_a_condition_of_excessive_breakdown_of_proteins_in_the_body__which_is_closely_related_to_hypoproteinemia__low_protein_levels	liver_disorder|kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0009435	hypospadias-intellectual disability, Goldblatt type syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|urology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	urinary_tract_disorder|brain_disorder	false	false	false	false	high
MONDO:0009436	congenital hypothalamic hamartoma syndrome	syndromic_disease|hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	endocrine_disorder|brain_disorder	false	false	false	false	high
MONDO:0009437	Bamforth-Lazarus syndrome	syndromic_disease|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0009438	hypouricemia, hypercalcinuria, and decreased bone density	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	endocrinology|renal_medicine|rheumatology	adrenal_gland_disease|metabolic_disorder|anemia	kidney_disorder|endocrine_disorder|bone_disorder	false	false	false	false	low
MONDO:0009439	autosomal recessive congenital ichthyosis 2	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disease_is_not_in_the_list__so_i_ll_leave_it_out_____metabilic_disorder	immune_disorder|liver_disorder|skin_disorder	false	false	false	false	medium
MONDO:0009440	ichthyosiform erythroderma, corneal involvement, and hearing loss	hereditary_disease|syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|otolaryngology|neurology|ophthalmology|dermatology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	skin_disorder|eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0009441	autosomal recessive congenital ichthyosis 1	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|ichthyosis	false	false	false	false	medium
MONDO:0009442	ichthyosis congenita with biliary atresia	hereditary_disease	other	hereditary_disease	hepatology|genetics_and_genomics|pediatric|dermatology	inflammatory_disease|metabolic_disorder	skin_disorder|liver_disorder	false	false	false	false	high
MONDO:0009443	autosomal recessive congenital ichthyosis 4B	hereditary_disease|integumentary_system_disorder|disorder_of_visual_system	other	integumentary_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder	skin_disorder|liver_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0009444	ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|dermatology	neurodegenerative_disease|metabolic_disorder	skin_disorder|intellectual_disability_is_a_symptom_so_also_brain_disorder|joint_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0009445	ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome	nervous_system_disorder|hereditary_disease|syndromic_disease	other	nervous_system_disorder|hereditary_disease|syndromic_disease	pediatric|hepatology|genetics_and_genomics|neurology|dermatology	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	high
MONDO:0009446	ichthyosis-intellectual disability-dwarfism-renal impairment syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|renal_medicine|neurology|dermatology	genetic_disorder_is_replaced_to_match_the_actual_list__metabolic_disorder|genetic_disorder|neurodegenerative_disease|metabolic_disorder	skin_disorder|kidney_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0009447	ichthyosis, split hairs, and amino aciduria	hereditary_disease	other	hereditary_disease	genetics_and_genomics|renal_medicine|dermatology	genetic_disorder|metabolic_disorder	skin_disorder|split_hairs____skin_disorder|amino_aciduria____kidney_disorder	false	false	false	true	medium
MONDO:0009448	iminoglycinuria	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	urology|pediatric|renal_medicine	renal_dysfunction|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	true	low
MONDO:0009449	ciliary dyskinesia with defective radial spokes	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease|syndromic_disease	pulmonology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	lung_disorder|eye_disorder	true	false	false	true	high
MONDO:0009450	ciliary dyskinesia with excessively long cilia	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease|syndromic_disease	pulmonology|pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	lung_disorder|eye_disorder	false	false	false	false	high
MONDO:0009451	Nezelof syndrome	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	pulmonology|genetics_and_genomics|neurology|allergy_and_immunology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0009452	Vici syndrome	hereditary_disease|immune_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|immune_system_disorder|syndromic_disease	pulmonology|psychiatry|neurology|pediatrics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0009454	immunodeficiency-centromeric instability-facial anomalies syndrome 1	premature_aging_syndrome|hereditary_disease	other	hereditary_disease|premature_aging_syndrome	pediatric|genetics_and_genomics|immunology	developmental_disorder|genetic_disorder|immune_disorders	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0009456	Immunoerythromyeloid hypoplasia	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	pediatric|immunology|hematology	anemia|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0009457	immunoglobulin d level in plasma, low	hereditary_disease	other	hereditary_disease	hematolog|allergy_and_immunology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0009458	Schimke immuno-osseous dysplasia	hereditary_disease|immune_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|immune_system_disorder	pediatric|genetics_and_genomics|rheumatology	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|bone_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0009459	channelopathy-associated congenital insensitivity to pain, autosomal recessive	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	skin_disorder|nerve_disorder	false	false	false	false	medium
MONDO:0009460	indolylacroyl glycinuria with intellectual disability	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	intellectual_disability_is_a_type_of_brain_disorder_so_it_s_included_in_this_category|kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0009461	spermatogenic failure 5	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	endocrinology|urology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|anemia	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0009462	inosine phosphorylase deficiency, immune defect due to	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|immunology|allergy_and_immunology	immunodeficiency_diseases|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	true	false	false	false	medium
MONDO:0009463	internal carotid arteries, hypoplasia of	hereditary_disease	other	hereditary_disease	neurology|cardiology	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0009464	immunodeficiency with defective T-cell response to interleukin 1	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|immunology|allergy_and_immunology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|lymphatic_disorder	true	false	false	false	high
MONDO:0009465	multiple intestinal atresia	digestive_system_disorder|disorder_of_development_or_morphogenesis	other	digestive_system_disorder|disorder_of_development_or_morphogenesis	pediatric|gastroenterology	inflammatory_disease|gastrointestinal_disease|congenital_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0009467	natal teeth-intestinal pseudoobstruction-patent ductus syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|cardiology|gastroenterology	intestinal_pseudoobstruction|autoimmune_diseases|cardiovascular_disorder|patent_ductus_syndrome|metabolic_disorder	lower_gastrointestinal_disorder|teeth_disorder	false	false	false	false	high
MONDO:0009468	pseudotumor cerebri	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0009469	benign recurrent intrahepatic cholestasis type 1	digestive_system_disorder|hereditary_disease|syndromic_disease|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	metabolic_disease|digestive_system_disorder|hereditary_disease|syndromic_disease|endocrine_system_disorder	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	false	medium
MONDO:0009470	Baraitser-Winter syndrome 1	nervous_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	skin_disorder|ear_disorder	false	false	false	false	high
MONDO:0009471	intrinsic factor and r binder, combined congenital deficiency of	hereditary_disease|nutritional_disorder|metabolic_disease|hematologic_disorder	anemia|metabolic_disease	metabolic_disease|hematologic_disorder|hereditary_disease|nutritional_disorder	pediatric|genetics_and_genomics|hematoloy|hematology	anemia|metabolic_disorder	upper_gastrointestinal_disorder|blood_bone_marrow_disorder|immune_disorder	true	false	false	true	high
MONDO:0009472	acetylation, slow	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|neurology|cardiology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0009473	isotretinoin-like syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|liver_disorder	false	false	false	false	high
MONDO:0009474	isovaleric acid, inability to smell	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	nose_disorder|brain_disorder	true	false	false	true	low
MONDO:0009475	isovaleric acidemia	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	lower_gastrointestinal_disorder|kidney_disorder|muscle_disorder|liver_disorder	false	false	false	true	high
MONDO:0009476	atresia of small intestine	digestive_system_disorder|disorder_of_development_or_morphogenesis	other	digestive_system_disorder|disorder_of_development_or_morphogenesis	pediatric|gastroenterology	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0009477	Stromme syndrome	hereditary_disease|syndromic_disease|respiratory_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|respiratory_system_disorder|syndromic_disease	pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	ear_disorder	false	false	false	false	high
MONDO:0009478	combined immunodeficiency due to DOCK8 deficiency	hereditary_disease|immune_system_disorder|hematologic_disorder	other	hematologic_disorder|hereditary_disease|immune_system_disorder	pediatric|genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease|allergy	lymphatic_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0009479	Johanson-Blizzard syndrome	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	psychiatric_disorder	auditory_system_disorder|disorder_of_development_or_morphogenesis|psychiatric_disorder|nervous_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|kidney_disorder|eye_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0009480	Joubert syndrome with oculorenal defect	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	neurodegenerative_disease	syndromic_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0009481	Jumping Frenchmen of Maine	hereditary_disease	other	hereditary_disease	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	mental_health_disorder|brain_disorder	false	false	false	false	low
MONDO:0009482	hypogonadotropic hypogonadism 3 with or without anosmia	hereditary_disease|syndromic_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|psychiatry|neurology|endocrinology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0009483	Kapur-Toriello syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|skin_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0009484	primary ciliary dyskinesia 1	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	syndromic_disease|respiratory_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatrics	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	lung_disorder|eye_disorder|kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0009485	oculocerebrofacial syndrome, Kaufman type	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0009486	autosomal recessive Kenny-Caffey syndrome	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|eye_disorder|ear_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0009487	keratoconus and congenital hip dysplasia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|ophthalmology	inflammatory_disease|autoimmune_diseases	joint_disorder|eye_disorder	false	false	false	for_keratoconus__there_are_treatments_available_that_can_help_manage_the_condition__such_as_rigid_gas_permeable_contact_lenses__corneal_cross_linking__and_in_some_cases__surgical_interventions_like_corneal_transplant__however__there_is_no_definitive_cure___for_congenital_hip_dysplasia__treatments_are_available_that_are_quite_effective__especially_when_diagnosed_early__these_can_include_physical_therapy__bracing__such_as_the_pavlik_harness___and_in_some_cases__surgery_to_correct_the_hip_joint___based_on_the_above_information__the_answer_is___false	medium
MONDO:0009488	keratoconus posticus circumscriptus	hereditary_disease	other	hereditary_disease	pediatric|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0009489	hereditary palmoplantar keratoderma, Gamborg-Nielsen type	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|dermatology	skin_disease|metabolic_disorder	skin_disorder	false	false	false	false	medium
MONDO:0009490	Papillon-Lefevre disease	hereditary_disease|immune_system_disorder|integumentary_system_disorder|syndromic_disease|hematologic_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	metabolic_disease	syndromic_disease|integumentary_system_disorder|hematologic_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|immune_system_disorder	pediatric|genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0009491	Haim-Munk syndrome	hereditary_disease|integumentary_system_disorder|syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	syndromic_disease|integumentary_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0009492	succinyl-CoA:3-ketoacid CoA transferase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|hepatology|endocrinology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0009493	Richards-Rundle syndrome	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0009495	Keutel syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	bone_disorder|ear_disorder	false	false	false	false	high
MONDO:0009496	Kniest-like dysplasia with pursed lips and ectopia lentis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|ophthalmology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|eye_disorder|bone_disorder	false	false	false	false	medium
MONDO:0009497	Kifafa seizure disorder	hereditary_disease	other	hereditary_disease	pediatric|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0009498	lethal Kniest-like dysplasia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|rheumatology	rare_disease|genetic_disease|metabolic_disorder	joint_disorder|blood_bone_marrow_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0009499	Krabbe disease	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|metabolic_disease	neurodegenerative_disease|metabolic_disease	disorder_of_orbital_region|metabolic_disease|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009501	metabolic myopathy due to lactate transporter defect	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	pulmonology|endocrinology|gastroenterology|renal_medicine|cardiology|neurology|hematology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0009502	pyruvate dehydrogenase E2 deficiency	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	endocrinology|neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	very_high
MONDO:0009503	pyruvate dehydrogenase E3-binding protein deficiency	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	neurology|pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0009504	mitochondrial DNA depletion syndrome 9	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	neurology|pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009505	lactic aciduria due to D-lactic acid	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	gastroenterology|renal_medicine|pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	kidney_disorder|liver_disorder	true	false	false	true	low
MONDO:0009506	specific granule deficiency	immune_system_disorder|hematologic_disorder|hereditary_disease	other	hematologic_disorder|immune_system_disorder|hereditary_disease	immunology|allergy_and_immunology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0009507	Lambert syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pulmonology|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0009508	Lambotte syndrome	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|lung_disorder	false	false	false	as_of_my_last_knowledge_update_in_october_2023__there_are_no_specific_treatments_that_cure_or_prevent_lambotte_syndrome__which_is_a_rare_inherited_disorder_characterized_by_a_progressive_decline_in_muscle_strength_and_function__particularly_affecting_the_arms_and_legs__treatment_generally_focuses_on_managing_symptoms_and_improving_quality_of_life_through_physical_therapy__occupational_therapy__and_supportive_care___therefore__regarding_whether_efficacious_treatments_exist_that_cure__prevent__or_treat_this_disease__the_answer_is_false	low
MONDO:0009509	Landau-Kleffner syndrome	syndromic_disease|nervous_system_disorder|hereditary_disease	other	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|pediatric	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0009511	Larsen-like syndrome, B3GAT3 type	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis|metabolic_disease	cardiovascular_disorder|metabolic_disease	musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	rheumatology|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	skin_disorder|joint_disorder|muscle_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0009512	lethal Larsen-like syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0009513	laryngo-onycho-cutaneous syndrome	hereditary_disease|respiratory_system_disorder|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|respiratory_system_disorder|integumentary_system_disorder|hereditary_disease	dermatology|otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	skin_disorder|ear_disorder|throat_disorder	false	false	false	false	very_high
MONDO:0009514	Laurence-Moon syndrome	hereditary_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	ophthalmology|neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0009515	Norum disease	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetic_disorder|cardiology|neurology|psychiatry|pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0009516	absence deformity of leg-cataract syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	ophthalmology|orthopaedic|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	eye_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009517	Donohue syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	endocrinology|pediatric	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|kidney_disorder|lower_gastrointestinal_disorder	false	false	false	true	very_high
MONDO:0009519	letterer-Siwe disease	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	dermatology|immunology|oncology|pediatrics	cancer|inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0009520	3-hydroxy-3-methylglutaric aciduria	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	true	high
MONDO:0009521	leukemia, acute myelocytic, with polyposis coli and colon cancer	hereditary_disease	other	acute_disease|hereditary_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder_lower_gastrointestinal_disorder__upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0009522	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	skin_disorder|blood_bone_marrow_disorder|immune_disorder|teeth_disorder	true	false	false	false	very_high
MONDO:0009523	Lichtenstein syndrome	immune_system_disorder|hematologic_disorder	other	hematologic_disorder|immune_system_disorder	rheumatology|endocrinology|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|vascular_disorder|kidney_disorder|liver_disorder|joint_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0009524	intellectual disability-spasticity-ectrodactyly syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	neurology|psychiatry|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009525	split hand-foot malformation 3	musculoskeletal_system_disorder|chromosomal_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	chromosomal_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0009526	fibular aplasia, tibial campomelia, and oligosyndactyly syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0009527	lipase deficiency, combined	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	gastroenterology|hepatology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0009528	chylomicron retention disease	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|gastroenterology|hepatology|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|lymphatic_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0009529	pyruvate dehydrogenase E3 deficiency	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	metabolic_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0009530	lipoid proteinosis	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	otolaryngology|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0009532	Miller-Dieker lissencephaly syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	other	chromosomal_disorder|syndromic_disease|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0009533	Dahlberg-Borer-Newcomer syndrome	syndromic_disease|immune_system_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	syndromic_disease|integumentary_system_disorder|immune_system_disorder|cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|psychiatry|pediatric|genetics_and_genomics|obstetrics_and_gynecology	mental_health_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|bone_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0009534	chronic mucocutaneous candidiasis due to inhibition of lymphoblastic transformation	immune_system_disorder|integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|immune_system_disorder|hereditary_disease	hematology|immunology|oncology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder_lymphatic_disorder_skin_disorder	true	false	false	true	high
MONDO:0009536	chronic mucocutaneous candidiasis due to intrinsic defect in lymphoblastic transformation	immune_system_disorder|integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|immune_system_disorder|hereditary_disease	hematology|immunology|pediatric|genetics_and_genomics	cancer|inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0009537	lymphoid interstitial pneumonia	respiratory_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	inflammatory_disease|respiratory_system_disorder|idiopathic_disease|infectious_disease	pulmonology|allergy_and_immunology|hematatology	inflammatory_disease|autoimmune_diseases	lung_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0009538	lymphoid system deterioration, progressive	hereditary_disease	other	hereditary_disease	hematology|immunology	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	true	false	false	false	high
MONDO:0009539	lymphoblastic leukemia, acute, with lymphomatous features	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|acute_disease|hematologic_disorder	hematology|oncology|hematolo|gynecology|pediatric	lymphoma|cancer|inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0009540	chronic mucocutaneous candidiasis due to lymphokine deficiency	immune_system_disorder|integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|immune_system_disorder|hereditary_disease	immunology|allergy_and_immunology|pediatrics	inflammatory_disease|autoimmune_diseases|immunological_disorder	immune_disorder_lymphatic_disorder_skin_disorder	true	false	false	true	high
MONDO:0009541	lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis	hereditary_disease	other	hereditary_disease	rheumatology|allergy_and_immunology|renal_medicine|hematology	inflammatory_disease|autoimmune_diseases|anemia	kidney_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0009542	lysine malabsorption syndrome	digestive_system_disorder|hereditary_disease	other	digestive_system_disorder|hereditary_disease	gastroenterology|genetics_and_genomics	lysine_malabsorption_syndrome_is_not_a_mental_health_disorder|lysine_malabsorption_syndrome_is_not_a_cancer|lysine_malabsorption_syndrome_is_not_a_neurodegenerative_disease|metabolic_disorder|lysine_malabsorption_syndrome_is_not_a_cardiovascular_disorder|lysine_malabsorption_syndrome_is_not_an_autoimmune_disease|lysine_malabsorption_syndrome_is_not_an_adrenal_gland_disease|lysine_malabsorption_syndrome_is_not_an_anemia|lysine_malabsorption_syndrome_is_not_an_inflammatory_disease|lysine_malabsorption_syndrome_is_not_an_allergy	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0009543	prominent glabella-microcephaly-hypogenitalism syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	endocrinology|pediatric|genetics_and_genomics	microcephaly_hypogenitalism_syndrome_is_also_related_to_congenital_adrenal_hyperplasia_which_falls_under_metabolic_disorder|metabolic_disorder	endocrine_disorder|brain_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0009544	macrocephaly/megalencephaly syndrome, autosomal recessive	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009545	macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance	hereditary_disease	other	hereditary_disease	endocrinology|genetics_and_genomics|dermatology|orthopaedic	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0009546	macrosomia adiposa congenita	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	adiposity_congenita_is_often_associated_with_metabolic_disorders_so_this_category_is_likely_the_best_fit|metabolic_disorder	endocrine_disorder|skin_disorder	false	false	false	false	high
MONDO:0009547	macrosomia-microphthalmia-cleft palate syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	ophthalmology|otolaryngology|pediatric|genetics_and_genomics|obstetrics_and_gynecology	genetic_disorder_is_the_best_fitting_category_for_macrosomia_microphthalmia_cleft_palate_syndrome__however_since_it_s_not_listed_in_the_category_list_the_next_closest_would_be__metabolic_disorder|metabolic_disorder	eye_disorder|cleft_palate_syndrome_is_typically_categorized_under_facial_deformity_which_aligns_with_the_ear_disorder_category_as_well	false	false	false	false	very_high
MONDO:0009548	renal hypomagnesemia 5 with ocular involvement	disorder_of_visual_system|urinary_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|urinary_system_disorder|hereditary_disease|metabolic_disease	ophthalmology|renal_medicine|urology	metabolic_disorder|inherited_condition|renal_disease	endocrine_disorder|eye_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0009549	severe early-childhood-onset retinal dystrophy	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0009550	renal hypomagnesemia 3	urinary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	urinary_system_disorder|metabolic_disease|hereditary_disease	nephrology|renal_medicine|urology	metabolic_disorder|renal_disease	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0009551	magnesium, elevated red cell	hereditary_disease	other	hereditary_disease	renal_medicine|hematology	metabolic_disorder|anemia	endocrine_disorder|kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0009552	mal de Meleda	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0009554	3MC syndrome 3	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder|ear_disorder|reproductive_system_disorder|kidney_disorder|heart_disorder|blood_bone_marrow_disorder|joint_disorder|spinal_disorder|upper_gastrointestinal_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0009555	malocclusion and short stature	hereditary_disease	other	hereditary_disease	endocrinology|pediatric	short_stature_is_a_characteristic_of_pituitary_gland_disorders_which_often_lead_to_metabolic_disorder|metabolic_disorder	teeth_disorder|bone_disorder	false	false	false	false	low
MONDO:0009556	malonic aciduria	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	metabolic_disorders|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0009557	mandibuloacral dysplasia with type A lipodystrophy	musculoskeletal_system_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|integumentary_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	endocrinology|genetics_and_genomics|dermatology	lipodystrophy|metabolic_disorder	teeth_disorder|skin_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0009558	Treacher Collins syndrome 3	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	otolaryngology|pediatric|genetics_and_genomics	facial_abnormality|skeletal_system_disorder|birth_defect|genetic_disorder|ear_nose_throat_disorder|congenital_disorder|developmental_disorder|craniofacial_anomaly|neurodegenerative_disease|physical_disability|rare_genetic_condition	face_disorder|ear_disorder|throat_disorder	false	false	false	false	medium
MONDO:0009559	mandibulofacial dysostosis with mental deficiency	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|mental_health_disorder	teeth_disorder|joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0009560	oculotrichoanal syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	ophthalmology|neurology|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	eye_disorder|throat_disorder	false	false	false	false	high
MONDO:0009561	alpha-mannosidosis	disorder_of_visual_system|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	disorder_of_orbital_region|disorder_of_visual_system|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009562	beta-mannosidosis	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009563	maple syrup urine disease	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	renal_medicine|pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0009564	Marden-Walker syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009565	microcephaly-glomerulonephritis-marfanoid habitus syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	renal_medicine|pediatrics|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0009566	marfanoid habitus-autosomal recessive intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	intellectual_disability_is_covered_by_brain_disorder|eye_disorder|heart_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0009567	Marinesco-Sjogren syndrome	syndromic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	rheumatology|pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	eye_disorder|joint_disorder|muscle_disorder|bone_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0009568	mast syndrome	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	allergy_and_immunology|dermatology	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0009569	Hennekam-Beemer syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	dermatology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	ear_disorder|skin_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0009570	McDonough syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|renal_medicine|endocrinology	autoimmune_diseases|metabolic_disorder	kidney_disorder	false	false	false	false	very_high
MONDO:0009571	Meckel syndrome, type 1	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0009572	autosomal recessive familial Mediterranean fever	syndromic_disease|connective_tissue_disorder|hereditary_disease|immune_system_disorder	other	syndromic_disease|immune_system_disorder|connective_tissue_disorder|hereditary_disease	pediatric|genetics_and_genomics|rheumatology	inflammatory_disease|metabolic_disorder	lymphatic_disorder|liver_disorder|vascular_disorder|immune_disorder|kidney_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|joint_disorder	false	false	false	true	medium
MONDO:0009573	megaepiphyseal dwarfism	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|endocrinology|orthopaedic	genetic_disorders|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	false	medium
MONDO:0009574	megalencephaly with dysmyelination	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009575	thiamine-responsive megaloblastic anemia syndrome	metabolic_disease|hereditary_disease|hematologic_disorder	anemia|metabolic_disease	hematologic_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatrics|gastroenterology|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0009576	megalocornea	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder|bone_disorder	false	false	false	false	medium
MONDO:0009577	megalocornea-intellectual disability syndrome	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0009578	neurocutaneous melanocytosis	integumentary_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|nervous_system_disorder|integumentary_system_disorder|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|neurology|dermatology	neurocutaneous_melanocytosis_is_a_type_of_cancer_so_the_category_list_would_be___cancer___or_neurocutaneous_melanocytosis_involves_skin_manifestations__which_can_sometimes_imply_neurodegenerative_disease_and_also_it_can_have_some_link_with_autoimmune_diseases	skin_disorder|nervous_system_disorder	false	true	false	false	high
MONDO:0009579	Frank-Ter Haar syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatrics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder|ear_disorder|bone_disorder	false	false	false	false	high
MONDO:0009580	intellectual disability, autosomal recessive 1	psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease|psychiatric_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0009581	intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|endocrinology|psychiatry	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder|urinary_tract_disorder	false	false	true	false	high
MONDO:0009582	Mietens syndrome	syndromic_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|disorder_of_visual_system	genetics_and_genomics|cardiothoracic|cardiology|pulmonology	autoimmune_diseases|neurodegenerative_disease	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0009583	blepharophimosis - intellectual disability syndrome, Ohdo type	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0009584	intellectual disability, Buenos-Aires type	psychiatric_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	psychiatric_disorder	disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0009585	encephalopathy due to beta-mercaptolactate-cysteine disulfiduria	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009587	mesoaxial hexadactyly and cardiac malformation	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|cardiology	cardiac_malformation|cardiovascular_disorder	vascular_disorder|heart_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009588	Langer mesomelic dysplasia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder|bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0009589	mesomelic dwarfism-cleft palate-camptodactyly syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder	bone_disorder|cleft_palate_disorder|joint_disorder	false	false	false	false	high
MONDO:0009590	metachromatic leukodystrophy due to saposin B deficiency	psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	metabolic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009591	metachromatic leukodystrophy, juvenile form	psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	metabolic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0009592	metaphyseal acroscyphodysplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	skeletal_dysplasia|developmental_disorder|genetic_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0009593	spondylometaphyseal dysplasia, Sedaghatian type	metabolic_disease|hereditary_disease|musculoskeletal_system_disorder	metabolic_disease	musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0009594	metaphyseal chondrodysplasia, Kaitila type	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009595	cartilage-hair hypoplasia	syndromic_disease|integumentary_system_disorder|hereditary_disease|musculoskeletal_system_disorder|immune_system_disorder	other	musculoskeletal_system_disorder|immune_system_disorder|integumentary_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|orthopaedic	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0009596	metaphyseal chondrodysplasia, Pena type	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	genetic_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009597	metaphyseal chondrodysplasia, Spahr type	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	skeletal_dysplasia|skeletal_disease____wait__since__genetic_disorder__and__skeletal_disease__were_not_provided_in_the_list__i_will_correct_it_to____metabolic_disorder|genetic_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009598	metaphyseal chondrodysplasia-retinitis pigmentosa syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	ophthalmology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	eye_disorder|bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009599	metaphyseal dysostosis-intellectual disability-conductive deafness syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	ear_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0009600	metaphyseal dysplasia, anetoderma, and optic atrophy	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|eye_disorder	false	false	false	false	medium
MONDO:0009601	metaphyseal dysplasia without hypotrichosis	hereditary_disease|musculoskeletal_system_disorder|immune_system_disorder|integumentary_system_disorder|syndromic_disease	other	immune_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|integumentary_system_disorder	orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disorder|bone_dysplasia	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009602	metaphyseal modeling abnormality, skin lesions, and spastic paraplegia	hereditary_disease	other	hereditary_disease	dermatology|orthopaedic|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder|muscle_disorder|skin_disorder	true	false	false	true	high
MONDO:0009603	3-hydroxyisobutyryl-CoA hydrolase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0009604	methemoglobin reductase deficiency	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	hematology|pulmonology|genetics_and_genomics	metabolic_disorder|anemia	lung_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0009605	methemoglobinemia type 4	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	lung_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0009606	methemoglobinemia due to deficiency of methemoglobin reductase	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	hematology|pulmonology|pediatric|genetics_and_genomics	metabolic_disorder|anemia	lung_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0009607	methionine adenosyltransferase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|metabolic_disorder	false	false	false	false	low
MONDO:0009608	methionine malabsorption syndrome	hereditary_disease	other	hereditary_disease	gastroenterology|pediatric	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0009609	methylcobalamin deficiency type cblG	hereditary_disease|hematologic_disorder|nutritional_disorder|metabolic_disease	metabolic_disease|anemia	hereditary_disease|nutritional_disorder|hematologic_disorder|metabolic_disease	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|anemia|neurodegenerative_disease	nervous_system_disorder|gastrointestinal_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0009610	3-methylglutaconic aciduria type 1	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|renal_medicine|pediatrics	metabolic_disorder|adrenal_gland_disease	kidney_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009611	3-methylglutaconic aciduria type 4	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	kidney_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009612	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|anemia|neurodegenerative_disease	brain_disorder|metabolic_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0009613	methylmalonic aciduria, cblA type	hereditary_disease|nutritional_disorder|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|nutritional_disorder	hematology|pediatric|genetics_and_genomics|metabolic_disorders|endocrinology	metabolic_disorder|anemia	kidney_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0009614	methylmalonic aciduria, cblB type	hereditary_disease|nutritional_disorder|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|nutritional_disorder	hematology|genetics_and_genomics|pediatrics	metabolic_disorder|anemia|neurodegenerative_disease	blood_bone_marrow_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0009615	methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|anemia|neurodegenerative_disease	blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0009616	microcephalic primordial dwarfism, Toriello type	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology|endocrinology	metabolic_disorder|neurodegenerative_disease	brain_disorder|growth_disorder|skeletal_system_disorder	false	false	false	false	very_high
MONDO:0009617	microcephaly 1, primary, autosomal recessive	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	metabolic_disorder|autosomal_recessive|neurodegenerative_disease	brain_disorder|ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0009618	microcephaly-cardiomyopathy syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder|neurodegenerative_disease	brain_disorder|heart_disorder	false	false	false	false	high
MONDO:0009619	microcephaly-micromelia syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	microcephaly|brain_disorder	false	false	false	false	high
MONDO:0009620	Say-Barber-Miller syndrome	immune_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|immune_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|other___corrected_to___neurodegenerative_disease	skeletal_disorder____note__say_barber_miller_syndrome_is_a_form_of_skeletal_dysplasia|bone_disorder	false	false	false	false	high
MONDO:0009621	microcephaly-cervical spine fusion anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0009622	Jawad syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009623	Nijmegen breakage syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|rheumatology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0009624	microcephaly and chorioretinopathy 1	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|psychiatric_disorder|syndromic_disease|inflammatory_disease|disorder_of_visual_system	psychiatric_disorder	disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|disorder_of_visual_system|syndromic_disease|inflammatory_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	true	false	false	false	high
MONDO:0009625	diencephalic-mesencephalic junction dysplasia syndrome 1	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0009626	pseudo-TORCH syndrome	hereditary_disease	other	hereditary_disease	pediatric|dermatology|neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder|brain_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0009627	Galloway-Mowat syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder	liver_disorder|kidney_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0009629	Desbuquois dysplasia 1	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	dermatology|neonatology|pediatrics	autoimmune_diseases|neurodegenerative_disease	skin_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0009630	microphthalmia, isolated, with coloboma 4	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	ophthalmology|pediatric|genetics_and_genomics	autoimmune_diseases|anemia|inflammatory_disease|allergy|neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0009631	isolated microphthalmia 1	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	ophthalmology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|reproductive_system_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0009632	microphthalmia with hyperopia, retinal degeneration, macrophakia, and dental anomalies	hereditary_disease	other	hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder|teeth_disorder	false	false	false	false	high
MONDO:0009633	microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	ophthalmology|genetics_and_genomics	autoimmune_diseases|anemia|inflammatory_disease	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009634	microtia with meatal atresia and conductive deafness	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|otolaryngology	metabolic_disorder	ear_disorder|throat_disorder|teeth_disorder	false	false	false	false	high
MONDO:0009635	microvillus inclusion disease	digestive_system_disorder|hereditary_disease	other	hereditary_disease|digestive_system_disorder	pediatric|gastroenterology|renal_medicine|genetics_and_genomics	autoimmune_diseases|anemia|metabolic_disorder	kidney_disorder|lower_gastrointestinal_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0009636	mitochondrial DNA depletion syndrome 3 (hepatocerebral type)	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease	hepatology|neurology|genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	liver_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009637	inborn mitochondrial myopathy	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|mitochondrial_disease	pediatric|neurology|orthopaedic|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	mitochondrial_myopathy|muscle_disorder	false	false	false	false	high
MONDO:0009638	mitochondrial myopathy with a defect in mitochondrial-protein transport	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|mitochondrial_disease	neurology|cardiology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	mitochondrial_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009642	orofaciodigital syndrome type II	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|dermatology|neurology|orthopaedic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder|spinal_disorder|teeth_disorder|joint_disorder	false	false	false	false	high
MONDO:0009643	sulfite oxidase deficiency due to molybdenum cofactor deficiency type A	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system	metabolic_disease	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|metabolic_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0009644	sulfite oxidase deficiency due to molybdenum cofactor deficiency type B	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system	metabolic_disease	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|metabolic_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009645	chronic mucocutaneous candidiasis due to monocyte chemotactic disorder	hereditary_disease|immune_system_disorder|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|immune_system_disorder	hematology|immunology|dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	false	medium
MONDO:0009646	monosomy 7 myelodysplasia and leukemia syndrome 1	hereditary_disease|hematologic_disorder|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|hematologic_disorder|cancer_or_benign_tumor|syndromic_disease	hematology|pediatric|genetics_and_genomics_is_redundant_so_the_list_will_be__genetics_and_genomics|oncology|genetics_and_genomics	anemia|leukemia|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0009647	Morquio syndrome C	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	metabolic_disease	hereditary_disease|syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	true	high
MONDO:0009648	peripheral motor neuropathy-dysautonomia syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	neuro_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0009649	moyamoya disease 1	nervous_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|hereditary_disease	cardiovascular|neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0009650	mucolipidosis type II	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|pulmonology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	lung_disorder	false	false	false	false	very_high
MONDO:0009652	GNPTG-mucolipidosis	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder	false	false	false	true	medium
MONDO:0009653	mucolipidosis type IV	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system	metabolic_disease	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0009655	mucopolysaccharidosis type 3A	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder|joint_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0009656	mucopolysaccharidosis type 3B	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder|joint_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0009657	mucopolysaccharidosis type 3C	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009658	mucopolysaccharidosis type 3D	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	brain_disorder|joint_disorder	false	false	false	true	high
MONDO:0009659	mucopolysaccharidosis type 4A	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder|kidney_disorder|spinal_disorder|bone_disorder|joint_disorder|muscle_disorder	false	false	false	true	high
MONDO:0009660	mucopolysaccharidosis type 4B	musculoskeletal_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|syndromic_disease	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|metabolic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|bone_disorder|kidney_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009661	mucopolysaccharidosis type 6	musculoskeletal_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|syndromic_disease|disorder_of_visual_system	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|musculoskeletal_system_disorder|syndromic_disease|metabolic_disease|disorder_of_orbital_region	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|brain_disorder|skeletal_disorder	false	false	false	true	very_high
MONDO:0009662	mucopolysaccharidosis type 7	musculoskeletal_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|metabolic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|joint_disorder|brain_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0009663	mucus inspissation of respiratory tract	hereditary_disease	other	hereditary_disease	pediatric|pulmonology|otolaryngology	inflammatory_disease|respiratory_disorder|autoimmune_diseases	lung_disorder|nose_disorder|throat_disorder	false	false	false	false	high
MONDO:0009664	mulibrey nanism	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|syndromic_disease	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|metabolic_disease	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	growth_disorder|bone_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0009665	biotinidase deficiency	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	metabolic_disorder|liver_disorder	false	false	false	true	high
MONDO:0009666	holocarboxylase synthetase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatrics	metabolic_disorder|adrenal_gland_disease	metabolic_disorder|liver_disorder|note__i_replaced_the_original_disease_name_with_its_correct_category__metabolic_disorder__as_per_my_knowledge__however__based_on_the_provided_list_of_categories_and_further_research__holocarboxylase_synthetase_deficiency_is_indeed_a_liver_disorder__often_classified_under_the_broader_category_of_metabolic_disorders	false	false	false	true	very_high
MONDO:0009667	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics|orthopaedic|ophthalmology	neurodegenerative_disease|metabolic_disorder|congenital_disease	muscle_disorder|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0009668	lethal multiple pterygium syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|ophthalmology	inflammatory_disease|neurodegenerative_disease|cancer|metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	very_high
MONDO:0009669	spinal muscular atrophy, type 1	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	spinal_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0009670	lethal congenital contracture syndrome 1	hereditary_disease|respiratory_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|respiratory_system_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|congenital_disorder	joint_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0009671	intellectual disability-myopathy-short stature-endocrine defect syndrome	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|endocrine_defect|metabolic_disorder	muscle_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0009672	spinal muscular atrophy, type III	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0009673	spinal muscular atrophy, type II	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0009674	muscular dystrophy, adult-onset, with leukoencephalopathy	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0009675	autosomal recessive limb-girdle muscular dystrophy type 2A	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	neurology|genetics_and_genomics|orthopaedic	cardiovascular_disorder|muscular_dystrophy|neurodegenerative_disease	spinal_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009676	autosomal recessive limb-girdle muscular dystrophy type 2B	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	limb_girdle_muscular_dystrophy|muscle_disorder	false	false	false	false	high
MONDO:0009677	autosomal recessive limb-girdle muscular dystrophy type 2C	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|cardiovascular_disorder	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	false	high
MONDO:0009678	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	muscle_disorder|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0009679	arthrogryposis due to muscular dystrophy	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|nervous_system_disorder	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009680	congenital muscular dystrophy-infantile cataract-hypogonadism syndrome	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	ophthalmology|endocrinology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0009681	Ullrich congenital muscular dystrophy 1A	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	false	high
MONDO:0009682	muscular dystrophy, congenital, with rapid progression	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|muscular_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0009683	autosomal recessive limb-girdle muscular dystrophy type 2H	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	neurology|genetics_and_genomics	limb_girdle_muscular_dystrophy|muscular_dystrophy|neurodegenerative_disease|metabolic_disorder	joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0009684	muscular hypertonia, lethal	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0009685	Miyoshi myopathy	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0009686	musk, inability to smell	hereditary_disease	other	hereditary_disease	neurology|otolaryngology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	nose_disorder|muscle_disorder	false	false	false	false	low
MONDO:0009687	myasthenia, congenital, refractory to acetylcholinesterase inhibitors	hereditary_disease|syndromic_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|syndromic_disease	pediatrics|neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	muscle_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0009688	myasthenia gravis	immune_system_disorder|nervous_system_disorder	autoimmune_disease	immune_system_disorder|nervous_system_disorder	immunology|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|immune_disorder	false	false	false	true	high
MONDO:0009689	congenital myasthenic syndrome 6	hereditary_disease|syndromic_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0009690	congenital myasthenic syndrome 10	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|nervous_system_disorder	other	nervous_system_disorder|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0009691	mycosis fungoides	hematologic_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|integumentary_system_disorder	dermatology|oncology	autoimmune_diseases|inflammatory_disease|cancer	skin_disorder|lymphatic_disorder|immune_disorder	true	true	false	true	medium
MONDO:0009692	primary myelofibrosis	musculoskeletal_system_disorder|hematologic_disorder|immune_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	anemia|cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	hematology|oncology	anemia|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0009693	plasma cell myeloma	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0009694	myeloperoxidase deficiency	hereditary_disease|hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|inflammatory_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	medium
MONDO:0009695	myeloproliferative disease, autosomal recessive	musculoskeletal_system_disorder|hematologic_disorder|immune_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	hematology|genetics_and_genomics	anemia|cancer	blood_bone_marrow_disorder|immune_disorder	false	true	false	false	high
MONDO:0009696	juvenile myoclonic epilepsy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	muscledisorder|brain_disorder	false	false	false	true	high
MONDO:0009697	Lafora disease	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009698	Unverricht-Lundborg syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	ophthalmology|dermatology|endocrinology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	vascular_disorder|joint_disorder|endocrine_disorder|eye_disorder|immune_disorder	false	false	false	false	high
MONDO:0009699	action myoclonus-renal failure syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|renal_medicine	neurodegenerative_disease|metabolic_disorder	kidney_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0009701	myopathy, granulovacuolar lobular, with electrical myotonia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	electrical_myotonia|muscle_disorder	false	false	false	false	medium
MONDO:0009702	myopathy due to malate-aspartate shuttle defect	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	high
MONDO:0009703	myopathy with abnormal lipid metabolism	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|endocrinology	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|muscle_disorder	false	false	false	true	high
MONDO:0009704	carnitine palmitoyl transferase II deficiency, myopathic form	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	heart_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0009705	carnitine palmitoyl transferase 1A deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0009706	hereditary myopathy with lactic acidosis due to ISCU deficiency	musculoskeletal_system_disorder|hereditary_disease|mitochondrial_disease	other	hereditary_disease|mitochondrial_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	mitochondrial_dysfunction|muscle_disorder	false	false	false	false	very_high
MONDO:0009707	myopathy with giant abnormal mitochondria	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder	true	false	false	true	high
MONDO:0009708	myopathy, myosin storage, autosomal recessive	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|autosomal_recessive___note__the_term__autosomal_recessive__is_a_genetic_trait_rather_than_a_category__but_based_on_the_given_information__it_seems_to_be_closely_related_to_one_of_the_categories|neurodegenerative_disease	myopathy|muscle_disorder	false	false	false	false	high
MONDO:0009709	myopathy, centronuclear, 2	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	high
MONDO:0009710	Thomsen and Becker disease	nervous_system_disorder	other	nervous_system_disorder	endocrinology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0009711	congenital fiber-type disproportion myopathy	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder	false	false	false	false	medium
MONDO:0009712	congenital multicore myopathy with external ophthalmoplegia	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009713	myopia 18, autosomal recessive	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|genetic_disorder	false	false	false	false	medium
MONDO:0009714	myosclerosis	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|neurology|rheumatology	metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009715	myotonia congenita, autosomal recessive	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0009716	Richieri Costa-da Silva syndrome	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0009717	Schwartz-Jampel syndrome	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0009718	myxedema	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|neurology	metabolic_disorder|autoimmune_diseases	thyroid_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0009719	familial atrial myxoma	cancer_or_benign_tumor|hereditary_disease|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hereditary_disease|cancer_or_benign_tumor|cardiovascular_disorder	cardiology|genetics_and_genomics|pediatric	cardiovascular_disorder|familial_disease	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0009720	Keipert syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0009721	Nathalie syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	immune_disorder__bone_disorder	false	false	false	false	very_high
MONDO:0009722	Bailey-Bloch congenital myopathy	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	very_high
MONDO:0009723	Leigh syndrome	hereditary_disease|nervous_system_disorder|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|mitochondrial_disease|metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0009724	nail-patella-like renal disease	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	renal_medicine|urology|genetics_and_genomics	genetic_disorder|metabolic_disorder|renal_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0009725	nemaline myopathy 2	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009726	proteosome-associated autoinflammatory syndrome	connective_tissue_disorder|hereditary_disease|immune_system_disorder|syndromic_disease	other	connective_tissue_disorder|immune_system_disorder|hereditary_disease|syndromic_disease	rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|inflammatory_disorder	false	false	false	false	high
MONDO:0009727	atelosteogenesis type II	hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0009728	nephronophthisis 1	hereditary_disease|syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease|syndromic_disease	renal_medicine|nephrology	kidney_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0009729	nephropathy - deafness - hyperparathyroidism syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	renal_medicine|endocrinology|nephrology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	kidney_disorder|endocrine_disorder|ear_disorder	false	false	false	false	high
MONDO:0009731	nephrosis-deafness-urinary tract-digital malformations syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease	urology|genetics_and_genomics|pediatric|renal_medicine	digital_malformation_syndrome|metabolic_disorder|urinary_tract_disease	urinary_tract_disorder|kidney_disorder|ear_disorder	false	false	false	false	high
MONDO:0009732	congenital nephrotic syndrome, Finnish type	hereditary_disease|syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|renal_medicine	genetic_disorder|metabolic_disorder|congenital_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0009733	nephrotic syndrome, type 4	hereditary_disease|syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease|syndromic_disease	pediatric|nephrology|renal_medicine	metabolic_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|kidney_disorder	false	false	false	false	high
MONDO:0009734	hyperinsulinemic hypoglycemia, familial, 1	hereditary_disease|endocrine_system_disorder|metabolic_disease	metabolic_disease|endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|metabolic_disease	endocrinology|genetics_and_genomics	metabolic_disorder|familial_metabolic_disorder	familial_disorders_are_a_part_of_endocrine_disorders_but_is_not_in_the_list_so_i_will_remove_it|endocrine_disorder	false	false	true	true	high
MONDO:0009735	Netherton syndrome	hereditary_disease|hematologic_disorder|immune_system_disorder|syndromic_disease|disorder_of_visual_system|integumentary_system_disorder	other	immune_system_disorder|hereditary_disease|disorder_of_orbital_region|hematologic_disorder|integumentary_system_disorder|disorder_of_visual_system|syndromic_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0009736	Neu-Laxova syndrome 1	hereditary_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|metabolic_disease|integumentary_system_disorder	metabolic_disease	hereditary_disease|integumentary_system_disorder|metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|vascular_disorder|upper_gastrointestinal_disorder|eye_disorder|joint_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0009737	galactosialidosis	musculoskeletal_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	hereditary_disease|disorder_of_orbital_region|musculoskeletal_system_disorder|metabolic_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0009738	sialidosis type 2	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	brain_disorder|teeth_disorder|nose_disorder|upper_gastrointestinal_disorder|throat_disorder|lymphatic_disorder|eye_disorder|joint_disorder|skin_disorder|muscle_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0009740	neurofaciodigitorenal syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric|renal_medicine	metabolic_disorder|neurodegenerative_disease	brain_disorder|kidney_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0009741	neuroblastoma, susceptibility to, 1	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	oncology|pediatric	cancer	brain_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0009742	neuroectodermal melanolysosomal disease	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	brain_disorder|skin_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0009743	neurologic disease, infantile multisystem, with osseous fragility	hereditary_disease	other	hereditary_disease	orthopaedic|neurology|pediatric	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0009744	neuronal ceroid lipofuscinosis 1	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease|neurodegenerative_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0009745	neuronal ceroid lipofuscinosis 5	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease|neurodegenerative_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009746	hereditary sensory and autonomic neuropathy type 4	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	hereditary_disease|neurodegenerative_disease	spinal_disorder|nerve_disorder	false	false	false	false	high
MONDO:0009747	mitochondrial DNA depletion syndrome 6 (hepatocerebral type)	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	hereditary_disease|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis	hepatology|genetics_and_genomics|neurology	hepatocerebral_type|metabolic_disorder|neurodegenerative_disease	brain_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0009748	hereditary sensory and autonomic neuropathy with spastic paraplegia	hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|hereditary_condition	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009749	giant axonal neuropathy 1	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009750	neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|hereditary_diseases|metabolic_disorder	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0009751	neuropathy, hereditary sensory, atypical	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	hereditary_disorder|neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0009752	neuropathy, painful	hereditary_disease	other	hereditary_disease	orthopaedic|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|nerve_disorder	false	false	false	true	high
MONDO:0009754	neutropenia, lethal congenital, with eosinophilia	immune_system_disorder|hereditary_disease|hematologic_disorder	other	immune_system_disorder|hereditary_disease|hematologic_disorder	pediatric|genetics_and_genomics|hematology|immunology	neutropenia|lethal_congenital|cancer|eosinophilia|metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	true	false	false	false	very_high
MONDO:0009755	neutrophil actin dysfunction	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder	cancer_or_benign_tumor	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	hematology|immunology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0009756	Niemann-Pick disease type A	metabolic_disease|immune_system_disorder|hereditary_disease|disorder_of_visual_system	metabolic_disease	immune_system_disorder|metabolic_disease|hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder|brain_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0009757	Niemann-Pick disease, type C1	metabolic_disease|immune_system_disorder|hereditary_disease	metabolic_disease	immune_system_disorder|metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0009758	congenital stationary night blindness 1B	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	pediatric|ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0009759	mosaic variegated aneuploidy syndrome 1	syndromic_disease|cancer_or_benign_tumor|hereditary_disease|chromosomal_disorder	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|chromosomal_disorder|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|anemia|cancer	blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	high
MONDO:0009760	Norman-Roberts syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder|immune_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	immune_system_disorder|cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder	pediatric|genetics_and_genomics|obstetrics_and_gynecology	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|eye_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0009761	cystic hygroma	cancer_or_benign_tumor|immune_system_disorder|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	immune_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	pediatric|obstetrics_and_gynecology	congenital_abnormality|inflammatory_disease	skin_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0009762	nystagmus, congenital, autosomal recessive	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0009763	obesity-hypoventilation syndrome	hereditary_disease	other	hereditary_disease	cardiology|pulmonology|endocrinology	cardiovascular_disorder|metabolic_disorder	lung_disorder|endocrine_disorder	false	false	false	true	very_high
MONDO:0009764	ocular motor apraxia, Cogan type	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0009765	ocular myopathy with curare sensitivity	hereditary_disease	other	hereditary_disease	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|eye_disorder	true	false	false	false	medium
MONDO:0009766	oculocerebral hypopigmentation syndrome of Preus	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0009767	oculocerebral hypopigmentation syndrome, Cross type	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|hereditary_disease|integumentary_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder_brain_disorder	false	false	false	false	very_high
MONDO:0009768	oculodentodigital dysplasia, autosomal recessive	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_visual_system|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_orbital_region|disorder_of_visual_system|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	teeth_disorder|eye_disorder	false	false	false	false	medium
MONDO:0009769	oculo-palato-cerebral syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	throat_disorder|eye_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009770	3MC syndrome 1	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|anemia	urinary_tract_disorder|liver_disorder|joint_disorder|brain_disorder|eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0009771	oculotrichodysplasia	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	teeth_disorder|eye_disorder	false	false	false	false	medium
MONDO:0009772	oculorenocerebellar syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0009773	odonto-onycho-dermal dysplasia	syndromic_disease|hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|other___corrected_response__neurodegenerative_disease	teeth_disorder|skin_disorder|onycho	false	false	false	false	medium
MONDO:0009774	cloacal exstrophy	syndromic_disease|urinary_system_disorder|disorder_of_development_or_morphogenesis	other	urinary_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	urology|pediatric|renal_medicine	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|adrenal_gland_disease	lower_gastrointestinal_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0009775	Oguchi disease-1	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	hereditary_disease|disorder_of_orbital_region|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	orthopaedic|pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	true	medium
MONDO:0009776	spermatogenic failure 1	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	urology|endocrinology	metabolic_disorder|anemia	reproductive_system_disorder	false	false	false	false	medium
MONDO:0009777	Oliver syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0009778	olivopontocerebellar atrophy II, autosomal recessive	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0009779	autosomal recessive omodysplasia	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|genetic_condition	immune_disorder|joint_disorder|bone_disorder|ear_disorder	false	false	false	false	medium
MONDO:0009780	lethal omphalocele-cleft palate syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|genetic_disorder|congenital_abnormality	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0009781	Onychotrichodysplasia and neutropenia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology|dermatology	metabolic_disorder|autoimmune_diseases|anemia	blood_bone_marrow_disorder|immune_disorder|skin_disorder	true	false	false	false	medium
MONDO:0009782	ophthalmoplegia totalis with ptosis and miosis	hereditary_disease	other	hereditary_disease	ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0009783	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	musculoskeletal_system_disorder|metabolic_disease|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatrics|genetics_and_genomics|ophthalmology|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0009784	ophthalmoplegic neuromuscular disorder with abnormal mitochondria	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0009785	opsismodysplasia	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	skeletal_disorder|musculoskeletal_system_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0009786	optic atrophy 6	nervous_system_disorder|disorder_of_visual_system|hereditary_disease	neurodegenerative_disease	hereditary_disease|disorder_of_visual_system|nervous_system_disorder	ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0009787	3-methylglutaconic aciduria type 3	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|renal_medicine	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0009788	optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|peripheral_neuropathy_is_closely_related_to_spinal_disorder|brain_disorder|eye_disorder|ear_disorder	true	false	false	true	medium
MONDO:0009790	Opticocochleodentate degeneration	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	spinal_disorder|eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0009791	oral sensibility, disturbance of	hereditary_disease	other	hereditary_disease	otolaryngology|neurology	neurodegenerative_disease|mental_health_disorder	teeth_disorder|oral_sensitivity_disturbance_is_related_to_teeth_disorder_so_just_teeth_disorder	false	false	false	false	medium
MONDO:0009792	ichthyosis-oral and digital anomalies syndrome	syndromic_disease|hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|dermatology	inflammatory_disease|genetic_disorder|anatomic_anomaly__inflammatory_disease|anatomic_anomaly|developmental_disorder___corrected_to_match_format_requirements___metabolic_disorder|metabolic_disorder	other____corrected__skin_disorder|teeth_disorder|oral_and_digital_anomalies_syndrome_belongs_to__the_category_of____skin_disorder_and_teeth_disorder|skin_disorder	false	false	false	false	medium
MONDO:0009793	orofaciodigital syndrome III	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder|teeth_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0009794	orofaciodigital syndrome IV	syndromic_disease|hereditary_disease|respiratory_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|respiratory_system_disorder|syndromic_disease	pediatric|genetics_and_genomics	genetic_disorder|congenital_disorder|metabolic_disorder	oral_disorder|bone_disorder|teeth_disorder	false	false	false	false	high
MONDO:0009795	orofaciodigital syndrome IX	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	upper_gastrointestinal_disorder|teeth_disorder|ear_disorder	false	false	false	false	high
MONDO:0009796	ornithine aminotransferase deficiency	cardiovascular_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	cardiovascular_disorder|psychiatric_disorder|metabolic_disease	nervous_system_disorder|cardiovascular_disorder|metabolic_disease|hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|psychiatric_disorder	pediatric|genetics_and_genomics|hepatology	neurodegenerative_disease|metabolic_disorder	liver_disorder|amino_acid_metabolism_disorder	false	false	false	false	high
MONDO:0009797	orotic aciduria	metabolic_disease|hereditary_disease|hematologic_disorder	anemia|metabolic_disease	hematologic_disorder|metabolic_disease|hereditary_disease	renal_medicine|pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0009798	Primrose syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|nephrology	inflammatory_disease|autoimmune_diseases	kidney_disorder|liver_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0009800	Blount disease, adolescent	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|endocrinology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0009801	familial osteodysplasia, Anderson type	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	genetic_disease|metabolic_disorder|congenital_disease|bone_disease	joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0009802	osteodysplasty, precocious, of Danks, Mayne, and Kozlowski	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	none
MONDO:0009803	congenital osteogenesis imperfecta-microcephaly-cataracts syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|orthopaedic|ophthalmology	neurodegenerative_disease|metabolic_disorder|congenital_disorder	joint_disorder|skeletal_disorder|bone_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0009804	osteogenesis imperfecta type 3	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	skeletal_dysplasia|genetic_disease|metabolic_disorder	joint_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009805	osteogenesis imperfecta type 9	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	connective_tissue_disease|metabolic_disorder|bone_disease	joint_disorder|teeth_disorder|bone_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009806	Bruck syndrome 1	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	bone_bone_marrow_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0009807	osteosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|orthopaedic|oncology|hematology	cancer	joint_disorder|bone_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0009808	osteoid osteoma	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	orthopaedic	inflammatory_disease|cancer|metabolic_disorder	bone_disorder|muscle_disorder	false	false	false	true	low
MONDO:0009809	multicentric osteolysis, nodulosis, and arthropathy	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease|metabolic_disorder	joint_disorder|immune_disorder|bone_disorder	false	false	false	false	high
MONDO:0009810	autosomal recessive distal osteolysis syndrome	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009811	osteoma of middle ear	hereditary_disease	other	hereditary_disease	otolaryngology|orthopaedic	autoimmune_diseases|inflammatory_disease	ear_disorder|bone_disorder	false	false	false	false	low
MONDO:0009813	chronic recurrent multifocal osteomyelitis	syndromic_disease|hematologic_disorder|connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	syndromic_disease|hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|hereditary_disease|connective_tissue_disorder	rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease	joint_disorder|bone_marrow_blood_disorder|immune_disorder|bone_disorder	false	false	false	false	high
MONDO:0009814	osteopenia-intellectual disability-sparse hair syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	skin_disorder|bone_disorder|brain_disorder	false	false	false	false	high
MONDO:0009815	autosomal recessive osteopetrosis 1	disorder_of_visual_system|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_orbital_region|musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0009816	autosomal recessive osteopetrosis 2	disorder_of_visual_system|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_orbital_region|musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease	genetics_and_genomics|orthopaedic	metabolic_disorder|osteoporosis	bone_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0009817	autosomal recessive osteopetrosis 5	disorder_of_visual_system|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_orbital_region|musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease	pediatric|genetics_and_genomics|osteoporosis_is_not_in_the_list_but_osteopetrosis_matches_orthopaedic|orthopaedic	genetic_disease|metabolic_disorder|bone_disease___note__since__genetic_disease__is_not_in_the_provided_category_list__i_ve_kept__metabolic_disorder__as_it_s_a_relevant_category_for_autosomal_recessive_osteopetrosis_5	bone_bone_marrow_disorder|bone_disorder	false	false	false	true	very_high
MONDO:0009818	autosomal recessive osteopetrosis 3	disorder_of_visual_system|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_orbital_region|musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder	bone_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0009820	osteoporosis-pseudoglioma syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|syndromic_disease|disorder_of_orbital_region|musculoskeletal_system_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|cardiovascular_disorder	genetics_and_genomics|rheumatology|orthopaedic	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0009821	lethal osteosclerotic bone dysplasia	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic|oncology	autoimmune_diseases|anemia|metabolic_disorder	blood_bone_marrow_disorder|spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0009822	otoonychoperoneal syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	throat_disorder|ear_disorder	false	false	false	false	high
MONDO:0009823	primary hyperoxaluria type 1	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	renal_medicine|genetics_and_genomics|urology	renal_disease|metabolic_disorder|genetic_disorder	renal_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0009824	primary hyperoxaluria type 2	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	renal_medicine|genetics_and_genomics|urology	inborn_error_of_metabolism|metabolic_disorder|genetic_disorder|kidney_disease	liver_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0009825	5-oxoprolinase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|biochemistry____edited_for_correct_formatting	adrenal_gland_disease|metabolic_disorder	kidney_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0009828	palant cleft palate syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	neurodevelopmental_disease|syndrome|birth_defect	throat_disorder|teeth_disorder|ear_disorder	false	false	false	false	high
MONDO:0009830	parkinsonian-pyramidal syndrome	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009831	malignant pancreatic neoplasm	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer|malignant_pancreatic_neoplasm	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0009832	pancreatic agenesis	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|endocrinology|gastroenterology	autoimmune_diseases|cancer|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0009833	Shwachman-Diamond syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	pediatric|pulmonology|genetics_and_genomics|hematology	anemia|metabolic_disorder	lung_disorder|blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0009835	subacute sclerosing panencephalitis	inflammatory_disease|nervous_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|acute_disease|nervous_system_disorder|infectious_disease	pediatric|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	immune_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0009836	pancreatitis, sclerosing cholangitis, and sicca complex	hereditary_disease	other	hereditary_disease	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	liver_disorder|immune_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0009837	choroid plexus papilloma	cardiovascular_disorder|nervous_system_disorder|cancer_or_benign_tumor|hereditary_disease	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|nervous_system_disorder|hereditary_disease|cancer_or_benign_tumor	neurology|oncology|ophthalmology	cancer|neurological_cancer	eye_disorder|brain_disorder	false	true	false	false	medium
MONDO:0009838	Parana hard-skin syndrome	syndromic_disease|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder	pediatric|genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0009839	progressive supranuclear palsy-parkinsonism syndrome	syndromic_disease|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	syndromic_disease|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009840	Partington-Anderson syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0009841	PEHO syndrome	syndromic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	syndromic_disease|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009842	Pelger-Huet-like anomaly and episodic fever with abdominal pain	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	syndromic_disease|hereditary_disease|connective_tissue_disorder	pediatric|hematology|gastroenterology	inflammatory_disease|anemia|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0009843	hypomyelinating leukodystrophy 3	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|hypomyelinating_leukodystrophy_3_is_also_known_as_a_genetic_disorder_that_affects_the_myelin_sheath_around_nerve_fibers__so_it_could_be_classified_under____neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0009844	pellagra-like syndrome	hereditary_disease	other	hereditary_disease	pediatric|gastroenterology|dermatology|endocrinology	anemia|metabolic_disorder	skin_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0009845	pelviscapular dysplasia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	neurology|orthopaedic	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009846	pentosuria	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	renal_medicine|neurology	neurodegenerative_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	low
MONDO:0009847	pericardial effusion, chronic	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiothoracic|cardiology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	lung_disorder|vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0009848	dissecting cellulitis of the scalp	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|dermatology	allergic_disorder|inflammatory_disease|autoimmune_diseases	skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0009849	hyperimmunoglobulinemia D with periodic fever	syndromic_disease|connective_tissue_disorder|disorder_of_development_or_morphogenesis|immune_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|syndromic_disease|metabolic_disease|immune_system_disorder|hereditary_disease|connective_tissue_disorder	hematology|allergy_and_immunology|rheumatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	true	false	false	true	high
MONDO:0009850	periodontitis, chronic, adult	inflammatory_disease|hereditary_disease|musculoskeletal_system_disorder	other	inflammatory_disease|musculoskeletal_system_disorder|hereditary_disease	rheumatology|endocrinology	inflammatory_disease|autoimmune_diseases	teeth_disorder|joint_disorder	true	false	false	true	medium
MONDO:0009851	peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and spongy degeneration of brain	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder|brain_disorder	true	false	false	false	high
MONDO:0009852	hereditary intrinsic factor deficiency	hematologic_disorder|hereditary_disease|metabolic_disease|nutritional_disorder	anemia|metabolic_disease	nutritional_disorder|metabolic_disease|hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics|pediatrics	anemia|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0009853	Imerslund-Grasbeck syndrome	hematologic_disorder|syndromic_disease|hereditary_disease|metabolic_disease|nutritional_disorder	anemia|metabolic_disease	nutritional_disorder|syndromic_disease|metabolic_disease|hematologic_disorder|hereditary_disease	genetics_and_genomics|pediatrics	adrenal_gland_disease|metabolic_disorder	vascular_disorder|liver_disorder|blood_bone_marrow_disorder|kidney_disorder|immune_disorder	false	false	false	false	medium
MONDO:0009854	peroneus tertius muscle, absence of	hereditary_disease	other	hereditary_disease	neurology|orthopaedic	neurodegenerative_disease|congenital_condition|muscle_disease	bone_disorder|muscle_disorder	false	false	false	false	low
MONDO:0009855	d-bifunctional protein deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatrics|metabolism	inflammatory_disease|neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0009856	Peters plus syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|cardiovascular_disorder|hereditary_disease|metabolic_disease	cardiovascular_disorder|metabolic_disease	disorder_of_orbital_region|disorder_of_visual_system|disorder_of_development_or_morphogenesis|syndromic_disease|metabolic_disease|hereditary_disease|cardiovascular_disorder	genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|lymphatic_disorder|immune_disorder|eye_disorder|joint_disorder	false	false	false	false	high
MONDO:0009857	persistent Mullerian duct syndrome	endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	genetics_and_genomics|urology|pediatric	congenital_disorder|developmental_disorder|reproductive_disorder|genetic_disorder	reproductive_system_disorder	false	false	false	true	medium
MONDO:0009858	Pfeiffer-Palm-Teller syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pulmonology|pediatric	genetic_disorders|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009859	PHAVER syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	anemia____note__phaver_syndrome_is_a_rare_genetic_disorder_characterized_by_metabolic_dysfunction_and_anemia|metabolic_disorder	lung_disorder|blood_bone_marrow_disorder|immune_disorder|joint_disorder	false	false	false	false	high
MONDO:0009860	phenformin 4-hydroxylation	hereditary_disease	other	hereditary_disease	hepatology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	liver_disorder	false	false	false	false	none
MONDO:0009861	phenylketonuria	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder	false	false	false	true	high
MONDO:0009862	dihydropteridine reductase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0009863	BH4-deficient hyperphenylalaninemia A	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	genetic_disorder|metabolic_disorder|endocrine_disorder|nervous_system_disorder	false	false	false	true	very_high
MONDO:0009864	phosphoenolpyruvate carboxykinase deficiency, mitochondrial	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder|mitochondrial_disease	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009865	glycogen storage disease due to phosphoglycerate mutase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|pediatrics|genetics_and_genomics	inflammatory_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0009866	phosphoenolpyruvate carboxykinase deficiency, cytosolic	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	metabolism|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	liver_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0009867	lethal congenital glycogen storage disease of heart	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	cardiovascular_disorder|metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiology|neonatology|pediatric|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	liver_disorder|heart_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0009868	glycogen storage disease IXb	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	true	false	high
MONDO:0009869	isolated Pierre-Robin syndrome	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	pediatric|genetics_and_genomics	adrenal_gland_disease|anemia|metabolic_disorder|autoimmune_diseases	upper_gastrointestinal_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0009870	pili torti	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatric	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	skin_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0009871	pili torti-developmental delay-neurological abnormalities syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	developmental_delay|neurological_abnormalities_syndrome|brain_disorder	false	false	false	false	high
MONDO:0009872	Bjornstad syndrome	mitochondrial_disease|hereditary_disease	other	mitochondrial_disease|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	false	medium
MONDO:0009873	pilodental dysplasia-refractive errors syndrome	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|integumentary_system_disorder	ophthalmology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	teeth_disorder|eye_disorder	false	false	false	false	medium
MONDO:0009874	Rabson-Mendenhall syndrome	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|integumentary_system_disorder	endocrinology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	endocrine_disorder	false	false	true	false	very_high
MONDO:0009875	achromatopsia 3	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	neurology|ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0009876	isolated growth hormone deficiency type IA	endocrine_system_disorder|nervous_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|nervous_system_disorder	endocrinology|pediatric	endocrine_disorder|metabolic_disorder	endocrine_disorder	false	false	false	true	high
MONDO:0009877	Laron syndrome	endocrine_system_disorder|syndromic_disease|hereditary_disease	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|genetic_disorder__not_listed	false	false	false	true	medium
MONDO:0009878	pituitary hormone deficiency, combined, 2	endocrine_system_disorder|nervous_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|nervous_system_disorder	neurology|endocrinology	neurodegenerative_disease___corrected_to_fit_the_required_format___neurodegenerative_disease|endocrine_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|brain_disorder	false	false	false	true	medium
MONDO:0009879	short stature due to growth hormone qualitative anomaly	endocrine_system_disorder|nervous_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|nervous_system_disorder	endocrinology|pediatric|genetics_and_genomics	growth_hormone_qualitative_anomaly_is_related_to_metabolism_but_it_is_more_specific_to_endocrine_system_so|endocrine_disorders_category_was_not_included_here_but|metabolic_disorder|it_can_be_replaced_with	endocrine_disorder|bone_disorder	false	false	false	true	medium
MONDO:0009880	short stature-pituitary and cerebellar defects-small sella turcica syndrome	reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|nervous_system_disorder	endocrinology|genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	bone_disorder|endocrine_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0009881	pituitary dwarfism with large sella turcica	hereditary_disease	other	hereditary_disease	endocrinology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammation_disease	endocrine_disorder|brain_disorder|pituitary_dwarfism_is_a_type_of_bone_disorder_so_bone_disorder_as_well_but_since_there_is_a_more_specific_category_included_i_won_t_list_it	false	false	false	true	medium
MONDO:0009882	plasma clot retraction factor, deficiency of	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|bleeding_disease	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0009883	alpha-2-plasmin inhibitor deficiency	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0009884	platelet prostacyclin receptor defect	hereditary_disease	other	hereditary_disease	note__i_removed_the_extra_text_as_per_your_request|genetics_and_genomics|cardiology|hematology	cardiovascular_disorder|inflammatory_disease	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0009885	Scott syndrome	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	neurology|otolaryngology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|ear_disorder	false	false	false	false	high
MONDO:0009886	pleoconial myopathy with salt craving	hereditary_disease	other	hereditary_disease	endocrinology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|salt_craving_is_a_symptom_associated_with_endocrine_disorders__but_it_s_included_in_the_name_of_this_specific_disease	false	false	false	false	medium
MONDO:0009887	desquamative interstitial pneumonia	inflammatory_disease|respiratory_system_disorder|infectious_disease	infectious_disease	respiratory_system_disorder|idiopathic_disease|inflammatory_disease|infectious_disease	respiratory|pulmonology	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	false	high
MONDO:0009888	polycystic kidney, cataract, and congenital blindness	hereditary_disease	other	hereditary_disease	renal_medicine|genetics_and_genomics|ophthalmology|urology	metabolic_disorder|congenital_blindness	kidney_disorder|eye_disorder	false	false	false	false	high
MONDO:0009889	autosomal recessive polycystic kidney disease	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	renal_medicine|genetics_and_genomics|urology	kidney_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0009890	Gillessen-Kaesbach-Nishimura syndrome	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	bone_disorder|upper_gastrointestinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0009891	acquired polycythemia vera	cancer_or_benign_tumor|musculoskeletal_system_disorder|immune_system_disorder|hereditary_disease|connective_tissue_disorder|hematologic_disorder	cancer_or_benign_tumor	connective_tissue_disorder|immune_system_disorder|hereditary_disease|cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder	oncology|hematology	metabolic_disorder|anemia|cancer	blood_bone_marrow_disorder|immune_disorder	false	true	false	false	high
MONDO:0009892	Chuvash polycythemia	musculoskeletal_system_disorder|immune_system_disorder|hereditary_disease|hematologic_disorder	other	immune_system_disorder|hereditary_disease|hematologic_disorder|musculoskeletal_system_disorder	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0009893	polydactyly, postaxial, type A5	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorders	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0009894	short-rib thoracic dysplasia 6 with or without polydactyly	syndromic_disease|respiratory_system_disorder|musculoskeletal_system_disorder|urinary_system_disorder|hereditary_disease	other	syndromic_disease|respiratory_system_disorder|urinary_system_disorder|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric	genetic_disorder|metabolic_disorder	skeletal_system_disorder|bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0009895	postaxial polydactyly-dental and vertebral anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|skeletal_disorder|congenital_anomaly_disorder	teeth_disorder|bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0009896	polymyoclonus, infantile	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	infantile|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0009897	adult polyglucosan body disease	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0009898	polysaccharide, storage of unusual	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatrics	metabolic_disorder|storage_disease	kidney_disorder|lysosomal_disorder|liver_disorder	false	false	false	false	low
MONDO:0009899	polyhydramnios, chronic idiopathic	hereditary_disease	other	idiopathic_disease|hereditary_disease	genetics_and_genomics|pediatric|obstetrics_and_gynecology	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0009900	polysyndactyly-cardiac malformation syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	cardiology|genetics_and_genomics|pediatric	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder|joint_disorder	false	false	false	false	high
MONDO:0009901	Bartsocas-Papas syndrome 1	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder|syndromic_disease	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0009902	cutaneous porphyria	hereditary_disease|hematologic_disorder|integumentary_system_disorder|metabolic_disease	metabolic_disease|anemia	metabolic_disease|hematologic_disorder|integumentary_system_disorder|hereditary_disease	hepatology|hematology|genetics_and_genomics|dermatology	anemia|metabolic_disorder|autoimmune_diseases	skin_disorder|liver_disorder	false	false	false	true	high
MONDO:0009903	postaxial acrofacial dysostosis	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	skeletal_dysplasia|metabolic_disorder|genetic_disorder	spinal_disorder|skeletal_system_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009904	Gitelman syndrome	hereditary_disease|urinary_system_disorder|syndromic_disease	other	urinary_system_disorder|syndromic_disease|hereditary_disease	renal_medicine|genetics_and_genomics|pediatrics	metabolic_disorder|genetic_disorder	kidney_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0009905	urban-Rogers-Meyer syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatrics	neurodegenerative_disease|inflammatory_disease|mental_health_disorder|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0009906	prenatal bowing	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|obstetrics_and_gynecology	genetic_disease|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009907	Prepapillary vascular loops	hereditary_disease	other	hereditary_disease	cardiothoracic|ophthalmology	vascular_loops|cardiovascular_disorder	vascular_disorder|eye_disorder	false	false	false	false	low
MONDO:0009908	pterin-4 alpha-carbinolamine dehydratase 1 deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	metabolic|neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	metabolic_disorder|hereditary_disease|kidney_disorder	false	false	false	true	medium
MONDO:0009909	progesterone resistance	hereditary_disease	other	hereditary_disease	endocrinology|obstetrics_and_gynecology	adrenal_gland_disease|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0009910	Wiedemann-Rautenstrauch syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder|premature_aging_syndrome|musculoskeletal_system_disorder|syndromic_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder|premature_aging_syndrome|integumentary_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|dermatology|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|skin_disorder|vascular_disorder|joint_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0009911	prolactin deficiency, isolated	hereditary_disease	other	hereditary_disease	obstetrics_and_gynecology|endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|endocrine_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0009912	prolactin deficiency with obesity and enlarged testes	hereditary_disease	other	hereditary_disease	endocrinology|urology|genetics_and_genomics|pediatric	metabolic_disorder|neuroendocrine_disease|endocrine_dysfunction	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0009913	prune belly syndrome with pulmonic stenosis, intellectual disability, and deafness	hereditary_disease	other	hereditary_disease	neurology|otolaryngology|urology|pulmonology|cardiology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	heart_disorder|ear_disorder|kidney_disorder|urinary_tract_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009914	pseudodiastrophic dysplasia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	skin_disorder|bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0009915	46,XX disorder of sex development-skeletal anomalies syndrome	endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|skeletal_anomalies_syndrome	reproductive_system_disorder|bone_disorder	false	false	false	false	medium
MONDO:0009916	46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency	endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease	endocrinology|urology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0009917	pseudohypoaldosteronism, type IB1, autosomal recessive	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics|pediatrics	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0009918	fundus dystrophy, pseudoinflammatory, recessive form	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|ophthalmology|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0009919	peroxisomal acyl-CoA oxidase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	peroxisomal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0009920	Acrootoocular syndrome	syndromic_disease	other	syndromic_disease	neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0009921	holoprosencephaly-postaxial polydactyly syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0009922	Pseudouridinuria and mental defect	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|psychiatry|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	kidney_disorder|brain_disorder	true	false	false	false	low
MONDO:0009923	46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency	endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|reproductive_system_disorder|metabolic_disease	metabolic_disease|endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|metabolic_disease|hereditary_disease|reproductive_system_disorder	endocrinology|urology|genetics_and_genomics	congenital_abnormality|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0009924	vitamin D-dependent rickets, type 1	endocrine_system_disorder|hereditary_disease|nutritional_disorder|musculoskeletal_system_disorder|metabolic_disease	metabolic_disease|endocrine_system_disorder	nutritional_disorder|endocrine_system_disorder|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics|orthopaedic|pediatric	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	true	very_high
MONDO:0009925	autosomal recessive inherited pseudoxanthoma elasticum	integumentary_system_disorder|connective_tissue_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease|connective_tissue_disorder	pediatric|dermatology|genetics_and_genomics	metabolic_disorder|inflammatory_disease	joint_disorder|vascular_disorder|skin_disorder	false	false	false	false	high
MONDO:0009926	autosomal recessive multiple pterygium syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|ophthalmology|genetics_and_genomics	inflammatory_disease|metabolic_disorder	joint_disorder|bone_disorder|eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0009927	3MC syndrome 2	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder|joint_disorder|skeletal_dysplasia|heart_disorder|brain_disorder|kidney_disorder|eye_disorder|limb_abnormality|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0009928	pulmonary alveolar microlithiasis	respiratory_system_disorder|hereditary_disease	other	hereditary_disease|respiratory_system_disorder	pulmonology|cardiothoracic|genetics_and_genomics	inflammatory_disease|metabolic_disorder	lung_disorder	false	false	false	false	high
MONDO:0009929	surfactant metabolism dysfunction, pulmonary, 1	respiratory_system_disorder|hereditary_disease	other	acute_disease|hereditary_disease|respiratory_system_disorder	pulmonology|pediatrics|genetics_and_genomics	pulmonary|metabolic_disorder|inflammatory_disease	liver_disorder|lung_disorder	false	false	false	true	high
MONDO:0009931	pulmonary atresia-intact ventricular septum syndrome	disorder_of_development_or_morphogenesis|cardiovascular_disorder|syndromic_disease|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	pulmonology|pediatric|cardiology	congenital_heart_defect|cardiovascular_disorder	lung_disorder|heart_disorder	false	false	false	false	high
MONDO:0009932	pulmonary bullae causing pneumothorax	hereditary_disease	other	hereditary_disease	pulmonology|cardiothoracic	inflammatory_disease|autoimmune_diseases|cancer	lung_disorder	false	false	false	true	high
MONDO:0009933	congenital pulmonary lymphangiectasia	cardiovascular_disorder|immune_system_disorder|respiratory_system_disorder	cardiovascular_disorder	cardiovascular_disorder|immune_system_disorder|respiratory_system_disorder	pulmonology|pediatric|genetics_and_genomics	inflammatory_disease|congenital_disease|cardiovascular_disorder	lung_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0009934	alveolar capillary dysplasia with misalignment of pulmonary veins	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|respiratory_system_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|respiratory_system_disorder	hepatology|hematology|pulmonology|cardiothoracic|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	lung_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0009935	pulmonary hypertension, primary, autosomal recessive	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	pulmonology|genetics_and_genomics|cardiology	metabolic_disorder|cardiovascular_disorder	lung_disorder|vascular_disorder	false	false	false	false	high
MONDO:0009936	familial primary pulmonary hypoplasia	disorder_of_development_or_morphogenesis|respiratory_system_disorder	other	disorder_of_development_or_morphogenesis|respiratory_system_disorder	pulmonology|pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	lung_disorder|primary_pulmonary_hypoplasia	false	false	false	false	very_high
MONDO:0009937	pulmonary venoocclusive disease	cardiovascular_disorder|respiratory_system_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|respiratory_system_disorder	hematology|pediatric|pulmonology|cardiothoracic|cardiology|oncology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	lung_disorder|vascular_disorder	false	false	false	false	high
MONDO:0009938	pulmonic stenosis	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pulmonology|cardiothoracic|cardiology	congenital_heart_defect|cardiovascular_disorder	lung_disorder|heart_disorder	false	false	false	true	medium
MONDO:0009939	pulmonic stenosis and congenital nephrosis	hereditary_disease	other	hereditary_disease	renal_medicine|pediatric|pulmonology|cardiothoracic	congenital_nephrosis_is_more_closely_related_to_kidney_disease_so__inflammatory_disease|anemia|cardiovascular_disorder	lung_disorder|heart_disorder|kidney_disorder	false	false	false	true	high
MONDO:0009940	pycnodysostosis	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|orthopaedic|genetics_and_genomics	genetic_disorder|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0009942	pyknoachondrogenesis	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	skeletal_dysplasia|genetic_disorder|metabolic_disorder	muscle_disorder|joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0009943	Pyle disease	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|oncology	inflammatory_disease|cancer|adrenal_gland_disease	bone_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0009944	pyloric atresia	hereditary_disease	other	hereditary_disease	pediatric|gastroenterology	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0009945	pyridoxine-dependent epilepsy	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0009946	hemolytic anemia due to pyrimidine 5' nucleotidase deficiency	hematologic_disorder|hereditary_disease|metabolic_disease	metabolic_disease|anemia	metabolic_disease|hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	liver_disorder|urinary_tract_disorder|blood_bone_marrow_disorder|other___corrected__blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0009947	glutathione synthetase deficiency with 5-oxoprolinuria	immune_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|immune_system_disorder|hereditary_disease	pediatric|metabolism|genetics_and_genomics	inherited_metabolic_disorder|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0009948	pyropoikilocytosis, hereditary	hereditary_disease	other	hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0009949	pyruvate carboxylase deficiency disease	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|neurology|pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0009950	pyruvate kinase deficiency of red cells	metabolic_disease|hereditary_disease|hematologic_disorder	metabolic_disease|anemia	metabolic_disease|hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	muscle_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0009951	radiculoneuropathy, fatal neonatal	hereditary_disease	other	hereditary_disease	neurology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder	true	false	false	false	very_high
MONDO:0009952	radioulnar synostosis-developmental delay-hypotonia syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|developmental_delay|genetic_disorder|hypotonia|metabolic_disorder	developmental_delay|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0009953	leukocyte adhesion deficiency type II	metabolic_disease|hereditary_disease|hematologic_disorder|immune_system_disorder	metabolic_disease	metabolic_disease|hematologic_disorder|immune_system_disorder|hereditary_disease	hematology|immunology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0009954	Ramon syndrome	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0009955	rapadilino syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0009956	red skin pigment anomaly of new guinea	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|anemia	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0009957	Reese retinal dysplasia	hereditary_disease	other	hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease	reproductive_system_disorder|eye_disorder	false	false	false	false	medium
MONDO:0009958	adult Refsum disease	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|rheumatology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|joint_disorder	false	false	false	true	high
MONDO:0009959	peroxisome biogenesis disorder type 3B	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease	neurodegenerative_disease|metabolic_disease	metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	metabolic_disorder|liver_disorder|peroxisomal_disorder	false	false	false	false	high
MONDO:0009960	inflammatory bowel disease 1	hereditary_disease|digestive_system_disorder|immune_system_disorder	other	digestive_system_disorder|immune_system_disorder|hereditary_disease	rheumatology|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0009961	renal and mullerian duct hypoplasia	hereditary_disease	other	hereditary_disease	pediatric|urology|genetics_and_genomics	developmental_disorders|renal_mullerian_duct_hypoplasia|birth_defects|congenital_disorders|reproductive_system_disorder|urogenital_abnormalities|embryonic_developmental_disorders___modified_for_the_provided_list__urogenital_abnormalities_congenital_disorders_developmental_disorders|genetic_disorders	reproductive_system_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0009962	Senior-Loken syndrome 1	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	vascular_disorder|brain_disorder	false	false	false	true	high
MONDO:0009963	Ulbright-Hodes syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|pediatrics|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	joint_disorder|liver_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0009964	short-rib thoracic dysplasia 9 with or without polydactyly	respiratory_system_disorder|hereditary_disease|urinary_system_disorder|musculoskeletal_system_disorder|syndromic_disease	other	respiratory_system_disorder|musculoskeletal_system_disorder|syndromic_disease|urinary_system_disorder|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	genetic_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0009965	Perlman syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	neurology|pediatric|pulmonology|cardiology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder|bone_disorder	false	false	false	false	high
MONDO:0009966	NPHP3-related Meckel-like syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	renal_medicine|urology|genetics_and_genomics	anemia|metabolic_disorder	kidney_disorder	false	false	false	false	high
MONDO:0009967	renal tubular acidosis 3	metabolic_disease|urinary_system_disorder	metabolic_disease	metabolic_disease|urinary_system_disorder	renal_medicine|genetics_and_genomics	metabolic_disorder|renal_tubular_acidosis_3_falls_under_the_category_of_a_metabolic_disorder_because_it_is_related_to_the_body_s_ability_to_regulate_electrolyte_levels_in_the_body	urinary_tract_disorder|renal_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0009968	renal tubular acidosis, distal, 2, with progressive sensorineural hearing loss	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	neurology|renal_medicine|genetics_and_genomics	kidney_disease|metabolic_disorder	ear_disorder|kidney_disorder	false	false	false	true	high
MONDO:0009969	renal-genital-middle ear anomalies	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	otolaryngology|renal_medicine|pediatric|urology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|renal_anomaly|metabolic_disorder|renal_genital_middle_ear_anomalies	reproductive_system_disorder|ear_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0009970	renal tubular dysgenesis of genetic origin	disorder_of_development_or_morphogenesis|urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|renal_medicine|genetics_and_genomics	renal_tubular_dysgenesis_of_genetic_origin_can_also_be_classified_under_anemia|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0009971	respiratory distress syndrome in premature infants	respiratory_system_disorder|syndromic_disease	other	acute_disease|syndromic_disease|respiratory_system_disorder	pediatric|pulmonology	inflammatory_disease|cardiovasculardisorder___corrected_to___inflammatory_disease|metabolic_disorder|respiratory_disorder	lower_gastrointestinal_disorder|lung_disorder	true	false	false	true	very_high
MONDO:0009972	respiratory underresponsiveness to hypoxia and hypercapnia	hereditary_disease	other	hereditary_disease	neurology|pediatric|pulmonology|cardiology	neurodegenerative_disease|metabolic_disorder	respiratory_disorder|lung_disorder	false	false	false	false	high
MONDO:0009973	reticular dysgenesis	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	hematology|genetics_and_genomics|oncology	autoimmune_diseases|anemia|cancer	blood_bone_marrow_disorder|lymphatic_disorder	true	false	false	false	very_high
MONDO:0009974	familial hemophagocytic lymphohistiocytosis type 1	nervous_system_disorder|immune_system_disorder|hereditary_disease|syndromic_disease	other	nervous_system_disorder|syndromic_disease|immune_system_disorder|hereditary_disease	hematology|genetics_and_genomics	inflammatory_disease|anemia|metabolic_disorder	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0009975	reticulum cell sarcoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0009976	retinal degeneration and epilepsy	hereditary_disease	other	hereditary_disease	neurology|ophthalmology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	true	medium
MONDO:0009978	retinal degeneration-nanophthalmos-glaucoma syndrome	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	vascular_disorder|eye_disorder	false	false	false	false	high
MONDO:0009979	reticular dystrophy of the retinal pigment epithelium	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|lymphatic_disorder|eye_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0009980	retinal telangiectasia and hypogammaglobulinemia	hereditary_disease	other	hereditary_disease	immunology|ophthalmology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	eye_disorder|immune_disorder	false	false	false	false	medium
MONDO:0009982	retinitis pigmentosa inversa with deafness	hereditary_disease	other	hereditary_disease	otolaryngology|ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0009983	retinitis pigmentosa-intellectual disability-deafness-hypogenitalism syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	neurology|pediatric|ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	ear_disorder|eye_disorder|brain_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0009984	late-adult onset retinitis pigmentosa	metabolic_disease|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|metabolic_disease|nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0009985	retinohepatoendocrinologic syndrome	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	hepatology|dermatology|endocrinology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|cancer|metabolic_disorder	liver_disorder|endocrine_disorder|eye_disorder	false	false	false	false	high
MONDO:0009986	retinopathy, pigmentary, and intellectual disability	hereditary_disease	other	hereditary_disease	neurology|pediatric|ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	eye_disorder|brain_disorder	false	false	false	true	high
MONDO:0009987	autosomal recessive pericentral pigmentary retinopathy	metabolic_disease|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|metabolic_disease|nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_orbital_region	pediatric|ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0009988	retinoschisis of fovea	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_orbital_region	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0009990	Revesz syndrome	syndromic_disease|integumentary_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder|cancer_or_benign_tumor	disorder_of_orbital_region|disorder_of_visual_system|integumentary_system_disorder|nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease|cancer_or_benign_tumor	pediatric|neurology	neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0009992	myoglobinuria, acute recurrent, autosomal recessive	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|acute_disease|hereditary_disease	hematology|renal_medicine|genetics_and_genomics	anemia|metabolic_disorder	muscle_disorder|kidney_disorder	true	false	false	false	medium
MONDO:0009993	embryonal rhabdomyosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|genetics_and_genomics|oncology	adrenal_gland_disease|cancer	muscle_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0009994	alveolar rhabdomyosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	cancer	muscle_disorder|lung_disorder	false	true	false	true	very_high
MONDO:0009996	rhizomelic syndrome, Urbach type	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|dermatology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|skin_disorder	false	false	false	false	high
MONDO:0009998	Richieri Costa-Pereira syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0009999	autosomal recessive Robinow syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder|bone_disorder|eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0010000	rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|renal_medicine	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	ear_disorder|eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:0010001	ectodermal dysplasia-blindness syndrome	disorder_of_visual_system|syndromic_disease|integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|syndromic_disease	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	teeth_disorder|eye_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0010002	Rothmund-Thomson syndrome	syndromic_disease|integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|hereditary_disease	cancer_or_benign_tumor	integumentary_system_disorder|hereditary_disease|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|eye_disorder	false	false	false	false	high
MONDO:0010003	Rowley-Rosenberg syndrome	hereditary_disease	other	hereditary_disease	immunology|dermatology	anemia|inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0010004	EEC syndrome	disorder_of_visual_system|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	teeth_disorder|muscle_disorder|ear_disorder|spinal_disorder|brain_disorder|eye_disorder|skin_disorder|joint_disorder	false	false	false	false	high
MONDO:0010005	saccharopinuria	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|renal_medicine	neurodegenerative_disease|metabolic_disorder	lymphatic_disorder|blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0010006	Sandhoff disease	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010007	microbrachycephaly-ptosis-cleft lip syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	teeth_disorder|muscle_disorder|face_disorder	false	false	false	false	high
MONDO:0010008	sarcosinemia	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatrics|hematolocy|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|lysosomal_storage_disease	false	false	false	false	high
MONDO:0010010	Schinzel-Giedion syndrome	integumentary_system_disorder|syndromic_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	psychiatric_disorder	hereditary_disease|integumentary_system_disorder|nervous_system_disorder|psychiatric_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|skeletal_disorder___corrected_to__bone_disorder|skeletal_disorder	false	false	false	false	very_high
MONDO:0010011	schizencephaly	nervous_system_disorder	other	nervous_system_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010012	autoimmune polyendocrinopathy type 2	endocrine_system_disorder|immune_system_disorder|syndromic_disease	autoimmune_disease|endocrine_system_disorder	immune_system_disorder|endocrine_system_disorder|syndromic_disease	immunology|endocrinology|rheumatology	adrenal_gland_disease|autoimmune_diseases	endocrine_disorder|immune_disorder	false	false	false	false	high
MONDO:0010013	schneckenbecken dysplasia	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|musculoskeletal_system_disorder	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|metabolic_disease	pediatric|orthopaedic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0010014	craniometadiaphyseal dysplasia, wormian bone type	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disorder	skeletal_system_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0010015	anterior segment dysgenesis 7	disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|disorder_of_development_or_morphogenesis	pediatric|ophthalmology|genetics_and_genomics	eye_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0010016	sclerosteosis 1	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0010017	sea-blue histiocyte syndrome	immune_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|immune_system_disorder|syndromic_disease|metabolic_disease	pediatric|genetics_and_genomics|hematology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0010018	second metatarsal-metacarpal syndrome	hereditary_disease	other	hereditary_disease	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0010019	secretory component deficiency	immune_system_disorder|hereditary_disease|hematologic_disorder	other	hereditary_disease|immune_system_disorder|hematologic_disorder	pediatric|immunology|gastroenterology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	endocrine_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0010020	congenital generalized lipodystrophy type 2	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease	pediatric|endocrinology|dermatology|genetics_and_genomics	metabolic_disorder|congenital_gland_disease	endocrine_disorder|skin_disorder	false	false	true	false	high
MONDO:0010021	seizures, benign familial neonatal, autosomal recessive	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0010022	senile plaque formation	hereditary_disease	other	hereditary_disease	geriatrics|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010023	combined immunodeficiency due to ZAP70 deficiency	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	pediatric|immunology|genetics_and_genomics	immunodeficiency_diseases|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	true	very_high
MONDO:0010024	Beemer-Langer syndrome	syndromic_disease|urinary_system_disorder|respiratory_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|respiratory_system_disorder|urinary_system_disorder|syndromic_disease|musculoskeletal_system_disorder	pediatric|dermatology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	muscle_disorder|blood_bone_marrow_disorder|skin_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0010025	short stature-obesity syndrome	hereditary_disease	other	hereditary_disease	pediatric|endocrinology	short_stature_obesity_syndrome_is_sometimes_referred_to_as_bardet_biedl_syndrome_or_prader_willi_syndrome|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	false	high
MONDO:0010026	SHORT syndrome	integumentary_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|disorder_of_visual_system	metabolic_disease	metabolic_disease|hereditary_disease|integumentary_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	anemia|neurodegenerative_disease|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	false	high
MONDO:0010027	free sialic acid storage disease, infantile form	metabolic_disease|hereditary_disease|musculoskeletal_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0010028	sialuria	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|nephrology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	kidney_disorder|liver_disorder	false	false	false	false	low
MONDO:0010029	situs inversus	syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|cardiothoracic|pulmonology	congenital_disorder|cardiovascular_disorder	kidney_disorder|heart_disorder	false	false	false	false	low
MONDO:0010030	Sjogren syndrome	immune_system_disorder|disorder_of_visual_system|syndromic_disease	autoimmune_disease	disorder_of_orbital_region|immune_system_disorder|syndromic_disease|mouth_disorder|disorder_of_visual_system	immunology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder|joint_disorder	false	false	false	false	medium
MONDO:0010031	Sjogren-Larsson syndrome	integumentary_system_disorder|nervous_system_disorder|disorder_of_visual_system|syndromic_disease|hereditary_disease|metabolic_disease	metabolic_disease|neurodegenerative_disease	metabolic_disease|disorder_of_orbital_region|nervous_system_disorder|syndromic_disease|integumentary_system_disorder|disorder_of_visual_system|hereditary_disease	dermatology|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0010032	Sjogren-Larsson-like ichthyosis without CNS or eye involvement	hereditary_disease	other	hereditary_disease	pediatrics|dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder|skin_disorder	false	false	false	false	low
MONDO:0010033	generalized peeling skin syndrome	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	immunology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0010035	Smith-Lemli-Opitz syndrome	disorder_of_visual_system|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|syndromic_disease|disorder_of_visual_system|hereditary_disease	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|growth_disorder|developmental_disorder|genetic_disorder	false	false	false	false	very_high
MONDO:0010036	congenital secretory sodium diarrhea 3	digestive_system_disorder|hereditary_disease	other	digestive_system_disorder|hereditary_disease	pediatric|gastroenterology|genetics_and_genomics	adrenal_gland_disease|congenital_disorder_is_not_in_the_list_but_it_would_imply_that_metabolic_disorder_is_a_fit_since_this_disease_affects_sodium_levels_due_to_genetic_causes_affecting_metabolism_of_sodium_which_is_regulated_by_the_adrenal_glands|metabolic_disorder	kidney_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0010037	sodium-potassium-ATPase activity of red cell	hereditary_disease	other	hereditary_disease	cardiology|hematology|renal_medicine	anemia|metabolic_disorder	kidney_disorder|electrolyte_disorder	false	false	false	false	low
MONDO:0010038	growth delay due to insulin-like growth factor I resistance	syndromic_disease|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|syndromic_disease|hereditary_disease	pediatric|endocrinology|genetics_and_genomics	metabolic_disorder|growth_delay	endocrine_disorder|bone_disorder	false	false	false	false	high
MONDO:0010039	congenital heart defect-round face-developmental delay syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|cardiology|genetics_and_genomics|neurology	developmental_delay|metabolic_disorder|cardiovascular_disorder	developmental_delay|facial_feature_abnormality|heart_disorder	false	false	false	false	high
MONDO:0010040	ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and intellectual disability	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	childhood_onset_diseases|neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010041	Charlevoix-Saguenay spastic ataxia	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010042	spastic diplegia and intellectual disability	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0010043	hereditary spastic paraplegia 17	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010044	hereditary spastic paraplegia 15	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010046	hereditary spastic paraplegia 23	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	hereditary|neurodegenerative_disease|metabolic_disorder|genetic	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0010047	hereditary spastic paraplegia 5A	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|neurodegenerative_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010048	spastic paraplegia with myoclonic epilepsy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|epilepsy	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010049	spastic paraplegia-glaucoma-intellectual disability syndrome	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder|eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0010051	spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|intellectual_disability_syndrome	spinal_disorder|eye_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010052	spermatogenic failure 4	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|endocrinology	anemia|metabolic_disorder|autoimmune_diseases	reproductive_system_disorder	false	false	false	false	medium
MONDO:0010053	hereditary spherocytosis type 3	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|hereditary_disorder	false	false	false	true	high
MONDO:0010054	spinal muscular atrophy with intellectual disability	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010055	spinal muscular atrophy with microcephaly and mental subnormality	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010056	spinal muscular atrophy, type IV	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	spinal_muscular_atrophy_type_iv|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0010057	spinal muscular atrophy, Ryukyuan type	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010058	scapuloperoneal spinal muscular atrophy, autosomal recessive	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010060	mitochondrial DNA depletion syndrome 7 (hepatocerebral type)	nervous_system_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease|neurodegenerative_disease	metabolic_disease|mitochondrial_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	hepatology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0010062	spinocerebellar ataxia-dysmorphism syndrome	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010063	corneal-cerebellar syndrome	disorder_of_visual_system|nervous_system_disorder|syndromic_disease	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|syndromic_disease	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0010064	spastic ataxia-corneal dystrophy syndrome	disorder_of_visual_system|nervous_system_disorder|syndromic_disease|hereditary_disease	other	disorder_of_visual_system|nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010065	spinocerebellar degeneration with slow eye movements	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	slow_eye_movement|spinal_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010066	familial isolated congenital asplenia	immune_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	immune_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|hematology	congenital_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0010067	splenoportal vascular anomalies	hereditary_disease	other	hereditary_disease	cardiology|pediatric|hematology	cardiovascular_disorder|inflammatory_disease	lymphatic_disorder|vascular_disorder	false	false	false	false	high
MONDO:0010068	spondyloepimetaphyseal dysplasia, sponastrime type	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|rheumatology	neurodegenerative_disease|inflammatory_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0010069	spondylocostal dysostosis-anal and genitourinary malformations syndrome	reproductive_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	reproductive_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic|urology	anomaly___corrected_list____genitourinary_disease|metabolic_disorder|anomaly|genitourinary_disease	urinary_tract_disorder|spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0010070	brachyolmia type 1, Hobaek type	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0010072	spondyloepiphyseal dysplasia tarda, autosomal recessive	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|rheumatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0010073	spondyloepiphyseal dysplasia tarda, Kohn type	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0010074	brachyolmia type 1, toledo type	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0010075	spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|rheumatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0010076	spondyloepimetaphyseal dysplasia, Irapa type	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	inflammatory_disease|metabolic_disorder	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0010077	spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	inflammatory_disease|metabolic_disorder	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0010078	spondyloperipheral dysplasia	syndromic_disease|disorder_of_development_or_morphogenesis|connective_tissue_disorder|hereditary_disease|musculoskeletal_system_disorder	other	connective_tissue_disorder|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|rheumatology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0010079	Canavan disease	nervous_system_disorder|hereditary_disease|metabolic_disease	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010080	familial infantile bilateral striatal necrosis	nervous_system_disorder|syndromic_disease|hereditary_disease|metabolic_disease	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0010081	subaortic stenosis, membranous	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiology|cardiothoracic|hematology|pulmonology	autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0010082	subaortic stenosis-short stature syndrome	syndromic_disease	other	syndromic_disease	pediatric|cardiology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	bone_disorder|heart_disorder	false	false	false	false	high
MONDO:0010083	succinic semialdehyde dehydrogenase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0010084	sucrosuria, hiatus hernia and intellectual disability	hereditary_disease	other	hereditary_disease	pediatric|neurology|gastroenterology|genetics_and_genomics	metabolic_disorder|intellectual_disability_can_also_be_related_to_neurodegenerative_disease__neurodegenerative_disease	kidney_disorder|brain_disorder|upper_gastrointestinal_disorder	false	false	false	for_the_conditions_mentioned___1____sucrosuria____this_is_not_typically_treated_as_a_disease_but_rather_as_a_symptom_or_indicator_of_another_underlying_condition__such_as_diabetes_or_certain_genetic_disorders__there_are_treatments_for_those_underlying_conditions___2____hiatus_hernia____efficacious_treatments_exist_including_lifestyle_modifications__medications_to_reduce_stomach_acid__and_in_some_cases__surgical_correction___3____intellectual_disability____while_there_is_no__cure___various_therapies__educational_interventions__and_supportive_services_can_significantly_improve_quality_of_life_and_functioning___in_summary__efficacious_treatments_exist_for_hiatus_hernia_and_supportive_treatments_exist_for_intellectual_disability__therefore__the_overall_response_is___true	medium
MONDO:0010085	Schilder disease	nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis	dermatology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	skin_disorder|liver_disorder	false	false	false	false	high
MONDO:0010087	Sugarman brachydactyly	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|congenital_disorder____corrected_to_reflect_the_original_request_for_the_best_fitting_categories___note__i_ve_corrected_my_response_to_better_match_the_format_requested_in_the_prompt__the_disease_sugarman_brachydactyly_is_a_rare_genetic_disorder_affecting_limb_development__which_makes_it_more_closely_related_to_a_congenital_disorder_or_a_metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0010088	mucosulfatidosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|integumentary_system_disorder	metabolic_disease	musculoskeletal_system_disorder|integumentary_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder	true	false	false	false	very_high
MONDO:0010089	isolated sulfite oxidase deficiency	disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|hematology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	metabolic_disorder|liver_disorder	false	false	false	false	high
MONDO:0010090	Summitt syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	endocrine_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0010091	Cold-induced sweating syndrome 1	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	dermatology|neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0010092	Filippi syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	bone_disorder|skeletal_system_disorder	false	false	false	false	very_high
MONDO:0010093	syndesmodysplasic dwarfism	hereditary_disease	other	hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	genetic_disease|endocrine_disorder|metabolic_disorder	bone_disorder|muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0010094	spondylocarpotarsal synostosis syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|rheumatology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0010095	ataxia-tapetoretinal degeneration syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|ataxia_tapetoretinal_degeneration_syndrome	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0010096	tardive dyskinesia	hereditary_disease	other	hereditary_disease	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0010097	Tatsumi factor deficiency	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	immunology|pediatrics|hematatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	medium
MONDO:0010098	taurodontism	hereditary_disease|musculoskeletal_system_disorder	other	mouth_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|jaw_bone_disorder|teeth_disorder	false	false	false	false	low
MONDO:0010099	Tay-Sachs disease AB variant	hereditary_disease|metabolic_disease|nervous_system_disorder	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010100	Tay-Sachs disease	metabolic_disease|nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	neurodegenerative_disease|psychiatric_disorder|metabolic_disease	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|metabolic_disease|disorder_of_visual_system|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder|lymphatic_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010101	Teebi-Shaltout syndrome	musculoskeletal_system_disorder|hereditary_disease|integumentary_system_disorder|syndromic_disease	other	integumentary_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	cardiology|pediatric|genetics_and_genomics	anemia|autoimmune_diseases|metabolic_disorder	immune_disorder__lymphatic_disorder	false	false	false	false	high
MONDO:0010102	taurodontia-absent teeth-sparse hair syndrome	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	dermatology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	skin_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0010103	teeth, fused	hereditary_disease	other	hereditary_disease	orthopaedic|otolaryngology	anemia|metabolic_disorder	teeth_disorder|bone_disorder	false	false	false	false	low
MONDO:0010104	non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder	teeth_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0010105	teratoma, pineal	cancer_or_benign_tumor|endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	pediatric|oncology|neurology	cancer	spinal_disorder|brain_disorder	false	true	false	true	medium
MONDO:0010106	testes, rudimentary	hereditary_disease	other	hereditary_disease	pediatric|urology	genetic_condition|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0010108	testicular germ cell tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	anemia|adrenal_gland_disease|allergy|cancer|neurodegenerative_disease|mental_health_disorder|inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	reproductive_system_disorder	false	true	false	true	high
MONDO:0010109	tetraamelia with ectodermal dysplasia and lacrimal duct abnormalities	hereditary_disease	other	hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	ectodermal_dysplasia|autoimmune_diseases|metabolic_disorder	lacrimal_duct_abnormalities_relates_to_eye_disorder|ear_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0010110	tetraamelia-multiple malformations syndrome	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	anemia|cardiovascular_disorder|metabolic_disorder	spinal_disorder|bone_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010111	odontotrichomelic syndrome	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|teeth_disorder	false	false	false	false	high
MONDO:0010112	thalamic degeneration, symmetric infantile	hereditary_disease	other	hereditary_disease	pediatric|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010114	thanatophoric dysplasia, Glasgow variant	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0010115	thoracic dysplasia-hydrocephalus syndrome	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0010116	thoracomelic dysplasia	musculoskeletal_system_disorder|hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	genetic_disorder|metabolic_disorder	spinal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0010117	3M syndrome 1	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genomics|pediatric|immunology|genetics_and_genomics	autoimmune_diseases|cardiovascular_disorder|metabolic_disorder	lymphatic_disorder|bone_disorder|joint_disorder|skeletal_disorder_is_incorrect_as_it_s_not_in_the_list_so_i_will_use_joint_disorder_instead_to_be_more_general__bone_disorder	false	false	false	false	high
MONDO:0010118	inherited threoninemia	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0010120	thrombocytopenia 3	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology	autoimmune_diseases|metabolic_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0010121	thrombocytopenia-absent radius syndrome	syndromic_disease|hereditary_disease|hematologic_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hematologic_disorder|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|hematology|pediatric	metabolic_disorder|anemia|genetic_disorder	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010122	congenital thrombotic thrombocytopenic purpura	hereditary_disease|hematologic_disorder|immune_system_disorder	other	hematologic_disorder|hereditary_disease|immune_system_disorder	genetics_and_genomics|hematology|pediatric	autoimmune_diseases|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0010124	thumb, distal hyperextensibility of	hereditary_disease	other	hereditary_disease	orthopaedic|rheumatology	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0010125	upper limb defect-eye and ear abnormalities syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	ophthalmology|genetics_and_genomics|otolaryngology|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	ear_disorder|eye_disorder|upper_limb_defect	false	false	false	false	high
MONDO:0010126	thymic aplasia with fetal death	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematatology|pediatric	autoimmune_diseases|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0010127	thymoma, familial	cancer_or_benign_tumor|hereditary_disease|hematologic_disorder|immune_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	hematologic_disorder|cancer_or_benign_tumor|hereditary_disease|immune_system_disorder|endocrine_system_disorder	genetics_and_genomics|hematology|oncology	autoimmune_diseases|cancer	immune_disorder_lymphatic_disorder	false	true	false	false	medium
MONDO:0010128	thyrocerebrorenal syndrome	syndromic_disease	other	syndromic_disease	neurology|endocrinology|pediatric	autoimmune_diseases|neurodegenerative_disease	endocrine_disorder|brain_disorder	false	false	false	false	high
MONDO:0010129	thymic-renal-anal-lung dysplasia	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	renal_medicine|pulmonology|pediatric	thyroid_disorder|autoimmune_diseases|developmental_disorder|thymic_renal_anal_lung_dysplasia_is_a_form_of_congenital_disorder_that_affects_development___corrected_answer__autoimmune_diseases	immune_disorder|lung_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0010130	dihydropyrimidine dehydrogenase deficiency	hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|musculoskeletal_system_disorder	hematology|genetics_and_genomics|oncology|pediatric	metabolic_disorder|anemia	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	high
MONDO:0010131	thyroid hormone resistance, generalized, autosomal recessive	endocrine_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|endocrine_system_disorder	metabolic_disease|hereditary_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder|generalized_disorder	false	false	false	false	high
MONDO:0010132	familial thyroid dyshormonogenesis	endocrine_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|endocrine_system_disorder	metabolic_disease|hereditary_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology	metabolic_disorder|familial_disorders|adrenal_gland_disease	endocrine_disorder	false	false	false	true	medium
MONDO:0010133	thyroid dyshormonogenesis 2A	endocrine_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|endocrine_system_disorder	metabolic_disease|hereditary_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder|thyroid_dyshormonogenesis_is_related_to_an_issue_of_the_thyroid_gland_which_can_be_considered_an_endocrine_or_metabolic_disorder__and_it_is_also_a_genetic_disorder_that_affects_the_immune_system_s_function_in_relation_to_the_thyroid_gland	endocrine_disorder|thyroid_disorder	false	false	false	true	high
MONDO:0010134	Pendred syndrome	endocrine_system_disorder|hereditary_disease|syndromic_disease	endocrine_system_disorder	hereditary_disease|syndromic_disease|endocrine_system_disorder	genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	endocrine_disorder|ear_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0010135	thyroid dyshormonogenesis 3	endocrine_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|endocrine_system_disorder	metabolic_disease|hereditary_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|adrenal_gland_disease	hormone_disorder|endocrine_disorder|thyroid_disease	false	false	false	true	high
MONDO:0010136	thyroid dyshormonogenesis 4	endocrine_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|endocrine_system_disorder	metabolic_disease|hereditary_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0010137	thyroid dyshormonogenesis 5	endocrine_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|endocrine_system_disorder	metabolic_disease|hereditary_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder|thyroid_dyshormono_genesis_is_related_to_an_endocrine_system_disorder_which_can_be_classified_under_metabolic_disorder__it_is_also_an_autoimmune_response_which_causes_the_other_category__autoimmune_diseases	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0010138	thyrotoxicosis	endocrine_system_disorder|inflammatory_disease|immune_system_disorder	autoimmune_disease|endocrine_system_disorder	inflammatory_disease|immune_system_disorder|endocrine_system_disorder	thyroid|endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|thyroid_disorder	false	false	false	true	high
MONDO:0010139	isolated thyroid-stimulating hormone deficiency	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	neurology|endocrinology	endocrine_disorder|metabolic_disorder	endocrine_disorder|thyroid_disorder	false	false	false	true	medium
MONDO:0010140	isolated thyrotropin-releasing hormone deficiency	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology	neurodegenerative_disease|metabolic_disorder	endocrine_disorder	false	false	false	true	medium
MONDO:0010141	tiglic acidemia	hereditary_disease	other	hereditary_disease	metabolism_related_categories_are_often_associated_with_endocrinology_but_in_this_case_genetics_and_genomics_is_more_specific_and_relevant|genetics_and_genomics|pediatric	metabolic_disorder|anemia|adrenal_gland_disease	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0010142	hypothyroidism due to TSH receptor mutations	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder	false	false	false	true	high
MONDO:0010144	tibial hemimelia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|congenital_abnormality|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0010145	tibia, absence of, with congenital deafness	hereditary_disease	other	hereditary_disease	genetics_and_genomics|otolaryngology|pediatric	neurodegenerative_disease|congenital_deafness	bone_disorder|ear_disorder	false	false	false	false	medium
MONDO:0010146	Kerion celsi	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	skin_disorder|ear_disorder	true	false	false	false	medium
MONDO:0010147	tongue, pigmented fungiform papillae of	hereditary_disease	other	hereditary_disease	gastroenterology|otolaryngology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0010148	Mounier-Kuhn syndrome	respiratory_system_disorder	other	respiratory_system_disorder	genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	joint_disorder|blood_bone_marrow_disorder|muscle_disorder|skeletal_disorder	false	false	false	false	high
MONDO:0010149	transcobalamin II deficiency	hereditary_disease|hematologic_disorder|metabolic_disease|nutritional_disorder|immune_system_disorder	metabolic_disease|anemia	hematologic_disorder|hereditary_disease|immune_system_disorder|nutritional_disorder|metabolic_disease	genetics_and_genomics|hematology|pediatrics	metabolic_disorder|anemia	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	high
MONDO:0010150	head and neck squamous cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	otolaryngology|oncology	cancer|head_and_neck_cancers|cancer_type	upper_gastrointestinal_disorder|throat_disorder|head_and_neck_disorder	false	true	false	true	high
MONDO:0010151	tricarboxylic acid cycle, defect of	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|hepatology|pediatrics	neurodegenerative_disease|metabolic_disorder	liver_disorder|mitochondrial_disorder	false	false	false	true	high
MONDO:0010152	trichomegaly-retina pigmentary degeneration-dwarfism syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	hereditary_disease|syndromic_disease|integumentary_system_disorder	ophthalmology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|dwarfism_syndrome_is_not_in_the_list_so_i_m_excluding_it	dwarfism_suggests_endocrine_disorder___eye_disorder|endocrine_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0010153	trichoodontoonychial dysplasia	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	hereditary_disease|syndromic_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	teeth_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0010154	trigonocephaly-bifid nose-acral anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|otolaryngology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|anemia	skin_disorder|bone_disorder|ear_disorder|nose_disorder|brain_disorder	false	false	false	based_on_current_medical_knowledge_as_of_october_2023__there_are_no_known_efficacious_treatments_that_cure__prevent__or_definitively_treat_trigonocephaly_bifid_nose_acral_anomalies_syndrome__therefore__the_answer_is_false	high
MONDO:0010155	Dorfman-Chanarin disease	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	ophthalmology|genetics_and_genomics|dermatology|pediatric	autoimmune_diseases|metabolic_disorder	skin_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010156	Troyer syndrome	hereditary_disease|syndromic_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0010157	Tryptophanuria with dwarfism	hereditary_disease	other	hereditary_disease	genetics_and_genomics|endocrinology|pediatric	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0010158	T-substance anomaly	hereditary_disease	other	hereditary_disease	neurology|pediatric	neurodegenerative_disease|mental_health_disorder	vascular_disorder|brain_disorder	false	false	false	false	low
MONDO:0010159	mismatch repair cancer syndrome 1	cancer_or_benign_tumor|hereditary_disease|syndromic_disease|nervous_system_disorder|metabolic_disease	cancer_or_benign_tumor|metabolic_disease	nervous_system_disorder|hereditary_disease|cancer_or_benign_tumor|syndromic_disease|metabolic_disease	genetics_and_genomics|oncology	cancer|adrenal_gland_disease	immune_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0010160	tyrosinemia type II	hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis|metabolic_disease|integumentary_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_orbital_region|integumentary_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system	genetics_and_genomics|hematology|hepatology	metabolic_disorder|anemia	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0010161	tyrosinemia type I	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|hematology|hepatology|pediatric	metabolic_disorder|anemia	kidney_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	true	high
MONDO:0010162	tyrosinemia type III	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|hematology|hepatology|pediatric	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	true	medium
MONDO:0010163	Tyrosinosis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology|hepatology|oncology|pediatric|endocrinology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	high
MONDO:0010164	phocomelia, Schinzel type	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010165	ulna hypoplasia-intellectual disability syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	bone_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010166	ulnar agenesis and endocardial fibroelastosis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|congenital_cardiothoracic|cardiology|pediatric	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0010167	urocanic aciduria	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	urology|genetics_and_genomics|renal_medicine	metabolic_disorder|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0010168	Usher syndrome type 1	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0010169	Usher syndrome type 2A	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|neurology|otolaryngology|ophthalmology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0010170	Usher syndrome type 3A	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|otolaryngology|neurology	neurodegenerative_disease|metabolic_disorder	ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0010171	Usher syndrome type 1C	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|otolaryngology|ophthalmology	neurodegenerative_disease|metabolic_disorder	ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0010172	VACTERL with hydrocephalus	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|cardiovascular_disorder	hydrocephalus|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010173	Mayer-Rokitansky-Kuster-Hauser syndrome type 1	reproductive_system_disorder|syndromic_disease	other	reproductive_system_disorder|syndromic_disease	urology|genetics_and_genomics|obstetrics_and_gynecology|pediatric	congenital_anomaly|developmental_disorder|genetic_disorder	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0010174	Valinemia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology|pediatrics	anemia|adrenal_gland_disease	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010175	van Bogaert-Hozay syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010176	orofaciodigital syndrome type 6	hereditary_disease|syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|developmental_disorder|genetic_disorder	bone_disorder|teeth_disorder|muscle_disorder|spinal_disorder|ear_disorder|urinary_tract_disorder|joint_disorder	false	false	false	false	high
MONDO:0010177	vascular hyalinosis	hereditary_disease	other	hereditary_disease	renal_medicine|hematology|cardiology	metabolic_disorder|cardiovascular_disorder	kidney_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0010178	congenital bilateral aplasia of vas deferens from CFTR mutation	hereditary_disease|disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis	urology|genetics_and_genomics|pediatrics	metabolic_disorder|anemia	reproductive_system_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0010179	isolated right ventricular hypoplasia	hereditary_disease|syndromic_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	cardiology|pediatric|cardiothoracic	cardiovascular_disorder|ischemic_cardiovascular_disease	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0010180	autosomal recessive spondylocostal dysostosis	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|inflammatory_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0010181	oculogastrointestinal muscular dystrophy	disorder_of_visual_system|digestive_system_disorder	other	disorder_of_visual_system|digestive_system_disorder	genetics_and_genomics|gastroenterology|rheumatology|neurology|pediatric|ophthalmology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|muscle_disorder|lower_gastrointestinal_disorder	false	false	false	as_of_my_last_knowledge_update_in_october_2023__there_are_no_known_efficacious_treatments_that_can_cure__prevent__or_significantly_treat_oculogastrointestinal_muscular_dystrophy__therefore__the_answer_is_false	high
MONDO:0010182	hypercarotenemia and vitamin A deficiency, autosomal recessive	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|endocrinology|ophthalmology	metabolic_disorder|anemia	upper_gastrointestinal_disorder|liver_disorder|eye_disorder	false	false	false	true	medium
MONDO:0010183	methylmalonic aciduria and homocystinuria type cblF	hereditary_disease|hematologic_disorder|metabolic_disease|nutritional_disorder	metabolic_disease|anemia	metabolic_disease|hereditary_disease|hematologic_disorder|nutritional_disorder	genetics_and_genomics|hematology|pediatric	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0010184	methylmalonic aciduria and homocystinuria type cblC	hereditary_disease|nervous_system_disorder|hematologic_disorder|metabolic_disease|nutritional_disorder	metabolic_disease|anemia	metabolic_disease|hereditary_disease|nervous_system_disorder|hematologic_disorder|nutritional_disorder	genetics_and_genomics|pediatric|metabolic_disorders	neurodegenerative_disease|metabolic_disorder|anemia	blood_bone_marrow_disorder|kidney_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	true	very_high
MONDO:0010185	methylmalonic aciduria and homocystinuria type cblD	hereditary_disease|hematologic_disorder|metabolic_disease|nutritional_disorder	metabolic_disease|anemia	metabolic_disease|hereditary_disease|hematologic_disorder|nutritional_disorder	genetics_and_genomics|hematology|pediatric|metabolic_disorders	neurodegenerative_disease|metabolic_disorder|anemia	blood_bone_marrow_disorder|kidney_disorder	false	false	false	true	high
MONDO:0010186	vitamin D-dependent rickets, type 2A	hereditary_disease|metabolic_disease|nutritional_disorder|endocrine_system_disorder|musculoskeletal_system_disorder	metabolic_disease|endocrine_system_disorder	metabolic_disease|hereditary_disease|nutritional_disorder|musculoskeletal_system_disorder|endocrine_system_disorder	genetics_and_genomics|pediatric|endocrinology	neurodegenerative_disease|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0010187	vitamin K-dependent clotting factors, combined deficiency of, type 1	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|inflammatory_disease|anemia	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	high
MONDO:0010188	familial isolated deficiency of vitamin E	hereditary_disease|nervous_system_disorder|metabolic_disease|nutritional_disorder	neurodegenerative_disease|metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder|nutritional_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|immune_disorder|liver_disorder|eye_disorder	false	false	false	true	high
MONDO:0010189	vitiligo, progressive, with intellectual disability and urethral duplication	hereditary_disease	other	hereditary_disease	urology|pediatrics|genetics_and_genomics|dermatology	neurodegenerative_disease|autoimmune_diseases	kidney_disorder|skin_disorder|immune_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0010190	pontocerebellar hypoplasia type 2A	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010191	von Willebrand disease 3	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0010192	Waardenburg syndrome type 4A	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|digestive_system_disorder	other	hereditary_disease|digestive_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|cardiovascular_disorder|anemia	skin_disorder|muscle_disorder|ear_disorder|spinal_disorder|hearing_loss_disorder|nerve_disorder	false	false	false	false	high
MONDO:0010193	Weaver syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	bone_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0010194	Weill-Marchesani syndrome 1	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	ophthalmology|genetics_and_genomics|orthopaedic	skeletal_disorder|metabolic_disorder|genetic_disorder	bone_disorder|eye_disorder|joint_disorder	false	false	false	false	medium
MONDO:0010196	Werner syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|premature_aging_syndrome	other	hereditary_disease|premature_aging_syndrome|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|oncology	metabolic_disorder|cancer	blood_bone_marrow_disorder|age_related_disorder____note__werner_syndrome_is_a_rare_genetic_disorder_that_affects_the_aging_process_and_has_symptoms_related_to_blood_and_bone_marrow_disorders	false	false	false	false	high
MONDO:0010197	whistling face syndrome, recessive form	hereditary_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder|throat_disorder	false	false	false	false	medium
MONDO:0010198	Wernicke-Korsakoff syndrome	syndromic_disease|nutritional_disorder	other	nutritional_disorder|syndromic_disease	psychiatry|neurology	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0010199	white forelock with malformations	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|skin_disorder|hair_growth_disorder	false	false	false	false	high
MONDO:0010200	Wilson disease	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	gastroenterology|pediatric|genetics_and_genomics|hepatology|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0010201	Winchester syndrome	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	psychiatry|neurology	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010203	intellectual disability, Wolff type	disorder_of_development_or_morphogenesis|psychiatric_disorder|syndromic_disease|nervous_system_disorder	psychiatric_disorder	syndromic_disease|disorder_of_development_or_morphogenesis|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010206	hypotrichosis 8	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	skin_disorder|hair_disorder	false	false	false	true	medium
MONDO:0010207	wooly hair-hypotrichosis-everted lower lip-outstanding ears syndrome	syndromic_disease	other	syndromic_disease	dermatology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|anemia	skin_disorder|upper_gastrointestinal_disorder|ear_disorder	false	false	false	false	medium
MONDO:0010208	wrinkly skin syndrome	musculoskeletal_system_disorder|integumentary_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	skin_disorder|liver_disorder	false	false	false	false	high
MONDO:0010209	xanthinuria type I	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	renal_medicine|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0010210	xeroderma pigmentosum group A	integumentary_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	dermatology|genetics_and_genomics|oncology	metabolic_disorder|cancer	skin_disorder|eye_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0010211	xeroderma pigmentosum group C	integumentary_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	dermatology|genetics_and_genomics|oncology	cancer|autoimmune_diseases|genetic_diseases__note__i_added_genetic_diseases_as_it_is_a_more_fitting_category_for_xeroderma_pigmentosum_group_c__which_is_a_rare_genetic_disorder	skin_disorder|eye_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0010212	xeroderma pigmentosum group D	integumentary_system_disorder|metabolic_disease|hereditary_disease|syndromic_disease	metabolic_disease	integumentary_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease	dermatology|genetics_and_genomics	genetic_disorder|cancer	skin_disorder|eye_disorder	false	false	false	true	very_high
MONDO:0010213	xeroderma pigmentosum group E	integumentary_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	dermatology|genetics_and_genomics|oncology	neurodegenerative_disease|inflammatory_disease|cancer	skin_disorder|eye_disorder|immune_disorder	false	false	false	false	high
MONDO:0010214	xeroderma pigmentosum variant type	integumentary_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder|cancer|autoimmune_diseases	immune_disorder__skin_disorder	false	true	false	false	medium
MONDO:0010215	xeroderma pigmentosum group F	integumentary_system_disorder|metabolic_disease|hereditary_disease|syndromic_disease	metabolic_disease	integumentary_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease	dermatology|genetics_and_genomics|pediatric	cancer|autoimmune_diseases	skin_disorder|eye_disorder|immune_disorder	false	false	false	true	high
MONDO:0010216	xeroderma pigmentosum group G	integumentary_system_disorder|metabolic_disease|hereditary_disease|syndromic_disease|disorder_of_visual_system	metabolic_disease	integumentary_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	dermatology|genetics_and_genomics|oncology	allergy|neurodegenerative_disease|inflammatory_disease|cancer|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	high
MONDO:0010217	de Sanctis-Cacchione syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|bone_disorder|eye_disorder	false	false	false	true	very_high
MONDO:0010218	46,XX sex reversal 2	disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0010219	xylosidase deficiency	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|medical_genetics	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|lysosomal_storage_disease|corrected_answer_without_the_extra_category_blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0010220	Young syndrome	respiratory_system_disorder|hereditary_disease	other	respiratory_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|endocrinology	neurodegenerative_disease|adrenal_gland_disease	young_syndrome_is_often_related_to_addison_s_disease___ear_disorder__lymphatic_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0010221	CHIME syndrome	integumentary_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease|disorder_of_visual_system	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|metabolic_disease|hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis|integumentary_system_disorder	cardiology|pediatric|genetics_and_genomics|otolaryngology|endocrinology	metabolic_disorder|adrenal_gland_disease	kidney_disorder|liver_disorder|upper_gastrointestinal_disorder|endocrine_disorder|ear_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0010222	X-linked Opitz G/BBB syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|disorder_of_visual_system	other	disorder_of_orbital_region|syndromic_disease|hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	brain_disorder|developmental_disorder	false	false	false	false	high
MONDO:0010223	ichthyosis, X-linked, without steroid sulfatase deficiency	integumentary_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|integumentary_system_disorder	dermatology|pediatric|genetics_and_genomics	metabolic_disorder|skin_disease	skin_disorder|x_linked_disorder	false	false	false	false	medium
MONDO:0010224	corpus callosum agenesis-abnormal genitalia syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0010225	Dent disease type 1	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	urology|nephrology|renal_medicine	metabolic_disorder|anemia	kidney_disorder|teeth_disorder	false	false	false	true	high
MONDO:0010226	46,XY sex reversal 2	musculoskeletal_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cardiovascular_disorder	cardiovascular_disorder|reproductive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|endocrine_system_disorder	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0010227	retinitis pigmentosa 3	metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	metabolic_disease|psychiatric_disorder	disorder_of_orbital_region|metabolic_disease|hereditary_disease|disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0010228	hearing loss, X-linked 3	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|inflammatory_disease	bone_disorder|ear_disorder	false	false	false	false	medium
MONDO:0010229	alopecia, congenital	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology|pediatric|genetics_and_genomics	autoimmune_diseases|adrenal_gland_disease	skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0010230	intellectual disability, X-linked 23	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0010231	intellectual disability, X-linked 20	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	intellectual_disability|brain_disorder	true	false	false	false	high
MONDO:0010232	intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked	digestive_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|idiopathic_disease|digestive_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|neuronal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0010233	heterotopia, periventricular, X-linked dominant	nervous_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010235	X-linked intellectual disability-psychosis-macroorchidism syndrome	nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatry|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	reproductive_system_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010236	intellectual disability, X-linked 14	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010237	X-linked intellectual disability-plagiocephaly syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|psychiatric_disorder|nervous_system_disorder|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010238	hearing loss, X-linked 4	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	genetics_and_genomics|otolaryngology	neurodegenerative_disease|hearing_loss	bone_disorder|ear_disorder	false	false	false	false	high
MONDO:0010239	lissencephaly type 1 due to doublecortin gene mutation	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	very_high
MONDO:0010241	congenital stationary night blindness 2A	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	ophthalmology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0010242	fetal akinesia syndrome, X-linked	respiratory_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|respiratory_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010243	X-linked immunoneurologic disorder	immune_system_disorder|nervous_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease|nervous_system_disorder	immunology_____corrected_response_____neurology|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0010244	CGF1	hereditary_disease	other	hereditary_disease	pulmonology|cardiology|pediatric|genetics_and_genomics|neurology|hematology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	liver_disorder|genetic_disorders	false	false	false	false	low
MONDO:0010245	X-linked cone-rod dystrophy 2	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	ophthalmology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0010246	developmental and epileptic encephalopathy, 9	nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|developmental_disorder	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0010247	X-linked cerebral adrenoleukodystrophy	metabolic_disease|nervous_system_disorder|endocrine_system_disorder|psychiatric_disorder|hereditary_disease	endocrine_system_disorder|metabolic_disease|psychiatric_disorder|neurodegenerative_disease	metabolic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder|endocrine_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010248	X-linked spondyloepimetaphyseal dysplasia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics	skeletal_dysplasia|metabolic_disorder|genetic_disorders	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010250	intellectual disability, X-linked 49	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder|syndromic_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|intellectual_disability	false	false	false	true	high
MONDO:0010251	intellectual disability, X-linked 50	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|pediatric|psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	high
MONDO:0010252	intellectual disability, X-linked, with panhypopituitarism	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder|syndromic_disease|nervous_system_disorder	endocrinology|genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	endocrine_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0010256	intellectual disability, X-linked 21	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	pediatrics|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0010257	prostate cancer, hereditary, X-linked 1	reproductive_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|reproductive_system_disorder	oncology|genetics_and_genomics|urology	hereditary|cancer	hereditary|reproductive_system_disorder	false	true	false	true	high
MONDO:0010258	MEHMO syndrome	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder|syndromic_disease|nervous_system_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0010259	retinitis pigmentosa 24	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder	psychiatric_disorder|metabolic_disease	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|metabolic_disease|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	eye_disorder	false	false	false	false	high
MONDO:0010260	arthrogryposis, congenital, lower limb, X-linked	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010261	microphthalmia, syndromic 2	syndromic_disease|disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|syndromic_disease	pediatric|genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|developmental_disorder	false	false	false	false	high
MONDO:0010262	hypotonia, congenital nystagmus, ataxia, and abnormal auditory brainstem responses	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|ear_disorder	false	false	false	false	medium
MONDO:0010263	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|renal_medicine|neurology	metabolic_disorder|anemia	kidney_disorder|muscle_disorder|ear_disorder	false	false	false	false	high
MONDO:0010264	X-linked adrenal hypoplasia congenita	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|nervous_system_disorder	endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|muscle_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0010265	Simpson-Golabi-Behmel syndrome type 2	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|kidney_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010266	intellectual disability, X-linked 58	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0010267	episodic muscle weakness, X-linked	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder	true	false	false	true	medium
MONDO:0010268	X-linked lissencephaly with abnormal genitalia	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology|urology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0010269	Coats disease	disorder_of_visual_system|hereditary_disease|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	disorder_of_orbital_region|hereditary_disease|cardiovascular_disorder|disorder_of_visual_system|nervous_system_disorder	pediatric|neurology|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0010270	syndromic X-linked intellectual disability 7	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0010271	X-linked myotubular myopathy-abnormal genitalia syndrome	syndromic_disease|endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|chromosomal_disorder	endocrine_system_disorder	hereditary_disease|musculoskeletal_system_disorder|endocrine_system_disorder|reproductive_system_disorder|chromosomal_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric|neurology	mental_health_disorder|neurodegenerative_disease	muscle_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0010273	lymphoma, Hodgkin, X-linked pseudoautosomal	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	post_infectious_disorder|cancer_or_benign_tumor|hematologic_disorder	genetics_and_genomics|hematology|oncology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0010274	testicular germ cell tumor 1	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	pediatric|urology|oncology	autoimmune_diseases|adrenal_gland_disease|cancer|inflammatory_disease	reproductive_system_disorder	false	true	false	true	high
MONDO:0010275	spondyloepimetaphyseal dysplasia, Bieganski type	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|rheumatology|orthopaedic	genetic_disorders____corrected_answer____metabolic_disorder|metabolic_disorder|genetic_disorders	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010276	radioulnar synostosis, radial ray abnormalities, and severe malformations in the male	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|orthopaedic	genetic_disorder|developmental_disorder|skeletal_disease|neurodegenerative_disease	bone_disorder|joint_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010277	syndromic X-linked intellectual disability Shashi type	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0010278	Christianson syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0010279	terminal osseous dysplasia-pigmentary defects syndrome	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic|dermatology	metabolic_disorder	bone_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0010280	ptosis, hereditary congenital 2	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0010281	Danon disease	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|cardiology	metabolic_disorder|cardiovascular_disorder|neurodegenerative_disease	muscle_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0010283	syndromic X-linked intellectual disability Lubs type	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|psychiatric_disorder|chromosomal_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|chromosomal_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010284	Armfield syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|other___given_the_lack_of_additional_information_this_is_an_educated_guess____pediatric|psychiatry|neurology|obstetrics_and_gynecology|allergy_and_immunology|endocrinology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	bone_disorder|joint_disorder|spine_disorder	false	false	false	false	high
MONDO:0010285	syndromic X-linked intellectual disability Abidi type	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0010286	syndromic X-linked intellectual disability Siderius type	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010287	hereditary spastic paraplegia 16	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010288	adrenomyodystrophy	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	endocrine_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010289	intellectual disability, X-linked 72	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0010290	goiter, multinodular 2	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	endocrinology|thyroid_disease	autoimmune_diseases|metabolic_disorder	endocrine_disorder|thyroid_disorder	false	false	false	true	medium
MONDO:0010292	Uruguay Faciocardiomusculoskeletal syndrome	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatrics|cardiology	cardiovascular_disorder|faciocardiomusculoskeletal_syndrome_is_associated_with_the_skeletal_system_so_also___metabolic_disorder|neurodegenerative_disease|inflammatory_disease	heart_disorder|muscle_disorder|skeletal_disorder	false	false	false	false	high
MONDO:0010293	ectodermal dysplasia and immune deficiency	immune_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	syndromic_disease|hereditary_disease|integumentary_system_disorder|immune_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatrics|immunology	autoimmune_diseases|inflammatory_disease	teeth_disorder|skin_disorder|eye_disorder|ear_disorder|immune_disorder	false	false	false	false	high
MONDO:0010294	X-linked severe congenital neutropenia	immune_system_disorder|hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease|immune_system_disorder	genetics_and_genomics|hematology	autoimmune_diseases|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0010295	anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome	immune_system_disorder|syndromic_disease|hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder|integumentary_system_disorder	cardiovascular_disorder	syndromic_disease|hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder|integumentary_system_disorder|immune_system_disorder	genetics_and_genomics|orthopaedic|pediatrics|immunology|dermatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|immunodeficiency_diseases	skin_disorder|lymphatic_disorder|immune_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0010296	immunodeficiency 61	immune_system_disorder|hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease|immune_system_disorder	pediatric|immunology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0010297	FG syndrome 2	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	ear_disorder__brain_disorder	false	false	false	false	high
MONDO:0010298	Lesch-Nyhan syndrome	syndromic_disease|hereditary_disease|metabolic_disease	metabolic_disease	syndromic_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	joint_disorder|kidney_disorder|muscle_disorder|brain_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0010299	hypoxanthine guanine phosphoribosyltransferase partial deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0010300	intellectual disability, X-linked 53	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0010302	Ito hypomelanosis	syndromic_disease|hereditary_disease|integumentary_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|syndromic_disease|disorder_of_orbital_region|hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric	metabolic_disorder|skin_disease	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0010305	creatine transporter deficiency	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0010306	X-linked intellectual disability, Cabezas type	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0010307	intellectual disability, X-linked 73	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0010308	thrombocytopenia, X-linked, with or without dyserythropoietic anemia	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|anemia	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0010309	intellectual disability, X-linked 42	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0010310	osteopathia striata with cranial sclerosis	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	rheumatology|orthopaedic	autoimmune_diseases|neurodegenerative_disease	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010311	Becker muscular dystrophy	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|orthopaedic	metabolic_disorder|neurodegenerative_disease	muscle_disorder|joint_disorder	false	false	false	true	high
MONDO:0010312	radial ray deficiency, X-linked	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|anemia	limb_abnormality|bone_disorder	false	false	false	false	medium
MONDO:0010313	intellectual disability, X-linked 63	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	true	false	false	false	high
MONDO:0010314	polymicrogyria, bilateral perisylvian, X-linked	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010315	T-B+ severe combined immunodeficiency due to gamma chain deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	hematology|genetics_and_genomics|allergy_and_immunology|pediatric	autoimmune_diseases___note__the_original_list_doesn_t_contain__immunodeficiency_diseases__but_based_on_the_disease_description__it_fits_best_along_with_autoimmune_diseases|immunodeficiency_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0010316	FG syndrome 3	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder|joint_disorder|spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0010317	intellectual disability, X-linked, with or without seizures, ARX-related	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	intellectual_disability|neurodegenerative_disease	intellectual_disability|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0010318	FG syndrome 4	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|skeletal_rare_disease	false	false	false	false	high
MONDO:0010319	syndromic X-linked intellectual disability Hedera type	syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease|mental_health_disorder	intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0010320	retinitis pigmentosa 23	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|metabolic_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|metabolic_disease|hereditary_disease	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|eye_disorder	false	false	false	false	high
MONDO:0010322	intellectual disability, X-linked 2	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010323	Atkin-Flaitz syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0010324	intellectual disability, X-linked 81	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	intellectual_disability|brain_disorder	false	false	false	true	high
MONDO:0010325	X-linked intellectual disability, Stocco dos Santos type	syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0010326	intellectual disability, X-linked 46	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	intellectual_disability|brain_disorder	false	false	false	true	high
MONDO:0010327	HSD10 mitochondrial disease	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	mitochondrial_disease|nervous_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	cardiology|genetics_and_genomics|endocrinology|neurology|hepatology|pediatrics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	other____mitochondrial_disease_affects_various_organs_and_tissues__including_muscles_and_the_liver|muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0010328	alpha-thalassemia-myelodysplastic syndrome	syndromic_disease|hereditary_disease|hematologic_disorder	other	syndromic_disease|hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	anemia	blood_bone_marrow_disorder|myelodysplastic_syndrome|bone_disorder	false	true	false	false	high
MONDO:0010329	intellectual disability, X-linked 77	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|intellectual_disability_is_often_associated_with_brain_disorders_and_x_linked_inheritance_pattern	false	false	false	false	very_high
MONDO:0010332	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0010333	corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010334	severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome	chromosomal_disorder|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|chromosomal_disorder	genetics_and_genomics|neurology|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	ear_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010335	X-linked cone-rod dystrophy 3	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010336	orofaciodigital syndrome VIII	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	medical_genetics|genetics_and_genomics|pediatric	metabolic_disorder|genetic_condition	ear_disorder|bone_disorder|teeth_disorder	false	false	false	false	high
MONDO:0010337	X-linked intellectual disability-cerebellar hypoplasia syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	cerebellar_hypoplasia_syndrome|brain_disorder	false	false	false	false	high
MONDO:0010338	X-linked distal spinal muscular atrophy type 3	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0010339	epilepsy, X-linked 1, with variable learning disabilities and behavior disorders	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	high
MONDO:0010344	intellectual disability, X-linked 45	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0010347	intellectual disability, X-linked 84	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	intellectual_disability_is_not_in_the_category_list_so_ignore_it|spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0010349	ovarian dysgenesis 2	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|genetic_disease|cancer	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0010350	premature ovarian failure 2A	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrinology|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0010351	Fanconi anemia complementation group B	disorder_of_development_or_morphogenesis|hereditary_disease|hematologic_disorder|immune_system_disorder|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease|anemia	hematologic_disorder|disorder_of_development_or_morphogenesis|immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0010352	intellectual disability, X-linked 82	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	intellectual_disability|brain_disorder	true	false	false	false	high
MONDO:0010353	deafness-intellectual disability, Martin-Probst type syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	ear_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0010354	Allan-Herndon-Dudley syndrome	hereditary_disease|syndromic_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|hereditary_disease|psychiatric_disorder	oncology|genetics_and_genomics|hematology|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0010355	syndromic X-linked intellectual disability Claes-Jensen type	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|developmental_disorder	false	false	false	false	high
MONDO:0010356	nephrogenic syndrome of inappropriate antidiuresis	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	pediatric|renal_medicine	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0010358	hypophosphatemic rickets, X-linked recessive	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|genetic_disease	bone_disorder|kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0010359	Dent disease type 2	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	genetics_and_genomics|nephrology|renal_medicine	metabolic_disorder|adrenal_gland_disease	kidney_disorder|teeth_disorder	false	false	false	true	high
MONDO:0010360	Parkinson disease 12	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0010361	intellectual disability, X-linked 30	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology|psychiatry|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0010362	glycogen storage disease IXd	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|hepatology	metabolic_disorder|glycogen_storage_disease	liver_disorder|muscle_disorder	false	false	true	false	medium
MONDO:0010363	intellectual disability, X-linked 91	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	intellectual_disability_is_a_type_of_brain_disorder|brain_disorder	false	false	false	true	high
MONDO:0010364	X-linked intellectual disability-retinitis pigmentosa syndrome	hereditary_disease|chromosomal_disorder|syndromic_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|hereditary_disease|psychiatric_disorder|chromosomal_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0010365	myopathy, congenital, with fiber-type disproportion, X-linked	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatrics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	muscle_disorder|congenital_disorder	false	false	false	true	high
MONDO:0010366	FG syndrome 5	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	ear_disorder|eye_disorder|joint_disorder|spine_disorder|brain_disorder	false	false	false	false	high
MONDO:0010367	SHOX-related short stature	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology|pediatric	growth_disorder|metabolic_disorder	bone_disorder|reproductive_system_disorder|growth_disorder	false	false	false	true	medium
MONDO:0010369	nystagmus 5, congenital, X-linked	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|ophthalmology|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	ear_disorder|eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0010370	Cornelia de Lange syndrome 2	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	bone_disorder|immune_disorder|joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0010371	Aland island eye disease	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder	true	false	false	false	high
MONDO:0010373	premature ovarian failure 2B	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	obstetrics_and_gynecology|endocrinology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0010374	retinitis pigmentosa 34	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|metabolic_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	genetics_and_genomics|ophthalmology	retinal_disease|eye_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0010375	developmental and epileptic encephalopathy, 8	hereditary_disease|syndromic_disease|psychiatric_disorder|metabolic_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	nervous_system_disorder|syndromic_disease|hereditary_disease|psychiatric_disorder|metabolic_disease	genetics_and_genomics|neurology|pediatric	developmental_and_epileptic_encephalopathy_has_some_overlap_with_this_category_is_not_a_clear_match_but_is_closest|neurodegenerative_disease	brain_disorder|developmental_disorder|epileptic_disorder	false	false	false	true	high
MONDO:0010377	myopia 13, X-linked	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	true	low
MONDO:0010378	X-linked hereditary sensory and autonomic neuropathy with hearing loss	hereditary_disease|psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology	hereditary_disease|neurodegenerative_disease	ear_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0010379	Brunner syndrome	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	liver_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0010380	cataract, ataxia, short stature, and intellectual disability	hereditary_disease	other	hereditary_disease	neurology|endocrinology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	brain_disorder|spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0010381	Tn polyagglutination syndrome	hereditary_disease	other	hereditary_disease	immunology|hematology	anemia|autoimmune_diseases|inflammatory_disease	liver_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0010382	fragile X-associated tremor/ataxia syndrome	syndromic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	syndromic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010383	fragile X syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|joint_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010384	hypospadias 1, X-linked	reproductive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	reproductive_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|urology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0010385	X-linked lymphoproliferative disease due to XIAP deficiency	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	pediatric|oncology|genetics_and_genomics|hematology	autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0010386	immunodeficiency 33	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	immunology|pediatrics|genetics_and_genomics|allergy_and_immunology	immunodeficiency|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0010388	rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	developmental_disorder|intellectual_disability|neurodegenerative_disease	speech_dyspraxia|brain_disorder|intellectual_disability	false	false	false	true	high
MONDO:0010390	ocular albinism with late-onset sensorineural deafness	hereditary_disease|metabolic_disease|disorder_of_visual_system	metabolic_disease	metabolic_disease|disorder_of_visual_system|hereditary_disease	ophthalmology|genetics_and_genomics|otolaryngology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0010391	angioma serpiginosum, X-linked	integumentary_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	dermatology|genetics_and_genomics	anemia|neurodegenerative_disease|autoimmune_diseases|cancer|cardiovascular_disorder	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0010392	glycogen storage disease due to phosphoglycerate kinase 1 deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	true	false	high
MONDO:0010393	intellectual disability, X-linked 93	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010395	phosphoribosylpyrophosphate synthetase superactivity	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|biochemistry	metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0010396	developmental and epileptic encephalopathy, 2	syndromic_disease|hereditary_disease|nervous_system_disorder	other	syndromic_disease|hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	developmental_disorder|neurodegenerative_disease|encephalopathy|epilepsy	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0010397	severe neonatal-onset encephalopathy with microcephaly	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|microcephaly	false	false	false	false	very_high
MONDO:0010398	syndromic X-linked intellectual disability 14	syndromic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|intellectual_disability	false	false	false	false	high
MONDO:0010399	chromosome Xp21 deletion syndrome	chromosomal_disorder|hereditary_disease|metabolic_disease	metabolic_disease	chromosomal_disorder|metabolic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	developmental_disorder|immune_disorder	false	false	false	false	high
MONDO:0010400	X-linked scapuloperoneal muscular dystrophy	nervous_system_disorder|hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder	neurology|pediatric|genetics_and_genomics|orthopaedic	muscular_dystrophy|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0010401	X-linked myopathy with postural muscle atrophy	nervous_system_disorder|hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010402	syndromic X-linked intellectual disability 94	psychiatric_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010403	albinism-hearing loss syndrome	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|integumentary_system_disorder|metabolic_disease	pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder|skin_disorder	false	false	false	false	high
MONDO:0010404	X-linked non progressive cerebellar ataxia	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0010405	prostate cancer, hereditary, X-linked 2	hereditary_disease|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	hereditary_disease|reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology|genetics_and_genomics	hereditary|cancer|x_linked_disorders	hereditary_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0010406	chromosome Xp11.22 duplication syndrome	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatrics|genomics|oncology|neurology|psychiatry|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0010407	intellectual disability, X-linked syndromic, Turner type	psychiatric_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0010408	syndactyly-telecanthus-anogenital and renal malformations syndrome	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	renal_medicine|urology|genetics_and_genomics|pediatric	metabolic_disorder|congenital_abnormality|developmental_disorder	joint_disorder|reproductive_system_disorder|kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0010409	syndromic X-linked intellectual disability Shrimpton type	psychiatric_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	intellectual_disability|brain_disorder	false	false	false	false	very_high
MONDO:0010410	alopecia, androgenetic, 2	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	endocrinology|dermatology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder|skin_disorder	false	false	false	true	low
MONDO:0010411	pyloric stenosis, infantile hypertrophic, 4	hereditary_disease|digestive_system_disorder	other	hereditary_disease|digestive_system_disorder	gastroenterology|pediatric	metabolic_disorder|infantile_hypertrophic_pyloric_stenosis_is_a_congenital_anomaly_of_the_pylorus_that_presents_as_an_obstruction_of_gastric_outflow__which_can_be_related_to_metabolic_functions	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0010412	X-linked intellectual disability-craniofacioskeletal syndrome	psychiatric_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	skeletal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010413	intellectual disability, X-linked 95	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	intellectual_disability|brain_disorder	false	false	false	true	high
MONDO:0010414	myopathy, reducing body, X-linked, early-onset, severe	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics|pediatric	muscular_dystrophy|neurodegenerative_disease	muscle_disorder	false	false	false	true	very_high
MONDO:0010415	myopathy, reducing body, X-linked, childhood-onset	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|x_linked_disorder_categories_not_present_in_the_list_but_myopathy_is_often_related_to_neurodegenerative_disease_and_metabolic_disorders|neurodegenerative_disease	muscle_disorder|childhood_onset	true	false	false	true	high
MONDO:0010416	deafness, cataract, retinitis pigmentosa, and sperm abnormalities	hereditary_disease	other	hereditary_disease	otolaryngology|urology|genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder|reproductive_system_disorder|ear_disorder	false	false	false	false	medium
MONDO:0010417	syndromic X-linked intellectual disability Najm type	disorder_of_development_or_morphogenesis|psychiatric_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	intellectual_disability|brain_disorder	false	false	false	false	very_high
MONDO:0010418	hereditary spastic paraplegia 34	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0010420	X-linked erythropoietic protoporphyria	endocrine_system_disorder|hereditary_disease|integumentary_system_disorder|metabolic_disease|digestive_system_disorder	endocrine_system_disorder|metabolic_disease	hereditary_disease|digestive_system_disorder|endocrine_system_disorder|integumentary_system_disorder|metabolic_disease	hematology|genetics_and_genomics|dermatology	metabolic_disorder|anemia	skin_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010421	Bruton-type agammaglobulinemia	hereditary_disease|hematologic_disorder|immune_system_disorder	other	hereditary_disease|hematologic_disorder|immune_system_disorder	immunology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0010422	Alzheimer disease 16	psychiatric_disorder|nervous_system_disorder	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	central_nervous_system_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010423	hypospadias 2, X-linked	disorder_of_development_or_morphogenesis|hereditary_disease|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|reproductive_system_disorder	urology|pediatric|genetics_and_genomics	metabolic_disorder|congenital_abnormality|developmental_disorder	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0010424	surfactant metabolism dysfunction, pulmonary, 4	hereditary_disease|respiratory_system_disorder	other	hereditary_disease|respiratory_system_disorder	pulmonology|pediatric	pulmonary|metabolic_disorder	liver_disorder|lung_disorder	false	false	false	true	high
MONDO:0010425	Lisch epithelial corneal dystrophy	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology	autoimmune_diseases|inflammatory_disease|corneal_dystrophy	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0010426	X-linked endothelial corneal dystrophy	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology	genetic_disorder|cardiovascular_disorder|ocular_disease	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0010427	syndromic X-linked intellectual disability Raymond type	psychiatric_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010428	chromosome Xp11.23-p11.22 duplication syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	inflammatory_disease|mental_health_disorder|neurodegenerative_disease	bone_disorder|immune_disorder	false	false	false	false	high
MONDO:0010429	intellectual disability, X-linked 96	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0010430	intellectual disability, X-linked 97	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	high
MONDO:0010431	Joubert syndrome 10	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0010432	thrombophilia, X-linked, due to factor 9 defect	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010434	synovial sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|rheumatology|orthopaedic	autoimmune_diseases|cancer|inflammatory_disease	bone_disorder|joint_disorder	false	true	false	true	very_high
MONDO:0010435	nystagmus 6, congenital, X-linked	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	congenital_disease|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0010436	chromosome Xq28 duplication syndrome	psychiatric_disorder|nervous_system_disorder|hereditary_disease|chromosomal_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	psychiatric_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|psychiatric_disorder|chromosomal_disorder	genetics_and_genomics|neurology|pediatrics	metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010437	severe X-linked mitochondrial encephalomyopathy	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010438	paroxysmal nocturnal hemoglobinuria 1	urinary_system_disorder|hematologic_disorder|metabolic_disease	anemia|metabolic_disease	urinary_system_disorder|metabolic_disease|hematologic_disorder	genetics_and_genomics|renal_medicine|hematology	anemia|metabolic_disorder	kidney_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0010439	cardiomyopathy, fatal fetal, due to myocardial calcification	hereditary_disease	other	hereditary_disease	pediatric|cardiology|obstetrics_and_gynecology	cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder|vascular_disorder	false	false	false	false	none
MONDO:0010441	CK syndrome	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	psychiatric_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010442	46,XX sex reversal 3	reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder	genetics_and_genomics|endocrinology|obstetrics_and_gynecology	genetic_disorder|adrenal_gland_disease|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0010443	macular degeneration, X-linked atrophic	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder	genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	x_linked_recessive_disorder|genetic_disorder|eye_disorder	false	false	false	false	high
MONDO:0010444	X-linked dyserythropoetic anemia with abnormal platelets and neutropenia	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	reproductive_system_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010446	X-linked cone dysfunction syndrome with myopia	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease|inflammatory_disease	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0010447	intellectual disability, X-linked 19	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0010448	moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome	nervous_system_disorder|hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|cardiovascular_disorder	pediatric|genetics_and_genomics|endocrinology	genetic_disorder|metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder|endocrine_disorder|vascular_disorder	false	false	false	false	high
MONDO:0010450	intellectual disability, X-linked 89	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	intellectual_disability|brain_disorder	false	false	false	true	very_high
MONDO:0010451	intellectual disability, X-linked 41	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0010452	intellectual disability, X-linked 90	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010453	intellectual disability, X-linked 92	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010454	intellectual disability, X-linked 88	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|intellectual_disability	false	false	false	true	high
MONDO:0010455	X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|immunology|oncology|allergy_and_immunology|pediatrics|pulmonology	autoimmune_diseases|metabolic_disorder|cancer|inflammatory_disease	immune_disorder|lymphatic_disorder|kidney_disorder	true	true	false	true	very_high
MONDO:0010456	renal cell carcinoma, Xp11-associated	urinary_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder|hereditary_disease	genetics_and_genomics|oncology|urology	renal_cell_carcinoma_xp11_associated_is_a_subcategory_of_renal_cell_carcinoma_and_therefore_falls_under_the_category__renal_cell_carcinoma__is_not_listed_so_i_removed_this_part|adrenal_gland_disease|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0010457	Ogden syndrome	syndromic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	psychiatric_disorder	disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease	gastroenterology|rheumatology	neurodegenerative_disease|inflammatory_disease	upper_gastrointestinal_disorder|joint_disorder|liver_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0010458	hypospadias 4, X-linked	reproductive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|urology	metabolic_disorder|genetic_condition	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0010459	amyotrophic lateral sclerosis type 15	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010460	syndromic X-linked intellectual disability 17	syndromic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	very_high
MONDO:0010461	syndromic X-linked intellectual disability Nascimento type	syndromic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010462	syndromic X-linked intellectual disability Chudley-Schwartz type	syndromic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010463	X-linked dominant chondrodysplasia, Chassaing-Lacombe type	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0010464	X-linked cerebral-cerebellar-coloboma syndrome syndrome	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010465	Kabuki syndrome 2	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|dermatology	genetic_disorders|metabolic_disorder	bone_disorder|skeletal_rdg_system_disorder|skin_disorder	false	false	false	false	high
MONDO:0010466	multiple congenital anomalies-hypotonia-seizures syndrome 2	syndromic_disease|nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|metabolic_disease|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|seizures	false	false	false	false	very_high
MONDO:0010467	Xq27.3q28 duplication syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology|developmental_delay_can_also_be_categorized_under_genetics_and_genomics__but_since_it_s_a_specific_subtype_of_the_disease__we_ll_prioritize_that_one	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	immune_disorder|brain_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010468	aneurysm, intracranial berry, 5	nervous_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|neurology	cardiovascular_disorder|intracranial_berry_is_a_subset_of_cardiovascular_disorder__neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0010471	Cornelia de Lange syndrome 5	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	immune_disorder|joint_disorder|skin_disorder|brain_disorder|developmental_disorder_is_not_present_in_the_list_so___brain_disorder	false	false	false	false	high
MONDO:0010472	developmental and epileptic encephalopathy, 36	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	epileptic_disease___note__the_list_of_categories_was_used_to_guide_this_response__but_the_actual_category_provided_is_developmental_and_epileptic_encephalopathy|neurodegenerative_disease|developmental_disorder	epileptic_disorder|brain_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0010473	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|syndromic_disease|hereditary_disease|psychiatric_disorder	pediatric|neurology|cardiology|cardiothoracic|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	heart_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010474	linear skin defects with multiple congenital anomalies 2	syndromic_disease|hereditary_disease|integumentary_system_disorder|disorder_of_visual_system	other	disorder_of_orbital_region|integumentary_system_disorder|syndromic_disease|hereditary_disease|disorder_of_visual_system	pediatric|dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	birth_defect|skin_disorder	true	false	false	false	high
MONDO:0010475	X-linked central congenital hypothyroidism with late-onset testicular enlargement	syndromic_disease|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|syndromic_disease|hereditary_disease	endocrinology|urology|genetics_and_genomics|pediatric	metabolic_disorder|endocrine_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0010476	neurodegeneration with brain iron accumulation 5	nervous_system_disorder|psychiatric_disorder|hereditary_disease|metabolic_disease	neurodegenerative_disease|metabolic_disease|psychiatric_disorder	nervous_system_disorder|metabolic_disease|hereditary_disease|psychiatric_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0010477	blepharophimosis - intellectual disability syndrome, MKB type	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	psychiatric_disorder	disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|hereditary_disease|psychiatric_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0010478	SLC35A2-congenital disorder of glycosylation	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder_of_glycosylation	brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0010479	Charcot-Marie-Tooth disease X-linked dominant 6	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	nerve_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0010480	anemia, nonspherocytic hemolytic, due to G6PD deficiency	hereditary_disease|hematologic_disorder|metabolic_disease	metabolic_disease|anemia	metabolic_disease|hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology|pediatric	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0010481	angioedema	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder|integumentary_system_disorder	immunology|pulmonology|hematology|dermatology|allergy_and_immunology	autoimmune_diseases|cardiovascular_disorder|allergy|inflammatory_disease	immune_disorder|skin_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0010482	X-linked parkinsonism-spasticity syndrome	nervous_system_disorder|syndromic_disease|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0010483	X-linked intellectual disability, Cantagrel type	nervous_system_disorder|syndromic_disease|hereditary_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0010484	hearing loss, X-linked 6	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|otolaryngology|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	ear_disorder|bone_disorder	false	false	false	false	high
MONDO:0010485	X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome	syndromic_disease|hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|disorder_of_orbital_region|syndromic_disease|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	spinal_disorder|muscle_disorder|joint_disorder|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0010486	Olmsted syndrome, X-linked	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	joint_disorder|brain_disorder|kidney_disorder|eye_disorder	false	false	false	false	high
MONDO:0010487	intellectual disability, X-linked 99	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	immune_disorder|brain_disorder	false	false	false	true	high
MONDO:0010488	intellectual disability, X-linked 100	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0010489	intellectual disability, X-linked 101	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	intellectual_disability|brain_disorder	false	false	false	false	very_high
MONDO:0010490	SSR4-congenital disorder of glycosylation	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder	ear_disorder|brain_disorder|kidney_disorder|eye_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0010491	X-linked acrogigantism due to Xq26 microduplication	chromosomal_disorder|hereditary_disease	other	chromosomal_disorder|hereditary_disease	endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0010492	pituitary adenoma, growth hormone-secreting, 2	nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|nervous_system_disorder|musculoskeletal_system_disorder|reproductive_system_disorder|connective_tissue_disorder|hereditary_disease	endocrinology|neurology	neurodegenerative_disease|cancer	endocrine_disorder|brain_disorder	false	false	false	true	medium
MONDO:0010493	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|anemia	bone_disorder|teeth_disorder|blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0010494	linear skin defects with multiple congenital anomalies 3	syndromic_disease|hereditary_disease|integumentary_system_disorder|disorder_of_visual_system	other	disorder_of_orbital_region|integumentary_system_disorder|syndromic_disease|hereditary_disease|disorder_of_visual_system	dermatology|genetics_and_genomics|pediatric	metabolic_disorder|congenital_anomalies	skin_disorder|multiple_congenital_anomalies	false	false	false	true	very_high
MONDO:0010495	trichothiodystrophy 5, nonphotosensitive	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|syndromic_disease|hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	skin_disorder|hair_disorder	false	false	false	false	high
MONDO:0010496	X-linked intellectual disability-short stature-overweight syndrome	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	psychiatric_disorder	disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|hereditary_disease|psychiatric_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	endocrine_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010497	intellectual disability, X-linked 102	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0010498	MEND syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|skeletal_system_disorder	false	false	false	false	high
MONDO:0010499	Ritscher-Schinzel syndrome 2	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0010500	intellectual disability, X-linked, syndromic 33	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|psychiatric_disorder|syndromic_disease|nervous_system_disorder	psychiatry|genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	intellectual_disability|brain_disorder	false	false	false	true	high
MONDO:0010501	syndromic X-linked intellectual disability 34	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|psychiatric_disorder|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010502	intellectual disability, X-linked 99, syndromic, female-restricted	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0010503	Bartter disease type 5	syndromic_disease|hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|renal_medicine|pediatric	electrolyte_imbalance_disorder|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0010504	immunodeficiency 47	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	immunology|pediatrics|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0010505	intellectual disability-balding-patella luxation-acromicria syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|neurology|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	endocrine_disorder|joint_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010506	intellectual disability, X-linked 61	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0010507	Xq25 microduplication syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	kidney_disorder|upper_gastrointestinal_disorder|immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0010508	intellectual disability, X-linked 103	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	spinal_disorder|intellectual_disability_x_linked_is_not_in_the_list_so__brain_disorder|brain_disorder	false	false	false	true	high
MONDO:0010509	intellectual disability, X-linked 104	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	intellectual_disability__x_linked_typically_falls_under_a_category_of_brain_disorder|brain_disorder	false	false	false	false	high
MONDO:0010510	intellectual disability, X-linked 105	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0010511	vas deferens, congenital bilateral aplasia of, X-linked	hereditary_disease|disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|urology	metabolic_disorder|anemia	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0010512	intellectual disability, X-linked, syndromic, Bain type	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	intellectual_disability_x_linked_bain_type|syndromic|brain_disorder	false	false	false	false	high
MONDO:0010514	combined immunodeficiency due to moesin deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|pediatric|immunology|hematology|allergy_and_immunology	metabolic_disorder|anemia|autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010515	Meester-Loeys syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	obstetrics_and_gynecology|dermatology|genetics_and_genomics|cardiology|pediatric|cardiothoracic|rheumatology|pulmonology	metabolic_disorder|cardiovascular_disorder|genetic_disorder	skin_disorder|vascular_disorder|joint_disorder	false	false	false	false	medium
MONDO:0010516	midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	otolaryngology|genetics_and_genomics|pediatric	metabolic_disorder|anemia|autoimmune_diseases	kidney_disorder|ear_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0010517	ciliary dyskinesia, primary, 36, X-linked	syndromic_disease|respiratory_system_disorder|hereditary_disease	other	hereditary_disease|respiratory_system_disorder|syndromic_disease	pulmonology|ophthalmology|genetics_and_genomics|pediatric	neurodegenerative_disease|genetic_disorder|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010518	Wiskott-Aldrich syndrome	syndromic_disease|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|hematologic_disorder|immune_system_disorder|syndromic_disease|cancer_or_benign_tumor	hematology|genetics_and_genomics|pediatric	autoimmune_diseases|anemia|immune_disorder|inflammatory_disease	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010519	alpha thalassemia-X-linked intellectual disability syndrome	endocrine_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|reproductive_system_disorder|psychiatric_disorder|hereditary_disease	endocrine_system_disorder|psychiatric_disorder	nervous_system_disorder|hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|psychiatric_disorder	genetics_and_genomics|neurology|pediatric	anemia|neurodegenerative_disease|mental_health_disorder	brain_disorder|reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010520	X-linked Alport syndrome	syndromic_disease|urinary_system_disorder|inflammatory_disease|hereditary_disease	other	urinary_system_disorder|hereditary_disease|inflammatory_disease|syndromic_disease	genetics_and_genomics|pediatric|renal_medicine	renal_disease|metabolic_disorder	eye_disorder|kidney_disorder|ear_disorder|urinary_tract_disorder|joint_disorder	false	false	false	false	high
MONDO:0010521	amelogenesis imperfecta type 1E	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	hematology|genetics_and_genomics|pediatric	anemia|metabolic_disorder	bone_disorder|teeth_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010522	X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	genetics_and_genomics|orthopaedic|pediatric|dermatology	anemia|metabolic_disorder	bone_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0010523	X-linked reticulate pigmentary disorder	syndromic_disease|integumentary_system_disorder|connective_tissue_disorder|hereditary_disease	other	connective_tissue_disorder|hereditary_disease|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|dermatology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0010524	X-linked sideroblastic anemia with ataxia	hematologic_disorder|mitochondrial_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|anemia	nervous_system_disorder|hereditary_disease|hematologic_disorder|mitochondrial_disease	hematology|genetics_and_genomics	anemia|neurodegenerative_disease|metabolic_disorder	spinal_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0010525	neural tube defects, X-linked	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatrics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010526	Fabry disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|nephrology|cardiology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	heart_disorder|kidney_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0010528	anosmia	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	neurology|otolaryngology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|nose_disorder	true	false	false	false	medium
MONDO:0010529	X-linked spinocerebellar ataxia type 3	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	autoimmune_diseases|cardiovascular_disorder|anemia|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010531	contractures-ectodermal dysplasia-cleft lip/palate syndrome	syndromic_disease|integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|otolaryngology|pediatric|rheumatology|dermatology	metabolic_disorder|genetic_disorders	teeth_disorder|eye_disorder|skin_disorder|upper_gastrointestinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0010532	infantile-onset X-linked spinal muscular atrophy	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|spinal_muscular_atrophy	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010533	Arts syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	psychiatry|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	articular_rheumatism_syndrome_does_not_fit_well_in_any_of_the_categories_above_but_is_closest_to___joint_disorder|bone_disorder	false	false	false	true	very_high
MONDO:0010534	X-linked spinocerebellar ataxia type 4	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010535	Bazex-Dupre-Christol syndrome	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|cancer|inflammatory_disease	skin_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0010536	tubulin, beta	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	tubulin_beta_related_diseases|neurodegenerative_disease	kidney_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0010537	Borjeson-Forssman-Lehmann syndrome	syndromic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	syndromic_disease|nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|kidney_disorder|bone_disorder	false	false	false	false	high
MONDO:0010538	Mononen-Karnes-Senac syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|rheumatology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0010539	X-linked mandibulofacial dysostosis	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|otolaryngology|orthopaedic|pediatric	skeletal_dysplasia|metabolic_disorder	teeth_disorder|lower_gastrointestinal_disorder|joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0010540	bullous dystrophy, macular type	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology|dermatology	autoimmune_diseases|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010541	X-linked calvarial hyperostosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|bone_disease	bone_disorder|spinal_disorder|muscle_disorder|reproductive_system_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0010542	dilated cardiomyopathy 3B	hereditary_disease|cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	nervous_system_disorder|hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0010543	Barth syndrome	hereditary_disease|hematologic_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease|syndromic_disease|cardiovascular_disorder|metabolic_disease|musculoskeletal_system_disorder|immune_system_disorder	metabolic_disease|cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|metabolic_disease|mitochondrial_disease	genetics_and_genomics|cardiology|pediatric	metabolic_disorder|cardiovascular_disorder	heart_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0010544	cataract 40	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	eye_disorder|vision_disorder	false	false	false	true	medium
MONDO:0010545	Nance-Horan syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|ear_disorder|joint_disorder	false	false	false	false	high
MONDO:0010546	central incisors, absence of	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	central_incisors_abnormality|teeth_disorder	false	false	false	false	high
MONDO:0010547	X-linked progressive cerebellar ataxia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010548	spinocerebellar ataxia, X-linked 2	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0010549	Charcot-Marie-Tooth disease X-linked dominant 1	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010550	Charcot-Marie-Tooth disease X-linked recessive 2	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0010551	Charcot-Marie-Tooth disease X-linked recessive 3	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010552	Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia cutis congenita	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|genetic_disorder	muscle_disorder|nerve_disorder	false	false	false	false	high
MONDO:0010553	Charcot-Marie-Tooth peroneal muscular atrophy and Friedreich ataxia, combined	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010554	Abruzzo-Erickson syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder|spinal_disorder|ear_disorder|joint_disorder	false	false	false	false	high
MONDO:0010555	X-linked chondrodysplasia punctata 1	disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease	dermatology|genetics_and_genomics|orthopaedic|pediatrics	metabolic_disorder|neurodegenerative_disease	bone_disorder|skin_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0010556	X-linked chondrodysplasia punctata	disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease	dermatology|genetics_and_genomics|orthopaedic	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	bone_disorder|skin_disorder|joint_disorder	false	false	false	false	high
MONDO:0010557	choroideremia	cardiovascular_disorder|nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder|hereditary_disease	psychiatric_disorder|cardiovascular_disorder	nervous_system_disorder|hereditary_disease|disorder_of_orbital_region|cardiovascular_disorder|disorder_of_visual_system|psychiatric_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0010558	choroideremia-deafness-obesity syndrome	nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|psychiatric_disorder	genetics_and_genomics|ophthalmology|pediatrics	metabolic_disorder|neurodegenerative_disease	eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0010559	MASA syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric	mental_health_disorder|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0010560	cleft palate with or without ankyloglossia, X-linked	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	throat_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0010561	Coffin-Lowry syndrome	syndromic_disease|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0010562	colonic atresia	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	gastroenterology|pediatric	metabolic_disorder|congenital_abnormality	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0010563	blue cone monochromacy	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|disorder_of_orbital_region	ophthalmology|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0010564	red-green color blindness	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	ophthalmology|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0010565	red color blindness	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|disorder_of_orbital_region	ophthalmology|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	eye_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0010566	X-linked cone-rod dystrophy 1	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|genetic_disorder|eye_disease	eye_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010567	cone dystrophy, X-linked, with tapetal-like sheen	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0010568	Aicardi syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	kidney_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010569	X-linked complicated corpus callosum dysgenesis	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010570	craniofrontonasal syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	mental_health_disorder|inflammatory_disease|autoimmune_diseases|neurodevelopmental_disease	craniofacial_disorder_is_not_in_the_list_but_it_would_also_be_a_good_fit|eye_disorder___removed_eye_disorder_as_it_doesn_t_quite_fit__reduced_to_just_brain_disorder|spinal_disorder|brain_disorder|nose_disorder	false	false	false	false	high
MONDO:0010571	otopalatodigital syndrome type 2	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|joint_disorder|ear_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0010572	occipital horn syndrome	disorder_of_development_or_morphogenesis|integumentary_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder|metabolic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0010573	cutis verticis gyrata, thyroid aplasia, and intellectual disability	hereditary_disease	other	hereditary_disease	neurology|psychiatry|genetics_and_genomics|pediatric|dermatology|endocrinology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|intellectual_disability_is_often_a_result_of_other_disorders_but_if_we_assume_the_question_is_asking_for_disorders_that_could_be_present_in_combination__then_endocrine_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0010574	syndromic X-linked intellectual disability 5	disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	disorder_of_development_or_morphogenesis|psychiatric_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010575	deafness-hypogonadism syndrome	syndromic_disease	other	syndromic_disease	otolaryngology|genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|ear_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0010576	X-linked mixed hearing loss with perilymphatic gusher	nervous_system_disorder|auditory_system_disorder|hereditary_disease|otorhinolaryngologic_disease|psychiatric_disorder	psychiatric_disorder	otorhinolaryngologic_disease|auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	ear_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0010577	hearing loss, X-linked 1	nervous_system_disorder|auditory_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|hearing_loss	ear_disorder|bone_disorder	false	false	false	false	medium
MONDO:0010578	deafness dystonia syndrome	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	otolaryngology|neurology	neurodegenerative_disease|metabolic_disorder	ear_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010579	X-linked corneal dermoid	syndromic_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|syndromic_disease	ophthalmology|genetics_and_genomics|pediatric	adrenal_gland_disease	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0010580	immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome	syndromic_disease|endocrine_system_disorder|immune_system_disorder|digestive_system_disorder|hereditary_disease	autoimmune_disease|endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|immune_system_disorder|digestive_system_disorder|syndromic_disease	gastroenterology|immunology|genetics_and_genomics|allergy_and_immunology|pediatric|endocrinology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|immune_disorder|endocrine_disorder	false	false	false	true	very_high
MONDO:0010581	diabetes insipidus, nephrogenic, X-linked	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	renal_medicine|genetics_and_genomics|endocrinology	kidney_disease|metabolic_disorder|genetic_condition	kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0010583	Dyggve-Melchior-Clausen syndrome, X-linked	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0010584	dyskeratosis congenita, X-linked	cancer_or_benign_tumor|integumentary_system_disorder|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|integumentary_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|pediatric|dermatology|genetic_medicine	neurodegenerative_disease|metabolic_disorder	skin_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0010585	X-linked hypohidrotic ectodermal dysplasia	integumentary_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|dermatology	cardiovascular_disorder|inflammatory_disease|neurodegenerative_disease|metabolic_disorder|anemia|autoimmune_diseases	skin_disorder|eye_disorder|joint_disorder|immune_disorder|urinary_tract_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010586	X-linked Ehlers-Danlos syndrome	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|dermatology	cardiovascular_disorder|metabolic_disorder	skin_disorder|joint_disorder|vascular_disorder|muscle_disorder	false	false	false	false	low
MONDO:0010587	epidermodysplasia verruciformis, X-linked	integumentary_system_disorder|immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder|integumentary_system_disorder	genetics_and_genomics|pediatric|dermatology	inflammatory_disease|neurodegenerative_disease|anemia|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0010588	exudative vitreoretinopathy 2, X-linked	nervous_system_disorder|cardiovascular_disorder|disorder_of_visual_system|hereditary_disease	cardiovascular_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|cardiovascular_disorder	ophthalmology|genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0010589	Aarskog-Scott syndrome, X-linked	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|joint_disorder|kidney_disorder|blood_bone_marrow_disorder|brain_disorder	false	false	false	false	medium
MONDO:0010590	FG syndrome 1	psychiatric_disorder|syndromic_disease|nervous_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0010591	fingerprint body myopathy	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0010592	focal dermal hypoplasia	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0010596	membranoproliferative glomerulonephritis, X-linked	inflammatory_disease|urinary_system_disorder	other	urinary_system_disorder|inflammatory_disease	renal_medicine|genetics_and_genomics|hematology	inflammatory_disease|anemia|autoimmune_diseases	immune_disorder|kidney_disorder|vascular_disorder	false	false	false	false	high
MONDO:0010597	glutamyl ribose-5-phosphate storage disease	hereditary_disease	other	hereditary_disease	genetics_and_genomics|endocrinology	inherited_metabolic_disorder|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0010598	glycogen storage disease IXa1	endocrine_system_disorder|digestive_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease|endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|digestive_system_disorder|metabolic_disease	genetics_and_genomics|hepatology	adrenal_gland_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	true	false	high
MONDO:0010599	granulomas, congenital cerebral	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	congenital_disease|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	immune_disorder|congenital_disorder|brain_disorder	false	false	false	false	high
MONDO:0010600	granulomatous disease, chronic, X-linked	hereditary_disease|inflammatory_disease|hematologic_disorder|immune_system_disorder	other	inflammatory_disease|immune_system_disorder|hereditary_disease|hematologic_disorder	genetics_and_genomics|rheumatology|immunology	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	true	false	false	true	high
MONDO:0010602	hemophilia A	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	joint_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0010603	hemophilia A with vascular abnormality	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	orthopaedic|hematology|genetics_and_genomics	vascular_abnormality|metabolic_disorder|cardiovascular_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010604	hemophilia B	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|blood_disorder	joint_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0010605	hemopoietic proliferation	hereditary_disease	other	hereditary_disease	hematogenetics_and_genomics|hematology|oncology	cancer|anemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010606	hernia, anterior diaphragmatic	hereditary_disease|respiratory_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|respiratory_system_disorder	general_surgery|pediatric	inflammatory_disease|cardiovascular_disorder	abdominal_disorder|muscle_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0010607	heterotaxy, visceral, 1, X-linked	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|cardiovascular_disorder	genetics_and_genomics|pediatric	metabolic_disorder|visceral	liver_disorder|kidney_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0010608	Hhhh syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0010610	holoprosencephaly-hypokinesia-congenital contractures syndrome	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|congenital_disorder__not_listed_but_implied_as_it_is_a_genetic_condition|neurodegenerative_disease	joint_disorder|spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010611	X-linked hydrocephalus with stenosis of the aqueduct of Sylvius	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	inflammatory_disease|neurodegenerative_disease	spinal_disorder|vascular_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010612	hydrocephaly-cerebellar agenesis syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010613	inborn glycerol kinase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|hepatology|pediatric	metabolic_disorder|inborn_error_of_metabolism	liver_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0010614	X-linked congenital generalized hypertrichosis	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	genetic_disease|metabolic_disorder|skin_condition	skin_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0010615	isolated growth hormone deficiency type III	hereditary_disease|endocrine_system_disorder|nervous_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|nervous_system_disorder	pediatric|endocrinology	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|pituitary_disorder	false	false	false	true	medium
MONDO:0010617	male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatrics|endocrinology	metabolic_disorder|genetic_disorder	intellectual_disability_is_associated_with_brain_disorder_but_this_was_a_very_specific_request_so_i_will_leave_it_out|reproductive_system_disorder|endocrine_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0010618	familial isolated hypoparathyroidism due to agenesis of parathyroid gland	hereditary_disease|endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010619	X-linked dominant hypophosphatemic rickets	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|hypophosphatemia_related_disorders	endocrine_disorder|kidney_disorder|bone_disorder	false	false	false	true	high
MONDO:0010620	hypouricemia, familial renal, due to tubular hypersecretion	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	hematology|genetics_and_genomics|renal_medicine	metabolic_disorder|renal_disease|genetic_condition	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0010621	CHILD syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder|integumentary_system_disorder|syndromic_disease|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|metabolic_disease	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|integumentary_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|bone_disorder	false	false	false	false	high
MONDO:0010622	recessive X-linked ichthyosis	hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	dermatology|genetics_and_genomics	metabolic_disorder|skin_condition	skin_disorder|reproductive_system_disorder|immune_disorder	false	false	false	true	medium
MONDO:0010623	ichthyosis and male hypogonadism	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	skin_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0010625	immunodeficiency, X-linked, with deficiency of 115,000 Dalton surface glycoprotein	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|immunology|pediatrics	metabolic_disorder|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0010626	hyper-IgM syndrome type 1	hereditary_disease|hematologic_disorder|immune_system_disorder	other	hematologic_disorder|hereditary_disease|immune_system_disorder	allergy_and_immunology|genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0010627	X-linked lymphoproliferative syndrome	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	hematology|genetics_and_genomics|pediatric|oncology	cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0010628	immunoglobulin M, level of	hereditary_disease	other	hereditary_disease	allergy_and_immunology|hematology	inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	none
MONDO:0010629	impacted teeth, multiple	hereditary_disease	other	hereditary_disease	orthopaedic|otolaryngology|neurology|oral_surgery|pediatric	inflammatory_disease|autoimmune_diseases	teeth_disorder	false	false	false	true	medium
MONDO:0010630	imprinting gene related to retinoblastoma	hereditary_disease	other	hereditary_disease	genetics_and_genomics|oncology	cancer	eye_disorder|cancer_disorder|hereditary_disorder|genetic_disorder	false	true	false	retinoblastoma_is_primarily_associated_with_mutations_in_the_rb1_gene__while_imprinting_itself_is_a_genetic_phenomenon_where_only_one_allele_of_a_gene_is_expressed__the_rb1_gene_is_not_known_to_be_imprinted__instead__it_is_a_tumor_suppressor_gene__and_its_inactivation__typically_through_biallelic_mutations__leads_to_the_development_of_retinoblastoma___as_for_treatments__there_are_efficacious_treatments_for_retinoblastoma__including___1____chemotherapy____used_to_shrink_tumors_before_surgery_or_to_treat_advanced_cases___2____surgery____removal_of_the_affected_eye__enucleation__in_severe_cases_or_laser_surgery_for_less_aggressive_forms___3____radiation_therapy____sometimes_employed_for_tumors_that_can_t_be_surgically_removed___4____cryotherapy____freezing_the_tumor_to_destroy_it___5____thermal_therapy____using_heat_to_destroy_cancer_cells___these_treatments_can_effectively_cure_or_control_the_disease_in_many_cases____so__to_answer_your_question__true	high
MONDO:0010631	incontinentia pigmenti	disorder_of_visual_system|hereditary_disease|integumentary_system_disorder|nervous_system_disorder|syndromic_disease	other	disorder_of_orbital_region|hereditary_disease|integumentary_system_disorder|nervous_system_disorder|disorder_of_visual_system|syndromic_disease	genetics_and_genomics|dermatology	neurodegenerative_disease|autoimmune_diseases	skin_disorder|joint_disorder|immune_disorder	false	false	false	false	high
MONDO:0010632	developmental and epileptic encephalopathy, 1	hereditary_disease|nervous_system_disorder|syndromic_disease	other	hereditary_disease|nervous_system_disorder|syndromic_disease	genetics_and_genomics|neurology|pediatric	epileptic_disorder|neurodegenerative_disease|developmental_disorder	epileptic_disorder|spinal_disorder|developmental_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0010633	iris hypoplasia with glaucoma	disorder_of_visual_system|hereditary_disease|nervous_system_disorder	other	disorder_of_orbital_region|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	genetics_and_genomics|ophthalmology|neurology|pediatric	inflammatory_disease|autoimmune_diseases	eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0010634	jaundice, familial obstructive, of infancy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hepatology|pediatrics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|biliary_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0010635	hypogonadotropic hypogonadism 1 with or without anosmia	endocrine_system_disorder|hereditary_disease|syndromic_disease|reproductive_system_disorder	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric|endocrinology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0010636	Kallmann syndrome with spastic paraplegia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|endocrinology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	spinal_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0010637	keratosis follicularis spinulosa decalvans, X-linked	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease	hereditary_disease|integumentary_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|skin_condition	skin_disorder	false	false	false	false	medium
MONDO:0010638	keratosis follicularis-dwarfism-cerebral atrophy syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	skin_disorder|brain_disorder	false	false	false	false	high
MONDO:0010639	laryngeal abductor paralysis-intellectual disability syndrome	syndromic_disease	other	syndromic_disease	otolaryngology|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	throat_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010641	X-linked diffuse leiomyomatosis-Alport syndrome	chromosomal_disorder|urinary_system_disorder	other	urinary_system_disorder|chromosomal_disorder	genetics_and_genomics|urology|renal_medicine	cardiovascular_disorder|cancer	kidney_disorder|vascular_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0010642	Lesch-Nyhan phenotype with normal HGPRT	hereditary_disease|metabolic_disease|syndromic_disease	metabolic_disease	syndromic_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology|pediatrics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder	false	false	false	the_lesch_nyhan_syndrome_is_a_genetic_disorder_caused_by_mutations_in_the_hgprt_gene__leading_to_a_deficiency_of_the_enzyme_hypoxanthine_guanine_phosphoribosyltransferase__hgprt___this_disorder_is_characterized_by_neurological_and_behavioral_symptoms_and_is_associated_with_hyperuricemia___if_you_are_referring_to_a_phenotype_of_lesch_nyhan_syndrome_but_with_normal_hgprt_levels__this_could_imply_an_atypical_presentation_or_a_different_disorder_altogether__as_the_classic_lesch_nyhan_syndrome_is_specifically_defined_by_the_hgprt_deficiency____regarding_efficacious_treatments__as_of_now__there_is_no_cure_for_lesch_nyhan_syndrome__the_management_is_focused_on_alleviating_symptoms_and_preventing_complications__such_as_the_use_of_allopurinol_to_manage_hyperuricemia__some_treatments_aim_to_address_behavioral_issues__but_these_do_not_cure_the_underlying_condition___thus__for_the_classic_lesch_nyhan_syndrome_and_the_specific_scenario_described__it_would_be_better_to_say___false	high
MONDO:0010643	acute leukemia	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|acute_disease	hematology|oncology	anemia|autoimmune_diseases|cancer	immune_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0010644	proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	urology|renal_medicine|endocrinology	kidney_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder|bone_disorder	false	false	false	false	high
MONDO:0010645	oculocerebrorenal syndrome	disorder_of_visual_system|hereditary_disease|metabolic_disease|urinary_system_disorder|syndromic_disease	metabolic_disease	syndromic_disease|disorder_of_orbital_region|urinary_system_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system	genetics_and_genomics|neurology|renal_medicine	neurodegenerative_disease|metabolic_disorder	eye_disorder|kidney_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010646	macular dystrophy, X-linked	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	genetics_and_genomics|ophthalmology|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0010647	spermatogenic failure, X-linked, 2	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	metabolic_disorder|anemia	spermatic_failure|reproductive_system_disorder	false	false	false	false	medium
MONDO:0010648	major affective disorder 2	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|psychiatry	major_affective_disorder|mental_health_disorder	mood_disorder|brain_disorder|mental_health_disorder	false	false	false	true	high
MONDO:0010649	isolated congenital megalocornea	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	ophthalmology|pediatric	metabolic_disorder|congenital_disorder	eye_disorder	false	false	false	false	medium
MONDO:0010650	Melnick-Needles syndrome	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|hematology|pediatric|oncology	neurodegenerative_disease|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0010651	Menkes disease	hereditary_disease|metabolic_disease|syndromic_disease	metabolic_disease	syndromic_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology|cardiology|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|skin_disorder|kidney_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0010652	X-linked intellectual disability-seizures-psoriasis syndrome	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	syndromic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|dermatology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0010653	Renpenning syndrome	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	psychiatric_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0010654	Partington syndrome	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	psychiatric_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0010655	X-linked intellectual disability with marfanoid habitus	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	psychiatric_disorder	disorder_of_development_or_morphogenesis|psychiatric_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	pediatrics|genetics_and_genomics|neurology|orthopaedic	metabolic_disorder|neurodegenerative_disease|cardiovascular_disorder	joint_disorder|muscle_disorder|bone_disorder|brain_disorder	false	false	false	true	high
MONDO:0010656	intellectual disability, X-linked 1	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010657	methylmalonic acidemia with homocystinuria, type cblX	hereditary_disease|hematologic_disorder|metabolic_disease|nervous_system_disorder|psychiatric_disorder|nutritional_disorder	metabolic_disease|anemia|psychiatric_disorder	psychiatric_disorder|hematologic_disorder|hereditary_disease|nutritional_disorder|metabolic_disease|nervous_system_disorder	pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|anemia	liver_disorder|kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010658	syndromic X-linked intellectual disability 12	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	psychiatric_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010659	FRAXE intellectual disability	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010660	intellectual disability, X-linked 9	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010661	severe X-linked intellectual disability, Gustavson type	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	psychiatric_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	intellectual_disability|brain_disorder	false	false	false	false	very_high
MONDO:0010662	paraplegia-intellectual disability-hyperkeratosis syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|intellectual_disability|muscle_disorder	false	false	false	false	high
MONDO:0010663	intellectual disability-hypotonic facies syndrome, X-linked, 1	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	psychiatric_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010664	syndromic X-linked intellectual disability Snyder type	hereditary_disease|metabolic_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	metabolic_disease|psychiatric_disorder	syndromic_disease|psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	very_high
MONDO:0010665	Wilson-Turner syndrome	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	psychiatric_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	endocrinology|genetics_and_genomics|cardiothoracic|hepatology	metabolic_disorder|neurodegenerative_disease	liver_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0010667	Prieto syndrome	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	psychiatric_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	dermatology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases|anemia	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0010668	skeletal dysplasia-intellectual disability syndrome	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	psychiatric_disorder|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|skeletal_disorder|bone_disorder	false	false	false	false	high
MONDO:0010669	syndactyly type 8	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|genetic_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0010670	X-linked intellectual disability-spastic quadriparesis syndrome	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	syndromic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|other___corrected_list__neurodegenerative_disease|mental_health_disorder	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010671	microphthalmia, syndromic 1	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	syndromic_disease|psychiatric_disorder|disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|teeth_disorder	false	false	false	false	high
MONDO:0010672	linear skin defects with multiple congenital anomalies	hereditary_disease|disorder_of_visual_system|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|disorder_of_orbital_region|hereditary_disease|integumentary_system_disorder|disorder_of_visual_system	genetics_and_genomics|dermatology|pediatric	metabolic_disorder|anemia|autoimmune_diseases	skin_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0010673	modifier, X-linked, for Neurofunctional defects	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	neurofunctional_defects|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0010674	mucopolysaccharidosis type 2	hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|syndromic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|liver_disorder|kidney_disorder|brain_disorder|joint_disorder	false	false	false	true	very_high
MONDO:0010675	muscular dystrophy, cardiac type	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|orthopaedic|pulmonology|cardiology|rheumatology	cardiovascular_disorder|muscular_dystrophy|cardiac_type	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010676	muscular dystrophy, Hemizygous lethal type	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|orthopaedic|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0010677	muscular dystrophy, Mabry type	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|orthopaedic	neurodegenerative_disease|muscular_dystrophy	muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0010678	muscular dystrophy, progressive Pectorodorsal	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|muscular_dystrophy	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010679	Duchenne muscular dystrophy	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010680	X-linked Emery-Dreifuss muscular dystrophy	hereditary_disease|cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder|nervous_system_disorder	pediatrics|genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|muscular_dystrophy	muscle_disorder|bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010681	myelolymphatic insufficiency	hereditary_disease	other	hereditary_disease	hematology|oncology	metabolic_disorder|anemia|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0010683	X-linked myotubular myopathy	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010684	X-linked myopathy with excessive autophagy	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0010685	myopia 1, X-linked	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|ophthalmology	allergy|neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	muscle_disorder|eye_disorder	false	false	false	true	medium
MONDO:0010686	N syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|syndromic_disease|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010687	nephrolithiasis, X-linked recessive, with renal failure	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	genetics_and_genomics|urology|renal_medicine	metabolic_disorder|kidney_disease	kidney_disorder|urinary_tract_disorder	false	false	false	true	very_high
MONDO:0010688	hereditary sensory neuropathy X-linked	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|hereditary	nerve_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010689	Charcot-Marie-Tooth disease X-linked recessive 4	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010690	congenital stationary night blindness 1A	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	pediatric|genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0010691	Norrie disease	hereditary_disease|disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	pulmonology|genetics_and_genomics|pediatrics|cardiology	neurodegenerative_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder|bone_bone_marrow_disorder	false	false	false	false	high
MONDO:0010692	nuclear ribonucleic acid	hereditary_disease	other	hereditary_disease	molecular_biology|cellular_biology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	false	none
MONDO:0010693	nystagmus 1, congenital, X-linked	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	congenital_disease|neurodegenerative_disease|genetic_disorder|eye_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0010694	nystagmus, myoclonic	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0010695	occipital hair, white lock of	hereditary_disease	other	hereditary_disease	dermatology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	ear_disorder	false	false	false	false	low
MONDO:0010696	omphalocele, X-linked	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|medical_genetics	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0010697	ophthalmoplegia, external, and myopia	hereditary_disease	other	hereditary_disease	neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0010698	optic atrophy 2	hereditary_disease|disorder_of_visual_system|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|disorder_of_visual_system	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0010699	Charcot-Marie-Tooth disease X-linked recessive 5	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010700	optic atrophy--spastic paraplegia syndrome	hereditary_disease	other	hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease	eye_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010702	orofaciodigital syndrome I	nervous_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|nervous_system_disorder|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|mental_health_disorder|inflammatory_disease|metabolic_disorder	ear_disorder|teeth_disorder|eye_disorder|joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0010703	ornithine carbamoyltransferase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|hepatology	metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0010704	otopalatodigital syndrome type 1	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder|skin_disorder|joint_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0010706	premature ovarian failure 1	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	obstetrics_and_gynecology|endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0010707	Paine syndrome	hereditary_disease	other	hereditary_disease	pediatrics|neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010708	Pallister-W syndrome	syndromic_disease	other	syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010709	early-onset parkinsonism-intellectual disability syndrome	nervous_system_disorder|hereditary_disease|psychiatric_disorder|syndromic_disease	psychiatric_disorder	syndromic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010710	Pierre Robin syndrome-faciodigital anomaly syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	teeth_disorder|bone_disorder|face_disorder|vascular_disorder|joint_disorder	false	false	false	false	medium
MONDO:0010711	TARP syndrome	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	dermatology|neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0010712	panhypopituitarism, X-linked	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	pediatric|endocrinology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0010713	properdin deficiency, X-linked	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatrics|immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0010714	Pelizeaus-Merzbacher spectrum disorder	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010716	X-linked lethal multiple pterygium syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	ophthalmology|pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder|skin_disorder|joint_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0010717	pyruvate dehydrogenase E1-alpha deficiency	mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder_muscle_disorder____liver_disorder	false	false	false	false	very_high
MONDO:0010718	absent radius-anogenital anomalies syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|obstetrics_and_gynecology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	absent_radius_anogenital_anomalies_syndrome|reproductive_system_disorder	false	false	false	false	high
MONDO:0010719	radiation sensitivity of natural killer activity	hereditary_disease	other	hereditary_disease	oncology|hematology|immunology	cancer|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0010720	partial androgen insensitivity syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|reproductive_system_disorder	urology|endocrinology|genetics_and_genomics	endocrine_disorder|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0010721	reticuloendotheliosis, X-linked	hereditary_disease	other	hereditary_disease	hematology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0010722	X-linked retinal dysplasia	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0010723	retinitis pigmentosa 2	disorder_of_visual_system|metabolic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|hereditary_disease|metabolic_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0010725	X-linked retinoschisis	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|hereditary_disease	ophthalmology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010726	Rett syndrome	hereditary_disease|psychiatric_disorder|syndromic_disease|nervous_system_disorder	psychiatric_disorder	syndromic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010727	Russell-silver syndrome, X-linked	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|chromosomal_disorder	other	syndromic_disease|hereditary_disease|chromosomal_disorder|disorder_of_development_or_morphogenesis	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|urinary_tract_disorder|endocrine_disorder|vascular_disorder|eye_disorder|lower_gastrointestinal_disorder|joint_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0010728	SCARF syndrome	syndromic_disease	other	syndromic_disease	dermatology|rhueumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0010729	X-linked intellectual disability, Schimke type	hereditary_disease|psychiatric_disorder|syndromic_disease|nervous_system_disorder	psychiatric_disorder	syndromic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0010730	combined immunodeficiency, X-linked	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatric|immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0010731	Simpson-Golabi-Behmel syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder|bone_disorder|lymphatic_disorder|kidney_disorder|vascular_disorder|endocrine_disorder|eye_disorder|lower_gastrointestinal_disorder|joint_disorder|skeletal_disorder|heart_disorder	false	false	false	false	high
MONDO:0010732	spastic paraparesis-deafness syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder|brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0010733	hereditary spastic paraplegia 2	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0010734	spatial visualization, aptitude for	hereditary_disease	other	hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	brain_disorder|eye_disorder|spatial_visualization_is_most_closely_associated_with_the_visual_system__so_it_would_be_best_to_categorize_it_as_eye_disorder_or_brain_disorder	false	false	false	false	none
MONDO:0010735	Kennedy disease	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010736	split hand-foot malformation 2	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric	congenital_abnormality|genetic_condition|metabolic_disorder|skeletal_dysplasia	joint_disorder|skin_disorder|bone_disorder	false	false	false	false	medium
MONDO:0010737	spondyloepiphyseal dysplasia tarda, X-linked	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	rheumatology|orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0010738	spondylometaphyseal dysplasia, Golden type	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0010739	Taqi polymorphism	hereditary_disease	other	hereditary_disease	genetics_and_genomics	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	immune_disorder|genetic_disorder	false	false	false	taqi_polymorphism_refers_to_a_specific_genetic_variation_in_the_human_genome__particularly_associated_with_the_dopamine_d2_receptor_gene__drd2___while_it_s_an_interesting_area_of_genetic_research__it_is_not_a_disease_itself__therefore__if_you_re_asking_about_efficacious_treatments_related_to_taqi_polymorphism__the_question_doesn_t_directly_apply_as_it_is_a_polymorphism_rather_than_a_disease_that_needs_treatment____thus__the_answer_would_be__false	none
MONDO:0010740	taurodontism, microdontia, and dens invaginatus	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	dens_invaginatus_is_not_in_list_so_removed___neurodegenerative_disease|metabolic_disorder|neurodegenerative_disease	teeth_disorder|bone_disorder	false	false	false	false	low
MONDO:0010741	tooth agenesis, selective, X-linked, 1	musculoskeletal_system_disorder|hereditary_disease	other	mouth_disorder|hereditary_disease|musculoskeletal_system_disorder	otolaryngology|orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases	teeth_disorder|bone_disorder	false	false	false	true	medium
MONDO:0010742	pentalogy of Cantrell	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|genetics_and_genomics|pediatric	metabolic_disorder|cardiovascular_disorder|neurodegenerative_disease	skeletal_system_disorder|spinal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0010743	thrombocytopenia 1	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	hematology	autoimmune_diseases|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0010744	thrombocytopenia with elevated serum IgA and renal disease	hereditary_disease	other	hereditary_disease	allergy_and_immunology|hematology|renal_medicine	autoimmune_diseases|anemia|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|kidney_disorder	true	false	false	false	very_high
MONDO:0010745	beta-thalassemia-X-linked thrombocytopenia syndrome	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0010746	thumbs, congenital Clasped	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	hand_anomaly|congenital_disease|metabolic_disorder|developmental_disorder	joint_disorder|skeletal_disorder|limb_disorder|hand_disorder	false	false	false	false	low
MONDO:0010747	X-linked dystonia-parkinsonism	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010748	torticollis-keloids-cryptorchidism-renal dysplasia syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric|urology	inflammatory_disease|autoimmune_diseases|renal_dysplasia	reproductive_system_disorder|muscle_disorder|kidney_disorder	false	false	false	false	high
MONDO:0010749	trigonocephaly-short stature-developmental delay syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|developmental_delay_is_not_in_the_list_so_ignore_it|pediatric	developmental_delay|metabolic_disorder|neurodegenerative_disease	developmental_delay|brain_disorder|short_stature|bone_disorder	false	false	false	false	high
MONDO:0010750	ulnar hypoplasia-split foot syndrome	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease	joint_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010751	unique green phenomenon	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	skin_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0010752	VACTERL association, X-linked, with or without hydrocephalus	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|heart_disorder	false	false	false	false	high
MONDO:0010753	cardiac valvular dysplasia, X-linked	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiology|cardiology_and_genetics_and_pediatric|genetics_and_genomics|pediatric	x_linked|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0010754	van den Bosch syndrome	syndromic_disease	other	syndromic_disease	oncology|genetics_and_genomics|pediatric	metabolic_disorder|cancer	immune_disorder|blood_bone_marrow_disorder|joint_disorder|vascular_disorder|bone_disorder	false	false	false	false	high
MONDO:0010755	vesicoureteral reflux, X-linked	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|urology	inflammatory_disease|neurodegenerative_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0010756	Von Willebrand disease, X-linked form	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0010757	widow's peak syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	low
MONDO:0010758	Wieacker-Wolff syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0010759	Wildervanck syndrome	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|skeletal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0010761	retinitis pigmentosa Y-linked	disorder_of_visual_system|psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	adrenal_gland_disease|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010762	lymphoma, Hodgkin, Y-linked pseudoautosomal	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	post_infectious_disorder|cancer_or_benign_tumor|hematologic_disorder	oncology|hematology|genetics_and_genomics	cancer|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0010763	spermatogenic failure, Y-linked, 1	reproductive_system_disorder|chromosomal_disorder|hereditary_disease	other	chromosomal_disorder|hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	metabolic_disorder|anemia	y_linked|reproductive_system_disorder	false	false	false	false	low
MONDO:0010764	hearing loss, Y-linked 1	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder|hereditary_disease	otolaryngology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	ear_disorder	false	false	false	false	medium
MONDO:0010765	46,XY complete gonadal dysgenesis	musculoskeletal_system_disorder|reproductive_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease	cardiovascular_disorder|endocrine_system_disorder	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder|cardiovascular_disorder|reproductive_system_disorder	endocrinology|genetics_and_genomics|urology	metabolic_disorder|anemia	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0010767	spermatogenic failure, Y-linked, 2	reproductive_system_disorder|chromosomal_disorder|hereditary_disease	other	chromosomal_disorder|hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	metabolic_disorder|anemia	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0010768	gonadoblastoma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	oncology|pediatric	adrenal_gland_disease|cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0010769	hairy ears, Y-linked	hereditary_disease	other	hereditary_disease	otolaryngology|genetics_and_genomics|pediatric	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	ear_disorder|skin_disorder	false	false	false	false	none
MONDO:0010770	ubiquitin-activating enzyme, Y-linked	hereditary_disease	other	hereditary_disease	genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder	false	false	false	false	none
MONDO:0010771	histiocytoid cardiomyopathy	musculoskeletal_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	cardiovascular_disorder|metabolic_disease	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiology|cardiothoracic	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010772	Leber optic atrophy and dystonia	disorder_of_visual_system|musculoskeletal_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease|nervous_system_disorder	cardiovascular_disorder|metabolic_disease|neurodegenerative_disease	metabolic_disease|mitochondrial_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|disorder_of_orbital_region|cardiovascular_disorder|musculoskeletal_system_disorder	ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010773	mitochondrial myopathy with diabetes	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	metabolic_disease	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	endocrinology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|muscle_disorder	false	false	true	false	high
MONDO:0010774	striatonigral degeneration, infantile, mitochondrial	syndromic_disease|metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|mitochondrial_diseases_are_not_listed_however_a_more_fitting_category_would_be_neurodegenerative_disease	mitochondrial|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010775	retinitis pigmentosa-deafness syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	otolaryngology|genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0010776	hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial	hereditary_disease	other	hereditary_disease	cardiology|endocrinology|nephrology|genetics_and_genomics|renal_medicine	mitochondrial|metabolic_disorder|cardiovascular_disorder	endocrine_disorder|vascular_disorder|muscle_disorder|kidney_disorder	false	false	false	true	high
MONDO:0010777	cardiomyopathy, infantile hypertrophic	hereditary_disease	other	hereditary_disease	cardiology|pediatric	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010778	cyclic vomiting syndrome	endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder	gastroenterology|neurology	metabolic_disorder|neurodegenerative_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0010779	mitochondrial non-syndromic sensorineural hearing loss	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	metabolic_disease	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease	otolaryngology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	ear_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0010780	mitochondrial myopathy with reversible cytochrome C oxidase deficiency	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease	metabolic_disease	musculoskeletal_system_disorder|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	heart_disorder|muscle_disorder|mitochondrial_diseases	false	false	false	false	high
MONDO:0010781	ataxia and polyneuropathy, adult-onset	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010782	myopathy, lactic acidosis, and sideroblastic anemia 3	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|hematologic_disorder|metabolic_disease|mitochondrial_disease	anemia|metabolic_disease	musculoskeletal_system_disorder|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|hematologic_disorder	neuromuscular__note__neuromuscular_was_not_in_the_list_but_it_is_the_best_fit|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010784	chloramphenicol toxicity	hereditary_disease	other	hereditary_disease	hematology|pediatric|hematotoxicity_can_be_associated_with_chloramphenicol_toxicity	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0010785	maternally-inherited diabetes and deafness	disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder|metabolic_disease|mitochondrial_disease|digestive_system_disorder	diabetes_mellitus|metabolic_disease|endocrine_system_disorder	digestive_system_disorder|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder	obstetrics_and_gynecology|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases	ear_disorder|endocrine_disorder	false	false	true	true	medium
MONDO:0010786	chronic diarrhea with villous atrophy	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease|digestive_system_disorder	metabolic_disease	digestive_system_disorder|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	gastroenterology|hepatology|endocrinology	inflammatory_disease|autoimmune_diseases|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0010787	Kearns-Sayre syndrome	musculoskeletal_system_disorder|disorder_of_visual_system|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder|metabolic_disease|mitochondrial_disease|nervous_system_disorder	cardiovascular_disorder|metabolic_disease	musculoskeletal_system_disorder|disorder_of_visual_system|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|nervous_system_disorder|cardiovascular_disorder	genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder|heart_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010788	Leber hereditary optic neuropathy	musculoskeletal_system_disorder|disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder|metabolic_disease|mitochondrial_disease|nervous_system_disorder	neurodegenerative_disease|cardiovascular_disorder|metabolic_disease	musculoskeletal_system_disorder|disorder_of_visual_system|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder|cardiovascular_disorder	ophthalmology|genetics_and_genomics|neurology	hereditary_disease|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0010789	MELAS syndrome	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease	metabolic_disease	musculoskeletal_system_disorder|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010790	MERRF syndrome	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease|nervous_system_disorder	metabolic_disease	musculoskeletal_system_disorder|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010791	myoglobinuria, recurrent	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hematology|renal_medicine	metabolic_disorder|anemia	kidney_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0010792	lethal infantile mitochondrial myopathy	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease	metabolic_disease	musculoskeletal_system_disorder|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	mitochondrial_myopathies|metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_myopathy	false	false	false	false	very_high
MONDO:0010793	nephropathy, chronic tubulointerstitial	hereditary_disease	other	hereditary_disease	nephrology|renal_medicine	inflammatory_disease|autoimmune_diseases	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0010794	NARP syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease|nervous_system_disorder	metabolic_disease	mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|nerve_disorder	false	false	false	false	high
MONDO:0010795	oncocytic neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics|hematology|neurology|pediatric	adrenal_gland_disease|cancer	kidney_disorder|blood_bone_marrow_disorder|reproductive_system_disorder	false	true	false	false	low
MONDO:0010796	Parkinson disease, mitochondrial	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	mitochondrial_disorders_is_not_in_the_list_so_this_should_be_removed____brain_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010797	Pearson syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|anemia	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0010798	proximal tubulopathy-diabetes mellitus-cerebellar ataxia syndrome	syndromic_disease	other	syndromic_disease	endocrinology|genetics_and_genomics|neurology|renal_medicine	metabolic_disorder|neurodegenerative_disease	kidney_disorder|endocrine_disorder|brain_disorder	true	false	true	false	very_high
MONDO:0010799	deafness, aminoglycoside-induced	auditory_system_disorder|psychiatric_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease	mitochondrial_disease|psychiatric_disorder|metabolic_disease|auditory_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	otolaryngology|neurology|pediatric	other____revised___neurodegenerative_disease|neurodegenerative_disease	ear_disorder	false	false	false	false	high
MONDO:0010800	Wolfram syndrome, mitochondrial form	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|endocrinology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	mitochondrial_form_is_not_a_category_so_it_has_been_omitted_from_the_selection|eye_disorder|kidney_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0010801	spondylocamptodactyly syndrome	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0010802	pancreatic hypoplasia-diabetes-congenital heart disease syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|cardiology|pediatric|endocrinology	metabolic_disorder|congenital_heart_disease|cardiovascular_disorder	heart_disorder|endocrine_disorder	false	false	true	false	very_high
MONDO:0010803	Eiken syndrome	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	neurology|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0010805	bladder exstrophy	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|urinary_system_disorder	pediatric|urology	metabolic_disorder|urological_disease|genetic_condition|kidney_disease|congenital_abnormality|bladder_problem|birth_defect	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0010806	retinitis pigmentosa 13	psychiatric_disorder|nervous_system_disorder|metabolic_disease|disorder_of_visual_system|hereditary_disease	metabolic_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|metabolic_disease|psychiatric_disorder|disorder_of_visual_system	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010807	autosomal recessive nonsyndromic hearing loss 2	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	otolaryngology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0010808	fatal familial insomnia	infectious_disease|nervous_system_disorder|hereditary_disease	infectious_disease|neurodegenerative_disease	sleep_disorder|hereditary_disease|nervous_system_disorder|infectious_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010809	familial chronic myelocytic leukemia-like syndrome	hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|connective_tissue_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|hematologic_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	hematoloy|genetics_and_genomics|oncology|hematology	cancer|anemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0010810	vitamin D hydroxylation-deficient rickets, type 1B	nutritional_disorder|musculoskeletal_system_disorder|metabolic_disease|endocrine_system_disorder|hereditary_disease	metabolic_disease|endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|musculoskeletal_system_disorder|metabolic_disease|nutritional_disorder	genetics_and_genomics|pediatric|endocrinology|orthopaedic	metabolic_disorder|vitamin_d_hydroxylation_deficient_rickets_type_1b	bone_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0010811	benign prostatic hyperplasia	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	urology|renal_medicine	metabolic_disorder|inflammatory_disease|cancer|cardiovascular_disorder	urinary_tract_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0010812	macrocytosis, familial	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0010813	pancreatic beta cell agenesis with neonatal diabetes mellitus	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|neonatal_diabetes	endocrine_disorder	false	false	true	false	high
MONDO:0010814	chondrodysplasia-pseudohermaphroditism syndrome	syndromic_disease|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder|syndromic_disease	pediatrics|genetics_and_genomics	metabolic_disorder	joint_disorder|reproductive_system_disorder|bone_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0010815	spondyloepiphyseal dysplasia tarda with characteristic facies	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0010816	Qazi Markouizos syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder|blood_bone_marrow_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0010817	autosomal dominant nonsyndromic hearing loss 2A	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	otolaryngology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	high
MONDO:0010818	retinitis pigmentosa 12	psychiatric_disorder|nervous_system_disorder|metabolic_disease|disorder_of_visual_system|hereditary_disease	metabolic_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|metabolic_disease|psychiatric_disorder|disorder_of_visual_system	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0010819	Stargardt disease 3	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|disorder_of_visual_system	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0010820	autosomal recessive juvenile Parkinson disease 2	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0010821	familial developmental dysphasia	syndromic_disease|nervous_system_disorder	other	nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010822	Warburg micro syndrome 1	syndromic_disease|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|nervous_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system|syndromic_disease	neurology|genetics_and_genomics|pediatric	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	liver_disorder|brain_disorder	false	false	false	false	high
MONDO:0010823	rhizomelic chondrodysplasia punctata type 3	musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|disorder_of_visual_system	metabolic_disease	hereditary_disease|disorder_of_orbital_region|musculoskeletal_system_disorder|metabolic_disease|disorder_of_visual_system	neurology|orthopaedic|genetics_and_genomics|dermatology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0010824	disorder of sex development-intellectual disability syndrome	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	neurology|psychiatry|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder|intellectual_disability_syndrome	false	false	false	true	very_high
MONDO:0010825	atrioventricular defect-blepharophimosis-radial and anal defect syndrome	syndromic_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|disorder_of_visual_system|syndromic_disease	genetics_and_genomics|cardiology|pediatric	congenital_abnormality|cardiovascular_disorder	joint_disorder|heart_disorder|eye_disorder	false	false	false	false	high
MONDO:0010826	childhood absence epilepsy	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric	mental_health_disorder|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0010827	retinitis pigmentosa 14	psychiatric_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease|disorder_of_visual_system	metabolic_disease|psychiatric_disorder	hereditary_disease|disorder_of_orbital_region|nervous_system_disorder|metabolic_disease|disorder_of_visual_system|psychiatric_disorder	genetics_and_genomics|ophthalmology	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0010828	retinitis pigmentosa 11	psychiatric_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease|disorder_of_visual_system	metabolic_disease|psychiatric_disorder	hereditary_disease|disorder_of_orbital_region|nervous_system_disorder|metabolic_disease|disorder_of_visual_system|psychiatric_disorder	genetics_and_genomics|ophthalmology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0010829	CARASIL syndrome	syndromic_disease|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|syndromic_disease	neurology|genetics_and_genomics	autoimmune_diseases|cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0010830	neuronal ceroid lipofuscinosis 8	psychiatric_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease|neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010831	familial caudal dysgenesis	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0010832	Bardet-Biedl syndrome 3	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	neurology|genetics_and_genomics|pediatric|ophthalmology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0010835	pterygium colli-intellectual disability-digital anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	joint_disorder|eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0010836	nanophthalmos 1	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	neurology|genetics_and_genomics|pediatric|ophthalmology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0010837	primary hyperparathyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|renal_medicine	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	true	high
MONDO:0010838	gonadal agenesis	hereditary_disease	other	hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics|urology	gonadal_dysgenesis_can_be_associated_with_disorders_of_sex_development_which_have_a_genetic_basis_related_to_hormone_production_in_the_body___metabolism_has_a_link_to_hormones_which_then_relates_to_sex_organs_and_their_development__so_this_category_is_relevant|metabolic_disorder	reproductive_system_disorder|gonadal_agenesis	false	false	false	false	medium
MONDO:0010839	neuronopathy, distal hereditary motor, autosomal dominant 8	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0010840	pachygyria-intellectual disability-epilepsy syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry|genetics_and_genomics|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010841	Waardenburg syndrome type 2B	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|spinal_disorder|ear_disorder|vascular_disorder|eye_disorder	false	false	false	false	medium
MONDO:0010842	multiple cutaneous and mucosal venous malformations	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	hematology|genetics_and_genomics|dermatology	vascular_malformation|cardiovascular_disorder	skin_disorder|lymphatic_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0010844	epiphyseal dysplasia, multiple, 2	musculoskeletal_system_disorder|connective_tissue_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0010846	exostoses, multiple, type III	syndromic_disease|musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|syndromic_disease	orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disease|bone_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0010847	spinocerebellar ataxia type 4	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics	adrenal_gland_disease_is_not_correct__however__the_category__adrenal_gland_disease__is_not_in_the_list_of_best_fitting_categories_for_spinocerebellar_ataxia_type_4____neurodegenerative_disease|inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010848	spinocerebellar ataxia type 5	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics	inflammatory_disease|cardiovascular_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0010849	palmoplantar keratoderma, Bothnian type	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0010850	Tessier number 4 facial cleft	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	otolaryngology|pediatric	congenital_disease|metabolic_disorder	facial_cleft|teeth_disorder	false	false	false	false	high
MONDO:0010851	Lowry-MacLean syndrome	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|disorder_of_visual_system|syndromic_disease	genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010852	chromosome 8Q12.1-q21.2 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|oncology	mental_health_disorder|cancer|neurodegenerative_disease	joint_disorder|spinal_disorder|lymphatic_disorder|immune_disorder|kidney_disorder|blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0010854	Toriello-Lacassie-Droste syndrome	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|dermatology|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	joint_disorder|skin_disorder|note__skeletal_system_disorder_is_not_in_the_original_list_but_it_s_a_more_accurate_categorization_than_bone_disorder__if_you_want_to_stick_strictly_to_the_given_categories__just_joint_disorder|skeletal_system_disorder|skin_disorder	false	false	false	false	high
MONDO:0010855	short tarsus-absence of lower eyelashes syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder	joint_disorder|eye_disorder	false	false	false	false	low
MONDO:0010856	autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis	chromosomal_disorder|urinary_system_disorder|hereditary_disease	other	chromosomal_disorder|urinary_system_disorder|hereditary_disease	renal_medicine|genetics_and_genomics|nephrology____urology|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|muscle_disorder|kidney_disorder|brain_disorder|tuberous_sclerosis	false	false	false	false	high
MONDO:0010857	semantic dementia	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	lower_gastrointestinal_disorder|joint_disorder|upper_gastrointestinal_disorder|spinal_disorder|lymphatic_disorder|vascular_disorder|immune_disorder|muscle_disorder|blood_bone_marrow_disorder|bone_disorder|brain_disorder	false	false	false	false	high
MONDO:0010858	macrocephaly-spastic paraplegia-dysmorphism syndrome	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0010860	autosomal recessive nonsyndromic hearing loss 3	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder|hereditary_disease	otolaryngology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder|autosomal_recessive_nonsyndromic_hearing_loss	false	false	false	true	medium
MONDO:0010865	pseudoaminopterin syndrome	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	hematology|renal_medicine|pediatrics|genetics_and_genomics|oncology	metabolic_disorder|autoimmune_diseases|anemia	blood_bone_marrow_disorder|eye_disorder	false	false	false	false	high
MONDO:0010866	infantile osteopetrosis with neuroaxonal dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	neurology|orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0010867	PARC syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|psychology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010868	rippling muscle disease 1	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	medium
MONDO:0010869	motor neuron disease with dementia and ophthalmoplegia	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	ophthalmology|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease|adrenal_gland_disease	eye_disorder|brain_disorder|spinal_disorder	true	false	false	false	very_high
MONDO:0010870	tibial muscular dystrophy	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics|neurology	muscular_dystrophy|neurodegenerative_disease	muscle_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0010871	succinic acidemia	hereditary_disease	other	hereditary_disease	pediatric|metabolic_disorders__note__the_original_list_does_not_have_a_direct_category_for_this__but_it_is_most_closely_related_to_genetics_and_genomics_and_pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0010872	parotid salivary glands, polycystic dysgenetic disease of	hereditary_disease	other	hereditary_disease	otolaryngology|endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	kidney_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0010873	band heterotopia of brain	nervous_system_disorder|syndromic_disease|hereditary_disease	other	nervous_system_disorder|syndromic_disease|hereditary_disease	pediatric|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0010874	enteropathy, familial, with villous edema and immunoglobulin G2 deficiency	hereditary_disease	other	hereditary_disease	immunology|genetics_and_genomics|gastroenterology	anemia|metabolic_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder_lower_gastrointestinal_disorder	true	false	false	false	high
MONDO:0010875	pachydermodactyly, familial	hereditary_disease	other	hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	inherited_condition|metabolic_disorder|genetic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0010876	recessive aplasia cutis congenita of limbs	integumentary_system_disorder	other	integumentary_system_disorder	pediatrics|dermatology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|skin_disorder	false	false	false	false	medium
MONDO:0010877	Charcot-Marie-Tooth disease type 5	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|nerve_disorder	false	false	false	false	high
MONDO:0010878	hereditary spastic paraplegia 6	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0010879	CODAS syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0010880	telangiectasia, hereditary hemorrhagic, type 2	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|dermatology|hematology	hereditary_hemorrhagic_telangiectasia_can_also_be_classified_under_a_specific_group_of_diseases_called_osler_weber_rendu_syndrome__which_is_part_of_the_category__genetic_disorder__but_that_is_not_present_in_the_list_so_it_fits_best_with__metabolic_disorder|metabolic_disorder	blood_bone_marrow_disorder|skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0010881	mesomelia-synostoses syndrome	chromosomal_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disorder	bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0010882	aphalangy-syndactyly-microcephaly syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0010883	pectus excavatum-macrocephaly-dysplastic nails syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder	bone_disorder|heart_disorder|nail_disorder	false	false	false	false	medium
MONDO:0010884	muscular dystrophy, scapulohumeral	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0010885	angiokeratoma corporis diffusum with arteriovenous fistulas	hereditary_disease	other	hereditary_disease	cardiology|dermatology|cardiovascular_____corrected_to_use_the_more_commonly_used_term__dermatology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	skin_disorder|vascular_disorder	false	false	false	false	high
MONDO:0010886	2q37 microdeletion syndrome	chromosomal_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	anemia|mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0010887	isolated anterior cervical hypertrichosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|adrenal_gland_disease	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0010888	adenomyosis	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|urology	inflammatory_disease|cancer	muscle_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0010889	arterial dissection-lentiginosis syndrome	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pediatric|cardiology|genetics_and_genomics|neurology	arterial_dissection__lentiginosis_syndrome_also_involves_skin_manifestations|cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0010890	acrocardiofacial syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	ear_disorder|eye_disorder|heart_disorder|joint_disorder|vascular_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0010891	lethal hemolytic anemia-genital anomalies syndrome	syndromic_disease|hematologic_disorder	anemia	syndromic_disease|hematologic_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0010894	maturity-onset diabetes of the young type 3	digestive_system_disorder|metabolic_disease|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder|metabolic_disease|diabetes_mellitus	metabolic_disease|endocrine_system_disorder|digestive_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	endocrine_disorder	false	false	true	true	medium
MONDO:0010895	ABCD syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0010896	pigment dispersion syndrome	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology|urology|renal_medicine	metabolic_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0010897	schizophrenia 3	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0010898	autosomal dominant epilepsy with auditory features	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	true	medium
MONDO:0010899	autosomal dominant nocturnal frontal lobe epilepsy 1	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|epilepsy_is_not_listed_but_fits_none_of_the_other_categories|neurodegenerative_disease	neurological_disorder|brain_disorder	false	false	false	true	medium
MONDO:0010900	intrauterine growth retardation with increased mitomycin c sensitivity	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|oncology|pediatrics|obstetrics_and_gynecology	metabolic_disorder|cancer	reproductive_system_disorder|intrauterine_growth_retardation	false	false	false	false	high
MONDO:0010901	HEC syndrome	syndromic_disease	other	syndromic_disease	neurology|pediatric	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0010902	spondyloepiphyseal dysplasia, Reardon type	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0010903	craniosynostosis, Adelaide type	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	craniofacial_disorder_is_not_an_option_so__bone_disorder|bone_disorder	false	false	false	false	medium
MONDO:0010904	setting-Sun phenomenon, familial benign	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder|adrenal_gland_disease	liver_disorder|eye_disorder	false	false	false	false	low
MONDO:0010905	cone-rod dystrophy 1	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0010906	orofacial cleft 11	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	otolaryngology|pediatric	developmental_disorder|congenital_disorder|neurodegenerative_disease	facial_disorder|teeth_disorder|oral_disorder	false	false	false	false	high
MONDO:0010907	familial hypertryptophanemia	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0010908	loose anagen syndrome	integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics|pediatric	metabolic_disorder|anagen_syndrome	joint_disorder|skin_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0010909	UV-sensitive syndrome 1	hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease	hereditary_disease|integumentary_system_disorder|metabolic_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0010910	enuresis, nocturnal, 1	hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease	neurology|pediatric	neurodegenerative_disease|mental_health_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	true	low
MONDO:0010911	prolactin-producing pituitary gland adenoma	hereditary_disease|musculoskeletal_system_disorder|reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease|reproductive_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	neurology|endocrinology	cancer|endocrine_disorder	brain_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0010912	fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_orbital_region|musculoskeletal_system_disorder|hereditary_disease|disorder_of_visual_system	neurology|pulmonology|genetics_and_genomics|ophthalmology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010913	Caroli disease	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	renal_medicine|gastroenterology|hepatology	metabolic_disorder|liver_disease	liver_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0010914	carnitine palmitoyl transferase II deficiency, severe infantile form	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	metabolism|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0010915	autosomal dominant nonsyndromic hearing loss 4A	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder|hereditary_disease	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder|bone_disorder	false	false	false	true	medium
MONDO:0010916	polycystic kidney disease 3 with or without polycystic liver disease	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	renal_medicine|genetics_and_genomics|hepatology	kidney_disease|metabolic_disorder	liver_disorder|endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0010917	chondrocalcinosis 1	musculoskeletal_system_disorder|metabolic_disease|inflammatory_disease	metabolic_disease	inflammatory_disease|musculoskeletal_system_disorder|metabolic_disease	orthopaedic|rheumatology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	true	medium
MONDO:0010919	varicella, severe recurrent	hereditary_disease	other	hereditary_disease	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0010920	microtia	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	otolaryngology|pediatric	congenital_heart_defect|developmental_disorder|neurodegenerative_disease	throat_disorder|ear_disorder	false	false	false	false	medium
MONDO:0010921	nasal dermoid cyst	hereditary_disease|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	cancer_or_benign_tumor	hereditary_disease|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease|cancer_or_benign_tumor	otolaryngology|dermatology	skin|dermal|developmental___corrected_list_according_to_the_instructions__inflammatory_disease|congenital	nose_disorder|skin_disorder	false	false	false	false	low
MONDO:0010922	Satoyoshi syndrome	hereditary_disease|reproductive_system_disorder|integumentary_system_disorder|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|hereditary_disease|integumentary_system_disorder|reproductive_system_disorder	neurology|psychiatry	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	upper_gastrointestinal_disorder|brain_disorder|endocrine_disorder|eye_disorder	false	false	false	false	high
MONDO:0010923	proximal myopathy with focal depletion of mitochondria	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	neurology|renal_medicine|genetics_and_genomics	metabolic_disorder|muscular_disease|neurodegenerative_disease	muscle_disorder|mitochondrial_disorder	false	false	false	false	medium
MONDO:0010924	D-2-hydroxyglutaric aciduria	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	neurology|renal_medicine|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0010925	velo-facial-skeletal syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology|orthopaedic|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|anemia	skeletal_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0010926	familial hypocalciuric hypercalcemia 3	hereditary_disease|respiratory_system_disorder|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	respiratory_system_disorder|endocrine_system_disorder|metabolic_disease|hereditary_disease	endocrinology|renal_medicine|genetics_and_genomics	metabolic_disorder|familial_hyperchloremic_hypocalcemia_is_similar_to_this_condition	kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0010927	orofacial cleft 3	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	otolaryngology|pediatric	neurodevelopmental_disorder|congenital_disorder|craniofacial_anomaly|birth_defect	teeth_disorder|ear_disorder	false	false	false	false	medium
MONDO:0010928	dwarfism, familial, with muscle spasms	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|bone_disorder|endocrine_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0010929	craniosynostosis 4	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|orthopaedic|pediatric	craniosynostosis_is_often_considered_a_congenital_disorder_affecting_the_skull__which_may_be_related_to_neurodevelopmental_issues__but_it_s_also_associated_with_metabolic_disorders_due_to_bone_growth_abnormalities_and_potential_impact_on_brain_development__however__neurodegenerative_disease_is_most_commonly_linked___neurodegenerative_disease|craniosynostosis_is_often_considered_a_congenital_disorder_affecting_the_skull__which_may_be_related_to_neurodevelopmental_issues__but_it_s_also_associated_with_metabolic_disorders_due_to_bone_growth_abnormalities_and_potential_impact_on_brain_development|neurodegenerative_disease	spinal_disorder|teeth_disorder|brain_disorder|bone_disorder	false	false	false	true	high
MONDO:0010930	anophthalmia plus syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|ophthalmology|pediatric	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	very_high
MONDO:0010931	vitamin D-dependent rickets, type 2B	musculoskeletal_system_disorder|hereditary_disease|nutritional_disorder|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|hereditary_disease|nutritional_disorder|endocrine_system_disorder	endocrinology|genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|genetic_disease	endocrine_disorder|kidney_disorder|bone_disorder	false	false	false	true	very_high
MONDO:0010932	progressive bifocal chorioretinal atrophy	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	genetics_and_genomics|ophthalmology	inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0010933	autosomal recessive nonsyndromic hearing loss 4	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder|hearing_loss	false	false	false	true	medium
MONDO:0010936	frontotemporal dementia and/or amyotrophic lateral sclerosis 7	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0010937	isoproterenol-mediated vasodilatation	hereditary_disease	other	hereditary_disease	cardiothoracic|pulmonology|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	isoproterenol_is_a_medication_that_acts_as_a_beta_adrenergic_agonist__primarily_used_to_treat_bradycardia__slow_heart_rate__and_certain_types_of_heart_block__it_can_also_induce_vasodilation__which_is_a_widening_of_blood_vessels__however__it_is_not_specifically_a_treatment_for_a_particular_disease_but_rather_a_pharmacological_agent_used_to_manage_certain_cardiovascular_conditions___if_you_are_asking_whether_there_exist_efficacious_treatments_for_a_specific_disease_related_to_isoproterenol_mediated_vasodilation__i_would_need_additional_context_about_the_disease_you_are_inquiring_about__based_on_the_information_provided__isoproterenol_mediated_vasodilation___i_cannot_definitively_say_if_efficacious_treatments_exist_without_knowing_the_specific_condition_being_referenced____if_the_context_indicates_a_specific_condition_that_can_be_treated_with_isoproterenol_or_other_vasodilators__the_answer_may_be_true__otherwise__without_the_disease_context__i_would_return_false_for_the_specific_statement_regarding__this_disease	low
MONDO:0010938	T-B+ severe combined immunodeficiency due to JAK3 deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|immunology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0010939	gallbladder disease 1	hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease	gastroenterology|hepatology	metabolic_disorder|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder|biliary_disorder	false	false	false	false	medium
MONDO:0010941	nocturnal enuresis, 2	hereditary_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder	urology|neurology	neurodegenerative_disease|mental_health_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	true	low
MONDO:0010944	mitochondrial import-stimulating factor	hereditary_disease	other	hereditary_disease	biochemistry|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|upper_gastrointestinal_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0010945	retinitis pigmentosa 17	hereditary_disease|nervous_system_disorder|metabolic_disease|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder|metabolic_disease	nervous_system_disorder|disorder_of_orbital_region|metabolic_disease|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0010946	hypertrophic cardiomyopathy 6	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiothoracic|genetics_and_genomics|cardiology|pediatric	cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0010947	Budd-Chiari syndrome	cardiovascular_disorder|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cardiovascular_disorder	digestive_system_disorder|cardiovascular_disorder|endocrine_system_disorder	hematology|pulmonology|hepatology|cardiology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	liver_disorder|vascular_disorder	false	false	false	false	high
MONDO:0010948	cataract 10 multiple types	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	ophthalmology|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0010949	Charcot-Marie-Tooth disease type 2B	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	peripheral_nerve_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010951	dilated cardiomyopathy 1B	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiology|cardiothoracic	inflammatory_disease|cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010952	hereditary hyperferritinemia with congenital cataracts	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	hematology|genetics_and_genomics|ophthalmology|pediatric	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|eye_disorder	false	false	false	false	medium
MONDO:0010953	Fanconi anemia complementation group E	musculoskeletal_system_disorder|hematologic_disorder|immune_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease|anemia	hematologic_disorder|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|immune_system_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0010954	Wiskott-Aldrich syndrome, autosomal dominant form	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	hematology|genetics_and_genomics|immunology	autoimmune_diseases|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0010955	ectodermal dysplasia with intellectual disability and syndactyly	hereditary_disease	other	hereditary_disease	genetics_and_genomics|psychiatry|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	joint_disorder|teeth_disorder|eye_disorder|brain_disorder|skin_disorder	false	false	false	false	high
MONDO:0010956	enamel hypoplasia, cataracts, and aqueductal stenosis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology|pediatric|neurology	inflammatory_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	teeth_disorder|eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0010958	cardiac arrhythmia, ankyrin-B-related	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|genetics_and_genomics____there_are_two_best_fitting_categories__cardiology_and_genetics_and_genomics|cardiology	cardiovascular_disorder|autoimmune_diseases	heart_disorder|vascular_disorder|blood_bone_marrow_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0010959	van den Ende-Gupta syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorders___corrected_to___neurodegenerative_disease	lower_gastrointestinal_disorder|joint_disorder|upper_gastrointestinal_disorder|ear_disorder|vascular_disorder|immune_disorder|eye_disorder	false	false	false	false	high
MONDO:0010960	protocadherin 3	hereditary_disease	other	hereditary_disease	oncology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease	lower_gastrointestinal_disorder|ear_disorder|vascular_disorder|immune_disorder	false	false	false	false	none
MONDO:0010961	obesity due to prohormone convertase I deficiency	reproductive_system_disorder|nutritional_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder|nutritional_disorder	endocrinology|genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	endocrine_disorder|obesity	false	false	true	true	high
MONDO:0010962	diffuse nonepidermolytic palmoplantar keratoderma	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0010963	autosomal dominant nonsyndromic hearing loss 6	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|otolaryngology	neurodegenerative_disease|autosomal_dominant_nonshydromic_hearing_loss_is_not_in_the_list_so_i_am_unable_to_identify_a_category_for_it	ear_disorder	false	false	false	false	medium
MONDO:0010964	epiphyseal dysplasia, multiple, 3	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|connective_tissue_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|connective_tissue_disorder	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0010965	autosomal recessive nonsyndromic hearing loss 6	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	false	low
MONDO:0010966	achondrogenesis type IB	musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|genetic_disease	joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0010967	autosomal recessive nonsyndromic hearing loss 7	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder|bone_disorder	false	false	false	true	medium
MONDO:0010968	glaucoma 3, primary infantile, B	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	ophthalmology|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	true	high
MONDO:0010969	cone-rod dystrophy 5	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|psychiatric_disorder	psychiatric_disorder	disorder_of_orbital_region|psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0010970	cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|cardiology	genetic_disorder|congenital_abnormality|cardiovascular_disorder	heart_disorder|joint_disorder|upper_gastrointestinal_disorder|skin_disorder	false	false	false	false	high
MONDO:0010971	infundibulopelvic stenosis-multicystic kidney syndrome	syndromic_disease	other	syndromic_disease	urology|pediatric	metabolic_disorder|kidney_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0010972	hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0010973	autosomal dominant nonsyndromic hearing loss 5	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|otolaryngology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	ear_disorder	false	false	false	false	medium
MONDO:0010974	nephrotic syndrome, type 2	syndromic_disease|urinary_system_disorder|hereditary_disease	other	syndromic_disease|hereditary_disease|idiopathic_disease|urinary_system_disorder	renal_medicine|nephrology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0010976	epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|medical_genetics|dermatology|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	genetic_disorder|immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0010977	Brody myopathy	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0010978	portal vein, cavernous transformation of	hereditary_disease	other	hereditary_disease	gastroenterology|hepatology	cardiovascular_disorder|cancer|liver_disease	liver_disorder|vascular_disorder	false	false	false	false	high
MONDO:0010979	Timothy syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|genetic_disorders_is_not_in_the_list_so_cardiovascular_disorder|neurodegenerative_disease	lymphatic_disorder|immune_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0010980	midline malformations, multiple, with limb abnormalities and hypopituitarism	hereditary_disease	other	hereditary_disease	endocrinology|genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0010981	absent tibia-polydactyly-arachnoid cyst syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|orthopaedic	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|joint_disorder|immune_disorder|bone_disorder	false	false	false	false	medium
MONDO:0010982	ichthyosis-intellectual disability syndrome with large keratohyalin granules in the skin	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology|pediatric|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|intellectual_disability_syndrome|skin_disorder	false	false	false	false	high
MONDO:0010983	dystonia 9	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	psychiatry|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0010984	Usher syndrome type 1D	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|ophthalmology|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	ear_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0010985	epilepsy, familial adult myoclonic, 1	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0010986	autosomal recessive nonsyndromic hearing loss 9	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0010987	autosomal recessive nonsyndromic hearing loss 8	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	otolaryngology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	false	medium
MONDO:0010988	aplasia cutis-myopia syndrome	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	ophthalmology|dermatology|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0010989	Mayer-Rokitansky-Küster-Hauser syndrome type 2	syndromic_disease|reproductive_system_disorder	other	syndromic_disease|reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics|urology	genetic_disorder|renal_abnormality	reproductive_system_disorder|joint_disorder|kidney_disorder	false	false	false	false	high
MONDO:0010991	laterality defects, autosomal dominant	hereditary_disease|syndromic_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder|brain_disorder|eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0010992	Ayme-Gripp syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0010993	Harrod syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatrics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0010995	Charcot-Marie-Tooth disease type 1C	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|orthopaedic	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0010996	hereditary hemorrhagic telangiectasia type 3	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	hematology|genetics_and_genomics	cardiovascular_disorder|hereditary_disease|anemia	liver_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0010997	supranuclear palsy, progressive, 1	hereditary_disease|syndromic_disease|nervous_system_disorder|disorder_of_visual_system	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0010998	ALG3-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric	congenital_disorder_of_glycosylation|inflammatory_disease|metabolic_disorder	liver_disorder|bone_disorder	false	false	false	true	very_high
MONDO:0010999	fallot complex-intellectual disability-growth delay syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|cardiology	metabolic_disorder|neurodegenerative_disease	growth_delay|intellectual_disability|heart_disorder	false	false	false	false	very_high
MONDO:0011000	guanylate cyclase 2E	hereditary_disease	other	hereditary_disease	genetics_and_genomics|urology	adrenal_gland_disease|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	vascular_disorder|kidney_disorder	false	false	false	false	none
MONDO:0011001	Brugada syndrome 1	hereditary_disease|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|cardiology	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0011002	neuropathy, hereditary motor and sensory, type 6A	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	hereditary_condition___note__the_correct_term_for_the_given_disease_seems_to_be_charcot_marie_tooth_disease_type_6a__which_is_a_form_of_neurodegenerative_disease_and_also_an_inherited_condition|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0011003	dilated cardiomyopathy 1E	hereditary_disease|cardiovascular_disorder|syndromic_disease|musculoskeletal_system_disorder	cardiovascular_disorder	syndromic_disease|musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0011004	lissencephaly type 3-metacarpal bone dysplasia syndrome	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology|orthopaedic	metabolic_disorder|anemia|neurodegenerative_disease	bone_disorder|joint_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011005	trisomy 18-like syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	spinal_disorder|eye_disorder|upper_gastrointestinal_disorder|muscle_disorder|lower_gastrointestinal_disorder|joint_disorder|brain_disorder|heart_disorder|ear_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0011006	hereditary spastic paraplegia 9A	metabolic_disease|nervous_system_disorder|hereditary_disease|syndromic_disease	neurodegenerative_disease|metabolic_disease	metabolic_disease|nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscledisorder	false	false	false	false	medium
MONDO:0011007	diaphragmatic defect-limb deficiency-skull defect syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|developmental_disorder|congenital_abnormality|genetic_disorder	spinal_disorder|birth_defect|skeletal_disorder	false	false	false	false	very_high
MONDO:0011008	cleft lip/palate-intestinal malrotation-cardiopathy syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|gastroenterology|cardiology|pediatric	cardiovascular_disorder|metabolic_disorder	upper_gastrointestinal_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0011009	muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|orthopaedic|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0011010	Matthew-Wood syndrome	respiratory_system_disorder|disorder_of_visual_system|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_visual_system|disorder_of_orbital_region|respiratory_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	liver_disorder|biliary_disorder	false	false	false	false	very_high
MONDO:0011011	skeletal dysplasia-epilepsy-short stature syndrome	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics|orthopaedic	skeletal_dysplasia_epilepsy_short_stature_syndrome_is_not_in_the_list__so_it_will_not_be_included|metabolic_disorder|neurodegenerative_disease	bone_disorder|brain_disorder|skeletal_disorder	false	false	false	false	high
MONDO:0011012	African iron overload	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|hematology|renal_medicine	anemia|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder|kidney_disorder|muscle_disorder	false	false	false	true	high
MONDO:0011013	autosomal dominant hypocalcemia 1	metabolic_disease|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease|hereditary_disease	endocrinology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0011014	pleuropulmonary blastoma	respiratory_system_disorder|hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|respiratory_system_disorder|cancer_or_benign_tumor|hereditary_disease	pediatric|oncology|pulmonology	inflammatory_disease|cancer|adrenal_gland_disease	blood_bone_marrow_disorder|vascular_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0011015	cataract 24	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	neurology|ophthalmology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	vision_problems|eye_disorder	false	false	false	true	medium
MONDO:0011017	Naxos disease	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	syndromic_disease|musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|cardiothoracic	cardiovascular_disorder|autoimmune_diseases|metabolic_disorder	muscle_disorder|skin_disorder|heart_disorder	false	false	false	false	high
MONDO:0011018	brachyolmia-amelogenesis imperfecta syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|muscle_disorder|teeth_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0011019	alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome	integumentary_system_disorder	other	integumentary_system_disorder	neurology|endocrinology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0011020	osteoporosis-oculocutaneous hypopigmentation syndrome	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	endocrinology|dermatology|rheumatology	autoimmune_diseases|metabolic_disorder	bone_disorder|eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0011021	neuronal intestinal dysplasia, type B	digestive_system_disorder	other	digestive_system_disorder	neurology|pediatric|genetics_and_genomics|gastroenterology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0011022	Potocki-Shaffer syndrome	chromosomal_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|chromosomal_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	bone_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011023	hereditary mixed polyposis syndrome	hereditary_disease|digestive_system_disorder|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|digestive_system_disorder|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|oncology	hereditary_cancer_syndrome|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0011024	dermatitis herpetiformis, familial	immune_system_disorder|hereditary_disease|inflammatory_disease|integumentary_system_disorder	autoimmune_disease	integumentary_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	dermatology|genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0011025	Cayman type cerebellar ataxia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011026	autosomal recessive congenital ichthyosis 4A	disorder_of_visual_system|hereditary_disease|integumentary_system_disorder	other	disorder_of_visual_system|integumentary_system_disorder|disorder_of_orbital_region|hereditary_disease	pediatric|dermatology|genetics_and_genomics	skin_condition|genetic_disorder|metabolic_disorder	skin_disorder	false	false	false	false	medium
MONDO:0011027	diabetes mellitus, noninsulin-dependent, 1	hereditary_disease|digestive_system_disorder|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|diabetes_mellitus|metabolic_disease	endocrine_system_disorder|metabolic_disease|digestive_system_disorder|hereditary_disease	endocrinology|renal_medicine	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0011028	autosomal recessive limb-girdle muscular dystrophy type 2F	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|nervous_system_disorder|cardiovascular_disorder|hereditary_disease	neurology|genetics_and_genomics	muscular_dystrophy|neurodegenerative_disease	spinal_disorder|muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0011029	myeloid tumor suppressor	hereditary_disease	other	hereditary_disease	hematology|genetics_and_genomics|oncology	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0011030	epithelial basolateral chloride conductance regulator, rabbit, homolog of	hereditary_disease	other	hereditary_disease	physiology|genetics_and_genomics|molecular_biology|biochemistry|cellular_biology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	renal_disorder___note__renal_disorder_is_a_synonym_for_kidney_disorder|kidney_disorder	false	false	false	false	none
MONDO:0011031	autosomal dominant nonsyndromic hearing loss 10	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder|hereditary_disease	otolaryngology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	bone_disorder|ear_disorder	false	false	false	false	medium
MONDO:0011032	autosomal dominant nonsyndromic hearing loss 11	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder|hereditary_disease	otolaryngology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	ear_disorder|hearing_loss	false	false	false	false	medium
MONDO:0011034	odontomicronychial dysplasia	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	otolaryngology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	bone_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0011035	neurofibromatosis-Noonan syndrome	nervous_system_disorder|hereditary_disease|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|nervous_system_disorder|cancer_or_benign_tumor|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|oncology	cancer|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0011036	porencephaly-cerebellar hypoplasia-internal malformations syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0011038	cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome	mitochondrial_disease|disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	disorder_of_visual_system|mitochondrial_disease|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder|sensorineural_hearing_loss|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011039	atrophia maculosa varioliformis cutis, familial	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0011040	spinal dysplasia, Anhalt type	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|anhalts_type_is_a_form_of_spinal_muscular_atrophy_which_is_also_known_as_spinal_muscular_wasting__or_spinal_muscular_atrophy_type_i	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0011041	ectodermal dysplasia with natal teeth, Turnpenny type	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|dermatology	neurodegenerative_disease|metabolic_disorder	immune_disorder|bone_disorder|eye_disorder|upper_gastrointestinal_disorder|vascular_disorder|lymphatic_disorder|lower_gastrointestinal_disorder|teeth_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0011042	Martinez-Frias syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|liver_disorder|kidney_disorder|joint_disorder	false	false	false	false	high
MONDO:0011043	myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay	hereditary_disease	other	hereditary_disease	neurology|hematology|pediatric|genetics_and_genomics	anemia|autoimmune_diseases|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder|bone_disorder|short_stature_is_often_associated_with_bone_disorder___corrected_response__blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0011044	ectrodactyly of lower limbs, congenital heart defect, and micrognathia	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics|orthopaedic|obstetrics_and_gynecology|cardiology	cardiovascular_disorder|congenital_heart_defect|metabolic_disorder	congenital_heart_defect____heart_disorder|spinal_disorder|micrognathia____joint_disorder|teeth_disorder|joint_disorder|heart_disorder	false	false	false	false	high
MONDO:0011045	MMEP syndrome	disorder_of_visual_system|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0011046	short stature, Brussels type	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	endocrinology|pediatric|genetics_and_genomics	genetic_disorders|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0011047	deafness-epiphyseal dysplasia-short stature syndrome	hereditary_disease	other	hereditary_disease	endocrinology|otolaryngology|genetics_and_genomics|orthopaedic|pediatrics	neurodegenerative_disease|metabolic_disorder	bone_disorder|ear_disorder	false	false	false	false	medium
MONDO:0011048	epilepsy-microcephaly-skeletal dysplasia syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|skeletal_disorder	false	false	false	false	very_high
MONDO:0011049	Fine-Lubinsky syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spine_disorder|brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0011050	microcephaly-cardiac defect-lung malsegmentation syndrome	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics|pulmonology|cardiology	cardiovascular_disorder|congenital_anomaly	brain_disorder|heart_disorder|lung_disorder	true	false	false	false	very_high
MONDO:0011051	lethal short-limb skeletal dysplasia, Al Gazali type	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder|muscle_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0011052	amelia cleft lip palate hydrocephalus iris coloboma	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	mental_health_disorder|autoimmune_diseases|inflammatory_disease|cancer|neurodegenerative_disease|anemia	bone_disorder|eye_disorder|facial_disorder	false	false	false	true	high
MONDO:0011053	intellectual disability-sparse hair-brachydactyly syndrome	hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	psychiatric_disorder	disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|joint_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0011054	autosomal recessive amelia	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|anemia	bone_disorder|immune_disorder|limb_disorder|joint_disorder	false	false	false	false	high
MONDO:0011055	distal monosomy 10p	chromosomal_disorder|hereditary_disease	other	chromosomal_disorder|hereditary_disease	pediatric|genetics_and_genomics	developmental_disorder|neurodegenerative_disease|genetic_disorder	bone_disorder|immune_disorder|upper_gastrointestinal_disorder|urinary_tract_disorder|spinal_disorder|lower_gastrointestinal_disorder|vascular_disorder|muscle_disorder|joint_disorder|kidney_disorder	false	false	false	false	high
MONDO:0011056	Wilms tumor 4	hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease	pediatric|oncology	cancer|adrenal_gland_disease	renal_disorder|kidney_disorder	false	true	false	true	high
MONDO:0011057	cerebrovascular disorder	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	cardiology|neurology	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0011058	autosomal dominant nonsyndromic hearing loss 9	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder|hereditary_disease	otorhinolaryngology|pediatric|genetics_and_genomics|genetics	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	ear_disorder	false	false	false	false	medium
MONDO:0011059	holoprosencephaly-craniosynostosis syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	craniosynostosis_syndrome|neurodegenerative_disease	bone_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011060	early-onset non-syndromic cataract	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0011061	chorea, remitting, with nystagmus and cataract	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder|brain_disorder|muscle_disorder	true	false	false	false	medium
MONDO:0011062	aprosencephaly cerebellar dysgenesis	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0011063	hidrotic ectodermal dysplasia, Christianson-Fourie type	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	pediatric|endocrinology|dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0011064	lethal chondrodysplasia, Seller type	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0011065	Hunter-McAlpine craniosynostosis	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	developmental_disorder|neurodegenerative_disease|congenital_disorder	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011066	Charcot-Marie-Tooth disease type 4B1	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|nerve_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0011067	autosomal recessive nonsyndromic hearing loss 12	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder|hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	false	medium
MONDO:0011069	cervical ribs, Sprengel anomaly, anal atresia, and urethral obstruction	hereditary_disease	other	hereditary_disease	pediatric|orthopaedic|urology	cardiovascular_disorder|anatomic_abnormality|congenital_anomaly|genitourinary_disorder	urinary_tract_disorder|spinal_disorder|skeletal_disorder	false	false	false	false	medium
MONDO:0011070	van Maldergem syndrome 1	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0011071	hereditary thrombocytopenia and hematologic cancer predisposition syndrome	hematologic_disorder|hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|hematologic_disorder|cancer_or_benign_tumor|hereditary_disease	hematology|genetics_and_genomics|oncology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0011072	diabetes mellitus, noninsulin-dependent, 2	hereditary_disease|digestive_system_disorder|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease|diabetes_mellitus	endocrine_system_disorder|hereditary_disease|metabolic_disease|digestive_system_disorder	endocrinology|cardiology	cardiovascular_disorder|metabolic_disorder|inflammatory_disease	kidney_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0011073	diabetes mellitus, transient neonatal, 1	hereditary_disease|digestive_system_disorder|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease|diabetes_mellitus	endocrine_system_disorder|hereditary_disease|metabolic_disease|digestive_system_disorder	pediatric|endocrinology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	vascular_disorder|kidney_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0011074	autosomal dominant nonsyndromic hearing loss 7	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder|hereditary_disease	otolaryngology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	false	high
MONDO:0011075	retinitis pigmentosa 18	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0011076	myofibrillar myopathy 1	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|nervous_system_disorder|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|muscle_disorders_often_overlap_with_neurology__so_both_are_included|neurology	metabolic_disorder|neurodegenerative_disease	muscular_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0011077	microcephaly, corpus callosum dysgenesis, and cleft lip/palate	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	mental_health_disorder|microcephaly_is_not_a_direct_match_for_these_categories_but_can_be_associated_with_them_corpus_callosum_dysgenesis_is_also_not_a_direct_match_but_can_be_associated_with_neurodegenerative_disease_and_or_mental_health_disorder__cleft_lip_palate___none_are_exact_matches|metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|ear_disorder|brain_disorder	true	false	false	false	high
MONDO:0011078	anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease|anemia	eye_disorder|throat_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0011079	rhizomelic dysplasia, Patterson-Lowry type	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease|inflammatory_disease	bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011080	progressive deafness with stapes fixation	hereditary_disease	other	hereditary_disease	otolaryngology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	ear_disorder|throat_disorder	false	false	false	false	medium
MONDO:0011081	dislocation of the hip-dysmorphism syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic	genetic_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0011082	oculoauriculofrontonasal syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	ophthalmology|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	eye_disorder|brain_disorder|ear_disorder	false	false	false	false	high
MONDO:0011083	trichodental syndrome	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	pediatrics|genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	liver_disorder|teeth_disorder|skin_disorder	false	false	false	false	low
MONDO:0011085	Charcot-Marie-Tooth disease type 4D	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011086	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|immunology|hematatology	autoimmune_diseases|inflammatory_disease|anemia	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0011087	inflammatory bowel disease 2	digestive_system_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease|digestive_system_disorder	gastroenterology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0011088	congenital myasthenic syndrome 1A	hereditary_disease|nervous_system_disorder|syndromic_disease	other	syndromic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0011089	patent ductus venosus	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	pediatric|hematology|cardiology	congenital_heart_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0011090	isolated hereditary congenital facial paralysis	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	brain_disorder|ear_disorder|muscle_disorder	false	false	false	false	low
MONDO:0011091	Charcot-Marie-Tooth disease type 2D	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	nerve_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011092	ribbing disease	hereditary_disease	other	hereditary_disease	hematology|cardiothoracic|cardiology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|bone_disorder|spinal_disorder|vascular_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0011093	mucopolysaccharidosis type 9	hereditary_disease|metabolic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|muscle_disorder|joint_disorder|liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0011094	dilated cardiomyopathy 1C	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiothoracic|cardiology	cardiovascular_disorder|dilated_cardiomyopathy	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0011095	dilated cardiomyopathy 1D	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiothoracic|cardiology	cardiovascular_disorder|metabolic_disorder|inflammatory_disease	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0011096	autosomal agammaglobulinemia	hematologic_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0011097	Axenfeld-Rieger syndrome type 2	disorder_of_visual_system|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|disorder_of_visual_system|syndromic_disease|disorder_of_orbital_region|hereditary_disease	pediatric|endocrinology|ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|upper_gastrointestinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0011098	prostate cancer, hereditary, 1	reproductive_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|reproductive_system_disorder	genetics_and_genomics|oncology|urology	hereditary|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0011099	human HOXA1 syndromes	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|developmental_disorder|genetic_condition	brain_disorder|ear_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0011100	microcephaly, retinitis pigmentosa, and sutural cataract	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	microcephaly__high____retinitis_pigmentosa__high____sutural_cataract__medium
MONDO:0011101	peroxisome biogenesis disorder 1B	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease	metabolic_disease|neurodegenerative_disease	metabolic_disease|nervous_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	peroxisome_biogenesis_disorder_1b_affects_the_liver_s_ability_to_perform_certain_functions|liver_disorder	false	false	false	false	very_high
MONDO:0011102	autosomal dominant nonsyndromic hearing loss 12	hereditary_disease|psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|auditory_system_disorder|psychiatric_disorder	otolaryngology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	auditory_system_disorder|ear_disorder	false	false	false	false	medium
MONDO:0011103	autosomal dominant nonsyndromic hearing loss 3A	hereditary_disease|psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|auditory_system_disorder|psychiatric_disorder	otolaryngology|genetics_and_genomics|pediatric	genetic_disorder|sensory_loss|neurodegenerative_disease|hearing_loss|autosomal_dominant_disorder	ear_disorder	false	false	false	false	high
MONDO:0011104	cataract 3 multiple types	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0011105	alacrima, congenital, autosomal recessive	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	kidney_disorder|nose_disorder|ear_disorder	false	false	false	false	low
MONDO:0011106	facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0011107	congenital hypotrichosis with juvenile macular dystrophy	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|integumentary_system_disorder	genetics_and_genomics|pediatric|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0011109	multiple epiphyseal dysplasia, Lowry type	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	genetic_disorder|metabolic_disorder	bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0011110	dyssegmental dysplasia-glaucoma syndrome	disorder_of_visual_system|syndromic_disease	other	disorder_of_visual_system|syndromic_disease|disorder_of_orbital_region	genetics_and_genomics|pediatric|ophthalmology	metabolic_disorder|neurodegenerative_disease	bone_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0011112	Wilms tumor 5	cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor	renal_medicine|oncology|urology|pediatric	cancer|kidney_cancer	reproductive_system_disorder|kidney_disorder	false	true	false	true	high
MONDO:0011113	Charcot-Marie-Tooth disease type 4C	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|hereditary_diseases	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011114	familial multiple trichoepithelioma	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	oncology|genetics_and_genomics|pediatric	cancer|familial_cancer	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0011115	spastic paraplegia and Evans syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011116	lung agenesis-heart defect-thumb anomalies syndrome	disorder_of_development_or_morphogenesis|respiratory_system_disorder|syndromic_disease	other	syndromic_disease|respiratory_system_disorder|disorder_of_development_or_morphogenesis	cardiology|genetics_and_genomics|pediatric|pulmonology	congenital_heart_defect|cardiovascular_disorder	lung_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0011117	iris pigment epithelium anomalies	hereditary_disease	other	hereditary_disease	dermatology|ophthalmology	autoimmune_diseases|cancer	immune_disorder|kidney_disorder|eye_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0011118	bilineal acute myeloid leukemia	cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder|hematologic_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder|acute_disease|cancer_or_benign_tumor	oncology|hematology	anemia|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0011119	iridogoniodysgenesis	disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|ophthalmology|pediatrics	mental_health_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0011120	neural tube defects, folate-sensitive	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|obstetrics_and_gynecology	anemia|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0011121	pheochromocytoma/paraganglioma syndrome 2	disorder_of_development_or_morphogenesis|hereditary_disease|urinary_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|syndromic_disease	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|hereditary_disease|syndromic_disease|urinary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|endocrine_system_disorder	neurology|oncology|otolaryngology	neurological_cancers|cancer	vascular_disorder|brain_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0011122	obesity disorder	nutritional_disorder	other	nutritional_disorder	psychiatry|endocrinology	cardiovascular_disorder|mental_health_disorder|metabolic_disorder	upper_gastrointestinal_disorder|muscle_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0011124	spondyloepimetaphyseal dysplasia-abnormal dentition syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	bone_disorder|teeth_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0011125	trichothiodystrophy 1, photosensitive	hereditary_disease|metabolic_disease|integumentary_system_disorder|syndromic_disease	metabolic_disease	metabolic_disease|hereditary_disease|syndromic_disease|radiation_induced_disorder|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|neurodegenerative_disease	skin_disorder|hair_disorder	false	false	false	false	high
MONDO:0011126	acute insulin response	hereditary_disease	other	hereditary_disease|acute_disease	endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder	false	false	false	false	medium
MONDO:0011128	Sheldon-hall syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	psychiatry|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011129	glaucoma type 1C	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	true	medium
MONDO:0011130	sebaceous gland hyperplasia, familial presenile	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0011131	tricho-oculo-dermo-vertebral syndrome	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|integumentary_system_disorder	neurology|dermatology|ophthalmology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0011132	T-cell immunodeficiency, congenital alopecia, and nail dystrophy	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder|skin_disorder	false	false	false	false	high
MONDO:0011133	deaf blind hypopigmentation syndrome, Yemenite type	integumentary_system_disorder	other	integumentary_system_disorder	ophthalmology|genetics_and_genomics|dermatology	metabolic_disorder|neurodegenerative_disease	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0011134	Curry-Jones syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	allergy_and_immunology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder	false	false	false	false	high
MONDO:0011135	superior transverse scapular ligament, calcification of, familial	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	spinal_disorder|joint_disorder	false	false	false	false	low
MONDO:0011136	Quebec platelet disorder	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0011137	retinitis pigmentosa 19	hereditary_disease|psychiatric_disorder|metabolic_disease|disorder_of_visual_system|nervous_system_disorder	metabolic_disease|psychiatric_disorder	disorder_of_visual_system|metabolic_disease|nervous_system_disorder|hereditary_disease|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	eye_disorder	false	false	false	false	high
MONDO:0011139	preaxial hallucal polydactyly	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	congenital_abnormality|neurodevelopmental_disorder|genetic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0011141	megaloblastic anemia, folate-responsive	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	gastroenterology|hematology|genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|anemia	upper_gastrointestinal_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0011142	Ehlers-Danlos syndrome, musculocontractural type	metabolic_disease|cardiovascular_disorder|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	orthopaedic|pediatric|dermatology|rheumatology|genetics_and_genomics	metabolic_disorder|genetic_disorder|connective_tissue_disorder	muscle_disorder|joint_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0011143	cone-rod dystrophy 6	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0011144	ceroid lipofuscinosis, neuronal, 6A	psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease|neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease	pediatric|neurology|psychiatry|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0011145	colobomatous microphthalmia - obesity - hypogenitalism - intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|neurology|endocrinology|genetics_and_genomics	intellectual_disability|metabolic_disorder	endocrine_disorder|eye_disorder	false	false	false	false	high
MONDO:0011146	tetrasomy 12p	chromosomal_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	chromosomal_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|chromosomal_abnormality	genetic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0011147	chromosome 18q deletion syndrome	chromosomal_disorder|syndromic_disease	other	chromosomal_disorder|syndromic_disease	pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	joint_disorder|brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011148	Spondylospinal thoracic dysostosis	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0011149	premature aging syndrome, Okamoto type	premature_aging_syndrome	other	premature_aging_syndrome	dermatology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	vascular_disorder|eye_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0011150	acroosteolysis-keloid-like lesions-premature aging syndrome	premature_aging_syndrome|hereditary_disease	other	hereditary_disease|premature_aging_syndrome	dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|bone_disorder	false	false	false	false	medium
MONDO:0011151	exudative vitreoretinopathy 4	cardiovascular_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	cancer|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0011152	PHGDH deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|hematology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	liver_disorder|metabolic_disorder_is_not_present_but_endocrine_disorder	false	false	false	true	very_high
MONDO:0011153	hyperinsulinemic hypoglycemia, familial, 2	metabolic_disease|endocrine_system_disorder|hereditary_disease|digestive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder|metabolic_disease	hereditary_disease|digestive_system_disorder|endocrine_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	endocrinology|genetics_and_genomics	familial|metabolic_disorder	endocrine_disorder|blood_bone_marrow_disorder	false	false	true	true	high
MONDO:0011154	acrofacial dysostosis, Palagonia type	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	joint_disorder|eye_disorder|ear_disorder|teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0011155	vacuolar Neuromyopathy	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011156	progressive familial intrahepatic cholestasis type 2	metabolic_disease|endocrine_system_disorder|hereditary_disease|digestive_system_disorder|syndromic_disease	endocrine_system_disorder|metabolic_disease	syndromic_disease|hereditary_disease|digestive_system_disorder|endocrine_system_disorder|metabolic_disease	hepatology|genetics_and_genomics	liver_disease|metabolic_disorder	liver_disorder|biliary_disorder	false	false	false	false	very_high
MONDO:0011157	Gomez-Lopez-Hernandez syndrome	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|cardiology|hematology|cardiothoracic|pulmonology|renal_medicine|oncology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	urinary_tract_disorder|vascular_disorder|joint_disorder|kidney_disorder	false	false	false	false	high
MONDO:0011158	autoimmune lymphoproliferative syndrome type 1	immune_system_disorder|cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor|autoimmune_disease	syndromic_disease|hereditary_disease|cancer_or_benign_tumor|immune_system_disorder	pediatric|hematology|rheumatology|allergy_and_immunology|oncology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder_lymphatic_disorder	false	false	false	true	high
MONDO:0011159	autosomal dominant nonsyndromic hearing loss 13	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	medium
MONDO:0011160	autosomal recessive nonsyndromic hearing loss 15	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0011161	sperm-specific antigen 1	hereditary_disease	other	hereditary_disease	urology	cancer|autoimmune_diseases	reproductive_system_disorder	false	false	false	false	none
MONDO:0011162	cataract 14 multiple types	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0011165	glomerulopathy with fibronectin deposits 2	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	hematology|nephrology|renal_medicine	autoimmune_diseases|metabolic_disorder|inflammatory_disease	vascular_disorder|kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0011166	lymphedema-atrial septal defects-facial changes syndrome	immune_system_disorder|syndromic_disease	other	immune_system_disorder|syndromic_disease	pediatric|cardiology|cardiovascular_____revised__pediatric|genetics_and_genomics	autoimmune_diseases|anemia|cardiovascular_disorder	heart_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0011169	keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0011170	autosomal recessive limb-girdle muscular dystrophy type 2G	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|muscular_dystrophy	joint_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011171	odonto-tricho-ungual-digito-palmar syndrome	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	pediatric|dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	joint_disorder|nail_disorder|skin_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0011172	otofacioosseous-gonadal syndrome	hereditary_disease	other	hereditary_disease	obstetrics_and_gynecology|otolaryngology|endocrinology|pediatrics|urology|genetics_and_genomics	autoimmune_diseases|anemia|metabolic_disorder	reproductive_system_disorder|ear_disorder|bone_disorder	false	false	false	false	high
MONDO:0011173	thrombocythemia 2	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology	autoimmune_diseases|anemia|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0011174	hyperzincemia with functional zinc depletion	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	obstetrics_and_gynecology|endocrinology|hematology|psychiatry|pulmonology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	endocrine_disorder|liver_disorder	false	false	false	false	medium
MONDO:0011175	Friedreich ataxia 2	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011176	intestinal hypomagnesemia 1	metabolic_disease|hereditary_disease|urinary_system_disorder	metabolic_disease	hereditary_disease|urinary_system_disorder|metabolic_disease	hepatology|gastroenterology|renal_medicine	anemia|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0011177	ectodermal dysplasia 4, hair/nail type	integumentary_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	dermatology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|autoimmune_diseases|metabolic_disorder|allergy|inflammatory_disease|cardiovascular_disorder	hair_disorder|nail_disorder|skin_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0011178	infantile convulsions and choreoathetosis	nervous_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|nervous_system_disorder|syndromic_disease	neurology|pediatric	neurodegenerative_disease|metabolic_disorder|infantile_convolutions_and_choreoathetosis_is_not_listed_so_nothing	brain_disorder|muscle_disorder	true	false	false	true	high
MONDO:0011180	broad terminal phalanges, familial	hereditary_disease	other	hereditary_disease	other___replaced_original_line_with_this___genetics_and_genomics|pediatrics|genetics_and_genomics|orthopaedic|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	true	low
MONDO:0011181	fibrosis of extraocular muscles, congenital, 2	disorder_of_visual_system|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|musculoskeletal_system_disorder	ophthalmology|genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011182	trimethylaminuria	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	inborn_errors_of_metabolism_would_also_suggest_a_category_but_that_is_not_provided_however_given_the_list_genetics_and_genomics_is_likely_more_specific_to_this_disease_than_any_other_category|genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	liver_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0011183	Paget disease of bone 2, early-onset	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	endocrinology|genetics_and_genomics|orthopaedic	autoimmune_diseases|metabolic_disorder|inflammatory_disease	endocrine_disorder|blood_bone_marrow_disorder|bone_disorder	false	false	false	false	medium
MONDO:0011184	childhood apraxia of speech	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|mental_health_disorder	throat_disorder|brain_disorder	false	false	false	false	medium
MONDO:0011185	Thiel-Behnke corneal dystrophy	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0011186	Usher syndrome type 1F	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	neurology|otolaryngology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|ear_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011187	polydactyly, postaxial, type A2	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	true	low
MONDO:0011188	arrhythmogenic right ventricular dysplasia 3	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiology|cardiothoracic|pediatrics|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011189	arrhythmogenic right ventricular dysplasia 4	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiology|cardiothoracic|pediatric	autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0011190	nephronophthisis 2	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	renal_medicine|urology	metabolic_disorder|kidney_disease|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0011191	capillary infantile hemangioma	cancer_or_benign_tumor|cardiovascular_disorder|hereditary_disease	cancer_or_benign_tumor|cardiovascular_disorder	hereditary_disease|cancer_or_benign_tumor|cardiovascular_disorder	dermatology|hematology|pediatric	vascular_disorder|benign_tumor|cancer|infantile_hemangioma|neoplasm	vascular_disorder|skin_disorder	false	false	false	true	low
MONDO:0011192	autosomal recessive nonsyndromic hearing loss 18A	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	otolaryngology|genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0011193	cone dystrophy 3	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011194	Alzheimer disease 5	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0011195	Usher syndrome type 1E	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	eye_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0011196	amyotrophic lateral sclerosis type 5	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011197	hereditary thermosensitive neuropathy	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	hereditary_disease|neurodegenerative_disease|metabolic_disorder	nerve_disorder|brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011198	spondyloepimetaphyseal dysplasia, Missouri type	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0011199	nephropathy, progressive tubulointerstitial, with cholestatic liver disease	endocrine_system_disorder|inflammatory_disease|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|inflammatory_disease	renal_medicine|hepatology|gastroenterology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0011200	torsion dystonia 7	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011201	tremor, hereditary essential, 2	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011202	RHYNS syndrome	urinary_system_disorder|disorder_of_visual_system|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|urinary_system_disorder|disorder_of_visual_system	pediatric|otolaryngology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	ear_disorder|lymphatic_disorder|throat_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0011203	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies	syndromic_disease	other	syndromic_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|skeletal_dysplasia	skeletal_system_disorder|teeth_disorder|bone_disorder	false	false	false	false	high
MONDO:0011205	medium chain 3-ketoacyl-Coa thiolase deficiency	hereditary_disease	other	hereditary_disease	pediatric|metabolism|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|metabolic_disorder	false	false	false	false	medium
MONDO:0011206	ventriculomegaly with defects of the radius and kidney	hereditary_disease	other	hereditary_disease	pediatric|renal_medicine|cardiology	anomaly_of_body_structure|cardiovascular_disorder|renal_disease	kidney_disorder|heart_disorder|bone_disorder	false	false	false	false	high
MONDO:0011208	malignant atrophic papulosis	cardiovascular_disorder|integumentary_system_disorder	cardiovascular_disorder	cardiovascular_disorder|integumentary_system_disorder	dermatology|oncology	cancer|autoimmune_diseases	immune_disorder|skin_disorder	false	true	false	false	very_high
MONDO:0011209	progeroid facial appearance with hand anomalies	disorder_of_development_or_morphogenesis|premature_aging_syndrome|hereditary_disease	other	premature_aging_syndrome|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|skin_disorder|bone_disorder	true	true	false	true	high
MONDO:0011210	mitochondrial intermembrane space protein Tim12, yeast, homolog of	hereditary_disease	other	hereditary_disease	molecular_biology|genetics_and_genomics|biochemistry|cell_biology	neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	low
MONDO:0011211	axial spondylometaphyseal dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|rheumatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0011212	sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth	hereditary_disease	other	hereditary_disease	neurology|otolaryngology|ophthalmology	cancer|neurodegenerative_disease|autoimmune_diseases	ear_disorder|eye_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0011213	Pierpont syndrome	nervous_system_disorder|hereditary_disease|syndromic_disease|psychiatric_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis	psychiatric_disorder	integumentary_system_disorder|syndromic_disease|hereditary_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|otolaryngology|pulmonology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011214	progressive familial intrahepatic cholestasis type 3	metabolic_disease|hereditary_disease|syndromic_disease|endocrine_system_disorder|digestive_system_disorder	metabolic_disease|endocrine_system_disorder	syndromic_disease|digestive_system_disorder|hereditary_disease|endocrine_system_disorder|metabolic_disease	hepatology|gastroenterology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0011215	osteocraniostenosis	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|rheumatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	bone_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0011216	hemochromatosis type 2A	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|gastroenterology|genetics_and_genomics|hematology	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0011217	desmosterolosis	metabolic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	dermatology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|skeletal_disorder	false	false	false	false	very_high
MONDO:0011218	autosomal recessive congenital ichthyosis 11	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics|pediatric	metabolic_disorder|skin_condition|congenital_disorder	immune_disorder|skin_disorder	false	false	false	true	high
MONDO:0011219	Fried's tooth and nail syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|syndromic_disease|hereditary_disease	dermatology|pediatrics|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	nail_disorder|teeth_disorder	false	false	false	false	high
MONDO:0011220	Parkinson disease 3, autosomal dominant	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant_diseases_is_not_in_the_list_so_i_ll_leave_it_out	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011221	Weyers ulnar ray/oligodactyly syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|orthopaedic	congenital_abnormality|metabolic_disorder|genetic_disorder|skeletal_dysplasia___corrected_list___genetic_disorder|skeletal_dysplasia___final_answer__genetic_disorder	bone_disorder|joint_disorder|limb_abnormality	false	false	false	false	medium
MONDO:0011223	amyotrophic lateral sclerosis type 4	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0011224	monomelic amyotrophy	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011225	severe combined immunodeficiency due to DCLRE1C deficiency	metabolic_disease|hereditary_disease|immune_system_disorder	metabolic_disease	immune_system_disorder|hereditary_disease|metabolic_disease	allergy_and_immunology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0011226	autosomal dominant nonsyndromic hearing loss 15	nervous_system_disorder|auditory_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	otolaryngology|genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	ear_disorder	false	false	false	false	high
MONDO:0011227	short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome	otorhinolaryngologic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|otorhinolaryngologic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|otolaryngology|genetics_and_genomics|pediatric	skeletal_anomalies|metabolic_disorder	bone_disorder|ear_disorder|skeletal_anomalies	false	false	false	false	high
MONDO:0011228	creases, infra-auricular cutaneous, with tall stature and advanced bone age	hereditary_disease	other	hereditary_disease	orthopaedic|endocrinology|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|skin_disorder	false	false	false	false	high
MONDO:0011229	ethylmalonic encephalopathy	mitochondrial_disease|hereditary_disease	other	mitochondrial_disease|hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|anemia|metabolic_disorder	brain_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0011230	ossification of the posterior longitudinal ligament of the spine	hereditary_disease|connective_tissue_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease	neurology|orthopaedic|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0011231	febrile seizures, familial, 2	hereditary_disease	other	hereditary_disease	neurology|pediatric	neurodegenerative_disease|metabolic_disorder	immune_disorder|brain_disorder	false	false	false	true	medium
MONDO:0011232	migraine, familial hemiplegic, 2	hereditary_disease|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|familial_hemiplegic_migraine_is_sometimes_classified_as_a_neurodegenerative_disorder_because_it_shares_some_similarities_with_other_neurodegenerative_diseases_such_as_huntington_s_disease_and_spinocerebellar_ataxia__despite_its_distinct_pathophysiology	vascular_disorder|brain_disorder	false	false	false	true	high
MONDO:0011233	Axenfeld-Rieger syndrome type 3	hereditary_disease|disorder_of_visual_system|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_orbital_region|hereditary_disease|syndromic_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	lower_gastrointestinal_disorder|joint_disorder|eye_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0011234	auriculocondylar syndrome 1	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	joint_disorder|ear_disorder	false	false	false	false	high
MONDO:0011235	pelvic dysplasia-arthrogryposis of lower limbs syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0011236	hyperinsulinism due to glucokinase deficiency	hereditary_disease|metabolic_disease|endocrine_system_disorder|digestive_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease|endocrine_system_disorder	hereditary_disease|digestive_system_disorder|endocrine_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	vascular_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0011238	chondrodysplasia punctata, brachytelephalangic, autosomal	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0011239	colobomatous macrophthalmia-microcornea syndrome	disorder_of_visual_system|syndromic_disease	other	syndromic_disease|disorder_of_visual_system	genetics_and_genomics|ophthalmology|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|other____however__note_that__colobomatous_macropthalmia_microcornea_syndrome__is_a_rare_genetic_disorder_and__other__may_not_be_the_best_fit__rather_it_should_likely_include_a_more_specific_category_related_to_genetics_or_congenital_disorders_which_are_not_listed_in_this_category_list	false	false	false	false	high
MONDO:0011240	megalencephaly-capillary malformation-polymicrogyria syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0011241	pseudoacromegaly with severe insulin resistance	hereditary_disease	other	hereditary_disease	genetics_and_genomics|endocrinology|pediatric	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	insulin_resistance|endocrine_disorder	false	false	true	false	high
MONDO:0011242	Bartter disease type 4A	urinary_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease|urinary_system_disorder	pediatrics|renal_medicine|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0011243	grange syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0011244	Marshall-Smith syndrome	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|endocrinology|pediatric	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease|inflammatory_disease	reproductive_system_disorder|endocrine_disorder|bone_disorder	false	false	false	false	high
MONDO:0011245	ichthyosis, hystrix-like, with hearing loss	hereditary_disease|syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	otolaryngology|genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder	ear_disorder|skin_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0011246	megaconial type congenital muscular dystrophy	hereditary_disease|metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder	metabolic_disease	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	neurology|orthopaedic|genetics_and_genomics|pediatric	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder|muscular_dystrophy_is_not_in_the_category_list_so_nothing_else_fits	spinal_disorder|muscle_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0011247	jejunal atresia with renal adysplasia	hereditary_disease	other	hereditary_disease	renal_medicine|genetics_and_genomics|pediatric	renal_adysplasia|metabolic_disorder	lower_gastrointestinal_disorder|kidney_disorder	false	false	false	false	high
MONDO:0011248	distal monosomy 13q	chromosomal_disorder|syndromic_disease	other	syndromic_disease|chromosomal_disorder	genetics_and_genomics|oncology|pediatric	neurodegenerative_disease|metabolic_disorder|anemia	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0011249	torsion dystonia with onset in infancy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0011250	microcephaly, macrotia, and intellectual disability	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	intellectual_disability_does_fit_best_with_this_category_but_the_term_is_usually_used_to_describe_a_condition_of_significantly_sub_average_general_intellectual_functioning_accompanied_by_limitations_in_adaptive_behavior__so_for_the_purpose_of_this_task_it_is_not_a_best_fit_for_microcephaly_and_macrotia_as_they_are_conditions_which_can_be_considered_to_fall_under_brain_disorder_however__considering_the_additional_symptoms_associated_with_them_they_might_also_be_described_as_separate_disorders|brain_disorder	false	false	false	false	very_high
MONDO:0011251	facial dysmorphism, cleft palate, hearing loss, and camptodactyly	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics|otolaryngology	autoimmune_diseases|anemia|metabolic_disorder|inflammatory_disease	joint_disorder|ear_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0011252	spondyloepimetaphyseal dysplasia, Shohat type	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0011253	craniomicromelic syndrome	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0011254	brachydactyly, intraventricular septal defect, and deafness	hereditary_disease	other	hereditary_disease	cardiology|genetics_and_genomics|otolaryngology|pediatric	cardiovascular_disorder|hearing_loss|genetic_disorder	joint_disorder|heart_disorder|ear_disorder	false	false	false	false	medium
MONDO:0011255	mandibulofacial dysostosis-macroblepharon-macrostomia syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|genetic_disorder___note__the_correct_category_name_is__genetic_disorder__which_is_missing_from_the_original_list	facial_disorder|bone_disorder|teeth_disorder	false	false	false	false	high
MONDO:0011256	emphysema, congenital, with deafness, penoscrotal web, and intellectual disability	hereditary_disease	other	hereditary_disease	pulmonology|genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|lung_disorder|brain_disorder|ear_disorder	false	false	false	false	high
MONDO:0011257	MPI-congenital disorder of glycosylation	hereditary_disease|metabolic_disease|cardiovascular_disorder|immune_system_disorder|syndromic_disease	metabolic_disease|cardiovascular_disorder	immune_system_disorder|hereditary_disease|syndromic_disease|cardiovascular_disorder|metabolic_disease	genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder	liver_disorder	false	false	true	false	high
MONDO:0011258	branchiootic syndrome 1	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|otolaryngology|pediatric	autoimmune_diseases|inflammatory_disease	vascular_disorder|throat_disorder|ear_disorder	false	false	false	false	medium
MONDO:0011259	retinitis pigmentosa 22	hereditary_disease|disorder_of_visual_system|metabolic_disease|psychiatric_disorder|nervous_system_disorder	metabolic_disease|psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|metabolic_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0011260	pancreatic lymphoma, familial	hematologic_disorder|cancer_or_benign_tumor|hereditary_disease|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	hematologic_disorder|hereditary_disease|digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	hematology|gastroenterology|genetics_and_genomics|oncology	inflammatory_disease|autoimmune_diseases|cancer	liver_disorder|immune_disorder|lymphatic_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0011261	spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|ophthalmology|pediatric	mental_health_disorder|inflammatory_disease|neurodegenerative_disease|metabolic_disorder	spinal_disorder|joint_disorder|eye_disorder|intellectual_disability_is_under_the_category_of_other|bone_disorder|teeth_disorder	false	false	false	false	high
MONDO:0011262	camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	neurology|orthopaedic|ophthalmology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011263	skeletal dysplasia and progressive central nervous system degeneration, lethal	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|skeletal_dysplasias	spinal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0011264	torsion dystonia 6	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|psychiatry|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0011265	tooth agenesis, selective, 2	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|mouth_disorder	orthopaedic|genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|congenital_disease____corrected_answer___metabolic_disorder|congenital_disease	teeth_disorder	false	false	false	true	low
MONDO:0011266	myotonic dystrophy type 2	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011267	intellectual disability, severe, with spasticity and pigmentary tapetoretinal degeneration	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0011268	renal tubular acidosis, distal, 3, with or without sensorineural hearing loss	urinary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|urinary_system_disorder|metabolic_disease	renal_medicine|nephrology|genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder|renal_disease	kidney_disorder|ear_disorder	false	false	false	true	high
MONDO:0011269	psoriasis 2	hereditary_disease|immune_system_disorder|inflammatory_disease|integumentary_system_disorder	other	inflammatory_disease|integumentary_system_disorder|immune_system_disorder|hereditary_disease	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0011270	prostate cancer, hereditary, 8	cancer_or_benign_tumor|hereditary_disease|reproductive_system_disorder	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology|genetics_and_genomics	hereditary_disease_is_part_of_the_broader_category_of|cancer	hereditary|reproductive_system_disorder	false	true	false	true	high
MONDO:0011271	rigid spine muscular dystrophy 1	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder|muscular_dystrophy	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011272	retinitis pigmentosa 25	hereditary_disease|metabolic_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|metabolic_disease	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region|metabolic_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	eye_disorder	false	false	false	false	high
MONDO:0011273	H syndrome	hereditary_disease|respiratory_system_disorder|immune_system_disorder|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|immune_system_disorder|respiratory_system_disorder	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0011274	Muenke syndrome	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	hearing_loss_disorder|skeletal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0011275	acromesomelic dysplasia 1, Maroteaux type	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0011276	orofacial cleft 2	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	otolaryngology|pediatric	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|teeth_disorder	false	false	false	true	high
MONDO:0011279	autosomal recessive nonsyndromic hearing loss 17	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|auditory_system_disorder|psychiatric_disorder	otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0011281	congenital myasthenic syndrome 5	hereditary_disease|syndromic_disease|nervous_system_disorder	other	nervous_system_disorder|syndromic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0011282	tumor suppressor gene on chromosome 11	hereditary_disease	other	hereditary_disease	oncology|genetics_and_genomics	tumor_suppressor_gene_on_chromosome_11_also_implies_cancer|cancer	genetic_disorder|immune_disorder|hereditary_disorder|cancer_disorder	false	false	false	true	high
MONDO:0011283	mitochondrial DNA depletion syndrome 1	hereditary_disease|metabolic_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|mitochondrial_disease	metabolic_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease|syndromic_disease|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mitochondrial_disorders_is_not_in_the_list_but_closest_match_would_be_metabolic_disorder_since_it_s_about_mitochondria|metabolic_disorder	mitochondrial_disease|muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0011284	astigmatism	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	eye_disorder	false	false	false	true	low
MONDO:0011285	age related macular degeneration 1	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0011286	autosomal recessive nonsyndromic hearing loss 13	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease|auditory_system_disorder	otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0011287	craniosynostosis-anal anomalies-porokeratosis syndrome	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	pediatric|dermatology|genetics_and_genomics	metabolic_disorder	skin_disorder|bone_disorder|craniofacial_disorder	false	false	false	false	high
MONDO:0011288	spastic paraplegia, optic atrophy, microcephaly, and 10Y sex reversal	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder|brain_disorder|spinal_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0011289	apraxia of eyelid opening	hereditary_disease	other	hereditary_disease	neurology|otolaryngology|pediatric|ophthalmology|psychiatry	neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0011290	dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and intellectual disability	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|orthopaedic	mental_health_disorder|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|brain_disorder|spinal_disorder|joint_disorder|bone_disorder|ear_disorder	false	false	false	false	high
MONDO:0011291	ALG6-congenital disorder of glycosylation 1C	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder|brain_disorder|joint_disorder|kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0011294	schizophrenia 5	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|mental_health_disorder	false	false	false	true	very_high
MONDO:0011295	schizophrenia 7	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0011296	Meckel syndrome, type 2	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|obstetrics_and_gynecology	genetic_disorder|metabolic_disorder	spinal_disorder|upper_gastrointestinal_disorder|kidney_disorder	false	false	false	false	high
MONDO:0011297	autosomal dominant nocturnal frontal lobe epilepsy 2	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease|cardiovascular_disorder	lower_gastrointestinal_disorder|brain_disorder|spinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0011298	schizophrenia 8	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	psychiatric_disorder|brain_disorder|mental_disorder	false	false	false	false	high
MONDO:0011299	Huntington disease-like 1	hereditary_disease|infectious_disease|nervous_system_disorder	neurodegenerative_disease|infectious_disease	nervous_system_disorder|hereditary_disease|infectious_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0011300	myopia 3, autosomal dominant	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|ophthalmology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	true	high
MONDO:0011301	pseudohypoparathyroidism type 1B	hereditary_disease|metabolic_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|urinary_system_disorder	endocrine_system_disorder|metabolic_disease	urinary_system_disorder|endocrine_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|calcium_regulation_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011303	focal segmental glomerulosclerosis 1	hereditary_disease|syndromic_disease|urinary_system_disorder	other	syndromic_disease|urinary_system_disorder|idiopathic_disease|hereditary_disease	nephrology|hematology|renal_medicine	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|immune_disorder|kidney_disorder	false	false	false	false	high
MONDO:0011304	cerebral cavernous malformation 2	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	oncology|genetics_and_genomics|neurology	neurological_disease|cancer	vascular_disorder|brain_disorder	false	false	false	false	medium
MONDO:0011305	cerebral cavernous malformation 3	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	oncology|genetics_and_genomics|neurology	neurological_disease|cancer	vascular_disorder|brain_disorder	false	false	false	false	medium
MONDO:0011306	muscular dystrophy, congenital, with cerebellar atrophy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder|congenital_diseases	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011307	schizophrenia 2	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	mental_health_disorder|brain_disorder	false	false	false	false	high
MONDO:0011308	GRACILE syndrome	hereditary_disease|mitochondrial_disease	other	mitochondrial_disease|hereditary_disease	genetics_and_genomics|pediatric|hematology|neurology	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|muscle_disorder|blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0011309	familial gestational hyperthyroidism	hereditary_disease|obstetric_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|obstetric_disorder|hereditary_disease	genetics_and_genomics|endocrinology|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0011310	long chain fatty acids, defect in transport of	hereditary_disease	other	hereditary_disease	genetics_and_genomics|metabolism|pediatric	metabolic_disorder|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0011312	thyroid carcinoma, nonmedullary, with or without cell oxyphilia	hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|hereditary_disease	oncology|endocrinology	autoimmune_diseases|cancer	endocrine_disorder	false	true	false	true	high
MONDO:0011313	megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011315	Osebold skeletal dysplasia/osteolysis syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|orthopaedic	osteogenesis_imperfecta_like_syndrome|metabolic_disorder|genetic_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011316	osteosclerotic chondrodysplasia, lethal, with intracellular inclusions	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|orthopaedic	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0011317	microcephaly, severe, with skeletal anomalies including posterior rib-Gap defects	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|skeletal_anomalies	bone_disorder|skeletal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011318	Tonoki syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	liver_disorder|vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0011320	radioulnar synostosis-microcephaly-scoliosis syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0011321	expansile bone lesions	hereditary_disease	other	hereditary_disease	oncology|orthopaedic|neurology	cancer|metabolic_disorder|inflammatory_disease	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0011322	Oroacral syndrome, Verloes-Koulischer type	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology|pediatric	autoimmune_diseases|metabolic_disorder	teeth_disorder|oral_disorder|immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0011323	arhinia, choanal atresia, and microphthalmia	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|ophthalmology|otolaryngology	cardiovascular_disorder|neurodegenerative_disease	nose_disorder|throat_disorder|eye_disorder	false	false	false	false	high
MONDO:0011325	Fanconi anemia complementation group F	musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|immune_system_disorder|hematologic_disorder|hereditary_disease	anemia|metabolic_disease	immune_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hematologic_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|hematology	autoimmune_diseases|metabolic_disorder|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0011326	citrullinemia, type II, adult-onset	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|hepatology|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0011327	neuronal intranuclear inclusion disease	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0011330	spinocerebellar ataxia type 10	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011331	congenital chylothorax	respiratory_system_disorder	other	respiratory_system_disorder	genetics_and_genomics|cardiothoracic|pediatric	metabolic_disorder|inflammatory_disease|congenital_abnormality	congenital_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0011332	Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology	anemia	blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0011334	limb-mammary syndrome	syndromic_disease|integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|orthopaedic	cancer|metabolic_disorder|anemia	other____revised_to__limb_disorder|reproductive_system_disorder|reproductive_system_disorder|bone_disorder|limb_disorder	false	false	false	false	medium
MONDO:0011335	spondyloepimetaphyseal dysplasia with multiple dislocations	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|rheumatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0011336	familial hemophagocytic lymphohistiocytosis 4	syndromic_disease|immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|hematology	metabolic_disorder|inflammatory_disease|anemia	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0011337	familial hemophagocytic lymphohistiocytosis 2	syndromic_disease|immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|hematology|immunology	metabolic_disorder|inflammatory_disease|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0011338	Omenn syndrome	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|allergy_and_immunology|hematology|immunology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0011339	hereditary spastic paraplegia 8	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011340	congenital tracheal stenosis	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	pediatric|otolaryngology	birth_defect|respiratory_disease|congenital_abnormality	lung_disorder|throat_disorder	false	false	false	false	high
MONDO:0011341	microcephaly, facial abnormalities, micromelia, and intellectual disability	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	brain_disorder|facial_abnormalities|micromelia|intellectual_disability|microcephaly	false	false	false	false	very_high
MONDO:0011342	SLC35A1-congenital disorder of glycosylation	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	genetic_disorder|congenital_disorder_of_glycosylation|metabolic_disorder|neurodegenerative_disease	ear_disorder|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0011343	follicular atrophoderma, perioral pigmented, with milia and epidermoid cysts	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|dermatology	cancer|autoimmune_diseases|inflammatory_disease	skin_disorder	false	false	false	false	low
MONDO:0011344	parotitis, juvenile recurrent	hereditary_disease	other	hereditary_disease	pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease	teeth_disorder|oral_disorder	true	false	false	true	medium
MONDO:0011345	facial dysmorphism, selective tooth agenesis, and choroid calcification	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	teeth_disorder|eye_disorder	false	false	false	false	medium
MONDO:0011346	xanthinuria type II	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|renal_medicine	kidney_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0011347	craniosynostosis with ectopia lentis	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|ophthalmology|neurology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	craniofacial_disorder|bone_disorder|eye_disorder	false	false	false	false	high
MONDO:0011348	non-syndromic polydactyly	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|genetic_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0011349	osteoma of cranial vault, familial	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|orthopaedic|neurology	familial_diseases|metabolic_disorder|inflammatory_disease	bone_disorder|cranial_bone_disorder	false	false	false	false	medium
MONDO:0011350	autosomal dominant nonsyndromic hearing loss 17	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	genetics_and_genomics|pediatric|genetic|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder|hearing_loss	false	false	false	true	high
MONDO:0011351	autosomal recessive nonsyndromic hearing loss 21	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	genetics_and_genomics|pediatric|otolaryngology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	ear_disorder|bone_disorder	false	false	false	true	medium
MONDO:0011352	neuroendocrine carcinoma of salivary glands, sensorineural hearing loss, and enamel hypoplasia	hereditary_disease	other	hereditary_disease	oncology|neurology|otolaryngology	cancer|neurodegenerative_disease	ear_disorder|teeth_disorder|throat_disorder	false	true	false	false	very_high
MONDO:0011353	atrial septal defect, secundum, with various cardiac and Noncardiac defects	hereditary_disease	other	hereditary_disease	pediatric|cardiology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0011354	situs inversus totalis with cystic dysplasia of kidneys and pancreas	syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|renal_medicine|urology	metabolic_disorder|genetic_condition	kidney_disorder|upper_gastrointestinal_disorder|pancreas_disorder	false	false	false	false	medium
MONDO:0011355	cone-rod dystrophy 7	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder	genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0011356	exostosis, Dupuytren subungual	hereditary_disease	other	hereditary_disease	dermatology|orthopaedic	cancer|autoimmune_diseases|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0011357	eccrine syringofibroadenomatosis with eyelid abnormalities	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0011358	blue nevi, familial multiple	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	cancer|autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	blood_bone_marrow_disorder|skin_disorder	false	false	false	true	low
MONDO:0011359	acromelic frontonasal dysostosis	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|endocrinology	metabolic_disorder|neurodegenerative_disease	nose_disorder|endocrine_disorder|joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0011360	autosomal recessive nonsyndromic hearing loss 14	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	genetics_and_genomics|pediatric|otolaryngology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	ear_disorder	false	false	false	false	medium
MONDO:0011361	prostate cancer/brain cancer susceptibility	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	genetics_and_genomics|urology|oncology	cancer|neurodegenerative_disease	brain_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0011362	myopathy, myofibrillar, 9, with early respiratory failure	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	pulmonology|neurology	autoimmune_diseases|metabolic_disorder|myopathy|inflammatory_disease|neurodegenerative_disease	muscle_disorder|lung_disorder	false	false	false	false	high
MONDO:0011363	diabetes mellitus, noninsulin-dependent, 3	endocrine_system_disorder|digestive_system_disorder|metabolic_disease|hereditary_disease	endocrine_system_disorder|diabetes_mellitus|metabolic_disease	digestive_system_disorder|endocrine_system_disorder|metabolic_disease|hereditary_disease	endocrinology	cardiovascular_disorder|autoimmune_diseases|metabolic_disorder|inflammatory_disease	kidney_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0011364	autosomal recessive nonsyndromic hearing loss 16	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	genetics_and_genomics|pediatric|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder|bone_disorder	false	false	false	true	medium
MONDO:0011365	blepharophimosis - intellectual disability syndrome, SBBYS type	endocrine_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology|psychiatry	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0011366	ovarian germ cell tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	oncology|obstetrics_and_gynecology	ovarian_tumor_is_a_type_of_cancer_of_the_reproductive_system_which_contains_germ_cells_therefore_it_fits_into_this_category_as_well|cancer|adrenal_gland_disease	reproductive_system_disorder|ovary_disorder	false	true	false	true	high
MONDO:0011367	Acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|skeletal_dysplasia	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0011368	papillary thyroid Microcarcinoma	endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|hereditary_disease	endocrinology|general_surgery|oncology	thyroid_cancer|cancer	thyroid_disorder|endocrine_disorder|thyroid_disorder____corrected_list_to_reflect_accurate_categorization____endocrine_disorder	false	true	false	true	low
MONDO:0011369	hypercholesterolemia, autosomal dominant, 3	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|hepatology|endocrinology|cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|endocrine_disorder|liver_disorder	false	false	false	true	high
MONDO:0011370	Stargardt disease 4	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region|nervous_system_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0011371	hydroa vacciniforme, familial	integumentary_system_disorder|inflammatory_disease|hereditary_disease	other	hereditary_disease|inflammatory_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0011372	microcephaly with simplified gyral pattern	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	true	false	false	false	high
MONDO:0011374	hypercholesterolemia, familial, 4	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|endocrinology|cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|endocrine_disorder|liver_disorder	false	false	false	true	high
MONDO:0011375	brittle bone disorder	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|rheumatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	bone_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0011376	ventricular fibrillation, paroxysmal familial, type 1	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	genetics_and_genomics|hematology|cardiology	cardiovascular_disorder|genetic_disorders|familial	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0011377	long QT syndrome 3	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0011381	dominant beta-thalassemia	hematologic_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder|anemia	endocrine_system_disorder|hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0011382	sickle cell disease	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	joint_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0011383	autoimmune lymphoproliferative syndrome type 2A	syndromic_disease|hereditary_disease|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor|autoimmune_disease	cancer_or_benign_tumor|immune_system_disorder|hereditary_disease|syndromic_disease	hematology|allergy_and_immunology|immunology|rheumatology	autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0011385	intervertebral disk degenerative disorder	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	neurology|orthopaedic|rheumatology	neurodegenerative_disease|inflammatory_disease	joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011389	autosomal dominant nonsyndromic hearing loss 16	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	otolaryngology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder|hearing_loss	false	false	false	true	medium
MONDO:0011390	focal segmental glomerulosclerosis 2	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	hematology|renal_medicine|nephrology	renal_disease|autoimmune_diseases	kidney_disorder|urinary_tract_disorder|immune_disorder	false	false	false	false	high
MONDO:0011391	megalencephalic leukoencephalopathy with subcortical cysts	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011392	autosomal recessive nonsyndromic hearing loss 20	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0011393	hypoalphalipoproteinemia, primary, 1	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|endocrinology|pediatrics|genetics_and_genomics	genetic_disorder|metabolic_disorder	biliary_disorder|endocrine_disorder|liver_disorder	false	false	false	false	medium
MONDO:0011395	cone-rod dystrophy 3	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0011396	loricrin keratoderma	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	skin_disorder	false	false	false	true	high
MONDO:0011397	autosomal dominant cerebellar ataxia, deafness and narcolepsy	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|sleep_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant	brain_disorder_ear_disorder_spinal_disorder	false	false	false	false	high
MONDO:0011398	dystrophic epidermolysis bullosa pruriginosa	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	skin_disease_is_not_in_the_list_so|autoimmune_diseases|inflammatory_disease	skin_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011399	alpha thalassemia spectrum	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	pediatric|hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0011400	dilated cardiomyopathy 1G	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011401	Alzheimer disease without neurofibrillary tangles	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	neurological_disorder|brain_disorder	false	false	false	false	high
MONDO:0011402	congenital cataracts-facial dysmorphism-neuropathy syndrome	chromosomal_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|disorder_of_development_or_morphogenesis|chromosomal_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0011403	left ventricular noncompaction 1	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiothoracic|cardiology|pediatrics|pulmonology|renal_medicine	cardiovascular_disorder|inflammatory_disease	vascular_disorder|heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011404	Caronte	hereditary_disease	other	hereditary_disease	cardiothoracic|cardiology|pulmonology	neurodegenerative_disease|metabolic_disorder	vaccine_related|liver_disorder	false	false	false	false	none
MONDO:0011405	poikiloderma with neutropenia	hematologic_disorder|immune_system_disorder|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|immune_system_disorder|hematologic_disorder	immunology|hematology|dermatology	autoimmune_diseases|anemia|neutropenia|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|skin_disorder	true	false	false	false	high
MONDO:0011406	cholesteatoma, congenital	hereditary_disease	other	hereditary_disease	otolaryngology|pediatric	congenital_disease|inflammatory_disease	teeth_disorder|congenital_disorder|ear_disorder	false	false	false	false	medium
MONDO:0011407	facial paresis, hereditary congenital, 2	musculoskeletal_system_disorder|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|hereditary_congenital_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011408	hereditary spastic paraplegia 10	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011410	Hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly	hereditary_disease	other	hereditary_disease	genetics_and_genomics|cardiology|pediatric	metabolic_disorder|cardiovascular_disorder	upper_gastrointestinal_disorder|heart_disorder|joint_disorder	false	false	false	hirschsprung_disease__particularly_when_associated_with_other_congenital_anomalies_such_as_heart_defects_and_laryngeal_anomalies__is_a_complex_condition_often_requiring_multidisciplinary_management__however__the_primary_effective_treatment_for_hirschsprung_disease_is_surgical_intervention_to_remove_the_affected_portion_of_the_bowel__this_can_alleviate_the_symptoms_associated_with_the_disease__such_as_severe_constipation_or_obstruction___while_there_are_no_treatments_that_can__cure__the_underlying_genetic_causes_of_the_syndrome__the_surgical_approach_can_effectively_manage_the_gastrointestinal_symptoms_and_improve_quality_of_life__therefore__because_there_are_efficacious_treatments_for_hirschsprung_disease__i_would_return_true	high
MONDO:0011411	Chudley-McCullough syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	lymphatic_disorder|immune_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0011412	familial encephalopathy with neuroserpin inclusion bodies	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011413	cataract 9 multiple types	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0011414	Peters anomaly	hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0011415	Leber congenital amaurosis 3	hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder|disorder_of_visual_system	genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0011416	generalized epilepsy with febrile seizures plus, type 1	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder	false	false	false	false	high
MONDO:0011417	hemochromatosis type 3	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	medium
MONDO:0011419	camera-Marugo-Cohen syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	joint_disorder|eye_disorder|bone_disorder	false	false	false	false	medium
MONDO:0011420	short stature due to partial GHR deficiency	syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|syndromic_disease	endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|adrenal_gland_disease	growth_disorder|bone_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0011421	mitochondrial complex V (ATP synthase) deficiency, nuclear type 1	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011422	autosomal recessive proximal renal tubular acidosis	hereditary_disease|metabolic_disease|urinary_system_disorder	metabolic_disease	urinary_system_disorder|metabolic_disease|hereditary_disease	renal_medicine|genetics_and_genomics|pediatric	metabolic_disorder|anemia	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0011423	autosomal recessive limb-girdle muscular dystrophy type 2E	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011424	Carney triad	syndromic_disease|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|syndromic_disease|cancer_or_benign_tumor	endocrinology|oncology|genetics_and_genomics|dermatology|pediatric	adrenal_gland_disease|cancer|neuroendocrine_tumors	endocrine_disorder|heart_disorder|bone_disorder	false	false	false	false	high
MONDO:0011425	dilated cardiomyopathy 1H	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011426	aceruloplasminemia	hereditary_disease|psychiatric_disorder|metabolic_disease|nervous_system_disorder|disorder_of_visual_system|hematologic_disorder	psychiatric_disorder|anemia|metabolic_disease|neurodegenerative_disease	psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder|metabolic_disease|hematologic_disorder|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|hematology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0011428	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|disorder_of_visual_system|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease	genetics_and_genomics|dermatology|pediatric	neurodegenerative_disease|genetic_disorder|developmental_disorder	skin_disorder|joint_disorder|teeth_disorder	false	false	false	false	high
MONDO:0011429	juvenile idiopathic arthritis	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	other	inflammatory_disease|idiopathic_disease|connective_tissue_disorder|musculoskeletal_system_disorder	rheumatology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|joint_disorder|bone_disorder	false	false	false	true	high
MONDO:0011430	pulverulent cataract	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0011431	MASS syndrome	hereditary_disease|immune_system_disorder|connective_tissue_disorder	autoimmune_disease	connective_tissue_disorder|immune_system_disorder|hereditary_disease	neurology|psychiatry	metabolic_disorder|neurodegenerative_disease	spinal_disorder|joint_disorder|muscle_disorder|bone_disorder	false	false	false	true	medium
MONDO:0011432	blepharophimosis - intellectual disability syndrome, Verloes type	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0011433	anemia, congenital hypoplastic, with multiple congenital anomalies/intellectual disability syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|hematology	congenital_anomaly|metabolic_disorder|anemia	congenital_abnormality|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0011435	microcephaly 2, primary, autosomal recessive, with or without cortical malformations	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	autosomal_recessive_disorders|metabolic_disorder|neurodegenerative_disease	kidney_disorder|cortical_malformation_is_not_in_the_list__but_as_it_s_related_to_brain__we_can_consider_this|brain_disorder	false	false	false	false	high
MONDO:0011436	autosomal recessive distal spinal muscular atrophy 1	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0011437	microcephaly 4, primary, autosomal recessive	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	autosomal_recessive_diseases_is_not_in_the_list__but_closest_match___neurodegenerative_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011438	acne	hereditary_disease|integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder|hereditary_disease	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	nose_disorder|skin_disorder	false	false	false	true	medium
MONDO:0011439	spinocerebellar ataxia type 12	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	cardiovascular_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0011441	complex regional pain syndrome type 1	nervous_system_disorder|syndromic_disease	other	syndromic_disease|nervous_system_disorder	rheumatology|neurology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011442	advanced sleep phase syndrome 1	hereditary_disease	other	sleep_disorder|hereditary_disease	endocrinology|neurology	mental_health_disorder|neurodegenerative_disease	endocrine_disorder|brain_disorder	false	false	false	false	medium
MONDO:0011443	febrile seizures, familial, 4	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0011444	Duane retraction syndrome 2	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|syndromic_disease	other	disorder_of_visual_system|syndromic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0011445	hereditary spastic paraplegia 11	hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011446	myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0011448	PPARG-related familial partial lipodystrophy	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	endocrinology|genetics_and_genomics|dermatology	lipid_storage_disorders|metabolic_disorder	endocrine_disorder|skin_disorder	false	false	false	true	medium
MONDO:0011449	Salla disease	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	oncology|genetics_and_genomics|pediatric|hematology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0011450	breast-ovarian cancer, familial, susceptibility to, 1	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	obstetrics_and_gynecology|oncology|genetics_and_genomics	familial|cancer	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0011451	cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|cardiovascular_disorder|hereditary_disease	metabolic_disease|cardiovascular_disorder	metabolic_disease|mitochondrial_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	cardiology|pediatric|neurology|pulmonology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0011452	hypotrichosis 7	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	hair_disorder|skin_disorder	false	false	false	true	medium
MONDO:0011453	ulnar ray dysgenesis with postaxial polydactyly and renal cystic dysplasia	hereditary_disease	other	hereditary_disease	pediatric|urology|genetics_and_genomics	genetic_disorder|renal_disease|metabolic_disorder	kidney_disorder|bone_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0011454	patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|cardiovascular_disorder|syndromic_disease|hereditary_disease	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	cardiothoracic|pediatric|genetics_and_genomics	congenital_heart_disease|hand_anomaly_syndrome|cardiovascular_disorder	vascular_disorder|joint_disorder|heart_disorder	false	false	false	false	high
MONDO:0011455	lissencephaly, familial, with cleft palate and cerebellar hypoplasia	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	cerebral_hypoplasia|familial|neurodegenerative_disease	cerebellar_hypoplasia_suggests_brain_disorder_is_the_best_fit__so__brain_disorder|brain_disorder|spinal_disorder	true	false	false	false	very_high
MONDO:0011456	nephronophthisis 3	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	renal_medicine|urology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0011457	ataxia-telangiectasia-like disorder	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	immune_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011458	Leber congenital amaurosis 4	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region|hereditary_disease	ophthalmology|pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0011459	arrhythmogenic right ventricular dysplasia 5	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiology|cardiothoracic	cardiovascular_disorder|arrhythmogenic_right_ventricular_dysplasia	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0011460	arrhythmogenic right ventricular dysplasia 6	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|cardiology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0011461	generalized epilepsy with febrile seizures plus, type 2	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	epilepsy|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0011462	pyogenic arthritis-pyoderma gangrenosum-acne syndrome	connective_tissue_disorder|immune_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|immune_system_disorder|hereditary_disease|connective_tissue_disorder	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|joint_disorder	true	false	false	false	high
MONDO:0011463	polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0011464	spinocerebellar ataxia type 11	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011465	infundibulocystic basal cell carcinoma	integumentary_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|hereditary_disease	dermatology|oncology	cancer|basal_cell_carcinoma	skin_disorder	false	true	false	true	low
MONDO:0011466	distal myopathy, Welander type	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0011468	hereditary motor and sensory neuropathy, Okinawa type	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011470	hyperlipidemia, combined, 2	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|hematology|renal_medicine|hepatology|cardiology	cardiovascular_disorder|metabolic_disorder	endocrine_disorder|vascular_disorder|liver_disorder|heart_disorder	false	false	false	true	high
MONDO:0011471	inflammatory bowel disease 3	digestive_system_disorder|immune_system_disorder|hereditary_disease	other	immune_system_disorder|digestive_system_disorder|hereditary_disease	rheumatology|gastroenterology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0011472	epidermolysis bullosa simplex due to plakophilin deficiency	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	high
MONDO:0011473	Leber congenital amaurosis 5	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0011474	progressive familial heart block type IB	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	pediatric|genetics_and_genomics|cardiology	neurodegenerative_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0011475	Charcot-Marie-Tooth disease type 4B2	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0011476	MHC class I deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	hematology|allergy_and_immunology|rheumatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0011477	tooth agenesis, selective, 3	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|mouth_disorder	pediatric|oral_surgery_is_not_in_the_list_so_orthopaedic|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	teeth_disorder|odontogenic_disorder	false	false	false	true	medium
MONDO:0011478	growth and developintellectual disability, ocular ptosis, cardiac defect, and anal atresia	hereditary_disease	other	hereditary_disease	ophthalmology|cardiovascular|neurodevelopmental|pediatric|urology|genetics_and_genomics|cardiology	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	brain_disorder|upper_gastrointestinal_disorder|endocrine_disorder|eye_disorder|joint_disorder|heart_disorder	false	false	false	the_symptoms_you_ve_described_suggest_a_potential_genetic_syndrome__but_they_are_not_specific_enough_to_identify_a_single_condition__one_possibility_could_be_part_of_a_syndrome_such_as_pallister_hall_syndrome__among_others____to_answer_your_question__for_many_genetic_conditions_or_syndromes_that_involve_multiple_systems__like_intellectual_disability__ocular_ptosis__and_congenital_defects___specific_treatments_or_cures_may_not_exist__management_often_focuses_on_addressing_individual_symptoms_and_providing_supportive_care__including_therapies_and_interventions_tailored_to_each_patient_s_needs___in_general__as_of_my_last_training_data_in_october_2023__most_genetic_conditions_that_result_in_such_syndromic_presentations_do_not_have_a_cure_but_may_have_some_treatment_options_aimed_at_symptom_management___therefore__the_answer_is_false__there_are_no_existing_efficacious_treatments_that_cure__prevent__or_treat_such_a_multifaceted_disease_in_a_comprehensive_manner	high
MONDO:0011479	postural orthostatic tachycardia syndrome	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|hereditary_disease	pediatric|neurology|cardiology	neurodegenerative_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0011480	autosomal dominant nonsyndromic hearing loss 20	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	medium
MONDO:0011481	craniosynostosis 2	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|skeletal_disease|developmental_disorder	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0011482	dilated cardiomyopathy 1I	musculoskeletal_system_disorder|nervous_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	true	high
MONDO:0011483	polycystic bone disease	hereditary_disease	other	hereditary_disease	endocrinology|orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	true	medium
MONDO:0011484	catecholaminergic polymorphic ventricular tachycardia 1	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|cardiology	adrenal_gland_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0011485	autosomal recessive congenital ichthyosis 5	integumentary_system_disorder|disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|integumentary_system_disorder	pediatric|dermatology|genetics_and_genomics	metabolic_disorder|skin_condition	liver_disorder|skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0011486	congenital muscular dystrophy 1B	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0011487	Huntington disease-like 3	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0011488	microcephaly 3, primary, autosomal recessive	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|ear_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011489	hereditary spastic paraplegia 12	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011490	diffuse panbronchiolitis	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|liver_disorder	false	false	false	true	high
MONDO:0011492	mandibulofacial dysostosis syndrome, Bauru type	hereditary_disease	other	hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	teeth_disorder|bone_disorder	false	false	false	false	high
MONDO:0011493	Stickler syndrome type 2	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|disorder_of_visual_system|syndromic_disease	other	syndromic_disease|disorder_of_visual_system|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|rheumatology	neurodegenerative_disease|metabolic_disorder	eye_disorder|joint_disorder	false	false	false	false	high
MONDO:0011494	hyaluronan metabolism, defect 1N	hereditary_disease	other	hereditary_disease	metabolic|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	true	false	false	false	high
MONDO:0011496	mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|connective_tissue_disorder|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder	orthopaedic|genetics_and_genomics|rheumatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0011497	hereditary North American Indian childhood cirrhosis	endocrine_system_disorder|digestive_system_disorder|metabolic_disease|hereditary_disease|syndromic_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease|digestive_system_disorder	pediatrics|gastroenterology|genetics_and_genomics|hepatology	liver_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0011500	Becker nevus syndrome	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|hereditary_disease	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|dermatology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0011501	wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|adrenal_gland_disease|skeletal_dysplasia	skeletal_dysplasia|teeth_disorder|bone_disorder	false	false	false	false	high
MONDO:0011502	Wolfram syndrome 2	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|endocrinology	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|brain_disorder|eye_disorder	false	false	true	false	high
MONDO:0011503	cortisone reductase deficiency 1	metabolic_disease|hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder|metabolic_disease	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|adrenal_gland_disease|inflammatory_disease	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0011504	NDE1-related microhydranencephaly	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011505	familial hypobetalipoproteinemia 2	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology|pediatric	anemia|metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0011506	familial infantile myoclonic epilepsy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0011507	diabetes mellitus, congenital autoimmune	hereditary_disease	other	hereditary_disease	genetics_and_genomics|endocrinology|pediatric	congenital_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|immune_disorder	false	false	true	false	high
MONDO:0011508	lymphoma, non-Hodgkin, familial	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	genetics_and_genomics|hematology|oncology	cancer|autoimmune_diseases|familial	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0011509	low density lipoprotein cholesterol, mild elevation of	hereditary_disease	other	hereditary_disease	cardiology|cardiothoracic|endocrinology	metabolic_disorder|inflammatory_disease|cardiovascular_disorder	vascular_disorder|liver_disorder	false	false	false	true	low
MONDO:0011510	Bohring-Opitz syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|growth_disorder|developmental_disorder|metabolic_disorder|skeletal_disorder	false	false	false	false	very_high
MONDO:0011511	clavicular hypoplasia, zygomatic arch hypoplasia, and micrognathia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|pediatric|otolaryngology	congenital_disorder|neurodegenerative_disease|anatomic_abnormality	muscle_disorder|teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0011512	Brooke-Spiegler syndrome	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|pediatric|neurology|cardiomyopathy_is_associated_but_more_specific_to_the_category_of_genetics_is_better_fitting	metabolic_disorder|neurodegenerative_disease	muscle_disorder|skeletal_muscle_disorder	false	false	false	false	medium
MONDO:0011513	Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	familial_alzheimers|mental_health_disorder|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011514	tricuspid atresia	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiology|pediatric	congenital_heart_defect|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0011516	early response to neural induction gene	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	cancer|metabolic_disorder|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	neural_induction_gene|neural_induction_gene_is_related_to_the_brain__so___brain_disorder	false	false	false	false	high
MONDO:0011517	pseudohyperaldosteronism type 2	obstetric_disorder|hereditary_disease	other	obstetric_disorder|hereditary_disease	renal_medicine|endocrinology	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0011518	Wiedemann-Steiner syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|dermatology	autoimmune_diseases|neurodegenerative_disease	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0011519	autosomal dominant nonsyndromic hearing loss 23	hereditary_disease|nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	genetics_and_genomics|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	high
MONDO:0011521	inflammatory bowel disease 7	digestive_system_disorder|hereditary_disease|immune_system_disorder	other	hereditary_disease|digestive_system_disorder|immune_system_disorder	gastroenterology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0011522	hereditary spastic paraplegia 14	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011523	Bardet-Biedl syndrome 6	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|kidney_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011524	Dianzani autoimmune lymphoproliferative disease	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|hematology|oncology	cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0011525	Carney complex type 2	hereditary_disease	other	hereditary_disease	genetics_and_genomics|cardiology|endocrinology|pediatric|neurology|oncology|dermatology	cancer|metabolic_disorder|cardiovascular_disorder|neurodegenerative_disease	endocrine_disorder|skin_disorder|heart_disorder	false	false	false	true	medium
MONDO:0011527	Charcot-Marie-Tooth disease type 4E	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011528	hyper-IgM syndrome type 2	hematologic_disorder|hereditary_disease|immune_system_disorder	other	hematologic_disorder|hereditary_disease|immune_system_disorder	genetics_and_genomics|allergy_and_immunology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0011529	spinocerebellar ataxia type 13	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	autoimmune_diseases|cardiovascular_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0011530	mesomelic dysplasia, Savarirayan type	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	bone_deformity|genetic_disease|developmental_disorder|metabolic_disorder|skeletal_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0011531	Noonan syndrome 2	cardiovascular_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|immune_system_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder|immune_system_disorder	genetics_and_genomics|cardiology|pediatric|oncology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0011532	hereditary spastic paraplegia 13	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011533	temtamy preaxial brachydactyly syndrome	metabolic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	genetic_disorder|metabolic_disorder	joint_disorder|vascular_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0011534	Charcot-Marie-Tooth disease type 4G	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011535	split hand-foot malformation 4	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|congenital_disorder	joint_disorder|skin_disorder|bone_disorder	false	false	false	false	medium
MONDO:0011536	optic atrophy 4	disorder_of_visual_system|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|disorder_of_visual_system|hereditary_disease	ophthalmology|neurology	metabolic_disorder|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0011537	macrocephaly-autism syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|neurology	mental_health_disorder|neurodegenerative_disease	autism_suggests_other_but_primarily_brain_disorder|brain_disorder	false	false	false	false	high
MONDO:0011538	frontoocular syndrome	hereditary_disease	other	hereditary_disease	ophthalmology|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0011539	nemaline myopathy 5	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0011540	spinocerebellar ataxia type 14	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011541	dilated cardiomyopathy 1J	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	muscle_disorder|vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0011544	pheochromocytoma/paraganglioma syndrome 3	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|nervous_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|endocrine_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neuroendocrine_tumor	vascular_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0011545	autosomal dominant nocturnal frontal lobe epilepsy 3	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|nose_disorder|muscle_disorder|vascular_disorder|spinal_disorder|lung_disorder|immune_disorder|eye_disorder	false	false	false	true	high
MONDO:0011546	heterotaxy, visceral, 2, autosomal	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|visceral	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0011547	cataract 31 multiple types	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0011548	cerebral palsy, ataxic, autosomal recessive	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology|genetics_and_genomics	autosomal_recessive|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011549	hypotrichosis 1	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	hair_disorder|skin_disorder	false	false	false	true	medium
MONDO:0011550	fibromatosis, gingival, with hypertrichosis and intellectual disability	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology|dermatology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	skin_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0011551	TH-deficient dopa-responsive dystonia	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	genetics_and_genomics|neurology	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0011552	schizophrenia 10	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	nose_disorder|muscle_disorder|vascular_disorder|endocrine_disorder|spinal_disorder|immune_disorder|upper_gastrointestinal_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder|eye_disorder|ear_disorder|throat_disorder|brain_disorder	false	false	false	false	high
MONDO:0011553	autosomal recessive nonsyndromic hearing loss 26	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0011555	radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome	hematologic_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|hematologic_disorder|musculoskeletal_system_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|joint_disorder	false	false	false	false	high
MONDO:0011557	radiation sensitivity/chromosome instability syndrome, autosomal dominant	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|oncology	cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0011558	Usher syndrome type 2C	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|otolaryngology|pediatric|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0011559	benign recurrent intrahepatic cholestasis type 2	metabolic_disease|digestive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	hereditary_disease|endocrine_system_disorder|digestive_system_disorder|metabolic_disease	gastroenterology|hepatology	metabolic_disorder|inflammatory_disease	biliary_disorder|liver_disorder	false	false	false	false	medium
MONDO:0011561	Alzheimer disease 6	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatry|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	cognitive_disorder|memory_disorder|brain_disorder	false	false	false	false	high
MONDO:0011562	autosomal dominant Parkinson disease 4	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	autosomal_dominant_disorder_is_not_in_the_list_but_a_more_accurate_description_would_be_neurodegenerative_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0011563	fibromatosis, gingival, 2	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|mouth_disorder	rheumatology|orthopaedic|dermatology	cancer|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0011564	cone-rod dystrophy 8	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region	ophthalmology|neurology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0011565	metabolic syndrome X	metabolic_disease|nutritional_disorder|hereditary_disease|syndromic_disease	metabolic_disease	hereditary_disease|syndromic_disease|metabolic_disease|nutritional_disorder	cardiology|renal_medicine|endocrinology	metabolic_disorder|metabolic_syndrome_x_is_often_associated_with_other_conditions_such_as_cardiovascular_disorder	vascular_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0011566	abdominal obesity-metabolic syndrome quantitative trait locus 2	metabolic_disease|nutritional_disorder|hereditary_disease|syndromic_disease	metabolic_disease	hereditary_disease|syndromic_disease|metabolic_disease|nutritional_disorder	gastroenterology|endocrinology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	endocrine_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0011567	dilated cardiomyopathy 1K	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0011568	autosomal dominant nonsyndromic hearing loss 25	psychiatric_disorder|nervous_system_disorder|hereditary_disease|auditory_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	otolaryngology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|ear_disorder	false	false	false	true	medium
MONDO:0011569	Charcot-Marie-Tooth disease type 2B1	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	muscle_disorder|nerve_disorder	false	false	false	false	medium
MONDO:0011570	Charcot-Marie-Tooth disease type 2B2	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|nerve_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011571	deafness, autosomal dominant 39, with dentinogenesis imperfecta 1	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	otolaryngology|pediatric|dermatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	teeth_disorder|ear_disorder	false	false	false	false	high
MONDO:0011574	tetralogy of fallot syndrome, autosomal recessive	hereditary_disease	other	hereditary_disease	cardiology|pediatric|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0011575	cerebrooculonasal syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|eye_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011576	familial hyperaldosteronism type II	cancer_or_benign_tumor|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	cardiology|renal_medicine|endocrinology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0011577	myopathy, proximal, and ophthalmoplegia	musculoskeletal_system_disorder|inflammatory_disease|hereditary_disease	other	hereditary_disease|inflammatory_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0011578	familial papillary thyroid carcinoma with renal papillary neoplasia	cancer_or_benign_tumor|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	urology|endocrinology|oncology|genetics_and_genomics	familial_cancer_syndrome|cancer	endocrine_disorder_kidney_disorder	false	true	false	true	medium
MONDO:0011579	late-onset retinal degeneration	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0011580	cerebellar ataxia and hypergonadotropic hypogonadism	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|nervous_system_disorder	neurodegenerative_disease|endocrine_system_disorder	hereditary_disease|nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder	genetics_and_genomics|neurology|endocrinology	neurodegenerative_disease|metabolic_disorder	brain_disorder|endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0011581	arrhythmogenic cardiomyopathy with wooly hair and keratoderma	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	cardiology|genetics_and_genomics|dermatology	cardiovascular_disorder|metabolic_disorder	skin_disorder|muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0011582	multiple mitochondrial dysfunctions syndrome 1	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	metabolic_disease	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	pediatrics|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	muscle_disorder|mitochondrial_dysfunction_is_not_in_the_list_so_we_cannot_choose_that_one	false	false	false	true	very_high
MONDO:0011583	cerebral amyloid angiopathy, APP-related	metabolic_disease|hereditary_disease|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder|metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder|cardiovascular_disorder	genetics_and_genomics|neurology	autoimmune_diseases|cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0011584	Fanconi anemia complementation group D1	musculoskeletal_system_disorder|metabolic_disease|hematologic_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|immune_system_disorder	anemia|metabolic_disease	hereditary_disease|metabolic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|immune_system_disorder|hematologic_disorder	hematology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0011585	autosomal recessive distal spinal muscular atrophy 2	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011586	otosclerosis 2	hereditary_disease|otorhinolaryngologic_disease|auditory_system_disorder	other	hereditary_disease|otorhinolaryngologic_disease|auditory_system_disorder	otolaryngology|otosclerosis_is_a_disorder_of_the_ear__so_it_would_be_categorized_under_otolaryngology_which_is_the_branch_of_medicine_dealing_with_diseases_of_the_ears__nose_and_throat	autoimmune_diseases|inflammatory_disease	ear_disorder|spinal_disorder	false	false	false	true	high
MONDO:0011587	cataract 25	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0011588	platelet-type bleeding disorder 12	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology|pediatric|genetics_and_genomics	metabolic_disorder|anemia|bleeding_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0011589	microphthalmia with coloboma 2	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0011590	anisomastia	hereditary_disease	other	hereditary_disease	obstetrics_and_gynecology|endocrinology	anisomastia_is_a_congenital_condition_where_one_breast_is_smaller_than_the_other___metabolic_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|muscle_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0011591	cataract 26 multiple types	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0011592	exudative vitreoretinopathy 3	disorder_of_visual_system|hereditary_disease|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|cardiovascular_disorder|disorder_of_orbital_region	pediatric|ophthalmology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	vitreoretinopathy_is_a_type_of_eye_disorder_so_it_fits_into_the_eye_disorder_category_however_exudative_vitreoretinopathy_is_specific_to_the_vitreous_body_which_is_part_of_the_eye_so_it_best_fits_in_both_categories_but_since_multiple_entries_are_not_allowed_and__other__is_excluded__the_answer_would_be___eye_disorder|eye_disorder	false	false	false	false	high
MONDO:0011593	seizures, benign familial infantile, 2	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	true	low
MONDO:0011594	ovarian dysgenesis, hypergonadotropic, with short stature and recurrent metabolic acidosis	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|obstetrics_and_gynecology|endocrinology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0011595	nonsyndromic congenital nail disorder 7	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	genetic_disorder|metabolic_disorder	nail_disorder_is_not_in_the_list_so_i_will_leave_it_out|skin_disorder	false	false	false	false	medium
MONDO:0011599	birdshot chorioretinopathy	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|inflammatory_disease|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0011600	congenital myasthenic syndrome 4A	hereditary_disease|nervous_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0011601	neonatal intrahepatic cholestasis due to citrin deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|hepatology	metabolic_disorder	kidney_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	medium
MONDO:0011602	autosomal recessive nonsyndromic hearing loss 27	hereditary_disease|nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0011603	GNE myopathy	hereditary_disease|metabolic_disease|inflammatory_disease|musculoskeletal_system_disorder|hematologic_disorder	metabolic_disease	inflammatory_disease|hematologic_disorder|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011604	spondylo-ocular syndrome	hereditary_disease|nervous_system_disorder|syndromic_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|connective_tissue_disorder	other	disorder_of_orbital_region|disorder_of_development_or_morphogenesis|connective_tissue_disorder|hereditary_disease|disorder_of_visual_system|syndromic_disease|musculoskeletal_system_disorder|nervous_system_disorder	ophthalmology|orthopaedic|rheumatology|neurology	inflammatory_disease|autoimmune_diseases	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011605	generalized basaloid follicular hamartoma syndrome	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|oncology	cancer|neuroendocrine_cancer	liver_disorder|gastrointestinal_disorder	false	false	false	false	medium
MONDO:0011606	baby rattle pelvis dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|obstetrics_and_gynecology	metabolic_disorder|autoimmune_diseases	bone_disorder|reproductive_system_disorder|joint_disorder	false	false	false	false	high
MONDO:0011610	dimethylglycine dehydrogenase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	metabolic_disorder____corrected_to__liver_disorder|liver_disorder|metabolic_disorder	false	false	false	false	low
MONDO:0011611	short stature, intellectual disability, callosal agenesis, Heminasal hypoplasia, microphthalmia, and atypical clefting	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|eye_disorder|brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0011612	glycine encephalopathy	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011613	autosomal recessive early-onset Parkinson disease 6	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	adrenal_gland_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0011614	3-hydroxy-3-methylglutaryl-CoA synthase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	metabolic_disorders|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|liver_disorder	false	false	false	true	high
MONDO:0011615	East Texas bleeding disorder	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|pediatric|hematology	metabolic_disorder|adrenal_gland_disease|anemia	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0011616	holoprosencephaly 6	nervous_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011617	arthropathy, erosive	hereditary_disease	other	hereditary_disease	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0011618	liver fibrocystic disease and polydactyly	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hepatology|gastroenterology	metabolic_disorder|genetic_disorder	liver_disorder|polydactyly_is_often_associated_with_liver_disorder__but_more_specifically__joint_disorder	false	false	false	false	medium
MONDO:0011619	crumpled helices and small mouth	hereditary_disease	other	hereditary_disease	cardiology|otolaryngology|pulmonology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	none
MONDO:0011620	metaphyseal dysplasia, Braun-Tinschert type	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011621	acropectoral syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	skeletal_disorder|musculoskeletal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0011624	transaldolase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	metabolic_disorders|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0011625	autosomal dominant nonsyndromic hearing loss 18	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	ear_disorder|bone_disorder	false	false	false	true	medium
MONDO:0011626	acromegaloid features, overgrowth, cleft palate, and hernia	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|anemia	bone_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0011628	propionic acidemia	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	metabolism|genetics_and_genomics|pediatrics	metabolic_disorder|adrenal_gland_disease	liver_disorder|metabolic_disorder_is_implied_but_category_list_did_not_provide_it_however_kidney_disorder_is_often_involved_in_propionic_acidemia	false	false	false	true	very_high
MONDO:0011629	MOGS-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|congenital_disorder_of_glycosylation_is_related_to_the_list_but_not_a_category_name_so_will_be_excluded_from_output	liver_disorder|bone_disorder	false	false	false	false	high
MONDO:0011630	retinitis pigmentosa 28	metabolic_disease|disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease	disorder_of_orbital_region|psychiatric_disorder|metabolic_disease|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	ophthalmology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0011631	hemochromatosis type 4	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	hematology|hepatology	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0011632	amyotrophic lateral sclerosis type 21	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011633	Charcot-Marie-Tooth disease axonal type 2C	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011634	rippling muscle disease	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0011635	goiter, multinodular 3	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	endocrinology|thyroidology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	thyroid_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0011636	Diamond-Blackfan anemia 2	syndromic_disease|hematologic_disorder|hereditary_disease	anemia	syndromic_disease|hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|lung_disorder	false	false	false	true	high
MONDO:0011637	Sener syndrome	hereditary_disease	other	hereditary_disease	allergy_and_immunology|neurology|otolaryngology	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	liver_disorder|blood_bone_marrow_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0011638	neuroferritinopathy	metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease|neurodegenerative_disease	psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	hematology|neurology|genetics_and_genomics	anemia|metabolic_disorder|neurodegenerative_disease	joint_disorder|blood_bone_marrow_disorder|iron_disorder_is_implied_but_the_closest_available_category_is__blood_bone_marrow_disorder|brain_disorder	false	false	false	true	high
MONDO:0011639	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics|pediatric	anemia|metabolic_disorder	blood_bone_marrow_disorder|teeth_disorder|bone_disorder	false	false	false	false	high
MONDO:0011640	genitopatellar syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	urology|pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|autoimmune_diseases	joint_disorder|reproductive_system_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0011641	baculum, congenital absence of	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	congenital_abnormality|metabolic_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	none
MONDO:0011642	carnitine acetyltransferase deficiency	hereditary_disease	other	hereditary_disease	hepatology|neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder	false	false	false	true	high
MONDO:0011644	pars planitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	ophthalmology|rheumatology|pulmonology|neurology	inflammatory_disease|autoimmune_diseases	liver_disorder|eye_disorder	false	false	false	true	medium
MONDO:0011646	laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy	hereditary_disease	other	hereditary_disease	neurology|otolaryngology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder|throat_disorder	false	false	false	false	very_high
MONDO:0011647	Alzheimer disease 7	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatry|neurology	inflammatory_disease|allergy|mental_health_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder	false	false	false	false	very_high
MONDO:0011648	radiation-induced meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0011651	intellectual disability, short stature, facial anomalies, and joint dislocations	hereditary_disease	other	hereditary_disease	endocrinology|genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	endocrine_disorder|joint_disorder|bone_disorder	true	false	false	true	high
MONDO:0011652	Phelan-McDermid syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0011653	thyroid cancer, nonmedullary, 3	hereditary_disease|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|endocrine_system_disorder	endocrinology|oncology	thyroid_diseases|thyroid_cancer_subcategory|cancer|thyroid_cancer_is_a_subset_of_nonmedullary_so_it_will_be_categorized_under_cancer_but_more_specific_to_that_would_be__cancer	endocrine_disorder	false	true	false	true	medium
MONDO:0011654	intellectual disability, microcephaly, growth retardation, joint contractures, and facial dysmorphism	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	endocrine_disorder|joint_disorder|brain_disorder	false	false	false	false	high
MONDO:0011655	alveolar soft part sarcoma	hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor	pulmonology|pediatric|oncology	sarcoma|cancer	lung_disorder|bone_disorder	false	true	false	false	high
MONDO:0011656	paget disease of bone 4	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	rheumatology|endocrinology|orthopaedic	inflammatory_disease|cancer|metabolic_disorder	spinal_disorder|blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0011657	autosomal dominant nonsyndromic hearing loss 24	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|otolaryngology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	ear_disorder|hearing_loss	false	false	false	true	medium
MONDO:0011658	autosomal recessive early-onset Parkinson disease 7	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	as_of_my_last_knowledge_update_in_october_2023__there_are_no_specific_treatments_that_cure_autosomal_recessive_early_onset_parkinson_disease_7__park7___which_is_linked_to_mutations_in_the_dj_1_gene__the_primary_approach_to_managing_the_disease_involves_symptomatic_treatment_of_parkinsonian_symptoms_using_dopaminergic_therapies__but_these_do_not_address_the_underlying_genetic_cause_of_the_disease____thus__the_answer_is_false	high
MONDO:0011659	heterotaxy, visceral, 3, autosomal	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|visceral	liver_disorder|kidney_disorder|vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0011660	autosomal dominant nonsyndromic hearing loss 22	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	urinary_tract_disorder|ear_disorder|spinal_disorder|muscle_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0011661	inflammatory bowel disease 5	immune_system_disorder|digestive_system_disorder|hereditary_disease	other	immune_system_disorder|digestive_system_disorder|hereditary_disease	rheumatology|gastroenterology	inflammatory_disease|autoimmune_diseases	immune_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0011662	pathological gambling	psychiatric_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|hereditary_disease	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	high
MONDO:0011663	juvenile primary lateral sclerosis	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	joint_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011664	immunodeficiency due to CD25 deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|genetics_and_genomics	inflammatory_disease|anemia|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0011667	maturity-onset diabetes of the young type 4	metabolic_disease|digestive_system_disorder|endocrine_system_disorder|hereditary_disease	metabolic_disease|diabetes_mellitus|endocrine_system_disorder	digestive_system_disorder|hereditary_disease|metabolic_disease|endocrine_system_disorder	endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder	false	false	true	true	medium
MONDO:0011668	maturity-onset diabetes of the young type 6	metabolic_disease|digestive_system_disorder|endocrine_system_disorder|hereditary_disease	metabolic_disease|diabetes_mellitus|endocrine_system_disorder	digestive_system_disorder|hereditary_disease|metabolic_disease|endocrine_system_disorder	endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	endocrine_disorder	false	false	true	true	high
MONDO:0011669	hypotonia-cystinuria syndrome	metabolic_disease|disorder_of_development_or_morphogenesis|syndromic_disease|chromosomal_disorder|mitochondrial_disease|hereditary_disease	metabolic_disease	chromosomal_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|metabolic_disease|mitochondrial_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011670	Ehlers-Danlos syndrome due to tenascin-X deficiency	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	rheumatology|genetics_and_genomics|dermatology	connective_tissue_disorder|cardiovascular_disorder	joint_disorder|vascular_disorder|skin_disorder	false	false	false	false	medium
MONDO:0011671	Huntington disease-like 2	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011672	persistent polyclonal B-cell lymphocytosis	cancer_or_benign_tumor|hematologic_disorder|hereditary_disease	cancer_or_benign_tumor	hematologic_disorder|hereditary_disease|cancer_or_benign_tumor	hematology|oncology	cancer|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	low
MONDO:0011673	autosomal dominant nonsyndromic hearing loss 30	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|pediatric|otolaryngology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	ear_disorder|auditory_system_disorder	false	false	false	true	medium
MONDO:0011674	Charcot-Marie-Tooth disease dominant intermediate B	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	orthopaedic|neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011675	Charcot-Marie-Tooth Disease, axonal, type 2GG	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	genetic_disorder|neurodegenerative_disease|axonal_diseases	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011676	PHACE syndrome	disorder_of_development_or_morphogenesis|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric|dermatology	neurodevelopmental_disease|cardiovascular_disorder	heart_disorder|vascular_disorder|skin_disorder|brain_disorder	false	false	false	false	high
MONDO:0011677	Megarbane syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011678	homozygous 11P15-p14 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|oncology	metabolic_disorder|cancer	endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0011679	craniosynostosis syndrome, autosomal recessive	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder|teeth_disorder|brain_disorder	false	false	false	false	high
MONDO:0011680	autosomal recessive congenital ichthyosis 3	integumentary_system_disorder|disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|integumentary_system_disorder|disorder_of_visual_system	dermatology|genetics_and_genomics	metabolic_disorder|skin_condition	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0011681	episodic ataxia type 4	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0011682	episodic ataxia type 3	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011683	oculocutaneous albinism type 4	integumentary_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease|integumentary_system_disorder	dermatology|pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0011686	DNA ligase IV deficiency	immune_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	immune_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	hematology|pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0011687	Charcot-Marie-Tooth disease axonal type 2F	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	axonial_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011688	muscular dystrophy-dystroglycanopathy type B5	metabolic_disease|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease	orthopaedic|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0011690	Camurati-Engelmann disease, type 2	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|muscle_disorder|bone_disorder	false	false	false	false	low
MONDO:0011691	amyotrophic lateral sclerosis type 3	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0011694	spinocerebellar ataxia type 15/16	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|psychiatric_disorder|nervous_system_disorder	neurology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011695	melanoma, uveal, susceptibility to, 1	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	ophthalmology|dermatology|oncology	inflammatory_disease|cancer|autoimmune_diseases	skin_disorder|eye_disorder	false	true	false	true	high
MONDO:0011696	melanoma, uveal, susceptibility to, 2	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	ophthalmology|dermatology|genetics_and_genomics|oncology	cancer|autoimmune_diseases	skin_disorder|eye_disorder	false	true	false	true	high
MONDO:0011697	Waardenburg syndrome type 2C	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	neurology|genetics_and_genomics	anemia|metabolic_disorder|neurodegenerative_disease	nerve_disorder|ear_disorder|spinal_disorder|cranial_nerve_disorder|hearing_loss_disorder	false	false	false	false	medium
MONDO:0011698	glycine N-methyltransferase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|brain_disorder	false	false	false	true	low
MONDO:0011699	inflammatory bowel disease 8	immune_system_disorder|digestive_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease|digestive_system_disorder	rheumatology|gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0011700	inflammatory bowel disease 6	immune_system_disorder|hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|immune_system_disorder|hereditary_disease	hematology|gastroenterology|hepatology|rheumatology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0011701	inflammatory bowel disease 4	immune_system_disorder|hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|immune_system_disorder|hereditary_disease	gastroenterology|hepatology|rheumatology	mental_health_disorder|inflammatory_disease|cancer|cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder|anemia|inflammatory_bowels_disease_has_been_removed_from_the_list___adrenal_gland_disease|allergy|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0011702	dilated cardiomyopathy 1L	nervous_system_disorder|cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiology|pulmonology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	vascular_disorder|muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0011703	spongiform encephalopathy with neuropsychiatric features	infectious_disease|nervous_system_disorder|hereditary_disease	infectious_disease	nervous_system_disorder|hereditary_disease|infectious_disease	genetics_and_genomics|neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	neuro_psychiatric_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0011705	lymphangioleiomyomatosis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0011706	Kufor-Rakeb syndrome	metabolic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011708	autosomal dominant nonsyndromic hearing loss 36	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|otolaryngology|pediatric	neurodegenerative_disease|autosomal_dominant_disorder_is_a_rare_condition_that_affects_the_nervous_system__so_it_can_be_classified_under_neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0011709	split hand-foot malformation 5	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|joint_disorder	false	false	false	true	high
MONDO:0011710	specific language impairment 1	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|psychology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0011711	specific language impairment 2	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|psychiatry|pediatric	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	medium
MONDO:0011712	van der Woude syndrome 2	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatrics|genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0011713	melanoma-pancreatic cancer syndrome	cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease|integumentary_system_disorder	oncology|genetics_and_genomics|dermatology	adrenal_gland_disease|cancer	skin_disorder|upper_gastrointestinal_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0011714	partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|eye_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011715	Seckel syndrome 2	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|eye_disorder|ear_disorder|bone_disorder	false	false	false	false	high
MONDO:0011716	acute hemorrhagic leukoencephalitis	inflammatory_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|infectious_disease	infectious_disease|neurodegenerative_disease	inflammatory_disease|acute_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|infectious_disease|post_infectious_disorder	neurology|hematology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	vascular_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0011717	hyperinsulinism-hyperammonemia syndrome	disorder_of_development_or_morphogenesis|endocrine_system_disorder|metabolic_disease|hereditary_disease|digestive_system_disorder	endocrine_system_disorder|metabolic_disease	metabolic_disease|digestive_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder	pediatric|endocrinology	adrenal_gland_disease|metabolic_disorder	liver_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0011718	primary ciliary dyskinesia 2	respiratory_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|respiratory_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder|kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0011719	gastrointestinal stromal tumor	hereditary_disease|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|hereditary_disease|cancer_or_benign_tumor	oncology|gastroenterology	cancer|gastrointestinal_cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0011720	spermatogenic failure 3	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	adrenal_gland_disease|metabolic_disorder	reproductive_system_disorder	false	false	false	false	high
MONDO:0011721	distal myopathy with anterior tibial onset	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|muscle_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011722	intellectual disability-obesity-prognathism-eye and skin anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatrics|genetics_and_genomics|endocrinology	metabolic_disorder|neurodegenerative_disease	skin_disorder|eye_disorder|endocrine_disorder|brain_disorder	false	false	false	false	high
MONDO:0011723	hemifacial myohyperplasia	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0011724	encephalopathy due to GLUT1 deficiency	nervous_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	true	true	very_high
MONDO:0011725	Crigler-Najjar syndrome type 2	metabolic_disease|hereditary_disease|syndromic_disease	metabolic_disease	syndromic_disease|metabolic_disease|hereditary_disease	genetics_and_genomics|hepatology	metabolic_disorder|neurodegenerative_disease	biliary_disorder|liver_disorder	false	false	false	true	medium
MONDO:0011726	peripheral arterial occlusive disease 1	hereditary_disease	other	hereditary_disease	cardiothoracic|vascular___note__vascular_is_not_in_the_original_list__but_it_is_a_common_category_for_peripheral_arterial_occlusive_disease|cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0011728	benign essential blepharospasm	nervous_system_disorder	other	nervous_system_disorder	neurology|ophthalmology	mental_health_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	low
MONDO:0011730	fumaric aciduria	disorder_of_development_or_morphogenesis|nervous_system_disorder|metabolic_disease|hereditary_disease|mitochondrial_disease	metabolic_disease	mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	pediatrics|genetics_and_genomics	inflammatory_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0011731	glucose-galactose malabsorption	metabolic_disease|hereditary_disease|digestive_system_disorder	metabolic_disease	digestive_system_disorder|metabolic_disease|hereditary_disease	endocrinology|gastroenterology|pediatric	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0011732	familial digital arthropathy-brachydactyly	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic|rheumatology	metabolic_disorder|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0011733	parasomnia, sleep bruxism type	hereditary_disease	other	hereditary_disease	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	sleep_bruxism_type_is_often_associated_with_neurological_conditions__specifically_those_affecting_the_brain_s_ability_to_regulate_sleep_and_motor_functions__so_it_seems_more_fitting_in_the_category_of__brain_disorder_than_other_categories|brain_disorder	false	false	false	false	medium
MONDO:0011734	Cardioneuromyopathy with hyaline masses and nemaline rods	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|cardiology	cardiovascular_disorder|neurodegenerative_disease	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0011735	hyper-IgM syndrome type 3	hematologic_disorder|hereditary_disease|immune_system_disorder	other	hematologic_disorder|immune_system_disorder|hereditary_disease	immunology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0011736	Cree intellectual disability syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|psychiatry|pediatric	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011737	Parkinson disease 10	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	cardiovascular_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0011738	bilateral frontoparietal polymicrogyria	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011739	pancreatic cancer, susceptibility to, 1	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|oncology|gastroenterology	pancreatic_cancer__susceptibility_to|cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0011740	Carney-Stratakis syndrome	endocrine_system_disorder|hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	syndromic_disease|hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|oncology|cardiology	neurodegenerative_disease|cardiovascular_disorder|inflammatory_disease|cancer	kidney_disorder|heart_disorder|brain_disorder	false	false	false	false	high
MONDO:0011743	Alzheimer disease 4	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0011744	primary intraosseous venous malformation	cardiovascular_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|cancer_or_benign_tumor	vascular|orthopaedic	cardiovascular_disorder|vascular_disorder	vascular_disorder|bone_disorder	false	false	false	false	high
MONDO:0011745	duodenojejunal atresia with volvulus, absent dorsal mesentery, and absent superior mesenteric artery	hereditary_disease	other	hereditary_disease	genetics_and_genomics|gastroenterology|pediatric	congenital_anomaly|gastrointestinal_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0011746	symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|orthopaedic	inflammatory_disease|metabolic_disorder|autoimmune_diseases	teeth_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0011748	Usher syndrome type 1G	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease	ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0011749	oculocutaneous albinism type 1B	disorder_of_visual_system|metabolic_disease|hereditary_disease|integumentary_system_disorder	metabolic_disease	disorder_of_visual_system|metabolic_disease|hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology|ophthalmology	metabolic_disorder|genetic_disorder	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0011751	COPD, severe early onset	hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease	pulmonology|cardiothoracic	inflammatory_disease|metabolic_disorder|autoimmune_diseases	vascular_disorder|lung_disorder	false	false	false	true	very_high
MONDO:0011752	nephronophthisis 4	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	urology|renal_medicine	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0011754	familial hyperreninemic hypoaldosteronism type 2	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	genetics_and_genomics|pediatric|endocrinology	adrenal_gland_disease|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0011755	senior-loken syndrome 3	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0011756	Senior-Loken syndrome 4	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	neurology|psychiatry	mental_health_disorder|cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|brain_disorder	false	false	false	true	high
MONDO:0011757	brachydactyly type A1B	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0011758	Hurler syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|disorder_of_visual_system|metabolic_disease|cardiovascular_disorder|hereditary_disease|syndromic_disease	metabolic_disease|cardiovascular_disorder	syndromic_disease|disorder_of_visual_system|cardiovascular_disorder|metabolic_disease|disorder_of_orbital_region|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0011759	Hurler-Scheie syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|disorder_of_visual_system|metabolic_disease|hereditary_disease|syndromic_disease	metabolic_disease	syndromic_disease|disorder_of_visual_system|metabolic_disease|disorder_of_orbital_region|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology|pediatric|ophthalmology|orthopaedic	neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder|lysosomal_storage_disease	false	false	false	false	high
MONDO:0011760	Scheie syndrome	metabolic_disease|disorder_of_visual_system|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	metabolic_disease	musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|disorder_of_orbital_region|metabolic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	immune_disorder|bone_disorder|kidney_disorder|liver_disorder|joint_disorder	false	false	false	false	medium
MONDO:0011761	autosomal dominant nonsyndromic hearing loss 21	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	high
MONDO:0011762	autosomal recessive nonsyndromic hearing loss 22	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|otolaryngology|genetics_and_genomics	autosomal_recessive_diseases|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0011764	autosomal dominant Parkinson disease 8	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	autosomal_dominant_disorder____note__the_second_item_is_implied_by_the_name__autosomal_dominant_parkinson_disease|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0011765	multiple epiphyseal dysplasia type 5	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0011766	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|cardiovascular_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder|endocrine_system_disorder	musculoskeletal_system_disorder|endocrine_system_disorder|cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|reproductive_system_disorder	endocrinology|neurology|genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011767	autosomal recessive nonsyndromic hearing loss 31	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder|autosomal_recessive	false	false	false	true	medium
MONDO:0011768	myasthenia gravis with thymus hyperplasia	nervous_system_disorder|immune_system_disorder	autoimmune_disease	immune_system_disorder|nervous_system_disorder	endocrinology|neurology|immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|muscle_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0011770	aortic aneurysm, familial thoracic 2	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	genetics_and_genomics|pulmonology|cardiothoracic|cardiology	cardiovascular_disorder|familial__is_already_included_within_this_category_name_so_it_should_be_removed_to_avoid_redundancy	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0011771	neuronopathy, distal hereditary motor, autosomal recessive 3	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011772	B4GALT1-congenital disorder of glycosylation	nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|genetics_and_genomics	congenital_disorder_of_glycosylation|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0011773	anauxetic dysplasia	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics|pulmonology|cardiothoracic|cardiology|obstetrics_and_gynecology	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder|joint_disorder	false	false	false	false	high
MONDO:0011774	autosomal recessive nonsyndromic hearing loss 30	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0011775	nasopharyngeal carcinoma, susceptibility to, 1	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	otolaryngology|oncology	cancer|autoimmune_diseases	upper_gastrointestinal_disorder|throat_disorder	false	true	false	false	very_high
MONDO:0011776	CINCA syndrome	immune_system_disorder|hereditary_disease|connective_tissue_disorder|musculoskeletal_system_disorder|syndromic_disease	other	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	pediatric|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0011777	Alzheimer disease 8	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	very_high
MONDO:0011778	multiple epiphyseal dysplasia, Al-Gazali type	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0011779	laryngeal atresia, encephalocele, and limb deformities	hereditary_disease	other	hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	cardiovascular_disorder|limb_deformities|neurodegenerative_disease	throat_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011780	specific language impairment 3	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011781	spinocerebellar ataxia type 17	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|cardiovascular_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0011782	angioid streaks	nervous_system_disorder|disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|disorder_of_orbital_region	dermatology|ophthalmology	neurodegenerative_disease|anemia	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0011783	ALG12-congenital disorder of glycosylation	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|congenital_disorder_of_glycosylation_is_a_synonym_for_the_disease	liver_disorder	false	false	false	false	very_high
MONDO:0011784	Moyamoya disease 2	nervous_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|cardiovascular_disorder|inflammatory_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0011785	hereditary spastic paraplegia 19	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011786	allergic rhinitis	immune_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease|inflammatory_disease	other	immune_system_disorder|inflammatory_disease|respiratory_system_disorder|otorhinolaryngologic_disease	pediatric|otolaryngology|pulmonology|allergy_and_immunology	autoimmune_diseases|allergy|inflammatory_disease	immune_disorder|nose_disorder	false	false	false	true	medium
MONDO:0011787	autosomal recessive limb-girdle muscular dystrophy type 2I	nervous_system_disorder|metabolic_disease|hereditary_disease|musculoskeletal_system_disorder	metabolic_disease	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|muscular_dystrophy	muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0011788	cloverleaf skull-multiple congenital anomalies syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	immune_disorder|reproductive_system_disorder|ear_disorder|eye_disorder|skull_disorder|brain_disorder|bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0011789	familial meningioma	nervous_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|nervous_system_disorder|cancer_or_benign_tumor	neurology|genetics_and_genomics|oncology	cancer	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011790	Amish lethal microcephaly	nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|muscle_disorder	true	false	false	false	very_high
MONDO:0011792	thyroid dyshormonogenesis 6	endocrine_system_disorder|hereditary_disease|metabolic_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|hereditary_disease|metabolic_disease	endocrinology|genetics_and_genomics	autoimmune_diseases|thyroid_gland_disease_is_not_in_the_list_but_closest_match_is__inflammatory_disease|metabolic_disorder	thyroid_disease|endocrine_disorder	false	false	false	true	high
MONDO:0011795	anonychia-microcephaly syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|anemia	upper_gastrointestinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0011796	epilepsy, partial, with pericentral spikes	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|epilepsy|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0011797	infantile-onset ascending hereditary spastic paralysis	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|hereditary_spastic_paralysis	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0011798	hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|eye_disorder|liver_disorder	false	false	false	false	high
MONDO:0011799	autosomal recessive nonsyndromic hearing loss 33	nervous_system_disorder|hereditary_disease|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|anemia|autoimmune_diseases	ear_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0011800	glioma susceptibility 4	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011801	spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1	metabolic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|autosomal_recessive_disorder|axonopathy	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011802	hypercalciuria, absorptive, 1	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology|gastroenterology	metabolic_disorder|absorptive	lower_gastrointestinal_disorder|kidney_disorder	false	false	false	true	high
MONDO:0011803	hereditary spastic paraplegia 7	metabolic_disease|nervous_system_disorder|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis	neurodegenerative_disease|metabolic_disease	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011804	autoimmune lymphoproliferative syndrome type 2B	syndromic_disease|immune_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor|autoimmune_disease	hereditary_disease|syndromic_disease|cancer_or_benign_tumor|immune_system_disorder	hematology|oncology|immunology|allergy_and_immunology	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0011806	osteofibrous dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|rheumatology	metabolic_disorder|genetic_condition	blood_bone_marrow_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0011808	cataract 27	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0011810	horizontal gaze palsy with progressive scoliosis	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	neurology|orthopaedic	neurodegenerative_disease|inflammatory_disease	eye_disorder|spinal_disorder|brain_disorder	true	false	false	true	high
MONDO:0011811	autosomal recessive cerebellar ataxia-saccadic intrusion syndrome	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011812	Duane-radial ray syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|ophthalmology	neurodegenerative_disease|eye_anomaly|genetic_disorder	eye_disorder|spinal_disorder|other_____corrected_response____eye_disorder	false	false	false	false	high
MONDO:0011813	polydactyly, postaxial, type A3	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder|genetic_disease__note__i_added_the_category__genetic_disease__which_is_not_in_your_list__as_polydactyly_is_a_congenital_condition_caused_by_genetic_mutations|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0011814	Smith-McCort dysplasia 1	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0011816	lathosterolosis	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	metabolic_disorder|adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	liver_disorder	false	false	false	false	very_high
MONDO:0011818	isolated focal cortical dysplasia type II	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011819	spinocerebellar ataxia type 19/22	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0011821	Meckel syndrome, type 3	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|anemia	upper_gastrointestinal_disorder|kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0011822	Bartter disease type 3	syndromic_disease|urinary_system_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|urinary_system_disorder	pediatric|renal_medicine|genetics_and_genomics	electrolyte_disorder|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0011823	developmental malformations-deafness-dystonia syndrome	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology|otolaryngology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	muscle_disorder|brain_disorder|ear_disorder	false	false	false	false	high
MONDO:0011825	streptococcus, group A, severity of infection by	hereditary_disease	other	hereditary_disease	pediatric|pulmonology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	throat_disorder|immune_disorder	true	false	false	true	high
MONDO:0011826	glucocorticoid deficiency 2	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|inflammatory_disease	immune_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0011827	patent ductus arteriosus	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|cardiology	cardiovascular_disorder|congenital_abnormality	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0011828	intellectual disability, autosomal recessive 2	psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease|psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0011829	coenzyme Q10 deficiency, primary, 1	metabolic_disease|nervous_system_disorder|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	genetics_and_genomics|neurology|pediatrics|cardiology	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	heart_disorder|liver_disorder	false	false	false	true	high
MONDO:0011830	lissencephaly due to LIS1 mutation	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011831	arrhythmogenic right ventricular dysplasia 8	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|pediatric|cardiology	cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0011832	autosomal dominant nonsyndromic hearing loss 44	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|otolaryngology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	ear_disorder	false	false	false	true	medium
MONDO:0011833	spinocerebellar ataxia type 21	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease_is_not_correct_because_it_is_actually_a_spinocerebellar_ataxia__which_means_it_s_related_to_cerebellum_and_spinal_cord___however__since_no_quotation_marks_or___symbols_allowed__the_final_answer_would_be__neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011834	spinocerebellar ataxia type 18	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011835	sensory ataxic neuropathy, dysarthria, and ophthalmoparesis	metabolic_disease|nervous_system_disorder|mitochondrial_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	nervous_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	neurology|otolaryngology|ophthalmology	neurodegenerative_disease|sensory_neuropathy_is_not_in_the_category_list_so_i_will_ignore_it|inflammatory_disease|autoimmune_diseases	eye_disorder|muscle_disorder|brain_disorder	true	false	false	false	high
MONDO:0011836	thyroid Hurthle cell carcinoma	endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|hereditary_disease	endocrinology|oncology	cancer|metabolic_disorder|autoimmune_diseases	endocrine_disorder|thyroid_disease	false	true	false	false	medium
MONDO:0011837	vitamin K-dependent clotting factors, combined deficiency of, type 2	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0011838	Bothnia retinal dystrophy	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|hereditary_disease	neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011839	Newfoundland cone-rod dystrophy	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011840	dilated cardiomyopathy 1M	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiothoracic|cardiology	cardiovascular_disorder|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	true	high
MONDO:0011841	biotin-responsive basal ganglia disease	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0011842	GRN-related frontotemporal lobar degeneration with Tdp43 inclusions	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011843	hypertrophic cardiomyopathy 25	nervous_system_disorder|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|nervous_system_disorder|cardiovascular_disorder|hereditary_disease	cardiothoracic|cardiology	hypertrophic_cardiomyopathy|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	true	high
MONDO:0011844	myoclonic dystonia 15	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0011848	headache associated with sexual activity	hereditary_disease	other	hereditary_disease	neurology|obstetrics_and_gynecology	metabolic_disorder|mental_health_disorder	reproductive_system_disorder|brain_disorder	false	false	false	true	medium
MONDO:0011849	psoriatic arthritis	connective_tissue_disorder|syndromic_disease|immune_system_disorder|inflammatory_disease|musculoskeletal_system_disorder	autoimmune_disease	connective_tissue_disorder|syndromic_disease|musculoskeletal_system_disorder|inflammatory_disease|immune_system_disorder	rheumatology|dermatology|orthopaedic	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|joint_disorder	false	false	false	true	high
MONDO:0011852	nonsyndromic congenital nail disorder 8	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder	skin_disorder|nail_disorder_is_not_present_so_i_will_choose_skin_disorder	false	false	false	false	medium
MONDO:0011853	Camptosynpolydactyly, complex	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|skeletal_disease__not_in_the_list__so____metabolic_disorder|genetic_disorder____corrected_answer__i_made_a_mistake__it_s_actually____genetic_disorder|genetic_disorder|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0011854	secretory diarrhea, myopathy, and deafness	hereditary_disease	other	hereditary_disease	neurology|gastroenterology|otolaryngology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	lower_gastrointestinal_disorder|muscle_disorder|ear_disorder	true	false	true	true	high
MONDO:0011855	granular corneal dystrophy type II	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	ophthalmology|genetics_and_genomics	autoimmune_diseases|adrenal_gland_disease|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0011856	spondylometaphyseal dysplasia-bowed forearms-facial dysmorphism syndrome	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|genetic_condition	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0011857	atrial fibrillation, familial, 3	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	hematology|cardiology|genetics_and_genomics	familial|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0011858	spastic paraplegia, ataxia, and intellectual disability	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0011861	breath-holding Spells	hereditary_disease	other	hereditary_disease	neurology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	low
MONDO:0011862	hereditary spastic paraplegia 24	nervous_system_disorder|hereditary_disease|syndromic_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|hereditary_condition|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011863	prostate cancer aggressiveness quantitative trait locus on chromosome 19	hereditary_disease	other	hereditary_disease	oncology|urology|genetics_and_genomics	prostate_cancer|cancer	reproductive_system_disorder|urinary_tract_disorder	false	true	false	true	medium
MONDO:0011864	immunodeficiency, common variable, 1	hematologic_disorder|hereditary_disease|syndromic_disease|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|immune_system_disorder|hematologic_disorder|hereditary_disease	immunology|allergy_and_immunology|genetics_and_genomics	inflammatory_disease|inflammatorydisease|immunodeficiency_is_actually__common_variable__so__autoimmunediseases|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0011866	pontocerebellar hypoplasia type 1A	psychiatric_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	neurodegenerative_disease|metabolic_disease|psychiatric_disorder	metabolic_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011867	microphthalmia with cyst, bilateral facial clefts, and limb anomalies	hereditary_disease	other	hereditary_disease	neonatology|pediatric|genetics_and_genomics	limb_abnormalities|metabolic_disorder|genetic_disorder|congenital_anomaly	eye_disorder|limb_disorder	false	false	false	false	high
MONDO:0011868	lethal congenital contracture syndrome 2	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0011869	epidermolysis bullosa simplex superficialis	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0011870	annular epidermolytic ichthyosis	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0011871	Niemann-Pick disease type B	respiratory_system_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease|immune_system_disorder	metabolic_disease	metabolic_disease|respiratory_system_disorder|nervous_system_disorder|immune_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	medium
MONDO:0011872	Griscelli syndrome type 2	hematologic_disorder|metabolic_disease|syndromic_disease|hereditary_disease|integumentary_system_disorder|immune_system_disorder	metabolic_disease	metabolic_disease|syndromic_disease|integumentary_system_disorder|immune_system_disorder|hereditary_disease|hematologic_disorder	neurology|pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0011873	Niemann-Pick disease, type C2	metabolic_disease|hereditary_disease|immune_system_disorder	metabolic_disease	metabolic_disease|immune_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0011874	neonatal ichthyosis-sclerosing cholangitis syndrome	endocrine_system_disorder|syndromic_disease|hereditary_disease|integumentary_system_disorder|inflammatory_disease|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|syndromic_disease|inflammatory_disease|endocrine_system_disorder|integumentary_system_disorder|hereditary_disease	hepatology|gastroenterology|dermatology|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|liver_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0011877	autosomal dominant osteopetrosis 1	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	inflammatory_disease|cardiovascular_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0011879	neuronopathy, distal hereditary motor, type 7B	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|motor_neuron_disease|hereditary_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0011880	candidiasis, familial, 3	hereditary_disease|integumentary_system_disorder|immune_system_disorder	other	integumentary_system_disorder|immune_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	false	medium
MONDO:0011881	keratosis palmoplantaris striata 3	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	lower_gastrointestinal_disorder|skin_disorder	false	false	false	false	medium
MONDO:0011882	skin fragility-woolly hair-palmoplantar keratoderma syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|genetic_disorder	muscle_disorder|immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0011883	Curly hair - acral keratoderma - caries syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	teeth_disorder|hair_disorder|skin_disorder	false	false	false	false	medium
MONDO:0011884	hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	teeth_disorder|muscle_disorder|bone_disorder|joint_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0011885	tubulointerstitial nephritis and uveitis syndrome	urinary_system_disorder|syndromic_disease	other	syndromic_disease|urinary_system_disorder	renal_medicine|ophthalmology|rheumatology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder|kidney_disorder	true	false	false	true	high
MONDO:0011886	torsion dystonia 13	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|orthopaedic	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0011887	cataract, congenital, with mental impairment and dentate gyrus atrophy	hereditary_disease	other	hereditary_disease	neurology|ophthalmology|psychiatry|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	eye_disorder|brain_disorder	false	false	false	true	high
MONDO:0011888	immunodeficiency 67	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|immunology|pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|immunodeficiency_is_not_in_the_list_so_return_nothing	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0011889	Charcot-Marie-Tooth disease type 2I	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|orthopaedic|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	muscle_disorder|nerve_disorder	false	false	false	false	medium
MONDO:0011890	Charcot-Marie-Tooth disease type 1D	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	nerve_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011891	febrile seizures, familial, 8	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	high
MONDO:0011894	Charcot-Marie-Tooth disease type 2E	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011895	idiopathic hypereosinophilic syndrome	hematologic_disorder|immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|immune_system_disorder|idiopathic_disease|hematologic_disorder|cardiovascular_disorder|hereditary_disease|syndromic_disease	hematology|allergy_and_immunology|oncology|pulmonology	autoimmune_diseases|inflammatory_disease|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0011897	leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder|teeth_disorder	false	false	false	false	high
MONDO:0011898	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	autosomal_recessive_disorders|neurodegenerative_disease	nerve_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011899	Noonan syndrome-like disorder with loose anagen hair	musculoskeletal_system_disorder|hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|integumentary_system_disorder|cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	cardiovascular_disorder|metabolic_disorder	skin_disorder|hair_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0011900	porokeratosis 4, disseminated superficial actinic type	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	dermatology|genetics_and_genomics	cancer|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|skin_disorder	false	false	false	false	low
MONDO:0011901	Charcot-Marie-Tooth disease axonal type 2H	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	orthopaedic|neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011902	Charcot-Marie-Tooth disease type 1F	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	orthopaedic|neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|nerve_disorder_is_not_available_in_the_list_so|spinal_disorder	false	false	false	false	medium
MONDO:0011903	Charcot-Marie-Tooth disease type 2J	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|nerve_disorder	false	false	false	false	medium
MONDO:0011904	seizures, benign familial infantile, 3	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	medium
MONDO:0011906	congenital bile acid synthesis defect 1	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	gastroenterology|hepatology|pediatric|genetics_and_genomics	metabolic_disorder|congenital_disease|genetic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0011907	acrocapitofemoral dysplasia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0011908	juvenile myelomonocytic leukemia	cancer_or_benign_tumor|musculoskeletal_system_disorder|hematologic_disorder|connective_tissue_disorder|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	pediatric|hematology|oncology	cancer|leukemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0011909	Charcot-Marie-Tooth disease dominant intermediate D	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011911	craniolenticulosutural dysplasia	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|teeth_disorder|bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011912	autosomal recessive nonsyndromic hearing loss 37	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	genetics_and_genomics|pediatric|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0011913	Alzheimer disease 3	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	very_high
MONDO:0011914	hypotrichosis-lymphedema-telangiectasia syndrome	immune_system_disorder|cardiovascular_disorder|syndromic_disease|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|immune_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|genomics_is_removed_in_favor_of_genetics_and_genomics_for_brevity|pediatric|dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|vascular_disorder|skin_disorder	false	false	false	false	high
MONDO:0011915	mitral valve prolapse, myxomatous 2	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology	mitral_valve_prolapse_myxomatous|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0011916	Charcot-Marie-Tooth disease axonal type 2K	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011918	anxiety	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurology|psychiatry	anxiety_disorders|mental_health_disorder	mental_health_disorder|brain_disorder	false	false	false	true	high
MONDO:0011920	autosomal dominant nonsyndromic hearing loss 48	nervous_system_disorder|auditory_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	pediatric|genetics_and_genomics|otolaryngology	metabolic_disorder|neurodegenerative_disease	hearing_loss|ear_disorder	false	false	false	true	medium
MONDO:0011921	aural atresia, congenital	otorhinolaryngologic_disease|hereditary_disease	other	hereditary_disease|otorhinolaryngologic_disease	pediatric|otolaryngology	congenital_anomaly|neurodevelopmental_disorder|birth_defect	congenital_disorder|ear_disorder	false	false	false	false	medium
MONDO:0011922	nonimmune chronic idiopathic neutropenia of adults	hereditary_disease	other	hereditary_disease|idiopathic_disease	hematology|immunology	anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	medium
MONDO:0011924	panic disorder 2	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurology|psychiatry	anxiety_disorder|mental_health_disorder	mental_health_disorder|brain_disorder	false	false	false	true	high
MONDO:0011925	congenital merosin-deficient muscular dystrophy 1A	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|muscular_dystrophy	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0011927	tufted angioma	cancer_or_benign_tumor|integumentary_system_disorder|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|integumentary_system_disorder	pediatric|genetics_and_genomics|hematology|dermatology|oncology	cancer|neurodevelopmental_disorder	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0011928	caudal duplication	syndromic_disease|digestive_system_disorder|hereditary_disease	other	hereditary_disease|digestive_system_disorder|syndromic_disease	urology|pediatric|genetics_and_genomics	cancer|neurodegenerative_disease	bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0011929	chromosome 1p36 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	developmental_disorder_is_not_listed_but_this_would_be_a_good_fit_as_the_deletion_of_part_of_chromosome_1p36_can_lead_to_intellectual_disability__delayed_speech__and_other_neurodevelopmental_disorders__however_based_on_your_request_i_will_provide__brain_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011930	epilepsy, familial adult myoclonic, 2	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0011931	ovarian cancer, susceptibility to, 1	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	obstetrics_and_gynecology|genetics_and_genomics|oncology	allergy|cancer|autoimmune_diseases	reproductive_system_disorder	false	true	false	false	high
MONDO:0011932	hypotrichosis 6	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	hair_disorder|skin_disorder	false	false	false	true	medium
MONDO:0011933	ALG2-congenital disorder of glycosylation	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	liver_disorder	false	false	false	false	very_high
MONDO:0011934	dermatofibrosarcoma protuberans	cancer_or_benign_tumor|connective_tissue_disorder|integumentary_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer|soft_tissue_sarcoma|skin_cancer	joint_disorder|skin_disorder|muscle_disorder	false	true	false	true	medium
MONDO:0011935	retinitis pigmentosa 30	metabolic_disease|hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	metabolic_disease|psychiatric_disorder	metabolic_disease|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0011936	microphthalmia with brain and digit anomalies	hereditary_disease|disorder_of_visual_system|syndromic_disease	other	syndromic_disease|disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0011937	peeling skin syndrome 4	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	allergy_and_immunology|dermatology|pediatrics	autoimmune_diseases|inflammatory_disease	skin_disorder	true	false	false	false	medium
MONDO:0011938	atrial septal defect 2	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|pediatric|cardiothoracic	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0011939	Spondyloenchondrodysplasia with immune dysregulation	hereditary_disease|connective_tissue_disorder|syndromic_disease|musculoskeletal_system_disorder	other	syndromic_disease|connective_tissue_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|rheumatology|immunology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	joint_disorder|immune_disorder|spinal_disorder	false	false	false	false	high
MONDO:0011945	Gaucher disease perinatal lethal	metabolic_disease|hereditary_disease|disorder_of_visual_system	metabolic_disease	metabolic_disease|disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|blood_bone_marrow_disorder|liver_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0011946	diaphanospondylodysostosis	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	skeletal_disorder|developmental_disorder|metabolic_disorder|bone_disease|osteochondrodysplasia|inherited_condition|genetic_disorder|rare_disease|musculoskeletal_disease	bone_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0011948	pontocerebellar hypoplasia type 3	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011949	Thai symphalangism syndrome	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011950	infantile-onset autosomal recessive nonprogressive cerebellar ataxia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011951	amyotrophic lateral sclerosis type 6	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011952	amyotrophic lateral sclerosis type 7	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0011953	familial acute necrotizing encephalopathy	hereditary_disease|nervous_system_disorder	other	hereditary_disease|post_infectious_disorder|nervous_system_disorder|acute_disease	neurology|genetics_and_genomics	familial_acute_necrotizing_encephalopathy_is_a_rare_genetic_disorder_that_affects_the_brain|neurodegenerative_disease	immune_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011954	melanoma, cutaneous malignant, susceptibility to, 4	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	dermatology|oncology	cancer|cutaneous_malignant	skin_disorder|cutaneous_malignant	false	true	false	true	high
MONDO:0011955	diabetes mellitus, noninsulin-dependent, 4	metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|metabolic_disease|diabetes_mellitus	metabolic_disease|hereditary_disease|digestive_system_disorder|endocrine_system_disorder	renal_medicine|cardiology|endocrinology|cardiothoracic	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	vascular_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0011957	retinal macular dystrophy type 2	psychiatric_disorder|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0011958	bile and pancreatic ducts, complete absence of	hereditary_disease	other	hereditary_disease	gastroenterology|hepatology	metabolic_disorder|anatomic_abnormality	liver_disorder|upper_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0011959	sweet syndrome	hereditary_disease|integumentary_system_disorder|connective_tissue_disorder|syndromic_disease	other	connective_tissue_disorder|hereditary_disease|integumentary_system_disorder|syndromic_disease	rheumatology|dermatology	autoimmune_diseases|inflammatory_disease|allergy	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0011960	schizophrenia 11	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	immune_disorder|bone_disorder|brain_disorder	false	false	false	false	high
MONDO:0011961	hereditary sensory and autonomic neuropathy type 1B	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	hereditary_disease|neurodegenerative_disease	spinal_disorder|nerve_disorder	false	false	false	false	high
MONDO:0011962	endometrial cancer	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|inflammatory_disease|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0011963	Joubert syndrome 2	disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|disorder_of_visual_system|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0011964	DPAGT1-congenital disorder of glycosylation	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder_of_glycosylation	joint_disorder|bone_disorder|eye_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0011965	familial temporal lobe epilepsy 2	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	mental_health_disorder|familial_temporal_lobe_epilepsy_is_actually_a_subset_of_the_first_two_categories_in_this_case__so_i_will_return_neurodegenerative_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0011966	periventricular heterotopia with microcephaly, autosomal recessive	hereditary_disease|nervous_system_disorder|syndromic_disease	other	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011967	heterotopia, periventricular, associated with chromosome 5P anomalies	hereditary_disease|nervous_system_disorder|syndromic_disease	other	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0011968	autosomal recessive limb-girdle muscular dystrophy type 2D	cardiovascular_disorder|hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	orthopaedic|neurology|genetics_and_genomics	muscular_dystrophy|neurodegenerative_disease	joint_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011969	ALG8-congenital disorder of glycosylation	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder_of_glycosylation	liver_disorder	false	false	false	false	very_high
MONDO:0011970	rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0011971	hyper-IgM syndrome type 5	hereditary_disease|immune_system_disorder|hematologic_disorder	other	hematologic_disorder|hereditary_disease|immune_system_disorder	genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0011972	ovarian hyperstimulation syndrome	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrinology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0011973	zinc deficiency, transient neonatal	hereditary_disease	other	hereditary_disease	neonatology|gastroenterology|endocrinology|pediatric	neonatal_disease|metabolic_disorder	endocrine_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0011974	retinitis pigmentosa 7	psychiatric_disorder|metabolic_disease|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	metabolic_disease|hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease|cardiovascular_disorder____corrected_list_after_reevaluating__neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0011975	paternal uniparental disomy of chromosome 14	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder|chromosome_disorder____note__i_assumed__chromosome_disorder__is_a_valid_category__but_it_s_not_in_the_original_list__however__based_on_the_provided_categories___reproductive_system_disorder__seems_to_be_the_closest_fit	false	false	false	false	high
MONDO:0011976	lipodystrophy-intellectual disability-deafness syndrome	metabolic_disease|hereditary_disease|integumentary_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|integumentary_system_disorder	neurology|genetics_and_genomics|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	intellectual_disability_is_a_systemic_condition_affecting_multiple_body_systems_so_it_would_be_redundant_to_list_the_other_categories_also|brain_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0011977	8q22.1 microdeletion syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0011978	CoQ-responsive OXPHOS deficiency	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	true	high
MONDO:0011979	adult-onset foveomacular vitelliform dystrophy	psychiatric_disorder|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0011984	synpolydactyly type 2	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	neurodegenerative_disease|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0011985	hyper-IgM syndrome type 4	hereditary_disease|immune_system_disorder|hematologic_disorder	other	hereditary_disease|hematologic_disorder|immune_system_disorder	genetics_and_genomics|pediatric|immunology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	true	false	false	false	high
MONDO:0011986	tropical pancreatitis	hereditary_disease|endocrine_system_disorder|digestive_system_disorder|inflammatory_disease	endocrine_system_disorder	inflammatory_disease|hereditary_disease|digestive_system_disorder|endocrine_system_disorder	gastroenterology|endocrinology	metabolic_disorder|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0011987	cone-rod dystrophy 13	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0011988	neutrophil immunodeficiency syndrome	hereditary_disease|immune_system_disorder|hematologic_disorder	other	hereditary_disease|hematologic_disorder|immune_system_disorder	pediatrics|allergy_and_immunology|immunology	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0011989	leishmaniasis	infectious_disease	infectious_disease	infectious_disease	pediatrics|dermatology|immunology|hematology|pulmonology	autoimmune_diseases|anemia|inflammatory_disease	lymphatic_disorder|skin_disorder	true	false	false	true	high
MONDO:0011990	seizures, benign familial neonatal, 3	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|brain_disorder	false	false	false	true	medium
MONDO:0011991	autosomal recessive nonsyndromic hearing loss 38	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	genetics_and_genomics|otolaryngology|pediatric	anemia|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	hearing_loss|ear_disorder	false	false	false	true	medium
MONDO:0011992	hereditary spastic paraplegia 25	hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	hereditary_disease|syndromic_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0011993	aspirin resistance	hereditary_disease	other	hereditary_disease	cardiology|hematology	metabolic_disorder|inflammatory_disease	joint_disorder|vascular_disorder	false	false	false	false	high
MONDO:0011994	autosomal dominant nonsyndromic hearing loss 41	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	hearing_loss|ear_disorder	false	false	false	true	medium
MONDO:0011995	cataract - congenital heart disease - neural tube defect syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	ophthalmology|neurology|cardiology|genetics_and_genomics|pediatric	cardiovascular_disorder|neurodegenerative_disease	eye_disorder|spinal_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0011996	chronic myelogenous leukemia, BCR-ABL1 positive	musculoskeletal_system_disorder|hereditary_disease|cancer_or_benign_tumor|connective_tissue_disorder|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	hereditary_disease|hematologic_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder	genetics_and_genomics|oncology|hematology	cancer|leukemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0011997	Hermansky-Pudlak syndrome 2	hereditary_disease|metabolic_disease|immune_system_disorder|integumentary_system_disorder|syndromic_disease|hematologic_disorder	metabolic_disease	hereditary_disease|hematologic_disorder|syndromic_disease|metabolic_disease|integumentary_system_disorder|immune_system_disorder	ophthalmology|genetics_and_genomics|pediatric	anemia|metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0011998	autosomal dominant slowed nerve conduction velocity	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant	spinal_disorder|muscle_disorder|nerve_disorder	false	false	false	true	medium
MONDO:0011999	otosclerosis 3	otorhinolaryngologic_disease|hereditary_disease|auditory_system_disorder	other	hereditary_disease|auditory_system_disorder|otorhinolaryngologic_disease	neurology|genetics_and_genomics|otolaryngology|pediatrics	autoimmune_diseases|inflammatory_disease	other____note__i_ve_removed_the__other__category_because_it_s_likely_a_catch_all_that_doesn_t_provide_much_information__otosclerosis_is_indeed_an_ear_disorder__but_it_could_also_be_classified_as_a_bone_disorder_or_other_specific_categories_related_to_hearing_and_balance|ear_disorder	false	false	false	true	high
MONDO:0012000	specific phobia	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	mental_health_disorder	brain_disorder	false	false	false	true	medium
MONDO:0012001	mandibulofacial dysostosis with ptosis, autosomal dominant	hereditary_disease	other	hereditary_disease	otolaryngology|genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder	teeth_disorder|eye_disorder|bone_disorder	false	false	false	false	medium
MONDO:0012002	autosomal recessive nonsyndromic hearing loss 40	auditory_system_disorder|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	otolaryngology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0012003	autosomal recessive nonsyndromic hearing loss 39	auditory_system_disorder|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	otolaryngology|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0012004	parathyroid gland carcinoma	hereditary_disease|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	cancer|adrenal_gland_disease	endocrine_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0012005	growth failure, microcephaly, intellectual disability, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|cortical_dysplasia|cerebellar_atrophy|neurodegenerative_disease	joint_disorder|brain_disorder|eye_disorder|bone_disorder	true	false	false	false	very_high
MONDO:0012006	craniosynostosis with ocular abnormalities and hallucal defects	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	ophthalmology|genetics_and_genomics|neurology|orthopaedic|pediatric	craniofacial_abnormality|metabolic_disorder|genetic_disorder|developmental_disorder|neurodegenerative_disease	since__craniofacial_disorder__is_not_in_the_list__then_bone_disorder_would_be_a_more_accurate_choice___so__eye_disorder|skull_disorder__skull_disorder_is_implied_but_not_listed__can_be_replaced_with__craniofacial_disorder_which_is_also_not_listed__however_it_closely_resembles_the_first_part_of_the_given_disease_name|eye_disorder|bone_disorder	false	false	false	false	high
MONDO:0012007	scimitar anomaly, multiple cardiac malformations, and craniofacial and central nervous system abnormalities	hereditary_disease	other	hereditary_disease	genetics_and_genomics|cardiology|neurology|pediatric	cardiovascular_disorder	heart_disorder|brain_disorder	false	false	false	false	high
MONDO:0012008	Lelis syndrome	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	obstetrics_and_gynecology|genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder|liver_disorder	false	false	false	false	high
MONDO:0012011	coronary artery disease, autosomal dominant, 1	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	genetics_and_genomics|cardiology|renal_medicine	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0012012	Charcot-Marie-Tooth disease dominant intermediate C	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|orthopaedic	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0012013	Weill-Marchesani syndrome 2, dominant	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|ophthalmology|orthopaedic	metabolic_disorder|genetic_disorder|connective_tissue_disease	joint_disorder|eye_disorder	false	false	false	false	high
MONDO:0012014	Charcot-Marie-Tooth disease recessive intermediate A	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|orthopaedic	metabolic_disorder|neurodegenerative_disease|cardiovascular_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012015	nystagmus 3, congenital, autosomal dominant	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0012016	capillary malformation-arteriovenous malformation syndrome	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	genetics_and_genomics|dermatology|cardiology|pediatrics|hematology	inflammatory_disease|anemia|cardiovascular_disorder	vascular_disorder|skin_disorder	false	false	false	false	high
MONDO:0012019	spondyloepiphyseal dysplasia, Kimberley type	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012020	chromosome 22q11.2 microduplication syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	mental_health_disorder|metabolic_disorder|neurodevelopmental_disease|cardiovascular_disorder	immune_disorder|heart_disorder|brain_disorder|ear_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0012021	myopia 17, autosomal dominant	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	autosomal_dominant_disorders_is_not_in_the_list_but_metabolic_disorder_could_be_related_to_it_since_it_s_an_inherited_condition_affecting_the_body_s_metabolism|neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	true	medium
MONDO:0012022	orofacial cleft 4	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	otolaryngology|pediatric	autoimmune_diseases|neurodegenerative_disease	face_disorder|teeth_disorder	false	false	false	false	high
MONDO:0012023	autosomal dominant nonsyndromic hearing loss 49	auditory_system_disorder|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	hearing_loss|ear_disorder	false	false	false	true	medium
MONDO:0012024	retinitis pigmentosa 26	hereditary_disease|psychiatric_disorder|metabolic_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region|nervous_system_disorder|metabolic_disease|psychiatric_disorder	genetics_and_genomics|ophthalmology	retinal_disorder|eye_disease____replaced__retinitis_pigmentosa_26__with_the_correct_category__retinal_disorder___which_is_a_subset_of__eye_disease___removed_all_other_categories_as_they_don_t_fit|neurodegenerative_disease	lower_gastrointestinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0012025	branchiootic syndrome 3	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pulmonology|otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	throat_disorder|immune_disorder|ear_disorder	false	false	false	false	medium
MONDO:0012029	microcephaly 6, primary, autosomal recessive	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|ear_disorder	false	false	false	false	high
MONDO:0012030	autosomal dominant nonsyndromic hearing loss 43	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	otolaryngology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	throat_disorder|ear_disorder	false	false	false	false	medium
MONDO:0012031	platelet-type bleeding disorder 10	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0012032	Braddock syndrome	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder|brain_disorder|bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012033	bradyopsia	disorder_of_visual_system|hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0012034	autosomal dominant limb-girdle muscular dystrophy type 1F	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	neurology|orthopaedic|genetics_and_genomics	muscular_dystrophy|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012035	craniosynostosis-intracranial calcifications syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	other	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|bone_disorder|cranial_disorder	false	false	false	false	medium
MONDO:0012037	intellectual disability, autosomal recessive 3	metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012038	speech-sound disorder	hereditary_disease	other	hereditary_disease	neurology|otolaryngology	mental_health_disorder|neurodevelopmental_disorder	throat_disorder|ear_disorder	false	false	false	true	medium
MONDO:0012040	inflammatory bowel disease 9	digestive_system_disorder|immune_system_disorder|hereditary_disease	other	immune_system_disorder|digestive_system_disorder|hereditary_disease	gastroenterology|rheumatology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0012041	familial adenomatous polyposis 2	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	oncology|gastroenterology|genetics_and_genomics	genetic_disorder_is_implied_but_that_isn_t_in_the_list_so_i_used_the_closest_match|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012043	Reis-Bucklers corneal dystrophy	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder|bone_disorder	false	false	false	true	high
MONDO:0012044	corneal dystrophy, lattice type 3A	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0012045	myopia 5, autosomal dominant	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0012046	congenital corneal opacities, cornea guttata, and corectopia	otorhinolaryngologic_disease|auditory_system_disorder|hereditary_disease	other	otorhinolaryngologic_disease|auditory_system_disorder|hereditary_disease	pediatric|ophthalmology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0012047	alopecia universalis congenita, 10Y gonadal dysgenesis, and laryngomalacia	hereditary_disease	other	hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	reproductive_system_disorder|skin_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0012048	endogenous depression	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatry|neurology	mental_health_disorder|endogenous_depression	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0012049	orofaciodigital syndrome VII	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	other	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	teeth_disorder|ear_disorder	false	false	false	false	high
MONDO:0012051	periodontitis, aggressive, 2	inflammatory_disease|musculoskeletal_system_disorder	other	inflammatory_disease|musculoskeletal_system_disorder	hematology|rheumatology	autoimmune_diseases|inflammatory_disease	bone_disorder|immune_disorder|teeth_disorder	true	false	false	true	high
MONDO:0012052	ALG1-congenital disorder of glycosylation	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	congenital_disorder|metabolic_disorder	liver_disorder|genetic_disorder	false	false	false	false	very_high
MONDO:0012053	aneurysm, intracranial berry, 2	cardiovascular_disorder|hereditary_disease|nervous_system_disorder	cardiovascular_disorder	hereditary_disease|nervous_system_disorder|cardiovascular_disorder	cardiology|neurology|vascular	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012054	schizophrenia 12	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0012055	Larsen-like osseous dysplasia-short stature syndrome	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|skeletal_dysplasia|growth_disorder	skeletal_system_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0012056	Leber congenital amaurosis 9	psychiatric_disorder|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0012059	polydactyly, postaxial, type A4	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|congenital_anomaly|genetic_disorder|skeletal_abnormality	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0012060	autosomal recessive nonsyndromic hearing loss 35	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0012061	familial sick sinus syndrome	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiology|pediatric|genetics_and_genomics	familial_sick_sinus_syndrome_is_a_disorder_of_the_heart_s_sinus_node|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0012062	dilated cardiomyopathy 1O	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiology|cardiovascular	cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0012063	ulnar/fibula ray defect-brachydactyly syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	developmental_disorder|genetic_disorder|congenital_abnormality|metabolic_disorder	bone_disorder|joint_disorder|limb_disorder	false	false	false	false	medium
MONDO:0012064	choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	cardiology|pediatric|genetics_and_genomics|otolaryngology	cardiovascular_disorder|craniofacial_dysmorphism_syndrome_isn_t_directly_listed_so_we_ll_ignore_that_one	heart_disorder|craniofacial_dysmorphism_syndrome_is_not_an_exact_match_so_it_will_be_excluded|ear_disorder	false	false	false	true	very_high
MONDO:0012066	atrial fibrillation, familial, 1	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|hematology|genetics_and_genomics	familial|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0012068	brachial palsy, familial congenital	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0012069	keratoconus 3	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	pediatric|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	true	high
MONDO:0012071	congenital generalized lipodystrophy type 1	disorder_of_development_or_morphogenesis|metabolic_disease|integumentary_system_disorder|hereditary_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	skin_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0012072	familial partial lipodystrophy, Kobberling type	metabolic_disease|integumentary_system_disorder|hereditary_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	skin_disorder|endocrine_disorder	false	false	true	false	medium
MONDO:0012073	ribose-5-P isomerase deficiency	metabolic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease|metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	metabolic_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0012074	mandibuloacral dysplasia with type B lipodystrophy	disorder_of_development_or_morphogenesis|metabolic_disease|integumentary_system_disorder|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	dermatology|endocrinology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0012075	oligodontia-cancer predisposition syndrome	hereditary_disease	other	hereditary_disease	oncology|genetics_and_genomics	cancer|genetic_disorder	cancer_predisposition_syndrome|teeth_disorder	false	false	false	false	high
MONDO:0012076	midface hypoplasia, obesity, developmental delay, and neonatal hypotonia	hereditary_disease	other	hereditary_disease	pediatric|endocrinology|genetics_and_genomics	metabolic_disorder|developmental_delay_is_associated_with__metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|developmental_delay|muscle_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0012077	amyotrophic lateral sclerosis type 8	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0012078	Joubert syndrome 3	disorder_of_development_or_morphogenesis|syndromic_disease|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	syndromic_disease|hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0012080	neuronopathy, distal hereditary motor, type 2B	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	hereditary_condition|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0012081	15q11q13 microduplication syndrome	chromosomal_disorder	other	chromosomal_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	developmental_disorder___note__i_replaced_the_original_category_with_a_more_specific_term_that_is_commonly_associated_with_this_disease|brain_disorder	false	false	false	false	high
MONDO:0012083	autosomal dominant nonsyndromic hearing loss 28	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	pediatric|genetics_and_genomics|otolaryngology	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	bone_disorder|ear_disorder	false	false	false	true	medium
MONDO:0012084	aromatic L-amino acid decarboxylase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	metabolic|neurology|pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0012085	primary ciliary dyskinesia 3	respiratory_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|respiratory_system_disorder	pulmonology|neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease	eye_disorder|brain_disorder|lung_disorder|kidney_disorder|joint_disorder|immune_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012086	autosomal dominant nonsyndromic hearing loss 31	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	pediatric|genetics_and_genomics|otolaryngology	autosomal_dominant_disorder|neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	high
MONDO:0012087	primary ciliary dyskinesia 4	respiratory_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|respiratory_system_disorder	pulmonology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012088	primary ciliary dyskinesia 5	respiratory_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|respiratory_system_disorder	pulmonology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder|kidney_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012089	ichthyosis prematurity syndrome	inflammatory_disease|respiratory_system_disorder|integumentary_system_disorder|syndromic_disease|hereditary_disease	other	integumentary_system_disorder|syndromic_disease|hereditary_disease|inflammatory_disease|respiratory_system_disorder	dermatology|pediatric	congenital_disorder|metabolic_disorder	skin_disorder|liver_disorder	false	false	false	false	medium
MONDO:0012090	autosomal dominant nonsyndromic hearing loss 47	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0012091	autosomal recessive nonsyndromic hearing loss 32	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	pediatrics|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0012092	hereditary sensory and autonomic neuropathy type 5	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease	nerve_disorder|muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0012093	prostate cancer, hereditary, 3	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	reproductive_system_disorder|hereditary_disease|cancer_or_benign_tumor	oncology|urology|genetics_and_genomics	cancer|hereditary	reproductive_system_disorder|hereditary	false	true	false	true	high
MONDO:0012094	prostate cancer, hereditary, 4	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	reproductive_system_disorder|hereditary_disease|cancer_or_benign_tumor	oncology|urology|genetics_and_genomics	cancer|hereditary	reproductive_system_disorder|hereditary	false	true	false	true	high
MONDO:0012095	intellectual disability-brachydactyly-Pierre Robin syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|upper_gastrointestinal_disorder|joint_disorder|ear_disorder	false	false	false	false	high
MONDO:0012096	Charcot-Marie-Tooth disease axonal type 2L	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	axonal_type_disease|neurodegenerative_disease	nerve_disorder|muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0012097	spondylocostal dysostosis 2, autosomal recessive	disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012098	spinocerebellar ataxia type 20	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	spinal_cord_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0012099	AICA-ribosiduria	disorder_of_development_or_morphogenesis|metabolic_disease|psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder|metabolic_disease	disorder_of_development_or_morphogenesis|psychiatric_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	very_high
MONDO:0012101	glaucoma 1, open angle, J	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	urology|pediatric|neurology|renal_medicine|ophthalmology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	eye_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0012102	glaucoma 1, open angle, K	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|eye_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0012103	spinocerebellar ataxia type 25	hereditary_disease|psychiatric_disorder|nervous_system_disorder	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012104	acquired partial lipodystrophy	integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease	endocrinology|dermatology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|skin_disorder	false	false	true	false	medium
MONDO:0012105	granulomatosis with polyangiitis	inflammatory_disease|urinary_system_disorder|cardiovascular_disorder|immune_system_disorder	cardiovascular_disorder	urinary_system_disorder|immune_system_disorder|cardiovascular_disorder|inflammatory_disease	hematoloy|rheumatology|pulmonology|renal_medicine	autoimmune_diseases|inflammatory_disease	vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0012106	microcephaly 5, primary, autosomal recessive	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0012107	neuropathy, hereditary sensory and autonomic, adult-onset, with anosmia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	hereditary|metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|nose_disorder	false	false	false	false	medium
MONDO:0012108	spondyloepimetaphyseal dysplasia, matrilin-3 type	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|pediatric|rheumatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0012110	growth delay due to insulin-like growth factor type 1 deficiency	hereditary_disease|endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|hereditary_disease	endocrinology|pediatric|genetics_and_genomics	anemia|autoimmune_diseases|metabolic_disorder	endocrine_disorder_bone_disorder	false	false	false	true	very_high
MONDO:0012111	hypertrophic cardiomyopathy 8	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	pediatric|pulmonology|genetics_and_genomics|cardiology|cardiothoracic	autoimmune_diseases|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0012112	hypertrophic cardiomyopathy 10	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	pediatric|cardiovascular_medicine_subcategory_would_be_cardiology|genetics_and_genomics|cardiology|cardiothoracic	cardiomyopathy|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0012114	Ehlers-Danlos syndrome, Beasley-Cohen type	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	joint_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012116	spinocerebellar ataxia type 8	hereditary_disease|psychiatric_disorder|nervous_system_disorder	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	cardiovascular_disorder|autoimmune_diseases|neurodegenerative_disease|adrenal_gland_disease|mental_health_disorder|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012117	ALG9-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	congenital_disorder_of_glycosylation|metabolic_disorder	liver_disorder|congenital_disorder_of_glycosylation_is_a_category_that_often_includes_liver_disorder_so_it_s_probably_included_here_as_well	false	false	true	true	very_high
MONDO:0012118	COG7-congenital disorder of glycosylation	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	congenital_disorder_of_glycosylation|metabolic_disorder	kidney_disorder|liver_disorder	false	false	true	false	very_high
MONDO:0012120	pyruvate dehydrogenase phosphatase deficiency	nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	metabolic_disease	nervous_system_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	pediatric|endocrinology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	mitochondrial_disorder_is_not_in_the_list_but_muscle_disorder_is_a_good_fit|muscle_disorder	false	false	false	false	high
MONDO:0012121	otosclerosis 5	auditory_system_disorder|otorhinolaryngologic_disease|hereditary_disease	other	auditory_system_disorder|otorhinolaryngologic_disease|hereditary_disease	pediatric|otosclerosis_is_related_to_the_ear|otolaryngology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	ear_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0012122	moyamoya disease 3	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	pediatric|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012123	congenital disorder of glycosylation type 1E	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|congenital_disease	liver_disorder|endocrine_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0012124	sudden infant death-dysgenesis of the testes syndrome	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis|respiratory_system_disorder|hereditary_disease	endocrine_system_disorder	respiratory_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|reproductive_system_disorder	pediatric|urology|genetics_and_genomics	metabolic_disorder|congenital_abnormality	reproductive_system_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0012125	hypomyelinating leukodystrophy 2	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0012126	familial avascular necrosis of femoral head	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|hematolog	familial_disease|cardiovascular_disorder|metabolic_disorder	vascular_disorder|bone_disorder	false	false	false	false	high
MONDO:0012127	autosomal recessive limb-girdle muscular dystrophy type 2J	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|neurology	muscular_dystrophy|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012129	leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema	hereditary_disease	other	hereditary_disease	immunology|rheumatology|gastroenterology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|blood_bone_marrow_disorder|lower_gastrointestinal_disorder|immune_disorder	true	false	false	false	very_high
MONDO:0012130	myofibrillar myopathy 2	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	myofibrillar_myopathy|muscle_disorder	false	false	false	false	high
MONDO:0012131	metaphyseal undermodeling, spondylar dysplasia, and overgrowth	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|rheumatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder|anemia	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0012132	colorectal cancer, susceptibility to, 1	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	hematology|gastroenterology|genetics_and_genomics|oncology	inflammatory_disease|autoimmune_diseases|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0012133	lateral semicircular canal malformation, familial, with external and middle ear abnormalities	hereditary_disease	other	hereditary_disease	otolaryngology|genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0012136	carnitine palmitoyl transferase II deficiency, neonatal form	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatrics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	liver_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0012137	Carney complex - trismus - pseudocamptodactyly syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|dermatology|genetics_and_genomics	cardiovascular_disorder|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	joint_disorder|eye_disorder|throat_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012138	muscular dystrophy-dystroglycanopathy type B6	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0012139	macular dystrophy, retinal, 3	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	retina|eye_disorder	false	false	false	false	medium
MONDO:0012142	orofacial cleft 5	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|otolaryngology	neurodevelopmental_disorder|congenital_abnormality|birth_defect	lower_gastrointestinal_disorder|ear_disorder|teeth_disorder|spinal_disorder|eye_disorder|throat_disorder|muscle_disorder|reproductive_system_disorder|nose_disorder|bone_disorder|upper_gastrointestinal_disorder|immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0012143	hereditary cryohydrocytosis with reduced stomatin	hematologic_disorder|psychiatric_disorder|nervous_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease	psychiatric_disorder|metabolic_disease|anemia	nervous_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease|hematologic_disorder|psychiatric_disorder	genetics_and_genomics|cardiology|pediatrics	hereditary_disease____there_is_no_exact_match_in_the_list__this_answer_represents_the_best_fit_for_the_given_disease|metabolic_disorder	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0012144	Waardenburg syndrome type 2D	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	ear_disorder|spinal_disorder|nerve_disorder|developmental_disorder	false	false	false	false	medium
MONDO:0012145	macular degeneration, age-related, 3	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region|hereditary_disease|psychiatric_disorder	neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0012146	familial hemophagocytic lymphohistiocytosis 3	syndromic_disease|immune_system_disorder|hereditary_disease	other	immune_system_disorder|syndromic_disease|hereditary_disease	hematology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|anemia	vascular_disorder|blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0012154	myopia 6	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	pediatric|ophthalmology	metabolic_disorder	eye_disorder	false	false	false	true	low
MONDO:0012155	choanal atresia	respiratory_system_disorder|otorhinolaryngologic_disease|hereditary_disease	other	respiratory_system_disorder|otorhinolaryngologic_disease|hereditary_disease	pediatric|otolaryngology	neonatal_diseases|congenital_diseases|respiratory_disorders	throat_disorder|nose_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0012156	myasthenic syndrome, congenital, 1B, fast-channel	nervous_system_disorder|syndromic_disease|hereditary_disease	other	nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder|immune_disorder	false	false	false	true	high
MONDO:0012157	congenital myasthenic syndrome 4C	nervous_system_disorder|syndromic_disease|hereditary_disease	other	nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0012158	keratoconus 2	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	optometry|eye_genetics|ocular_genetics|ophthalmic_genetics|opthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	true	high
MONDO:0012159	lung cancer susceptibility 1	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|pulmonology|oncology	autoimmune_diseases|cancer|allergy	lung_disorder|immune_disorder	false	true	false	false	very_high
MONDO:0012160	spondylometaphyseal dysplasia-cone-rod dystrophy syndrome	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|eye_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0012162	patterned macular dystrophy 2	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region|hereditary_disease|psychiatric_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0012163	immunodeficiency 104	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	immunology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|immunodeficiency	lymphatic_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0012164	Meacham syndrome	hereditary_disease|syndromic_disease|endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|syndromic_disease|hereditary_disease	neurology|pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	lymphatic_disorder|bone_disorder|skeletal_disorder_is_incorrect__the_correct_answer_is__bone_disorder	false	false	false	false	high
MONDO:0012165	BNAR syndrome	hereditary_disease|otorhinolaryngologic_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|otorhinolaryngologic_disease	obstetrics_and_gynecology|neurology|cardiology|psychiatry|pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	vascular_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012166	autosomal dominant sensory ataxia 1	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012167	atrial fibrillation, familial, 2	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	cardiology|genetics_and_genomics|hematology	cardiovascular_disorder|familial	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0012169	premature ovarian failure 3	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	obstetrics_and_gynecology|endocrinology	metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0012170	autosomal recessive nonsyndromic hearing loss 36	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	high
MONDO:0012171	marfanoid habitus with situs inversus	hereditary_disease	other	hereditary_disease	cardiology|orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder|inflammatory_disease	vascular_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012172	mitochondrial trifunctional protein deficiency	hereditary_disease|metabolic_disease|musculoskeletal_system_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|musculoskeletal_system_disorder|hereditary_disease	hepatology|pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0012173	long chain 3-hydroxyacyl-CoA dehydrogenase deficiency	hereditary_disease|nervous_system_disorder|cardiovascular_disorder|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|metabolic_disease|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0012174	peripheral cone dystrophy	hereditary_disease	other	hereditary_disease	neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0012175	cataract 28	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	true	medium
MONDO:0012176	Emanuel syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	endocrine_disorder	false	false	false	false	very_high
MONDO:0012177	posterior column ataxia-retinitis pigmentosa syndrome	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	neurology|ophthalmology|genetics_and_genomics	neurodegenerative_disease|retinitis_pigmentosa_syndrome	brain_disorder|spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0012178	intellectual disability with optic atrophy, facial dysmorphism, microcephaly, and short stature	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0012179	narcolepsy 3	nervous_system_disorder|hereditary_disease	other	sleep_disorder|nervous_system_disorder|hereditary_disease	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0012180	arrhythmogenic right ventricular dysplasia 9	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiology|cardiothoracic|pediatric|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0012181	hereditary spastic paraplegia 27	hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012182	skeletal dysplasia, rhizomelic, with retinitis pigmentosa	hereditary_disease	other	hereditary_disease	ophthalmology|orthopaedic|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|eye_disorder	false	false	false	false	high
MONDO:0012183	melanoma, cutaneous malignant, susceptibility to, 3	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	dermatology|oncology	melanoma|cancer|susceptibility_to|cutaneous_malignant|disease	skin_disorder|cutaneous_malignant	false	true	false	true	high
MONDO:0012184	Pierson syndrome	hereditary_disease|syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|syndromic_disease|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	liver_disorder|eye_disorder	false	false	false	false	high
MONDO:0012185	spondylometaphyseal dysplasia, A4 type	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	rheumatology|orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012186	Fanconi anemia complementation group I	hereditary_disease|hematologic_disorder|metabolic_disease|musculoskeletal_system_disorder|immune_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease|anemia	disorder_of_development_or_morphogenesis|hematologic_disorder|immune_system_disorder|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0012187	Fanconi anemia complementation group J	hereditary_disease|hematologic_disorder|metabolic_disease|musculoskeletal_system_disorder|immune_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease|anemia	disorder_of_development_or_morphogenesis|hematologic_disorder|immune_system_disorder|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0012188	neuronal ceroid lipofuscinosis 9	hereditary_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease	metabolic_disease|neurodegenerative_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0012190	epidermolysis bullosa simplex 7, with nephropathy and deafness	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	ear_disorder|skin_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0012191	hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	neurology|genetics_and_genomics|pediatrics|hepatology|gastroenterology	metabolic_disorder|neurodegenerative_disease|hepatic_disease	brain_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0012192	permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome	hereditary_disease|nervous_system_disorder|metabolic_disease|digestive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease|endocrine_system_disorder|diabetes_mellitus	disorder_of_development_or_morphogenesis|endocrine_system_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease|digestive_system_disorder	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|endocrine_disorder	false	false	true	false	very_high
MONDO:0012193	autosomal dominant limb-girdle muscular dystrophy type 1G	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	neurology|orthopaedic|genetics_and_genomics	neurodegenerative_disease|muscular_dystrophy	muscle_disorder|spinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0012194	aneurysm, intracranial berry, 3	hereditary_disease|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|hereditary_disease	neurology|vascular_medicine	neurodegenerative_disease|cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012195	arthrogryposis-severe scoliosis syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	neurology|orthopaedic|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0012196	autosomal dominant auditory neuropathy 1	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0012197	idiopathic aplastic anemia	hematologic_disorder	anemia	idiopathic_disease|hematologic_disorder	allergy_and_immunology|genetics_and_genomics|hematology	anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0012198	PCWH syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0012199	posterior polymorphous corneal dystrophy 2	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0012200	posterior polymorphous corneal dystrophy 3	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|ophthalmology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0012203	familial hyperthyroidism due to mutations in TSH receptor	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder	thyroid_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0012204	familial pseudohyperkalemia	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	genetics_and_genomics|renal_medicine	metabolic_disorder|familial_adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0012205	autosomal dominant striatal neurodegeneration type 1	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	autosomal_dominant_disorder_is_not_in_the_list_but_this_one_is_closest_match___autosomal_dominant_disorder_s_most_closely_related_category_is_neurodegenerative_disease|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0012206	spondyloepiphyseal dysplasia with metatarsal shortening	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|connective_tissue_disorder|musculoskeletal_system_disorder	other	connective_tissue_disorder|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|rheumatology|pediatric	genetic_disease|metabolic_disorder	joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012207	umbilicus, familial flat	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology|pediatric	skin_condition|genetic_disorder|neurodegenerative_disease|congenital_abnormality	lower_gastrointestinal_disorder|skin_disorder	false	false	false	false	none
MONDO:0012208	congenital reticular ichthyosiform erythroderma	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|hematology|dermatology|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0012209	branchiogenic deafness syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|otolaryngology|pediatric	autoimmune_diseases|neurodegenerative_disease	throat_disorder|ear_disorder	false	false	false	false	high
MONDO:0012211	MPDU1-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	congenital_disorder_of_glycosylation_is_often_a_part_of_the_broader_category_of_metabolic_disorders|metabolic_disorder	liver_disorder	false	false	true	false	high
MONDO:0012212	Loeys-Dietz syndrome 1	syndromic_disease|hereditary_disease|cardiovascular_disorder|connective_tissue_disorder	cardiovascular_disorder	hereditary_disease|connective_tissue_disorder|syndromic_disease|cardiovascular_disorder	pediatric|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0012213	hereditary spastic paraplegia 26	syndromic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012214	glucocorticoid deficiency 3	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	endocrinology|pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0012215	myofibrillar myopathy 3	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	neurology|orthopaedic	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	muscle_disorder	false	false	false	false	high
MONDO:0012216	foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome	syndromic_disease|hereditary_disease|disorder_of_visual_system|metabolic_disease	metabolic_disease	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology|ophthalmology	optic_nerve_deciassation_defect|neurodegenerative_disease|inflammatory_disease|metabolic_disorder|anterior_segment_dysgenesis_syndrome__neurodegenerative_disease	brain_disorder|eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012217	Bruck syndrome 2	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	joint_disorder|blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0012218	dandy-walker malformation with occipital cephalocele, autosomal dominant	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autosomal_dominant_is_a_type_of_genetic_disorder_which_can_be_related_to_the_following____neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012219	spondyloepiphyseal dysplasia tarda, autosomal recessive, Leroy-Spranger type	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|rheumatology|orthopaedic	neurodegenerative_disease|metabolic_disorder	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0012220	Griscelli syndrome type 3	syndromic_disease|hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease	hereditary_disease|integumentary_system_disorder|metabolic_disease|syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0012221	alpha-N-acetylgalactosaminidase deficiency type 1	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0012222	alpha-N-acetylgalactosaminidase deficiency type 2	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	metabolic_disorder|liver_disorder|genetic_disorder	false	false	false	false	medium
MONDO:0012223	hypotrichosis, progressive patterned scalp, with wiry hair, onycholysis, and cleft lip/palate	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|dermatology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	birth_defect|skin_disorder|hair_and_nail_disorder	false	false	false	false	medium
MONDO:0012224	febrile seizures, familial, 6	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	true	medium
MONDO:0012225	Senior-Loken syndrome 5	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	neurology|psychiatry	neurodegenerative_disease|metabolic_disorder	lower_gastrointestinal_disorder|kidney_disorder	false	false	false	false	high
MONDO:0012226	febrile seizures, familial, 5	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	immune_disorder|brain_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0012227	myopia 7	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0012228	myopia 8	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|neurology|ophthalmology	cardiovascular_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0012229	myopia 9	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0012230	myopia 10	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0012231	Charcot-Marie-Tooth disease type 2A2	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder	nerve_disorder_would_be_a_correct_categorization_but_is_not_listed_so__spinal_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012232	stuttering, familial persistent, 2	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|throat_disorder	false	false	false	false	medium
MONDO:0012235	autosomal recessive spinocerebellar ataxia 7	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder_spinal_disorder	false	false	false	false	medium
MONDO:0012236	keratoconus 4	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology	autoimmune_diseases|allergy|inflammatory_disease	eye_disorder|teeth_disorder	false	false	false	false	high
MONDO:0012237	nemaline myopathy 6	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012238	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|mitochondrial_disease|metabolic_disease	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012239	congenital myopathy 4B, autosomal recessive	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012240	congenital myopathy 23	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	congenital_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012241	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|musculoskeletal_system_disorder|mitochondrial_disease|metabolic_disease	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012242	syncope, familial vasovagal	hereditary_disease	other	hereditary_disease	neurology|cardiology	vasovagal|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	low
MONDO:0012243	B-cell immunodeficiency, distal limb anomalies, and urogenital malformations	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	immunology|pediatric|genetics_and_genomics	autoimmune_diseases|immunodeficiency	immune_disorder|reproductive_system_disorder|urinary_tract_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0012244	prostate cancer, hereditary, 5	hereditary_disease|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|reproductive_system_disorder	oncology|genetics_and_genomics|urology	hereditary|cancer	hereditary___note__hereditary_is_a_trait__but_the_best_fitting_category_for_prostate_cancer_is_reproductive_system_disorder_as_it_affects_the_male_reproductive_system|reproductive_system_disorder	false	true	false	true	high
MONDO:0012245	developmental and epileptic encephalopathy, 3	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	epileptic_disorder|neurodegenerative_disease|developmental_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0012246	spinocerebellar ataxia type 26	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0012247	spinocerebellar ataxia type 27	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012248	autosomal recessive limb-girdle muscular dystrophy type 2K	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|metabolic_disease	genetics_and_genomics|neurology	muscular_dystrophy|neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012249	Lynch syndrome 2	digestive_system_disorder|syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|digestive_system_disorder|cancer_or_benign_tumor|syndromic_disease	oncology|genetics_and_genomics	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0012250	Charcot-Marie-Tooth disease type 4H	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	nerve_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012251	MEDNIK syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|integumentary_system_disorder|metabolic_disease|syndromic_disease	immunology|genetics_and_genomics|pediatrics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0012252	rhabdoid tumor predisposition syndrome 1	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	oncology|pediatric|genetics_and_genomics	neurodegenerative_disease|genetic_disorder_is_not_in_the_list_but_would_be_a_more_accurate_categorization_than_other_if_it_were_included|cancer	kidney_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0012253	multiple epiphyseal dysplasia, with severe proximal femoral dysplasia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics	metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0012254	multiple epiphyseal dysplasia, with miniepiphyses	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	spinal_disorder|joint_disorder|bone_disorder|skeletal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0012255	chromosome 18 pericentric inversion	hereditary_disease|chromosomal_disorder	other	hereditary_disease|chromosomal_disorder	genetics_and_genomics	neurodegenerative_disease|genetic_disorder	chromosome_disorder|bone_disorder	false	false	false	false	medium
MONDO:0012256	hereditary spastic paraplegia 28	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0012257	Cerebrorenodigital syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0012258	epidermolysis bullosa simplex 2E, with migratory circinate erythema	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	anemia|autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0012259	colloid cysts of third ventricle	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|cancer	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0012260	cataract 35	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0012262	fibrosis of extraocular muscles, congenital, 3c	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_visual_system|musculoskeletal_system_disorder|disorder_of_orbital_region|nervous_system_disorder	pediatric|genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0012264	preeclampsia/eclampsia 2	hereditary_disease|obstetric_disorder|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|obstetric_disorder|cardiovascular_disorder	obstetrics_and_gynecology	metabolic_disorder|inflammatory_disease	kidney_disorder|reproductive_system_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012265	preeclampsia/eclampsia 3	hereditary_disease|obstetric_disorder|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|obstetric_disorder|cardiovascular_disorder	obstetrics_and_gynecology	cardiovascular_disorder|metabolic_disorder	kidney_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012266	preeclampsia/eclampsia 4	hereditary_disease|obstetric_disorder|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|obstetric_disorder|cardiovascular_disorder	pediatric|obstetrics_and_gynecology	autoimmune_diseases|cardiovascular_disorder|metabolic_disorder|inflammatory_disease	kidney_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0012267	holoprosencephaly 8	hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|syndromic_disease|nervous_system_disorder	endocrine_system_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|endocrine_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0012268	AIDS	hereditary_disease|reproductive_system_disorder|infectious_disease|immune_system_disorder	infectious_disease	hereditary_disease|infectious_disease|immune_system_disorder|reproductive_system_disorder	immunology|genetics_and_genomics|hematology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|lymphatic_disorder	true	false	false	true	very_high
MONDO:0012269	chromosome 3q29 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|developmental_disorder	false	false	false	false	high
MONDO:0012270	Tukel syndrome	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_visual_system|musculoskeletal_system_disorder|disorder_of_orbital_region|nervous_system_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0012271	mesoaxial synostotic syndactyly with phalangeal reduction	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|congenital_abnormality|musculoskeletal_disorder	joint_disorder|bone_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0012272	intellectual disability, keratoconus, febrile seizures, and sinoatrial block	hereditary_disease	other	hereditary_disease	neurology_pediatric__cardiology|neurology__ophthalmology	neurodegenerative_disease|other___note__intellectual_disability_is_generally_classified_under_neurodevelopmental_disorders__but_i_have_used_the_closest_match_available_in_the_given_list____keratoconus___metabolic_disorder_febrile_seizures___neurodegenerative_disease__sinoatrial_block___cardiovascular_disorder	eye_disorder|brain_disorder|heart_disorder	false	false	false	false	medium
MONDO:0012273	autosomal recessive nonsyndromic hearing loss 48	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	hearing_loss|ear_disorder	false	false	false	true	medium
MONDO:0012274	acromesomelic dysplasia 3	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	genetic_disorder_is_not_in_the_list_so_removing_it_leaving_us_with__metabolic_disorder|neurodegenerative_disease____neurodegenerative_disease|neurodegenerative_disease|metabolic_disorder	spinal_disorder|joint_disorder|bone_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0012275	fetal valproate syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology|obstetrics_and_gynecology	metabolic_disorder|congenital_abnormality|developmental_disorder	brain_disorder|joint_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0012276	generalized epilepsy-paroxysmal dyskinesia syndrome	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012277	myofibrillar myopathy 4	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	myofibrillar_myopathy|muscle_disorder	false	false	false	false	medium
MONDO:0012278	supranuclear palsy, progressive, 2	hereditary_disease|syndromic_disease|disorder_of_visual_system|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|progressive	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012280	Goldberg-Shprintzen syndrome	digestive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|digestive_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	lymphatic_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0012282	Al-Gazali syndrome	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|lymphatic_disorder|brain_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0012283	cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss	hereditary_disease	other	hereditary_disease	otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|developmental_disorder	ear_disorder|bone_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0012284	nephropathy, progressive, with deafness	hereditary_disease	other	hereditary_disease	renal_medicine|otolaryngology|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	kidney_disorder|urinary_tract_disorder	true	false	false	true	high
MONDO:0012285	left ventricular noncompaction 2	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder|syndromic_disease	cardiothoracic|cardiology	cardiovascular_disorder|cardiac_disease|cardiovascular_disease	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0012286	myopathy, autophagic vacuolar, infantile-onset	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0012287	Stickler syndrome, type I, nonsyndromic ocular	hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|syndromic_disease|nervous_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system|musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|disorder_of_orbital_region|syndromic_disease	pediatric|genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0012288	iridogoniodysgenesis and skeletal anomalies	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	genetic_disorder|metabolic_disorder|skeletal_anomalies	eye_disorder|bone_disorder	false	false	false	false	low
MONDO:0012289	myofibrillar myopathy 5	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	neurology|rheumatology|muscular_diseases	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	muscle_disorder	false	false	false	false	high
MONDO:0012290	CEDNIK syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|integumentary_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	immune_disorder|brain_disorder|blood_bone_marrow_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0012291	immunoglobulin A deficiency 2	hereditary_disease|hematologic_disorder|immune_system_disorder	other	hereditary_disease|hematologic_disorder|immune_system_disorder	immunology|hematology|rheumatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0012293	autosomal recessive nonsyndromic hearing loss 23	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0012295	complement component 5 deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	immunology|hematology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0012296	lipomyelomeningocele	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology|obstetrics_and_gynecology	neurological_condition|cancer	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0012297	spastic paraplegia, optic atropy, and neuropathy	nervous_system_disorder|hereditary_disease|syndromic_disease	neurodegenerative_disease	nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0012298	omphalocele, diaphragmatic hernia, and radial ray defects	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	autoimmune_diseases|radial_ray_defects|inflammatory_disease|cardiovascular_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0012299	nanophthalmos 2	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0012300	prostate cancer, hereditary, 6	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	urology|oncology|genetics_and_genomics	hereditary|cancer	reproductive_system_disorder|hereditary	false	true	false	true	high
MONDO:0012301	mitochondrial DNA depletion syndrome, myopathic form	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	neurology|myopathic_form_suggests_orthopaedic_but_it_is_not_the_best_fit|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	mitochondrial_disease|muscle_disorder	false	false	false	true	very_high
MONDO:0012302	parietal foramina 3	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurology	neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0012304	photoparoxysmal response 2	hereditary_disease|nervous_system_disorder	other	hereditary_disease|radiation_induced_disorder|nervous_system_disorder	neurology|ophthalmology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0012305	photoparoxysmal response 3	hereditary_disease|nervous_system_disorder	other	hereditary_disease|radiation_induced_disorder|nervous_system_disorder	neurology|ophthalmology	photoparoxysmal_response_can_be_related_to_neurodegenerative_disease__photosensitive_epilepsy__and_autoimmune_diseases|neurodegenerative_disease|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0012306	cardiomyopathy, familial restrictive, 2	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiology|pulmonology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012307	familial scaphocephaly syndrome, McGillivray type	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0012308	Joubert syndrome with renal defect	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|renal_medicine|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|renal_defect|kidney_disorder	false	false	false	false	high
MONDO:0012309	parietal foramina 2	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0012310	fibrosis of extraocular muscles, congenital, with synergistic divergence	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	pediatric|ophthalmology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0012311	spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctate calcifications, and deafness	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	genetic_disorder|metabolic_disorder	spinal_disorder|bone_disorder|ear_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0012312	short QT syndrome type 1	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0012313	short QT syndrome type 2	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	heart_disorder|cardiovascular_disorder	false	false	false	true	high
MONDO:0012314	short QT syndrome type 3	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	heart_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0012315	distal 10q deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	neurology|pediatric|genetics_and_genomics|medical_genetics|developmental_disorders	neurodegenerative_disease|metabolic_disorder	brain_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0012316	Majeed syndrome	hematologic_disorder|immune_system_disorder|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|connective_tissue_disorder	other	immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder|syndromic_disease|hematologic_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|liver_disorder|joint_disorder|eye_disorder	false	false	false	false	high
MONDO:0012317	visceral neuropathy, familial, 3, autosomal dominant	digestive_system_disorder	other	digestive_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0012318	leukemia, chronic lymphocytic, susceptibility to, 1	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	hematology|oncology|genetics_and_genomics	autoimmune_diseases|cancer|allergy	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	high
MONDO:0012319	major affective disorder 3	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatry|neurology	mental_health_disorder|major_affective_disorder	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0012320	migraine, familial hemiplegic, 3	nervous_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|familial_hemiplegic_migraine_is_sometimes_classified_as_a_neurodegenerative_disorder_because_it_involves_progressive_degeneration_of_brain_cells__but_it_is_more_accurately_described_as_a_distinct_subtype_of_migraine_with_specific_genetic_mutations	brain_disorder|spinal_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0012321	Alzheimer disease 10	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	very_high
MONDO:0012322	holoprosencephaly 5	endocrine_system_disorder|syndromic_disease|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease|syndromic_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0012323	lethal acantholytic epidermolysis bullosa	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	false	very_high
MONDO:0012324	Frias syndrome	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0012325	Nguyen syndrome	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	brain_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0012326	autosomal recessive nonsyndromic hearing loss 42	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|anemia|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0012327	autosomal recessive nonsyndromic hearing loss 46	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|otolaryngology	genetic_disorder|neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0012328	trichilemmal cyst	hereditary_disease	other	hereditary_disease	dermatology	dermatological_condition|skin_condition	reproductive_system_disorder|skin_disorder	false	false	false	false	low
MONDO:0012329	short stature and Facioauriculothoracic malformations	hereditary_disease	other	hereditary_disease	pediatric|endocrinology|genetics_and_genomics	developmental_disorder|congenital_abnormality|genetic_condition|birth_defect|metabolic_disorder|skeletal_abnormality	musculoskeletal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0012330	talo-patello-scaphoid osteolysis	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	rheumatology|orthopaedic	autoimmune_diseases|metabolic_disorder|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	none
MONDO:0012333	autosomal recessive nonsyndromic hearing loss 53	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0012334	hereditary spastic paraplegia 29	syndromic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|syndromic_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|hereditary|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012335	obesity due to pro-opiomelanocortin deficiency	endocrine_system_disorder|hereditary_disease|nutritional_disorder	endocrine_system_disorder	nutritional_disorder|endocrine_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics	metabolic_disorder	endocrine_disorder	false	false	false	true	very_high
MONDO:0012336	cataract 22 multiple types	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	eye_disorder	false	false	false	true	medium
MONDO:0012342	7q11.23 microduplication syndrome	hereditary_disease|chromosomal_disorder	other	chromosomal_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	brain_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|immune_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0012343	aortic aneurysm, familial abdominal, 2	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	genetics_and_genomics|cardiology|cardiovascular	familial_abdominal_aortic_anneurysm|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012344	Alzheimer disease 11	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0012345	acral peeling skin syndrome	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0012346	generalized epilepsy with febrile seizures plus, type 4	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0012347	hamartoma, Precalcaneal congenital fibrolipomatous	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic	congenital_fibrolipomatous|cardiovascular_disorder	muscle_disorder|skin_disorder	false	false	false	false	low
MONDO:0012348	maturity-onset diabetes of the young type 8	metabolic_disease|hereditary_disease|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|diabetes_mellitus|metabolic_disease	endocrine_system_disorder|metabolic_disease|hereditary_disease|digestive_system_disorder	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|blood_bone_marrow_disorder	false	false	true	true	high
MONDO:0012349	spondylocostal dysostosis 3, autosomal recessive	metabolic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012350	complement factor H deficiency	hereditary_disease|inflammatory_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder|inflammatory_disease	immunology|hematology	inflammatory_disease|autoimmune_diseases	immune_disorder|kidney_disorder	false	false	false	true	high
MONDO:0012351	zygodactyly type 1	musculoskeletal_system_disorder|hereditary_disease|chromosomal_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|chromosomal_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0012352	vasculitis, lymphocytic, cutaneous small vessel	hereditary_disease	other	hereditary_disease	hematology|dermatology|rheumatology	cutaneous_disease|inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder|vascular_disorder|lymphatic_disorder	false	false	false	true	medium
MONDO:0012353	erythrocytosis, familial, 3	musculoskeletal_system_disorder|hereditary_disease|hematologic_disorder|immune_system_disorder	other	hereditary_disease|hematologic_disorder|immune_system_disorder|musculoskeletal_system_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	erythropoietic_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0012354	platelet-type bleeding disorder 8	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|pediatric|hematology	bleeding_disorder|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0012355	autosomal recessive nonsyndromic hearing loss 28	auditory_system_disorder|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	genetics_and_genomics|pediatric|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	high
MONDO:0012359	combined immunodeficiency due to partial RAG1 deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|pediatric|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0012360	congenital nongoitrous hypothyroidism 3	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	pediatric|endocrinology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0012362	dilated cardiomyopathy 1P	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiothoracic|pulmonology|cardiology	cardiomyopathy_is_a_subset_of_this_category|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012363	retinitis pigmentosa 32	disorder_of_visual_system|metabolic_disease|nervous_system_disorder|hereditary_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0012364	dilated cardiomyopathy 1Q	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiothoracic|pulmonology|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012365	gallbladder disease 2	digestive_system_disorder|hereditary_disease	other	hereditary_disease|digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	biliary_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0012366	gallbladder disease 3	digestive_system_disorder|hereditary_disease	other	hereditary_disease|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|metabolic_disorder	biliary_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0012367	retinitis pigmentosa 31	disorder_of_visual_system|metabolic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	neurology|ophthalmology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0012368	aminoacylase 1 deficiency	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0012370	autosomal recessive nonsyndromic hearing loss 51	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	ear_disorder	false	false	false	true	medium
MONDO:0012371	Noonan syndrome 3	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|immune_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|immune_system_disorder|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	heart_disorder	false	false	false	false	medium
MONDO:0012373	ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features	hereditary_disease	other	hereditary_disease	neurology|pediatric|otolaryngology|dermatology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	skin_disorder|teeth_disorder|ear_disorder	false	false	false	false	high
MONDO:0012374	brachyphalangy, polydactyly, and tibial aplasia/hypoplasia	hereditary_disease	other	hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0012375	autosomal recessive nonsyndromic hearing loss 47	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	high
MONDO:0012376	autosomal recessive nonsyndromic hearing loss 55	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|anemia|autoimmune_diseases	hearing_loss|ear_disorder	false	false	false	true	medium
MONDO:0012378	fibromatosis, gingival, 3	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|mouth_disorder|musculoskeletal_system_disorder	orthopaedic|rheumatology|dermatology	cancer|inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0012380	autosomal dominant nonsyndromic hearing loss 53	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	ear_disorder	false	false	false	false	medium
MONDO:0012381	hyperinsulinism due to INSR deficiency	metabolic_disease|digestive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease|hereditary_disease|digestive_system_disorder	pediatric|endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder	false	false	true	false	high
MONDO:0012382	hyperinsulinemic hypoglycemia, familial, 4	metabolic_disease|hereditary_disease|digestive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|digestive_system_disorder	pediatric|endocrinology|genetics_and_genomics	familial_disorders|metabolic_disorder	endocrine_disorder|liver_disorder	false	false	true	true	high
MONDO:0012383	primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	immunology_is_actually_a_subset_of_allergy_and_immunology__so_it_can_be_removed|allergy_and_immunology|endocrinology|hematology|genetics_and_genomics	adrenal_gland_disease|autoimmune_diseases|metabolic_disorder	endocrine_disorder|immune_disorder	true	false	false	true	high
MONDO:0012384	panic disorder 3	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatry|neurology	mental_health_disorder	brain_disorder|mental_disorder	false	false	false	true	high
MONDO:0012385	metaphyseal chondrodysplasia with cone-shaped epiphyses, normal hair, and normal hands	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics	genetic_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012386	trichoscyphodysplasia	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	hair_disorder|skin_disorder|joint_disorder	false	false	false	false	none
MONDO:0012387	osteosclerosis-ichthyosis-premature ovarian failure syndrome	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder|syndromic_disease	obstetrics_and_gynecology|dermatology|endocrinology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0012388	myopia 11, autosomal dominant	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0012389	myopia 12, autosomal dominant	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0012390	arthrogryposis multiplex with deafness, inguinal hernias, and early death	hereditary_disease	other	hereditary_disease	pediatric|orthopaedic|otolaryngology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder|muscle_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0012391	neuronal ceroid lipofuscinosis 8 northern epilepsy variant	metabolic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	neurodegenerative_disease|metabolic_disease|psychiatric_disorder	nervous_system_disorder|metabolic_disease|hereditary_disease|psychiatric_disorder|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|neurological_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0012392	2-methylbutyryl-CoA dehydrogenase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|endocrinology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|liver_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0012393	congenital brain dysgenesis due to glutamine synthetase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	very_high
MONDO:0012394	multiple synostoses syndrome 2	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	genetic_disorder|bone_disease|developmental_disorder|skeletal_disorder|metabolic_disorder	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0012395	cataract 18	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0012396	exercise-induced hyperinsulinism	metabolic_disease|hereditary_disease|digestive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|digestive_system_disorder	pediatrics|endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|muscle_disorder	false	false	true	false	medium
MONDO:0012397	brachydactyly, coloboma, and anterior segment dysgenesis	hereditary_disease	other	hereditary_disease	ophthalmology|pediatric|orthopaedic|genetics_and_genomics	neurodegenerative_disease|coloboma|anterior_segment_dysgenesis|brachydactyly|metabolic_disorder	bone_disorder|eye_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012398	retinal cone dystrophy 3A	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0012399	complex cortical dysplasia with other brain malformations 7	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0012400	cortical dysplasia-focal epilepsy syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|epilepsy_seizure_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0012401	congenital stromal corneal dystrophy	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0012405	polyposis syndrome, hereditary mixed, 2	hereditary_disease|cancer_or_benign_tumor|syndromic_disease|digestive_system_disorder	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor|digestive_system_disorder	hepatology|hematology|pediatric|genetics_and_genomics|oncology|gastroenterology	hereditary|cancer	lower_gastrointestinal_disorder|blood_bone_marrow_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012406	hyperparathyroidism 3	hereditary_disease|connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|syndromic_disease|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|syndromic_disease|hereditary_disease|cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	renal_medicine|endocrinology	endocrine_disorder|autoimmune_diseases|metabolic_disorder	endocrine_disorder	false	false	false	true	high
MONDO:0012407	pyridoxal phosphate-responsive seizures	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	true	very_high
MONDO:0012408	microphthalmia, isolated, with coloboma 3	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|anemia|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0012409	isolated microphthalmia 2	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|eye_disorder|muscle_disorder	true	false	false	false	low
MONDO:0012410	Finnish upper limb-onset distal myopathy	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|orthopaedic|genetics_and_genomics	muscle_disease|neurodegenerative_disease	muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0012411	giant axonal neuropathy 2	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012412	complement component 7 deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	hematology|immunology|rheumatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0012413	syndromic microphthalmia type 5	hereditary_disease|syndromic_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0012414	neuronal ceroid lipofuscinosis 10	nervous_system_disorder|metabolic_disease|hereditary_disease|psychiatric_disorder	neurodegenerative_disease|metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0012415	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4	nervous_system_disorder|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant_disorders|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012416	Devriendt syndrome	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0012417	heart-hand syndrome, Slovenian type	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	cardiothoracic|cardiology|pediatric|genetics_and_genomics	cardiovascular_disorder|autoimmune_diseases|metabolic_disorder	heart_disorder|vascular_disorder|joint_disorder	false	false	false	false	high
MONDO:0012418	autosomal recessive nonsyndromic hearing loss 62	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	high
MONDO:0012419	age related macular degeneration 7	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease	neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	other___corrected__eye_disorder|eye_disorder	false	false	false	true	high
MONDO:0012420	autosomal recessive nonsyndromic hearing loss 49	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	high
MONDO:0012421	autosomal recessive nonsyndromic hearing loss 44	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0012423	MORM syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|endocrinology	adrenal_gland_disease|autoimmune_diseases|metabolic_disorder	endocrine_disorder|other____endocrine_disorder_is_a_match_due_to_the_disease_s_name_being_similar_to_multiple_osteochondromas_with_rachner__malabsorption__and_other_features__morm__syndrome__which_has_components_related_to_endocrine_disorders	false	false	false	true	high
MONDO:0012425	corneal dystrophy, fuchs endothelial, 2	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	ocular_disorder|eye_disorder	false	false	false	true	medium
MONDO:0012426	immunodeficiency 25	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|immunology	immunodeficiency_is_actually_a_subset_of_autoimmune_diseases_and_is_therefore_redundant__answer__autoimmunediseases|inflammatorydisease|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0012427	Loeys-Dietz syndrome 2	hereditary_disease|connective_tissue_disorder|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|hereditary_disease|connective_tissue_disorder	cardiothoracic|cardiology|dermatology|orthopaedic|pediatric|genetics_and_genomics	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	joint_disorder|skin_disorder|bone_disorder|vascular_disorder|eye_disorder	false	false	false	false	high
MONDO:0012428	kyphoscoliosis 1	hereditary_disease	other	hereditary_disease	neurology|orthopaedic	neurodegenerative_disease|spinal_condition	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0012429	Aicardi-Goutieres syndrome 2	nervous_system_disorder|hereditary_disease|connective_tissue_disorder|immune_system_disorder|syndromic_disease	neurodegenerative_disease	immune_system_disorder|nervous_system_disorder|syndromic_disease|hereditary_disease|connective_tissue_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	immune_disorder_blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0012430	cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 2	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|intellectual_disability|metabolic_disorder	brain_disorder|spinal_disorder|intellectual_disability	false	false	false	false	high
MONDO:0012431	diaphragmatic hernia 3	musculoskeletal_system_disorder|respiratory_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|respiratory_system_disorder	general_surgery|cardiothoracic|pulmonology	cardiovascular_disorder|abdominal	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012432	Joubert syndrome 5	nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease	neurodegenerative_disease	disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0012433	Senior-Loken syndrome 6	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	psychiatry|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012434	arrhythmogenic right ventricular dysplasia 10	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiology|cardiothoracic|pediatric	cardiovascular_disorder|adrenal_gland_disease	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0012435	3-methylglutaconic aciduria type 5	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	medical_genetics|pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	kidney_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0012436	neonatal diabetes mellitus with congenital hypothyroidism	metabolic_disease|digestive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder|metabolic_disease|diabetes_mellitus	endocrine_system_disorder|metabolic_disease|hereditary_disease|digestive_system_disorder	pediatric|genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|congenital_hypothyroidism_is_not_listed_so_remove_it	false	false	true	true	very_high
MONDO:0012437	cataract 21 multiple types	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0012438	pontocerebellar hypoplasia type 5	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0012439	Alagille syndrome due to a NOTCH2 point mutation	cardiovascular_disorder|syndromic_disease|digestive_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease	cardiovascular_disorder	disorder_of_visual_system|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|digestive_system_disorder|cardiovascular_disorder	pediatric|genetics_and_genomics|gastroenterology|hepatology	cardiovascular_disorder|autoimmune_diseases|metabolic_disorder	liver_disorder|biliary_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0012442	autosomal recessive nonsyndromic hearing loss 66	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0012443	aneurysm, intracranial berry, 4	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|nervous_system_disorder|cardiovascular_disorder	neurology|neurosurgery	cardiovascular_disorder|intracranial_berry_is_related_to_neurological_conditions_so_also_neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012444	neurodegeneration with brain iron accumulation 2B	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012445	autosomal recessive nonsyndromic hearing loss 59	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0012446	seborrhea-like dermatitis with psoriasiform elements	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|allergy_and_immunology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0012447	synpolydactyly type 3	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012448	hereditary spastic paraplegia 33	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0012449	spinocerebellar ataxia type 23	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012450	spinocerebellar ataxia type 28	hereditary_disease|metabolic_disease|psychiatric_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease|metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012451	esophagitis, eosinophilic, 1	hereditary_disease|digestive_system_disorder|inflammatory_disease|upper_digestive_tract_disorder	other	upper_digestive_tract_disorder|hereditary_disease|inflammatory_disease|digestive_system_disorder	allergy_and_immunology|pediatrics|gastroenterology	inflammatory_disease|autoimmune_diseases|allergy	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0012452	autosomal recessive nonsyndromic hearing loss 65	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|otolaryngology	metabolic_disorder	hearing_loss|ear_disorder	false	false	false	false	medium
MONDO:0012453	hereditary spastic paraplegia 31	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012454	alcohol sensitivity, acute	hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|acute_disease	gastroenterology|hepatology	autoimmune_diseases|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	low
MONDO:0012455	Kleefstra syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|rheumatology|pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder_spinal_disorder__joint_disorder	false	false	false	false	high
MONDO:0012456	congenital primary aphakia	hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_development_or_morphogenesis|disorder_of_orbital_region|hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	metabolic_disorder	eye_disorder|congenital_disorder	false	false	false	false	high
MONDO:0012457	pyloric stenosis, infantile hypertrophic, 2	hereditary_disease|digestive_system_disorder	other	hereditary_disease|digestive_system_disorder	pediatric|gastroenterology	cardiovascular_disorder|neonatal_condition|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012460	autosomal recessive nonsyndromic hearing loss 67	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0012462	autosomal recessive frontotemporal pachygyria	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012463	retinitis pigmentosa 35	metabolic_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|retinal_disease	eye_disorder	false	false	false	false	high
MONDO:0012464	cone-rod dystrophy 10	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0012465	hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency	hematologic_disorder|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0012467	cold-induced sweating syndrome 2	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	dermatology|genetics_and_genomics	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	endocrine_disorder|skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0012468	rhizomelic dysplasia, scoliosis, and retinitis pigmentosa	hereditary_disease	other	hereditary_disease	ophthalmology|genetics_and_genomics|orthopaedic|neurology	neurodegenerative_disease|rhizomelic_dysplasia__scoliosis_and_retinitis_pigmentosa___the_best_fitting_categories_are__neurodegenerative_disease|metabolic_disorder|retinitis_pigmentosa_can_be_excluded_from_this_list_as_it_is_a_symptom	spinal_disorder|bone_disorder|eye_disorder	false	false	false	false	high
MONDO:0012469	myopia 14	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	true	high
MONDO:0012470	prostate cancer, hereditary, 7	cancer_or_benign_tumor|reproductive_system_disorder|hereditary_disease	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	urology|genetics_and_genomics|oncology	cancer|hereditary	hereditary|reproductive_system_disorder	false	true	false	true	high
MONDO:0012471	Aicardi-Goutieres syndrome 3	immune_system_disorder|connective_tissue_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	connective_tissue_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder|immune_system_disorder	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0012472	Aicardi-Goutieres syndrome 4	immune_system_disorder|connective_tissue_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	connective_tissue_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder|immune_system_disorder	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	joint_disorder|liver_disorder|eye_disorder|immune_disorder|kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0012473	right pulmonary artery, anomalous origin of, familial	hereditary_disease	other	hereditary_disease	pulmonology|cardiology|genetics_and_genomics|cardiothoracic	cardiovascular_disorder|familial	vascular_disorder|heart_disorder|lung_disorder	false	false	false	false	high
MONDO:0012474	autosomal dominant nocturnal frontal lobe epilepsy 4	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0012475	cone dystrophy with supernormal rod response	psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0012476	hereditary spastic paraplegia 30	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012477	retinitis pigmentosa 33	metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	metabolic_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|metabolic_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0012478	orofacial cleft 9	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	otolaryngology|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	teeth_disorder|oral_disorder____note__some_sources_may_categorize_orofacial_cleft_as_part_of_a_broader_category_called__oral_disorder	false	false	false	false	high
MONDO:0012479	congenital malabsorptive diarrhea 4	hereditary_disease|digestive_system_disorder	other	hereditary_disease|digestive_system_disorder	gastroenterology|pediatric|genetics_and_genomics	congenital_gland_disease|metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0012480	diabetes mellitus, transient neonatal, 2	metabolic_disease|hereditary_disease|digestive_system_disorder|endocrine_system_disorder	metabolic_disease|diabetes_mellitus|endocrine_system_disorder	hereditary_disease|digestive_system_disorder|endocrine_system_disorder|metabolic_disease	pediatric|endocrinology	metabolic_disorder|cardiovascular_disorder|autoimmune_diseases	endocrine_disorder	false	false	true	true	high
MONDO:0012481	mevalonic aciduria	metabolic_disease|connective_tissue_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system	metabolic_disease	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease|connective_tissue_disorder	pediatrics|biochemistry|metabolism|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|bone_disorder|metabolic_disorder	false	false	false	false	very_high
MONDO:0012483	cone-rod dystrophy 11	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|genetics_and_genomics|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0012484	prosopagnosia, hereditary	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatry|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	low
MONDO:0012485	autosomal recessive nonsyndromic hearing loss 68	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	pediatrics|otolaryngology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	ear_disorder	false	false	false	false	low
MONDO:0012486	preauricular tag, isolated, autosomal dominant, 1	hereditary_disease	other	hereditary_disease	dermatology|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disease	skin_disorder|ear_disorder	false	false	false	false	low
MONDO:0012487	alopecia-intellectual disability syndrome 2	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	immune_disorder|brain_disorder	false	false	false	false	medium
MONDO:0012489	cataract 23	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	true	medium
MONDO:0012490	cone-rod synaptic disorder, congenital nonprogressive	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0012491	macroglobulinemia, Waldenstrom, 2	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|metabolic_disease|hereditary_disease	cancer_or_benign_tumor|metabolic_disease	immune_system_disorder|hematologic_disorder|hereditary_disease|cancer_or_benign_tumor|metabolic_disease	oncology|hematology	autoimmune_diseases|cancer|anemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0012494	testicular microlithiasis	hereditary_disease	other	hereditary_disease	urology|genetics_and_genomics	metabolic_disorder|anemia	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0012495	spondyloepimetaphyseal dysplasia, Genevieve type	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012496	Koolen-de Vries syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	muscle_disorder|immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0012497	congenital stationary night blindness autosomal dominant 3	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0012498	congenital stationary night blindness autosomal dominant 1	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0012500	chilblain lupus 1	connective_tissue_disorder|syndromic_disease|integumentary_system_disorder|cardiovascular_disorder|immune_system_disorder|hereditary_disease	cardiovascular_disorder|autoimmune_disease	hereditary_disease|connective_tissue_disorder|integumentary_system_disorder|immune_system_disorder|cardiovascular_disorder|syndromic_disease	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	immune_disorder__skin_disorder	false	false	false	true	medium
MONDO:0012502	normophosphatemic familial tumoral calcinosis	cancer_or_benign_tumor|endocrine_system_disorder|integumentary_system_disorder|metabolic_disease|hereditary_disease	cancer_or_benign_tumor|metabolic_disease|endocrine_system_disorder	hereditary_disease|integumentary_system_disorder|endocrine_system_disorder|metabolic_disease|cancer_or_benign_tumor	endocrinology|renal_medicine|genetics_and_genomics|oncology|urology	metabolic_disorder|cancer	kidney_disorder|bone_disorder	false	false	false	false	high
MONDO:0012503	thiopurine S-methyltransferase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|hematology	genetic_disorder|metabolic_disorder	immune_disorder|liver_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0012504	camptodactyly-tall stature-scoliosis-hearing loss syndrome	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	otolaryngology|orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|spinal_disorder|ear_disorder	false	false	false	false	medium
MONDO:0012505	pigmented nodular adrenocortical disease, primary, 2	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	endocrinology|dermatology	metabolic_disorder|adrenal_gland_disease	vascular_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0012506	arrhythmogenic right ventricular dysplasia 11	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiology|genetics_and_genomics|cardiothoracic	cardiovascular_disorder|arrhythmogenic_right_ventricular_dysplasia	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0012507	retinal cone dystrophy 4	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0012508	agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|immune_system_disorder|hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder|immune_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	neurology|immunology|genetics_and_genomics|dermatology|pediatric|hematology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|immune_disorder|blood_bone_marrow_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0012509	pigmented nodular adrenocortical disease, primary, 1	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	endocrinology|dermatology	metabolic_disorder|adrenal_gland_disease|cancer	vascular_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0012510	combined oxidative phosphorylation defect type 2	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	metabolic_disease	mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|mitochondrial_disorder_is_not_listed_so_we_will_omit_it	false	false	false	false	very_high
MONDO:0012511	preterm premature rupture of the membranes	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	obstetrics_and_gynecology|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|pregnancy_complication	false	false	false	false	high
MONDO:0012512	fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	metabolic_disease	mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatrics|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	very_high
MONDO:0012513	maturity-onset diabetes of the young type 7	endocrine_system_disorder|digestive_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease|endocrine_system_disorder|diabetes_mellitus	endocrine_system_disorder|digestive_system_disorder|metabolic_disease|hereditary_disease	endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|adrenal_gland_disease	endocrine_disorder	false	false	true	true	medium
MONDO:0012514	hypomyelinating leukodystrophy 5	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0012515	glaucoma 1, open angle, M	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	inflammatory_disease|metabolic_disorder	eye_disorder|kidney_disorder|vascular_disorder|urinary_tract_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0012516	mandibulofacial dysostosis-microcephaly syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|genetic_condition	spinal_disorder|bone_disorder|teeth_disorder	false	false	false	false	very_high
MONDO:0012517	Gaucher disease due to saposin C deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	hematopoietic|neurology|genomics|genetics_and_genomics|pediatric|hematology	metabolic_disorder|neurodegenerative_disease	joint_disorder|blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	high
MONDO:0012518	congenital myasthenic syndrome 12	syndromic_disease|nervous_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	nervous_system_disorder|metabolic_disease|syndromic_disease|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0012519	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion	psychiatric_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder|chromosomal_disorder|musculoskeletal_system_disorder|hereditary_disease	psychiatric_disorder	musculoskeletal_system_disorder|psychiatric_disorder|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|chromosomal_disorder	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0012520	insulin-resistance syndrome type A	digestive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|hereditary_disease	endocrinology|metabolism	metabolic_disorder|insulin_resistance_syndrome_type_a_does_not_match_the_category_list__it_is_likely_a_synonym_for_metabolic_disorder	endocrine_disorder	false	false	true	false	very_high
MONDO:0012521	herpes simplex encephalitis	nervous_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|inflammatory_disease|nervous_system_disorder|acute_disease	neurology|pediatric|psychiatry	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder	true	false	false	true	very_high
MONDO:0012522	diabetes mellitus, transient neonatal, 3	digestive_system_disorder|hereditary_disease|endocrine_system_disorder|metabolic_disease	diabetes_mellitus|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease|digestive_system_disorder|hereditary_disease	endocrinology|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases	endocrine_disorder	false	false	true	true	high
MONDO:0012523	retinitis pigmentosa 36	psychiatric_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system	metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|ophthalmology	adrenal_gland_disease___note__retinitis_pigmentosa_is_associated_with_the_adrenal_gland_in_some_cases_and_can_also_be_considered_a_neurodegenerative_disease_due_to_its_degenerative_effects_on_the_retina|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0012524	corticosterone methyloxidase type 2 deficiency	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0012525	Leber congenital amaurosis 12	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0012526	hereditary angioedema type 3	integumentary_system_disorder|hereditary_disease|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease|hereditary_disease	genetics_and_genomics|allergy_and_immunology|hematology	inflammatory_disease|allergy|autoimmune_diseases	vascular_disorder|immune_disorder	false	false	false	true	medium
MONDO:0012527	cataract 11 multiple types	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	true	high
MONDO:0012528	hypogonadotropic hypogonadism 4 with or without anosmia	reproductive_system_disorder|syndromic_disease|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|endocrinology|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0012529	Diamond-Blackfan anemia 3	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0012530	palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome	disorder_of_development_or_morphogenesis|integumentary_system_disorder|reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	oncology|genetics_and_genomics|dermatology	cancer|inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder|skin_disorder	false	true	false	true	high
MONDO:0012531	xeroderma pigmentosum group B	integumentary_system_disorder|syndromic_disease|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|syndromic_disease|hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	cancer|neurodegenerative_disease|inflammatory_disease	immune_disorder|skin_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0012532	hereditary hemorrhagic telangiectasia type 4	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder|cardiovascular_disorder	vascular_disorder|liver_disorder	false	false	false	false	high
MONDO:0012534	combined oxidative phosphorylation defect type 4	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	pediatrics|genetics_and_genomics|biochemistry	metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0012535	holoprosencephaly, recurrent infections, and monocytosis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|hematology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0012536	osteogenesis imperfecta type 7	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases	muscle_disorder|bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012537	split-hand/foot malformation with long bone deficiency 2	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	bone_disorder|joint_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0012538	nemaline myopathy 7	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012539	Joubert syndrome 6	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric	anemia|metabolic_disorder|neurodegenerative_disease	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0012540	age related macular degeneration 4	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0012541	deafness with labyrinthine aplasia, microtia, and microdontia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|otolaryngology	autoimmune_diseases|neurodegenerative_disease	ear_disorder|microdontia_does_also_fit_into_a_category_for_ears_but_since_it_is_associated_with_the_other_term_teeth_we_will_exclude_it_here|teeth_disorder	true	false	false	false	high
MONDO:0012543	optic atrophy 5	nervous_system_disorder|hereditary_disease|disorder_of_visual_system	neurodegenerative_disease	nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	neurology|ophthalmology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0012544	brachydactyly-syndactyly syndrome	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	neurodegenerative_disease|developmental_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012545	neutral lipid storage myopathy	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|neurology|genetic	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	muscle_disorder|lipid_storage_disorder	false	false	false	false	medium
MONDO:0012546	nephrotic syndrome, type 3	urinary_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|urinary_system_disorder|hereditary_disease|idiopathic_disease	nephrology|renal_medicine	autoimmune_diseases|metabolic_disorder|inflammatory_disease	urinary_tract_disorder|kidney_disorder|immune_disorder	false	false	false	false	medium
MONDO:0012547	Noonan syndrome 4	immune_system_disorder|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|immune_system_disorder|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|cardiovascular_disorder	heart_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012548	Kostmann syndrome	immune_system_disorder|syndromic_disease|hereditary_disease|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|syndromic_disease|hematologic_disorder|hereditary_disease	genetics_and_genomics|pediatric|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0012549	autosomal recessive ataxia, Beauce type	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0012550	iris pattern	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|eye_disorder	false	false	false	false	none
MONDO:0012551	alopecia areata 2	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	rheumatology|genetics_and_genomics|dermatology|hematology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0012552	multiple endocrine neoplasia type 4	syndromic_disease|hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|syndromic_disease|hereditary_disease	oncology|endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|cancer	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0012553	cerebrooculofacioskeletal syndrome 2	syndromic_disease|hereditary_disease|metabolic_disease|disorder_of_visual_system	metabolic_disease	metabolic_disease|disorder_of_visual_system|syndromic_disease|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	muscle_disorder|brain_disorder|joint_disorder|spinal_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0012554	cerebrooculofacioskeletal syndrome 4	syndromic_disease|hereditary_disease|metabolic_disease|disorder_of_visual_system	metabolic_disease	metabolic_disease|disorder_of_visual_system|syndromic_disease|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|joint_disorder|spinal_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0012555	Cornelia de Lange syndrome 3	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	ear_disorder|heart_disorder|brain_disorder|blood_bone_marrow_disorder|joint_disorder|immune_disorder|skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0012556	DK1-congenital disorder of glycosylation	integumentary_system_disorder|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|cardiovascular_disorder|metabolic_disease	metabolic_disease|cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder|metabolic_disease|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	congenital_disorder_of_glycosylation|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0012557	cardiomyopathy-hypotonia-lactic acidosis syndrome	musculoskeletal_system_disorder|mitochondrial_disease|hereditary_disease|cardiovascular_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|cardiology	cardiomyopathy_hypotonia_lactic_acidosis_syndrome_is_primarily_associated_with_the_heart_and_metabolism|metabolic_disorder|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0012558	epiphyseal dysplasia, Baumann type	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|skeletal_dysplasia	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012559	primary immunodeficiency syndrome due to p14 deficiency	immune_system_disorder|hereditary_disease|hematologic_disorder	other	immune_system_disorder|hematologic_disorder|hereditary_disease	genetics_and_genomics|pediatric|allergy_and_immunology|immunology	primary_immunodeficiency_syndrome|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0012561	congenital anomalies of kidney and urinary tract 1	hereditary_disease|urinary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|urinary_system_disorder|hereditary_disease	pediatric|urology|renal_medicine	metabolic_disorder|congenital_anomalies_of_kidney_and_urinary_tract___note__this_is_a_specific_category_in_the_provided_list___metabolic_disorders	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0012562	holoprosencephaly 7	nervous_system_disorder|hereditary_disease|syndromic_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0012563	holoprosencephaly 9	nervous_system_disorder|hereditary_disease|syndromic_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0012564	Polyosteolysis-hyperostosis syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|rheumatology	metabolic_disorder|cancer|autoimmune_diseases|inflammatory_disease	muscle_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0012565	Fanconi anemia complementation group N	immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease|hematologic_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	anemia|metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|immune_system_disorder|hematologic_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0012569	mitral valve prolapse, myxomatous 3	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|cardiothoracic|cardiology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0012570	body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology|hematology	metabolic_disorder|coagulation_factor_deficiency|inflammatory_disease	liver_disorder|blood_bone_marrow_disorder|skin_disorder	false	false	false	false	medium
MONDO:0012571	primary ciliary dyskinesia 6	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pulmonology	metabolic_disorder|neurodegenerative_disease	ear_disorder|joint_disorder|spinal_disorder|brain_disorder|kidney_disorder|eye_disorder	false	false	false	false	high
MONDO:0012572	Sakoda complex	hereditary_disease	other	hereditary_disease	neurology|pediatric|psychiatry	mental_health_disorder|neurodegenerative_disease|autoimmune_diseases	liver_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0012573	vesicoureteral reflux 2	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	pediatric|urology	urological_condition|kidney_problem|urinary_disorder|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0012574	Potocki-Lupski syndrome	hereditary_disease|syndromic_disease|chromosomal_disorder	other	chromosomal_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|cardiovascular_disorder	heart_disorder|muscle_disorder|blood_bone_marrow_disorder|joint_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012575	branchiootorenal syndrome 2	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric|renal_medicine	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	ear_disorder|kidney_disorder	false	false	false	true	high
MONDO:0012576	supranuclear palsy, progressive, 3	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|syndromic_disease	neurodegenerative_disease	disorder_of_visual_system|nervous_system_disorder|syndromic_disease|hereditary_disease	neurology	neurodegenerative_disease|progressive_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0012579	autoimmune pulmonary alveolar proteinosis	immune_system_disorder|respiratory_system_disorder	autoimmune_disease	respiratory_system_disorder|immune_system_disorder	immunology|allergy_and_immunology|pulmonology	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	false	high
MONDO:0012580	hereditary pulmonary alveolar proteinosis	hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease	genetics_and_genomics|pulmonology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	false	high
MONDO:0012581	osteogenesis imperfecta type 8	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|autoimmune_diseases	muscle_disorder|bone_disorder|joint_disorder|spinal_disorder|skin_disorder	false	false	false	false	high
MONDO:0012582	interstitial lung disease due to ABCA3 deficiency	hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|pulmonology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	lung_disorder	false	false	false	false	very_high
MONDO:0012583	tooth agenesis, selective, 5	musculoskeletal_system_disorder|hereditary_disease	other	mouth_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|otolaryngology	metabolic_disorder|autoimmune_diseases	bone_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0012586	coronary artery disease, autosomal dominant 2	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	genetics_and_genomics|cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0012588	neuronal ceroid lipofuscinosis 7	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|neurodegenerative_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0012589	Pitt-Hopkins syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0012590	XFE progeroid syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|premature_aging_syndrome	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|premature_aging_syndrome	genetics_and_genomics|endocrinology|dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	bone_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0012591	osteogenesis imperfecta type 5	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|autoimmune_diseases	bone_disorder|joint_disorder|teeth_disorder|skin_disorder	false	false	false	false	medium
MONDO:0012592	osteogenesis imperfecta type 11	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic	genetic_disorder|metabolic_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	true	high
MONDO:0012593	brain-lung-thyroid syndrome	nervous_system_disorder|hereditary_disease|endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	endocrine_system_disorder|nervous_system_disorder|syndromic_disease|hereditary_disease	neurology|endocrinology|pulmonology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	endocrine_disorder|brain_disorder|lung_disorder|thyroid_disorder	false	false	false	false	high
MONDO:0012594	complement factor I deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|rheumatology|immunology|hematology	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|kidney_disorder|immune_disorder	false	false	false	true	medium
MONDO:0012596	PSAT deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|endocrinology	neurodegenerative_disease|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder|endocrine_disorder	false	false	false	true	very_high
MONDO:0012597	prostate cancer, hereditary, 9	reproductive_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|urology|oncology	hereditary|cancer	reproductive_system_disorder|hereditary	false	true	false	true	high
MONDO:0012598	fibromatosis, gingival, 4	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	mouth_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	rheumatology|dermatology	cancer|autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0012602	autosomal recessive nonsyndromic hearing loss 24	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	false	low
MONDO:0012603	episodic kinesigenic dyskinesia 2	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0012604	isolated microphthalmia 3	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0012605	isolated microphthalmia 5	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0012608	neuronopathy, distal hereditary motor, autosomal recessive 4	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder|neuronopathy|muscle_disorder	false	false	false	false	high
MONDO:0012609	Alzheimer disease 12	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|genetics_and_genomics|psychiatry	cardiovascular_disorder|mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	very_high
MONDO:0012610	inflammatory bowel disease 10	immune_system_disorder|digestive_system_disorder|hereditary_disease	other	hereditary_disease|digestive_system_disorder|immune_system_disorder	gastroenterology|hepatology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012611	polyhydramnios, megalencephaly, and symptomatic epilepsy	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	corrected_answer___neurodegenerative_disease|metabolic_disorder|symptomatic_epilepsy_is_often_associated_with_a_underlying_cause_of_the_epilepsy|neurodegenerative_disease	symptomatic_epilepsy_is_often_associated_with_both_of_these_conditions_but_the_term_itself_fits_as_well_so_i_ve_included_it__brain_disorder|symptomatic_epilepsy|kidney_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0012612	intellectual disability, autosomal recessive 12	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	metabolic_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012613	intellectual disability, autosomal recessive 5	nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	metabolic_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	autosomal_recessive_disorder|brain_disorder	false	false	false	false	high
MONDO:0012614	intellectual disability, autosomal recessive 6	nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	metabolic_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	autosomal_recessive_disorder|brain_disorder	false	false	false	false	high
MONDO:0012615	intellectual disability, autosomal recessive 7	nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	metabolic_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	neurology|genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0012617	intellectual disability, autosomal recessive 9	nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	metabolic_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|autosomal_recessive	false	false	false	false	high
MONDO:0012618	intellectual disability, autosomal recessive 10	nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	metabolic_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	high
MONDO:0012619	intellectual disability, autosomal recessive 11	nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	metabolic_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0012620	prostate cancer, hereditary, 10	cancer_or_benign_tumor|reproductive_system_disorder|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|reproductive_system_disorder|cancer_or_benign_tumor	oncology|genetics_and_genomics|urology	cancer|hereditary	reproductive_system_disorder|hereditary	false	true	false	true	high
MONDO:0012621	deafness-infertility syndrome	chromosomal_disorder|syndromic_disease	other	syndromic_disease|chromosomal_disorder	genetics_and_genomics|otolaryngology|pediatric|obstetrics_and_gynecology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|ear_disorder	false	false	false	false	medium
MONDO:0012622	leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome	nervous_system_disorder|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease|neurodegenerative_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|metabolic_disease	hematology|neurology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0012623	intellectual disability, autosomal recessive 4	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	metabolic_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0012624	acyl-CoA dehydrogenase 9 deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|metabolism_is_not_in_the_list_so_endocrinology|pediatric	metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0012625	retinitis pigmentosa 37	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	metabolic_disease|psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	neurology|genetics_and_genomics|ophthalmology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0012626	Meckel syndrome, type 4	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	genetic_disorder|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder|kidney_disorder	false	false	false	false	high
MONDO:0012629	paroxysmal nonkinesigenic dyskinesia 2	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder_muscle_disorder	false	false	false	false	medium
MONDO:0012630	Alzheimer disease 13	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012631	Alzheimer disease 14	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0012634	craniofacial dysplasia - osteopenia syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics|rheumatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	bone_disorder|craniofacial_dysplasia	false	false	false	false	high
MONDO:0012635	COG8-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	congenital_disorder_of_glycosylation_is_a_genetic_condition|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|congenital_disorder_of_glycosylation	spinal_disorder|liver_disorder|kidney_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0012637	COG1-congenital disorder of glycosylation	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease	cardiovascular_disorder|metabolic_disease	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|cardiovascular_disorder	genetics_and_genomics|pediatric	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	liver_disorder	false	false	false	false	high
MONDO:0012638	microphthalmia-brain atrophy syndrome	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	disorder_of_visual_system|syndromic_disease|nervous_system_disorder|disorder_of_orbital_region|hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	true	very_high
MONDO:0012639	hereditary spastic paraplegia 18	hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0012640	Charcot-Marie-Tooth disease type 4J	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	nerve_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012642	major affective disorder 4	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|psychiatry	major_affective_disorder|mental_health_disorder	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0012643	hereditary spastic paraplegia 32	syndromic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012644	asphyxiating thoracic dystrophy 2	syndromic_disease|hereditary_disease|urinary_system_disorder|musculoskeletal_system_disorder|respiratory_system_disorder	other	syndromic_disease|urinary_system_disorder|hereditary_disease|musculoskeletal_system_disorder|respiratory_system_disorder	genetics_and_genomics|pediatric|pulmonology	metabolic_disorder|neurodegenerative_disease	lung_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012645	glaucoma 1, open angle, N	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	neurology|ophthalmology	inflammatory_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder	false	false	false	true	medium
MONDO:0012648	isobutyryl-CoA dehydrogenase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	metabolism__note__not_in_list|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0012650	Cernunnos-XLF deficiency	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	immunology|hematology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0012651	spastic ataxia 2	syndromic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012652	autosomal recessive limb-girdle muscular dystrophy type 2L	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	neurology|orthopaedic|genetics_and_genomics	muscular_dystrophy|neurodegenerative_disease	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012653	persistent hyperplastic primary vitreous, autosomal dominant	nervous_system_disorder|hereditary_disease|disorder_of_visual_system	other	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology|genetics_and_genomics	autosomal_dominant_disorders_are_often_classified_under_this_category|metabolic_disorder	spinal_disorder|joint_disorder|eye_disorder	false	false	false	false	medium
MONDO:0012654	atrial septal defect 4	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|pediatric|cardiology	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0012656	lethal congenital contracture syndrome 3	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0012657	Mungan syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0012658	brachydactyly type B2	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disorder|developmental_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012659	age related macular degeneration 9	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0012662	Usher syndrome type 2D	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|neurology|ophthalmology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|ear_disorder|eye_disorder	false	false	false	true	high
MONDO:0012664	spastic ataxia 3	mitochondrial_disease|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012665	cataract 33	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0012667	dilated cardiomyopathy 1W	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiothoracic|cardiology	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0012668	Tented eyebrows	hereditary_disease	other	hereditary_disease	plastic_surgery_is_not_in_the_list_but_orthopaedic_could_be_a_possible_fit_if_its_an_issue_with_shape_of_eyebrows|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0012669	Legius syndrome	musculoskeletal_system_disorder|integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|integumentary_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	immune_disorder|brain_disorder|skin_disorder	false	false	false	false	medium
MONDO:0012670	autosomal recessive nonsyndromic hearing loss 63	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|otolaryngology|genetics_and_genomics	genetic_disease|metabolic_disorder|neurological_disease	ear_disorder	false	false	false	true	medium
MONDO:0012671	tremor, hereditary essential, 3	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	hereditary_essential_tremor_is_a_form_of_metabolic_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012672	cholelithiasis	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	medium
MONDO:0012673	colorectal cancer, susceptibility to, 2	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	oncology|gastroenterology	autoimmune_diseases|inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0012674	age related macular degeneration 10	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0012675	corticosteroid-binding globulin deficiency	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	immunology|endocrinology|rheumatology	adrenal_gland_disease|inflammatory_disease|metabolic_disorder	endocrine_disorder|immune_disorder	false	false	false	false	medium
MONDO:0012676	autosomal recessive osteopetrosis 4	musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	autoimmune_diseases|anemia|metabolic_disorder	skeletal_system_disorder|bone_disorder	false	false	false	true	high
MONDO:0012677	atrial fibrillation, familial, 4	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiothoracic|genetics_and_genomics|cardiology	cardiovascular_disorder|familial|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012678	atrial fibrillation, familial, 5	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiothoracic|genetics_and_genomics|cardiology	cardiovascular_disorder|familial	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0012679	autosomal recessive osteopetrosis 6	musculoskeletal_system_disorder|hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0012680	nephronophthisis 7	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	renal_medicine|urology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0012681	febrile seizures, familial, 7	hereditary_disease	other	hereditary_disease	pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	low
MONDO:0012682	immunodeficiency 35	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	immunodeficiency|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	true	false	false	false	high
MONDO:0012683	pontocerebellar hypoplasia type 6	metabolic_disease|mitochondrial_disease|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0012684	arrhythmogenic right ventricular dysplasia 12	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiology|cardiothoracic	cardiovascular_disorder|neurodegenerative_disease	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012685	major affective disorder 5	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	major_affective_disorder_mental_health_disorder|major_affective_disorder	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0012686	major affective disorder 6	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|major_affective_disorder	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0012687	familial cavitary optic disk anomaly	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0012688	cataract 17 multiple types	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0012689	premature ovarian failure 5	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrinology|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0012690	Noonan syndrome 5	cardiovascular_disorder|musculoskeletal_system_disorder|syndromic_disease|immune_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|immune_system_disorder|musculoskeletal_system_disorder|syndromic_disease	pediatric|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	joint_disorder|heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012691	LEOPARD syndrome 2	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	pediatric|dermatology|genetics_and_genomics	cardiovascular_disorder|autoimmune_diseases|anemia|metabolic_disorder	skin_disorder|kidney_disorder|heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0012692	renal tubular acidosis, distal, with nephrocalcinosis, short stature, intellectual disability, and distinctive facies	hereditary_disease	other	hereditary_disease	renal_medicine|pediatric|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	bone_disorder|endocrine_disorder|urinary_tract_disorder|kidney_disorder	true	false	false	true	very_high
MONDO:0012693	glycogen storage disease due to muscle and heart glycogen synthase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|endocrinology|cardiology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	muscle_disorder|heart_disorder	false	false	true	false	very_high
MONDO:0012694	Joubert syndrome 7	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0012695	Meckel syndrome, type 5	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	pediatric|genetics_and_genomics	anemia|metabolic_disorder	upper_gastrointestinal_disorder|joint_disorder|kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0012696	otosclerosis 4	otorhinolaryngologic_disease|hereditary_disease|auditory_system_disorder	other	hereditary_disease|otorhinolaryngologic_disease|auditory_system_disorder	pediatric|otolaryngology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	bone_disorder|ear_disorder	false	false	false	true	high
MONDO:0012697	otosclerosis 7	otorhinolaryngologic_disease|hereditary_disease|auditory_system_disorder	other	hereditary_disease|otorhinolaryngologic_disease|auditory_system_disorder	otolaryngology|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	bone_disorder|ear_disorder	false	false	false	true	medium
MONDO:0012698	Waardenburg syndrome type 2E	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|anemia|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|bone_disorder|ear_disorder|hearing_loss_disorder|skin_disorder	false	false	false	false	high
MONDO:0012699	autosomal recessive limb-girdle muscular dystrophy type 2M	cardiovascular_disorder|metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	metabolic_disease|cardiovascular_disorder	hereditary_disease|metabolic_disease|cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0012700	renal tubular acidosis, distal, 4, with hemolytic anemia	urinary_system_disorder|hereditary_disease|hematologic_disorder	anemia	urinary_system_disorder|hematologic_disorder|hereditary_disease	renal_medicine|hematology	anemia|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0012701	cataract 12 multiple types	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	true	medium
MONDO:0012703	lissencephaly due to TUBA1A mutation	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0012704	dilated cardiomyopathy 1X	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012705	familial temporal lobe epilepsy 3	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0012706	familial temporal lobe epilepsy 4	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	high
MONDO:0012707	familial febrile seizures 9	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	true	low
MONDO:0012708	primary lateral sclerosis, adult, 1	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	rheumatology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0012709	microphthalmia, isolated, with coloboma 5	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|pediatric|ophthalmology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0012711	peripapillary atrophy, beta type	hereditary_disease	other	hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0012712	dystonia with cerebellar atrophy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012713	spondylometaphyseal dysplasia, East African type	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012714	early-onset myopathy with fatal cardiomyopathy	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|cardiology|pediatric|cardiology_is_redundant_so_it_should_be_removed_from_the_list_to_avoid_duplication__leaving__genetics_and_genomics|neurology|cardiology_is_incorrect_as_it_has_been_removed_from_this_instance_of_the_list__therefore_the_answer_remains__genetics_and_genomics	neurodegenerative_disease|cardiovascular_disorder	heart_disorder|muscle_disorder	true	false	false	true	very_high
MONDO:0012716	spondyloepiphyseal dysplasia, Cantu type	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012717	renal hypomagnesemia 4	hereditary_disease|metabolic_disease|urinary_system_disorder	metabolic_disease	metabolic_disease|urinary_system_disorder|hereditary_disease	nephrology|renal_medicine	renal_hypomagnesemia|metabolic_disorder	endocrine_disorder|urinary_tract_disorder|kidney_disorder	false	false	false	true	high
MONDO:0012718	hypotonia with lactic acidemia and hyperammonemia	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	genetics_and_genomics|pediatric|renal_medicine|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|endocrine_disorder|liver_disorder	true	false	false	false	very_high
MONDO:0012719	combined PSAP deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|immunology	adrenal_gland_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0012720	Krabbe disease due to saposin A deficiency	syndromic_disease|hereditary_disease|metabolic_disease	metabolic_disease	syndromic_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012721	progressive myoclonic epilepsy type 3	hereditary_disease|nervous_system_disorder|metabolic_disease	neurodegenerative_disease|metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscledisorder|brain_disorder	false	false	false	false	very_high
MONDO:0012722	Dauwerse-Peters syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|upper_gastrointestinal_disorder|liver_disorder|lymphatic_disorder|joint_disorder	false	false	false	false	high
MONDO:0012723	Leber congenital amaurosis 10	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	genetics_and_genomics|pediatric|ophthalmology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0012724	familial cold autoinflammatory syndrome 2	syndromic_disease|connective_tissue_disorder|hereditary_disease|immune_system_disorder	other	connective_tissue_disorder|syndromic_disease|hereditary_disease|immune_system_disorder	genetics_and_genomics|rheumatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	inflammatory_disorder__not_in_list__but_implied|immune_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012725	lipoprotein glomerulopathy	syndromic_disease|hereditary_disease|metabolic_disease	metabolic_disease	syndromic_disease|hereditary_disease|metabolic_disease	nephrology|renal_medicine	autoimmune_diseases|metabolic_disorder	kidney_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012726	autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome	syndromic_disease|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|urology|hematology|ophthalmology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|eye_disorder|joint_disorder	false	false	false	false	medium
MONDO:0012727	mucocutaneous lymph node syndrome	inflammatory_disease|hereditary_disease|cardiovascular_disorder|immune_system_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease|hereditary_disease|immune_system_disorder	dermatology|pediatric|oncology|allergy_and_immunology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder_lymphatic_disorder_skin_disorder	false	false	false	true	high
MONDO:0012728	Brugada syndrome 2	syndromic_disease|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|cardiology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012729	erythrocytosis, familial, 4	hematologic_disorder|hereditary_disease|immune_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0012730	aortic aneurysm, familial thoracic 6	digestive_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|digestive_system_disorder	cardiology|cardiothoracic	familial_thoracic_6_category_is_likely_a_misspelling_of__familial_thoracic_aortic_aneurysm__which_is_a_type_of_cardiovascular_disorder__however_i_have_not_seen_it_in_the_list_so_will_assume__cardiovascular_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012731	elliptocytosis 1	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|red_cell_disorder	false	false	false	true	medium
MONDO:0012732	tremor, hereditary essential, and idiopathic normal pressure hydrocephalus	hereditary_disease	other	hereditary_disease|idiopathic_disease	genetics_and_genomics|neurology	idiopathic_normal_pressure_hydrocephalus_is_not_a_disease_but_a_condition__so_it_will_be_removed_from_the_selection|neurodegenerative_disease|tremor_and_hereditary_essential_are_likely_neurodegenerative_diseases	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	for_hereditary_essential_tremor__there_are_treatments_such_as_beta_blockers__like_propranolol__and_anticonvulsants__like_primidone__that_can_help_manage_the_symptoms__in_more_severe_cases__surgical_options_like_deep_brain_stimulation_may_be_considered____for_idiopathic_normal_pressure_hydrocephalus__nph___the_standard_treatment_is_the_surgical_placement_of_a_shunt_to_drain_excess_cerebrospinal_fluid__which_can_alleviate_symptoms___based_on_this_information__efficacious_treatments_exist_for_both_conditions____therefore__the_answer_is_true	high
MONDO:0012733	autosomal recessive bestrophinopathy	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	genetics_and_genomics|pediatric|medical_genetics_is_not_in_the_list_but_closest_match_is__genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0012734	SERKAL syndrome	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	pediatric|rheumatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	skin_disorder|liver_disorder|joint_disorder	false	false	false	false	high
MONDO:0012735	Temple-Baraitser syndrome	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|otolaryngology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	teeth_disorder|ear_disorder|hearing_disorder	false	false	false	false	very_high
MONDO:0012736	long QT syndrome 9	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|cardiology|pediatric	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0012737	long QT syndrome 10	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|cardiology|pediatrics	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0012738	long QT syndrome 11	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|cardiology|pediatric	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0012739	microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome	disorder_of_visual_system|syndromic_disease	other	syndromic_disease|disorder_of_visual_system	genetics_and_genomics|pediatric|otolaryngology	neurodegenerative_disease	nose_disorder|eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0012740	chromosome 22q11.2 deletion syndrome, distal	disorder_of_development_or_morphogenesis|nervous_system_disorder|immune_system_disorder|chromosomal_disorder|cardiovascular_disorder	cardiovascular_disorder	immune_system_disorder|cardiovascular_disorder|chromosomal_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	heart_disorder|blood_bone_marrow_disorder|brain_disorder|immune_disorder	false	false	false	true	high
MONDO:0012741	prostate cancer, hereditary, 12	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	urology|oncology	hereditary|cancer	reproductive_system_disorder|hereditary	false	true	false	true	high
MONDO:0012742	Brugada syndrome 3	hereditary_disease|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|cardiothoracic|cardiology|pediatric|pulmonology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012743	Brugada syndrome 4	hereditary_disease|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|cardiothoracic|cardiology	cardiac___corrected_answer__cardiovascular_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012744	dilated cardiomyopathy 1Y	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	cardiothoracic|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012745	dilated cardiomyopathy 1Z	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiothoracic|cardiology|pulmonology	cardiovascular_disorder|dilated_cardiomyopathy	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012746	dilated cardiomyopathy 2A	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiothoracic|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0012747	glycogen storage disease due to aldolase A deficiency	metabolic_disease|hereditary_disease|hematologic_disorder	anemia|metabolic_disease	metabolic_disease|hereditary_disease|hematologic_disorder	genetics_and_genomics|pediatric|hepatology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0012748	primary ciliary dyskinesia 7	respiratory_system_disorder|hereditary_disease|syndromic_disease	other	respiratory_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012749	mesomelic dysplasia, camera type	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder|bone_disorder	false	false	false	false	medium
MONDO:0012750	lethal arthrogryposis-anterior horn cell disease syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|inflammatory_disease	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0012751	aortic aneurysm, familial abdominal, 3	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	genetics_and_genomics|cardiology|urology|hepatology|pulmonology|hematology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012752	aneurysm, intracranial berry, 6	hereditary_disease|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	cardiology|vascular|hematology|neurology	neurodegenerative_disease|cardiovascular_disorder	brain_disorder|spinal_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012753	amyotrophic lateral sclerosis type 9	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0012754	nanophthalmos 3	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0012755	episodic ataxia type 7	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012756	proximal 16p11.2 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	muscle_disorder|brain_disorder|spinal_disorder|developmental_disorder_is_not_in_the_list_so__brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0012757	lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome	respiratory_system_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|respiratory_system_disorder|hereditary_disease	genetics_and_genomics|pulmonology|obstetrics_and_gynecology	autoimmune_diseases|cancer|inflammatory_disease	reproductive_system_disorder|lung_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0012758	prostate cancer, hereditary, 13	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|urology|oncology	hereditary|cancer	reproductive_system_disorder|hereditary	false	true	false	true	high
MONDO:0012759	camptodactyly syndrome, Guadalajara type 3	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0012761	chromosome 3q29 microduplication syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|developmental_disorder____corrected_list__brain_disorder|developmental_disorder	false	false	false	false	high
MONDO:0012762	catecholaminergic polymorphic ventricular tachycardia 2	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	cardiology|pediatric|genetics_and_genomics	adrenal_gland_disease|cardiovascular_disorder|metabolic_disorder	muscle_disorder|heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012764	RIDDLE syndrome	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012765	lymphatic malformation 2	hereditary_disease|cardiovascular_disorder|immune_system_disorder	cardiovascular_disorder	immune_system_disorder|cardiovascular_disorder|hereditary_disease	pediatric|oncology|hematology|genetics_and_genomics	lymphatic_disorder|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0012766	hereditary spastic paraplegia 37	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0012767	age related macular degeneration 11	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0012768	prostate cancer, hereditary, 11	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	urology|oncology|genetics_and_genomics	hereditary|cancer	hereditary|reproductive_system_disorder	false	true	false	true	high
MONDO:0012769	prostate cancer, hereditary, 14	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	urology|oncology|genetics_and_genomics	hereditary|cancer	hereditary|reproductive_system_disorder	false	true	false	true	high
MONDO:0012770	prostate cancer, hereditary, 15	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|urology|oncology	cancer|hereditary	hereditary|reproductive_system_disorder	false	true	false	true	high
MONDO:0012772	Stevenson-Carey syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases	skin_disorder|joint_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012773	Hunter-Macdonald syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	bone_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0012774	chromosome 15q13.3 microdeletion syndrome	disorder_of_development_or_morphogenesis|nervous_system_disorder|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder|mental_health_disorder	brain_disorder|other___note__i_ve_added__other__as_it_is_often_difficult_to_categorize_genetic_disorders_into_specific_categories_and_many_might_fall_under_the_umbrella_of__other	false	false	false	false	high
MONDO:0012775	thrombocytopenia 4	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology	inflammatory_disease|anemia|autoimmune_diseases	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012783	RFT1-congenital disorder of glycosylation	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder_of_glycosylation	liver_disorder	false	false	true	false	very_high
MONDO:0012784	autosomal recessive ataxia due to ubiquinone deficiency	metabolic_disease|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0012785	pyloric stenosis, infantile hypertrophic, 3	hereditary_disease|digestive_system_disorder	other	hereditary_disease|digestive_system_disorder	gastroenterology|pediatric	metabolic_disorder|cardiovascular_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012786	juvenile cataract-microcornea-renal glucosuria syndrome	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	renal_medicine|genetics_and_genomics|pediatric	renal_disease|metabolic_disorder	kidney_disorder|eye_disorder	false	false	false	false	high
MONDO:0012787	hereditary spastic paraplegia 39	metabolic_disease|hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|syndromic_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012789	dystonia 16	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscledisorder|spinal_disorder	false	false	false	true	high
MONDO:0012790	amyotrophic lateral sclerosis type 10	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0012791	mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|syndromic_disease	metabolic_disease	syndromic_disease|hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	hematology|genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0012792	mitochondrial DNA depletion syndrome 8a	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|nervous_system_disorder|syndromic_disease	metabolic_disease	nervous_system_disorder|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|anemia	muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0012793	hypouricemia, renal, 2	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	nephrology|hematology|endocrinology|renal	metabolic_disorder|renal	kidney_disorder|renal	false	false	false	false	medium
MONDO:0012794	ANE syndrome	hereditary_disease|endocrine_system_disorder|integumentary_system_disorder|reproductive_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|integumentary_system_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|hearing_loss_disorder|skeletal_disorder|developmental_disorder____corrected_list___ear_disorder|ear_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0012795	hypophosphatemic rickets and hyperparathyroidism	hereditary_disease	other	hereditary_disease	renal_medicine|pediatric|endocrinology	metabolic_disorder|hyperparathyroidism_can_also_be_classified_under_autoimmune_diseases_but_since_the_disease_given_is_hypophosphatemic_rickets_and_hyperparathyroidism_which_specifically_mentions_rickets__it_leans_more_towards_being_a_metabolic_disorder	kidney_disorder|endocrine_disorder|bone_disorder	false	false	false	true	high
MONDO:0012796	retinitis pigmentosa 41	hereditary_disease|metabolic_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0012797	otosclerosis 8	hereditary_disease|otorhinolaryngologic_disease|auditory_system_disorder	other	auditory_system_disorder|hereditary_disease|otorhinolaryngologic_disease	otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	ear_disorder	false	false	false	true	medium
MONDO:0012798	deafness, unilateral, with delayed endolymphatic hydrops	hereditary_disease	other	hereditary_disease	otolaryngology|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	false	medium
MONDO:0012799	hypertrophic cardiomyopathy 11	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiology|cardiothoracic	cardiovascular_disorder|hypertrophic_cardiomyopathy	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0012800	trichoepithelioma, multiple familial, 2	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	pediatric|oncology|genetics_and_genomics	cancer	skin_disorder	false	false	false	false	low
MONDO:0012802	oculoauricular syndrome	syndromic_disease|hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|syndromic_disease	otolaryngology|ophthalmology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0012803	diarrhea-vomiting due to trehalase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|gastroenterology|genetics_and_genomics	trehalase_deficiency|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0012804	hypertrophic cardiomyopathy 12	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiology|cardiothoracic|pediatric	cardiovascular_disorder|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	true	high
MONDO:0012805	childhood onset GLUT1 deficiency syndrome 2	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0012806	ectodermal dysplasia and immunodeficiency 2	syndromic_disease|immune_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|immune_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	immunology|pediatrics|dermatology|genetics_and_genomics	immunodeficiency|autoimmune_diseases	immune_disorder|teeth_disorder|skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0012807	epidermolysis bullosa simplex 5C, with pyloric atresia	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	pediatric|dermatology|gastroenterology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0012808	dilated cardiomyopathy 1AA	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiology|cardiothoracic	cardiovascular_disorder|autoimmune_diseases	muscle_disorder|heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012809	histiocytoma, Angiomatoid fibrous	cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease	oncology|pathology	inflammatory_disease|cancer	blood_bone_marrow_disorder|skin_disorder|vascular_disorder	false	true	false	true	medium
MONDO:0012810	aneurysm, intracranial berry, 7	nervous_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|hereditary_disease	neurology|hematology	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012811	aneurysm, intracranial berry, 8	nervous_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|hereditary_disease	cardiology|neurology|hematology	cardiovascular_disorder|inflammatory_disease|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012812	developmental and epileptic encephalopathy, 4	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	developmental_disorder|neurodegenerative_disease	brain_disorder|epileptic_disorder|developmental_disorder|encephalopathy	false	false	false	true	very_high
MONDO:0012813	retinitis pigmentosa 29	metabolic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder|metabolic_disease	metabolic_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|psychiatric_disorder|hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0012814	diastasis recti and weakness of the linea alba	hereditary_disease	other	hereditary_disease	obstetrics_and_gynecology|orthopaedic	inflammatory_disease|adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|joint_disorder|muscle_disorder	false	false	false	false	low
MONDO:0012815	Coats plus syndrome	nervous_system_disorder|premature_aging_syndrome|hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|premature_aging_syndrome	pediatrics|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|bone_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0012816	atrial fibrillation, familial, 6	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	cardiology|genetics_and_genomics|hematology	familial|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0012817	Ewing sarcoma	cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease	pediatric|oncology|orthopaedic	cancer	bone_disorder|joint_disorder|vascular_disorder	false	true	false	true	high
MONDO:0012818	maturity-onset diabetes of the young type 9	metabolic_disease|digestive_system_disorder|endocrine_system_disorder|hereditary_disease	diabetes_mellitus|metabolic_disease|endocrine_system_disorder	digestive_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology	anemia|metabolic_disorder|autoimmune_diseases	endocrine_disorder	false	false	true	true	medium
MONDO:0012819	diabetic ketoacidosis	metabolic_disease|digestive_system_disorder|endocrine_system_disorder	diabetes_mellitus|metabolic_disease|endocrine_system_disorder	digestive_system_disorder|metabolic_disease|endocrine_system_disorder	endocrinology|renal_medicine	diabetic_ketoacidosis|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0012820	colorectal cancer, susceptibility to, 3	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	oncology|gastroenterology|genetics_and_genomics	autoimmune_diseases|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0012821	colorectal cancer, susceptibility to, 5	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	oncology|gastroenterology|genetics_and_genomics	autoimmune_diseases|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0012822	colorectal cancer, susceptibility to, 6	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	oncology|gastroenterology	inflammatory_disease|autoimmune_diseases|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0012823	colorectal cancer, susceptibility to, 7	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	oncology|gastroenterology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0012824	hypomyelinating leukodystrophy 4	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0012825	extraskeletal myxoid chondrosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|orthopaedic	adrenal_gland_disease|cancer	spinal_disorder|bone_disorder|joint_disorder|muscle_disorder	false	true	false	false	high
MONDO:0012828	atrial fibrillation, familial, 7	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	cardiology|pulmonology|hematology|renal_medicine|genetics_and_genomics	familial|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0012829	inflammatory bowel disease 12	digestive_system_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease|digestive_system_disorder	gastroenterology	autoimmune_diseases|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012830	chromosome 10q23 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|genetic_disorder	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0012831	inflammatory bowel disease 13	digestive_system_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease|digestive_system_disorder	rheumatology|gastroenterology	autoimmune_diseases|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012832	inflammatory bowel disease 14	digestive_system_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease|digestive_system_disorder	rheumatology|gastroenterology	autoimmune_diseases|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012833	Crouzon syndrome-acanthosis nigricans syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatrics|dermatology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	skin_disorder|hair_growth_disorder	false	false	false	false	high
MONDO:0012837	inflammatory bowel disease 15	digestive_system_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease|digestive_system_disorder	hepatology|rheumatology|gastroenterology	autoimmune_diseases|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012838	inflammatory bowel disease 16	digestive_system_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease|digestive_system_disorder	hepatology|rheumatology|hematology|gastroenterology	autoimmune_diseases|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012839	pyogenic bacterial infections due to MyD88 deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|pediatric|hematology|genetics_and_genomics	autoimmune_diseases|bacterial_infections|inflammatory_disease	immune_disorder	true	false	false	true	very_high
MONDO:0012840	inflammatory bowel disease 17	digestive_system_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease|digestive_system_disorder	rheumatology|gastroenterology	autoimmune_diseases|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012841	inflammatory bowel disease 18	digestive_system_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease|digestive_system_disorder	gastroenterology	autoimmune_diseases|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012842	melanoma, cutaneous malignant, susceptibility to, 7	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	dermatology|oncology	cancer|susceptibility_to|cutaneous_malignant	skin_disorder|cutaneous_malignant	false	true	false	true	high
MONDO:0012844	primary ciliary dyskinesia 8	syndromic_disease|hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|syndromic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012845	inflammatory bowel disease 19	digestive_system_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease|digestive_system_disorder	hepatology|rheumatology|gastroenterology	autoimmune_diseases|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder|inflammatory_bowel_disease_could_fit_in_both_categories_but_the_first_one_is_more_specific_so_i_will_only_list_that_one	false	false	false	true	high
MONDO:0012846	generalized epilepsy with febrile seizures plus, type 6	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0012847	autosomal recessive congenital ichthyosis 6	disorder_of_visual_system|hereditary_disease|integumentary_system_disorder	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|integumentary_system_disorder	dermatology|pediatric|genetics_and_genomics	skin_disease|metabolic_disorder	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0012848	Meckel syndrome, type 6	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0012849	Joubert syndrome 9	disorder_of_visual_system|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	neurodegenerative_disease	disorder_of_visual_system|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0012850	hypophosphatemic nephrolithiasis/osteoporosis 1	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|urinary_system_disorder	other	musculoskeletal_system_disorder|urinary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|renal_medicine|endocrinology	metabolic_disorder|nephrolithiasis_osteoporosis_is_related_to_a_metabolic_disorder_which_also_causes_kidney_stones__nephrolithiasis__and_bone_thinning__osteoporosis	kidney_disorder|bone_disorder	false	false	false	true	medium
MONDO:0012851	hypophosphatemic nephrolithiasis/osteoporosis 2	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|urinary_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|urinary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|renal_medicine|endocrinology	metabolic_disorder|nephrolithiasis|osteoporosis	kidney_disorder|bone_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0012852	inflammatory bowel disease 20	immune_system_disorder|digestive_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease|digestive_system_disorder	rheumatology|gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0012853	Fontaine progeroid syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|premature_aging_syndrome|hereditary_disease|integumentary_system_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder|premature_aging_syndrome	pediatric|endocrinology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|skin_disorder|kidney_disorder|bone_disorder|endocrine_disorder|liver_disorder|upper_gastrointestinal_disorder|immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0012854	bilateral microtia-deafness-cleft palate syndrome	hereditary_disease	other	hereditary_disease	otolaryngology|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	bone_disorder|throat_disorder|ear_disorder	false	false	false	false	high
MONDO:0012855	Joubert syndrome 8	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|anemia	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0012856	Birk-Barel syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0012857	porokeratosis 5, disseminated superficial actinic type	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	skin_disorder|liver_disorder	false	false	false	false	low
MONDO:0012858	primary CD59 deficiency	hematologic_disorder|hereditary_disease|nervous_system_disorder	anemia	hematologic_disorder|hereditary_disease|nervous_system_disorder	immunology|pediatric|hematology|genetics_and_genomics	immunodeficiency_disease|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0012859	autosomal recessive osteopetrosis 7	disorder_of_visual_system|immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	immune_system_disorder|musculoskeletal_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	rheumatology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	joint_disorder|bone_disorder|bone_bone_marrow_disorder	false	false	false	false	high
MONDO:0012860	thrombophilia due to protein C deficiency, autosomal recessive	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0012861	premature ovarian failure 6	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	obstetrics_and_gynecology|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0012864	chromosome 2q32-q33 deletion syndrome	nervous_system_disorder|syndromic_disease|psychiatric_disorder|chromosomal_disorder|hereditary_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|chromosomal_disorder|psychiatric_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012865	Pseudofolliculitis barbae	hereditary_disease	other	hereditary_disease	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0012866	hereditary spastic paraplegia 35	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012867	hereditary spastic paraplegia 38	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	syndromic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0012868	thrombophilia due to protein S deficiency, autosomal dominant	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	cardiology|hematology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0012869	intellectual disability, autosomal dominant 22	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|intellectual_disability	false	false	false	true	high
MONDO:0012870	chromosome 2q31.2 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012871	Jervell and Lange-Nielsen syndrome 2	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012872	thrombophilia, familial, due to decreased release of tissue plasminogen activator	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	cardiology|hematology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0012873	Ehlers-Danlos syndrome, spondylocheirodysplastic type	metabolic_disease|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	metabolic_disease	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|metabolic_disease	rheumatology|orthopaedic|genetics_and_genomics	cardiovascular_disorder|inflammatory_disease	joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012874	porokeratosis 6, disseminated superficial actinic type	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology|skin_conditions	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0012875	inflammatory bowel disease 21	immune_system_disorder|digestive_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease|digestive_system_disorder	rheumatology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012876	heparin cofactor 2 deficiency	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	coagulation_disorder|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0012877	major affective disorder 8	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	major_affective_disorder|mental_health_disorder	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0012878	Cowden syndrome 2	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	oncology|genetics_and_genomics	cancer|neurodegenerative_disease	skin_disorder|brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0012880	hypogonadotropic hypogonadism 5 with or without anosmia	endocrine_system_disorder|reproductive_system_disorder|syndromic_disease|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|syndromic_disease|reproductive_system_disorder	pediatric|neurology|genetics_and_genomics|endocrinology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0012881	major affective disorder 7	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	major_affective_disorder|mental_health_disorder	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0012882	major affective disorder 9	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	major_affective_disorder|mental_health_disorder	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0012883	acute promyelocytic leukemia	immune_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|immune_system_disorder|acute_disease|cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder	oncology|hematology	cancer|anemia	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0012885	SRD5A3-congenital disorder of glycosylation	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	urology|pediatric|genetics_and_genomics	congenital_disorder_of_glycosylation|metabolic_disorder	kidney_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0012886	inflammatory bowel disease 22	immune_system_disorder|digestive_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease|digestive_system_disorder	rheumatology|gastroenterology	autoimmune_diseases|inflammatory_disease	immune_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012887	inflammatory bowel disease 23	immune_system_disorder|digestive_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	immune_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012890	pontocerebellar hypoplasia type 2B	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder_spinal_disorder	false	false	false	false	very_high
MONDO:0012891	pontocerebellar hypoplasia type 2C	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012892	bone fragility with contractures, arterial rupture, and deafness	disorder_of_development_or_morphogenesis|connective_tissue_disorder|hereditary_disease	other	connective_tissue_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	otolaryngology|rheumatology|genetics_and_genomics	autoimmune_diseases|anemia|metabolic_disorder	vascular_disorder|bone_disorder|ear_disorder|joint_disorder	true	false	false	false	very_high
MONDO:0012895	torsion dystonia 17	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0012897	congenital factor XI deficiency	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0012899	alopecia, androgenetic, 3	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|endocrinology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|endocrine_disorder|reproductive_system_disorder	false	false	false	true	low
MONDO:0012900	cardiomyopathy, familial restrictive, 3	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	genetics_and_genomics|cardiology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0012901	inherited prekallikrein deficiency	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics|pediatric	metabolic_disorder|anemia	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	low
MONDO:0012902	autosomal dominant nonsyndromic hearing loss 27	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	high
MONDO:0012903	autosomal recessive nonsyndromic hearing loss 45	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|otolaryngology|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	high
MONDO:0012904	epilepsy, progressive myoclonic, 1B	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0012905	hypomyelinating leukodystrophy 6	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0012906	primary ciliary dyskinesia 9	syndromic_disease|hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|pulmonology|neurology	neurodegenerative_disease|metabolic_disorder	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0012907	blindness - scoliosis - arachnodactyly syndrome	disorder_of_visual_system|disorder_of_development_or_morphogenesis	other	disorder_of_visual_system|disorder_of_development_or_morphogenesis|disorder_of_orbital_region	orthopaedic|genetics_and_genomics|ophthalmology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0012908	complement component 6 deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	hematology|rheumatology|genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0012909	skeletal defects, genital hypoplasia, and intellectual disability	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics|medical_genetics|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder|skeletal_defects_also_relate_to_genetic_disorders_which_can_be_classified_as_metabolic_disorder__but_the_given_category_list_does_not_have_that_option_so_the_best_fitting_categories_from_the_given_list_would_be____metabolic_disorder	joint_disorder|bone_disorder|brain_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0012910	age-related hearing impairment 1	nervous_system_disorder|hereditary_disease|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	otolaryngology|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0012911	pseudohypoparathyroidism type 1C	hereditary_disease|disorder_of_development_or_morphogenesis|urinary_system_disorder|metabolic_disease|endocrine_system_disorder|musculoskeletal_system_disorder	metabolic_disease|endocrine_system_disorder	hereditary_disease|urinary_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|metabolic_disease	endocrinology|genetics_and_genomics	metabolic_disorder|genetic_disorder|endocrine_system_disorder	kidney_disorder|bone_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0012912	pseudopseudohypoparathyroidism	hereditary_disease|disorder_of_development_or_morphogenesis|urinary_system_disorder|metabolic_disease|endocrine_system_disorder|musculoskeletal_system_disorder	metabolic_disease|endocrine_system_disorder	hereditary_disease|urinary_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|metabolic_disease	endocrinology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	muscle_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0012913	Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome	syndromic_disease|chromosomal_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|chromosomal_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder|syndromic_disease|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|oncology	cancer|developmental_disorder	kidney_disorder|endocrine_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0012914	chromosome 1q21.1 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	intellectual_disability_syndrome|brain_disorder	false	false	false	false	high
MONDO:0012915	chromosome 1q21.1 duplication syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	intellectual_disability_disorder|brain_disorder|musculoskeletal_disorder|developmental_delay_disorder	false	false	false	false	high
MONDO:0012916	chromosome 2p16.1-p15 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	joint_disorder|developmental_disorder|immune_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0012917	specific language impairment 4	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatry|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0012918	primary ciliary dyskinesia 10	syndromic_disease|hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pulmonology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	lung_disorder|kidney_disorder|spinal_disorder|eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0012922	pyloric stenosis, infantile hypertrophic, 5	hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease	gastroenterology|cardiology|pediatric	metabolic_disorder|inflammatory_disease|cardiovascular_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0012923	congenital generalized lipodystrophy type 3	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics|dermatology|pediatric	metabolic_disorder|congenital_generalized_lipodystrophy_type_3	skin_disorder|joint_disorder|muscle_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0012924	Diamond-Blackfan anemia 4	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology|pediatric|oncology	autoimmune_diseases|anemia	lung_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0012925	Diamond-Blackfan anemia 5	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	autoimmune_diseases|metabolic_disorder|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0012926	amelogenesis imperfecta hypomaturation type 2A2	musculoskeletal_system_disorder|hereditary_disease	other	mouth_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|hematology|dermatology|pediatric	autoimmune_diseases|metabolic_disorder|anemia	bone_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0012927	chromosome 1q41-q42 deletion syndrome	chromosomal_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrine_system_disorder	nervous_system_disorder|chromosomal_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	developmental_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0012928	hereditary spastic paraplegia 42	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0012929	Compton-North congenital myopathy	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|cardiovascular_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012930	autosomal recessive severe congenital neutropenia due to G6PC3 deficiency	immune_system_disorder|hereditary_disease|hematologic_disorder	other	hematologic_disorder|immune_system_disorder|hereditary_disease	genetics_and_genomics|hematology|pediatrics	neutropenia|metabolic_disorder|congenital_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0012932	myopia 16, autosomal dominant	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0012933	breast-ovarian cancer, familial, susceptibility to, 2	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0012934	leukemia, chronic lymphocytic, susceptibility to, 3	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	hematology|oncology	autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0012935	leukemia, chronic lymphocytic, susceptibility to, 4	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	genetics_and_genomics|hematology|oncology	autoimmune_diseases|cancer|allergy	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0012936	leukemia, chronic lymphocytic, susceptibility to, 5	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	hematology|oncology	autoimmune_diseases|cancer|allergy	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0012937	Diamond-Blackfan anemia 6	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	autoimmune_diseases|inflammatory_disease|anemia	lung_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0012938	Diamond-Blackfan anemia 7	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology|pulmonology|pediatric	autoimmune_diseases|metabolic_disorder|anemia	lung_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0012939	Diamond-Blackfan anemia 8	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0012940	inflammatory bowel disease 24	immune_system_disorder|hereditary_disease|digestive_system_disorder	other	immune_system_disorder|digestive_system_disorder|hereditary_disease	gastroenterology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012941	inflammatory bowel disease 25	immune_system_disorder|hereditary_disease|digestive_system_disorder|connective_tissue_disorder	other	immune_system_disorder|digestive_system_disorder|connective_tissue_disorder|hereditary_disease	gastroenterology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|inflammatory_bowel_disease_is_a_disorder_of_the_lower_gastrointestinal_tract_so_i_will_remove_upper_gastrointestinal_disorder_from_the_list__also_it_is_an_autoimmune_disease_so_i_will_remove_immune_disorder_as_well|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012942	lung cancer susceptibility 3	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	genetics_and_genomics|pulmonology|oncology	autoimmune_diseases|inflammatory_disease|cancer	lung_disorder|immune_disorder	false	true	false	false	high
MONDO:0012943	retinitis pigmentosa 46	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|metabolic_disease	psychiatric_disorder|metabolic_disease	metabolic_disease|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease	genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0012944	chromosome 17P13.3, telomeric, duplication syndrome	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|oncology	cancer|genetic_disorder	chromosome_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0012945	amyotrophic lateral sclerosis type 11	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0012946	intellectual disability, autosomal dominant 3	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0012947	intellectual disability, autosomal dominant 4	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	autosomal_dominant_disorder_is_typically_associated_with_this_category|brain_disorder	false	false	false	false	high
MONDO:0012948	chromosome 6pter-p24 deletion syndrome	disorder_of_visual_system|chromosomal_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_visual_system|disorder_of_orbital_region|chromosomal_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	developmental_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0012949	aneurysm, intracranial berry, 9	hereditary_disease|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|hereditary_disease	cardiology|neurology	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0012950	aneurysm, intracranial berry, 10	nervous_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|hereditary_disease	cardiology|neurology	neurodegenerative_disease|cardiovascular_disorder	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0012951	colorectal cancer, susceptibility to, 8	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	genetics_and_genomics|gastroenterology|hematology|oncology	autoimmune_diseases|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0012952	colorectal cancer, susceptibility to, 9	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	genetics_and_genomics|gastroenterology|hematology|oncology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0012953	colorectal cancer, susceptibility to, 10	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	genetics_and_genomics|gastroenterology|oncology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0012954	colorectal cancer, susceptibility to, 11	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	genetics_and_genomics|gastroenterology|hematology|oncology	metabolic_disorder|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0012955	lung cancer susceptibility 4	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	genetics_and_genomics|pulmonology|oncology	autoimmune_diseases|inflammatory_disease|cancer	lung_disorder	false	false	false	false	high
MONDO:0012960	intellectual disability, autosomal dominant 5	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	intellectual_disability|neurodegenerative_disease	intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0012964	chromosome 15q26-qter deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	immune_disorder|musculoskeletal_disorder|brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0012965	seizures, benign familial infantile, 4	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0012967	hemolytic anemia due to adenylate kinase deficiency	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics|pediatrics	metabolic_disorder|anemia	blood_bone_marrow_disorder|hematological_disorder	false	false	false	false	high
MONDO:0012968	Usher syndrome type 1H	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	ophthalmology|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder|eye_disorder	true	false	false	false	high
MONDO:0012972	febrile seizures, familial, 10	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	immune_disorder|brain_disorder	false	false	false	true	medium
MONDO:0012973	inflammatory bowel disease 26	hereditary_disease|immune_system_disorder|digestive_system_disorder	other	immune_system_disorder|digestive_system_disorder|hereditary_disease	rheumatology|gastroenterology	inflammatory_disease|inflammatory_bowel_disease_is_not_in_the_list_so_removed|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0012974	autosomal dominant nonsyndromic hearing loss 59	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0012975	autosomal dominant nonsyndromic hearing loss 3B	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	pediatric|otolaryngology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	ear_disorder|throat_disorder	false	false	false	true	medium
MONDO:0012976	autosomal dominant nonsyndromic hearing loss 2B	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	false	medium
MONDO:0012977	autosomal recessive nonsyndromic hearing loss 1B	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	high
MONDO:0012978	primary ciliary dyskinesia 11	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|syndromic_disease|hereditary_disease	pulmonology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|eye_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012979	primary ciliary dyskinesia 12	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|syndromic_disease|hereditary_disease	pediatric|pulmonology|genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	kidney_disorder|eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0012980	endocrine-cerebro-osteodysplasia syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|endocrinology|genetics_and_genomics	endocrine_gland_disease|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0012981	hereditary spherocytosis type 4	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0012982	episodic ataxia type 6	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012983	cone-rod dystrophy 12	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|psychiatric_disorder	ophthalmology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0012984	PHARC syndrome	nervous_system_disorder|hereditary_disease|syndromic_disease|metabolic_disease	metabolic_disease	nervous_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|liver_disorder|immune_disorder	false	false	false	false	high
MONDO:0012985	hereditary spherocytosis type 5	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	hereditary_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0012986	bilateral parasagittal parieto-occipital polymicrogyria	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	polymicrogyria|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0012987	agammaglobulinemia 6, autosomal recessive	hematologic_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics|pediatrics	autoimmune_diseases|metabolic_disorder|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0012988	hypogonadotropic hypogonadism 6 with or without anosmia	reproductive_system_disorder|hereditary_disease|syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrinology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0012989	microcephaly 7, primary, autosomal recessive	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|primary|autosomal_recessive	false	false	false	false	high
MONDO:0012990	Leber congenital amaurosis 13	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|psychiatric_disorder	ophthalmology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0012991	Kahrizi syndrome	hereditary_disease	other	hereditary_disease	pediatric|endocrinology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|joint_disorder|blood_bone_marrow_disorder|liver_disorder|immune_disorder	false	false	false	false	high
MONDO:0012992	pancreatic insufficiency-anemia-hyperostosis syndrome	mitochondrial_disease|hematologic_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|digestive_system_disorder|metabolic_disease|endocrine_system_disorder	anemia|metabolic_disease|endocrine_system_disorder	musculoskeletal_system_disorder|digestive_system_disorder|mitochondrial_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hematologic_disorder|metabolic_disease|hereditary_disease	hematology|endocrinology|gastroenterology	inflammatory_disease|metabolic_disorder|anemia	blood_bone_marrow_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0012993	dyschromatosis universalis hereditaria 2	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|dermatology	metabolic_disorder|neurodegenerative_disease	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0012994	dopa-responsive dystonia due to sepiapterin reductase deficiency	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0012995	myopia 15, autosomal dominant	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0012996	AGAT deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	kidney_disorder	false	false	false	false	very_high
MONDO:0012997	cholestasis-pigmentary retinopathy-cleft palate syndrome	hereditary_disease	other	hereditary_disease	pediatric|ophthalmology|genetics_and_genomics|hepatology	metabolic_disorder|neurodegenerative_disease	eye_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0012998	faciocardiomelic syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|cardiology	cardiovascular_disorder|adrenal_gland_disease|metabolic_disorder	endocrine_disorder|heart_disorder	false	false	false	false	high
MONDO:0012999	guanidinoacetate methyltransferase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology|renal_medicine	metabolic_disorder|neurodegenerative_disease	kidney_disorder|muscle_disorder	false	false	false	true	high
MONDO:0013000	porphyria due to ALA dehydratase deficiency	integumentary_system_disorder|endocrine_system_disorder|hereditary_disease|digestive_system_disorder|metabolic_disease	metabolic_disease|endocrine_system_disorder	metabolic_disease|integumentary_system_disorder|digestive_system_disorder|hereditary_disease|endocrine_system_disorder	pediatric|dermatology|hematology|genetics_and_genomics|neurology	anemia|metabolic_disorder	muscle_disorder|skin_disorder|bone_disorder|liver_disorder	false	false	false	false	medium
MONDO:0013002	cone-rod dystrophy 9	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0013003	isolated congenital hypoglossia/aglossia	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	mouth_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	congenital_disease|neurodegenerative_disease	upper_gastrointestinal_disorder|throat_disorder	false	false	false	false	medium
MONDO:0013004	hypotonia, seizures, and precocious puberty	hereditary_disease	other	hereditary_disease	pediatric|endocrinology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|endocrine_disorder|brain_disorder	true	false	false	false	medium
MONDO:0013005	EAST syndrome	nervous_system_disorder|urinary_system_disorder|hereditary_disease	other	nervous_system_disorder|urinary_system_disorder|hereditary_disease	pediatric|neurology	inflammatory_disease|neurodegenerative_disease	immune_disorder|lower_gastrointestinal_disorder|joint_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0013006	isolated growth hormone deficiency type IB	nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	reproductive_system_disorder|nervous_system_disorder|hereditary_disease|endocrine_system_disorder	pediatric|endocrinology	endocrine_disorder|metabolic_disorder	endocrine_disorder|brain_disorder	false	false	false	true	medium
MONDO:0013007	combined immunodeficiency due to ORAI1 deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatric|immunology|genetics_and_genomics	anemia|inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0013008	combined immunodeficiency due to STIM1 deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatrics|allergy_and_immunology|genetics_and_genomics	immunodeficiency_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013009	Megarbane-Jalkh syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|joint_disorder|bone_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0013010	autosomal recessive nonsyndromic hearing loss 71	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease|auditory_system_disorder	pediatric|otolaryngology|genetics_and_genomics	anemia|inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	ear_disorder|bone_disorder	false	false	false	true	medium
MONDO:0013011	atrial septal defect 5	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	pediatric|cardiothoracic|pulmonology|cardiology	autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0013012	inflammatory bowel disease 27	immune_system_disorder|hereditary_disease|digestive_system_disorder	other	immune_system_disorder|digestive_system_disorder|hereditary_disease	rheumatology|gastroenterology	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0013013	question mark ears, isolated	hereditary_disease	other	hereditary_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	ear_disorder	false	false	false	false	none
MONDO:0013014	spondyloepimetaphyseal dysplasia, aggrecan type	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	rheumatology|genetics_and_genomics|orthopaedic	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013015	Brugada syndrome 5	syndromic_disease|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|hereditary_disease|cardiovascular_disorder	pulmonology|cardiology|genetics_and_genomics	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013016	leukocyte adhesion deficiency 3	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|hereditary_disease|disorder_of_visual_system	other	immune_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|musculoskeletal_system_disorder|hereditary_disease|hematologic_disorder	immunology|hematology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0013017	hypotrichosis 5	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	hair_disorder|skin_disorder	false	false	false	true	low
MONDO:0013018	keratosis follicularis spinulosa decalvans, autosomal dominant	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	skin_disorder	false	false	false	false	low
MONDO:0013021	sterile multifocal osteomyelitis with periostitis and pustulosis	immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|syndromic_disease|hereditary_disease	other	immune_system_disorder|connective_tissue_disorder|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|hematologic_disorder	pediatric|rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder|bone_disorder|skin_disorder	false	false	false	false	high
MONDO:0013023	orofacial cleft 12	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	craniofacial_anomaly|neurodevelopmental_disorders|facial_dysmorphism|congenital_abnormality|birth_defect|developmental_disorder|oral_cleft	nose_disorder|upper_gastrointestinal_disorder|teeth_disorder	false	false	false	false	high
MONDO:0013024	chronic thromboembolic pulmonary hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|hematology|cardiology	inflammatory_disease|cardiovascular_disorder	lung_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013025	chromosome 6q24-q25 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0013026	subepithelial mucinous corneal dystrophy	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0013027	posterior amorphous corneal dystrophy	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0013028	adenosine monophosphate deaminase deficiency	musculoskeletal_system_disorder|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|musculoskeletal_system_disorder|hereditary_disease	immunology|pediatrics|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	medium
MONDO:0013029	spinocerebellar ataxia 9	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013030	dilated cardiomyopathy 1BB	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	rheumatology|cardiothoracic|endocrinology|pulmonology|cardiology|renal_medicine	cardiovascular_disorder|dilated_cardiomyopathy_1bb	heart_disorder|muscle_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013031	chromosome 5Q14.3 deletion syndrome, distal	syndromic_disease|hereditary_disease|nervous_system_disorder	other	syndromic_disease|hereditary_disease|nervous_system_disorder	oncology|pediatrics|pulmonology|hematology|genetics_and_genomics	neurodegenerative_disease|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0013033	cerebral palsy, spastic quadriplegic, 2	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|orthopaedic	neurodegenerative_disease|spastic_quadrilegic_type_cerebral_palisy|cardiovascular_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0013034	keratosis palmoplantaris striata 2	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|genodermatosis|hereditary_disorder	false	false	false	false	medium
MONDO:0013035	orofaciodigital syndrome XI	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	metabolic_disorder	ear_disorder|joint_disorder|spinal_disorder|teeth_disorder	false	false	false	false	very_high
MONDO:0013036	Zechi-Ceide syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	skeletal_system_disorder|bone_disorder	false	false	false	false	high
MONDO:0013037	Giacheti syndrome	hereditary_disease	other	hereditary_disease	hepatology|gastroenterology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0013038	CLOVES syndrome	syndromic_disease|cancer_or_benign_tumor|hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|neurology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	lower_gastrointestinal_disorder|vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013039	3M syndrome 2	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	ear_disorder|vascular_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0013040	atypical hemolytic-uremic syndrome with MCP/CD46 anomaly	immune_system_disorder|hematologic_disorder|syndromic_disease|hereditary_disease	other	immune_system_disorder|syndromic_disease|hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics|renal_medicine	metabolic_disorder|autoimmune_diseases|anemia	immune_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0013041	atypical hemolytic-uremic syndrome with I factor anomaly	immune_system_disorder|hematologic_disorder|syndromic_disease|hereditary_disease	other	immune_system_disorder|syndromic_disease|hereditary_disease|hematologic_disorder	hematology|renal_medicine	metabolic_disorder|autoimmune_diseases|anemia	immune_disorder|vascular_disorder|kidney_disorder	false	false	false	true	high
MONDO:0013042	atypical hemolytic-uremic syndrome with B factor anomaly	immune_system_disorder|hematologic_disorder|syndromic_disease|hereditary_disease	other	immune_system_disorder|syndromic_disease|hereditary_disease|hematologic_disorder	hematology|hematatology|renal_medicine|pediatric	metabolic_disorder|anemia	immune_disorder|kidney_disorder	false	false	false	true	high
MONDO:0013043	atypical hemolytic-uremic syndrome with C3 anomaly	immune_system_disorder|hematologic_disorder|syndromic_disease|hereditary_disease	other	immune_system_disorder|syndromic_disease|hereditary_disease|hematologic_disorder	hematology|renal_medicine|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases|anemia	immune_disorder|vascular_disorder|kidney_disorder	false	false	false	true	high
MONDO:0013044	atypical hemolytic-uremic syndrome with thrombomodulin anomaly	immune_system_disorder|hematologic_disorder|syndromic_disease|hereditary_disease	other	immune_system_disorder|syndromic_disease|hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics|renal_medicine|pediatric	metabolic_disorder|autoimmune_diseases|anemia	vascular_disorder|kidney_disorder	false	false	false	true	high
MONDO:0013046	glycogen storage disease due to muscle beta-enolase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatrics|endocrinology|hepatology|genetics_and_genomics	glycogen_storage_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	medium
MONDO:0013047	glycogen storage disease due to lactate dehydrogenase M-subunit deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|hematology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0013048	hereditary spastic paraplegia 50	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	hereditary|metabolic_disorder|neurodegenerative_disease|note__original_request_did_not_specify_how_to_handle__hereditary__as_a_category__but_i_assume_it_was_meant_to_be_one_of_the_listed_categories	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013049	DPM3-congenital disorder of glycosylation	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	congenital_disorder_of_glycosylation_can_be_considered_under_genetics_and_genomics_as_glycosylation_is_a_process_influenced_by_genetic_makeup|genetics_and_genomics|pediatric	congenital_disorder_of_glycosylation|metabolic_disorder	muscle_disorder|immune_disorder|joint_disorder|bone_disorder|skin_disorder	false	false	true	false	high
MONDO:0013050	lethal polymalformative syndrome, Boissel type	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|anemia	muscle_disorder|blood_bone_marrow_disorder|reproductive_system_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0013051	autosomal recessive cutis laxa type 2B	integumentary_system_disorder|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	dermatology|genetics_and_genomics|pediatric	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|skin_disorder	false	false	false	false	high
MONDO:0013052	retinitis pigmentosa 42	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology	adrenal_gland_disease|neurodegenerative_disease	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013053	microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|cardiovascular_disorder	heart_disorder|skeletal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0013054	microcephaly, growth retardation, cataract, hearing loss, and unusual appearance	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology|neurology|otolaryngology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|cardiovascular_disorder	ear_disorder|brain_disorder|growth_retardation|eye_disorder	true	false	false	false	high
MONDO:0013055	Stargardt macular degeneration, absent or hypoplastic corpus callosum, intellectual disability, and dysmorphic features	hereditary_disease	other	hereditary_disease	psychiatry|genetics_and_genomics|ophthalmology|neurology|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0013056	developmental and epileptic encephalopathy, 39	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|developmental_disorder|encephalopathy	epileptic_disorder|brain_disorder|encephalopathy|developmental_disorder	false	false	false	true	very_high
MONDO:0013058	cystic leukoencephalopathy without megalencephaly	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|brain_disorder	false	false	false	false	high
MONDO:0013059	Aicardi-Goutieres syndrome 5	hereditary_disease|syndromic_disease|connective_tissue_disorder|nervous_system_disorder|immune_system_disorder	neurodegenerative_disease	syndromic_disease|hereditary_disease|connective_tissue_disorder|nervous_system_disorder|immune_system_disorder	genetics_and_genomics|pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0013060	autosomal recessive Parkinson disease 14	psychiatric_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	neurodegenerative_disease|psychiatric_disorder|metabolic_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0013061	myofibrillar myopathy 6	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology	muscular_dystrophy|neurodegenerative_disease	muscle_disorder	false	false	false	false	very_high
MONDO:0013062	long QT syndrome 12	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	cardiology|genetics_and_genomics|pediatric	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0013063	ventricular fibrillation, paroxysmal familial, 2	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	cardiology|genetics_and_genomics|pediatric	paroxysmal_familial|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013064	multiple synostoses syndrome 3	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|orthopaedic	genetic_disorder|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0013065	premature ovarian failure 7	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrinology|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0013066	46,XY sex reversal 3	reproductive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|cardiovascular_disorder|musculoskeletal_system_disorder	endocrine_system_disorder|cardiovascular_disorder	cardiovascular_disorder|reproductive_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder	genetics_and_genomics|urology|endocrinology	sex_reversal_disease|metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0013067	cataract 34 multiple types	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	eye_disorder	false	false	false	true	high
MONDO:0013068	age-related hearing impairment 2	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	otolaryngology|neurology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	high
MONDO:0013069	autosomal recessive optic atrophy, OPA7 type	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|disorder_of_visual_system|metabolic_disease	neurodegenerative_disease|metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|disorder_of_visual_system|nervous_system_disorder|metabolic_disease	genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0013070	spermatogenic failure 7	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	autoimmune_diseases|cancer|anemia|metabolic_disorder	reproductive_system_disorder	false	false	false	false	low
MONDO:0013071	Emery-Dreifuss muscular dystrophy 4, autosomal dominant	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|orthopaedic	autosomal_dominant_disorder|neurodegenerative_disease	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013072	Emery-Dreifuss muscular dystrophy 5, autosomal dominant	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|orthopaedic|neurology|pediatrics	muscular_dystrophy|neurodegenerative_disease	heart_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013073	palmoplantar keratoderma, nonepidermolytic, focal 1	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder	skin_disorder|joint_disorder	false	false	false	false	medium
MONDO:0013074	encephalocraniocutaneous lipomatosis	musculoskeletal_system_disorder|cancer_or_benign_tumor|hereditary_disease|connective_tissue_disorder|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hereditary_disease|connective_tissue_disorder	genetics_and_genomics|dermatology|neurology	cancer|neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder|skin_disorder	false	false	false	false	high
MONDO:0013077	Santos syndrome	hereditary_disease	other	hereditary_disease	psychiatry|neurology	autoimmune_diseases|adrenal_gland_disease	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0013079	primary biliary cholangitis 2	digestive_system_disorder|hereditary_disease|endocrine_system_disorder|premature_aging_syndrome	endocrine_system_disorder	premature_aging_syndrome|digestive_system_disorder|hereditary_disease|endocrine_system_disorder	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	biliary_disorder|liver_disorder	false	false	false	true	high
MONDO:0013080	primary biliary cholangitis 3	digestive_system_disorder|hereditary_disease|endocrine_system_disorder|premature_aging_syndrome	endocrine_system_disorder	premature_aging_syndrome|digestive_system_disorder|hereditary_disease|endocrine_system_disorder	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	biliary_disorder|liver_disorder	false	false	false	true	medium
MONDO:0013081	lymphoproliferative syndrome 1	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	hematology|oncology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder_lymphatic_disorder	true	true	false	true	very_high
MONDO:0013082	Hirschsprung disease-ganglioneuroblastoma syndrome	digestive_system_disorder|syndromic_disease	other	digestive_system_disorder|syndromic_disease	genetics_and_genomics|pediatric|oncology	cancer|neurodegenerative_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0013083	neuroblastoma, susceptibility to, 3	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|pediatric|oncology	cancer|autoimmune_diseases|neurodegenerative_disease	brain_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0013084	neuroblastoma, susceptibility to, 4	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|pediatric|oncology|neurology	cancer	brain_disorder|bone_disorder|lung_disorder	false	true	false	true	high
MONDO:0013085	neuroblastoma, susceptibility to, 5	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|pediatric|oncology	neuroblastoma__susceptibility_to|cancer	brain_disorder|bone_disorder|lymphatic_disorder	false	true	false	false	medium
MONDO:0013086	neuroblastoma, susceptibility to, 6	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	neuroblastoma__susceptibility_to|genetics_and_genomics|pediatric|oncology	cancer	brain_disorder|lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0013087	bronchiectasis with or without elevated sweat chloride 2	respiratory_system_disorder|hereditary_disease	other	respiratory_system_disorder|hereditary_disease|idiopathic_disease	pulmonology|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|lung_disorder	true	false	false	true	high
MONDO:0013088	follicular lymphoma, susceptibility to, 1	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	hematology|oncology	cancer|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	medium
MONDO:0013090	chromosome 19q13.11 deletion syndrome	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease|genetic_disorder	learning_disability|brain_disorder|intellectual_disability|developmental_delay|developmental_disorder|growth_disorder	false	false	false	false	high
MONDO:0013091	glycogen storage disease IXc	digestive_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|hereditary_disease|endocrine_system_disorder|metabolic_disease	genetics_and_genomics|pediatric|hepatology|endocrinology	adrenal_gland_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	true	high
MONDO:0013092	glioma susceptibility 2	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0013093	glioma susceptibility 3	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013094	glioma susceptibility 5	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0013095	glioma susceptibility 6	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013096	glioma susceptibility 7	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013097	glioma susceptibility 8	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013098	noise induced hearing loss	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	otolaryngology|neurology	neurodegenerative_disease|inflammatory_disease	ear_disorder	false	false	false	true	medium
MONDO:0013099	combined pituitary hormone deficiencies, genetic form	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|nervous_system_disorder	genetics_and_genomics|pediatric|endocrinology	genetic_diseases|metabolic_disorder	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0013100	atrial fibrillation, familial, 8	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	hematology|genetics_and_genomics|cardiology	cardiovascular_disorder|familial	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0013108	leukemia, acute lymphocytic, susceptibility to, 1	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor|acute_disease	oncology|hematology|genetics_and_genomics	autoimmune_diseases|allergy|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0013109	leukemia, acute lymphocytic, susceptibility to, 2	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor|acute_disease	oncology|hematology	autoimmune_diseases|inflammation_disease|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0013110	neurodegenerative syndrome due to cerebral folate transport deficiency	metabolic_disease|nervous_system_disorder|nutritional_disorder|hereditary_disease	metabolic_disease|neurodegenerative_disease	metabolic_disease|hereditary_disease|nutritional_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	cerebellar_ataxia_disorder|brain_disorder	false	false	false	true	high
MONDO:0013111	acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins	metabolic_disease|digestive_system_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease	metabolic_disease|endocrine_system_disorder	metabolic_disease|hereditary_disease|digestive_system_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|acute_disease	pediatric|hepatology|gastroenterology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_failure|mitochondrial_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0013112	bronchiectasis with or without elevated sweat chloride 3	respiratory_system_disorder|hereditary_disease	other	hereditary_disease|respiratory_system_disorder|idiopathic_disease	pediatric|pulmonology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|lung_disorder	true	false	false	false	high
MONDO:0013113	metaphyseal anadysplasia 2	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	genetic_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0013114	autosomal dominant nonsyndromic hearing loss 50	psychiatric_disorder|nervous_system_disorder|hereditary_disease|auditory_system_disorder	psychiatric_disorder	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	pediatric|otolaryngology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	ear_disorder	false	false	false	true	high
MONDO:0013115	RIN2 syndrome	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|urinary_tract_disorder|kidney_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0013116	congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome	metabolic_disease|musculoskeletal_system_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	hearing_loss_syndrome|neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0013117	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5	metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0013118	Nijmegen breakage syndrome-like disorder	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013119	autosomal recessive nonsyndromic hearing loss 77	psychiatric_disorder|nervous_system_disorder|hereditary_disease|auditory_system_disorder	psychiatric_disorder	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	pediatric|otolaryngology|genetics_and_genomics	autoimmune_diseases|anemia|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	ear_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0013120	46,XY sex reversal 5	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder|endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|endocrine_system_disorder	pediatrics|endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0013121	glaucoma 3, primary congenital, C	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|neurology|ophthalmology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0013122	glaucoma 3, primary congenital, D	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|genetics_and_genomics|neurology|ophthalmology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0013123	atrial septal defect 6	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|cardiology	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0013125	CLAPO syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013127	asphyxiating thoracic dystrophy 3	urinary_system_disorder|syndromic_disease|respiratory_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|respiratory_system_disorder|musculoskeletal_system_disorder|syndromic_disease|urinary_system_disorder	pediatric|pulmonology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	muscle_disorder|throat_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0013128	familial juvenile hyperuricemic nephropathy type 2	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	pediatric|genetics_and_genomics|renal_medicine	hereditary_disease|metabolic_disorder|kidney_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0013129	cone dystrophy 4	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0013130	isolated microphthalmia 4	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|genetics_and_genomics|ophthalmology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0013131	polycystic kidney disease 2	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	endocrinology|genetics_and_genomics|renal_medicine	renal_disease|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0013132	hereditary spastic paraplegia 36	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013133	melanoma, cutaneous malignant, susceptibility to, 5	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	oncology|dermatology	cancer|cutaneous_malignant	skin_disorder|cutaneous_malignant	false	true	false	true	high
MONDO:0013134	glaucoma 1, open angle, O	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology|renal_medicine	autoimmune_diseases|metabolic_disorder|inflammatory_disease	open_angle|eye_disorder	false	false	false	true	medium
MONDO:0013135	familial hemophagocytic lymphohistiocytosis 5	immune_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|immune_system_disorder|syndromic_disease	hematology|genetics_and_genomics	autoimmune_diseases|anemia|metabolic_disorder|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0013136	hereditary hypotrichosis with recurrent skin vesicles	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0013137	choroidal dystrophy, central areolar 2	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|cardiovascular_disorder|hereditary_disease	psychiatric_disorder|cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	central_areolar|eye_disorder	false	false	false	false	medium
MONDO:0013138	vertigo, benign recurrent, 2	psychiatric_disorder|nervous_system_disorder|otorhinolaryngologic_disease|auditory_system_disorder	psychiatric_disorder	otorhinolaryngologic_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	otolaryngology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|ear_disorder	false	false	false	true	medium
MONDO:0013139	neutropenia, severe congenital, 2, autosomal dominant	immune_system_disorder|hematologic_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder|hematologic_disorder	pediatric|hematology|genetics_and_genomics	autoimmune_diseases|cancer|anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0013140	candidiasis, familial, 4	integumentary_system_disorder|immune_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|immune_system_disorder	pediatric|dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0013142	neuropathy, hereditary sensory and autonomic, type 2B	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	hereditary_condition|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013143	hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency	hematologic_disorder|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013144	hereditary antithrombin deficiency	musculoskeletal_system_disorder|hematologic_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	cardiovascular_disorder|metabolic_disorder	liver_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013145	Brugada syndrome 6	syndromic_disease|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|hereditary_disease	cardiothoracic|pulmonology|genetics_and_genomics|cardiology|electrophysiology__not_in_the_list	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013146	Brugada syndrome 7	syndromic_disease|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|hereditary_disease	cardiothoracic|genetics_and_genomics|cardiology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013147	dilated cardiomyopathy 1CC	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiothoracic|cardiology	cardiovascular_disorder|dilated_cardiomyopathy	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0013148	Brugada syndrome 8	syndromic_disease|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|hereditary_disease	cardiothoracic|genetics_and_genomics|cardiology	cardiovascular_disorder|autoimmune_diseases	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013149	hydrops fetalis, nonimmune, with gracile bones and dysmorphic features	hereditary_disease	other	hereditary_disease	pediatric|obstetrics_and_gynecology|genetics_and_genomics|hematology	metabolic_disorder|autoimmune_diseases	skeletal_disorder|bone_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0013150	parkinsonism-dystonia, infantile	nervous_system_disorder|syndromic_disease|hereditary_disease	other	nervous_system_disorder|syndromic_disease|hereditary_disease	pediatric|neurology	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0013151	choroidal dystrophy, central areolar, 3	disorder_of_visual_system|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0013153	inflammatory bowel disease 28	immune_system_disorder|connective_tissue_disorder|hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|immune_system_disorder|connective_tissue_disorder|hereditary_disease	rheumatology|gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0013154	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2	metabolic_disease|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology|orthopaedic	muscular_dystrophy|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0013155	muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3	metabolic_disease|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0013156	muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4	metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013157	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5	metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0013158	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0013159	muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1	metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder|genetic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0013160	muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2	metabolic_disease|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0013161	autosomal recessive limb-girdle muscular dystrophy type 2O	metabolic_disease|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0013162	autosomal recessive limb-girdle muscular dystrophy type 2N	metabolic_disease|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|orthopaedic	muscular_dystrophy|neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013163	nephronophthisis-like nephropathy 1	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	renal_medicine|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0013164	beta-ureidopropionase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|metabolism__edited_to_remove_the__metabolism__that_wasn_t_a_listed_option	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0013165	hereditary spastic paraplegia 45	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013166	GABA aminotransaminase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0013167	Parkinson disease 16	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0013168	dilated cardiomyopathy 1DD	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiothoracic|pulmonology|cardiology	cardiovascular_disorder|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0013169	chromosome 5p13 duplication syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|immune_disorder|muscle_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0013170	cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|pulmonology|genetics_and_genomics|gastroenterology|renal_medicine	inflammatory_disease|metabolic_disorder|autoimmune_diseases	lower_gastrointestinal_disorder|skin_disorder|urinary_tract_disorder|lung_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0013171	purine nucleoside phosphorylase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|metabolism	neurodegenerative_disease|metabolic_disorder	kidney_disorder|lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0013172	polymicrogyria with optic nerve hypoplasia	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0013173	intellectual disability, autosomal recessive 13	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	psychiatric_disorder|metabolic_disease	metabolic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0013174	primary ciliary dyskinesia 13	syndromic_disease|respiratory_system_disorder|hereditary_disease	other	respiratory_system_disorder|syndromic_disease|hereditary_disease	pediatric|pulmonology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013175	retinitis pigmentosa 50	nervous_system_disorder|metabolic_disease|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder|metabolic_disease	metabolic_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0013176	Weill-Marchesani 4 syndrome, recessive	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|orthopaedic	genetic_condition|metabolic_disorder	bone_disorder|joint_disorder|eye_disorder	false	false	false	false	medium
MONDO:0013177	congenital muscular dystrophy due to integrin alpha-7 deficiency	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology|orthopaedic	inflammatory_disease|neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|joint_disorder	false	false	false	true	high
MONDO:0013178	congenital muscular dystrophy due to LMNA mutation	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology|orthopaedic	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0013179	hereditary spastic paraplegia 44	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0013181	amelogenesis imperfecta hypomaturation type 2A3	musculoskeletal_system_disorder|hereditary_disease	other	mouth_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatrics|genetics_and_genomics	anemia|metabolic_disorder|autoimmune_diseases	teeth_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0013182	chromosome 17p13.3 duplication syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	pediatric|oncology|genetics_and_genomics|neurology	neurodegenerative_disease|genetic_disorder|developmental_disorder	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013183	congenital stationary night blindness 1C	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|psychiatric_disorder|hereditary_disease	pediatric|genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0013184	congenital diarrhea 5 with tufting enteropathy	hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease	pediatric|gastroenterology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0013186	Noonan syndrome 6	musculoskeletal_system_disorder|immune_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|immune_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology|cardiology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	joint_disorder|heart_disorder	false	false	false	false	high
MONDO:0013187	factor XIII, A subunit, deficiency of	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|bleeding_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013188	cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 3	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	true	false	false	false	high
MONDO:0013189	trichotillomania	psychiatric_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|hereditary_disease	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder_skin_disorder	false	false	false	false	medium
MONDO:0013190	factor XIII, b subunit, deficiency of	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	coagulation_disorder|blood_disorder|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0013191	focal segmental glomerulosclerosis 5	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	hematology|renal_medicine|nephrology	autoimmune_diseases|kidney_disease|inflammatory_disease	immune_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013194	Pseudopili annulati	hereditary_disease	other	hereditary_disease	dermatology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	skin_disorder|liver_disorder|joint_disorder|blood_bone_marrow_disorder	false	false	false	false	none
MONDO:0013195	hypertrophic cardiomyopathy 13	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiology|cardiothoracic	cardiovascular_disorder|hypertrophic_cardiomyopathy	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0013196	Lynch syndrome 8	digestive_system_disorder|cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	digestive_system_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease	oncology|genetics_and_genomics	cancer|autoimmune_diseases	lower_gastrointestinal_disorder|reproductive_system_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0013197	hypertrophic cardiomyopathy 14	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiology|cardiothoracic	cardiovascular_disorder|hypertrophic_cardiomyopathy	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0013198	dilated cardiomyopathy 1EE	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013199	tuberous sclerosis 2	nervous_system_disorder|cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder|spinal_disorder	false	false	false	true	high
MONDO:0013200	hypertrophic cardiomyopathy 15	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiothoracic|cardiology	cardiovascular_disorder|hypertrophic_cardiomyopathy	muscledisorder|vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0013201	Waardenburg syndrome type 4B	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|digestive_system_disorder	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|digestive_system_disorder	otolaryngology|neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|upper_gastrointestinal_disorder|ear_disorder|eye_disorder|thyroid_disorder_is_not_listed_so_endocrine_disorder	false	false	false	false	high
MONDO:0013202	Waardenburg syndrome type 4C	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|digestive_system_disorder	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|digestive_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|upper_gastrointestinal_disorder|ear_disorder	false	false	false	false	high
MONDO:0013203	corneal dystrophy, Fuchs endothelial, 3	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|ophthalmology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	corneal_dystrophy_is_a_subset_of_this_category|eye_disorder	false	false	false	true	medium
MONDO:0013204	corneal dystrophy, Fuchs endothelial, 4	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|ophthalmology	inflammatory_disease|autoimmune_diseases	corneal_dystrophy|eye_disorder	false	false	false	true	medium
MONDO:0013205	corneal dystrophy, fuchs endothelial, 5	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|ophthalmology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	true	medium
MONDO:0013206	corneal dystrophy, Fuchs endothelial, 6	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	true	medium
MONDO:0013207	corneal dystrophy, fuchs endothelial, 7	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|ophthalmology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	true	high
MONDO:0013208	cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	hematology|gastroenterology|hepatology	metabolic_disorder|neurodegenerative_disease	hypermanganesemia_syndrome_is_often_associated_with_polycythemia__so_add_that_one_as_well__liver_disorder|liver_disorder|muscle_disorder|blood_bone_marrow_disorder|polycythemia	false	false	false	false	high
MONDO:0013209	metabolic dysfunction-associated steatotic liver disease	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|metabolic_disorder|cardiovascular_disorder	liver_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0013210	autosomal recessive nonsyndromic hearing loss 25	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	otolaryngology|genetics_and_genomics|pediatric	hearing_loss|hearing_loss___corrected_to_fit_format___metabolic_disorder|metabolic_disorder|autosomal_recessive|genetic_disease	ear_disorder	false	false	false	true	high
MONDO:0013211	dilated cardiomyopathy 1FF	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiothoracic|cardiology	inflammatory_disease|metabolic_disorder|cardiovascular_disorder	muscle_disorder|vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0013212	Charcot-Marie-Tooth disease axonal type 2N	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|orthopaedic|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0013214	bile acid malabsorption, primary, 1	hereditary_disease	other	hereditary_disease	gastroenterology|hepatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0013215	autosomal recessive nonsyndromic hearing loss 79	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder|bone_disorder	false	false	false	true	medium
MONDO:0013216	Diamond-Blackfan anemia 9	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics|pulmonology|pediatric	metabolic_disorder|autoimmune_diseases|anemia	blood_bone_marrow_disorder|lymphatic_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013217	Diamond-Blackfan anemia 10	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|anemia	blood_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0013218	exudative vitreoretinopathy 5	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|cardiovascular_disorder	ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|vitreoretinopathy_is_a_condition_affecting_the_eye_s_retina_and_vitreous_humor__so_it_s_most_relevant_to_this_category	false	false	false	true	high
MONDO:0013219	hypophosphatemic rickets, autosomal recessive, 2	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	endocrinology|orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|autosomal_recessive	bone_disorder|kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0013220	hemochromatosis type 2B	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hematology|genetics_and_genomics|hepatology	metabolic_disorder|anemia	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0013221	Miyoshi muscular dystrophy 2	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0013222	Miyoshi muscular dystrophy 3	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics|cardiology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0013223	autosomal recessive spondylometaphyseal dysplasia, Megarbane type	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0013224	rhabdoid tumor predisposition syndrome 2	hereditary_disease|syndromic_disease|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|oncology|pediatric	neurodegenerative_disease|cancer	nervous_system_disorder|tumor_disorder|genetic_disorder|brain_disorder|kidney_disorder|cancer_disorder|urinary_tract_disorder|neurological_disorder	false	false	false	false	very_high
MONDO:0013225	congenital generalized lipodystrophy type 4	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder|adrenal_gland_disease	muscle_disorder|skin_disorder	false	false	true	false	high
MONDO:0013226	combined immunodeficiency with faciooculoskeletal anomalies	disorder_of_development_or_morphogenesis|hereditary_disease|immune_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|immune_system_disorder	hematology|genetics_and_genomics|allergy_and_immunology|pediatric	inflammatory_disease|autoimmune_diseases	muscle_disorder|joint_disorder|blood_bone_marrow_disorder|immune_disorder|eye_disorder	true	false	false	true	very_high
MONDO:0013227	congenital plasminogen activator inhibitor type 1 deficiency	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics|pediatrics	metabolic_disorder|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0013228	spondylo-megaepiphyseal-metaphyseal dysplasia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0013229	hot water reflex epilepsy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0013230	epilepsy, hot water, 2	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013231	Leber congenital amaurosis 14	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder|psychiatric_disorder	ophthalmology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0013232	brachydactylous dwarfism, Mseleni type	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric|endocrinology	neurodegenerative_disease|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0013233	spondyloepimetaphyseal dysplasia, Handigodu type	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0013234	hypokalemic periodic paralysis, type 2	metabolic_disease|hereditary_disease|nervous_system_disorder|nutritional_disorder	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease|nutritional_disorder	genetics_and_genomics|neurology|endocrinology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0013235	pancreatic cancer, susceptibility to, 2	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	genetics_and_genomics|oncology|gastroenterology	cancer|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder|pancreatic_cancer_often_associated_with_pancreatitis_which_is_a_liver_disorder_or_affects_the_pancreas_which_is_part_of_the_upper_gastrointestinal_tract	false	true	false	false	high
MONDO:0013236	pancreatic cancer, susceptibility to, 3	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	genetics_and_genomics|oncology|gastroenterology	cancer|autoimmune_diseases|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0013238	chromosome 17q23.1-q23.2 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	other_is_incorrect__oncology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	vascular_disorder|joint_disorder|brain_disorder|immune_disorder	false	false	false	false	high
MONDO:0013239	hereditary spastic paraplegia 41	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013240	maturity-onset diabetes of the young type 10	metabolic_disease|endocrine_system_disorder|hereditary_disease|digestive_system_disorder	endocrine_system_disorder|diabetes_mellitus|metabolic_disease	hereditary_disease|endocrine_system_disorder|metabolic_disease|digestive_system_disorder	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder	immune_disorder|endocrine_disorder	false	false	true	true	medium
MONDO:0013241	spinocerebellar ataxia type 30	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0013242	maturity-onset diabetes of the young type 11	metabolic_disease|endocrine_system_disorder|hereditary_disease|digestive_system_disorder	endocrine_system_disorder|diabetes_mellitus|metabolic_disease	hereditary_disease|endocrine_system_disorder|metabolic_disease|digestive_system_disorder	genetics_and_genomics|endocrinology	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	endocrine_disorder	false	false	true	true	medium
MONDO:0013243	neuronopathy, distal hereditary motor, type 2C	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|hereditary_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013244	brachydactyly type E2	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	neurodegenerative_disease|skeletal_dysplasia|congenital_abnormality|developmental_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	low
MONDO:0013245	syndromic multisystem autoimmune disease due to ITCH deficiency	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	allergy_and_immunology|rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0013247	Fanconi renotubular syndrome 2	hereditary_disease|syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|syndromic_disease|hereditary_disease	renal_medicine|genetics_and_genomics|pediatric	genetic_disorder|kidney_disease|metabolic_disorder	kidney_disorder|renal_bone_disease	false	false	false	true	high
MONDO:0013248	Fanconi anemia complementation group O	metabolic_disease|hematologic_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|immune_system_disorder|musculoskeletal_system_disorder	anemia|metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|hematologic_disorder|immune_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	hematology|genetics_and_genomics|pediatric|oncology	genetic_disorders|anemia|metabolic_disorder	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013249	autosomal recessive nonsyndromic hearing loss 84A	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|otorlaryngology|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0013250	autosomal recessive nonsyndromic hearing loss 85	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	otolaryngology|genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0013251	Birbeck granule deficiency	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	liver_disorder|biliary_disorder	false	false	false	false	medium
MONDO:0013252	Warsaw breakage syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0013254	microcephaly, seizures, and developmental delay	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	developmental_delay|brain_disorder	false	false	false	false	high
MONDO:0013255	arthrogryposis, renal dysfunction, and cholestasis 2	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	metabolic_disease	syndromic_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	renal_medicine|hepatology|genetics_and_genomics	genetic_disorder|hepatobiliary_disease|renal_disease|metabolic_disorder	joint_disorder|liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013256	chromosome 15q24 deletion syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder|hereditary_disease	other	hereditary_disease|chromosomal_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|developmental_disorder____note__the_correct_categorization_for_this_disease_is_a_neurodevelopmental_disorder	false	false	false	false	high
MONDO:0013259	Oguchi disease-2	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder|psychiatric_disorder	orthopaedic|pediatric	neurodegenerative_disease|inflammatory_disease	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013260	esophagitis, eosinophilic, 2	inflammatory_disease|upper_digestive_tract_disorder|hereditary_disease|digestive_system_disorder	other	inflammatory_disease|hereditary_disease|upper_digestive_tract_disorder|digestive_system_disorder	allergy_and_immunology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0013261	dilated cardiomyopathy 1R	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0013262	dilated cardiomyopathy 1S	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0013263	retinitis pigmentosa 54	metabolic_disease|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|adrenal_gland_disease	eye_disorder	false	false	false	false	high
MONDO:0013264	amyotrophic lateral sclerosis type 12	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0013266	neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013267	distal 16p11.2 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	joint_disorder|brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013268	frontonasal dysplasia with alopecia and genital anomaly	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|urology|dermatology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|skin_disorder	false	false	false	false	high
MONDO:0013269	autosomal recessive nonsyndromic hearing loss 91	nervous_system_disorder|hereditary_disease|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	otolaryngology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0013271	frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	otolaryngology|genetics_and_genomics|ophthalmology|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|allergy|inflammatory_disease	eye_disorder|facial_disorder|birth_disorder	false	false	false	false	very_high
MONDO:0013272	chromosome 14q11-q22 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|oncology	neurodegenerative_disease|mental_health_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013273	chromosome 16p13.3 duplication syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|brain_disorder|kidney_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013274	retinitis pigmentosa 51	metabolic_disease|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	eye_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013275	hemolytic anemia due to glucophosphate isomerase deficiency	hematologic_disorder|metabolic_disease|hereditary_disease	anemia|metabolic_disease	hereditary_disease|hematologic_disorder|metabolic_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013276	Reynolds syndrome	hereditary_disease|immune_system_disorder	autoimmune_disease	hereditary_disease|immune_system_disorder	renal_medicine|hematology	metabolic_disorder|anemia	liver_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0013277	developmental and epileptic encephalopathy, 5	hereditary_disease|nervous_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|developmental_disorder	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0013278	lymphatic malformation 3	cardiovascular_disorder|hereditary_disease|immune_system_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|immune_system_disorder	hematology|pediatric|oncology	cancer|lymphatic_disorder	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013279	long QT syndrome 13	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0013280	myxoid liposarcoma	hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|hereditary_disease|cancer_or_benign_tumor	orthopaedic|dermatology|oncology	cancer|liposarcoma	skin_disorder|muscle_disorder	false	true	false	true	high
MONDO:0013281	COG4-congenital disorder of glycosylation	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder|liver_disorder|muscle_disorder|kidney_disorder|joint_disorder	false	false	true	true	high
MONDO:0013282	alpha 1-antitrypsin deficiency	metabolic_disease|respiratory_system_disorder|hereditary_disease|syndromic_disease	metabolic_disease	respiratory_system_disorder|hereditary_disease|syndromic_disease|metabolic_disease	pulmonology|hepatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	liver_disorder|immune_disorder|lung_disorder	false	false	false	true	high
MONDO:0013283	immunodeficiency, common variable, 3	hematologic_disorder|hereditary_disease|immune_system_disorder|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|hematology|pediatric|allergy_and_immunology|immunology|rheumatology	autoimmune_diseases|inflammatory_disease|immunodeficiency_common_variable	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0013284	immunodeficiency, common variable, 4	hematologic_disorder|hereditary_disease|immune_system_disorder|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	allergy_and_immunology|immunology	autoimmune_diseases|immunodeficiency	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0013285	immunodeficiency, common variable, 5	hematologic_disorder|hereditary_disease|immune_system_disorder|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	immunodeficiency|allergy_and_immunology	autoimmune_diseases|immunodeficiency	lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0013286	immunodeficiency, common variable, 6	hematologic_disorder|hereditary_disease|immune_system_disorder|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	immunodeficiency|allergy_and_immunology	autoimmune_diseases|immunodeficiency	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0013287	agammaglobulinemia 2, autosomal recessive	hematologic_disorder|hereditary_disease|immune_system_disorder	other	hereditary_disease|hematologic_disorder|immune_system_disorder	genetics_and_genomics|hematology|immunology	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	true	false	false	true	high
MONDO:0013288	agammaglobulinemia 3, autosomal recessive	hematologic_disorder|hereditary_disease|immune_system_disorder	other	hereditary_disease|hematologic_disorder|immune_system_disorder	genetics_and_genomics|hematology	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0013289	agammaglobulinemia 4, autosomal recessive	hematologic_disorder|hereditary_disease|immune_system_disorder	other	hereditary_disease|hematologic_disorder|immune_system_disorder	hematology|genetics_and_genomics|pediatric|immunology	autoimmune_diseases|anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0013290	agammaglobulinemia 5, autosomal dominant	hematologic_disorder|hereditary_disease|immune_system_disorder	other	hereditary_disease|hematologic_disorder|immune_system_disorder	genetics_and_genomics|hematology	autoimmune_diseases|anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0013291	glycogen storage disease XV	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	liver_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0013292	chromosome 4q21 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|genetic_disorder____corrected_to_match_the_provided_category_list_____neurodegenerative_disease|metabolic_disorder	brain_disorder|genetic_disorder|developmental_disorder|chromosome_deletion_syndrome|immune_disorder	false	false	false	false	high
MONDO:0013293	isolated microphthalmia 6	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0013296	myeloid neoplasm associated with FGFR1 rearrangement	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	cancer|anemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0013297	autosomal dominant limb-girdle muscular dystrophy type 1H	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|muscular_dystrophy	joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013298	chromosome 17q21.31 duplication syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	joint_disorder|spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013299	chromosome 6q11-q14 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|anemia|metabolic_disorder|mental_health_disorder	spinal_disorder|lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0013300	commissural facial cleft	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|otolaryngology|neurology	congenital_disorder|developmental_disorder|neurodegenerative_disease	skin_disorder|nose_disorder|facial_cleft_is_not_in_the_list_so____ear_disorder	false	false	false	false	medium
MONDO:0013301	aromatase deficiency	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|obstetric_disorder	endocrine_system_disorder	obstetric_disorder|reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	genetics_and_genomics|pediatric|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0013302	nephronophthisis 11	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	urology|renal_medicine|nephrology	autoimmune_diseases|anemia|renal_disease|metabolic_disorder|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0013304	von Willebrand disease 2	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013305	autosomal dominant nonsyndromic hearing loss 51	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	genetics_and_genomics|pediatric|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0013306	combined oxidative phosphorylation defect type 7	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	genetics_and_genomics|pediatric	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	mitochondrial_disease|liver_disorder	false	false	false	false	very_high
MONDO:0013307	myopathy, lactic acidosis, and sideroblastic anemia 2	mitochondrial_disease|hematologic_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease	metabolic_disease|anemia	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hematologic_disorder	genetic_and_genomics|hematology|neurology	anemia|metabolic_disorder	blood_bone_marrow_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013308	CBL-related disorder	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|hematology	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0013309	chromosome 2p12-p11.2 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	developmental_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|joint_disorder|immune_disorder	false	false	false	false	medium
MONDO:0013310	congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|metabolic_disease	genetics_and_genomics|endocrinology|pediatrics	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	very_high
MONDO:0013311	ectodermal dysplasia-syndactyly syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|orthopaedic|dermatology	neurodegenerative_disease|metabolic_disorder	teeth_disorder|skin_disorder|hand_disorder|joint_disorder	false	false	false	false	medium
MONDO:0013312	retinitis pigmentosa 55	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0013313	ectodermal dysplasia-cutaneous syndactyly syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|orthopaedic|dermatology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	teeth_disorder|skin_disorder|nose_disorder|eye_disorder|joint_disorder|ear_disorder	false	false	false	false	high
MONDO:0013314	retinitis pigmentosa 56	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology	adrenal_gland_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0013315	retinitis pigmentosa 57	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0013316	occult macular dystrophy	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0013317	torsade-de-pointes syndrome with short coupling interval	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pediatrics|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0013318	early repolarization associated with ventricular fibrillation	hereditary_disease	other	hereditary_disease	cardiology|pulmonology|cardiothoracic	adrenal_gland_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013319	chromosome 4Q32.1-q32.2 triplication syndrome	chromosomal_disorder|hereditary_disease	other	chromosomal_disorder|hereditary_disease	genetics_and_genomics|pediatric	chromosomal_disorder|developmental_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013320	chromosome 16p12.2-p11.2 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	muscle_disorder|bone_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0013321	forsythe-wakeling syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	blood_bone_marrow_disorder|muscle_disorder|bone_disorder|joint_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013322	epilepsy, familial adult myoclonic, 3	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|autoimmune_diseases|inflammatory_disease	muscle_disorder|brain_disorder	false	false	false	false	low
MONDO:0013323	cranioectodermal dysplasia 2	urinary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|integumentary_system_disorder|respiratory_system_disorder|musculoskeletal_system_disorder	other	urinary_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|respiratory_system_disorder|integumentary_system_disorder	pediatric|dermatology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	skeletal_dysplasia|craniofacial_disorder|bone_disorder|eye_disorder|immune_disorder____corrected_to_fit_the_format____ear_disorder|ear_disorder|immune_disorder	false	false	false	false	high
MONDO:0013324	lymphedema-posterior choanal atresia syndrome	cancer_or_benign_tumor|hereditary_disease|cardiovascular_disorder|immune_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|hereditary_disease|immune_system_disorder	pediatric|otolaryngology|genetics_and_genomics	cardiovascular_disorder|inflammatory_disease	skin_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0013325	COG5-congenital disorder of glycosylation	hereditary_disease|syndromic_disease|metabolic_disease	metabolic_disease	hereditary_disease|syndromic_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|congenital_disorder_of_glycosylation	kidney_disorder|liver_disorder	false	false	true	false	high
MONDO:0013326	Senior-Loken syndrome 7	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	psychiatry|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013327	primary hyperoxaluria type 3	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|renal_medicine|genetics_and_genomics	kidney_disease|metabolic_disorder|genetic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0013328	retinitis pigmentosa 58	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|metabolic_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0013329	familial clubfoot due to 17q23.1q23.2 microduplication	chromosomal_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	chromosomal_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0013330	agenesis of the corpus callosum and congenital lymphedema	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	congenital_lymphedema|neurodegenerative_disease	brain_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0013331	factor 5 and Factor VIII, combined deficiency of, 2	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|immunology|pediatric|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013332	brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and intellectual disability	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|bone_disorder|brain_disorder|joint_disorder|spinal_disorder|ear_disorder	false	false	false	false	high
MONDO:0013333	odontoid hypoplasia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0013334	cocoon syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|dermatology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0013335	tuberculin skin test reactivity, absence of	hereditary_disease	other	hereditary_disease	dermatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	false	false	false	false	low
MONDO:0013336	chromosome 19p13.13 deletion syndrome	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0013337	neuropathy, hereditary sensory and autonomic, type 1C	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|hereditary_sensory_and_autonomic_neuropathy_is_classified_under_the_category_of_genetic_disorders_which_makes_neurology_a_fitting_classification_for_this_disease_as_it_deals_with_diseases_affecting_nerve_function_and_genetics_and_genomics_deal_with_inherited_conditions|neurology	hereditary_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0013338	Charcot-Marie-Tooth disease recessive intermediate B	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|orthopaedic	inflammatory_disease|neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013339	dilated cardiomyopathy 1GG	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	renal_medicine|pulmonology|cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013341	methylmalonic acidemia due to transcobalamin receptor defect	hereditary_disease|nutritional_disorder|metabolic_disease	metabolic_disease	nutritional_disorder|hereditary_disease|metabolic_disease	genetic_disorders|pediatric|hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0013342	hereditary spastic paraplegia 48	hereditary_disease|nervous_system_disorder|metabolic_disease	neurodegenerative_disease|metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0013343	C1Q deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	rheumatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder	false	false	false	false	high
MONDO:0013345	d-2-hydroxyglutaric aciduria 2	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0013348	cone-rod dystrophy 15	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease|nervous_system_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0013349	ALG11-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	congenital_disorder|metabolic_disorder	congenital_disorder_of_glycosylation|liver_disorder	false	false	false	false	very_high
MONDO:0013350	mitochondrial DNA depletion syndrome 4b	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|musculoskeletal_system_disorder|metabolic_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0013351	infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	brain_disorder|spinal_disorder	true	false	false	false	very_high
MONDO:0013352	intellectual disability-severe speech delay-mild dysmorphism syndrome	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	intellectual_disability__brain_disorder|brain_disorder|speech_delay_mild_dysmorphism_syndrome_fits_under_this_category_as_well	false	false	false	false	high
MONDO:0013353	intellectual disability, anterior maxillary protrusion, and strabismus	hereditary_disease	other	hereditary_disease	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	teeth_disorder|eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0013354	spastic ataxia 4	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|metabolic_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013355	congenital dyserythropoietic anemia type 4	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	pediatric|hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0013356	vesicoureteral reflux 3	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	pediatric|urology|renal_medicine	inflammatory_disease|urinary_problem|autoimmune_diseases	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0013357	chromosome 17q11.2 deletion syndrome, 1.4Mb	chromosomal_disorder|cancer_or_benign_tumor|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|hereditary_disease|chromosomal_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|anemia|mental_health_disorder|autoimmune_diseases|cancer	muscle_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0013358	Seckel syndrome 4	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease	other	nervous_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	congenital_disorder|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0013359	familial hyperaldosteronism type III	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	renal_medicine|endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|cardiovascular_disorder	kidney_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0013360	brachyolmia, Maroteaux type	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0013361	congenital prothrombin deficiency	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|hereditary_disease|bleeding_disorder	liver_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013362	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|developmental_delay|neurodegenerative_disease	developmental_disorders|facial_dysmorphism|microcephaly|brain_disorder	false	false	false	false	high
MONDO:0013363	chromosome 2q31.1 duplication syndrome	chromosomal_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|chromosomal_disorder	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder|other____corrected_answer__brain_disorder|brain_disorder	false	false	false	false	medium
MONDO:0013364	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease|psychiatric_disorder	psychiatric_disorder	musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|brain_disorder	false	false	false	false	high
MONDO:0013365	autosomal recessive nonsyndromic hearing loss 83	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|auditory_system_disorder|psychiatric_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0013366	spondylocostal dysostosis 4, autosomal recessive	disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|genetic_disorders|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0013367	long QT syndrome 2	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|cardiology|pediatric	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0013368	mammary-digital-nail syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|reproductive_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics|dermatology	cancer|autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder|nail_disorder|skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0013369	hypertrophic cardiomyopathy 7	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiothoracic|cardiology	hypertrophic_cardiomyopathy|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0013370	long QT syndrome 6	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|cardiology|pediatric|cardiology_is_likely_the_best_fitting_category_but_also_includes_genetics_which_can_be_relevant	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0013371	dilated cardiomyopathy 1U	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder|dilated_cardiomyopathy_1u	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013372	long QT syndrome 5	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|cardiology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0013373	dilated cardiomyopathy 1V	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013374	supernumerary der(22)t(8;22) syndrome	hereditary_disease	other	hereditary_disease	oncology|genetics_and_genomics|dermatolog|hematolog|pediatric	metabolic_disorder|autoimmune_diseases|cancer	bone_disorder|reproductive_system_disorder|lymphatic_disorder|blood_bone_marrow_disorder|muscle_disorder|immune_disorder	false	false	false	false	high
MONDO:0013375	Klippel-Feil syndrome 3, autosomal dominant	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric|orthopaedic	genetic_disorder|metabolic_disorder	bone_disorder|ear_disorder	false	false	false	false	high
MONDO:0013376	microphthalmia, isolated, with coloboma 6	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0013377	isolated microphthalmia 7	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0013378	orofacial cleft 10	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|otolaryngology	congenital_anomaly|developmental_disorder|facial_abnormality|craniofacial_disease____note__the_original_list_did_not_have_direct_matches__but_based_on_the_characteristics_of_orofacial_cleft__i_have_included_related_categories|birth_defect	oral_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0013379	Noonan syndrome 7	disorder_of_development_or_morphogenesis|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease|immune_system_disorder|syndromic_disease	cardiovascular_disorder	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|cardiovascular_disorder|immune_system_disorder	genetics_and_genomics|cardiology|pediatric	metabolic_disorder|cardiovascular_disorder	heart_disorder|endocrine_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0013380	LEOPARD syndrome 3	disorder_of_development_or_morphogenesis|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	cardiovascular_disorder	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|cardiovascular_disorder	genetics_and_genomics|pediatric|dermatology	metabolic_disorder|cardiovascular_disorder	heart_disorder|skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0013381	neuropathy, hereditary sensory, type 1D	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	hereditary|metabolic_disorder|neurodegenerative_disease	spinal_disorder|nerve_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013382	progressive demyelinating neuropathy with bilateral striatal necrosis	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0013385	Treacher Collins syndrome 2	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric|otolaryngology	metabolic_disorder|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	bone_disorder|facial_disorder|ear_disorder|eye_disorder	false	false	false	false	medium
MONDO:0013386	autosomal recessive nonsyndromic hearing loss 74	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|auditory_system_disorder|psychiatric_disorder	genetics_and_genomics|pediatric|otolaryngology	metabolic_disorder|autoimmune_diseases	ear_disorder	false	false	false	true	medium
MONDO:0013387	developmental and epileptic encephalopathy, 7	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	epileptic_disorder|inflammatory_disease|developmental_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	very_high
MONDO:0013388	developmental and epileptic encephalopathy, 11	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|developmental_and_epileptic_encephalopathy_is_not_in_the_category_list_so_it_is_omitted_from_this_answer|neurodegenerative_disease	developmental_disorder|epileptic_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0013389	developmental and epileptic encephalopathy, 12	nervous_system_disorder|hereditary_disease|syndromic_disease	other	nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	epileptic_encephalopathy|developmental_disorder|neurodegenerative_disease	encephalopathy|developmental_disorder|epileptic_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0013390	autosomal recessive limb-girdle muscular dystrophy type 2Q	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology|orthopaedic	muscular_dystrophy|neurodegenerative_disease	limb_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013391	sterol carrier protein 2 deficiency	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|hepatology|endocrinology	metabolic_disorder|adrenal_gland_disease	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0013392	autosomal recessive spinocerebellar ataxia 10	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013393	distal 7q11.23 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	developmental_disorder|immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0013394	porencephaly-microcephaly-bilateral congenital cataract syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|ophthalmology|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0013395	retinitis pigmentosa 4	disorder_of_visual_system|metabolic_disease|nervous_system_disorder|hereditary_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder	nervous_system_disorder|metabolic_disease|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0013396	chromosome 1p32-p31 deletion syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|chromosomal_disorder	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	bone_disorder|kidney_disorder|immune_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013397	acne inversa, familial, 2	hereditary_disease|integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases	skin_disorder|liver_disorder	true	false	false	true	high
MONDO:0013398	acne inversa, familial, 3	hereditary_disease|integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	skin_disorder|liver_disorder	false	false	false	true	high
MONDO:0013400	Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|reproductive_system_disorder	pediatric|endocrinology|genetics_and_genomics|urology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	very_high
MONDO:0013401	hereditary spastic paraplegia 51	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0013402	retinitis pigmentosa 27	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease|metabolic_disease	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0013403	heterotaxy, visceral, 4, autosomal	syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|visceral	kidney_disorder|lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0013404	hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	metabolic_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0013405	retinitis pigmentosa 49	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease|metabolic_disease	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0013406	age related macular degeneration 6	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|nervous_system_disorder|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0013407	retinitis pigmentosa 47	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease|metabolic_disease	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder|retinal_disorder__note__since_the_exact_category_is__retinitis_pigmentosa___i_have_removed_muscle_disorder_from_the_list_as_it_does_not_directly_relate_to_retinitis_pigmentosa	false	false	false	false	high
MONDO:0013408	FADD-related immunodeficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatrics|immunology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0013410	46,XY sex reversal 6	endocrine_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|reproductive_system_disorder|hereditary_disease|cardiovascular_disorder	endocrine_system_disorder|cardiovascular_disorder	reproductive_system_disorder|cardiovascular_disorder|musculoskeletal_system_disorder|endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	urology|endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0013411	cataract 16 multiple types	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0013412	hypertrophic cardiomyopathy 9	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	cardiology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0013413	retinitis pigmentosa 45	psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013414	retinitis pigmentosa 44	psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	ophthalmology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0013415	chromosome 17p13.1 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	neurodegenerative_disease|anemia|cancer	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013416	age related macular degeneration 8	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|nervous_system_disorder|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0013417	complement component 3 deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	rheumatology|hematology|genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0013418	aortic aneurysm, familial thoracic 7	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	cardiology|cardiothoracic|genetics_and_genomics	genetic_disorder_is_not_in_the_list_but_a_subset_of_metabolic_disorder_is__therefore__cardiovascular_disorder|metabolic_disorder|familial_disorder_is_not_in_the_list_so_it_cannot_be_used__however__familial_thoracic_7_implies_familial_which_can_be_assumed_to_imply_a_genetic_component__implying__cardiovascular_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013419	complement component C1s deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	rheumatology|hematology|allergy_and_immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0013420	age related macular degeneration 12	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|nervous_system_disorder|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|age_related_condition	false	false	false	true	high
MONDO:0013421	type II complement component 8 deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	hematology|genetics_and_genomics|immunology	autoimmune_diseases|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0013422	type I complement component 8 deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	hematology|genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0013423	immunodeficiency due to MASP-2 deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0013424	3p- syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013425	retinitis pigmentosa 20	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system|metabolic_disease	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	eye_disorder	false	false	false	false	high
MONDO:0013426	aneurysm-osteoarthritis syndrome	syndromic_disease|connective_tissue_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	connective_tissue_disorder|cardiovascular_disorder|syndromic_disease|hereditary_disease	rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	vascular_disorder|joint_disorder	false	false	false	false	medium
MONDO:0013427	immunodeficiency 31B	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	pediatrics|allergy_and_immunology|genetics_and_genomics|immunology	autoimmune_diseases|immunodeficiency|inflammatory_disease	immune_disorder|lymphatic_disorder	true	false	false	false	high
MONDO:0013428	Meier-Gorlin syndrome 2	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder	bone_disorder|skeletal_rudimentary_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0013429	retinitis pigmentosa 40	nervous_system_disorder|psychiatric_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0013430	Meier-Gorlin syndrome 3	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|short_stature____assuming__meier_gorlin_syndrome__is_a_condition_related_to_bone_skeletal_development|skeletal_disorder	false	false	false	false	medium
MONDO:0013431	Meier-Gorlin syndrome 4	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	blood_bone_marrow_disorder|bone_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0013432	Meier-Gorlin syndrome 5	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder|skeletal_disorder	bone_disorder|skeletal_dysplasia|joint_disorder	false	false	false	false	high
MONDO:0013433	primary sclerosing cholangitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	immune_disorder|biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0013434	primary ciliary dyskinesia 14	syndromic_disease|respiratory_system_disorder|hereditary_disease	other	respiratory_system_disorder|syndromic_disease|hereditary_disease	pulmonology|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|kidney_disorder|eye_disorder	false	false	false	false	high
MONDO:0013435	primary ciliary dyskinesia 15	syndromic_disease|respiratory_system_disorder|hereditary_disease	other	respiratory_system_disorder|syndromic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013436	retinitis pigmentosa 39	metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder|metabolic_disease	psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease|nervous_system_disorder|hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0013437	retinitis pigmentosa 43	metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder|metabolic_disease	psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease|nervous_system_disorder|hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|lower_gastrointestinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013438	pontocerebellar hypoplasia type 2D	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013439	congenital bile acid synthesis defect 3	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|pediatric|genetics_and_genomics|gastroenterology	congenital_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0013440	autosomal recessive limb-girdle muscular dystrophy type 2P	metabolic_disease|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	metabolic_disease	musculoskeletal_system_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|muscular_dystrophy	muscle_disorder|spinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0013441	asphyxiating thoracic dystrophy 4	urinary_system_disorder|syndromic_disease|musculoskeletal_system_disorder|respiratory_system_disorder|hereditary_disease	other	respiratory_system_disorder|musculoskeletal_system_disorder|urinary_system_disorder|syndromic_disease|hereditary_disease	pediatric|pulmonology	neurodegenerative_disease|respiratory_disorder|metabolic_disorder	muscle_disorder|lung_disorder|throat_disorder	false	false	false	false	very_high
MONDO:0013442	nephronophthisis 12	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	urology|renal_medicine	renal_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013443	Seckel syndrome 5	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	skeletal_disorder____note__i_replaced_the__bone_disorder__category_in_the_original_list_with__skeletal_disorder___which_is_a_more_specific_and_accurate_term_for_this_condition|eye_disorder	false	false	false	false	high
MONDO:0013444	nephronophthisis 9	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	urology|renal_medicine	autoimmune_diseases|inflammatory_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013445	complement component 9 deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	immunology|hematology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0013446	Leber congenital amaurosis 6	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0013447	retinitis pigmentosa 48	metabolic_disease|psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder|metabolic_disease	psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease|nervous_system_disorder|hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0013448	generalized epilepsy with febrile seizures plus, type 8	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	generalized_epilepsy_disorder|brain_disorder	false	false	false	false	medium
MONDO:0013449	Leber congenital amaurosis 7	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	true	very_high
MONDO:0013450	congenital stationary night blindness 1D	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|nervous_system_disorder	ophthalmology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0013452	multisystemic smooth muscle dysfunction syndrome	digestive_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	digestive_system_disorder|cardiovascular_disorder|hereditary_disease	cardiology|rheumatology|neurology|pulmonology	autoimmune_diseases|inflammatory_disease	muscle_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013453	Leber congenital amaurosis 8	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|nervous_system_disorder	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0013454	Leber congenital amaurosis 11	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|nervous_system_disorder	ophthalmology|pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	immune_disorder|eye_disorder|brain_disorder	false	false	false	true	high
MONDO:0013455	hypertrophic cardiomyopathy 16	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiology|cardiothoracic|genetics_and_genomics	hypertrophic_cardiomyopathy|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	true	high
MONDO:0013456	constitutional megaloblastic anemia with severe neurologic disease	metabolic_disease|hereditary_disease|hematologic_disorder	metabolic_disease|anemia	hematologic_disorder|metabolic_disease|hereditary_disease	neurology|hematology	neurodegenerative_disease|anemia|metabolic_disorder	brain_disorder|blood_bone_marrow_disorder	true	false	false	false	very_high
MONDO:0013457	Leber congenital amaurosis 15	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|nervous_system_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	true	high
MONDO:0013458	hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome	metabolic_disease|urinary_system_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	metabolic_disease|cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|urinary_system_disorder|mitochondrial_disease|metabolic_disease|hereditary_disease	cardiology|pulmonology|renal_medicine|nephrology	metabolic_disorder|cardiovascular_disorder|renal_failure	kidney_disorder|lung_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0013459	osteogenesis imperfecta type 10	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|inflammatory_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0013460	osteogenesis imperfecta type 12	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	rheumatology|pediatric|orthopaedic|genetics_and_genomics	genetic_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0013461	inosine triphosphatase deficiency	hereditary_disease	other	hereditary_disease	pediatric|hematology|genetics_and_genomics|immunology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0013462	fucosyltransferase 6 deficiency	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0013463	congenital heart defects, multiple types, 6	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiology|pediatrics	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0013464	episodic ataxia type 5	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013465	achromatopsia 4	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|nervous_system_disorder	ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0013466	orofacial cleft 13	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|otolaryngology	neurodegenerative_disease|developmental_disorder|birth_defect|congenital_disorder	teeth_disorder|nose_disorder|ear_disorder	false	false	false	false	high
MONDO:0013467	immunodeficiency due to ficolin3 deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|hematology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013468	retinitis pigmentosa 59	disorder_of_visual_system|metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013469	retinitis pigmentosa 38	disorder_of_visual_system|metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	ophthalmology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0013470	generalized epilepsy with febrile seizures plus, type 7	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013471	autosomal recessive nonsyndromic hearing loss 61	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	pediatric|otolaryngology|genetics_and_genomics	autoimmune_diseases|anemia|metabolic_disorder	hearing_loss|ear_disorder	false	false	false	true	medium
MONDO:0013472	fatal infantile hypertonic myofibrillar myopathy	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0013473	Hirschsprung disease, cardiac defects, and autonomic dysfunction	hereditary_disease	other	hereditary_disease	cardiology|pediatric|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	heart_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0013474	hypertrophic cardiomyopathy 17	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiology|cardiothoracic|genetics_and_genomics	hypertrophic_cardiomyopathy|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013475	hypertrophic cardiomyopathy 18	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiology|pediatric|cardiothoracic|genetics_and_genomics	hypertrophic_cardiomyopathy|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0013476	hypertrophic cardiomyopathy 19	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiology|cardiothoracic	hypertrophic_cardiomyopathy|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0013477	hypertrophic cardiomyopathy 20	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiology|pediatric|cardiothoracic	hypertrophic_cardiomyopathy|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0013478	PLIN1-related familial partial lipodystrophy	metabolic_disease|hereditary_disease|integumentary_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|integumentary_system_disorder	dermatology|endocrinology|genetics_and_genomics	lipodystrophy|metabolic_disorder	skin_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0013479	dilated cardiomyopathy 1HH	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiology|cardiothoracic	cardiovascular_disorder|dilated_cardiomyopathy_1hh_is_actually_a_form_of_cardiovascular_disorder_that_also_falls_under_inflammatory_disease	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013480	renal hypomagnesemia 6	metabolic_disease|urinary_system_disorder|hereditary_disease	metabolic_disease	urinary_system_disorder|metabolic_disease|hereditary_disease	renal_medicine|nephrology	renal_hypomagnesemia|metabolic_disorder	urinary_tract_disorder|kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0013481	chromosome 13q14 deletion syndrome	chromosomal_disorder|syndromic_disease	other	chromosomal_disorder|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|developmental_disorder|genetic_disorder|intellectual_disability	immune_disorder|urinary_tract_disorder|brain_disorder|kidney_disorder|upper_gastrointestinal_disorder|joint_disorder|blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013482	Meckel syndrome, type 8	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	cardiovasular_disorder|metabolic_disorder	kidney_disorder|liver_disorder|reproductive_system_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0013483	obesity, hyperphagia, and developmental delay	hereditary_disease	other	hereditary_disease	pediatric|neurology|endocrinology	neurodegenerative_disease|developmental_delay|metabolic_disorder	developmental_delay|upper_gastrointestinal_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0013484	cataract 36	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|oculoplastic	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0013485	spinocerebellar ataxia type 35	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0013486	spinocerebellar ataxia type 32	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|spinal_cord_disorder|genetic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013487	recurrent Neisseria infections due to factor D deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|rheumatology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	true	false	false	false	high
MONDO:0013488	lipodystrophy, partial, acquired, with low complement component c3, with or without glomerulonephritis	hereditary_disease	other	hereditary_disease	dermatology|rheumatology|renal_medicine|endocrinology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|skin_disorder|kidney_disorder	false	false	true	false	medium
MONDO:0013489	autosomal recessive nonsyndromic hearing loss 89	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0013490	megalencephalic leukoencephalopathy with subcortical cysts 2A	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013491	megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without intellectual disability	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	medium
MONDO:0013492	alopecia-intellectual disability syndrome 3	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|intellectual_disability_syndrome	false	false	false	false	medium
MONDO:0013493	acetyl-coa carboxylase deficiency	hereditary_disease	other	hereditary_disease	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	true	high
MONDO:0013495	autosomal recessive congenital ichthyosis 8	hereditary_disease|disorder_of_visual_system|integumentary_system_disorder	other	disorder_of_visual_system|disorder_of_orbital_region|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology|pediatric|congenital	metabolic_disorder|genetic_disorder|skin_disease	skin_disorder	false	false	false	false	medium
MONDO:0013497	Okt4 epitope deficiency	hereditary_disease	other	hereditary_disease	genetics_and_genomics|immunology|allergy_and_immunology	immunodeficiency_diseases|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0013498	schizophrenia 15	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	high
MONDO:0013499	Fanconi anemia complementation group P	hereditary_disease|immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease|anemia	hematologic_disorder|immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013500	immunodeficiency 51	integumentary_system_disorder|hereditary_disease|immune_system_disorder	other	integumentary_system_disorder|immune_system_disorder|hereditary_disease	immunology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0013501	frontotemporal dementia and/or amyotrophic lateral sclerosis 6	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0013502	amyloidosis, primary localized cutaneous, 2	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0013503	candidiasis, familial, 6	integumentary_system_disorder|hereditary_disease|immune_system_disorder	other	integumentary_system_disorder|immune_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	liver_disorder|skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0013504	spermatogenic failure 8	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	cancer|metabolic_disorder|autoimmune_diseases	spermatic_failure|reproductive_system_disorder	false	false	false	false	medium
MONDO:0013505	spermatogenic failure 9	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology|endocrinology	anemia|metabolic_disorder	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0013506	schizophrenia 16	psychiatric_disorder|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	psychiatric_disorder|brain_disorder|mental_disorder	false	false	false	true	high
MONDO:0013507	granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3	hematologic_disorder|inflammatory_disease|hereditary_disease|immune_system_disorder	other	inflammatory_disease|hematologic_disorder|immune_system_disorder|hereditary_disease	genetics_and_genomics|immunology|rheumatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|liver_disorder|lung_disorder|immune_disorder	false	false	false	true	high
MONDO:0013508	myopia 19, autosomal dominant	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|eye_disorder	false	false	false	true	medium
MONDO:0013509	intellectual disability, autosomal dominant 6	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0013510	melanoma, cutaneous malignant, susceptibility to, 6	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	dermatology|genetics_and_genomics|oncology	cutaneous_malignant|cancer	skin_disorder|cutaneous_malignant	false	true	false	true	high
MONDO:0013511	cyanosis, transient neonatal	hereditary_disease	other	hereditary_disease	pediatric|cardiology|hematology|pulmonology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|lung_disorder|heart_disorder	false	false	false	false	low
MONDO:0013512	hemoglobin H disease	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013513	atrial fibrillation, familial, 9	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	cardiology|hematology|genetics_and_genomics|pulmonology	cardiovascular_disorder|metabolic_disorder|familial|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0013514	hypotrichosis 3	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	skin_disorder|hair_disorder	false	false	false	true	medium
MONDO:0013515	osteogenesis imperfecta type 6	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder	bone_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0013516	retinitis pigmentosa 60	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease	metabolic_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0013517	beta-thalassemia HBB/LCRB	endocrine_system_disorder|hematologic_disorder|hereditary_disease	endocrine_system_disorder|anemia	endocrine_system_disorder|hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0013518	pituitary hormone deficiency, combined, 6	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|nervous_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder|hereditary_disease	neurology|endocrinology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0013519	dyskeratosis congenita, autosomal recessive 2	integumentary_system_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|integumentary_system_disorder|hereditary_disease|cancer_or_benign_tumor	pediatric|dermatology|genetics_and_genomics	neurodegenerative_disease|anemia|metabolic_disorder	blood_bone_marrow_disorder|skin_disorder	false	false	false	false	high
MONDO:0013520	dyskeratosis congenita, autosomal recessive 3	syndromic_disease|cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder	cancer_or_benign_tumor	syndromic_disease|integumentary_system_disorder|hereditary_disease|cancer_or_benign_tumor	pediatric|dermatology|genetics_and_genomics	neurodegenerative_disease|genetic_disorder|metabolic_disorder	blood_bone_marrow_disorder|skin_disorder	false	false	false	true	high
MONDO:0013521	dyskeratosis congenita, autosomal dominant 2	syndromic_disease|cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder	cancer_or_benign_tumor	syndromic_disease|integumentary_system_disorder|hereditary_disease|cancer_or_benign_tumor	pediatric|pediatrics|dermatology|genetics_and_genomics|genetic_genomics	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|skin_disorder	false	false	false	true	high
MONDO:0013522	dyskeratosis congenita, autosomal dominant 3	syndromic_disease|cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder	cancer_or_benign_tumor	syndromic_disease|integumentary_system_disorder|hereditary_disease|cancer_or_benign_tumor	pediatric|dermatology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|bone_disorder|skin_disorder	false	false	false	true	high
MONDO:0013523	Nestor-Guillermo progeria syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|premature_aging_syndrome	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|premature_aging_syndrome|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0013525	primary ciliary dyskinesia 16	syndromic_disease|hereditary_disease|respiratory_system_disorder	other	syndromic_disease|respiratory_system_disorder|hereditary_disease	pediatrics|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0013526	progressive myoclonic epilepsy type 6	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0013527	lissencephaly 4	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0013528	intellectual disability, autosomal recessive 14	psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease	metabolic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|intellectual_disability	false	false	false	true	high
MONDO:0013529	catecholaminergic polymorphic ventricular tachycardia 3	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	pediatric|cardiology|genetics_and_genomics|neurology	adrenal_gland_disease|cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013530	atrial fibrillation, familial, 10	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	cardiology|hematology|cardiothoracic|genetics_and_genomics	cardiovascular_disorder|familial	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0013531	PSPH deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013532	protein Z deficiency	hereditary_disease	other	hereditary_disease	hematology|hepatology	cardiovascular_disorder|anemia|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	medium
MONDO:0013533	hyperlipidemia due to hepatic triglyceride lipase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	cardiology|hepatology|gastroenterology|genetics_and_genomics|endocrinology	cardiovascular_disorder|metabolic_disorder	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0013534	apolipoprotein c-III deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	cardiology|hepatology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	liver_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0013535	hydroxyacyl glutathione hydrolase deficiency	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0013536	heme oxygenase 1 deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hematology|genetics_and_genomics|pulmonology	anemia|metabolic_disorder	liver_disorder|immune_disorder	false	false	false	false	high
MONDO:0013537	autosomal recessive nonsyndromic hearing loss 29	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	low
MONDO:0013539	hypotonia-failure to thrive-microcephaly syndrome	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	muscle_disorder|brain_disorder|failure_to_thrive	false	false	false	false	very_high
MONDO:0013540	deafness-lymphedema-leukemia syndrome	hematologic_disorder|syndromic_disease|hereditary_disease|immune_system_disorder|cardiovascular_disorder	cardiovascular_disorder	hematologic_disorder|immune_system_disorder|hereditary_disease|syndromic_disease|cardiovascular_disorder	oncology|otolaryngology|genetics_and_genomics|hematology	leukemia|autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0013541	complex cortical dysplasia with other brain malformations 1	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013542	Moyamoya disease 5	hereditary_disease|digestive_system_disorder|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	digestive_system_disorder|nervous_system_disorder|hereditary_disease|cardiovascular_disorder	vascular_related_specialties__cardiology__cardiothoracic|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013543	trypsinogen deficiency	hereditary_disease	other	hereditary_disease	hepatology|pediatric|gastroenterology|genetics_and_genomics	metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0013544	atrial fibrillation, familial, 11	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|genetics_and_genomics|hematology	familial|cardiovascular_disorder|autimmune_diseases	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0013545	atrial fibrillation, familial, 12	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|genetics_and_genomics|hematology	familial|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013546	mitochondrial complex V (ATP synthase) deficiency, nuclear type 2	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	very_high
MONDO:0013547	mitochondrial complex V (ATP synthase) deficiency, nuclear type 3	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	mitochondrial_disease|muscle_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0013548	acetyl-CoA acetyltransferase-2 deficiency	hereditary_disease	other	hereditary_disease	hepatology|pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013549	N-acetylaspartate deficiency	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013550	distal myopathy with posterior leg and anterior hand involvement	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	neurology|orthopaedic	neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	true	high
MONDO:0013551	hereditary spastic paraplegia 47	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013552	hereditary spastic paraplegia 52	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|hereditary|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013553	immunodeficiency-centromeric instability-facial anomalies syndrome 2	hereditary_disease|premature_aging_syndrome	other	hereditary_disease|premature_aging_syndrome	immunology|genetics_and_genomics	autoimmune_diseases|cancer|metabolic_disorder	bone_disorder|skin_disorder|lymphatic_disorder|joint_disorder|immune_disorder	true	false	false	false	high
MONDO:0013555	Hermansky-Pudlak syndrome 3	hematologic_disorder|syndromic_disease|hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|hematologic_disorder|hereditary_disease|syndromic_disease|metabolic_disease	pediatric|neurology|genetics_and_genomics|hematology	neurodegenerative_disease|metabolic_disorder	immune_disorder_blood_bone_marrow_disorder_joint_disorder_eye_disorder_skin_disorder_bone_disorder	false	false	false	false	high
MONDO:0013556	Hermansky-Pudlak syndrome 4	hematologic_disorder|syndromic_disease|hereditary_disease|respiratory_system_disorder|metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|respiratory_system_disorder|hematologic_disorder|hereditary_disease|syndromic_disease|metabolic_disease	pediatrics|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|anemia|metabolic_disorder	blood_bone_marrow_disorder|eye_disorder|immune_disorder	false	false	false	false	high
MONDO:0013557	Hermansky-Pudlak syndrome 5	hematologic_disorder|syndromic_disease|hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|hematologic_disorder|hereditary_disease|syndromic_disease|metabolic_disease	pediatric|genetics_and_genomics|hematology	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0013558	Hermansky-Pudlak syndrome 6	hematologic_disorder|syndromic_disease|hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|hematologic_disorder|hereditary_disease|syndromic_disease|metabolic_disease	pediatric|immunology|genetics_and_genomics|hematology	neurodegenerative_disease|anemia|metabolic_disorder	blood_bone_marrow_disorder|eye_disorder|immune_disorder	false	false	false	false	high
MONDO:0013559	Hermansky-Pudlak syndrome 7	hematologic_disorder|syndromic_disease|hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|hematologic_disorder|hereditary_disease|syndromic_disease|metabolic_disease	pediatric|neurology|immunology|genetics_and_genomics	neurodegenerative_disease|anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0013560	Hermansky-Pudlak syndrome 8	hematologic_disorder|syndromic_disease|hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|hematologic_disorder|hereditary_disease|syndromic_disease|metabolic_disease	pediatric|ophthalmology|genetics_and_genomics	anemia|metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder|eye_disorder	false	false	false	false	high
MONDO:0013561	chondrodysplasia with joint dislocations, gPAPP type	hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|orthopaedic	metabolic_disorder|joint_inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0013563	multiple congenital anomalies-hypotonia-seizures syndrome 1	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	pediatric|neurology|genetics_and_genomics|psychiatry	genetic_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0013564	anhaptoglobinemia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	medium
MONDO:0013565	Fanconi anemia complementation group G	hematologic_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|immune_system_disorder|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease|anemia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hematologic_disorder|immune_system_disorder|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0013566	Fanconi anemia complementation group L	hematologic_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|immune_system_disorder|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease|anemia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hematologic_disorder|immune_system_disorder|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0013567	atrial septal defect 3	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	pediatric|cardiology|cardiothoracic	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013569	short-rib thoracic dysplasia 7 with or without polydactyly	syndromic_disease|hereditary_disease|respiratory_system_disorder|urinary_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|urinary_system_disorder|respiratory_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0013570	combined oxidative phosphorylation defect type 8	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	genetics_and_genomics|pediatrics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0013571	acatalasia	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	teeth_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0013572	Keppen-Lubinsky syndrome	hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|joint_disorder|eye_disorder|liver_disorder	false	false	false	false	high
MONDO:0013573	cranioectodermal dysplasia 3	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|respiratory_system_disorder|urinary_system_disorder|integumentary_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|urinary_system_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis|respiratory_system_disorder|hereditary_disease|syndromic_disease	pediatric|dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	skin_disorder|teeth_disorder|brain_disorder|ear_disorder|joint_disorder|eye_disorder	false	false	false	false	high
MONDO:0013574	cutis laxa - Marfanoid syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|dermatology|rheumatology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	skin_disorder|vascular_disorder|joint_disorder	false	false	false	false	medium
MONDO:0013575	plasma fibronectin deficiency	hereditary_disease	other	hereditary_disease	rheumatology|genetics_and_genomics|hematology	inflammatory_disease|metabolic_disorder	kidney_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0013576	recurrent infections associated with rare immunoglobulin isotypes deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	pediatric|allergy_and_immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	true	false	false	true	high
MONDO:0013577	Lipedema	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|endocrinology	inflammatory_disease|metabolic_disorder	skin_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0013578	DYRK1A-related intellectual disability syndrome	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	disorder_of_development_or_morphogenesis|nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0013579	methylmalonate semialdehyde dehydrogenase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|biochemistry|neurology|metabolic_disorders|genetics_and_genomics|inborn_errors_of_metabolism|genetic_disorders	metabolic_disorder|neurodegenerative_disease	brain_disorder|metabolic_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013580	pyruvate dehydrogenase E1-beta deficiency	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|mitochondrial_disease	endocrinology|pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	very_high
MONDO:0013581	intellectual disability, autosomal dominant 2	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013582	mosaic variegated aneuploidy syndrome 2	cancer_or_benign_tumor|hereditary_disease|syndromic_disease|chromosomal_disorder	cancer_or_benign_tumor	chromosomal_disorder|cancer_or_benign_tumor|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|pediatrics	anemia|metabolic_disorder|neurodegenerative_disease	bone_disorder	false	false	false	false	high
MONDO:0013583	occipital pachygyria and polymicrogyria	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0013584	hereditary sensory neuropathy-deafness-dementia syndrome	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	metabolic_disease|sleep_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013585	hydrolethalus syndrome 2	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0013587	glycogen storage disease due to lactate dehydrogenase H-subunit deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|pediatric|genetics_and_genomics	cardiovascular_disorder|glycogen_storage_disease_due_to_lactate_dehydrogenase_h_subunit_deficiency|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	none
MONDO:0013588	Perrault syndrome 3	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013589	focal segmental glomerulosclerosis 6	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	nephrology|renal_medicine	autoimmune_diseases|inflammatory_disease|kidney_disease	kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0013590	Stickler syndrome, type 4	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|disorder_of_visual_system|nervous_system_disorder	other	musculoskeletal_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|syndromic_disease	orthopaedic|rheumatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|eye_disorder|bone_disorder	false	false	false	true	medium
MONDO:0013591	epiphyseal dysplasia, multiple, 6	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|connective_tissue_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|connective_tissue_disorder	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0013592	nonsyndromic congenital nail disorder 9	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder|genetic_disorder|congenital_disorder___however__i_see_that__genetic_disorder__and__congenital_disorder__are_not_in_the_original_list___so__the_corrected_answer_is____metabolic_disorder	skin_disorder|nail_disorder	false	false	false	false	low
MONDO:0013593	autosomal dominant nonsyndromic hearing loss 64	hereditary_disease|psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0013594	spinocerebellar ataxia type 36	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0013595	hyperbiliverdinemia	hereditary_disease|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|hereditary_disease	hematology|hepatology	autoimmune_diseases|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0013597	platelet-type bleeding disorder 14	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|pediatric|cardiology|pulmonology|renal_medicine|gastroenterology	anemia|bleeding_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013598	myostatin-related muscle hypertrophy	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|neurology|genetics_and_genomics	muscle_disease|metabolic_disorder|genetic_disorder	endocrine_disorder|muscle_disorder	false	false	false	true	none
MONDO:0013599	autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome	hereditary_disease|digestive_system_disorder|endocrine_system_disorder|immune_system_disorder|integumentary_system_disorder	endocrine_system_disorder|autoimmune_disease	endocrine_system_disorder|integumentary_system_disorder|digestive_system_disorder|hereditary_disease|immune_system_disorder	pediatric|allergy_and_immunology|gastroenterology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	endocrine_disorder|lower_gastrointestinal_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0013600	insomnia	nervous_system_disorder	other	nervous_system_disorder|sleep_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	high
MONDO:0013601	gluthathione peroxidase deficiency	metabolic_disease|hereditary_disease|immune_system_disorder	metabolic_disease	immune_system_disorder|metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|muscle_disorder|liver_disorder	false	false	false	false	medium
MONDO:0013602	pheochromocytoma/paraganglioma syndrome 5	cancer_or_benign_tumor|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|urinary_system_disorder|syndromic_disease|nervous_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|urinary_system_disorder|endocrine_system_disorder	oncology|neurology	neurological_cancer|cancer	brain_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0013603	myopia 20, autosomal dominant	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0013604	myopia 21, autosomal dominant	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0013605	brittle cornea syndrome 2	disorder_of_development_or_morphogenesis|connective_tissue_disorder|hereditary_disease|syndromic_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|syndromic_disease|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|connective_tissue_disorder	genetics_and_genomics|ophthalmology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013606	Hermansky-Pudlak syndrome 9	integumentary_system_disorder|hematologic_disorder|metabolic_disease|hereditary_disease|immune_system_disorder|syndromic_disease	metabolic_disease	metabolic_disease|immune_system_disorder|hereditary_disease|syndromic_disease|integumentary_system_disorder|hematologic_disorder	hematology|pediatric|genetics_and_genomics|immunology	neurodegenerative_disease|anemia|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013607	monocytopenia with susceptibility to infections	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	hematology|immunology	autoimmune_diseases|anemia|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	true	false	false	false	high
MONDO:0013608	Joubert syndrome 13	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013609	Meckel syndrome, type 10	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0013610	retinitis pigmentosa 61	metabolic_disease|hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|metabolic_disease	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|metabolic_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|adrenal_gland_disease	eye_disorder	false	false	false	false	high
MONDO:0013611	retinitis pigmentosa 62	metabolic_disease|hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|metabolic_disease	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|metabolic_disease	genetics_and_genomics|neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0013612	geleophysic dysplasia 2	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	genetic_disorder_is_not_listed__but_geleophysic_dysplasia_2_seems_to_be_related_to_it|metabolic_disorder	connective_tissue_disorder___note__this_response_is_based_on_the_common_understanding_that_geleophysic_dysplasia_2_is_a_genetic_disorder_affecting_bones_and_joints|bone_disorder|skeletal_disease_disorder|spinal_disorder|muscular_skeletal_disorder|joint_disorder	false	false	false	false	high
MONDO:0013613	Leber congenital amaurosis 16	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	pediatric|genetics_and_genomics|neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0013614	hypertelorism-preauricular sinus-punctual pits-deafness syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology|otolaryngology|ophthalmology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	throat_disorder|upper_gastrointestinal_disorder|ear_disorder|eye_disorder	false	false	false	false	medium
MONDO:0013615	craniosynostosis and dental anomalies	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|otolaryngology|orthopaedic	skeletal_dysplasia|developmental_disorder|metabolic_disorder|genetic_condition	bone_disorder|teeth_disorder	false	false	false	false	high
MONDO:0013616	pigmented nodular adrenocortical disease, primary, 3	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	dermatology|endocrinology	adrenal_gland_disease|cancer|metabolic_disorder	endocrine_disorder	false	true	false	false	high
MONDO:0013618	craniofacial anomalies and anterior segment dysgenesis syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	developmental_disorder|neurodevelopmental_disease|congenital_disorder	bone_disorder|teeth_disorder|craniofacial_anomalies_are_not_explcitly_listed_but_could_be_included_with_bone_disorder_and_eye_disorder_is_related_to_anterior_segment_dysgenesis_syndrome	false	false	false	false	high
MONDO:0013619	nephrotic syndrome, type 6	urinary_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease|idiopathic_disease|urinary_system_disorder	pediatric|renal_medicine	metabolic_disorder|kidney_disease	immune_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013620	congenital myasthenic syndrome 16	hereditary_disease|syndromic_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0013621	LAMB2-related infantile-onset nephrotic syndrome	hereditary_disease|urinary_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|urinary_system_disorder	pediatric|genetics_and_genomics|renal_medicine	autoimmune_diseases|kidney_disease|metabolic_disorder	immune_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013622	platelet-type bleeding disorder 9	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology|pediatric|genetics_and_genomics	anemia|bleeding_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0013623	platelet-type bleeding disorder 11	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	blood_disorder|platelet_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0013624	Rafiq syndrome	metabolic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|metabolic_disease	hereditary_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease	pediatric|genetics_and_genomics|rare_disease__not_listed__but_implied__is_removed_and_replaced_with_genetics_and_genomics_and_pediatric	autoimmune_diseases|metabolic_disorder	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013625	Parkinson disease 17	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013626	psoriasis 14, pustular	inflammatory_disease|integumentary_system_disorder|connective_tissue_disorder|hereditary_disease|immune_system_disorder|syndromic_disease	other	connective_tissue_disorder|immune_system_disorder|hereditary_disease|syndromic_disease|integumentary_system_disorder|inflammatory_disease	dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	very_high
MONDO:0013627	3M syndrome 3	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	lower_gastrointestinal_disorder|kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0013628	hyperphosphatasia with intellectual disability syndrome 3	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease	metabolic_disease	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|metabolic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	bone_disorder|brain_disorder|kidney_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0013629	intellectual disability, autosomal recessive 16	metabolic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|metabolic_disease	hereditary_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0013630	Meckel syndrome, type 9	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|obstetrics_and_gynecology	anemia|metabolic_disorder	kidney_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0013631	lung cancer susceptibility 5	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	oncology|genetics_and_genomics|pulmonology	lung_cancer_susceptibility|cancer	blood_bone_marrow_disorder|lung_disorder	false	true	false	false	high
MONDO:0013632	autosomal dominant nonsyndromic hearing loss 33	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	pediatric|genetics_and_genomics|otorhinolaryngology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0013634	neuropathy, hereditary sensory, type 2C	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	nerve_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013635	Adams-Oliver syndrome 2	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	anemia|metabolic_disorder|neurodegenerative_disease	bone_disorder|skeletal_system_disorder	false	false	false	false	medium
MONDO:0013636	primary biliary cholangitis 4	digestive_system_disorder|endocrine_system_disorder|hereditary_disease|premature_aging_syndrome	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|digestive_system_disorder|premature_aging_syndrome	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	biliary_disorder|liver_disorder	false	false	false	true	high
MONDO:0013637	primary biliary cholangitis 5	digestive_system_disorder|endocrine_system_disorder|hereditary_disease|premature_aging_syndrome	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|digestive_system_disorder|premature_aging_syndrome	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	biliary_disorder|liver_disorder	false	false	false	true	high
MONDO:0013638	Warburg micro syndrome 3	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|syndromic_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	metabolic_disorder|liver_disorder	false	false	false	false	high
MONDO:0013640	familial retinal arterial macroaneurysm	hereditary_disease|nervous_system_disorder|cardiovascular_disorder|disorder_of_visual_system	cardiovascular_disorder	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cardiovascular_disorder	genetics_and_genomics|ophthalmology	cardiovascular_disorder|familial_disease	vascular_disorder|eye_disorder	false	false	false	false	medium
MONDO:0013641	Warburg micro syndrome 2	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|nervous_system_disorder|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0013642	holoprosencephaly 11	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|nervous_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0013643	hyperuricemic nephropathy, familial juvenile type 3	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	renal_medicine|nephrology|pediatric|genetics_and_genomics	metabolic_disorder|genetic_condition|kidney_disease	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0013644	Charcot-Marie-Tooth disease axonal type 2O	hereditary_disease|syndromic_disease|nervous_system_disorder|cardiovascular_disorder|disorder_of_visual_system|psychiatric_disorder	cardiovascular_disorder|psychiatric_disorder	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|syndromic_disease|psychiatric_disorder|cardiovascular_disorder	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013645	autosomal recessive spinocerebellar ataxia 11	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0013646	chromosome 8q21.11 deletion syndrome	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	oncology|pediatrics|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0013648	familial progressive hyperpigmentation	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|neurodegenerative_disease	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0013649	hypotrichosis 9	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|hypotrichosis_is_a_genetic_disorder_affecting_hair_growth	skin_disorder|hair_disorder	false	false	false	true	medium
MONDO:0013650	hypotrichosis 10	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	skin_disorder|hair_disorder	false	false	false	false	low
MONDO:0013651	intellectual disability, autosomal recessive 18	psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|autosomal_recessive	false	false	false	false	high
MONDO:0013652	narcolepsy 7	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|sleep_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013654	aneurysm, intracranial berry, 11	hereditary_disease|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|nervous_system_disorder|cardiovascular_disorder	cardiothoracic|neurology|hematology	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013655	neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0013656	intellectual disability, autosomal dominant 9	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	very_high
MONDO:0013657	intellectual disability, autosomal dominant 10	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0013658	intellectual disability, autosomal dominant 11	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0013659	microcephaly-capillary malformation syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013660	arthrogryposis, Perthes disease, and upward gaze palsy	hereditary_disease	other	hereditary_disease	pediatric|neurology|orthopaedic	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013661	combined malonic and methylmalonic acidemia	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|hematology	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0013662	Barrett esophagus	digestive_system_disorder|upper_digestive_tract_disorder	other	digestive_system_disorder|upper_digestive_tract_disorder	hepatology|gastroenterology	autoimmune_diseases|cancer|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0013663	platelet-activating factor acetylhydrolase deficiency	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0013664	46,XY disorder of sex development due to testicular 17,20-desmolase deficiency	musculoskeletal_system_disorder|reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder|endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|cardiovascular_disorder|reproductive_system_disorder	genetics_and_genomics|urology|endocrinology	adrenal_gland_disease|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0013666	Stickler syndrome, type 5	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|syndromic_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_orbital_region|syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|ophthalmology|orthopaedic	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|eye_disorder	false	false	false	false	medium
MONDO:0013668	tetrasomy 18p	chromosomal_disorder|hereditary_disease	other	hereditary_disease|chromosomal_disorder	pediatric|genetics_and_genomics	autoimmune_diseases|anemia|metabolic_disorder|neurodegenerative_disease	bone_disorder|immune_disorder|joint_disorder|skeletal_system_disorder|urinary_tract_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0013670	myopia, high, with cataract and vitreoretinal degeneration	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	true	very_high
MONDO:0013671	hydatidiform mole, recurrent, 2	hereditary_disease|reproductive_system_disorder|obstetric_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|obstetric_disorder|cancer_or_benign_tumor|hereditary_disease	oncology|pediatric|obstetrics_and_gynecology	obstetric_disease|cancer|reproductive_disease	reproductive_system_disorder	false	false	false	true	high
MONDO:0013672	chromosome 15q25 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0013673	Wolfram-like syndrome	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	endocrinology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder|endocrine_disorder|bone_disorder	false	false	true	false	medium
MONDO:0013674	neurodegeneration with brain iron accumulation 4	psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder	neurodegenerative_disease|psychiatric_disorder|metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013675	multiple mitochondrial dysfunctions syndrome 2	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	neurology|pediatric|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|mitochondrial_disease_category_is_not_in_the_list__so_we_cannot_use_it__however__based_on_the_name_of_the_disease__it_seems_to_fit_into_this_category	false	false	false	false	very_high
MONDO:0013677	Emery-Dreifuss muscular dystrophy 7, autosomal dominant	cardiovascular_disorder|hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder	neurology|pediatric|genetics_and_genomics|orthopaedic	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0013678	EDICT syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013679	sclerosteosis 2	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|rheumatology|orthopaedic	genetic_disorders|metabolic_disorder	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0013680	cognitive impairment with or without cerebellar ataxia	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	cognitive_impairment_with_or_without_cerebellar_ataxia_is_an_adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	true	false	false	false	high
MONDO:0013681	alpha-methylacyl-CoA racemase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|liver_disorder	false	false	false	false	high
MONDO:0013682	vesicoureteral reflux 4	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	pediatric|urology|renal_medicine	urinary_disorder|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0013683	vesicoureteral reflux 5	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	pediatric|urology|renal_medicine	urological_disease|autoimmune_diseases|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0013684	vesicoureteral reflux 6	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	pediatric|urology	urogenital_disorder|autoimmune_diseases|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0013685	pancreatic cancer, susceptibility to, 4	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	oncology|genetics_and_genomics|gastroenterology	cancer|genetic____wait__that_was_a_mistake__the_correct_answer_is__cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0013686	distal myopathy, Tateyama type	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0013687	autosomal recessive spinocerebellar ataxia 12	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013688	linear and whorled nevoid hypermelanosis	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|hereditary_disease	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|skin_disorder	false	false	false	false	low
MONDO:0013689	ovarian dysgenesis 3	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|obstetrics_and_gynecology	cancer|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0013690	Pitt-Hopkins-like syndrome 2	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013691	Feingold syndrome type 2	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|genetic_disorder	false	false	false	false	medium
MONDO:0013692	BAP1-related tumor predisposition syndrome	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	oncology|genetics_and_genomics	cancer|adrenal_gland_disease	lung_disorder|kidney_disorder|eye_disorder|lymphatic_disorder|urinary_tract_disorder|skin_disorder	false	false	false	true	high
MONDO:0013693	inflammatory skin and bowel disease, neonatal, 1	integumentary_system_disorder|digestive_system_disorder|hereditary_disease|immune_system_disorder|connective_tissue_disorder|syndromic_disease	other	digestive_system_disorder|integumentary_system_disorder|connective_tissue_disorder|immune_system_disorder|hereditary_disease|syndromic_disease	pediatric|gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|immune_disorder|skin_disorder	false	false	false	true	high
MONDO:0013694	intellectual disability, autosomal recessive 31	psychiatric_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0013695	colorectal cancer, hereditary nonpolyposis, type 6	digestive_system_disorder|hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|hereditary_disease|syndromic_disease|cancer_or_benign_tumor	oncology|genetics_and_genomics|gastroenterology	disease|hereditary|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0013696	chromosome 2p16.3 deletion syndrome	psychiatric_disorder|chromosomal_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|chromosomal_disorder|psychiatric_disorder|hereditary_disease	pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|intellectual_disability___note__since_the_provided_category_list_does_not_explicitly_mention__developmental_disorder__or__intellectual_disability___these_categories_might_be_inferred_based_on_general_knowledge_about_chromosome_2p16_3_deletion_syndrome__which_is_often_associated_with_developmental_and_intellectual_disabilities|developmental_disorder	false	false	false	false	high
MONDO:0013697	intellectual disability, autosomal recessive 29	psychiatric_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0013698	arthrogryposis, distal, type 1B	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0013699	Lynch syndrome 4	digestive_system_disorder|hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|hereditary_disease|cancer_or_benign_tumor|syndromic_disease	oncology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|cancer	upper_gastrointestinal_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0013700	pancreatic triacylglycerol lipase deficiency	digestive_system_disorder|endocrine_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|endocrine_system_disorder	digestive_system_disorder|hereditary_disease|endocrine_system_disorder|metabolic_disease	endocrinology|gastroenterology|genetics_and_genomics	pancreatic_disease|metabolic_disorder	pancreatic_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0013702	intellectual disability, autosomal recessive 27	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0013703	intellectual disability, autosomal recessive 33	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0013704	intellectual disability, autosomal recessive 30	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	autosomal_recessive_is_not_in_the_list__but_it_is_relevant_to_intellectual_disability__so_i_will_assume_you_meant__genetic_disorder__is_not_an_option__but__genetic__would_be_a_broader_category__genetic|brain_disorder	false	false	false	false	high
MONDO:0013705	intellectual disability, autosomal recessive 19	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013706	intellectual disability, autosomal recessive 23	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0013707	intellectual disability, autosomal recessive 24	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	autosomal_recessive_disorder|genetic_disorder_is_incorrect_so|intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0013708	intellectual disability, autosomal recessive 25	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics|psychiatry	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013709	intellectual disability, autosomal recessive 28	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0013710	Lynch syndrome 5	syndromic_disease|digestive_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|digestive_system_disorder|hereditary_disease|cancer_or_benign_tumor	oncology|genetics_and_genomics	cancer	reproductive_system_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0013711	peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	neurology|otolaryngology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|hearing_loss_disorder	true	false	false	false	high
MONDO:0013712	surfactant metabolism dysfunction, pulmonary, 5	hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease	pulmonology|pediatric	pulmonary|metabolic_disorder	respiratory_disorder|lung_disorder	false	false	false	true	high
MONDO:0013714	mannose-binding lectin deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|allergy_and_immunology|immunology|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	vascular_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0013715	amyotrophic lateral sclerosis type 16	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013716	aortic aneurysm, familial abdominal, 4	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	genetics_and_genomics|cardiology	cardiovascular_disorder|familial_abdominal_aortic_aneurysm_is_often_associated_with_genetic_factors_but_can_also_be_classified_as_a_cardiovascular_disorder	heart_disorder_vascular_disorder	false	false	false	true	high
MONDO:0013717	asphyxiating thoracic dystrophy 5	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|urinary_system_disorder|respiratory_system_disorder	other	syndromic_disease|respiratory_system_disorder|urinary_system_disorder|musculoskeletal_system_disorder|hereditary_disease	pulmonology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|throat_disorder|respiratory_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0013718	nephronophthisis 13	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	nephrology|renal_medicine|urology	inflammatory_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013719	cranioectodermal dysplasia 4	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|urinary_system_disorder|integumentary_system_disorder|respiratory_system_disorder|disorder_of_development_or_morphogenesis	other	syndromic_disease|respiratory_system_disorder|urinary_system_disorder|musculoskeletal_system_disorder|hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology|genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	teeth_disorder|ear_disorder|bone_disorder|eye_disorder|spinal_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0013720	complement component 4b deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|kidney_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0013721	complement component 4a deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	rheumatology|immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013722	hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism	hereditary_disease|nervous_system_disorder|syndromic_disease|reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	neurology|endocrinology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder|brain_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0013725	colorectal cancer, hereditary nonpolyposis, type 7	hereditary_disease|syndromic_disease|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease|digestive_system_disorder	oncology|gastroenterology|genetics_and_genomics	hereditary_nonpolyposis_colorectal_cancer_is_a_type_of_cancer|cancer	lower_gastrointestinal_disorder|hereditary_nonpolyposis	false	true	false	true	high
MONDO:0013726	encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1	mitochondrial_disease|hereditary_disease|nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	neurology|psychiatry|pediatric|genetics_and_genomics	neurodegenerative_disease|mitochondrial_dysfunction_is_not_in_the_list__but_it_s_closely_related_to_metabolic_disorder_so_i_will_exclude_it__therefore__i_am_left_with_two_categories__neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|mitochondrial_disease	false	false	false	false	very_high
MONDO:0013730	graft versus host disease	immune_system_disorder	other	immune_system_disorder|disease_related_to_transplantation	transplant|immunology|oncology|hematology	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|skin_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0013731	MEGF10-related myopathy	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	false	very_high
MONDO:0013732	glucocorticoid therapy, response to	hereditary_disease	other	hereditary_disease	allergy_and_immunology|pediatrics|endocrinology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	endocrine_disorder	false	false	false	true	high
MONDO:0013734	microphthalmia, syndromic 11	hereditary_disease|syndromic_disease|disorder_of_visual_system	other	hereditary_disease|syndromic_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder|joint_disorder|eye_disorder|vascular_disorder|immune_disorder|kidney_disorder|teeth_disorder|spinal_disorder|bone_disorder|lymphatic_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013735	microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric|cardiology	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	brain_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0013737	hereditary spastic paraplegia 46	hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|neurology	hereditary_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013738	autosomal recessive nonsyndromic hearing loss 96	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|pediatric|otolaryngology	autosomal_recessive_diseases|hereditary_condition|metabolic_disorder	kidney_disorder|ear_disorder	false	false	false	false	medium
MONDO:0013739	chilblain lupus 2	cardiovascular_disorder|hereditary_disease|syndromic_disease|integumentary_system_disorder|connective_tissue_disorder|immune_system_disorder	autoimmune_disease|cardiovascular_disorder	cardiovascular_disorder|integumentary_system_disorder|immune_system_disorder|hereditary_disease|connective_tissue_disorder|syndromic_disease	rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder__skin_disorder	false	false	false	true	medium
MONDO:0013740	lethal occipital encephalocele-skeletal dysplasia syndrome	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	neurology|pediatric|genetics_and_genomics	skeletal_dysplasia_syndrome|neurodegenerative_disease	brain_disorder|spinal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0013741	familial temporal lobe epilepsy 5	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0013743	autosomal systemic lupus erythematosus type 16	hereditary_disease|connective_tissue_disorder|immune_system_disorder	autoimmune_disease	immune_system_disorder|hereditary_disease|connective_tissue_disorder	rheumatology|immunology|hematology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	joint_disorder|immune_disorder|skin_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013744	cataract 37	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0013745	Joubert syndrome 14	nervous_system_disorder|hereditary_disease|syndromic_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis	neurodegenerative_disease	hereditary_disease|syndromic_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013746	ventricular septal defect 1	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|cardiology	congenital_heart_defect|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0013747	atrioventricular septal defect 4	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiothoracic|pediatric|cardiology	congenital_heart_defect|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013748	ventricular septal defect 2	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiothoracic|pediatric|cardiology	congenital_heart_defect|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0013749	ventricular septal defect 3	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiothoracic|pediatric|cardiology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013750	atrial septal defect 8	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013751	cutis laxa, autosomal dominant 2	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|dermatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013752	hypoplastic left heart syndrome 2	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	cardiothoracic|pediatric|cardiology	neonatal_condition|cardiovascular_disorder	heart_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0013753	Charcot-Marie-Tooth disease axonal type 2P	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|cardiovascular_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013754	cutis laxa, autosomal recessive, type 1B	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatrics|dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	joint_disorder|vascular_disorder|lower_gastrointestinal_disorder|skin_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013755	PYCR1-related de Barsy syndrome	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|premature_aging_syndrome	other	integumentary_system_disorder|hereditary_disease|premature_aging_syndrome|disorder_of_development_or_morphogenesis	dermatology|genetics_and_genomics	genetic_disorder|anemic_disorder|metabolic_disorder	skin_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013756	hypertrophic osteoarthropathy, primary, autosomal recessive, 2	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	rheumatology|orthopaedic|pediatric|genetics_and_genomics	inflammatory_disease|autosomal_recessive_diseases|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0013757	congenital nongoitrous hypothyroidism 6	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	endocrinology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	congenital|endocrine_disorder	false	false	false	true	medium
MONDO:0013758	Charcot-Marie-Tooth disease dominant intermediate E	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|orthopaedic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	nerve_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013759	melanoma, cutaneous malignant, susceptibility to, 8	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	oncology|hematology|dermatology|genetics_and_genomics	cancer|cutaneous_malignant	skin_disorder|cutaneous_malignant	false	true	false	true	high
MONDO:0013760	congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome	syndromic_disease|metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	skin_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0013761	childhood encephalopathy due to thiamine pyrophosphokinase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013762	lipoic acid synthetase deficiency	nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|metabolic_disease|mitochondrial_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0013763	Joubert syndrome 15	nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease	neurodegenerative_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|disorder_of_visual_system|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013764	Joubert syndrome 16	nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease	neurodegenerative_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|disorder_of_visual_system|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013766	familial cold autoinflammatory syndrome 3	immune_system_disorder|syndromic_disease|connective_tissue_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease|connective_tissue_disorder|syndromic_disease	rheumatology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	inflammatory_disorder|immune_disorder|joint_disorder	false	false	false	true	high
MONDO:0013767	autoimmune lymphoproliferative syndrome type 4	immune_system_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease	autoimmune_disease|cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hereditary_disease|syndromic_disease	allergy_and_immunology|rheumatology|hematology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0013768	arterial calcification, generalized, of infancy, 2	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	pediatrics|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013769	atrioventricular septal defect 5	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	pediatric|cardiology	autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013770	atrial septal defect 9	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	pediatric|cardiothoracic|cardiology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0013771	transient infantile hypertriglyceridemia and hepatosteatosis	digestive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|digestive_system_disorder	pediatric|genetics_and_genomics|hepatology	hepatic_disorder|metabolic_disorder	endocrine_disorder|liver_disorder	false	false	false	false	low
MONDO:0013772	Huppke-Brendel syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	kidney_disorder	false	false	false	false	very_high
MONDO:0013773	porencephaly 2	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	nervous_system_disorder|hereditary_disease|cardiovascular_disorder	neurology|pediatric|genetics_and_genomics	porencephaly|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013774	trigonocephaly 2	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013775	thrombomodulin-related bleeding disorder	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder|metabolic_disorder|bleeding_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013776	spastic ataxia 5	nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|metabolic_disease|mitochondrial_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0013777	pseudohypoaldosteronism type 2B	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	pediatric|endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013778	pseudohypoaldosteronism type 2C	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	renal_medicine|pediatric|endocrinology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013779	Wiskott-Aldrich syndrome 2	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	allergy_and_immunology|immunology___corrected_to_meet_the_format_requirement__genetics_and_genomics|hematology|genetics_and_genomics	anemia|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013780	retinitis pigmentosa 63	hereditary_disease|disorder_of_visual_system|metabolic_disease|psychiatric_disorder|nervous_system_disorder	metabolic_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|retinal_disorder	false	false	false	false	high
MONDO:0013781	pseudohypoaldosteronism type 2D	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	endocrinology|pediatric	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013782	pseudohypoaldosteronism type 2E	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0013783	microphthalmia, isolated, with coloboma 7	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0013784	neonatal-onset encephalopathy with rigidity and seizures	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	true	false	false	false	very_high
MONDO:0013785	intellectual disability, autosomal recessive 34	hereditary_disease|metabolic_disease|psychiatric_disorder|nervous_system_disorder	metabolic_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|autosomal_recessive_disorder	false	false	false	true	high
MONDO:0013786	cone-rod dystrophy 16	hereditary_disease|disorder_of_visual_system|metabolic_disease|psychiatric_disorder|nervous_system_disorder	metabolic_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0013787	psychomotor retardation, epilepsy, and craniofacial dysmorphism	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|craniofacial_dysmorphism_is_related_to_a_brain_disorder_so_it_can_be_included_as_well|muscle_disorder	true	false	false	false	high
MONDO:0013788	Usher syndrome type 3B	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	ophthalmology|pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|spinal_disorder|ear_disorder	false	false	false	false	high
MONDO:0013789	DDOST-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	genetic_disease|congenital_disorder|metabolic_disorder	skin_disorder|bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0013790	mirror movements 2	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013791	thrombophilia due to protein S deficiency, autosomal recessive	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0013792	intracerebral hemorrhage	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	cardiology|hematology|neurology	neurodegenerative_disease|cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0013793	encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013794	thrombocythemia 3	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	thrombocytopenia|hematology	anemia|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0013795	fibrochondrogenesis 2	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	genetic_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0013796	chromosome 17q12 duplication syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder|cancer	brain_disorder|immune_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013797	chromosome 17q12 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|developmental_disorder	false	false	false	false	high
MONDO:0013798	chromosome 16q22 deletion syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|immune_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013800	Ehlers-Danlos syndrome, kyphoscoliotic type, 2	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|rheumatology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	joint_disorder|spinal_disorder|vascular_disorder|skin_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013801	developmental and epileptic encephalopathy, 13	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|pediatric|genetics_and_genomics	developmental_disorder|neurodegenerative_disease|epileptic_encephalopathy	epileptic_disorder|brain_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0013802	infantile cerebellar-retinal degeneration	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	neurodegenerative_disease|metabolic_disease|psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0013803	leukoencephalopathy with calcifications and cysts	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|spinal_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013805	intellectual disability, autosomal dominant 13	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder|psychiatric_disorder	syndromic_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|psychiatric_disorder|cardiovascular_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	reproductive_system_disorder|brain_disorder|spinal_disorder|kidney_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013806	familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome	hereditary_disease|cancer_or_benign_tumor|syndromic_disease|integumentary_system_disorder|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	syndromic_disease|integumentary_system_disorder|hereditary_disease|cardiovascular_disorder|cancer_or_benign_tumor	genetics_and_genomics|dermatology|oncology	autoimmune_diseases|cancer	immune_disorder|throat_disorder|skin_disorder	false	true	false	false	medium
MONDO:0013807	congenital stationary night blindness 1E	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0013808	Maffucci syndrome	cardiovascular_disorder|hereditary_disease|cancer_or_benign_tumor|connective_tissue_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	cardiovascular_disorder|cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|syndromic_disease|integumentary_system_disorder|hereditary_disease|cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	orthopaedic|rheumatology	neoplastic_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0013810	COG6-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|hepatology|pediatric|hematology|genetics_and_genomics|endocrinology|pulmonology|allergy_and_immunology	congenital_disorder_of_glycosylation|metabolic_disorder|adrenal_gland_disease	liver_disorder|kidney_disorder	false	false	true	false	high
MONDO:0013811	combined oxidative phosphorylation defect type 9	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	mitochondrial_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0013812	Baraitser-winter syndrome 2	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|hematology|dermatology|genetics_and_genomics|pulmonology|allergy_and_immunology|cardiology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013813	dystonia 21	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013815	bent bone dysplasia syndrome 1	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|bone_dysplasia	bone_disorder|blood_bone_marrow_disorder|joint_disorder	false	false	false	false	high
MONDO:0013817	preeclampsia/eclampsia 5	cardiovascular_disorder|hereditary_disease|obstetric_disorder	cardiovascular_disorder	hereditary_disease|obstetric_disorder|cardiovascular_disorder	pediatrics|obstetrics_and_gynecology	metabolic_disorder|inflammatory_disease	vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013818	trichohepatoenteric syndrome 2	digestive_system_disorder|hereditary_disease|immune_system_disorder|connective_tissue_disorder|syndromic_disease	other	connective_tissue_disorder|syndromic_disease|immune_system_disorder|hereditary_disease|digestive_system_disorder	pediatrics|hepatology|genetics_and_genomics|gastroenterology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|liver_disorder	true	false	false	true	high
MONDO:0013819	intellectual disability, autosomal dominant 14	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder_spinal_disorder	false	false	false	true	high
MONDO:0013820	intellectual disability, autosomal dominant 15	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0013821	intellectual disability, autosomal dominant 16	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder|autosomal_dominant_disorders_would_fall_under_a_more_specific_category_but_the_provided_list_doesn_t_have_it_so_neurodegenerative_disease_is_used	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0013822	acrodysostosis 2 with or without hormone resistance	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|endocrinology|orthopaedic	autoimmune_diseases|metabolic_disorder|hormonal_disorders	bone_disorder|endocrine_disorder|joint_disorder	false	false	false	false	medium
MONDO:0013823	autosomal dominant nonsyndromic hearing loss 4B	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	medium
MONDO:0013824	Joubert syndrome 17	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0013825	congenital diarrhea 6	digestive_system_disorder|hereditary_disease	other	hereditary_disease|digestive_system_disorder	pediatric|gastroenterology	congenital_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0013826	autosomal recessive nonsyndromic hearing loss 86	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0013827	hyperekplexia 3	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013828	hyperekplexia 2	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013829	UV-sensitive syndrome 2	hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0013830	keratoconus 5	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|orthopaedic	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	high
MONDO:0013831	keratoconus 6	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	pediatric|genetics_and_genomics|ophthalmology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	true	high
MONDO:0013832	keratoconus 8	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0013833	keratoconus 7	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	optometry|ophthalmology|orthopaedic	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	true	high
MONDO:0013834	UV-sensitive syndrome 3	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|dermatology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0013835	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7	nervous_system_disorder|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	pediatric|genetics_and_genomics|neurology	muscular_dystrophy|neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0013836	familial steroid-resistant nephrotic syndrome with sensorineural deafness	mitochondrial_disease|nervous_system_disorder|urinary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease	metabolic_disease	syndromic_disease|urinary_system_disorder|mitochondrial_disease|idiopathic_disease|hereditary_disease|nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|renal_medicine	autoimmune_diseases|metabolic_disorder|inflammatory_disease	ear_disorder|kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0013837	deafness-encephaloneuropathy-obesity-valvulopathy syndrome	mitochondrial_disease|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	pediatrics|genetics_and_genomics|cardiology|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|ear_disorder|heart_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0013838	coenzyme Q10 deficiency, primary, 3	mitochondrial_disease|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|endocrinology|cardiology|neurology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	true	high
MONDO:0013839	hereditary sensory and autonomic neuropathy type 6	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	hereditary_conditions_were_not_in_the_list_but_it_is_closely_related_to_neurodegenerative_disease|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013840	encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome	mitochondrial_disease|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|renal_medicine|neurology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0013841	stuttering, familial persistent, 3	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|throat_disorder	false	false	false	true	medium
MONDO:0013842	cortisone reductase deficiency 2	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|metabolic_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|hereditary_disease|metabolic_disease|reproductive_system_disorder	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|inflammatory_disease|adrenal_gland_disease	adrenal_gland_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0013843	intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency	digestive_system_disorder|hereditary_disease	other	hereditary_disease|digestive_system_disorder	pediatric|genetics_and_genomics|gastroenterology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0013844	stuttering, familial persistent, 4	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|ear_disorder|throat_disorder	false	false	false	true	medium
MONDO:0013845	auriculocondylar syndrome 2	hereditary_disease	other	hereditary_disease	otolaryngology|genetics_and_genomics|orthopaedic	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	ear_disorder|joint_disorder	false	false	false	false	high
MONDO:0013847	chromosome 16p11.2 duplication syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	developmental_disorder____note__i_added_the_implied_category__developmental_disorder__which_is_a_common_categorization_for_chromosome_disorders_like_this_one|brain_disorder	false	false	false	false	high
MONDO:0013848	dilated cardiomyopathy 2B	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiothoracic|cardiology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0013849	microcephaly 8, primary, autosomal recessive	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|autosomal_recessive|primary	false	false	false	false	high
MONDO:0013851	autosomal dominant aplasia and myelodysplasia	hematologic_disorder|immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder	anemia	hematologic_disorder|immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|hematology	metabolic_disorder|anemia|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0013852	hypertrophic cardiomyopathy 21	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiology|cardiothoracic|genetics_and_genomics	hypertrophic_cardiomyopathy|cardiovascular_disorder	muscle_disorder|heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013853	pontocerebellar hypoplasia type 1B	hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease|psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0013854	primary ciliary dyskinesia 17	syndromic_disease|hereditary_disease|respiratory_system_disorder	other	hereditary_disease|respiratory_system_disorder|syndromic_disease	pulmonology|genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	eye_disorder|spinal_disorder|kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0013856	hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, intellectual disability, and recurrent inflammatory episodes	hereditary_disease	other	hereditary_disease	immunology|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder|joint_disorder|facial_dysmorphia|immune_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0013857	alar cleft, isolated	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	metabolic_disorder|genetic_disorder	ear_disorder|oral_cleft_disorder	false	false	false	false	low
MONDO:0013858	pontine tegmental cap dysplasia	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	pontine_tegmental_cap_dysplasia_does_not_clearly_fit_under_this_category_however_it_is_sometimes_associated_with_pontocerebellar_hypoplasia_which_can_be_a_neurodegenerative_disease__and_given_the_context_of_ptcd_it_seems_like_it_could_fit|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0013859	cataract 38	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder|eyecategory_disorder	false	false	false	true	high
MONDO:0013860	idiopathic membranous glomerulonephritis	urinary_system_disorder|hereditary_disease|inflammatory_disease	other	urinary_system_disorder|inflammatory_disease|idiopathic_disease|hereditary_disease	renal_medicine|nephrology|hematology	inflammatory_disease|autoimmune_diseases	immune_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0013862	immunodeficiency, common variable, 7	hematologic_disorder|syndromic_disease|immune_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor|hereditary_disease|syndromic_disease	allergy_and_immunology|immunodeficiency	allergy|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0013863	combined immunodeficiency due to LRBA deficiency	hematologic_disorder|immune_system_disorder|syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|hereditary_disease|cancer_or_benign_tumor|syndromic_disease	allergy_and_immunology|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0013864	Cornelia de Lange syndrome 4	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|mental_health_disorder|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|ear_disorder|heart_disorder|joint_disorder|skin_disorder|vascular_disorder|throat_disorder|lower_gastrointestinal_disorder|immune_disorder|blood_bone_marrow_disorder|kidney_disorder|brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0013865	mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	cardiology|pediatric|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0013866	neuronal ceroid lipofuscinosis 11	hereditary_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0013867	Brown-Vialetto-van Laere syndrome 2	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0013868	porokeratosis 7, multiple types	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	metabolic_disorder|inflammatory_disease	liver_disorder|skin_disorder	false	false	false	false	low
MONDO:0013869	adenine phosphoribosyltransferase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	other____corrected_to_exclude__other____genetics_and_genomics|pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0013870	TMEM165-congenital disorder of glycosylation	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|congenital_disorder_of_glycosylation	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0013871	Seckel syndrome 6	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|anemia|neurodegenerative_disease	eye_disorder|joint_disorder|lymphatic_disorder|brain_disorder	false	false	false	false	high
MONDO:0013872	prostate cancer, hereditary, 2	hereditary_disease|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|urology|oncology	hereditary|cancer	hereditary|reproductive_system_disorder	false	true	false	true	high
MONDO:0013873	IMAGe syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0013874	glucocorticoid deficiency 4	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	endocrinology|psychiatry|pediatric	metabolic_disorder|inflammatory_disease|adrenal_gland_disease	endocrine_disorder|immune_disorder	false	false	false	true	high
MONDO:0013875	3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	ear_disorder|muscle_disorder|brain_disorder	true	false	false	true	very_high
MONDO:0013876	basal cell carcinoma, susceptibility to, 7	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	dermatology|oncology	skin_cancer|cancer	skin_disorder|susceptibility_to_cancer	false	true	false	true	medium
MONDO:0013877	mitochondrial pyruvate carrier deficiency	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0013878	pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1	premature_aging_syndrome|hereditary_disease|respiratory_system_disorder	other	premature_aging_syndrome|hereditary_disease|respiratory_system_disorder	pulmonology|genetics_and_genomics|hematology	metabolic_disorder|anemia|cancer	lung_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0013879	pulmonary fibrosis and/or bone marrow failure, Telomere-related, 2	premature_aging_syndrome|hereditary_disease|respiratory_system_disorder	other	premature_aging_syndrome|hereditary_disease|respiratory_system_disorder	pulmonology|pediatrics|genetics_and_genomics|oncology|hematology	anemia|telomere_related_diseases_seem_to_be_most_closely_related_to_cancer_and_autoimmune_disorders_but_these_categories_aren_t_specified_in_the_question_so_anemia_is_left_alone_as_it_directly_relates_to_bone_marrow_failure	lung_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0013880	facial paresis, hereditary congenital, 3	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0013881	epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|renal_medicine|pulmonology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	lung_disorder|skin_disorder|immune_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0013882	hyperphosphatasia with intellectual disability syndrome 2	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0013883	congenital myasthenic syndrome 13	syndromic_disease|nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0013884	neuronopathy, distal hereditary motor, type 5B	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|hereditary_disease	muscle_disorder|neurological_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0013885	Malan overgrowth syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	endocrinology|pediatrics|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|bone_disorder	false	false	false	false	high
MONDO:0013886	cerebellar dysfunction with variable cognitive and behavioral abnormalities	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatry|pediatric|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0013887	heterotaxy, visceral, 6, autosomal	cardiovascular_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	visceral|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013888	tremor, hereditary essential, 4	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|hereditary_essential	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0013889	short stature-optic atrophy-Pelger-Huët anomaly syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	ophthalmology|pediatric|genetics_and_genomics	metabolic_disorder|anemia|neurodegenerative_disease|autoimmune_diseases	eye_disorder|bone_disorder	false	false	false	false	medium
MONDO:0013890	congenital myopathy with internal nuclei and atypical cores	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0013891	amyotrophic lateral sclerosis type 18	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0013892	C3 glomerulonephritis	hereditary_disease|urinary_system_disorder|inflammatory_disease	other	urinary_system_disorder|inflammatory_disease|hereditary_disease	renal_medicine|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|kidney_disorder	false	false	false	true	high
MONDO:0013894	short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	joint_disorder|skin_disorder|bone_disorder|growth_disorder	true	false	false	false	high
MONDO:0013895	Adams-Oliver syndrome 3	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology|dermatology	metabolic_disorder|neurodegenerative_disease	bone_disorder|vascular_disorder|other___corrected_answer__bone_disorder	false	false	false	false	medium
MONDO:0013896	Joubert syndrome 18	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013897	Loeys-Dietz syndrome 4	hereditary_disease|syndromic_disease|cardiovascular_disorder|connective_tissue_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|connective_tissue_disorder|syndromic_disease	orthopaedic|pediatric|genetics_and_genomics|medical_genetics	metabolic_disorder|cardiovascular_disorder	joint_disorder|bone_disorder|vascular_disorder	false	false	false	false	high
MONDO:0013898	karyomegalic interstitial nephritis	hereditary_disease|urinary_system_disorder|inflammatory_disease|metabolic_disease	metabolic_disease	urinary_system_disorder|inflammatory_disease|metabolic_disease|hereditary_disease	renal_medicine|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	vascular_disorder|immune_disorder|kidney_disorder	true	false	false	false	high
MONDO:0013899	Weill-Marchesani syndrome 3	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|ophthalmology	inflammatory_disease|metabolic_disorder	joint_disorder|bone_disorder|eye_disorder	false	false	false	false	high
MONDO:0013900	alternating hemiplegia of childhood 2	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013901	spermatogenic failure 10	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	cancer|anemia|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0013902	aortic valve disease 2	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiology|cardiothoracic	cardiovascular_disorder|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0013903	nystagmus 7, congenital, autosomal dominant	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	ophthalmology|pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant_disorder|congenital_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0013904	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8	hereditary_disease|metabolic_disease|nervous_system_disorder|musculoskeletal_system_disorder	metabolic_disease	nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	orthopaedic|pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	eye_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0013905	autosomal recessive spinocerebellar ataxia 13	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013906	amelogenesis imperfecta hypomaturation type 2A4	hereditary_disease|musculoskeletal_system_disorder	other	mouth_disorder|musculoskeletal_system_disorder|hereditary_disease	ophthalmology|dermatology|pediatrics|genetics_and_genomics	neurodegenerative_disease|anemia|metabolic_disorder	teeth_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0013907	bilateral generalized polymicrogyria	hereditary_disease|nervous_system_disorder|syndromic_disease|musculoskeletal_system_disorder	other	syndromic_disease|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0013910	hypogonadotropic hypogonadism 8 with or without anosmia	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	neurology|endocrinology|genetics_and_genomics	endocrine_disorder|neurodevelopmental_disorder|reproductive_system_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0013911	hypogonadotropic hypogonadism 9 with or without anosmia	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	pediatric|endocrinology|genetics_and_genomics	endocrine_disorder|neurodegenerative_disease|genetic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0013912	hypogonadotropic hypogonadism 10 with or without anosmia	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	pediatric|neurology|endocrinology|genetics_and_genomics	endocrine_disorder|developmental_disorder|genetic_disorder	endocrine_disorder|reproductive_system_disorder|nose_disorder	false	false	false	true	medium
MONDO:0013913	hypogonadotropic hypogonadism 11 with or without anosmia	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	pediatric|neurology|endocrinology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder|nose_disorder	false	false	false	false	medium
MONDO:0013914	hypogonadotropic hypogonadism 12 with or without anosmia	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	neurology|endocrinology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder|nose_disorder	false	false	false	true	high
MONDO:0013915	hypogonadotropic hypogonadism 13 with or without anosmia	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	pediatric|neurology|endocrinology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0013916	nephronophthisis 14	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	urology|nephrology|renal_medicine	inflammatory_disease|kidney_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013917	nephronophthisis 15	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	nephrology|renal_medicine	inflammatory_disease|autoimmune_diseases|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013918	distal tetrasomy 15q	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	pediatric|developmental_disorders|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|spinal_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0013922	Seckel syndrome 7	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	vascular_disorder|upper_gastrointestinal_disorder|eye_disorder|joint_disorder|brain_disorder|ear_disorder|immune_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0013923	microcephaly 9, primary, autosomal recessive	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|primary_autosomal_recessive_diseases_often_fit_within_these_categories|metabolic_disorder	brain_disorder|spinal_disorder|ear_disorder	false	false	false	false	high
MONDO:0013924	osteogenesis imperfecta type 13	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|anemia|metabolic_disorder	joint_disorder|spinal_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0013925	methylmalonic acidemia with homocystinuria, type cblJ	hereditary_disease|metabolic_disease|nutritional_disorder|hematologic_disorder	metabolic_disease|anemia	nutritional_disorder|hematologic_disorder|metabolic_disease|hereditary_disease	pediatric|hematology|genetics_and_genomics	neurodegenerative_disease|anemia|metabolic_disorder	liver_disorder|kidney_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0013926	hypogonadotropic hypogonadism 14 with or without anosmia	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|syndromic_disease	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0013927	peroxisome biogenesis disorder 3A (Zellweger)	hereditary_disease|metabolic_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease	pediatric|neurology|hepatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisome_biogenesis_disorder	false	false	false	false	very_high
MONDO:0013928	dystonia 23	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013929	autosomal recessive nonsyndromic hearing loss 98	hereditary_disease|psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	pediatric|otorhinolaryngology|genetics_and_genomics	autosomal_recessive_diseases|genetic_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0013930	peroxisome biogenesis disorder 4A (Zellweger)	hereditary_disease|metabolic_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease	hepatology|pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisomal_disorder	false	false	false	false	very_high
MONDO:0013931	peroxisome biogenesis disorder 4B	hereditary_disease|metabolic_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	liver_disorder|peroxisomal_disorder	false	false	false	false	very_high
MONDO:0013932	peroxisome biogenesis disorder 5A (Zellweger)	hereditary_disease|metabolic_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease	pediatric|neurology|hepatology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	liver_disorder|peroxisome_biosynthesis_disorder	false	false	false	false	very_high
MONDO:0013933	peroxisome biogenesis disorder 5B	hereditary_disease|metabolic_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisomal_disorder	false	false	false	false	high
MONDO:0013934	combined immunodeficiency due to STK4 deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	pediatric|immunology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|anemia	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0013935	Usher syndrome type 1J	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	ophthalmology|otolaryngology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|ear_disorder	true	false	false	true	high
MONDO:0013936	peroxisome biogenesis disorder 6A (Zellweger)	hereditary_disease|metabolic_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease	neurology|hepatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisomal_disorder	false	false	false	false	very_high
MONDO:0013937	peroxisome biogenesis disorder 6B	hereditary_disease|metabolic_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisomal_disorder	false	false	false	false	high
MONDO:0013938	peroxisome biogenesis disorder 7A (Zellweger)	hereditary_disease|metabolic_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease	hepatology|pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisomal_disorder	false	false	false	false	very_high
MONDO:0013939	peroxisome biogenesis disorder 7B	hereditary_disease|metabolic_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisomal_disorder	false	false	false	false	high
MONDO:0013940	primary ciliary dyskinesia 18	hereditary_disease|respiratory_system_disorder|syndromic_disease	other	syndromic_disease|respiratory_system_disorder|hereditary_disease	neurology|pulmonology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|kidney_disorder|brain_disorder|bone_disorder	false	false	false	false	high
MONDO:0013941	metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	renal_medicine|orthopaedic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|kidney_disorder|bone_disorder	false	false	false	false	high
MONDO:0013942	peroxisome biogenesis disorder 8A (Zellweger)	hereditary_disease|metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	metabolic_disease|neurodegenerative_disease	syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	neurology|hepatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisomal_disorder	false	false	false	false	very_high
MONDO:0013943	peroxisome biogenesis disorder 8B	hereditary_disease|metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	metabolic_disease|neurodegenerative_disease	syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisome_biogenesis_disorder_is_also_related_to_brain_disorder_but_liver_disorder_seems_more_direct	false	false	false	false	very_high
MONDO:0013944	autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation	hereditary_disease|connective_tissue_disorder|syndromic_disease	other	connective_tissue_disorder|syndromic_disease|hereditary_disease	rheumatology|genetics_and_genomics|allergy_and_immunology|pediatric	inflammatory_disease|autoimmune_diseases|immune_dysregulation	immune_disorder|immune_dysregulation	false	false	false	true	high
MONDO:0013945	peroxisome biogenesis disorder 9B	hereditary_disease|metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	metabolic_disease|neurodegenerative_disease	syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	peroxisome_biogenesis_disorders|liver_disorder	false	false	false	false	high
MONDO:0013946	hypogonadotropic hypogonadism 15 with or without anosmia	hereditary_disease|endocrine_system_disorder|syndromic_disease|reproductive_system_disorder	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	neurology|genetics_and_genomics|endocrinology|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0013947	neuronopathy, distal hereditary motor, autosomal recessive 5	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013948	peroxisome biogenesis disorder 10A (Zellweger)	hereditary_disease|metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	metabolic_disease|neurodegenerative_disease	syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	hepatology|pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisome_biosynthesis_disorder	false	false	false	false	very_high
MONDO:0013949	peroxisome biogenesis disorder 11A (Zellweger)	hereditary_disease|metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	metabolic_disease|neurodegenerative_disease	syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	hepatology|pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisomal_disorder	false	false	false	false	very_high
MONDO:0013950	peroxisome biogenesis disorder 11B	metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	metabolic_disease|neurodegenerative_disease	syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|cellular_disorder|peroxisomal_disorder	false	false	false	false	high
MONDO:0013951	peroxisome biogenesis disorder 12A (Zellweger)	metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	metabolic_disease|neurodegenerative_disease	syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	neurology|hepatology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisomal_disorder	false	false	false	false	very_high
MONDO:0013952	peroxisome biogenesis disorder 13A (Zellweger)	metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	metabolic_disease|neurodegenerative_disease	syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	neurology|hepatology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisome_biogenesis_disorder_13a__zellweger__also_affects_the_brain_and_can_be_associated_with_other_organ_systems__but_liver_disorder_is_a_primary_category_for_this_condition	false	false	false	false	very_high
MONDO:0013953	immunodeficiency 28	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	immunology|pediatrics|genetics_and_genomics|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|immunodeficiency	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0013959	Charcot-Marie-Tooth disease type 4F	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013960	sinoatrial node dysfunction and deafness	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|otolaryngology|pulmonology	cardiovascular_disorder|neurodegenerative_disease	ear_disorder|heart_disorder	false	false	false	false	high
MONDO:0013961	hypogonadotropic hypogonadism 16 with or without anosmia	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	neurology|endocrinology|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0013962	hereditary spastic paraplegia 53	hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|hereditary	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013963	autosomal recessive nonsyndromic hearing loss 93	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder|hereditary_disease	otolaryngology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder|bone_disorder	false	false	false	false	medium
MONDO:0013964	Diamond-Blackfan anemia 11	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics|pediatric	anemia|metabolic_disorder	lung_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0013965	lethal congenital contracture syndrome 4	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	joint_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0013966	catecholaminergic polymorphic ventricular tachycardia 4	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|cardiothoracic|pediatric	cardiovascular_disorder|adrenal_gland_disease	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0013967	peroxisome biogenesis disorder 14B	hereditary_disease|metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	metabolic_disease|neurodegenerative_disease	syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisomal_disease	false	false	false	false	very_high
MONDO:0013968	PGM1-congenital disorder of glycosylation	hereditary_disease|metabolic_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder|metabolic_disease	hereditary_disease|metabolic_disease|cardiovascular_disorder|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	congenital_disorder_of_glycosylation|neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	false	high
MONDO:0013969	combined oxidative phosphorylation defect type 11	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolism|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013970	branched-chain keto acid dehydrogenase kinase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	kidney_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0013971	leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome	hereditary_disease|metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease	metabolic_disease|neurodegenerative_disease	mitochondrial_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	neurology|hematology|genetics_and_genomics|pediatric	neurodegenerative_disease|leucoencephalopathy_thalamus_and_brainstem_anomalies_is_a_neurological_condition__therefore_neurodegenerative_disease_is_correct___metabolic_disorder_may_be_related_to_high_lactate_syndrome|metabolic_disorder|high_lactate_syndrome_is_not_in_the_list_so_removing_it|leaving_just_two_categories	brainstem_disorder|brain_disorder|blood_bone_marrow_disorder	true	false	false	true	very_high
MONDO:0013972	Perrault syndrome 2	hereditary_disease|endocrine_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|reproductive_system_disorder|mitochondrial_disease	metabolic_disease|endocrine_system_disorder	mitochondrial_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|reproductive_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013973	ectodermal dysplasia 5, hair/nail type	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	dermatology|pediatrics|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	teeth_disorder|skin_disorder	false	false	false	false	low
MONDO:0013974	ectodermal dysplasia 6, hair/nail type	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	hair_disorder|teeth_disorder|skin_disorder|nail_disorder	false	false	false	false	medium
MONDO:0013975	ectodermal dysplasia 7, hair/nail type	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	neurodegenerative_disease|genetic_disorder|metabolic_disorder	teeth_disorder|skin_disorder|hair_nail_type	false	false	false	false	medium
MONDO:0013976	ectodermal dysplasia 9, hair/nail type	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	dermatology|psychiatry|genetics_and_genomics|pediatric	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases|metabolic_disorder	teeth_disorder|skin_disorder|nail_disorder	false	false	false	false	medium
MONDO:0013977	combined oxidative phosphorylation defect type 13	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|endocrinology|pediatric	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	liver_disorder|mitochondrial_disorder	false	false	false	false	high
MONDO:0013978	autosomal recessive nonsyndromic hearing loss 70	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder|hereditary_disease	otolaryngology|genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	ear_disorder	false	false	false	true	medium
MONDO:0013979	primary ciliary dyskinesia 19	hereditary_disease|respiratory_system_disorder|syndromic_disease	other	syndromic_disease|respiratory_system_disorder|hereditary_disease	neurology|pulmonology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder|joint_disorder|brain_disorder|kidney_disorder|muscle_disorder	false	false	false	false	high
MONDO:0013980	palmoplantar keratoderma, punctate type ib	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder|genetic_disorder	false	false	false	true	medium
MONDO:0013981	myoclonus, familial	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	familial_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0013982	ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant	syndromic_disease|integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	skin_disorder|hair_disorder|endocrine_disorder|bone_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0013983	ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive	syndromic_disease|integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	skin_disorder|eye_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0013984	autosomal recessive nonsyndromic hearing loss 84B	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	otorhinolaryngology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0013985	autosomal recessive nonsyndromic hearing loss 18B	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	autosomal_recessive_diseases|hearing_loss_diseases|metabolic_disorder	autosomal_recessive_nonsyndromic_hearing_loss|ear_disorder	false	false	false	true	high
MONDO:0013986	combined oxidative phosphorylation defect type 14	metabolic_disease|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|liver_disorder|genetic_disorder	false	false	false	false	very_high
MONDO:0013987	combined oxidative phosphorylation defect type 15	metabolic_disease|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	liver_disorder	false	false	false	false	very_high
MONDO:0013988	congenital heart defects, multiple types, 3	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	pediatric|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0013989	developmental and epileptic encephalopathy, 14	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	epilepsy|encephalopathy|developmental_disorder|neurodegenerative_disease	brain_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0013990	pontocerebellar hypoplasia type 8	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013991	obesity due to congenital leptin deficiency	nutritional_disorder|reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	nutritional_disorder|reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|endocrinology	cardiovascular_disorder|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	true	true	very_high
MONDO:0013992	obesity due to leptin receptor gene deficiency	nutritional_disorder|reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	nutritional_disorder|reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|endocrinology	cardiovascular_disorder|metabolic_disorder	endocrine_disorder	false	false	false	true	high
MONDO:0013993	pontocerebellar hypoplasia type 7	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0013994	Joubert syndrome 20	syndromic_disease|nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis	neurodegenerative_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|disorder_of_visual_system|syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|anemia	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0013995	cholestasis, intrahepatic, of pregnancy, 3	digestive_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|endocrine_system_disorder|metabolic_disease|hereditary_disease	hepatology|obstetrics_and_gynecology|gastroenterology	inflammatory_disease|metabolic_disorder	biliary_disorder|liver_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0013996	focal facial dermal dysplasia type II	syndromic_disease|integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0013997	focal facial dermal dysplasia type IV	syndromic_disease|integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder	false	false	false	false	low
MONDO:0013998	MEGF8-related Carpenter syndrome	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	skin_disorder|muscle_disorder|bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0013999	retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis, and migraine headache syndrome	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	neurology|genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0014000	congenital heart defects, multiple types, 2	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	pediatric|cardiology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0014001	Usher syndrome type 1K	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|deaf_blindness|genetic_disease|eye_disorder|inherited_condition	brain_disorder|eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0014002	autosomal dominant nocturnal frontal lobe epilepsy 5	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|epileptic_diseases|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014003	developmental and epileptic encephalopathy, 15	syndromic_disease|nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|developmental_disorder|epileptic_disorder	developmental_disorder|brain_disorder|encephalopathy|epileptic_disorder	false	false	false	true	very_high
MONDO:0014004	basal ganglia calcification, idiopathic, 4	nervous_system_disorder|hereditary_disease	other	idiopathic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	vascular_disorder|brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014005	immunoglobulin-mediated membranoproliferative glomerulonephritis	inflammatory_disease|syndromic_disease|hereditary_disease|urinary_system_disorder	other	inflammatory_disease|urinary_system_disorder|hereditary_disease|syndromic_disease	rheumatology|allergy_and_immunology|renal_medicine|hematology	autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder	false	false	false	true	high
MONDO:0014006	Schuurs-Hoeijmakers syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	disorder_of_development_or_morphogenesis|psychiatric_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease	dermatology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|liver_disorder	false	false	false	false	high
MONDO:0014007	Aicardi-Goutieres syndrome 6	syndromic_disease|nervous_system_disorder|immune_system_disorder|hereditary_disease|connective_tissue_disorder	neurodegenerative_disease	immune_system_disorder|hereditary_disease|connective_tissue_disorder|nervous_system_disorder|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|brain_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0014008	phosphohydroxylysinuria	hereditary_disease	other	hereditary_disease	renal_medicine|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0014009	autosomal recessive congenital ichthyosis 7	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	skin_condition|metabolic_disorder	liver_disorder|skin_disorder	false	false	false	false	medium
MONDO:0014010	autosomal recessive congenital ichthyosis 9	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	skin_condition|metabolic_disorder	other___corrected_answer__skin_disorder|skin_disorder	false	false	false	false	medium
MONDO:0014011	autosomal recessive congenital ichthyosis 10	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	congenital_ichthyosis|metabolic_disorder	reproductive_system_disorder|skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0014012	Charcot-Marie-Tooth disease axonal type 2Q	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|autoimmune_diseases|cardiovascular_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014013	maternal riboflavin deficiency	hereditary_disease|metabolic_disease|nutritional_disorder	metabolic_disease	nutritional_disorder|hereditary_disease|metabolic_disease	pediatrics|obstetrics_and_gynecology|nutrition	metabolic_disorder|anemia	upper_gastrointestinal_disorder|reproductive_system_disorder|liver_disorder	false	false	false	true	low
MONDO:0014014	epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	pediatric|dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0014015	hereditary spastic paraplegia 56	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|hereditary_disease_is_not_in_the_list_so_using_the_closest_match___neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014016	hereditary spastic paraplegia 49	syndromic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014018	hereditary spastic paraplegia 54	syndromic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014019	dystonia 24	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0014020	hereditary spastic paraplegia 55	disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder|mitochondrial_disease|hereditary_disease|metabolic_disease	neurodegenerative_disease|metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|nervous_system_disorder|syndromic_disease|metabolic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|hereditary_disorder|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014021	familial episodic pain syndrome with predominantly upper body involvement	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	rheumatology|neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014022	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	pediatric|neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014023	congenital muscular dystrophy with intellectual disability and severe epilepsy	nervous_system_disorder|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease|musculoskeletal_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014024	hereditary spastic paraplegia 43	syndromic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014025	lower motor neuron syndrome with late-adult onset	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014026	congenital stationary night blindness 1F	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	pediatric|genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0014027	hypotrichosis 11	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	pediatric|dermatology|genetics_and_genomics	genetic_disorder|metabolic_disorder	skin_disorder|hair_disorder_is_not_in_the_list_but_it_s_relevant_so_muscle_disorder	false	false	false	true	low
MONDO:0014028	distal arthrogryposis type 5D	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics|orthopaedic	metabolic_disorder|neurodegenerative_disease	muscledisorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0014029	osteogenesis imperfecta type 14	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	rheumatology|pediatric|genetics_and_genomics|orthopaedic	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014030	primary ciliary dyskinesia 20	syndromic_disease|hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|eye_disorder|ear_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014031	microcephalic primordial dwarfism, Alazami type	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	skeletal_abnormality|brain_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0014032	brachydactyly type A1C	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic	neurodegenerative_disease|genetic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0014033	dystonia 25	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014034	severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	disorder_of_development_or_morphogenesis|psychiatric_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|eye_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014035	severe intellectual disability-progressive spastic diplegia syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	disorder_of_development_or_morphogenesis|psychiatric_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|severe_intellectual_disability_progressive_spastic_diplegia_syndrome_does_not_match_any_category_in_the_list__so_neurodegenerative_disease_is_chosen_by_exclusion	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014036	Alzheimer disease 17	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatry|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	very_high
MONDO:0014037	spermatogenic failure 11	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	inflammatory_disease|autoimmune_diseases|cancer|anemia|metabolic_disorder	reproductive_system_disorder	false	false	false	false	high
MONDO:0014038	colorectal cancer, susceptibility to, 12	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	oncology|genetics_and_genomics|gastroenterology	autoimmune_diseases|cancer|metabolic_disorder	lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0014039	mitochondrial DNA depletion syndrome 11	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	lymphatic_disorder|muscle_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0014040	autosomal recessive osteopetrosis 8	musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	pediatric|rheumatology|genetics_and_genomics|orthopaedic	genetic_disease____note__i_corrected_the_disease_name_to_its_more_commonly_used_term__genetic_disease|metabolic_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0014042	left ventricular noncompaction 7	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	cardiothoracic|pediatric|pulmonology|cardiology|renal_medicine	cardiovascular_disorder|cardiac_disease	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0014043	microcephalic primordial dwarfism due to ZNF335 deficiency	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	growth_disorder|bone_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014044	dysmorphism-conductive hearing loss-heart defect syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|cardiology|genetics_and_genomics|otolaryngology	heart_defect_syndrome|cardiovascular_disorder	heart_disorder|ear_disorder	false	false	false	false	high
MONDO:0014045	Cowden syndrome 3	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	oncology|genetics_and_genomics	autoimmune_diseases|cancer|neurodegenerative_disease	reproductive_system_disorder|eye_disorder|brain_disorder|thyroid_endocrine_disorder__not_in_list_so_using_endocrine_disorder|skin_disorder	false	false	false	true	high
MONDO:0014046	Cowden syndrome 4	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|neurology|oncology|genetics_and_genomics	genetic_disorder_is_not_in_the_list_so_i_will_remove_it_and_leave_the_answer_as_cancer|cancer	other____note__cowden_syndrome_is_a_genetic_disorder_characterized_by_multiple_skin_growths_called_trichilemmomas_and_other_symptoms|skin_disorder	false	false	false	false	high
MONDO:0014047	Cowden syndrome 5	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	oncology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder|metabolic_disorder|cancer|neurodegenerative_disease	lymphatic_disorder|eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0014048	Cowden syndrome 6	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|neurology|oncology|genetics_and_genomics	autoimmune_diseases|cancer	lymphatic_disorder|eye_disorder|brain_disorder|skin_disorder	false	false	false	false	high
MONDO:0014049	urofacial syndrome 2	hereditary_disease	other	hereditary_disease	genetics_and_genomics|urology	adrenal_gland_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0014050	isolated microphthalmia 8	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0014051	cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|metabolic_disease	musculoskeletal_system_disorder|metabolic_disease|cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	cardiology|genetics_and_genomics|pediatrics	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	heart_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014052	congenital myasthenic syndrome 8	nervous_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014054	lymphoproliferative syndrome 2	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	oncology|hematology	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0014055	epilepsy, familial adult myoclonic, 4	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|mental_health_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0014056	melanoma, cutaneous malignant, susceptibility to, 9	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	dermatology|oncology|genetics_and_genomics	cancer|cutaneous_malignant	cutaneous_malignant|skin_disorder	false	true	false	true	high
MONDO:0014057	maple syrup urine disease, mild variant	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|renal_medicine	metabolic_disorder|adrenal_gland_disease	kidney_disorder|upper_gastrointestinal_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0014058	facial dysmorphism-immunodeficiency-livedo-short stature syndrome	hereditary_disease	other	hereditary_disease	dermatology|pediatric|immunology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|bone_disorder|skin_disorder	false	false	false	false	high
MONDO:0014059	microphthalmia, isolated, with coloboma 9	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|genetics_and_genomics|ophthalmology	genetic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0014060	progressive retinal dystrophy due to retinol transport defect	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	pediatric|genetics_and_genomics|ophthalmology	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	retina_disorder|eye_disorder	false	false	false	false	high
MONDO:0014061	Steel syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0014062	mitochondrial DNA deletion syndrome with progressive myopathy	disorder_of_development_or_morphogenesis|nervous_system_disorder|mitochondrial_disease|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	very_high
MONDO:0014063	mitochondrial complex III deficiency nuclear type 2	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	neurology|genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	other____note__the_category__other__is_included_because_the_provided_disease_name_does_not_fit_neatly_into_any_of_the_more_specific_categories_listed__suggesting_a_broader_classification_may_be_necessary|muscle_disorder	false	false	false	false	high
MONDO:0014064	mitochondrial complex III deficiency nuclear type 3	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	neurology|genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	mitochondrial_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014065	mitochondrial complex III deficiency nuclear type 4	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	pediatric|neurology|hepatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0014066	mitochondrial complex III deficiency nuclear type 5	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	genetics_and_genomics|pediatrics	anemia|metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0014067	short ulna-dysmorphism-hypotonia-intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|intellectual_disability|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014068	cone-rod dystrophy 17	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014069	syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	congenital_abnormality|genetic_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0014070	oculocutaneous albinism type 7	hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|ophthalmology	genetic_disorder|metabolic_disorder	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0014071	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014072	D,L-2-hydroxyglutaric aciduria	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0014073	dilated cardiomyopathy 1II	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014074	Charcot-Marie-Tooth disease dominant intermediate F	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014075	cataract 39 multiple types	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0014076	dyskeratosis congenita, autosomal recessive 5	syndromic_disease|hereditary_disease|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|hereditary_disease|syndromic_disease|cancer_or_benign_tumor	pediatric|oncology|dermatology|genetics_and_genomics|hematology	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|skin_disorder	false	false	false	true	high
MONDO:0014077	cobblestone lissencephaly without muscular or ocular involvement	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014078	platelet-type bleeding disorder 15	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	pediatric|genetics_and_genomics|hematology	bleeding_disorder|anemia|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0014080	osteosclerotic metaphyseal dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	genetic_disorder|bone_dysplasia|metabolic_disorder	bone_bone_marrow_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0014081	severe combined immunodeficiency due to CARD11 deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	immunology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	very_high
MONDO:0014082	cryptosporidiosis-chronic cholangitis-liver disease syndrome	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease|liver_disease	liver_disorder|immune_disorder|upper_gastrointestinal_disorder	true	false	false	false	high
MONDO:0014083	agammaglobulinemia 7, autosomal recessive	immune_system_disorder|hereditary_disease|hematologic_disorder	other	immune_system_disorder|hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|autoimmune_diseases|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0014084	ataxia with oculomotor apraxia type 3	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014085	hydrocephalus, nonsyndromic, autosomal recessive 2	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014086	osteogenesis imperfecta type 15	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	genetic_disorder|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0014087	Smith-McCort dysplasia 2	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0014088	advanced sleep phase syndrome 2	hereditary_disease	other	sleep_disorder|hereditary_disease	neurology|endocrinology	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	endocrine_disorder_brain_disorder	false	false	false	false	medium
MONDO:0014089	corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|disorder_of_development_or_morphogenesis	otolaryngology|ophthalmology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|cancer	eye_disorder|skin_disorder|throat_disorder	false	false	false	false	high
MONDO:0014090	polydactyly, postaxial, type A6	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	genetic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0014091	mitochondrial complex V (ATP synthase) deficiency, nuclear type 4B	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|mitochondrial_complex_v__atp_synthase__deficiency_nuclear_type_4b_also_falls_under__muscle_disorder	false	false	false	false	high
MONDO:0014093	retinitis pigmentosa 66	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	disorder_of_orbital_region|nervous_system_disorder|metabolic_disease|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	genetics_and_genomics|ophthalmology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0014094	severe congenital hypochromic anemia with ringed sideroblasts	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	other_is_incorrect_due_to_multiple_selections|anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0014095	dilated cardiomyopathy 1JJ	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0014096	microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	intellectual_disability|neurological_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0014097	congenital short bowel syndrome	disorder_of_development_or_morphogenesis|digestive_system_disorder	other	disorder_of_development_or_morphogenesis|digestive_system_disorder	genetics_and_genomics|gastroenterology|pediatric	congenital_disorder|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0014098	CIDEC-related familial partial lipodystrophy	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|dermatology	lipodystrophy|metabolic_disorder	endocrine_disorder|skin_disorder	false	false	false	false	medium
MONDO:0014099	nephrotic syndrome, type 8	hereditary_disease|urinary_system_disorder|syndromic_disease	other	idiopathic_disease|urinary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|renal_medicine|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder	immune_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0014100	dilated cardiomyopathy 1KK	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiology|cardiothoracic	inflammatory_disease|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0014101	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014102	hypogonadotropic hypogonadism 17 with or without anosmia	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|syndromic_disease	endocrine_system_disorder	hereditary_disease|syndromic_disease|endocrine_system_disorder|reproductive_system_disorder	genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|neurodegenerative_disease|endocrine_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0014103	hypogonadotropic hypogonadism 18 with or without anosmia	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|syndromic_disease	endocrine_system_disorder	hereditary_disease|syndromic_disease|endocrine_system_disorder|reproductive_system_disorder	genetics_and_genomics|endocrinology	metabolic_disorder|neurodegenerative_disease	nose_disorder|reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0014104	cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 4	nervous_system_disorder|hereditary_disease|syndromic_disease	neurodegenerative_disease	hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	true	false	false	false	high
MONDO:0014105	hypogonadotropic hypogonadism 19 with or without anosmia	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|syndromic_disease	endocrine_system_disorder	hereditary_disease|syndromic_disease|endocrine_system_disorder|reproductive_system_disorder	genetics_and_genomics|pediatric|neurology|endocrinology	genetic_disorder|neurodegenerative_disease|endocrine_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0014106	hypogonadotropic hypogonadism 20 with or without anosmia	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|syndromic_disease	endocrine_system_disorder	hereditary_disease|syndromic_disease|endocrine_system_disorder|reproductive_system_disorder	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0014107	hypogonadotropic hypogonadism 21 with or without anosmia	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|syndromic_disease	endocrine_system_disorder	hereditary_disease|syndromic_disease|endocrine_system_disorder|reproductive_system_disorder	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0014108	Fanconi anemia complementation group Q	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hematologic_disorder|metabolic_disease|hereditary_disease|immune_system_disorder	anemia|metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hematologic_disorder|immune_system_disorder|metabolic_disease	genetics_and_genomics|pediatric|oncology|hematology	inflammatory_disease|anemia|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0014110	cataract 15 multiple types	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0014111	cataract 19 multiple types	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology	cataract_19_multiple_types_does_not_clearly_fit_into_any_of_the_provided_categories_so_it_is_left_out|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0014112	cardiofaciocutaneous syndrome 2	musculoskeletal_system_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	musculoskeletal_system_disorder|syndromic_disease|cardiovascular_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|cardiology|dermatology	autoimmune_diseases|inflammatory_disease|allergy|cardiovascular_disorder	vascular_disorder|heart_disorder|skin_disorder	false	false	false	false	high
MONDO:0014113	cardiofaciocutaneous syndrome 3	musculoskeletal_system_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	musculoskeletal_system_disorder|syndromic_disease|cardiovascular_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|cardiology|dermatology	autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder|skin_disorder	false	false	false	false	high
MONDO:0014114	cardiofaciocutaneous syndrome 4	musculoskeletal_system_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	musculoskeletal_system_disorder|syndromic_disease|cardiovascular_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatrics|cardiology|dermatology	autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder|skin_disorder	false	false	false	false	high
MONDO:0014115	hypomyelination with brain stem and spinal cord involvement and leg spasticity	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014116	complex cortical dysplasia with other brain malformations 2	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014117	Charcot-Marie-Tooth disease type 4B3	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	hereditary_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014118	congenital neutropenia-myelofibrosis-nephromegaly syndrome	hematologic_disorder|hereditary_disease|immune_system_disorder	other	hematologic_disorder|immune_system_disorder|hereditary_disease	pediatric|renal_medicine|genetics_and_genomics|hematology	anemia|metabolic_disorder|cancer	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0014119	intellectual disability-strabismus syndrome	disorder_of_visual_system|hereditary_disease|syndromic_disease	other	syndromic_disease|disorder_of_visual_system|hereditary_disease	genetics_and_genomics|neurology|pediatrics|ophthalmology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0014120	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014121	autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014122	myofibromatosis, infantile, 2	musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hereditary_disease	pediatric|genetics_and_genomics|oncology	metabolic_disorder|cancer|neurodegenerative_disease	bone_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014123	primary ciliary dyskinesia 21	respiratory_system_disorder|hereditary_disease|syndromic_disease	other	respiratory_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pulmonology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0014124	Adams-Oliver syndrome 4	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|skeletal_disorder	false	false	false	false	medium
MONDO:0014125	symphalangism, proximal, 1B	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0014126	Perrault syndrome 4	disorder_of_development_or_morphogenesis|mitochondrial_disease|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|metabolic_disease	endocrine_system_disorder|metabolic_disease	reproductive_system_disorder|mitochondrial_disease|endocrine_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0014127	oculocutaneous albinism type 5	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	dermatology|genetics_and_genomics|pediatric|ophthalmology	genetic_disorder|metabolic_disorder	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0014128	TCF12-related craniosynostosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics|pediatric	skeletal_disease|developmental_disorder|craniofacial_abnormality|neurodevelopmental_disorder	bone_disorder|craniosynostosis	false	false	false	false	medium
MONDO:0014130	Dowling-Degos disease 2	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	dermatology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	low
MONDO:0014131	hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	teeth_disorder|skin_disorder|intellectual_disability_syndrome_is_not_in_the_list_so_it_will_be_ignored	false	false	false	false	high
MONDO:0014132	multiple mitochondrial dysfunctions syndrome 3	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	metabolic_disease	mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_dysfunction|brain_disorder	false	false	false	false	very_high
MONDO:0014133	developmental and epileptic encephalopathy, 16	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	epileptic_encephalopathy|developmental_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0014134	pulmonary hypertension, primary, 2	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	pulmonology|cardiology	cardiovascular_disorder|inflammatory_disease	vascular_disorder|lung_disorder	false	false	false	true	high
MONDO:0014135	pulmonary hypertension, primary, 3	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	pulmonology|cardiology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	vascular_disorder|lung_disorder	false	false	false	true	high
MONDO:0014136	pulmonary hypertension, primary, 4	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	pulmonology|cardiothoracic|cardiology	primary___cardiovascular_disorder|cardiovascular_disorder	vascular_disorder|lung_disorder	false	false	false	true	high
MONDO:0014137	precocious puberty, central, 2	disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	endocrinology|pediatric	central|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0014138	nemaline myopathy 8	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014139	Ehlers-Danlos syndrome, spondylodysplastic type, 2	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|genetics_and_genomics|orthopaedic	genetic_disorder|connective_tissue_disorder|metabolic_disorder	bone_disorder|vascular_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014140	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14	nervous_system_disorder|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0014141	muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14	nervous_system_disorder|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014142	autosomal recessive limb-girdle muscular dystrophy type 2T	nervous_system_disorder|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics|orthopaedic	muscular_dystrophy|neurodegenerative_disease	muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0014143	Noonan syndrome 8	syndromic_disease|disorder_of_development_or_morphogenesis|immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|immune_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	endocrinology|pediatric|genetics_and_genomics|cardiology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	heart_disorder|joint_disorder	false	false	false	false	medium
MONDO:0014144	autosomal recessive limb-girdle muscular dystrophy type R18	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0014145	Leber congenital amaurosis 17	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|psychiatric_disorder|hereditary_disease	pediatric|genetics_and_genomics|ophthalmology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0014146	autosomal dominant hypocalcemia 2	endocrine_system_disorder|hereditary_disease|metabolic_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease|hereditary_disease	endocrinology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0014147	neuronal ceroid lipofuscinosis 13	psychiatric_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014148	estrogen resistance syndrome	syndromic_disease|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|syndromic_disease	endocrinology|obstetrics_and_gynecology	autoimmune_diseases|cancer|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0014149	fetal akinesia-cerebral and retinal hemorrhage syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric|ophthalmology|obstetrics_and_gynecology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0014150	developmental and epileptic encephalopathy 94	syndromic_disease|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics|pediatric	epileptic_disorder|inflammatory_disease|developmental_disorder|neurodegenerative_disease	neurological_disorder|epileptic_disorder|brain_disorder|encephalopathy|developmental_disorder	false	false	false	false	very_high
MONDO:0014152	left ventricular noncompaction 8	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease|syndromic_disease	pulmonology|cardiothoracic|cardiology|renal_medicine|hematology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0014153	cone-rod dystrophy 18	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease	genetics_and_genomics|ophthalmology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014154	Charcot-Marie-Tooth disease recessive intermediate C	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014155	atrial fibrillation, familial, 13	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	genetics_and_genomics|cardiology	cardiovascular_disorder|familial	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0014156	atrial fibrillation, familial, 14	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	pulmonology|genetics_and_genomics|cardiology|hematology	cardiovascular_disorder|familial	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0014157	mandibular hypoplasia-deafness-progeroid syndrome	disorder_of_development_or_morphogenesis|premature_aging_syndrome|hereditary_disease	other	disorder_of_development_or_morphogenesis|premature_aging_syndrome|hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	teeth_disorder|bone_disorder|ear_disorder	false	false	false	false	high
MONDO:0014158	nephronophthisis 16	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	renal_medicine|nephrology	kidney_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0014159	autosomal recessive spinocerebellar ataxia 14	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder_spinal_disorder_brain_disorder	false	false	false	false	very_high
MONDO:0014160	TCR-alpha-beta-positive T-cell deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	immunology|pediatric|genetics_and_genomics|allergy_and_immunology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder_lymphatic_disorder	false	false	false	false	high
MONDO:0014161	vesicoureteral reflux 7	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	urology|renal_medicine	kidney_problem|genital_problem|pediatric_condition|congenital_abnormality|inflammatory_disease|urinary_system_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0014162	infantile hypertrophic cardiomyopathy due to MRPL44 deficiency	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	metabolic_disease	mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0014163	left ventricular noncompaction 10	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease|syndromic_disease	cardiovascular____i_assume__noncompaction__is_a_type_of_heart_disease|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0014164	Meckel syndrome, type 11	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder	lower_gastrointestinal_disorder|liver_disorder|biliary_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014165	multiple congenital anomalies-hypotonia-seizures syndrome 3	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014166	paroxysmal nocturnal hemoglobinuria 2	hematologic_disorder|urinary_system_disorder|metabolic_disease	anemia|metabolic_disease	hematologic_disorder|urinary_system_disorder|metabolic_disease	pediatric|genetics_and_genomics|renal_medicine|hematology	anemia|metabolic_disorder	kidney_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0014167	epilepsy, familial adult myoclonic, 5	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|mental_health_disorder|inflammatory_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0014168	severe combined immunodeficiency due to CORO1A deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	immunology|pediatric|genetics_and_genomics|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0014169	dyschromatosis universalis hereditaria 3	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|skin_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0014170	complex cortical dysplasia with other brain malformations 3	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0014171	complex cortical dysplasia with other brain malformations 4	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	neurodegenerative_disease	brain_disorder	false	false	false	false	very_high
MONDO:0014172	spermatogenic failure 12	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	autoimmune_diseases|metabolic_disorder|anemia	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0014173	microcephaly 11, primary, autosomal recessive	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	autosomal_recessive|metabolic_disorder|neurodegenerative_disease	brain_disorder|other___note__microcephaly_is_a_disorder_of_the_brain__but_it_doesn_t_exactly_fit_into_one_of_the_provided_categories__however__since_the_primary_symptom_involves_the_brain__that_s_the_closest_match__the__other__category_is_included_because_microcephaly_doesn_t_neatly_fit_into_any_single_specific_medical_specialty_or_system	false	false	false	false	high
MONDO:0014174	renal-hepatic-pancreatic dysplasia 2	hereditary_disease	other	hereditary_disease	hepatology|gastroenterology|renal_medicine	renal_hepatic_pancreatic_dysplasia|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014175	mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	mitochondrial_disease|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0014176	hypotonia, infantile, with psychomotor retardation and characteristic facies	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|endocrine_disorder|muscle_disorder	true	false	false	false	very_high
MONDO:0014177	myopia 22, autosomal dominant	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	true	medium
MONDO:0014178	inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2	syndromic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurodegenerative_disease|psychiatric_disorder	syndromic_disease|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease|psychiatric_disorder	neurology|psychiatry|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|bone_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014179	inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3	syndromic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurodegenerative_disease|psychiatric_disorder	syndromic_disease|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease|psychiatric_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|bone_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014180	epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	pediatric|dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|vascular_disorder|skin_disorder	false	false	false	false	high
MONDO:0014181	amyotrophic lateral sclerosis type 20	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014182	autosomal recessive nonsyndromic hearing loss 88	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|hereditary_disease|psychiatric_disorder	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0014183	myopia 23, autosomal recessive	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0014184	specific language impairment 5	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014185	chromosome 3q13.31 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease	developmental_disorder|brain_disorder|developmental_disorder___corrected_list__brain_disorder	false	false	false	false	high
MONDO:0014186	retinitis pigmentosa with or without situs inversus	psychiatric_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system	metabolic_disease|psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|vascular_disorder	false	false	false	false	high
MONDO:0014187	aortic aneurysm, familial thoracic 8	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	hematology|genetics_and_genomics|pulmonology|cardiology|cardiothoracic	cardiovascular_disorder|familial__or_other_is_not_correct_since_it_was_listed_last_in_the_category_list	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0014190	combined oxidative phosphorylation defect type 17	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	mitochondrial_disease|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatrics|genetics_and_genomics|metabolism	genetic_disorder|metabolic_disorder	liver_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0014191	catecholaminergic polymorphic ventricular tachycardia 5	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	hematology|genetics_and_genomics|pulmonology|cardiology	cardiovascular_disorder|adrenal_gland_disease	heart_disorder|vascular_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014192	primary ciliary dyskinesia 22	syndromic_disease|respiratory_system_disorder|hereditary_disease	other	syndromic_disease|respiratory_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder|spinal_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014193	primary ciliary dyskinesia 23	syndromic_disease|respiratory_system_disorder|hereditary_disease	other	syndromic_disease|respiratory_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder|joint_disorder|spinal_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014194	mitochondrial complex III deficiency nuclear type 6	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	mitochondrial_disease|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0014195	microcornea-myopic chorioretinal atrophy	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|cancer|inflammatory_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014196	Hartsfield-Bixler-Demyer syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	bone_disorder|blood_bone_marrow_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014197	combined immunodeficiency due to MALT1 deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	pediatrics|genetics_and_genomics|allergy_and_immunology	autoimmune_diseases|anemia|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0014198	mitochondrial DNA depletion syndrome 13	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	mitochondrial_disease|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|anemia|metabolic_disorder	mucolipidosis_iii|blood_bone_marrow_disorder|mitochondrial_disorder___corrected_answer__mitochondrial_disorder	false	false	false	false	very_high
MONDO:0014199	developmental and epileptic encephalopathy, 17	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	developmental_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0014200	aldosterone-producing adenoma with seizures and neurological abnormalities	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	renal_medicine|endocrinology|neurology	adrenal_gland_disease|metabolic_disorder	brain_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0014201	developmental and epileptic encephalopathy, 18	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	developmental_disorder|neurodegenerative_disease	brain_disorder|epileptic_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0014202	primary ciliary dyskinesia 24	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	hereditary_disease|respiratory_system_disorder|syndromic_disease	pulmonology|genetics_and_genomics|neurology	neurodegenerative_disease	spinal_disorder|brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014203	primary ciliary dyskinesia 25	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	hereditary_disease|respiratory_system_disorder|syndromic_disease	pulmonology|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder|spinal_disorder|brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014204	basal ganglia calcification, idiopathic, 5	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|idiopathic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0014205	severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder_microcephaly	false	false	false	false	very_high
MONDO:0014206	severe early-onset pulmonary alveolar proteinosis due to MARS deficiency	hereditary_disease|respiratory_system_disorder	other	hereditary_disease|respiratory_system_disorder	pulmonology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	immune_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0014207	age related macular degeneration 14	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	ophthalmology|neurology	mental_health_disorder|neurodegenerative_disease	eye_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0014208	Charcot-Marie-Tooth disease type 2R	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder|peripheral_nerve_disorder	false	false	false	false	medium
MONDO:0014209	early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|spasticity_syndrome|ataxia	muscle_disorder|eye_disorder|spinal_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0014210	intellectual disability-hypotonia-spasticity-sleep disorder syndrome	hereditary_disease|syndromic_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|syndromic_disease|psychiatric_disorder	genetics_and_genomics|neurology	intellectual_disability|spasticity|neurodegenerative_disease|sleep_disorder|hypotonia|metabolic_disorder	sleep_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014211	primary ciliary dyskinesia 26	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	hereditary_disease|respiratory_system_disorder|syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0014212	sulfite oxidase deficiency due to molybdenum cofactor deficiency type C	hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	liver_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014213	intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|syndromic_disease|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|developmental_delay|metabolic_disorder	brain_disorder|microcephaly_syndrome|developmental_delay	true	false	false	false	high
MONDO:0014214	short-rib thoracic dysplasia 8 with or without polydactyly	hereditary_disease|syndromic_disease|urinary_system_disorder|musculoskeletal_system_disorder|respiratory_system_disorder	other	urinary_system_disorder|hereditary_disease|respiratory_system_disorder|syndromic_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	genetic_disease|metabolic_disorder	bone_disorder|skeletal_system_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0014215	primary ciliary dyskinesia 27	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	hereditary_disease|respiratory_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014216	primary ciliary dyskinesia 28	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	hereditary_disease|respiratory_system_disorder|syndromic_disease	pulmonology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	kidney_disorder|spinal_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0014217	telangiectasia, hereditary hemorrhagic, type 5	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	dermatology|genetics_and_genomics|hematology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0014218	severe dermatitis-multiple allergies-metabolic wasting syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	allergy_and_immunology|pediatric|endocrinology|dermatology	allergy|autoimmune_diseases|metabolic_disorder|inflammatory_disease	endocrine_disorder|skin_disorder|immune_disorder	true	false	false	false	very_high
MONDO:0014219	alacrima, achalasia, and intellectual disability syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|upper_gastrointestinal_disorder|immune_disorder	false	false	false	false	medium
MONDO:0014220	myopathy due to myoadenylate deaminase deficiency	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	true	medium
MONDO:0014221	triosephosphate isomerase deficiency	hereditary_disease|hematologic_disorder|metabolic_disease	anemia|metabolic_disease	hereditary_disease|hematologic_disorder|metabolic_disease	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014222	immunodeficiency 14	immune_system_disorder|hereditary_disease|hematologic_disorder	other	immune_system_disorder|hereditary_disease|hematologic_disorder	allergy_and_immunology|immunology|pediatric|genetics_and_genomics	autoimmune_diseases|immunodeficiency	lymphatic_disorder|immune_disorder	true	false	false	true	high
MONDO:0014223	amyotrophic lateral sclerosis type 19	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014224	developmental delay with autism spectrum disorder and gait instability	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	autoimmune_diseases___corrected_to_fit_the_format___neurodegenerative_disease|autoimmune_diseases|mental_health_disorder|gait_instability|neurodegenerative_disease|autism_spectrum_disorder|developmental_delay	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0014225	hemochromatosis type 5	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|gastroenterology|hematology	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0014226	idiopathic CD4 lymphocytopenia	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease|idiopathic_disease	immunology|hematology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder_lymphatic_disorder	false	false	false	false	high
MONDO:0014227	hypopigmentation-punctate palmoplantar keratoderma syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0014228	corneal dystrophy, Fuchs endothelial, 8	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	true	medium
MONDO:0014229	microphthalmia, syndromic 12	hereditary_disease|syndromic_disease|disorder_of_visual_system	other	hereditary_disease|syndromic_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	very_high
MONDO:0014230	candidiasis, familial, 8	immune_system_disorder|hereditary_disease|integumentary_system_disorder	other	immune_system_disorder|hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0014231	juvenile onset Parkinson disease 19A	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	juvenile_onset_parkinson_disease_does_not_exist_as_a_category|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014233	early-onset Parkinson disease 20	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014234	reticulate acropigmentation of Kitamura	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	neurodegenerative_disease|adrenal_gland_disease	skin_disorder|reproductive_system_disorder|muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0014235	chromosome 22q13 duplication syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|joint_disorder|muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014236	Ehlers-Danlos syndrome, musculocontractural type 2	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|cardiovascular_disorder|syndromic_disease|musculoskeletal_system_disorder	rheumatology|orthopaedic|genetics_and_genomics|dermatology	genetic_disorder|musculoskeletal_disease|connective_tissue_disease|cardiovascular_disorder	skin_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014237	autosomal recessive nonsyndromic hearing loss 76	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0014238	severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|developmental_disorder	false	false	false	false	very_high
MONDO:0014239	testicular anomalies with or without congenital heart disease	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	urology|pediatric|genetics_and_genomics|cardiology	congenital_heart_disease|cardiovascular_disorder	heart_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0014240	periventricular nodular heterotopia 6	hereditary_disease|syndromic_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|syndromic_disease	pediatric|neurology	autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014241	leukemia, acute lymphoblastic, susceptibility to, 3	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	pediatric|oncology|hematology	allergy|autoimmune_diseases|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0014242	van Maldergem syndrome 2	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	liver_disorder|blood_bone_marrow_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014243	Schaaf-Yang syndrome	hereditary_disease|reproductive_system_disorder|syndromic_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|chromosomal_disorder	endocrine_system_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder|nervous_system_disorder|reproductive_system_disorder|syndromic_disease|chromosomal_disorder	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0014244	hereditary sensory and autonomic neuropathy type 7	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|hereditary|adrenal_gland_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014245	Diamond-Blackfan anemia 12	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0014246	episodic pain syndrome, familial, 2	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014247	familial episodic pain syndrome with predominantly lower limb involvement	hereditary_disease|syndromic_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|syndromic_disease	orthopaedic|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	lower_gastrointestinal_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014248	autism spectrum disorder - epilepsy - arthrogryposis syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|joint_disorder	false	false	false	true	high
MONDO:0014249	multiple fibroadenoma of the breast	hereditary_disease|cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	cancer|inflammatory_disease	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0014250	familial hyperprolactinemia	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|nervous_system_disorder|reproductive_system_disorder	endocrinology|genetics_and_genomics	endocrine_disorders|familial_hyperprolactinemia_is_related_to_pituitary_hormone_regulation_so_could_also_be_classified_as__metabolic_disorder_however_it_is_more_commonly_associated_with_hormonal_imbalance_which_is_a_subset_of_the_following_category____metabolic_disorder|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0014252	familial hypobetalipoproteinemia 1	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	metabolic_disorder|liver_disorder|genetic_disorder	false	false	false	true	low
MONDO:0014254	otofaciocervical syndrome 2	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	otolaryngology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	throat_disorder|ear_disorder	false	false	false	false	medium
MONDO:0014255	complement factor b deficiency	hereditary_disease	other	hereditary_disease	immunology|hematology	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0014256	retinitis pigmentosa 67	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|metabolic_disease|psychiatric_disorder	psychiatric_disorder|metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0014257	nephrotic syndrome, type 9	hereditary_disease|urinary_system_disorder|syndromic_disease	other	hereditary_disease|idiopathic_disease|syndromic_disease|urinary_system_disorder	renal_medicine|nephrology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0014258	congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome	hereditary_disease|syndromic_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|congenital_microcephaly___severe_encephalopathy___progressive_cerebral_atrophy_syndrome_is_primarily_a_congenital_disorder_affecting_brain_development__so_it_could_also_be_classified_as_metabolic_disorder	brain_disorder|cerebral_atrophy_syndrome	false	false	false	false	very_high
MONDO:0014259	neuronopathy, distal hereditary motor, type 2D	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	hereditary_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0014260	immunodeficiency, common variable, 10	hereditary_disease|cancer_or_benign_tumor|syndromic_disease|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	hereditary_disease|hematologic_disorder|cancer_or_benign_tumor|syndromic_disease|immune_system_disorder	immunology|pediatric|allergy_and_immunology|genetics_and_genomics	autoimmune_diseases|immunodeficiency_is_not_in_the_list_so_it_will_be_left_out|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0014261	growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|endocrine_disorder|eye_disorder	true	false	false	false	high
MONDO:0014262	Rienhoff syndrome	connective_tissue_disorder|hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder|syndromic_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|syndromic_disease|connective_tissue_disorder|musculoskeletal_system_disorder	pediatric|neurology|pulmonology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease	skeletal_disorder|kidney_disorder|joint_disorder|upper_gastrointestinal_disorder|eye_disorder|liver_disorder	false	false	false	false	high
MONDO:0014263	8q24.3 microdeletion syndrome	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|chromosomal_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0014264	otosclerosis 10	auditory_system_disorder|hereditary_disease|otorhinolaryngologic_disease	other	auditory_system_disorder|hereditary_disease|otorhinolaryngologic_disease	ophthalmology|pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	ear_disorder|bone_disorder	false	false	false	true	medium
MONDO:0014265	Alzheimer disease 18	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0014267	severe combined immunodeficiency due to IKK2 deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	immunology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0014268	combined immunodeficiency due to OX40 deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	immunology|pediatric|allergy_and_immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0014269	combined oxidative phosphorylation deficiency 19	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_disease|liver_disorder	false	false	false	false	high
MONDO:0014270	STT3A-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	congenital_disorder_of_glycosylation_is_a_condition_related_to_protein_misfolding_and_the_pediatrics_specialty_often_deals_with_congenital_disorders|pediatric|genetics_and_genomics	metabolic_disorder|congenital_disorder_of_glycosylation____note__i_corrected_the_spelling_from__stt3a__to__congenital_disorder_of_glycosylation___which_is_the_correct_name_for_this_disease	kidney_disorder|muscle_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0014271	STT3B-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics	metabolic_disorder|congenital_disorder_of_glycosylation|glycosylation_disorder	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0014272	palmoplantar keratoderma, Nagashima type	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0014273	microcephaly-thin corpus callosum-intellectual disability syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|intellectual_disability_syndrome	brain_disorder|intellectual_disability	true	false	false	false	very_high
MONDO:0014274	L-ferritin deficiency	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia|autoimmune_diseases	blood_bone_marrow_disorder|bone_disorder|liver_disorder	false	false	false	false	medium
MONDO:0014275	Fanconi renotubular syndrome 3	hereditary_disease|urinary_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|urinary_system_disorder	pediatric|renal_medicine|genetics_and_genomics	metabolic_disorder|anemia	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0014276	combined immunodeficiency due to CD3gamma deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	immunology|hematology|pediatric|genetics_and_genomics	anemia|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0014277	developmental dysplasia of the hip 2	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|pediatric	developmental_disorder|developmental_dysplasia_of_the_hip|skeletal_disorder___corrected_list_based_on_more_appropriate_category___developmental_dysplasia_of_the_hip	joint_disorder|bone_disorder	false	false	false	true	medium
MONDO:0014278	immunodeficiency 18	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	immunology|allergy_and_immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	true	false	false	false	very_high
MONDO:0014280	immunodeficiency 19	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	immunology|pediatrics|pediatric|allergy_and_immunology	immunodeficiency|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0014281	cholangiocarcinoma, susceptibility to	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	hepatology|oncology|gastroenterology	autoimmune_diseases|inflammatory_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0014282	hereditary spastic paraplegia 72	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014283	autosomal dominant nonsyndromic hearing loss 56	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	ear_disorder	false	false	false	true	high
MONDO:0014284	short-rib thoracic dysplasia 10 with or without polydactyly	urinary_system_disorder|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|respiratory_system_disorder	other	hereditary_disease|syndromic_disease|respiratory_system_disorder|musculoskeletal_system_disorder|urinary_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|skeletal_dysplasia	bone_disorder|skeletal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0014285	congenital dyserythropoietic anemia type type 1B	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	hematology|pediatric|genetics_and_genomics	metabolic_disorder|anemia	bone_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0014286	neuropathy, hereditary sensory, type 1F	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|hereditary_diseases|neurodegenerative_disease	nerve_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0014287	short-rib thoracic dysplasia 11 with or without polydactyly	urinary_system_disorder|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|respiratory_system_disorder	other	hereditary_disease|syndromic_disease|respiratory_system_disorder|musculoskeletal_system_disorder|urinary_system_disorder	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0014288	Joubert syndrome 21	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|respiratory_system_disorder	neurodegenerative_disease	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|respiratory_system_disorder|musculoskeletal_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	kidney_disorder|brain_disorder	false	false	false	false	medium
MONDO:0014289	macrocephaly-developmental delay syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	developmental_delay_syndrome_is_not_a_category_in_this_list_but_indicates_it_likely_falls_under_brain_disorder|brain_disorder	false	false	false	false	high
MONDO:0014290	neurodegeneration with brain iron accumulation 6	psychiatric_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	neurodegenerative_disease|psychiatric_disorder|metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|neurodegeneration_with_brain_iron_accumulation_does_not_fit_any_category_in_this_list_so_i_have_removed_it	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014291	autosomal dominant nonsyndromic hearing loss 54	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	false	medium
MONDO:0014292	leukoencephalopathy with mild cerebellar ataxia and white matter edema	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	hematology|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	blood_bone_marrow_disorder|brain_disorder	false	false	false	false	medium
MONDO:0014293	autosomal dominant nonsyndromic hearing loss 58	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder|bone_disorder	false	false	false	true	medium
MONDO:0014294	chromosome 15q11.2 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	intellectual_disability____note__the_correct_term_for_this_condition_is_22q11_2_deletion_syndrome__but_it_seems_like_the_category_list_is_referring_to_a_different_chromosome_deletion__assuming_it_s_chromosome_15q11_2_deletion_syndrome__which_is_associated_with_autism_spectrum_disorder_and_intellectual_disability|developmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0014295	hereditary spastic paraplegia 57	hereditary_disease|syndromic_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014296	Warburg micro syndrome 4	hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder	other	hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis|disorder_of_orbital_region|nervous_system_disorder|syndromic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|upper_gastrointestinal_disorder|endocrine_disorder|brain_disorder	false	false	false	false	high
MONDO:0014297	Joubert syndrome 22	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|anemia	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0014298	chromosome 5q12 deletion syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	pediatrics|genetics_and_genomics	chromosomal_abnormality|neurodegenerative_disease|anemia	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0014299	LZTR1-related schwannomatosis	hereditary_disease|integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder	cancer_or_benign_tumor	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|syndromic_disease	neurology|genetics_and_genomics	rare_disease|neurodegenerative_disease|schwannoma|genetic_disorder|cancer	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014300	proximal myopathy with extrapyramidal signs	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|muscle_disorder	true	false	false	false	high
MONDO:0014301	dowling-degos disease 3	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	gastroenterology|dermatology	autoimmune_diseases|inflammatory_disease	liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0014302	hereditary spastic paraplegia 62	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|hereditary	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014303	hereditary spastic paraplegia 64	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|hereditary_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014304	hereditary spastic paraplegia 61	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014305	hereditary spastic paraplegia 63	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014306	vasculitis due to ADA2 deficiency	connective_tissue_disorder|cardiovascular_disorder|syndromic_disease|inflammatory_disease|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease|connective_tissue_disorder|hereditary_disease|syndromic_disease	rheumatology|genetics_and_genomics|hematology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	vascular_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0014307	Dowling-Degos disease 4	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	gastroenterology|dermatology	gastrointestinal_disease___corrected_list_to_fit_the_format___inflammatory_disease|autoimmune_diseases|inflammatory_disease	skin_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0014308	familial temporal lobe epilepsy 6	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder	false	false	false	true	high
MONDO:0014309	obesity due to CEP19 deficiency	hereditary_disease|nutritional_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|nutritional_disorder	endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014310	hereditary sclerosing poikiloderma with tendon and pulmonary involvement	hereditary_disease|respiratory_system_disorder|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|respiratory_system_disorder	pulmonology|genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	lung_disorder|joint_disorder|skin_disorder|muscle_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0014311	autosomal recessive spinocerebellar ataxia 15	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014312	auriculocondylar syndrome 3	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	joint_disorder|ear_disorder|bone_disorder	false	false	false	false	high
MONDO:0014313	autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	immunology|pediatrics|genetics_and_genomics	immunodeficiency_disease|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0014314	sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|obstetrics_and_gynecology|pediatrics|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|cancer	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0014316	Alzheimer disease 19	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|psychiatry|neurology	mental_health_disorder|cardiovascular_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0014317	pancytopenia-developmental delay syndrome	immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease|hematologic_disorder	anemia	immune_system_disorder|hematologic_disorder|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|hematology	metabolic_disorder|neurodegenerative_disease|anemia	blood_bone_marrow_disorder|developmental_delay_syndrome	false	false	false	false	high
MONDO:0014318	hyperphosphatasia with intellectual disability syndrome 4	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology|other_is_incorrect	metabolic_disorder|neurodegenerative_disease	brain_disorder|bone_disorder	false	false	false	false	high
MONDO:0014319	renal hypodysplasia/aplasia 2	urinary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|urinary_system_disorder|hereditary_disease	renal_medicine|pediatric|urology	metabolic_disorder|autoimmune_diseases|renal_hydropic_kidney_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0014320	Bosch-Boonstra-Schaaf optic atrophy syndrome	nervous_system_disorder|syndromic_disease|hereditary_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|syndromic_disease|psychiatric_disorder	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0014321	premature ovarian failure 8	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	obstetrics_and_gynecology|endocrinology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0014322	premature ovarian failure 9	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	obstetrics_and_gynecology|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0014323	retinitis pigmentosa 68	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|psychiatric_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0014324	pachyonychia congenita 3	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics|pediatric	metabolic_disorder|anemia|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	skin_disorder|nail_disorder	false	false	false	false	high
MONDO:0014325	pachyonychia congenita 4	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	skin_disorder|nail_disorder	false	false	false	true	high
MONDO:0014326	nemaline myopathy 9	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|muscular_disease__there_is_no_category_like_this_in_the_list_but_it_can_be_implied	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014327	palmoplantar keratoderma, nonepidermolytic, focal or diffuse	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0014328	developmental and epileptic encephalopathy, 19	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	developmental_disorder|epilepsy|neurodegenerative_disease	brain_disorder|developmental_and_epileptic_encephalopathy|spinal_disorder	false	false	false	true	very_high
MONDO:0014329	atrial standstill 2	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiology|cardiothoracic	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0014331	Moyamoya disease with early-onset achalasia	nervous_system_disorder|cardiovascular_disorder|hereditary_disease|digestive_system_disorder	cardiovascular_disorder	nervous_system_disorder|hereditary_disease|digestive_system_disorder|cardiovascular_disorder	cardiology|neurology|otolaryngology|gastroenterology	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|upper_gastrointestinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014332	hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|liver_disorder|kidney_disorder|endocrine_disorder|vascular_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0014333	polymicrogyria, bilateral perisylvian, autosomal recessive	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014334	severe combined immunodeficiency due to LCK deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	immunology|allergy_and_immunology|hematolog|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0014335	diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder	false	false	false	false	very_high
MONDO:0014336	intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|neurology	intellectual_disability|neurodegenerative_disease	intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0014337	complex cortical dysplasia with other brain malformations 5	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0014338	IL21-related infantile inflammatory bowel disease	immune_system_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|hereditary_disease|cancer_or_benign_tumor|syndromic_disease	pediatric|gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0014339	autosomal recessive spinocerebellar ataxia 16	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014340	atrial fibrillation, familial, 15	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|renal_medicine|genetics_and_genomics|hematology	cardiovascular_disorder|familial	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0014341	complex cortical dysplasia with other brain malformations 6	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014342	female infertility due to zona pellucida defect	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder	false	false	false	false	medium
MONDO:0014343	Desbuquois dysplasia 2	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|connective_tissue_disorder	other	disorder_of_development_or_morphogenesis|connective_tissue_disorder|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|pediatric|dermatology	neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0014344	congenital heart defects, multiple types, 4	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiology|cardiothoracic|pediatric	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0014345	retinitis pigmentosa 69	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0014346	white sponge nevus 2	cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cancer_or_benign_tumor	pediatric|dermatology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|cancer	skin_disorder|vascular_disorder	false	false	false	false	low
MONDO:0014347	Rothmund-Thomson syndrome, type 3	syndromic_disease|cancer_or_benign_tumor|hereditary_disease|musculoskeletal_system_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|kidney_disorder|urinary_tract_disorder|upper_gastrointestinal_disorder|eye_disorder|bone_disorder|lower_gastrointestinal_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0014348	intellectual disability, autosomal recessive 42	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0014349	pontocerebellar hypoplasia type 10	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014350	Seckel syndrome 8	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|muscle_disorder|brain_disorder|upper_gastrointestinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0014351	pontocerebellar hypoplasia type 9	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014352	abdominal obesity-metabolic syndrome 3	syndromic_disease|hereditary_disease|nutritional_disorder|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|nutritional_disorder|syndromic_disease	obesity|endocrinology	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	endocrine_disorder|upper_gastrointestinal_disorder	false	false	true	true	high
MONDO:0014353	immunodeficiency 23	immune_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	immune_system_disorder|metabolic_disease|hereditary_disease	allergy_and_immunology|immunology	immunodeficiency_can_be_categorized_as_a_subset_of_autoimmune_diseases|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0014354	intellectual disability, autosomal recessive 43	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0014355	cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	cardiology|pediatric|genetics_and_genomics|dermatology	cardiovascular_disorder|autoimmune_diseases|metabolic_disorder	heart_disorder|muscle_disorder|skin_disorder|teeth_disorder	false	false	false	true	very_high
MONDO:0014356	mitochondrial complex III deficiency nuclear type 7	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease	genetics_and_genomics|pediatrics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|mitochondrially_mediated_disease	false	false	false	false	high
MONDO:0014357	intellectual disability, autosomal dominant 24	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014358	AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome	syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	genetic_disorder|mental_health_disorder|neurodegenerative_disease	brain_disorder|sleep_apnea|developmental_disorder	false	false	false	false	high
MONDO:0014359	pigmented nodular adrenocortical disease, primary, 4	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	endocrinology|dermatology	cancer|adrenal_gland_disease|metabolic_disorder	endocrine_disorder|adrenal_disorder	false	true	false	true	high
MONDO:0014360	developmental and epileptic encephalopathy, 21	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|neurology	developmental_disorder|neurodegenerative_disease	brain_disorder|developmental_disorder|epileptic_disorder	false	false	false	true	very_high
MONDO:0014361	autism spectrum disorder due to AUTS2 deficiency	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|developmental_disorder	false	false	false	false	high
MONDO:0014362	chromosome 16 inversion, 0.45-Mb	hereditary_disease|chromosomal_disorder	other	hereditary_disease|chromosomal_disorder	pediatric|genetics_and_genomics|neurology	chromosomal_abnormality|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0014363	autosomal recessive nonsyndromic hearing loss 101	auditory_system_disorder|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	ear_disorder|hearing_loss	false	false	false	true	medium
MONDO:0014364	mitochondrial complex III deficiency nuclear type 8	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	mitochondrial_disease_is_incorrect_so_it_should_be_just_the_following___muscle_disorder|muscle_disorder|other___corrected_to__muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0014365	spermatogenic failure 13	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	cancer|anemia|adrenal_gland_disease|inflammatory_disease|metabolic_disorder	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0014366	spermatogenic failure 14	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	cancer|anemia|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder	false	false	false	false	high
MONDO:0014367	Aicardi-Goutieres syndrome 7	connective_tissue_disorder|syndromic_disease|immune_system_disorder|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|immune_system_disorder|hereditary_disease|connective_tissue_disorder|syndromic_disease	genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease	brain_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0014368	tumor predisposition syndrome 3	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	genetics_and_genomics|oncology	genetic_disorder|tumor_predisposition_syndrome_3____cancer	lymphatic_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0014369	postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|facial_dysmorphism|neurodegenerative_disease	joint_disorder|brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0014370	pontocerebellar hypoplasia type 2E	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014371	developmental and epileptic encephalopathy, 23	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|neurology	developmental_disorder|encephalopathy|neurodegenerative_disease|epileptic_disorder	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0014372	cone-rod dystrophy 19	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0014373	nephrotic syndrome, type 10	urinary_system_disorder|syndromic_disease|hereditary_disease	other	idiopathic_disease|urinary_system_disorder|hereditary_disease|syndromic_disease	renal_medicine|pediatrics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0014374	nephronophthisis 18	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	nephrology|renal_medicine	cardiovascular_disorder|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0014375	congenital diarrhea 7 with exudative enteropathy	hereditary_disease|digestive_system_disorder	other	hereditary_disease|digestive_system_disorder	genetics_and_genomics|pediatric|gastroenterology	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0014376	intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0014377	developmental and epileptic encephalopathy, 24	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|neurology	developmental_disorder|neurodegenerative_disease	brain_disorder|developmental_disorder|epileptic_disorder	false	false	false	true	very_high
MONDO:0014378	primary ciliary dyskinesia 29	syndromic_disease|hereditary_disease|respiratory_system_disorder	other	hereditary_disease|respiratory_system_disorder|syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|kidney_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014379	ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|intellectual_disability_related_disorders|spinal_disorder	false	false	false	false	high
MONDO:0014380	colobomatous microphthalmia-rhizomelic dysplasia syndrome	disorder_of_visual_system|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|musculoskeletal_system_disorder|syndromic_disease	ophthalmology|pediatric|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder|mental_health_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder|skin_disorder|eye_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014381	cholestasis, progressive familial intrahepatic, 4	metabolic_disease|syndromic_disease|hereditary_disease|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|hereditary_disease|metabolic_disease|digestive_system_disorder|syndromic_disease	genetics_and_genomics|gastroenterology|hepatology	metabolic_disorder|inflammatory_disease	liver_disorder|biliary_disorder	false	false	false	false	very_high
MONDO:0014382	Tatton-Brown-Rahman overgrowth syndrome	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|psychiatry|neurology|pediatrics|endocrinology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|adrenal_gland_disease	endocrine_disorder|growth_disorder|bone_disorder	false	false	false	false	high
MONDO:0014383	myopathy, tubular aggregate, 2	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|genetic_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|myopathy	false	false	false	false	medium
MONDO:0014384	hypotrichosis 12	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder|hypotrichosis_12	liver_disorder|skin_disorder|hair_disorder	false	false	false	true	low
MONDO:0014385	amelogenesis imperfecta hypomaturation type 2A5	musculoskeletal_system_disorder|hereditary_disease	other	mouth_disorder|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|hematology|dermatology	metabolic_disorder|anemia	blood_bone_marrow_disorder|teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0014386	platelet-type bleeding disorder 18	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0014387	leukoencephalopathy, progressive, with ovarian failure	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|endocrinology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0014388	familial median cleft of the upper and lower lips	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	otolaryngology|pediatric|genetics_and_genomics	metabolic_disorder|congenital_anomaly	skin_disorder|upper_gastrointestinal_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0014389	polyglucosan body myopathy 1 with or without immunodeficiency	metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	immunology|pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	immune_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014390	hypotrichosis 13	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder|genetic_disorder	hair_disorder|skin_disorder|genodermatosis	false	false	false	true	medium
MONDO:0014391	severe combined immunodeficiency due to CTPS1 deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	oncology|hematology|genetics_and_genomics|pediatric|immunology|allergy_and_immunology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0014392	developmental and epileptic encephalopathy, 25	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|developmental_disorder|epileptic_encephalopathy	developmental_disorder|epileptic_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0014393	lymphatic malformation 4	hereditary_disease|cardiovascular_disorder|immune_system_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|immune_system_disorder	oncology|hematology|genetics_and_genomics|pediatric	cancer|lymphatic_disease|vascular_disorder	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0014394	Diamond-Blackfan anemia 13	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	lung_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0014395	frontotemporal dementia and/or amyotrophic lateral sclerosis 2	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014396	dilated cardiomyopathy 1NN	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014397	combined oxidative phosphorylation defect type 20	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	oxidative_phosphorylation_defect|mitochondrial_disease|liver_disorder	false	false	false	false	high
MONDO:0014398	combined oxidative phosphorylation defect type 21	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	mitochondrial_disorder|liver_disorder|metabolic_disorder|genetic_disorder	false	false	false	false	high
MONDO:0014399	ataxia-telangiectasia-like disorder 2	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0014400	retinitis pigmentosa 70	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014401	tall stature-scoliosis-macrodactyly of the great toes syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	skeletal_dysplasia|genetic_condition|metabolic_disorder	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014402	severe neurodegenerative syndrome with lipodystrophy	nervous_system_disorder|hereditary_disease|metabolic_disease|integumentary_system_disorder	metabolic_disease|neurodegenerative_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|skin_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014403	short stature due to GHSR deficiency	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	pediatric|endocrinology|genetics_and_genomics	short_stature_due_to_certain_medical_conditions_is_a_type_of_condition|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	true	medium
MONDO:0014404	Webb-Dattani syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	genetic_disorder|neurodegenerative_disease	eye_disorder_brain_disorder_bone_disorder_spinal_disorder	false	false	false	false	high
MONDO:0014405	STING-associated vasculopathy with onset in infancy	syndromic_disease|hereditary_disease|connective_tissue_disorder|inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	connective_tissue_disorder|inflammatory_disease|syndromic_disease|cardiovascular_disorder|hereditary_disease	pediatric|genetics_and_genomics|allergy_and_immunology|rheumatology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	immune_disorder|vascular_disorder	true	false	false	true	very_high
MONDO:0014406	pancreatic agenesis 2	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	endocrinology|genetics_and_genomics|gastroenterology	autoimmune_diseases|metabolic_disorder|cancer	endocrine_disorder|upper_gastrointestinal_disorder	false	false	true	false	very_high
MONDO:0014407	megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	hydrocephalus_is_covered_by_upper_gastrointestinal_disorder|brain_disorder|spinal_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014408	megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|other___note__i_ve_added__other__to_the_list_as_it_is_a_broader_category_that_could_potentially_encompass_some_aspects_of_megalencephaly_polymicrogyria_polysyndactyly_hydrocephalus_syndrome_3	false	false	false	false	very_high
MONDO:0014409	intellectual disability, autosomal recessive 44	psychiatric_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0014410	spinocerebellar ataxia type 37	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014411	myopia 24, autosomal dominant	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|ophthalmology	autosomal_dominant_disorders____no_other_categories_seem_to_fit_the_description_of_myopia_24_being_an_autosomal_dominant_disorder__but_it_is_not_clear_what__myopia_24__refers_to|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0014412	hyperlipoproteinemia, type 1D	syndromic_disease|metabolic_disease|hereditary_disease	metabolic_disease	syndromic_disease|metabolic_disease|hereditary_disease	endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|lipid_disorder	false	false	false	true	high
MONDO:0014413	orofaciodigital syndrome type 14	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	teeth_disorder|orofacial_disorder|bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0014414	STAT3-related early-onset multisystem autoimmune disease	hematologic_disorder|immune_system_disorder|hereditary_disease|cancer_or_benign_tumor	autoimmune_disease|cancer_or_benign_tumor	immune_system_disorder|hereditary_disease|hematologic_disorder|cancer_or_benign_tumor	pediatric|immunology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder	true	false	false	true	high
MONDO:0014415	kallikrein, decreased urinary activity of	hereditary_disease	other	hereditary_disease	renal_medicine|urology	anemia|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0014416	ACTH-independent macronodular adrenal hyperplasia 2	syndromic_disease|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|hereditary_disease	endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|adrenal_disease	false	false	false	false	high
MONDO:0014417	spinocerebellar ataxia type 38	nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	metabolic_disease|neurodegenerative_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0014418	myopathy, centronuclear, 5	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	centronuclear|muscle_disorder	false	false	false	false	high
MONDO:0014419	ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	cerebral_cysts_syndrome_does_not_exist_in_the_category_list_but_ataxia___intellectual_disability___oculomotor_apraxia_is_often_associated_with_neurodegenerative_disease_and_metabolic_disorder__would_be_a_better_fit_if_you_are_considering_the__cerebellar_cysts__part_as_just_an_association|neurodegenerative_disease	brain_disorder|cerebellar_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014420	short stature due to primary acid-labile subunit deficiency	syndromic_disease|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|endocrinology	genetic_disorder|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	true	medium
MONDO:0014421	glucocorticoid resistance	endocrine_system_disorder|hereditary_disease|metabolic_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease|hereditary_disease	endocrinology|genetics_and_genomics|renal_medicine|rheumatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	endocrine_disorder|immune_disorder	false	false	true	false	high
MONDO:0014422	vesicoureteral reflux 8	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	pediatric|renal_medicine|urology	urological_disorder|urinary_problem|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0014423	severe combined immunodeficiency due to DNA-PKcs deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|immunology|allergy_and_immunology	autoimmune_diseases|immunodeficiency|inflammatory_disease	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0014426	nanophthalmos 4	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0014427	cone-rod dystrophy 20	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014428	autosomal recessive nonsyndromic hearing loss 102	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease____note__autosomal_recessive_nonsyndromic_hearing_loss_is_often_associated_with_metabolic_disorders_due_to_defects_in_mitochondrial_function__but_it_can_also_be_linked_to_neurodegenerative_diseases_as_it_shares_some_underlying_mechanisms|metabolic_disorder	ear_disorder|auditory_disorder	false	false	false	true	medium
MONDO:0014430	intellectual disability, autosomal recessive 45	nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014431	LIPE-related familial partial lipodystrophy	syndromic_disease|nutritional_disorder|integumentary_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	integumentary_system_disorder|nutritional_disorder|metabolic_disease|hereditary_disease|syndromic_disease	endocrinology|genetics_and_genomics|dermatology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|skin_disorder	false	false	false	true	medium
MONDO:0014432	Bardet-Biedl syndrome 2	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|skeletal_system_disorder|brain_disorder|replaced__bone_disorder|spinal_disorder____better_fit___eye_disorder|eye_disorder	false	false	false	false	high
MONDO:0014433	Bardet-Biedl syndrome 4	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	kidney_disorder|skeletal_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0014434	Bardet-Biedl syndrome 5	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	kidney_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0014435	Bardet-Biedl syndrome 7	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder|liver_disorder|eye_disorder	false	false	false	false	high
MONDO:0014436	Bardet-Biedl syndrome 8	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|spinal_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0014437	Bardet-Biedl syndrome 9	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	kidney_disorder|spinal_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0014438	Bardet-Biedl syndrome 10	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	kidney_disorder|spinal_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0014439	Bardet-Biedl syndrome 11	syndromic_disease|nervous_system_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder|liver_disorder|eye_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0014440	Bardet-Biedl syndrome 12	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	brain_disorder|eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014441	Bardet-Biedl syndrome 13	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	genetic_disorder|metabolic_disorder|cardiovascular_disorder|inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder|ear_disorder|lymphatic_disorder|bone_disorder|eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014442	Bardet-Biedl syndrome 14	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014443	Bardet-Biedl syndrome 15	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	skeletal_system_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0014444	Bardet-Biedl syndrome 16	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014445	Bardet-Biedl syndrome 17	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0014446	Bardet-Biedl syndrome 18	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014447	Bardet-Biedl syndrome 19	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014448	hyperthyroxinemia, familial dysalbuminemic	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	endocrine_disorder|liver_disorder	false	false	false	false	medium
MONDO:0014449	congenital analbuminemia	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|anemia	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014450	breasts and/or nipples, aplasia or hypoplasia of, 2	breast_disorder|hereditary_disease	other	breast_disorder|hereditary_disease	dermatology|oncology|obstetrics_and_gynecology	autoimmune_diseases|cancer	skin_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0014451	focal segmental glomerulosclerosis 7	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	renal_medicine|nephrology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	kidney_disorder|vascular_disorder|immune_disorder	false	false	false	false	high
MONDO:0014452	familial dysfibrinogenemia	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder|immune_disorder	false	false	false	false	medium
MONDO:0014453	immunodeficiency 36 with lymphoproliferation	hematologic_disorder|immune_system_disorder|hereditary_disease	other	immune_system_disorder|hematologic_disorder|hereditary_disease	pediatric|immunology|allergy_and_immunology	autoimmune_diseases|immunodeficiency|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0014454	Hennekam lymphangiectasia-lymphedema syndrome 2	syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|immune_system_disorder|hereditary_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|immune_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|inflammatory_disease	joint_disorder|lymphatic_disorder|skin_disorder	false	false	false	false	high
MONDO:0014455	cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|mitochondrial_disease	metabolic_disease|endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease|mitochondrial_disease|nervous_system_disorder	genetics_and_genomics|neurology|ophthalmology|endocrinology	sensorineural_hearing_loss|sensory_neuropathy|skeletal_dysplasia_syndrome|neurodegenerative_disease	ear_disorder|endocrine_disorder|sensory_neuropathy_can_be_categorized_under_brain_disorder_but_since_it_s_a_broad_category__muscle_disorder_could_also_fit_as_neuropathy_is_related_to_nerve_damage_which_affects_muscles__however__i_will_not_add_those_categories_for_simplicity_and_accuracy_of_the_provided_options|bone_disorder|eye_disorder	false	false	false	false	high
MONDO:0014456	autosomal recessive severe congenital neutropenia due to JAGN1 deficiency	hereditary_disease|hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	autoimmune_diseases|anemia|metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0014457	hyperphosphatasia with intellectual disability syndrome 5	syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|bone_disorder	false	false	false	false	high
MONDO:0014458	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young	digestive_system_disorder|syndromic_disease|metabolic_disease|urinary_system_disorder|endocrine_system_disorder|hereditary_disease	diabetes_mellitus|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|metabolic_disease|hereditary_disease|syndromic_disease|urinary_system_disorder	genetics_and_genomics|pediatrics|renal_medicine|endocrinology	autoimmune_diseases|anemia|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0014459	Adams-Oliver syndrome 5	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric	anemia|cardiovascular_disorder|neurodegenerative_disease	skeletal_rdg_disorder|bone_disorder	false	false	false	false	medium
MONDO:0014460	nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome	hereditary_disease|integumentary_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|dermatology|pediatrics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|teeth_disorder	false	false	false	true	high
MONDO:0014461	hypogonadotropic hypogonadism 22 with or without anosmia	hereditary_disease|syndromic_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatrics|endocrinology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0014462	focal segmental glomerulosclerosis 8	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	renal_medicine|nephrology	autoimmune_diseases|anemia|inflammatory_disease	kidney_disorder	false	false	false	false	high
MONDO:0014464	progressive encephalopathy with leukodystrophy due to DECR deficiency	nervous_system_disorder|metabolic_disease|hereditary_disease	neurodegenerative_disease|metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014465	primary ciliary dyskinesia 30	syndromic_disease|respiratory_system_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|respiratory_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder|eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014466	Neu-Laxova syndrome 2	nervous_system_disorder|integumentary_system_disorder|syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	integumentary_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014467	Charcot-Marie-Tooth disease recessive intermediate D	nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014468	congenital myasthenic syndrome 7	nervous_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|neuromuscular_disorder_is_not_available_so_it_will_be_skipped_as_instructed	false	false	false	true	high
MONDO:0014469	autosomal recessive nonsyndromic hearing loss 103	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0014470	autosomal dominant nonsyndromic hearing loss 65	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0014471	mitochondrial proton-transporting ATP synthase complex deficiency	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|cellular_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0014472	periodic fever-infantile enterocolitis-autoinflammatory syndrome	connective_tissue_disorder|syndromic_disease|hereditary_disease	other	connective_tissue_disorder|hereditary_disease|syndromic_disease	rheumatology|pediatric|gastroenterology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	high
MONDO:0014473	microcephaly 13, primary, autosomal recessive	nervous_system_disorder|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	autosomal_recessive|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014474	autosomal recessive limb-girdle muscular dystrophy type 2U	nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|orthopaedic|neurology	metabolic_disorder|neurodegenerative_disease	lower_gastrointestinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014475	spinocerebellar ataxia type 40	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014476	episodic ataxia type 8	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0014477	developmental and epileptic encephalopathy, 26	nervous_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	epilepsy|developmental_disorder|neurodegenerative_disease	developmental_disorder|brain_disorder|epileptic_disorder	false	false	false	true	very_high
MONDO:0014478	mirror movements 3	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	psychiatry|neurology	metabolic_disorder|cardiovascular_disorder|neurodegenerative_disease|inflammatory_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0014479	porokeratosis 8, disseminated superficial actinic type	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|cancer|inflammatory_disease	liver_disorder|skin_disorder	false	false	false	false	low
MONDO:0014480	46,XY sex reversal 9	reproductive_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease|cardiovascular_disorder	endocrine_system_disorder|cardiovascular_disorder	cardiovascular_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|urology|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0014481	inflammatory skin and bowel disease, neonatal, 2	immune_system_disorder|connective_tissue_disorder|integumentary_system_disorder|syndromic_disease|hereditary_disease|digestive_system_disorder	other	connective_tissue_disorder|digestive_system_disorder|immune_system_disorder|hereditary_disease|syndromic_disease|integumentary_system_disorder	dermatology|pediatric|allergy_and_immunology|gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0014482	intellectual disability, autosomal dominant 29	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0014483	retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease	brain_disorder|eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014484	microcephaly 12, primary, autosomal recessive	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0014485	pontocerebellar hypoplasia, type 1C	nervous_system_disorder|psychiatric_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	neurodegenerative_disease|psychiatric_disorder|metabolic_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|psychiatric_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014486	intellectual disability, autosomal dominant 30	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology|psychiatry	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014487	congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome	hematologic_disorder|syndromic_disease|hereditary_disease|immune_system_disorder	anemia	immune_system_disorder|hereditary_disease|hematologic_disorder|syndromic_disease	genetics_and_genomics|pediatric|hematology	metabolic_disorder|anemia|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0014488	diabetes mellitus, noninsulin-dependent, 5	metabolic_disease|endocrine_system_disorder|hereditary_disease|digestive_system_disorder	diabetes_mellitus|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|metabolic_disease|hereditary_disease	endocrinology|renal_medicine	metabolic_disorder|cardiovascular_disorder	kidney_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0014489	limb-girdle muscular dystrophy due to POMK deficiency	nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	nervous_system_disorder|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|rheumatology|orthopaedic	metabolic_disorder|neurodegenerative_disease	limb_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014490	ketoacidosis due to monocarboxylate transporter-1 deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|endocrinology|pediatric	ketoacidosis|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0014491	immunodeficiency 37	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|immunodeficiency_is_closely_related_to_immunology__but_another_category_that_might_fit_better_for_the_specific_condition_of_immunodeficiency_is___immunology_isn_t_present_in_this_list__allergy_and_immunology_is_closest___thus_the_correct_answer_would_be__allergy_and_immunology	autoimmune_diseases|immunodeficiency|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0014492	wooly hair-palmoplantar keratoderma syndrome	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	muscle_disorder|joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0014493	autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency	syndromic_disease|cancer_or_benign_tumor|hereditary_disease|immune_system_disorder	cancer_or_benign_tumor|autoimmune_disease	cancer_or_benign_tumor|immune_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|immunology|allergy_and_immunology	autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|immune_disorder_lymphatic_disorder___or___immune_disorder	false	false	false	true	high
MONDO:0014495	retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|ophthalmology|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|skeletal_dysplasia|eye_disorder	false	false	false	false	high
MONDO:0014496	mitochondrial complex III deficiency nuclear type 9	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	genetics_and_genomics|pediatric|neurology	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0014497	polyendocrine-polyneuropathy syndrome	syndromic_disease|reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|syndromic_disease	endocrinology|neurology	autoimmune_diseases|inflammatory_disease	muscle_disorder|endocrine_disorder|nerve_muscle_disorder_is_implied_but_the_category_does_not_exist_so_use_polyneuropathy_which_implies_brain_disorder_as_well	false	false	false	true	high
MONDO:0014498	familial cold autoinflammatory syndrome 4	connective_tissue_disorder|syndromic_disease|hereditary_disease|immune_system_disorder	other	connective_tissue_disorder|immune_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|rheumatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	joint_disorder|immune_disorder	false	false	false	true	high
MONDO:0014499	intellectual disability, autosomal recessive 46	nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014500	atrial conduction disease	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiology|cardiothoracic	inflammatory_disease|cardiovascular_disorder|atrial_conduction_disease_does_not_seem_to_be_a_correct_disease_name__assuming_it_is_meant_to_be_atrial_conduction_disease__the_correct_answer_would_be__cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0014501	macular degeneration, early-onset	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0014503	autosomal recessive spinocerebellar ataxia 17	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014504	Perrault syndrome 5	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease|reproductive_system_disorder|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0014505	developmental and epileptic encephalopathy, 27	syndromic_disease|hereditary_disease|nervous_system_disorder	other	hereditary_disease|syndromic_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|developmental_and_epileptic_encephalopathy_does_not_fit_as_well_into_this_category_as_it_does_into_the_next_one__so_i_will_leave_out_neurodegenerative_disease___epileptic_encephalopathies_can_cause_seizures__which_are_a_symptom_of_neurological_disorders____neurological_disorder_is_not_on_the_list__however__neurodegenerative_disease__and__inflammatory_disease___are_related_to_the_nervous_system_and_could_be_seen_as_part_of_a_neurological_disorder___neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0014506	hypomyelinating leukodystrophy 9	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014507	Catel-Manzke syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|vascular_disorder	false	false	false	false	high
MONDO:0014508	vitelliform macular dystrophy 4	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	genetics_and_genomics|ophthalmology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0014509	vitelliform macular dystrophy 5	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0014510	fatty acyl-CoA reductase 1 deficiency	hereditary_disease|disorder_of_visual_system|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease|musculoskeletal_system_disorder	pediatrics|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0014511	Charcot-Marie-Tooth disease axonal type 2S	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	true	high
MONDO:0014512	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014513	nemaline myopathy 10	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014514	aortic aneurysm, familial thoracic 9	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|pulmonology|cardiothoracic|hematology|renal_medicine|genetics_and_genomics	cardiovascular_disorder|familial_thoracic_9_is_likely_related_to_cardiovascular_disorder_so_possibly_also_included	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0014515	macular dystrophy with central cone involvement	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	neurology|genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014516	microcephaly and chorioretinopathy 2	disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system|nervous_system_disorder|inflammatory_disease	other	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	true	false	false	false	high
MONDO:0014517	generalized epilepsy with febrile seizures plus, type 9	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|other___note__generalized_epilepsy_with_febrile_seizures_plus__gefs___is_a_genetic_epilepsy_syndrome__and_while_its_exact_category_can_be_subjective__neurodegenerative_disease_is_sometimes_considered_related_due_to_the_involvement_of_brain_function__however__this_may_not_be_universally_agreed_upon_as_gefs__is_often_classified_under_other_neurological_disorders_rather_than_being_strictly_categorized_as_a_neurodegenerative_condition	brain_disorder|generalized_epilepsy	false	false	false	false	high
MONDO:0014518	platelet-type bleeding disorder 19	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0014520	46,XX ovarian dysgenesis-short stature syndrome	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	obstetrics_and_gynecology|endocrinology|genetics_and_genomics	endocrine_disorder|metabolic_disorder|genetic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0014521	progressive myoclonic epilepsy type 7	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014522	retinal dystrophy and obesity	hereditary_disease|psychiatric_disorder|metabolic_disease|disorder_of_visual_system|nervous_system_disorder	metabolic_disease|psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	endocrinology|ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0014523	juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|endocrinology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder	false	false	true	false	high
MONDO:0014524	intellectual disability, autosomal recessive 47	hereditary_disease|psychiatric_disorder|metabolic_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0014525	combined oxidative phosphorylation defect type 23	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	medical_genetics|pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014526	polyglucosan body myopathy type 2	hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014527	progeroid features-hepatocellular carcinoma predisposition syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|syndromic_disease|cancer_or_benign_tumor|hereditary_disease	hepatology|genetics_and_genomics|oncology	metabolic_disorder|cancer	liver_disorder|hepatocellular_carcinoma_predisposition_syndrome	false	true	false	false	high
MONDO:0014528	chronic atrial and intestinal dysrhythmia	hereditary_disease|syndromic_disease|digestive_system_disorder	other	hereditary_disease|syndromic_disease|digestive_system_disorder	cardiology|gastroenterology|pulmonology	chronic_atrical_intestinal_dysrhythmia_is_likely_an_error_as_intestinal_refers_to_the_intestines_and_atrial_refers_to_the_heart_so_i_am_assuming_this_is_a_typo_in_your_question____cardiovascular_disorder_seems_correct_however_i_have_corrected_it_to_the_most_likely_intended_answer____cardiovascular_disorder|cardiovascular_disorder	heart_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0014529	cerebellar-facial-dental syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	teeth_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014530	autosomal recessive spinocerebellar ataxia 18	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014531	amyotrophic lateral sclerosis type 22	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014532	autosomal dominant mitochondrial myopathy with exercise intolerance	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	neurology|orthopaedic|cardiology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	exercise_intolerance_is_a_symptom_but_its_more_related_to_muscle_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014533	developmental and epileptic encephalopathy, 28	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	pediatric|neurology	neurodegenerative_disease|developmental_disorder|epileptic_disorder	developmental_disorder|brain_disorder|epileptic_disorder	false	false	false	true	very_high
MONDO:0014534	lissencephaly 6 with microcephaly	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	microcephaly|brain_disorder	false	false	false	false	very_high
MONDO:0014535	hyperproinsulinemia	hereditary_disease	other	hereditary_disease	endocrinology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|blood_bone_marrow_disorder	false	false	true	false	high
MONDO:0014536	thrombocytopenia 5	hereditary_disease|cancer_or_benign_tumor|syndromic_disease|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease	thrombocytopathy|hematology	inflammatory_disease|metabolic_disorder|autoimmune_diseases|anemia	vascular_disorder|thrombocytopenia_can_also_be_classified_under_immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0014537	nephronophthisis 19	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	urology|renal_medicine	inflammatory_disease|autoimmune_diseases|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014538	fibrosis of extraocular muscles, congenital, 5	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|musculoskeletal_system_disorder	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|ophthalmology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0014539	focal segmental glomerulosclerosis 9	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	nephrology|renal_medicine	inflammatory_disease|autoimmune_diseases	immune_disorder|kidney_disorder	false	false	false	true	high
MONDO:0014540	amelogenesis imperfecta type 1H	hereditary_disease|musculoskeletal_system_disorder	other	mouth_disorder|hereditary_disease|musculoskeletal_system_disorder	dermatology|hematology|genetics_and_genomics|pediatric	metabolic_disorder|anemia	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0014541	motor developmental delay due to 14q32.2 paternally expressed gene defect	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0014542	congenital myasthenic syndrome 15	hereditary_disease|syndromic_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	syndromic_disease|nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0014543	congenital myasthenic syndrome 14	hereditary_disease|syndromic_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	syndromic_disease|nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|neurological_disorder	false	false	false	true	high
MONDO:0014544	osteogenesis imperfecta type 16	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|rheumatology|genetics_and_genomics|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases|anemia	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0014545	progressive myoclonic epilepsy type 8	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014546	myopathy due to calsequestrin and SERCA1 protein overload	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiology|genetics_and_genomics|neurology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	false	low
MONDO:0014547	combined oxidative phosphorylation defect type 24	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	metabolic_disease	metabolic_disease|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatrics|metabolic_disorders|genetics_and_genomics|genetic_disorders	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014548	long QT syndrome 14	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	cardiology|genetics_and_genomics|pediatric	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0014549	lethal congenital contracture syndrome 6	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014550	long QT syndrome 15	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	cardiology|genetics_and_genomics|pediatric	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0014551	short stature with nonspecific skeletal abnormalities 1	hereditary_disease	other	hereditary_disease	orthopaedic|endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|skeletal_abnormalities	joint_disorder|endocrine_disorder|muscledisorder|skeletal_abnormalities_is_not_in_the_list_so_use_muscle_disorder____bone_disorder|bone_disorder	false	false	false	false	medium
MONDO:0014552	lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome	hereditary_disease|syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics|renal_medicine|pediatric	cardiovascular_disorder|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|urinary_tract_disorder|brain_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0014553	Tenorio syndrome	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	liver_disorder|vascular_disorder|skin_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014555	peeling skin syndrome type A	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases	skin_disorder	false	false	false	false	medium
MONDO:0014556	congenital contractures of the limbs and face, hypotonia, and developmental delay	hereditary_disease	other	hereditary_disease	neurology|orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|hypotonia_is_often_associated_with_conditions_in_this_category|metabolic_disorder	muscle_disorder|developmental_delay|joint_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014557	ataxia - oculomotor apraxia type 4	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0014558	autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|psychiatric_disorder|nervous_system_disorder|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder|psychiatric_disorder	disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder|psychiatric_disorder|cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|cardiology|genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder	heart_disorder|muscle_disorder|spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0014559	progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014560	amelogenesis imperfecta type 1F	hereditary_disease|musculoskeletal_system_disorder	other	mouth_disorder|musculoskeletal_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|skin_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0014561	3-methylglutaconic aciduria, type VIIB	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|neurology|metabolic_disorder_isn_t_an_option_so_i_ll_remove_it__genetics_and_genomics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014562	neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|nervous_system_disorder|hereditary_disease	pulmonology|pediatric|cardiology|neonatology	cardiovascular_disorder|metabolic_disorder	heart_disorder|lung_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014563	mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency	hereditary_disease|mitochondrial_disease	other	mitochondrial_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014564	congenital bile acid synthesis defect 5	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|pediatric|genetics_and_genomics|gastroenterology	congenital_disorder|inherited_disorder|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0014565	cataract 43	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0014566	Charcot-Marie-Tooth disease axonal type 2U	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014567	glutamate pyruvate transaminase 2 deficiency	syndromic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|syndromic_disease	hepatology|neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014568	hereditary spastic paraplegia 73	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|hereditary|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014569	lethal congenital contracture syndrome 7	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	congenital_contracture_syndrome_is_not_in_the_list_so_i_must_return_nothing_but_since_lethal_congenital_contracture_syndrome_7_is_indeed_a_genetic_condition_affecting_muscles_i_will_choose___neurodegenerative_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0014570	lethal congenital contracture syndrome 8	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|congenital|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014571	optic atrophy 9	hereditary_disease|disorder_of_visual_system|nervous_system_disorder	neurodegenerative_disease	disorder_of_visual_system|nervous_system_disorder|hereditary_disease	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0014572	Lichtenstein-Knorr syndrome	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0014573	Cole-Carpenter syndrome 2	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	endocrinology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	brain_disorder|bone_disorder|eye_disorder	false	false	false	false	high
MONDO:0014574	peeling skin-leukonuchia-acral punctate keratoses-cheilitis-knuckle pads syndrome	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|joint_disorder	true	false	false	false	medium
MONDO:0014575	Singleton-Merten syndrome 2	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|connective_tissue_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|connective_tissue_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0014576	lipoyl transferase 1 deficiency	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	endocrinology|pediatric|metabolic__assumed_to_be_implied_by_hepatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0014577	short-rib thoracic dysplasia 13 with or without polydactyly	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|respiratory_system_disorder|urinary_system_disorder	other	urinary_system_disorder|musculoskeletal_system_disorder|hereditary_disease|respiratory_system_disorder|syndromic_disease	orthopaedic|pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	short_rib_polydactyly_syndrome_is_also_known_as__skeletal_disorder|bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0014578	congenital myasthenic syndrome 17	syndromic_disease|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014579	Senior-Loken syndrome 8	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	psychiatry|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0014580	intellectual disability, autosomal dominant 33	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014581	congenital myasthenic syndrome 2A	syndromic_disease|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014582	congenital myasthenic syndrome 2C	syndromic_disease|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014583	congenital myasthenic syndrome 3A	syndromic_disease|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014584	congenital myasthenic syndrome 3B	syndromic_disease|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	true	high
MONDO:0014585	congenital myasthenic syndrome 3C	syndromic_disease|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014586	congenital myasthenic syndrome 4B	syndromic_disease|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014587	congenital myasthenic syndrome 9	syndromic_disease|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014588	congenital myasthenic syndrome 11	syndromic_disease|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	true	high
MONDO:0014589	maturity-onset diabetes of the young type 13	hereditary_disease|digestive_system_disorder|metabolic_disease|endocrine_system_disorder	diabetes_mellitus|endocrine_system_disorder|metabolic_disease	digestive_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder	endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	endocrine_disorder|immune_disorder	false	false	true	true	medium
MONDO:0014590	congenital myasthenic syndrome 18	syndromic_disease|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014591	autosomal dominant Robinow syndrome 2	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|anemia|metabolic_disorder	skin_disorder|bone_disorder|vascular_disorder|joint_disorder|eye_disorder	false	false	false	false	medium
MONDO:0014592	microcephaly and chorioretinopathy 3	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|inflammatory_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	true	false	false	false	high
MONDO:0014593	developmental and epileptic encephalopathy, 29	hereditary_disease|nervous_system_disorder|metabolic_disease	neurodegenerative_disease|metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	epileptic_encephalopathy|neurodegenerative_disease|developmental_disorder	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0014594	autosomal dominant nonsyndromic hearing loss 67	hereditary_disease|psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0014595	developmental and epileptic encephalopathy, 30	syndromic_disease|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease	pediatric|neurology|genetics_and_genomics	epileptic_disorder|neurodegenerative_disease|developmental_disorder	brain_disorder|epileptic_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0014596	lissencephaly 7 with cerebellar hypoplasia	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|cerebellar_hyplasia	false	false	false	false	very_high
MONDO:0014597	immunodeficiency 39	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	immunology|allergy_and_immunology	immunodeficiency|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0014598	developmental and epileptic encephalopathy, 31A	syndromic_disease|hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease|syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|developmental_disorder	brain_disorder|epileptic_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0014599	intellectual disability, autosomal dominant 34	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	autosomal_dominant|brain_disorder	false	false	false	false	high
MONDO:0014600	dyskeratosis congenita, autosomal recessive 6	cancer_or_benign_tumor|hereditary_disease|syndromic_disease|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|dermatology|pediatric	metabolic_disorder|anemia	skin_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0014601	autosomal recessive spinocerebellar ataxia 20	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014602	Hogue-Janssens syndrome 1	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|syndromic_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|immune_disorder|skeletal_rack_disorder|bone_disorder	false	false	false	false	high
MONDO:0014603	autosomal dominant nonsyndromic hearing loss 40	auditory_system_disorder|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|auditory_system_disorder|psychiatric_disorder	genetics_and_genomics|otolaryngology|pediatric	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases|metabolic_disorder	ear_disorder	false	false	false	true	high
MONDO:0014604	Parkinson disease 21	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0014605	Houge-Janssens syndrome 2	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases|metabolic_disorder	immune_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0014606	intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|syndromic_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	eye_disorder|behavioral_abnormalities_syndrome_is_not_an_actual_category_so_i_am_removing_that_one_from_the_list|brain_disorder	false	false	false	false	very_high
MONDO:0014607	developmental and epileptic encephalopathy, 32	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0014608	mandibulofacial dysostosis with alopecia	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	other	integumentary_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|otolaryngology|dermatology|pediatric	inflammatory_disease|autoimmune_diseases	teeth_disorder|bone_disorder	false	false	false	false	high
MONDO:0014609	cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	cardiology|neurology|orthopaedic|genetics_and_genomics|endocrinology|pediatric|pulmonology	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	skeletal_dysplasia|heart_disorder|bone_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0014611	multiple mitochondrial dysfunctions syndrome 4	disorder_of_visual_system|hereditary_disease|metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease	neurodegenerative_disease|metabolic_disease	disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region|mitochondrial_disease|nervous_system_disorder|metabolic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|mitochondrial_dysfunction_is_not_in_the_list_so_this_is_as_good_as_it_gets	false	false	false	false	very_high
MONDO:0014612	pulmonary fibrosis and/or bone marrow failure, Telomere-related, 4	respiratory_system_disorder|premature_aging_syndrome|hereditary_disease	other	hereditary_disease|premature_aging_syndrome|respiratory_system_disorder	pulmonology|genetics_and_genomics|hematology	cancer|anemia	lung_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0014613	pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3	respiratory_system_disorder|cancer_or_benign_tumor|premature_aging_syndrome|hereditary_disease|syndromic_disease|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|hereditary_disease|syndromic_disease|premature_aging_syndrome|respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|genetics_and_genomics|hematology	cancer|metabolic_disorder|autoimmune_diseases|anemia|inflammatory_disease	lung_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0014614	congenital stationary night blindness 1G	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|ophthalmology|neurology	neurodegenerative_disease|congenital_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0014615	trichothiodystrophy 2, photosensitive	hereditary_disease|metabolic_disease|syndromic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|hereditary_disease|syndromic_disease|radiation_induced_disorder|metabolic_disease	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0014617	intellectual disability, autosomal dominant 38	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0014618	retinitis pigmentosa 71	disorder_of_visual_system|hereditary_disease|metabolic_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0014619	trichothiodystrophy 3, photosensitive	hereditary_disease|metabolic_disease|syndromic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|hereditary_disease|syndromic_disease|radiation_induced_disorder|metabolic_disease	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	hair_disorder|skin_disorder	false	false	false	false	high
MONDO:0014620	myoclonic dystonia 26	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014621	Brugada syndrome 9	hereditary_disease|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|syndromic_disease	cardiothoracic|cardiology|genetics_and_genomics	cardiovascular_disorder|cardiac	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0014622	isolated focal non-epidermolytic palmoplantar keratoderma	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immunodeficiency_related_disorder|genodermatosis|skin_disorder	false	false	false	true	medium
MONDO:0014623	microcephaly 14, primary, autosomal recessive	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0014624	Brown syndrome	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|ophthalmology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|anemia	eye_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0014625	developmental and epileptic encephalopathy, 33	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|epileptic_encephalopathy|developmental_disorder|metabolic_disorder|inflammatory_disease	epileptic_disorder|developmental_disorder|brain_disorder|spinal_disorder|encephalopathy	false	false	false	false	very_high
MONDO:0014626	spinocerebellar ataxia type 41	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|cerebellar_disorder|spinal_cord_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014627	dystonia 27	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014628	basal ganglia calcification, idiopathic, 6	hereditary_disease|nervous_system_disorder	other	idiopathic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014629	autoimmune interstitial lung disease-arthritis syndrome	connective_tissue_disorder|respiratory_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|connective_tissue_disorder|syndromic_disease|respiratory_system_disorder	rheumatology|pulmonology|allergy_and_immunology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder|joint_disorder	false	false	false	true	very_high
MONDO:0014630	familial adenomatous polyposis 3	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	oncology|genetics_and_genomics|gastroenterology	familial_adenomatous_polyposis_fits_into_this_category|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0014631	hypomagnesemia, seizures, and intellectual disability	hereditary_disease|metabolic_disease|urinary_system_disorder	metabolic_disease	hereditary_disease|metabolic_disease|urinary_system_disorder	pediatrics|genetics_and_genomics|endocrinology|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	endocrine_disorder|brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014632	hypomyelinating leukodystrophy 10	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014633	epilepsy with myoclonic atonic seizures	hereditary_disease|nervous_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0014634	46,XY sex reversal 10	musculoskeletal_system_disorder|hereditary_disease|reproductive_system_disorder|cardiovascular_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder|cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease|endocrine_system_disorder|musculoskeletal_system_disorder|reproductive_system_disorder	urology|genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0014635	microphthalmia, isolated, with coloboma 10	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|genetics_and_genomics|ophthalmology	metabolic_disorder|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0014636	combined oxidative phosphorylation defect type 25	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease	pediatrics|genetics_and_genomics|metabolic_disorders	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014637	DOCK2 deficiency	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0014638	Fanconi anemia complementation group T	immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease|hematologic_disorder|disorder_of_development_or_morphogenesis	anemia|metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder|hematologic_disorder|immune_system_disorder	genetics_and_genomics|hematology	metabolic_disorder|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0014639	familial temporal lobe epilepsy 7	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	familial_temporal_lobe_epilepsy_is_not_in_the_list_so_it_s_excluded|mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0014640	frontotemporal dementia and/or amyotrophic lateral sclerosis 3	hereditary_disease|metabolic_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|metabolic_disease|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder	psychiatry|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014641	frontotemporal dementia and/or amyotrophic lateral sclerosis 4	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014642	candidiasis, familial, 9	immune_system_disorder|hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|immune_system_disorder	dermatology|pediatrics|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	immune_disorder|other____note__i_corrected_the_response_to_remove__other__since_it_was_part_of_the_original_instruction|skin_disorder	true	false	false	true	medium
MONDO:0014643	congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	eye_disorder|brain_disorder|muscle_disorder|skin_disorder	true	false	false	false	very_high
MONDO:0014644	hereditary spastic paraplegia 74	hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014645	BENTA disease	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	pediatric|cardiology|hepatology|gastroenterology|genetics_and_genomics|cardiology_is_incorrect__replace_with__pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0014646	Zimmermann-Laband syndrome 2	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|ear_disorder	false	false	false	false	high
MONDO:0014647	developmental and epileptic encephalopathy, 50	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	pediatric|genetics_and_genomics|neurology	developmental_disorder|epileptic_disease|inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014648	Al-Raqad syndrome	hereditary_disease|metabolic_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder	pediatrics|genetics_and_genomics|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0014649	intellectual disability, autosomal recessive 50	hereditary_disease|metabolic_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder	pediatric|genetics_and_genomics|psychiatry|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|autosomal_recessive_disorder	false	false	false	false	high
MONDO:0014650	familial temporal lobe epilepsy 8	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	epilepsy|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0014651	acrofacial dysostosis Cincinnati type	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	genetic_disorder|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0014652	exudative vitreoretinopathy 6	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology	cancer|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0014653	retinitis pigmentosa 72	hereditary_disease|disorder_of_visual_system|metabolic_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|metabolic_disease	psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder|metabolic_disease	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0014654	Ullrich congenital muscular dystrophy 2	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	genetics_and_genomics|neurology	muscular_dystrophy_is_not_an_option_but_i_assume_this_is_the_closest_match_to_ullrich_congenital_muscular_dystrophy_2__however__it_s_not_in_the_provided_list_so_it_can_t_be_used|metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014656	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2	hereditary_disease|metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|nervous_system_disorder|metabolic_disease|musculoskeletal_system_disorder	ophthalmology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014657	primary ciliary dyskinesia 32	respiratory_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease|respiratory_system_disorder	genetics_and_genomics|pulmonology|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|spinal_disorder|brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014658	severe achondroplasia-developmental delay-acanthosis nigricans syndrome	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|dermatology|genetics_and_genomics|orthopaedic	developmental_disorder|metabolic_disorder|acanthosis_nigricans_syndrome___note__acanthosis_nigricans_syndrome_is_a_rare_skin_condition_that_can_be_associated_with_various_underlying_conditions__including_genetic_disorders_and_metabolic_syndromes|neurodegenerative_disease|inflammatory_disease	skin_disorder|joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0014659	infantile liver failure syndrome 2	hereditary_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|digestive_system_disorder	pediatric|hepatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	biliary_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0014660	microcephaly 15, primary, autosomal recessive	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0014661	epidermolysis bullosa simplex with nail dystrophy	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	skin_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014662	congenital insensitivity to pain-hypohidrosis syndrome	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatrics	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	skin_disorder|nerve_disorder|immune_disorder	false	false	false	false	high
MONDO:0014663	Silver-Russell syndrome 3	hereditary_disease|chromosomal_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|chromosomal_disorder	pediatric|genetics_and_genomics|endocrinology	genetic_disorder|metabolic_disorder|genetic_disorder___corrected_answer___metabolic_disorder	endocrine_disorder|growth_disorder	false	false	false	false	high
MONDO:0014664	Joubert syndrome 23	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014665	Charcot-Marie-Tooth disease axonal type 2V	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|orthopaedic	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014666	hypomyelinating leukodystrophy 11	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014667	cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3	hereditary_disease|metabolic_disease|musculoskeletal_system_disorder|cardiovascular_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|musculoskeletal_system_disorder	pediatric|cardiology|genetics_and_genomics|neurology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0014668	cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4	hereditary_disease|metabolic_disease|musculoskeletal_system_disorder|cardiovascular_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|musculoskeletal_system_disorder	pediatric|cardiology|genetics_and_genomics|neurology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0014669	cone-rod dystrophy 21	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0014670	lethal congenital contracture syndrome 9	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014671	neuropathy, hereditary motor and sensory, type 6B	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	hereditary_condition|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014672	osteogenesis imperfecta type 17	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	genetic_disorder|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder|teeth_disorder	false	false	false	false	high
MONDO:0014673	cataract 44	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0014674	maturity-onset diabetes of the young type 14	hereditary_disease|metabolic_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|metabolic_disease|diabetes_mellitus	hereditary_disease|endocrine_system_disorder|metabolic_disease|digestive_system_disorder	genetics_and_genomics|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|immune_disorder	false	false	true	true	medium
MONDO:0014675	autosomal recessive nonsyndromic hearing loss 104	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	false	medium
MONDO:0014676	Emery-Dreifuss muscular dystrophy 3, autosomal recessive	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|rheumatology|neurology|orthopaedic	metabolic_disorder|neurodegenerative_disease	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0014677	achromatopsia 7	psychiatric_disorder|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	genetics_and_genomics|ophthalmology|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0014678	intellectual disability, autosomal dominant 39	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	high
MONDO:0014679	polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology|orthopaedic	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014681	thyroid cancer, nonmedullary, 4	cancer_or_benign_tumor|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	thyroid_cancer__nonmedullary|cancer	thyroid_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0014682	thyroid cancer, nonmedullary, 5	cancer_or_benign_tumor|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	oncology|general_surgery|endocrinology	thyroid_cancer|cancer	endocrine_disorder	false	true	false	true	medium
MONDO:0014683	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology|orthopaedic	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014684	combined oxidative phosphorylation defect type 26	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	genetics_and_genomics|pediatrics	energy_production_disorder|mitochondrial_disease|genetic_disorder|metabolic_disorder|inherited_metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014685	progressive myoclonic epilepsy type 9	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	genetic_disorder|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014686	short stature, microcephaly, and endocrine dysfunction	syndromic_disease|hereditary_disease|reproductive_system_disorder|musculoskeletal_system_disorder|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|syndromic_disease|endocrine_system_disorder|musculoskeletal_system_disorder|reproductive_system_disorder	pediatric|genetics_and_genomics|neurology|endocrinology	endocrine_dysfunction|metabolic_disorder|adrenal_gland_disease	endocrine_disorder|bone_disorder	false	false	false	false	medium
MONDO:0014687	retinitis pigmentosa 73	psychiatric_disorder|disorder_of_visual_system|hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|metabolic_disease	genetics_and_genomics|ophthalmology|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0014688	short-rib thoracic dysplasia 14 with polydactyly	syndromic_disease|respiratory_system_disorder|hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|urinary_system_disorder	neurodegenerative_disease	hereditary_disease|urinary_system_disorder|syndromic_disease|nervous_system_disorder|respiratory_system_disorder|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	genetic_disorder|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0014689	Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|otolaryngology|genetics_and_genomics|neurology|orthopaedic	metabolic_disorder|neurodegenerative_disease	muscle_disorder|bone_disorder|facial_dysmorphism_is_not_in_the_category_list_so_it_will_be_omitted	false	false	false	false	high
MONDO:0014690	dyskeratosis congenita, autosomal dominant 6	cancer_or_benign_tumor|syndromic_disease|hereditary_disease|premature_aging_syndrome|integumentary_system_disorder|hematologic_disorder	cancer_or_benign_tumor	integumentary_system_disorder|hereditary_disease|syndromic_disease|premature_aging_syndrome|cancer_or_benign_tumor|hematologic_disorder	pediatric|dermatology|genetics_and_genomics	metabolic_disorder|anemia|neurodegenerative_disease	skin_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0014691	Noonan syndrome 9	syndromic_disease|hereditary_disease|immune_system_disorder|musculoskeletal_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	immune_system_disorder|cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	pediatric|cardiology|genetics_and_genomics|pulmonology|endocrinology	cardiovascular_disorder|metabolic_disorder	joint_disorder|lymphatic_disorder|heart_disorder	false	false	false	false	medium
MONDO:0014692	retinitis pigmentosa 74	psychiatric_disorder|disorder_of_visual_system|hereditary_disease|metabolic_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|metabolic_disease	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0014693	Noonan syndrome 10	disorder_of_development_or_morphogenesis|cardiovascular_disorder|immune_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|cardiovascular_disorder|immune_system_disorder|disorder_of_development_or_morphogenesis	cardiology|genetics_and_genomics|pediatric	metabolic_disorder|cardiovascular_disorder	joint_disorder|bone_disorder|heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0014694	spondylocostal dysostosis 6, autosomal recessive	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|genetic_disorder|skeletal_dysplasia___corrected_to___skeletal_dysplasia_is_replaced_by_a_more_specific_classification__metabolic_disorder	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0014696	cerebrooculofacioskeletal syndrome 3	disorder_of_visual_system|hereditary_disease|syndromic_disease|metabolic_disease	metabolic_disease	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|syndromic_disease|metabolic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	eye_disorder|bone_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0014697	immunodeficiency, common variable, 12	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	hereditary_disease|hematologic_disorder|syndromic_disease|immune_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|pediatric|allergy_and_immunology|immunology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0014698	microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	ear_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014699	intellectual disability, autosomal dominant 40	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0014700	Au-Kline syndrome	nervous_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	ear_disorder|muscle_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0014701	spondyloepiphyseal dysplasia, Stanescu type	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|connective_tissue_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|connective_tissue_disorder|hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0014702	autosomal recessive complex spastic paraplegia type 9B	nervous_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014703	Adams-Oliver syndrome 6	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|neurology|genetics_and_genomics	genetic_disorder|metabolic_disorder|neurodegenerative_disease	skeletal_disorder|congenital_abnormality___note__this_categorization_is_based_on_the_available_information_about_adams_oliver_syndrome__which_involves_abnormalities_of_the_skin_and_bones__often_in_combination_with_other_systemic_features__the_categories_listed_above_best_match_these_characteristics|bone_disorder	false	false	false	false	high
MONDO:0014704	skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|neurology|orthopaedic|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	joint_disorder|spinal_disorder|bone_disorder|skin_disorder	false	false	false	false	high
MONDO:0014705	craniosynostosis 6	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|neurology|orthopaedic	metabolic_disorder|neurodegenerative_disease	brain_disorder|bone_disorder	false	false	false	false	high
MONDO:0014706	cutis laxa, autosomal dominant 3	integumentary_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases|cardiovascular_disorder|neurodegenerative_disease	muscle_disorder|skin_disorder	false	false	false	false	high
MONDO:0014707	14q32 duplication syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|neurology|genetics_and_genomics	other___note__14q32_duplication_syndrome_is_a_rare_genetic_disorder_associated_with_neurodevelopmental_abnormalities_and_intellectual_disability__so_it_fits_into_the_category_of_neurodegenerative_disease__however__as_duplication_syndromes_often_have_overlapping_characteristics_across_different_categories__it_s_also_classified_under__other__due_to_its_complex_presentation|neurodegenerative_disease	brain_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0014708	ring chromosome 14	chromosomal_disorder	other	chromosomal_disorder	oncology|genetics_and_genomics	metabolic_disorder|cancer|neurodegenerative_disease	blood_bone_marrow_disorder|genetic_disorder	false	true	false	false	high
MONDO:0014711	autosomal dominant Charcot-Marie-Tooth disease type 2W	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	nerve_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014712	Senior-Loken syndrome 9	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	psychiatry|neurology	metabolic_disorder|neurodegenerative_disease	senior_loken_syndrome_is_not_a_real_medical_condition__but_i_assume_you_meant__sundowner_s_syndrome__which_can_affect_seniors_experiencing_dementia___brain_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0014713	porokeratosis 9, multiple types	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|skin_disorder	false	false	false	false	high
MONDO:0014714	progressive microcephaly-seizures-cortical blindness-developmental delay syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|developmental_delay_syndrome	brain_disorder|developmental_delay|eye_disorder|seizures	false	false	false	false	very_high
MONDO:0014715	primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatric|allergy_and_immunology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder	true	false	false	true	very_high
MONDO:0014716	macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	lung_disorder|brain_disorder|neurodevelopmental_disorder	true	false	false	true	very_high
MONDO:0014717	early-onset Lafora body disease	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0014718	developmental and epileptic encephalopathy, 34	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	developmental_disorder|neurodegenerative_disease|epileptic_disease	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0014719	developmental and epileptic encephalopathy, 35	nervous_system_disorder|metabolic_disease|hereditary_disease	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|developmental_disorder|neurodegenerative_disease|epileptic_disease	note__the_actual_disease_name_in_the_prompt_was_developmental_and_epileptic_encephalopathy__35__which_appears_to_be_a_duplicate_entry|brain_disorder|spinal_disorder|developmental_and_epileptic_encephalopathy	false	false	false	true	very_high
MONDO:0014720	autosomal dominant optic atrophy plus syndrome	nervous_system_disorder|disorder_of_visual_system|mitochondrial_disease|hereditary_disease	neurodegenerative_disease	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|mitochondrial_disease|nervous_system_disorder	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0014722	Roifman syndrome	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|immune_system_disorder|hereditary_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0014723	PMP22-RAI1 contiguous gene duplication syndrome	chromosomal_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|chromosomal_disorder|hereditary_disease	psychiatry|pediatric|neurology|genetics_and_genomics	genetic_disorder|neurodegenerative_disease	nerve_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014724	Joubert syndrome 24	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0014725	spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014726	Charcot-Marie-Tooth disease axonal type 2X	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014727	immunodeficiency 45	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatric|allergy_and_immunology|pulmonology|immunology	inflammatory_disease|immunodeficiency|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	true	false	false	true	high
MONDO:0014728	combined oxidative phosphorylation defect type 27	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|liver_disorder	false	false	false	false	very_high
MONDO:0014729	hereditary spastic paraplegia 75	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|syndromic_disease|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014730	microcephaly 16, primary, autosomal recessive	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014731	seizures-scoliosis-macrocephaly syndrome	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0014732	hypomyelinating leukodystrophy 12	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014733	Charcot-Marie-Tooth disease type 4K	nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	metabolic_disease	nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|peripheral_nerve_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014735	Charcot-Marie-Tooth disease type 2Y	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	nerve_disorder|muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014736	Charcot-Marie-Tooth disease axonal type 2Z	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|cardiovascular_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014737	dehydrated hereditary stomatocytosis 2	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	pediatric|hematology|genetics_and_genomics	metabolic_disorder|anemia	hereditary_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0014738	autosomal dominant nonsyndromic hearing loss 69	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	otolaryngology|pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0014739	autosomal recessive nonsyndromic hearing loss 97	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease|auditory_system_disorder	otolaryngology|pediatric|genetics_and_genomics	metabolic_disorder|autosomal_recessive_condition	ear_disorder	false	false	false	false	medium
MONDO:0014740	autosomal dominant nonsyndromic hearing loss 68	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease|auditory_system_disorder	genetics_and_genomics|pediatric|otolaryngology	autosomal_dominant|neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	true	medium
MONDO:0014741	DeSanto-Shinawi syndrome due to WAC point mutation	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatrics|obstetrics_and_gynecology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0014742	Parkinson disease 22, autosomal dominant	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autosomal_dominant_disorders__note__this_is_a_subcategory_implied_by_the_provided_information	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014743	rhizomelic chondrodysplasia punctata type 5	syndromic_disease|metabolic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_visual_system|nervous_system_disorder	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease	genetics_and_genomics|pediatric|dermatology	neurodegenerative_disease|metabolic_disorder	skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0014744	acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome	syndromic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|acute_disease|hereditary_disease|syndromic_disease	hepatology|genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|liver_disorder|muscle_disorder	true	false	false	false	very_high
MONDO:0014745	congenital myasthenic syndrome 19	syndromic_disease|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014746	SLC39A8-CDG	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|nervous_system_disorder	false	false	false	true	high
MONDO:0014747	familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome	syndromic_disease|hereditary_disease|disorder_of_visual_system	other	hereditary_disease|syndromic_disease|disorder_of_visual_system	ophthalmology|genetics_and_genomics|pediatric	congenital_disorder|neurodegenerative_disease	eye_disorder|congenital_disorder	false	false	false	false	high
MONDO:0014748	progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0014749	tooth agenesis, selective, 7	hereditary_disease|musculoskeletal_system_disorder	other	mouth_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	anemia|inflammatory_disease|metabolic_disorder|autoimmune_diseases	teeth_disorder	false	false	false	true	medium
MONDO:0014750	primary ciliary dyskinesia 33	syndromic_disease|respiratory_system_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|respiratory_system_disorder	pulmonology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder|eye_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014751	palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	facial_dysmorphism|palatal_anomalies|developmental_delay|metabolic_disorder	teeth_disorder|facial_dysmorphism|developmental_delay_syndrome	false	false	false	false	very_high
MONDO:0014752	nephrotic syndrome, type 11	syndromic_disease|urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder|syndromic_disease|idiopathic_disease	renal_medicine|pediatrics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0014754	primary coenzyme Q10 deficiency 8	nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology|cardiology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	liver_disorder|heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014755	skin creases, congenital symmetric circumferential, 2	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	congenital_symmetric_circumferential_skin_folds|congenital_skin_folding_disorder	skin_disorder|developmental_disorder|congenital_disorder	false	false	false	false	low
MONDO:0014756	tremor, hereditary essential, 5	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|hereditary_essential_fits_into_category___neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0014757	macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome	syndromic_disease|hematologic_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|hematologic_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	hematology|genetics_and_genomics|pediatric	anemia|developmental_delay|metabolic_disorder	lymphatic_disorder|blood_bone_marrow_disorder|joint_disorder|developmental_delay	false	false	false	false	high
MONDO:0014758	radioulnar synostosis with amegakaryocytic thrombocytopenia 2	hematologic_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|hematologic_disorder	genetics_and_genomics|hematology	anemia|autoimmune_diseases|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder|joint_disorder	false	false	false	false	high
MONDO:0014759	intellectual disability, autosomal recessive 51	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	psychiatric_disorder|metabolic_disease	nervous_system_disorder|psychiatric_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatrics	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014760	TFRC-related combined immunodeficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|immunology|pediatric	anemia|metabolic_disorder|autoimmune_diseases	immune_disorder_lymphatic_disorder_blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0014762	heterotaxy, visceral, 7, autosomal	disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|visceral____note__i_assumed__visceral__refers_to_a_type_of_heterotaxy__which_is_a_congenital_defect_affecting_the_position_of_organs_in_the_body__it_s_often_classified_as_a_type_of_metabolic_disorder_or_visceral_anomaly	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0014764	spastic paraplegia-severe developmental delay-epilepsy syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric|neurology	epilepsy_syndrome|neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	true	false	false	false	very_high
MONDO:0014765	wooly hair, autosomal recessive 3	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|pediatric	genetic_disease|metabolic_disorder	hair_disorder|skin_disorder	false	false	false	false	low
MONDO:0014766	leukodystrophy and acquired microcephaly with or without dystonia;	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014767	Seckel syndrome 9	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|pediatric	genetic_disorder|metabolic_disorder	lymphatic_disorder|muscle_disorder|immune_disorder|bone_disorder|eye_disorder|joint_disorder	false	false	false	false	high
MONDO:0014768	cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2	syndromic_disease|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|neurology	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0014769	inherited oocyte maturation defect	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|pediatric|obstetrics_and_gynecology	neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder	false	false	false	false	high
MONDO:0014770	Joubert syndrome 25	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014771	Joubert syndrome 26	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014772	orofacial cleft 15	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	teeth_disorder|oral_disorder	false	false	false	false	medium
MONDO:0014773	cardiac anomalies - developmental delay - facial dysmorphism syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|psychiatric_disorder|cardiovascular_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|cardiovascular_disorder	psychiatric_disorder|nervous_system_disorder|cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric|cardiology	facial_dysmorphism_syndrome_is_not_in_the_list__use__developmental_delay|cardiovascular_disorder|developmental_delay	heart_disorder|facial_dysmorphism_syndrome|developmental_delay	false	false	false	true	very_high
MONDO:0014774	neuroblastoma, susceptibility to, 7	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology|oncology	cancer	brain_disorder|lymphatic_disorder|bone_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0014775	combined oxidative phosphorylation deficiency 28	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	genetics_and_genomics|pediatric|neurology|metabolism_is_not_listed_so_all_of_the_above_are_incorrect	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0014776	spinocerebellar ataxia type 42	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014777	hypotonia, infantile, with psychomotor retardation and characteristic facies 2	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|muscle_disorder|endocrine_disorder	true	false	false	true	very_high
MONDO:0014778	Lamb-Shaffer syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0014779	Wilms tumor 6	cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease	pediatric|oncology	adrenal_gland_disease|cancer	kidney_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0014780	hyperphosphatasia with intellectual disability syndrome 6	disorder_of_development_or_morphogenesis|syndromic_disease|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0014781	combined oxidative phosphorylation deficiency 29	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease|metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	mitochondrial_disease|liver_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014782	autosomal recessive limb-girdle muscular dystrophy type 2X	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014784	severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|cardiology|pediatrics	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|heart_disorder|muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0014785	microcephaly, short stature, and impaired glucose metabolism 2	hereditary_disease	other	hereditary_disease	genetics_and_genomics|endocrinology|pediatric	neurodegenerative_disease|metabolic_disorder	short_stature_is_also_related_to_endocrine_disorder|brain_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0014787	severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	cerebellar_ataxia_suggests_inflammatory_disease|neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014788	autosomal recessive limb-girdle muscular dystrophy type 2W	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|muscular_dystrophy	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014789	CCDC115-CDG	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder	false	false	false	true	high
MONDO:0014790	TMEM199-CDG	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014791	Luscan-Lumish syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|neurology|pediatrics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	liver_disorder|biliary_disorder____based_on__luscan_lumish_syndrome__being_a_rare_genetic_disorder_primarily_affecting_the_liver	false	false	false	false	high
MONDO:0014792	Paget disease of bone 6	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	rheumatology|orthopaedic	metabolic_disorder|cancer|inflammatory_disease	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	medium
MONDO:0014793	microcephaly-congenital cataract-psoriasiform dermatitis syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology|dermatology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0014794	Meier-Gorlin syndrome 6	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	bone_disorder|skeletal_disorder	false	false	false	false	high
MONDO:0014795	exercise intolerance, riboflavin-responsive	hereditary_disease	other	hereditary_disease	pulmonology|other____removed|cardiology	metabolic_disorder|riboflavin_responsive_is_typically_associated_with_a_specific_metabolic_disorder_so_this_seems_to_be_the_best_category	heart_disorder|muscle_disorder|endocrine_disorder	true	false	false	true	medium
MONDO:0014796	autosomal recessive early-onset Parkinson disease 23	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014797	lymphatic malformation 6	immune_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	immune_system_disorder|cardiovascular_disorder|hereditary_disease	pediatric|hematology|oncology	cancer|lymphatic_disorder	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0014798	brachydactyly type A1D	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic	congenital_condition|genetic_condition|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0014799	cataract 45	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0014800	progressive scapulohumeroperoneal distal myopathy	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	orthopaedic|neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014801	even-plus syndrome	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	psychiatry|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0014802	Cowden syndrome 7	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|oncology|genetics_and_genomics	neurodegenerative_disease|cancer	endocrine_disorder|skin_disorder	false	false	false	false	high
MONDO:0014803	spasticity-ataxia-gait anomalies syndrome	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	metabolic_disease	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|ataxia	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014804	sideroblastic anemia 3	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hematologic_disorder	anemia|metabolic_disease	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|hematologic_disorder|hereditary_disease	oncology|hematology|genetics_and_genomics	blood_disorder|anemia|cancer	blood_bone_marrow_disorder|bone_disorder	false	false	false	true	high
MONDO:0014805	Hao-Fountain syndrome	nervous_system_disorder	other	nervous_system_disorder	dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0014806	spinal muscular atrophy with congenital bone fractures 1	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	orthopaedic|pediatric|neurology|genetics_and_genomics	congenital_bone_fractures_is_not_in_the_list_so_it_s_excluded|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014807	spinal muscular atrophy with congenital bone fractures 2	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|congenital_bone_fractions_disorder	muscle_disorder|spinal_disorder|bone_disorder	false	false	false	true	very_high
MONDO:0014808	congenital secretory sodium diarrhea 8	hereditary_disease|digestive_system_disorder	other	hereditary_disease|digestive_system_disorder	pediatric|gastroenterology	adrenal_gland_disease|metabolic_disorder	upper_gastrointestinal_disorder|endocrine_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0014809	DDX41-related hematologic malignancy predisposition syndrome	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	oncology|hematology|genetics_and_genomics	cancer|hematologic_malignancy	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0014810	pancytopenia due to IKZF1 mutations	syndromic_disease|hereditary_disease|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	syndromic_disease|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|hereditary_disease	oncology|hematology|genetics_and_genomics	anemia|cancer	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0014811	cerebellar atrophy, visual impairment, and psychomotor retardation;	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	true	false	false	false	high
MONDO:0014813	hypomyelinating leukodystrophy 13	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014814	advanced sleep phase syndrome 3	hereditary_disease	other	sleep_disorder|hereditary_disease	endocrinology|neurology	neurodegenerative_disease|metabolic_disorder	endocrine_disorder_brain_disorder	false	false	false	false	medium
MONDO:0014815	intellectual disability, autosomal recessive 52	hereditary_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	immune_disorder|upper_gastrointestinal_disorder|urinary_tract_disorder|brain_disorder|kidney_disorder|liver_disorder|muscle_disorder|lower_gastrointestinal_disorder|spinal_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0014816	split-foot malformation-mesoaxial polydactyly syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	anemia|metabolic_disorder|inflammatory_disease|autoimmune_diseases	skin_disorder|spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0014817	nephrotic syndrome, type 12	syndromic_disease|hereditary_disease|urinary_system_disorder	other	syndromic_disease|hereditary_disease|idiopathic_disease|urinary_system_disorder	pediatric|renal_medicine|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014818	nephrotic syndrome, type 13	syndromic_disease|hereditary_disease|urinary_system_disorder	other	syndromic_disease|hereditary_disease|idiopathic_disease|urinary_system_disorder	pediatric|renal_medicine	metabolic_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|kidney_disorder	false	false	false	false	high
MONDO:0014819	autosomal dominant Robinow syndrome 3	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	medical_genetics|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder|eye_disorder	false	false	false	false	medium
MONDO:0014820	mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type)	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	neurology|cardiology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	brain_disorder|heart_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014821	complex lethal osteochondrodysplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	osteochondrodysplasia|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0014822	15q14 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014823	hypotonia, infantile, with psychomotor retardation and characteristic facies 3	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0014825	chromosome 11p13 deletion syndrome, distal	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	immune_disorder|vascular_disorder|blood_bone_marrow_disorder|muscle_disorder|spinal_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0014827	autosomal recessive spastic paraplegia type 76	syndromic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014828	immunodeficiency-centromeric instability-facial anomalies syndrome 3	hereditary_disease|premature_aging_syndrome	other	hereditary_disease|premature_aging_syndrome	immunology|genetics_and_genomics	cancer|metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0014829	immunodeficiency-centromeric instability-facial anomalies syndrome 4	hereditary_disease|premature_aging_syndrome	other	hereditary_disease|premature_aging_syndrome	pediatric|immunology|genetics_and_genomics	anemia|metabolic_disorder|autoimmune_diseases	immune_disorder|bone_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0014830	platelet-type bleeding disorder 20	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	pediatric|oncology|cardiology|genetics_and_genomics|gastroenterology|hematology	platelet_type_bleeding_disorder|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0014831	progeroid and marfanoid aspect-lipodystrophy syndrome	hereditary_disease|connective_tissue_disorder|disorder_of_development_or_morphogenesis|premature_aging_syndrome	other	disorder_of_development_or_morphogenesis|connective_tissue_disorder|hereditary_disease|premature_aging_syndrome	genetics_and_genomics|dermatology	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	vascular_disorder|skin_disorder|joint_disorder	false	false	false	false	high
MONDO:0014832	intellectual disability, autosomal recessive 53	hereditary_disease|syndromic_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	autosomal_recessive_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014833	heart and brain malformation syndrome	hereditary_disease	other	hereditary_disease	pediatric|neurology|cardiology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	brain_disorder|heart_disorder	false	false	false	false	high
MONDO:0014835	striatal degeneration, autosomal dominant 2	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease|neurodegenerative_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014836	Charcot-Marie-Tooth disease axonal type 2CC	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|orthopaedic|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014837	thrombocytopenia 6	musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|connective_tissue_disorder|hereditary_disease	pediatric|obstetrics_and_gynecology|hematology	anemia|metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0014838	Coffin-Siris syndrome 5	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|oncology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0014839	chorea, childhood-onset, with psychomotor retardation	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|childhood_onset_diseases	brain_disorder|spinal_disorder	true	false	false	true	very_high
MONDO:0014840	agammaglobulinemia 8, autosomal dominant	hereditary_disease|hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|autoimmune_diseases|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0014841	trichothiodystrophy 6, nonphotosensitive	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	syndromic_disease|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	genetic_disorder|skin_disorder	false	false	false	false	high
MONDO:0014842	intellectual disability, autosomal dominant 41	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|autosomal_dominant_disorders_are_typically_classified_under_this_category_so___autosomal_dominant_disorders_is_not_in_the_list_but_it_can_be_related_to_neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0014843	premature ovarian failure 11	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrinology|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0014844	premature ovarian failure 12	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrinology|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0014845	spinocerebellar ataxia, autosomal recessive 22	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014846	spinocerebellar ataxia, autosomal recessive 23	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014847	spermatogenic failure 15	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	anemia|adrenal_gland_disease|metabolic_disorder	reproductive_system_disorder|spermatogenic_failure	false	false	false	false	high
MONDO:0014848	TELO2-related intellectual disability-neurodevelopmental disorder	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|chromosomal_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|neurodevelopmental_disorder	false	false	false	false	high
MONDO:0014850	retinitis pigmentosa and erythrocytic microcytosis	hereditary_disease	other	hereditary_disease	ophthalmology|genetics_and_genomics|hematology	anemia|neurodegenerative_disease	blood_bone_marrow_disorder|eye_disorder	false	false	false	for_retinitis_pigmentosa__there_are_currently_no_cures__but_there_are_treatments_aimed_at_managing_symptoms_and_slowing_progression__for_example__vitamin_a_supplementation_has_shown_some_promise_in_slowing_vision_loss_in_certain_individuals__additionally__gene_therapy_has_emerged_as_a_potential_treatment_for_specific_genetic_forms_of_retinitis_pigmentosa___for_erythrocytic_microcytosis__which_can_be_caused_by_various_conditions__treatment_focuses_on_addressing_the_underlying_cause__such_as_iron_deficiency__iron_supplementation_can_effectively_treat_microcytic_anemia_due_to_iron_deficiency___therefore__since_efficacious_treatments_exist_for_both_conditions__the_answer_is_true	medium
MONDO:0014851	hypercalcemia, infantile, 2	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|pediatric|renal_medicine	endocrine_system_disorder|metabolic_disorder|electrolyte_imbalance	calcium_disorder_is_not_listed_but_kidney_disorder|endocrine_disorder	false	false	false	true	very_high
MONDO:0014853	autosomal dominant nonsyndromic hearing loss 70	hereditary_disease|nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	hearing_loss|ear_disorder	false	false	false	false	high
MONDO:0014854	autosomal dominant nonsyndromic hearing loss 66	hereditary_disease|nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	hearing_loss|ear_disorder	false	false	false	true	medium
MONDO:0014855	intellectual disability, autosomal dominant 42	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|intellectual_disability|autosomal_dominant	false	false	false	true	very_high
MONDO:0014856	combined oxidative phosphorylation defect type 30	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	hepatology|ophthalmology|pediatric|endocrinology|neurology|oncology|renal_medicine|pulmonology|cardiology|genetics_and_genomics|otolaryngology	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	mitochondrial_disorder|liver_disorder|genetic_disorder	false	false	false	false	high
MONDO:0014857	neurodevelopmental disorder with or without anomalies of the brain, eye, or heart	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	heart_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0014858	intellectual disability, autosomal dominant 43	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|intellectual_disability	false	false	false	false	high
MONDO:0014859	developmental and epileptic encephalopathy, 37	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	epileptic_disorder|neurodegenerative_disease|developmental_disorder	brain_disorder|developmental_and_epileptic_encephalopathy_belongs_to_this_category_as_its_name_suggests_it_is_related_to_brain_disorders_and_encephalopathies	false	false	false	true	very_high
MONDO:0014860	polycystic liver disease 2	hereditary_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|hereditary_disease	hepatology|endocrinology|gastroenterology	metabolic_disorder|inflammatory_disease	liver_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0014861	autoimmune disease, multisystem, infantile-onset, 2	immune_system_disorder|hereditary_disease	autoimmune_disease	immune_system_disorder|hereditary_disease	pediatric|immunology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|multisystem|autoimmune_disease	false	false	false	false	very_high
MONDO:0014862	cerebral palsy, spastic quadriplegic, 3	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|orthopaedic	spastic_quadrilegic|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014863	macrocephaly, dysmorphic facies, and psychomotor retardation	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0014864	hypermanganesemia with dystonia 2	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0014865	autosomal recessive severe congenital neutropenia due to CSF3R deficiency	immune_system_disorder|hereditary_disease|hematologic_disorder	other	immune_system_disorder|hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0014866	Charcot-Marie-Tooth disease axonal type 2T	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0014867	spinocerebellar ataxia 43	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014868	developmental and epileptic encephalopathy, 38	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	epileptic_encephalopathy|neurodegenerative_disease|developmental_disorder|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0014869	hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	pediatric|endocrinology|hematology|genetics_and_genomics|neonatology___corrected_answer____hematology	anemia|multisystemic_failure_syndrome_can_sometimes_be_classified_as_a_subset_of_metabolic_disorders_so_this_may_also_fit_under_metabolic_disorder_but_for_clarity_i_will_include_both|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder|endocrine_disorder	true	false	false	false	very_high
MONDO:0014870	NEK9-related lethal skeletal dysplasia	disorder_of_development_or_morphogenesis|respiratory_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	respiratory_system_disorder|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric	skeletal_dysplasia_is_not_a_category_in_the_list_but_nek9_related_lethal_skeletal_dysplasia_implies_it_could_be_related_to__neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder|skeletal_dysplasia	false	false	false	false	very_high
MONDO:0014871	retinitis pigmentosa 75	nervous_system_disorder|psychiatric_disorder|metabolic_disease|disorder_of_visual_system|hereditary_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|metabolic_disease|nervous_system_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014872	congenital stationary night blindness 1H	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder	ophthalmology|genetics_and_genomics|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0014873	nevus comedonicus syndrome	integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder	skin_disorder	false	false	false	false	low
MONDO:0014874	pontocerebellar hypoplasia, type 2F	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurodegenerative_disease	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014875	hyperaldosteronism, familial, type IV	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	renal_medicine|endocrinology	adrenal_gland_disease|cardiovascular_disorder|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0014876	intellectual disability, autosomal recessive 54	nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	autosomal_recessive_disorder_is_not_in_the_list_so_i_am_omitting_it|brain_disorder	false	false	false	false	high
MONDO:0014877	myopathy, distal, 5	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	orthopaedic|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|myopathy	false	false	false	false	high
MONDO:0014878	patent ductus arteriosus 2	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiology|pulmonology|pediatric	inflammatory_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0014880	Duane retraction syndrome 3 with or without deafness	nervous_system_disorder|syndromic_disease|disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|syndromic_disease|nervous_system_disorder	ophthalmology|genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	ear_disorder|eye_disorder	false	false	false	false	medium
MONDO:0014881	transketolase deficiency	cardiovascular_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	cardiovascular_disorder|metabolic_disease	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0014882	hereditary spastic paraplegia 77	nervous_system_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	neurodegenerative_disease|metabolic_disease	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014883	hypertrophic cardiomyopathy 26	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014884	cholestasis, progressive familial intrahepatic, 5	syndromic_disease|endocrine_system_disorder|digestive_system_disorder|metabolic_disease|hereditary_disease	endocrine_system_disorder|metabolic_disease	hereditary_disease|endocrine_system_disorder|metabolic_disease|digestive_system_disorder|syndromic_disease	hepatology|gastroenterology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0014885	Hermansky-Pudlak syndrome 10	syndromic_disease|integumentary_system_disorder|hematologic_disorder|metabolic_disease|hereditary_disease	metabolic_disease	hematologic_disorder|hereditary_disease|integumentary_system_disorder|metabolic_disease|syndromic_disease	genetics_and_genomics|pediatrics	neurodegenerative_disease|anemia|metabolic_disorder	joint_disorder|blood_bone_marrow_disorder|eye_disorder|immune_disorder	false	false	false	false	high
MONDO:0014886	severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	ophthalmology|genetics_and_genomics|neurology|endocrinology|pediatric|dermatology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	skin_disorder|eye_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0014887	bone marrow failure syndrome 3	hematologic_disorder|immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|immune_system_disorder|hematologic_disorder|hereditary_disease	hematology|pediatric|oncology	anemia|blood|cancer|metabolic_disorder	blood_bone_marrow_disorder|bone_disorder	false	false	false	true	high
MONDO:0014888	MIRAGE syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	neurology|psychiatry	neurodegenerative_disease|autoimmune_diseases	immune_disorder|upper_gastrointestinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014889	striatonigral degeneration, childhood-onset	nervous_system_disorder|metabolic_disease|hereditary_disease	neurodegenerative_disease|metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0014890	PERCHING syndrome	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|pulmonology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	bone_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014891	hyperuricemic nephropathy, familial juvenile type 4	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	genetics_and_genomics|renal_medicine|pediatric	kidney_disease|metabolic_disorder	joint_disorder|kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0014892	micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	teeth_disorder|mild_intellectual_disability|immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0014893	Okur-Chung neurodevelopmental syndrome	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014894	Meier-Gorlin syndrome 7	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|skeletal_r_system_disorder	false	false	false	false	high
MONDO:0014895	developmental and epileptic encephalopathy, 40	hereditary_disease|nervous_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|developmental_and_epileptic_encephalopathy_is_more_closely_associated_with_neurodevelopmental_disorders_which_can_also_be_classified_as_a_type_of_neurodegenerative_disorder_or_sometimes_a_category_on_its_own_however_in_this_list_the_closest_matches_would_be|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0014896	congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|orthopaedic|pulmonology|pediatric|dermatology	neurodegenerative_disease|metabolic_disorder	joint_disorder|skin_disorder|lung_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014898	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease|musculoskeletal_system_disorder|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|nervous_system_disorder	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014899	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease|musculoskeletal_system_disorder|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014900	autosomal recessive limb-girdle muscular dystrophy type 2Y	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	neurology|genetics_and_genomics|orthopaedic	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease|anemia	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014901	tooth agenesis, selective, 8	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	genetics_and_genomics|oral_surgery|pediatric	autoimmune_diseases|metabolic_disorder|anemia	teeth_disorder	false	false	false	false	medium
MONDO:0014902	nasopharyngeal carcinoma, susceptibility to, 3	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	oncology|otolaryngology	allergy|cancer	lymphatic_disorder|throat_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0014903	seizures, benign familial infantile, 5	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0014904	congenital disorder of glycosylation, type IAA	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	other___note__the_category_list_is_not_exhaustive_for_this_disease__as_congenital_disorder_of_glycosylation__cdg__type_ia_can_manifest_in_various_systems_and_organs__however__considering_the_specific_type__liver_disorder_is_a_well_documented_manifestation_of_cdg_ia|liver_disorder	false	false	true	false	high
MONDO:0014905	encephalopathy due to defective mitochondrial and peroxisomal fission 2	metabolic_disease|hereditary_disease|nervous_system_disorder|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0014906	Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014907	short-rib thoracic dysplasia 15 with polydactyly	syndromic_disease|hereditary_disease|respiratory_system_disorder|musculoskeletal_system_disorder|urinary_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|respiratory_system_disorder|urinary_system_disorder	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0014908	microcephaly 17, primary, autosomal recessive	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0014909	primary ciliary dyskinesia 34	syndromic_disease|hereditary_disease|respiratory_system_disorder	other	hereditary_disease|syndromic_disease|respiratory_system_disorder	neurology|genetics_and_genomics|pediatric|pulmonology	metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014910	primary ciliary dyskinesia 35	syndromic_disease|hereditary_disease|respiratory_system_disorder	other	hereditary_disease|syndromic_disease|respiratory_system_disorder	neurology|genetics_and_genomics|pulmonology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0014911	growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	hepatology|neurology|endocrinology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease|hepatopathy_is_often_associated_with_several_categories_but_i_ll_exclude__hepatopathy__since_it_was_part_of_the_original_disease_description__thus__metabolic_disorder	growth_retardation_disorder|endocrine_disorder|brain_disorder|liver_disorder	true	false	false	true	very_high
MONDO:0014912	autoinflammation, panniculitis, and dermatosis syndrome, autosomal recessive	syndromic_disease|immune_system_disorder|hereditary_disease|connective_tissue_disorder	other	hereditary_disease|syndromic_disease|connective_tissue_disorder|immune_system_disorder	allergy_and_immunology|dermatology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|liver_disorder	false	false	false	false	high
MONDO:0014914	Dias-Logan syndrome	hereditary_disease	other	hereditary_disease	cardiology|pulmonology	cardiovascular_disorder|neurodegenerative_disease	joint_disorder|lower_gastrointestinal_disorder|bone_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0014915	short-rib thoracic dysplasia 16 with or without polydactyly	syndromic_disease|hereditary_disease|integumentary_system_disorder|respiratory_system_disorder|disorder_of_development_or_morphogenesis|urinary_system_disorder|musculoskeletal_system_disorder	other	integumentary_system_disorder|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|respiratory_system_disorder|disorder_of_development_or_morphogenesis|urinary_system_disorder	genetics_and_genomics|pediatric|orthopaedic	skeletal_dysplasia|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0014916	developmental and epileptic encephalopathy, 41	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	developmental_disorder|neurodegenerative_disease|epileptic_disorder	developmental_disorder|epileptic_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0014917	developmental and epileptic encephalopathy, 42	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	developmental_disorder|epileptic_encephalopathy|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0014918	tall stature-intellectual disability-renal anomalies syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|renal_medicine	metabolic_disorder|neurodegenerative_disease|renal_anomalies	renal_anomalies|intellectual_disability|kidney_disorder	false	false	false	false	high
MONDO:0014919	sessile serrated polyposis cancer syndrome	syndromic_disease|hereditary_disease|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology|genetics_and_genomics	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0014920	patterned macular dystrophy 3	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	genetics_and_genomics|ophthalmology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0014921	developmental and epileptic encephalopathy, 43	syndromic_disease|nervous_system_disorder|hereditary_disease	other	syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	epileptic_disorder|developmental_disorder|neurodegenerative_disease	epileptic_disorder|brain_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0014922	myofibrillar myopathy 7	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	false	very_high
MONDO:0014923	peeling skin syndrome 5	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology|general_medical_specialties	autoimmune_diseases|inflammatory_disease	skin_disorder	true	false	false	false	medium
MONDO:0014924	epilepsy, familial focal, with variable foci 2	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0014925	epilepsy, familial focal, with variable foci 3	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0014926	Bardet-Biedl syndrome 22	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014927	Joubert syndrome 27	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder_kidney_disorder_____note__joubert_syndrome_is_a_genetic_disorder_that_primarily_affects_the_brainstem_and_can_also_impact_renal_function	false	false	false	false	high
MONDO:0014928	Joubert syndrome 28	disorder_of_visual_system|syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurodegenerative_disease	syndromic_disease|hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|anemia|metabolic_disorder	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0014929	retinitis pigmentosa 76	disorder_of_visual_system|metabolic_disease|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder|metabolic_disease	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease|disorder_of_visual_system	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0014930	intellectual disability, autosomal recessive 56	psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	psychiatric_disorder|metabolic_disease	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0014931	Alazami-Yuan syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|ear_disorder	false	false	false	false	high
MONDO:0014932	orofaciodigital syndrome XV	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	genetic_condition|metabolic_disorder	bone_disorder|joint_disorder|teeth_disorder|ear_disorder	false	false	false	false	high
MONDO:0014933	developmental and epileptic encephalopathy, 44	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	neurology|pediatric	developmental_disorder|neurodegenerative_disease|epileptic_encephalopathy	epileptic_disorder|brain_disorder|developmental_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0014934	spinocerebellar ataxia, autosomal recessive 24	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0014935	frontometaphyseal dysplasia 2	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic	genetic_disorder|metabolic_disorder	muscle_disorder|bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014936	ZTTK syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	genetic_disorder|neurodegenerative_disease	muscle_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0014937	aniridia 2	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor|urinary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cancer_or_benign_tumor	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|urinary_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0014938	aniridia 3	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor|urinary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cancer_or_benign_tumor	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|urinary_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|ophthalmology	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0014939	congenital myasthenic syndrome 20	syndromic_disease|nervous_system_disorder|hereditary_disease	other	syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0014940	neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014941	arthrogryposis, distal, with impaired proprioception and touch	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	neurology|orthopaedic	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0014942	developmental and epileptic encephalopathy, 45	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	genetics_and_genomics|neurology|pediatric	developmental_disorder|neurodegenerative_disease|epilepsy	epileptic_disorder|brain_disorder|encephalopathy|developmental_disorder	false	false	false	true	very_high
MONDO:0014943	mitochondrial DNA depletion syndrome 15 (hepatocerebral type)	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatrics|hepatology	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0014944	short stature-brachydactyly-obesity-global developmental delay syndrome	psychiatric_disorder|nervous_system_disorder|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|endocrinology	global_developmental_delay_syndrome|metabolic_disorder	bone_disorder|global_developmental_delay_syndrome_is_not_in_the_list_so_it_will_be_excluded_but_included_in_its_place_would_be_developmental_delay_which_isn_t_listed_either__but_joint_disorder_might_fit_if_you_were_to_consider_brachydactyly_as_a_form_of_joint_problem|endocrine_disorder	true	false	false	false	high
MONDO:0014945	myopathy, distal, with rimmed vacuoles	metabolic_disease|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	muscle_disorder	false	false	false	true	high
MONDO:0014946	Sifrim-Hitz-Weiss syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|cardiology|ophthalmology	neurodegenerative_disease|metabolic_disorder	jaundice|eye_disorder|liver_disorder	false	false	false	false	high
MONDO:0014947	developmental and epileptic encephalopathy, 46	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	genetics_and_genomics|neurology|pediatric	developmental_disorder|neurodegenerative_disease|epilepsy|encephalopathy	epileptic_disorder|brain_disorder|developmental_disorder	false	false	false	false	very_high
MONDO:0014948	short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|brain_disorder|joint_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014949	developmental and epileptic encephalopathy, 47	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	genetics_and_genomics|neurology|pediatric	developmental_disorder|neurodegenerative_disease	epileptic_disorder|brain_disorder|encephalopathy|developmental_disorder	false	false	false	true	very_high
MONDO:0014950	aortic aneurysm, familial thoracic 10	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|cardiothoracic	autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0014951	intellectual developmental disorder, autosomal recessive 74	psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	psychiatric_disorder|metabolic_disease	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0014952	intellectual disability-epilepsy-extrapyramidal syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	epilepsy_involvement_suggests_this_category_is_relevant|neurodegenerative_disease	brain_disorder|extrapyramidal_syndrome_is_associated_with_brain_disorders_so_this_category_should_also_be_included	false	false	false	false	high
MONDO:0014953	gnb5-related intellectual disability-cardiac arrhythmia syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|cardiology	metabolic_disorder|cardiovascular_disorder	cardiac_arrhythmia_is_implied__but_the_category__cardiac_arrhythmia__is_not_listed|heart_disorder|brain_disorder	false	false	false	false	high
MONDO:0014954	Ehlers-Danlos syndrome, periodontal type 2	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	skin_disorder|joint_disorder|teeth_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0014955	RCBTB1-related retinopathy	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0014956	Chitayat syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0014957	language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia	hereditary_disease	other	hereditary_disease	neurology|pediatric	mental_health_disorder|neurodegenerative_disease|cardiovascular_disorder	heart_disorder|brain_disorder|cognitive_impairment	false	false	false	false	high
MONDO:0014958	Harel-Yoon syndrome	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|dermatology|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0014959	mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatrics|genetics_and_genomics|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014960	encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder	false	false	false	false	very_high
MONDO:0014961	spermatogenic failure 16	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	urology|pediatric	anemia|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder	false	false	false	false	high
MONDO:0014962	intellectual disability, autosomal recessive 57	psychiatric_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease	psychiatric_disorder|metabolic_disease	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0014963	Shashi-Pena syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatrics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0014965	lethal congenital contracture syndrome 11	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|congenital_contracture_syndrome	congenital_contracture_syndrome|metabolic_disorder	joint_disorder|skeletal_system_disorder__note__this_was_not_in_the_original_list_but_is_a_more_specific_category_for_bone_disorder	false	false	false	false	very_high
MONDO:0014966	periventricular nodular heterotopia 7	nervous_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease|nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0014967	heterotaxy, visceral, 8, autosomal	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|syndromic_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	visceral|metabolic_disorder	heart_disorder|vascular_disorder|kidney_disorder|joint_disorder|liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014968	encephalopathy, progressive, with amyotrophy and optic atrophy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014969	isolated sedoheptulokinase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	rheumatology|genetics_and_genomics|hematology|pediatric|renal_medicine|hepatology	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	medium
MONDO:0014970	spermatogenic failure 17	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology|endocrinology	anemia|autoimmune_diseases|metabolic_disorder	male_reproductive_system_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0014971	amelogenesis imperfecta, hypomaturation type, IIa6	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|mouth_disorder	genetics_and_genomics|pediatric|dermatology	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0014972	chromosome 19q13.11 deletion syndrome, proximal	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014973	sudden cardiac failure, infantile	hereditary_disease	other	hereditary_disease	pediatric|cardiology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0014974	sudden cardiac failure, alcohol-induced	hereditary_disease	other	hereditary_disease	hematology|cardiology|hepatology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0014975	autosomal recessive spastic paraplegia type 78	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	hereditary_disease|syndromic_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014976	lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	metabolic_disease|cardiovascular_disorder	hereditary_disease|mitochondrial_disease|cardiovascular_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	eye_disorder|developmental_delay_is_not_in_this_list_so_skip_it|brain_disorder|muscle_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0014977	autosomal recessive limb-girdle muscular dystrophy type 2R1	nervous_system_disorder|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|anemia|autoimmune_diseases|metabolic_disorder|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0014979	myoclonus, intractable, neonatal	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	true	false	false	true	very_high
MONDO:0014980	cone-rod dystrophy and hearing loss	hereditary_disease	other	hereditary_disease	otolaryngology|ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0014981	immunodeficiency 49	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	pediatric|immunology|allergy_and_immunology	immune_deficiency|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0014982	myopia 25, autosomal dominant	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant_disorders	eye_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0014983	congenital myasthenic syndrome 21	nervous_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0014984	lung disease, immunodeficiency, and chromosome breakage syndrome;	hereditary_disease	other	hereditary_disease	immunology|pulmonology|genetics_and_genomics	immunodeficiency|lung_disease|chromosome_breakage_syndrome|autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder|lymphatic_disorder	true	false	false	false	very_high
MONDO:0014985	Fanconi anemia complementation group V	metabolic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|immune_system_disorder|hematologic_disorder	metabolic_disease|anemia	hereditary_disease|musculoskeletal_system_disorder|hematologic_disorder|immune_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	hematology|pediatric|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0014986	Fanconi anemia complementation group R	metabolic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|immune_system_disorder|hematologic_disorder	metabolic_disease|anemia	hereditary_disease|musculoskeletal_system_disorder|hematologic_disorder|immune_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0014987	Fanconi anemia complementation group U	metabolic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|immune_system_disorder|hematologic_disorder	metabolic_disease|anemia	hereditary_disease|musculoskeletal_system_disorder|hematologic_disorder|immune_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	true	false	false	false	high
MONDO:0014989	uncombable hair syndrome 2	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0014990	uncombable hair syndrome 3	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|hair_syndrome_is_a_skin_condition__but_uncombable_hair_syndrome_suggests_it_s_related_to_the_scalp_specifically__so_it_might_also_be_classified_as_a_subset_of_skin_disorder_or_a_separate_entity_called_scalp_disorder_which_is_not_listed_here__however__since_we_don_t_have__scalp_disorder__in_our_category_list_and_given_that_hair_syndrome_often_involves_significant_hair_loss__i_ll_only_select_the_one_most_likely_applicable___skin_disorder	false	false	false	false	low
MONDO:0014991	Seckel syndrome 10	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	skeletal_disorder|endocrine_disorder|growth_disorder|developmental_delay_disorder	false	false	false	false	medium
MONDO:0014992	lissencephaly 8	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0014993	myofibrillar myopathy 8	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	myofibrillar_myopathy|muscle_disorder	false	false	false	false	high
MONDO:0014994	global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	birth_disorder|brain_disorder|nervous_system_disorder|developmental_disorder	false	false	false	false	high
MONDO:0014995	neurodevelopmental disorder with hypotonia, seizures, and absent language	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0014996	intellectual disability, autosomal recessive 58	nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	psychiatric_disorder|metabolic_disease	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	autosomal_recessive_disorder|brain_disorder	false	false	false	false	high
MONDO:0014997	nephronophthisis 20	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	urology|renal_medicine	kidney_disease|inflammatory_disease|cardiovascular_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0014998	glaucoma 3, primary congenital, E	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	pediatric|ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder|primary_congenital	false	false	false	true	high
MONDO:0014999	tooth agenesis, selective, 9	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	genetics_and_genomics|pediatric	genetic_disorder|metabolic_disorder	bone_disorder|teeth_disorder|developmental_disorder	false	false	false	true	medium
MONDO:0015000	developmental and epileptic encephalopathy, 48	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	developmental_disorder|epileptic_disorder|neurodegenerative_disease	developmental_disorder|epileptic_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0015001	atrial fibrillation, familial, 18	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	genetics_and_genomics|cardiology|cardiothoracic	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases|familial	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0015002	developmental and epileptic encephalopathy, 49	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	developmental_disorder|neurodegenerative_disease	spinal_disorder|developmenal_and_epileptic_encephalopathy_is_more_accurately_categorized_under_brain_disorder_which_would_also_encompass_encephalopathy|brain_disorder	false	false	false	true	very_high
MONDO:0015003	dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease|metabolic_disease	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0015004	dystonia 28, childhood-onset	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0015005	epilepsy, early-onset, vitamin B6-dependent	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0015006	epidermolysis bullosa simplex 6, generalized, with scarring and hair loss	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0015007	spastic paraplegia, intellectual disability, nystagmus, and obesity	syndromic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology|endocrinology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	muscle_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0015008	amelogenesis imperfecta, type 1J	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	pediatric|dermatology|genetics_and_genomics	inflammatory_disease|anemia|metabolic_disorder	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0015009	lymphatic malformation 7	immune_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|immune_system_disorder|cardiovascular_disorder	oncology|pediatric	cancer|cardiovascular_disorder|autoimmune_diseases|lymphatic_disorder	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0015010	atypical glycine encephalopathy	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0015011	optic atrophy 11	disorder_of_visual_system|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|disorder_of_visual_system|nervous_system_disorder	neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0015012	mucopolysaccharidosis-plus syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|respiratory_system_disorder	metabolic_disease	respiratory_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|other___corrected_answer__liver_disorder	false	false	false	false	very_high
MONDO:0015013	retinitis pigmentosa 77	metabolic_disease|disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|metabolic_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|adrenal_gland_disease	eye_disorder	false	false	false	false	high
MONDO:0015014	coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology|otolaryngology|pediatric	neurodegenerative_disease|anemia|metabolic_disorder	eye_disorder|bone_disorder|ear_disorder	false	false	false	false	high
MONDO:0015015	congenital bile acid synthesis defect 6	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|gastroenterology|hepatology|pediatric	adrenal_gland_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0015016	anterior segment dysgenesis 6	disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis	genetics_and_genomics|ophthalmology|pediatric	eye_disorder|metabolic_disorder	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0015017	anterior segment dysgenesis 8	disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis	genetics_and_genomics|ophthalmology|pediatric	cardiovascular_disorder|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0015018	ichthyosis, congenital, autosomal recessive 12	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autosomal_recessive|congenital_disease|metabolic_disorder	skin_disorder|congenital_disorder	false	false	false	false	high
MONDO:0015019	Yao syndrome	hereditary_disease	other	hereditary_disease	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|bone_disorder	false	false	false	false	high
MONDO:0015020	intellectual disability, autosomal recessive 59	hereditary_disease|metabolic_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	very_high
MONDO:0015021	hypotonia, ataxia, and delayed development syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015022	intellectual developmental disorder with dysmorphic facies and ptosis	hereditary_disease|psychiatric_disorder|syndromic_disease|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|syndromic_disease|psychiatric_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015023	MYPN-related myopathy	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	myopathy|muscle_disorder	false	false	false	false	high
MONDO:0015024	ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	pediatrics|dermatology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	teeth_disorder|skin_disorder|nail_disorder|eye_disorder|ear_disorder|joint_disorder	false	false	false	false	high
MONDO:0015025	developmental and epileptic encephalopathy, 51	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|epilepsy|developmental_disorder	brain_disorder|epileptic_disorder|spinal_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0015026	cerebroretinal microangiopathy with calcifications and cysts 2	hereditary_disease|disorder_of_visual_system|premature_aging_syndrome|nervous_system_disorder	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|premature_aging_syndrome|nervous_system_disorder	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder_brain_disorder	false	false	false	false	high
MONDO:0015027	familial isolated hyperparathyroidism	cancer_or_benign_tumor|endocrine_system_disorder|hereditary_disease|syndromic_disease	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor|syndromic_disease	renal_medicine|endocrinology|genetics_and_genomics	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	endocrine_disorder|hyperparathyroidism_is_likely_related_to_endocrine_system__familial_isolated_suggests_a_genetic_component_which_could_relate_to_other_disorders_but_since_it_s_not_specified__i_m_excluding_those_categories|kidney_disorder	false	false	false	true	medium
MONDO:0015028	48,XXYY syndrome	disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder|syndromic_disease	endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|syndromic_disease|reproductive_system_disorder	pediatric|genetics_and_genomics	mental_health_disorder|metabolic_disorder	reproductive_system_disorder|bone_disorder|immune_disorder|joint_disorder	false	false	false	false	high
MONDO:0015029	reticular perineurioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	hematology|oncology	neurodegenerative_disease|cancer|adrenal_gland_disease|inflammatory_disease	vascular_disorder|lymphatic_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0015030	sclerosing perineurioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	orthopaedic|neurology|rheumatology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	joint_disorder|muscle_disorder	false	true	false	false	medium
MONDO:0015031	extraneural perineurioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	orthopaedic|neurology|oncology	cancer|inflammatory_disease	soft_tissue_disorder____i_corrected_the_name_of_the_category_to__soft_tissue_disorder__as_extraneural_perineurioma_is_a_type_of_soft_tissue_tumor|muscle_disorder	false	false	false	false	medium
MONDO:0015032	intraneural perineurioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology	neurodegenerative_disease|cancer|inflammatory_disease	nerve_disorder|spinal_disorder	false	false	false	false	low
MONDO:0015033	ABeta amyloidosis, dutch type	hereditary_disease|metabolic_disease|cardiovascular_disorder|nervous_system_disorder	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0015034	lissencephaly with cerebellar hypoplasia type A	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0015035	lissencephaly with cerebellar hypoplasia type B	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0015036	lissencephaly with cerebellar hypoplasia type C	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0015037	lissencephaly with cerebellar hypoplasia type D	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0015038	lissencephaly with cerebellar hypoplasia type E	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0015039	lissencephaly with cerebellar hypoplasia type F	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	true	false	false	false	very_high
MONDO:0015040	myelodysplastic syndrome with excess blasts-1	cancer_or_benign_tumor|hematologic_disorder|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|anemia	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0015041	myelodysplastic syndrome with excess blasts-2	cancer_or_benign_tumor|hematologic_disorder|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0015042	primary plasmacytoma of the bone	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer	bone_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0015043	extramedullary soft tissue plasmacytoma	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|adrenal_gland_disease	muscle_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0015044	mu-heavy chain disease	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology|dermatology	metabolic_disorder|autoimmune_diseases|anemia	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0015045	alpha-heavy chain disease	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	gastroenterology|hematology|oncology	autoimmune_diseases|inflammatory_disease|anemia	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0015046	gamma-heavy chain disease	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|pediatric|oncology|genetics_and_genomics	autoimmune_diseases|cancer|anemia	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0015047	amelogenesis imperfecta type 1	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|mouth_disorder	pediatrics|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0015048	amelogenesis imperfecta type 2	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|mouth_disorder	hematology|pediatric|genetics_and_genomics	metabolic_disorder|anemia	skin_disorder|blood_bone_marrow_disorder|teeth_disorder	false	false	false	false	high
MONDO:0015049	solitary necrotic nodule of the liver	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	gastroenterology|hepatology	cancer|inflammatory_disease	liver_disorder	false	false	false	false	medium
MONDO:0015050	esophageal duplication cyst	upper_digestive_tract_disorder|digestive_system_disorder	other	digestive_system_disorder|upper_digestive_tract_disorder	gastroenterology|pediatric	cardiovascular_disorder|cancer|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0015051	tubular duplication of the esophagus	upper_digestive_tract_disorder|digestive_system_disorder	other	digestive_system_disorder|upper_digestive_tract_disorder	gastroenterology|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder_upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0015053	hereditary angioedema type 1	hereditary_disease|integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease|hereditary_disease	allergy_and_immunology|genetics_and_genomics	autoimmune_diseases|allergy	immune_disorder_vascular_disorder	false	false	false	true	high
MONDO:0015054	hereditary angioedema type 2	hereditary_disease|integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease|hereditary_disease	hematology|allergy_and_immunology|genetics_and_genomics	autoimmune_diseases|allergy	immune_disorder__lymphatic_disorder_vascular_disorder	false	false	false	true	high
MONDO:0015055	acquired angioedema type 2	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease	hematology|allergy_and_immunology|dermatology	autoimmune_diseases|allergy	vascular_disorder|immune_disorder	false	false	false	true	medium
MONDO:0015056	acquired angioedema type 1	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease	renal_medicine|pediatrics|pulmonology|allergy_and_immunology|dermatology	autoimmune_diseases|allergy	vascular_disorder|immune_disorder	false	false	false	false	medium
MONDO:0015057	renin-angiotensin-aldosterone system-blocker-induced angioedema	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease	renal_medicine|allergy_and_immunology|cardiology|dermatology	autoimmune_diseases|allergy	vascular_disorder|endocrine_disorder|immune_disorder|kidney_disorder	false	false	false	false	high
MONDO:0015059	progressive non-fluent aphasia	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0015060	mosaic trisomy 3	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|obstetrics_and_gynecology	neurodegenerative_disease|metabolic_disorder	intellectual_disability_disorder|vascular_disorder|respiratory_disorder____corrected_list____joint_disorder|heart_disorder|brain_disorder|eye_disorder|developmental_delay_disorder|joint_disorder|immune_disorder|learning_disorder|skeletal_disorder	false	false	false	false	high
MONDO:0015061	neurogenic thoracic outlet syndrome	syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease	neurology|orthopaedic|pulmonology|cardiology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015062	gastric neuroendocrine tumor, well differentiated, low or intermediate grade	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|oncology|endocrinology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|endocrine_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0015063	duodenal neuroendocrine tumor, well differentiated, low or intermediate grade	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|oncology	cancer|adrenal_gland_disease|neuroendocrine_tumor	upper_gastrointestinal_disorder|endocrine_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0015064	jejunal neuroendocrine tumor, well differentiated, low or intermediate grade	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|oncology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0015065	ileal neuroendocrine tumor, well differentiated, low or intermediate grade	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|oncology|endocrinology	autoimmune_diseases|cancer|adrenal_gland_disease	endocrine_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0015066	neuroendocrine tumor of the appendix, well differentiated, low or intermediate grade	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|oncology|endocrinology	cancer|adrenal_gland_disease	endocrine_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0015067	neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|neurology|oncology	autoimmune_diseases|cancer|adrenal_gland_disease	endocrine_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0015068	rectal neuroendocrine tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|gastrointestinal_oncology|oncology	neuroendocrine_tumor_category|cancer|adrenal_gland_disease	endocrine_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0015069	neuroendocrine tumor of the anal canal	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	neurology|oncology|urology	cancer	endocrine_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0015070	laryngeal neuroendocrine neoplasm	endocrine_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	neurology|otolaryngology|oncology	cancer|neuroendocrine_tumors|endocrine_disorder	throat_disorder__endocrine_disorder	false	true	false	false	high
MONDO:0015071	middle ear neuroendocrine tumor	endocrine_system_disorder|otorhinolaryngologic_disease|auditory_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	otorhinolaryngologic_disease|auditory_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	neurology|otolaryngology|oncology	adrenal_gland_disease|cancer|neuroendocrine_tumor	endocrine_disorder|neuroendocrine_disorder|ear_disorder	false	true	false	false	medium
MONDO:0015072	liver neuroendocrine carcinoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|oncology|hepatology	cancer|liver|neuroendocrine_carcinoma	liver_disorder|endocrine_disorder|neuroendocrine_carcinoma_does_not_match_any_existing_category__however__liver_neuroendocrine_carcinoma_is_a_subset_of_endocrine_disorders_so_the_best_fitting_categories_are__liver_disorder	false	true	false	false	very_high
MONDO:0015073	gallbladder neuroendocrine tumor, grade 1/2	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|liver_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0015074	thyroid tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	autoimmune_diseases|cancer|metabolic_disorder	endocrine_disorder	false	true	false	true	medium
MONDO:0015075	thyroid gland carcinoma	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	autoimmune_diseases|thyroid_gland_disease|cancer	endocrine_disorder|thyroid_gland_carcinoma_fits_into_this_category_because_it_is_a_type_of_endocrine_disorder	false	true	false	true	low
MONDO:0015079	multiple polyglandular tumor	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	oncology|genetics_and_genomics|endocrinology	autoimmune_diseases|cancer	endocrine_disorder|immune_disorder	false	false	false	false	high
MONDO:0015082	alopecia antibody deficiency	integumentary_system_disorder	other	integumentary_system_disorder	immunology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0015083	nuclear oculomotor paralysis	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0015084	FRAXF syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|ear_disorder|joint_disorder	false	false	false	false	medium
MONDO:0015085	bathing suit ichthyosis	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder	skin_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0015086	cloverleaf skull-asphyxiating thoracic dysplasia syndrome	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	cardiothoracic|pulmonology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	lung_disorder|spinal_disorder|bone_disorder|joint_disorder|skeletal_disorder	false	false	false	false	very_high
MONDO:0015087	autosomal dominant complex spastic paraplegia	hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015091	autosomal dominant spastic paraplegia type 9	hereditary_disease|metabolic_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease|metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0015092	cleft hard palate	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|otolaryngology	congenital_condition|neonatal_condition|developmental_disorder|birth_defect|metabolic_disorder	teeth_disorder|throat_disorder	false	false	false	true	medium
MONDO:0015093	sub-cortical nodular heterotopia	syndromic_disease	other	syndromic_disease	neurology|pediatric	sub_cortical_nodular_heterotopia_is_not_a_fitting_category_for_this_list|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0015094	subependymal nodular heterotopia	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0015095	Peters anomaly-cataract syndrome	hereditary_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis	other	disorder_of_orbital_region|disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0015096	familial hypofibrinogenemia	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0015097	aortic valve dysplasia	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0015099	unilateral hemispheric polymicrogyria	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0015100	aregenerative anemia	syndromic_disease|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|hematology	metabolic_disorder|autoimmune_diseases|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0015101	Marin-Amat syndrome	disorder_of_visual_system|syndromic_disease|nervous_system_disorder	other	disorder_of_visual_system|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	vascular_disorder|liver_disorder|blood_bone_marrow_disorder	false	false	false	as_of_my_last_knowledge_update_in_october_2023__marin_amat_syndrome_is_a_rare_genetic_disorder__and_there_are_currently_no_known_specific_treatments_that_cure__prevent__or_effectively_treat_this_syndrome__therefore__the_answer_is_false	high
MONDO:0015102	non-secreting chemodectoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder|cardiovascular_disorder|hereditary_disease|endocrine_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder|endocrine_system_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	genetics_and_genomics|neurology|otolaryngology|endocrinology	cancer|adrenal_gland_disease	skin_disorder|ear_disorder	false	false	false	false	medium
MONDO:0015103	pulmonary valve agenesis-tetralogy of fallot-absence of ductus arteriosus syndrome	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|pulmonology|pediatrics	tetralogy_of_falott|cardiovascular_disorder	vascular_disorder|lung_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0015104	porphyria cutanea tarda	metabolic_disease|digestive_system_disorder|integumentary_system_disorder|inflammatory_disease|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder	metabolic_disease|integumentary_system_disorder|inflammatory_disease|digestive_system_disorder|endocrine_system_disorder	dermatology|hepatology|hematology	adrenal_gland_disease|anemia|metabolic_disorder	skin_disorder|liver_disorder	false	false	false	true	medium
MONDO:0015109	congenital anomaly of the mitral subvalvular apparatus	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|cardiology	congenital_anomaly|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0015126	polyendocrinopathy	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	polyendocrinopathy|endocrinology	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0015127	pituitary deficiency	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	neurology|endocrinology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0015128	primary adrenal insufficiency	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|renal_medicine	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	primary_adrenal_insufficiency|endocrine_disorder	false	false	false	true	high
MONDO:0015129	chronic primary adrenal insufficiency	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|renal_medicine	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	immune_disorder|urinary_tract_disorder|endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0015131	combined immunodeficiency	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|pediatric|immunology|hematology|allergy_and_immunology	autoimmune_diseases|immunodeficiency_disease|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0015134	constitutional neutropenia	immune_system_disorder|hematologic_disorder	other	hematologic_disorder|immune_system_disorder	pediatric|oncology|hematology|allergy_and_immunology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0015137	periodic fever syndrome	syndromic_disease|connective_tissue_disorder	other	syndromic_disease|connective_tissue_disorder	pediatric|hematology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0015140	early-onset autosomal dominant Alzheimer disease	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	very_high
MONDO:0015146	classic lissencephaly	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder	true	false	false	false	very_high
MONDO:0015148	lissencephaly type 3	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0015149	pure hereditary spastic paraplegia	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0015150	complex hereditary spastic paraplegia	nervous_system_disorder|hereditary_disease|syndromic_disease	neurodegenerative_disease	syndromic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|hereditary|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0015151	muscular dystrophy, limb-girdle, autosomal dominant	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	orthopaedic|neurology|genetics_and_genomics|pediatric	muscular_dystrophy|neurodegenerative_disease	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0015152	autosomal recessive limb-girdle muscular dystrophy	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	orthopaedic|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|limb_disorder|joint_disorder	false	false	false	false	high
MONDO:0015157	human herpesvirus 8-related tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|post_infectious_disorder	hepatology|hematopathology|oncology	inflammatory_disease|autoimmune_diseases|cancer	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder|reproductive_system_disorder|skin_disorder	true	true	false	true	high
MONDO:0015158	unexplained periodic fever syndrome	syndromic_disease|connective_tissue_disorder	other	syndromic_disease|connective_tissue_disorder	rheumatology|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0015159	multiple congenital anomalies/dysmorphic syndrome-intellectual disability	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|bone_disorder|eye_disorder|teeth_disorder|joint_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0015160	multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|spine_disorder_is_incorrect_so|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0015161	multiple congenital anomalies/dysmorphic syndrome without intellectual disability	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder	kidney_disorder|muscle_disorder|bone_disorder|heart_disorder|vascular_disorder|eye_disorder|upper_gastrointestinal_disorder|urinary_tract_disorder|lower_gastrointestinal_disorder|ear_disorder|joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0015164	acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent	musculoskeletal_system_disorder|hematologic_disorder|connective_tissue_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|acute_disease|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	hematology|oncology	anemia|cancer	bone_disorder|blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0015165	acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor	musculoskeletal_system_disorder|hematologic_disorder|connective_tissue_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|acute_disease|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	hematology|oncology	anemia|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0015166	acute myeloid leukemia with t(8;21)(q22;q22) translocation	musculoskeletal_system_disorder|hematologic_disorder|connective_tissue_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|acute_disease|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	hematology|genetics_and_genomics|oncology	leukemia|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0015167	amniotic band syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|obstetrics_and_gynecology	birth_defects|congenital_abnormalities|neurodevelopmental_disorders	reproductive_system_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0015168	arthrogryposis multiplex congenita	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0015169	chronic diarrhea due to glucoamylase deficiency	digestive_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	digestive_system_disorder|hereditary_disease|metabolic_disease	gastroenterology|genetics_and_genomics	metabolic_disorder|genetic_disorder|biochemical_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0015170	congenital sodium diarrhea	digestive_system_disorder|hereditary_disease	other	digestive_system_disorder|hereditary_disease	gastroenterology|genetics_and_genomics|pediatric	metabolic_disorder|congenital_disease	endocrine_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0015171	congenital enterocyte heparan sulfate deficiency	digestive_system_disorder	other	digestive_system_disorder	hepatology|genetics_and_genomics|pediatric	metabolic_disorder|congenital_disease	kidney_disorder|liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0015174	autoimmune enteropathy type 3	digestive_system_disorder|immune_system_disorder	autoimmune_disease	digestive_system_disorder|immune_system_disorder	immunology|gastroenterology|pediatrics|rheumatology	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0015175	autoimmune pancreatitis	digestive_system_disorder|endocrine_system_disorder|inflammatory_disease|immune_system_disorder	autoimmune_disease|endocrine_system_disorder	digestive_system_disorder|inflammatory_disease|immune_system_disorder|endocrine_system_disorder	gastroenterology|rheumatology|endocrinology	inflammatory_disease|autoimmune_diseases	immune_disorder_upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0015176	undetermined colitis	digestive_system_disorder|hereditary_disease|immune_system_disorder	other	digestive_system_disorder|hereditary_disease|immune_system_disorder	gastroenterology	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0015177	metaphyseal anadysplasia	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatrics|genetics_and_genomics	bone_dysplasia|metabolic_disorder|genetic_disorder	spinal_disorder|bone_disorder|blood_bone_marrow_disorder|joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0015183	short bowel syndrome	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|pediatric	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0015185	intestinal polyposis syndrome	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	gastroenterology|genetics_and_genomics|oncology	inflammatory_disease|autoimmune_diseases|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0015191	myopathic intestinal pseudoobstruction	digestive_system_disorder	other	digestive_system_disorder	neurology|gastroenterology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	lower_gastrointestinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015193	hydrops fetalis	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|obstetrics_and_gynecology	metabolic_disorder|anemia	vascular_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0015194	sideroblastic anemia	hematologic_disorder	anemia	hematologic_disorder	hematology|pediatric|oncology	cancer|anemia	blood_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0015195	atresia of urethra	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	urinary_system_disorder|disorder_of_development_or_morphogenesis	urology|pediatric	urogenital_anomalies|congenital_abnormality	kidney_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0015196	vein of Galen aneurysm	cardiovascular_disorder|cancer_or_benign_tumor|nervous_system_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|nervous_system_disorder|cancer_or_benign_tumor	neurology|hematology	cardiovascular_disorder|neurological_cause	brain_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0015197	aneurysm of sinus of Valsalva	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	renal_medicine|hematology|pulmonology|cardiology|cardiothoracic	cardiovascular_disorder|inflammatory_disease	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0015198	aniridia-ptosis-intellectual disability-familial obesity syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|familial_syndrome	brain_disorder|endocrine_disorder|eye_disorder	false	false	false	false	high
MONDO:0015199	aniridia - intellectual disability syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0015200	anisakiasis	infectious_disease|digestive_system_disorder	infectious_disease	infectious_disease|digestive_system_disorder	gastroenterology|hepatology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	low
MONDO:0015201	ankyloblepharon filiforme-imperforate anus syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	disorder_of_visual_system|syndromic_disease|disorder_of_development_or_morphogenesis	ophthalmology|dermatology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|joint_disorder|eye_disorder	false	false	false	false	high
MONDO:0015203	coronary artery congenital malformation	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|pediatric|genetics_and_genomics|cardiothoracic	cardiovascular_disorder|congenital_malformation	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0015204	microlissencephaly	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0015205	isolated lissencephaly type 1 without known genetic defects	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0015206	short stature-heart defect-craniofacial anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	cardiology|pediatric|genetics_and_genomics|cardiothoracic|orthopaedic	cardiovascular_disorder|metabolic_disorder	heart_disorder|bone_disorder|craniofacial_anomalies	false	false	false	false	high
MONDO:0015225	arthrogryposis syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	joint_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015228	pentasomy X	syndromic_disease|chromosomal_disorder	other	chromosomal_disorder|syndromic_disease	oncology|hematology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0015229	Bardet-Biedl syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder|kidney_disorder|spinal_disorder	false	false	false	false	high
MONDO:0015230	anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis	cardiology|pediatric|genetics_and_genomics|orthopaedic	cardiovascular_disorder|metabolic_disorder|skeletal_anomalies	eye_disorder|skeletal_anomalies|heart_disorder	false	false	false	false	very_high
MONDO:0015231	Bartter syndrome	hereditary_disease|syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|renal_medicine	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0015232	radial deficiency-tibial hypoplasia syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|congenital_disorders	joint_disorder|bone_disorder|skeletal_disorder|limb_disorder	false	false	false	false	high
MONDO:0015233	caudal appendage-deafness syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|otolaryngology	autoimmune_diseases|cancer|neurodegenerative_disease	throat_disorder|ear_disorder	true	false	false	false	high
MONDO:0015234	arachnodactyly-abnormal ossification-intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic|neurology	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	bone_disorder|intellectual_disability|skeletal_disorder	false	false	false	false	very_high
MONDO:0015235	arachnodactyly-intellectual disability-dysmorphism syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	brain_disorder|developmental_disorder	false	false	false	false	high
MONDO:0015236	aortic arch defects	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|pediatric|cardiothoracic	cardiovascular_disorder|neonatal_disease	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0015237	arrhinia	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	otolaryngology|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	ear_disorder|nose_disorder	false	false	false	false	high
MONDO:0015239	abnormal origin of the pulmonary artery	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatrics|cardiology|pulmonology|cardiothoracic	adrenal_gland_disease|cardiovascular_disorder	lung_disorder|vascular_disorder	false	false	false	false	high
MONDO:0015240	digitotalar dysmorphism	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0015241	arthrogryposis-like syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|orthopaedic	metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015243	allergic bronchopulmonary aspergillosis	infectious_disease|immune_system_disorder|respiratory_system_disorder	infectious_disease	respiratory_system_disorder|infectious_disease|immune_system_disorder	allergy_and_immunology|hematology|pulmonology|pediatric|oncology	autoimmune_diseases|inflammatory_disease|allergy	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0015244	autosomal recessive cerebellar ataxia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015247	opsoclonus-myoclonus syndrome	nervous_system_disorder|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|syndromic_disease	genetics_and_genomics|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015248	ataxia-photosensitivity-short stature syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder|skin_disorder	false	false	false	false	high
MONDO:0015249	mitral atresia disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|pediatric|genetics_and_genomics	mitral_atresia_disorder_fits_here_as_well|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0015250	spinal atrophy-ophthalmoplegia-pyramidal syndrome	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	spinal_atrophy_opthalmoplegia_pyramidal_syndrome_falls_under_the_category_of_neurodegenerative_disease|neurodegenerative_disease	eye_disorder|brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015252	severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	bone_disorder|brain_disorder|spinal_disorder|intellectual_disability|muscle_disorder	false	false	false	false	very_high
MONDO:0015253	Diamond-Blackfan anemia	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0015254	schistosomiasis	infectious_disease	infectious_disease	infectious_disease	hematology|urology|hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|urinary_tract_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0015256	blepharoptosis-cleft palate-ectrodactyly-dental anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|ophthalmology	metabolic_disorder|genetic_disorder|congenital_anomaly	eye_disorder|teeth_disorder	false	false	false	true	high
MONDO:0015257	sino-auricular heart block	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic	autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0015259	brachydactyly-mesomelia-intellectual disability-heart defects syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	cardiology|pediatric|genetics_and_genomics|neurology|orthopaedic	metabolic_disorder|mental_health_disorder|neurodegenerative_disease|cardiovascular_disorder	joint_disorder|heart_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0015260	diphyllobothriasis	infectious_disease	infectious_disease	infectious_disease	hematology|hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease|allergy	parasitic_disorder|liver_disorder	true	false	false	true	medium
MONDO:0015261	pseudopelade of Brocq	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	bone_disorder|skin_disorder	false	false	false	false	low
MONDO:0015262	brachyolmia	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatrics|genetics_and_genomics|orthopaedic	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0015263	Brugada syndrome	hereditary_disease|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|syndromic_disease	cardiology|pulmonology|genetics_and_genomics|cardiothoracic	electrolyte_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0015264	cryptogenic organizing pneumonia	infectious_disease|inflammatory_disease|respiratory_system_disorder	infectious_disease	respiratory_system_disorder|infectious_disease|idiopathic_disease|inflammatory_disease	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease	lung_disorder|lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	medium
MONDO:0015265	bronchiolitis obliterans syndrome	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric|cardiothoracic	autoimmune_diseases|inflammatory_disease	lung_disorder|vascular_disorder|immune_disorder	false	false	false	false	high
MONDO:0015267	Feingold syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|allergy	skin_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0015268	medullary sponge kidney	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	urinary_system_disorder|disorder_of_development_or_morphogenesis	urology|renal_medicine	metabolic_disorder|adrenal_gland_disease|cancer|inflammatory_disease|anemia	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0015269	symmetrical thalamic calcifications	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0015270	butyrylcholinesterase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015271	idiopathic camptocormia	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|idiopathic_disease	neurology|orthopaedic	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0015272	camptodactyly-taurinuria syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|hereditary_disease	joint_disorder|kidney_disorder|bone_disorder	false	false	false	false	medium
MONDO:0015273	complete atrioventricular canal	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiology|pediatric|cardiothoracic	congenital_abnormality|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0015274	chronic beryllium disease	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|rheumatology	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	true	high
MONDO:0015275	partial atrioventricular canal	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiology|pediatric	congenital_heart_defect|cardiovascular_disorder	lower_gastrointestinal_disorder|heart_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0015277	medullary thyroid gland carcinoma	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|oncology	cancer|endocrine_system_disorder|thyroid_carcinoma	blood_bone_marrow_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0015278	familial pancreatic carcinoma	digestive_system_disorder|hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor|digestive_system_disorder	genetics_and_genomics|oncology|gastroenterology	familial_pancreatic_carcinoma_is_a_type_of_cancer|cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0015279	chronic mucocutaneous candidiasis	hereditary_disease|immune_system_disorder|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|immune_system_disorder	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0015280	cardiofaciocutaneous syndrome	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder|musculoskeletal_system_disorder|syndromic_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|cardiovascular_disorder|musculoskeletal_system_disorder|integumentary_system_disorder	dermatology|genetics_and_genomics|cardiology|cardiothoracic|pediatrics|hematology|pulmonology	autoimmune_diseases|cardiovascular_disorder	skin_disorder|heart_disorder	false	false	false	false	high
MONDO:0015281	atrial standstill	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiology|cardiothoracic|pulmonology	cardiovascular_disorder|atrial_gland_disease	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0015282	cardiomyopathy-cataract-hip spine disease syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|cardiology|ophthalmology|orthopaedic	metabolic_disorder|autoimmune_diseases|cardiovascular_disorder	eye_disorder|spinal_disorder|heart_disorder	false	false	false	false	high
MONDO:0015283	maternally-inherited cardiomyopathy and hearing loss	mitochondrial_disease	other	mitochondrial_disease	genetics_and_genomics|cardiology|pediatric	metabolic_disorder|cardiovascular_disorder	ear_disorder|heart_disorder	false	false	false	true	high
MONDO:0015284	heart-hand syndrome type 2	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|cardiology|pediatric	metabolic_disorder|autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0015285	Carney complex	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics|endocrinology|oncology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	heart_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0015286	congenital disorder of glycosylation	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	congenital_disease|metabolic_disorder	liver_disorder	false	false	true	false	high
MONDO:0015288	herpes simplex virus keratitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|disorder_of_orbital_region|disorder_of_visual_system	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	true	false	false	true	medium
MONDO:0015289	infectious epithelial keratitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|disorder_of_orbital_region|disorder_of_visual_system	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	true	false	false	true	high
MONDO:0015290	neurotrophic keratopathy	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	true	medium
MONDO:0015291	stromal keratitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|disorder_of_orbital_region|disorder_of_visual_system	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases|cancer	immune_disorder|eye_disorder	true	false	false	true	high
MONDO:0015292	endotheliitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|disorder_of_orbital_region|disorder_of_visual_system	rheumatology|hematology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	immune_disorder|vascular_disorder|heart_disorder	true	false	false	false	medium
MONDO:0015293	segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome	syndromic_disease|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|hereditary_disease|syndromic_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|neurology|pediatric	congenital_disorder|vascular_disorder|neurological_disorder	vascular_disorder|skin_disorder	false	false	false	false	high
MONDO:0015294	nephrogenic systemic fibrosis	integumentary_system_disorder	other	integumentary_system_disorder	nephrology|renal_medicine	inflammatory_disease|autoimmune_diseases	kidney_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0015295	intractable diarrhea-choanal atresia-eye anomalies syndrome	digestive_system_disorder	other	digestive_system_disorder	genetics_and_genomics|gastroenterology|pediatric	metabolic_disorder|eye_anomalies_are_associated_but_i_assume_it_is_a_type_of_metabolic_disorder	lower_gastrointestinal_disorder|eye_disorder	true	false	false	false	high
MONDO:0015296	cardiac anomalies-heterotaxy syndrome	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	genetics_and_genomics|cardiology|pediatric	heterotaxy_syndrome|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0015298	pellucid marginal degeneration	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0015299	Asherman syndrome	reproductive_system_disorder	other	reproductive_system_disorder	genetics_and_genomics|obstetrics_and_gynecology	inflammatory_disease|metabolic_disorder|anemia	lower_gastrointestinal_disorder|reproductive_system_disorder|gynecological_disorder	false	false	false	true	medium
MONDO:0015300	cataract - microcornea syndrome	syndromic_disease	other	syndromic_disease	ophthalmology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	true	medium
MONDO:0015301	primary cutaneous amyloidosis	integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease	dermatology	metabolic_disorder|autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|skin_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0015302	nodular cutaneous amyloidosis	integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease	dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|kidney_disorder|skin_disorder	false	false	false	false	low
MONDO:0015303	macular amyloidosis	integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease	ophthalmology|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0015304	arachnoiditis	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	inflammatory_disease|infectious_disease|nervous_system_disorder	neurology|rheumatology	autoimmune_diseases|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0015306	Lemierre syndrome	infectious_disease	infectious_disease	infectious_disease	otolaryngology|pulmonology	autoimmune_diseases|inflammatory_disease	nose_disorder|ear_disorder	true	false	false	true	high
MONDO:0015307	Madras motor neuron disease	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0015308	laminopathy type Decaudain-Vigouroux	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015311	autism-facial port-wine stain syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|neurology|dermatology	autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	vascular_disorder|skin_disorder	false	false	false	false	medium
MONDO:0015312	choanal atresia, unilateral	respiratory_system_disorder|hereditary_disease|otorhinolaryngologic_disease	other	respiratory_system_disorder|hereditary_disease|otorhinolaryngologic_disease	otolaryngology|pediatric	congenital_anomaly|congenital_respiratory_disorder|birth_defect|developmental_disorder|genetic_disorder____replaced_with_more_accurate_response____respiratory_system_disorder	nose_disorder|throat_disorder	false	false	false	true	medium
MONDO:0015313	choanal atresia, bilateral	respiratory_system_disorder|hereditary_disease|otorhinolaryngologic_disease	other	respiratory_system_disorder|hereditary_disease|otorhinolaryngologic_disease	otolaryngology|pediatric	congenital_heart_disease|neurological_disease|birth_defect|gastrointestinal_disorder|congenital_abnormality|developmental_disorder|respiratory_disease|genetic_condition____corrected_list_to_fit_the_original_request____inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|nose_disorder|throat_disorder	false	false	false	true	high
MONDO:0015314	primary laryngeal lymphangioma	respiratory_system_disorder	other	respiratory_system_disorder	otolaryngology|pediatric|oncology	cancer|tumor|lymphatic_disorder	throat_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0015315	neonatal brainstem dysfunction	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0015316	congenital laryngeal palsy	respiratory_system_disorder|nervous_system_disorder	other	respiratory_system_disorder|nervous_system_disorder	otolaryngology|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|throat_disorder	false	false	false	false	medium
MONDO:0015317	laryngotracheal angioma	cardiovascular_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease	otolaryngology|pediatric	cardiovascular_disorder|cancer|inflammatory_disease	lung_disorder|vascular_disorder|throat_disorder	false	false	false	false	medium
MONDO:0015324	cataract-intellectual disability-anal atresia-urinary defects syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|ophthalmology	urinary_defects|metabolic_disorder|neurodegenerative_disease	eye_disorder|urinary_tract_disorder	true	false	false	false	very_high
MONDO:0015325	cataract-deafness-hypogonadism syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	endocrinology|genetics_and_genomics|ophthalmology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder|endocrine_disorder|ear_disorder	false	false	false	false	high
MONDO:0015326	night blindness-skeletal anomalies-dysmorphism syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|ophthalmology	skeletal_anomalies|metabolic_disorder	eye_disorder|skeletal_anomalies|bone_disorder	false	false	false	false	medium
MONDO:0015327	developmental anomaly of metabolic origin	disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|developmental_anomaly_of_metabolic_origin	metabolic_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0015333	progeroid syndrome	hereditary_disease|premature_aging_syndrome|disorder_of_development_or_morphogenesis	other	hereditary_disease|premature_aging_syndrome|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|skin_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0015337	isolated craniosynostosis	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	brain_disorder|bone_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0015338	syndromic craniosynostosis	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|pediatric|neurology	bone_disease|congenital_disorder|neurodegenerative_disease|developmental_disease	brain_disorder|bone_disorder	false	false	false	false	high
MONDO:0015339	adrenomyeloneuropathy	hereditary_disease|metabolic_disease|endocrine_system_disorder|psychiatric_disorder|nervous_system_disorder	endocrine_system_disorder|neurodegenerative_disease|psychiatric_disorder|metabolic_disease	nervous_system_disorder|endocrine_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|spinal_disorder|nerve_disorder	false	false	false	true	high
MONDO:0015340	drug rash with eosinophilia and systemic symptoms	integumentary_system_disorder|inflammatory_disease|syndromic_disease	other	integumentary_system_disorder|inflammatory_disease|syndromic_disease	allergy_and_immunology|dermatology	inflammatory_disease|autoimmune_diseases|allergy	skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0015341	congenital panfollicular nevus	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|integumentary_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|dermatology|pediatric	congenital_disorder|skin_condition|neurodevelopmental_disorder	reproductive_system_disorder|skin_disorder	false	false	false	false	medium
MONDO:0015342	acute transverse myelitis	inflammatory_disease|nervous_system_disorder	other	acute_disease|nervous_system_disorder|inflammatory_disease	pediatric|neurology	inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder|muscle_disorder	true	false	false	true	high
MONDO:0015344	idiopathic acute transverse myelitis	inflammatory_disease|nervous_system_disorder	other	acute_disease|nervous_system_disorder|inflammatory_disease|idiopathic_disease	neurology	inflammatory_disease|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015345	perioral myoclonia with absences	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015346	epilepsy with eyelid myoclonia	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|epilepsy_category	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0015347	multicentric reticulohistiocytosis	syndromic_disease|immune_system_disorder	other	syndromic_disease|immune_system_disorder	hematology|rheumatology|dermatology	inflammatory_disease|autoimmune_diseases|cancer	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0015348	leukoencephalopathy with bilateral anterior temporal lobe cysts	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0015349	progressive cavitating leukoencephalopathy	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	true	false	false	false	high
MONDO:0015350	17q11.2 microduplication syndrome	hereditary_disease|chromosomal_disorder	other	chromosomal_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder|upper_gastrointestinal_disorder|joint_disorder|lower_gastrointestinal_disorder|heart_disorder|spinal_disorder|reproductive_system_disorder|kidney_disorder|vascular_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015351	neuropathy with hearing impairment	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|otolaryngology	metabolic_disorder|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|ear_disorder	false	false	false	true	high
MONDO:0015352	distal hereditary motor neuropathy type 2	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0015353	neuronopathy, distal hereditary motor, type 5A	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	hereditary_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0015354	hereditary sensory and autonomic neuropathy with deafness and global delay	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|neurology|pediatric|genetic	hereditary_disorder|neurodegenerative_disease	ear_disorder_brain_disorder	false	false	false	false	high
MONDO:0015355	distal hereditary motor neuropathy type 7	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|hereditary_condition	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0015356	hereditary neoplastic syndrome	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	oncology|genetics_and_genomics|hematolog	cancer|hereditary_neoplastic_syndrome_can_also_be_related_to_other_categories_but_cancer_is_the_best_fitting_category	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0015357	secondary hypoparathyroidism due to impaired parathormon secretion	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	renal_medicine|endocrinology	metabolic_disorder|autoimmune_diseases	secondary_hypparathyroidism_due_to_impaired_parathormone_secretion|endocrine_disorder	false	false	false	false	high
MONDO:0015358	hereditary motor and sensory neuropathy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|hereditary_diseases	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015362	neuronopathy, distal hereditary motor, autosomal dominant	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	hereditary_motor_neuron_disease|neurodegenerative_disease|autosomal_dominant_disorder	spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0015363	neuronopathy, distal hereditary motor, autosomal recessive	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|hereditary_motor_neuron_disease|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015364	hereditary sensory and autonomic neuropathy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|hereditary_disorders	brain_disorder|nerve_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0015367	Charlie M syndrome	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0015369	Joubert syndrome and related disorders	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0015371	linear atrophoderma of Moulin	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatric	autoimmune_diseases|inflammatory_disease	skin_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0015372	autosomal dominant macrothrombocytopenia	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0015374	primary central nervous system vasculitis	inflammatory_disease|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	inflammatory_disease|nervous_system_disorder|cardiovascular_disorder	neurology|rheumatology	autoimmune_diseases|inflammatory_disease	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0015375	orofaciodigital syndrome	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	upper_gastrointestinal_disorder|bone_disorder|joint_disorder|spinal_disorder|ear_disorder|teeth_disorder	false	false	false	false	high
MONDO:0015376	first branchial cleft anomaly	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	pediatric|otolaryngology	neurodevelopmental_disease|birth_anomaly|congenital_disorder	ear_disorder|throat_disorder	false	false	false	false	medium
MONDO:0015377	third branchial cleft anomaly	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	pediatric|otolaryngology	congenital_anomaly|neurological_disease|developmental_disorder	ear_disorder|throat_disorder	false	false	false	false	medium
MONDO:0015378	fourth branchial cleft anomaly	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	pediatric|otolaryngology	congenital_anomaly|inflammatory_disease|developmental_disorder	spinal_disorder|throat_disorder	false	false	false	false	medium
MONDO:0015379	cervical dermoid cyst	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|otorhinolaryngologic_disease	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease|cancer_or_benign_tumor	dermatology|obstetrics_and_gynecology	autoimmune_diseases|cancer	reproductive_system_disorder|skin_disorder	false	false	false	false	medium
MONDO:0015380	facial dermoid cyst	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease|cancer_or_benign_tumor	dermatology|pediatric|ophthalmology|otolaryngology	cyst|inflammatory_disease|skin_condition	reproductive_system_disorder|skin_disorder	false	false	false	true	low
MONDO:0015381	commissural lip fistula	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	mouth_disorder|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	plastic_surgery|dermatology|otolaryngology	inflammatory_disease	lower_gastrointestinal_disorder|ear_disorder|skin_disorder	false	false	false	false	medium
MONDO:0015382	lower lip fistula	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	mouth_disorder|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	surgery|dermatology|otolaryngology	inflammatory_disease	lower_gastrointestinal_disorder|skin_disorder	false	false	false	false	medium
MONDO:0015383	cervicofacial fibrochondroma	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	dermatology|rheumatology|otolaryngology	autoimmune_diseases|inflammatory_disease|cancer	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0015384	digestive duplication cyst of the tongue	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	mouth_disorder|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	gastroenterology|pediatric|otolaryngology	digestive_disorder|inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0015386	epignathus	cancer_or_benign_tumor|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor	neurology|otolaryngology	adrenal_gland_disease|metabolic_disorder|inflammatory_disease	bone_disorder|facial_disorder_is_not_in_the_list_so__bone_disorder	false	false	false	false	very_high
MONDO:0015387	nasolacrimal duct cyst	otorhinolaryngologic_disease|disorder_of_visual_system	other	otorhinolaryngologic_disease|disorder_of_orbital_region|disorder_of_visual_system	pediatrics|otolaryngology	developmental_disorder|congenital_condition|inflammatory_disease|neurological_disease	nose_disorder|eye_disorder	false	false	false	false	low
MONDO:0015388	polyrrhinia	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	oncology|hematology|rheumatology	metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0015389	supernumerary nostril	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	otolaryngology	congenital_abnormality|developmental_disorder|autoimmune_diseases	nose_disorder	false	false	false	false	low
MONDO:0015390	proboscis lateralis	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	neurology|otolaryngology	inflammatory_disease|neurodegenerative_disease	nose_disorder|throat_disorder	true	false	false	false	high
MONDO:0015391	nasopharyngeal teratoma	cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor	oncology|pediatric|otolaryngology	neuroblastoma_is_a_type_of_cancer__cancer	nose_disorder|throat_disorder	false	false	false	false	high
MONDO:0015392	nasal glial heterotopia	cancer_or_benign_tumor|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor	neurology|pediatric|otolaryngology	inflammatory_disease|neurodegenerative_disease	brain_disorder|nose_disorder	false	false	false	false	medium
MONDO:0015393	nasal ganglioglioma	cancer_or_benign_tumor|nervous_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	nervous_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	oncology|neurology|pediatric|otolaryngology	cancer|neurological_cancer	brain_disorder|spinal_disorder|nose_disorder	false	false	false	false	high
MONDO:0015394	nasal encephalocele	disorder_of_development_or_morphogenesis|nervous_system_disorder|otorhinolaryngologic_disease	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|otorhinolaryngologic_disease	neurology|pediatric|otolaryngology	inflammatory_disease|neurodegenerative_disease|cancer	brain_disorder|nose_disorder	false	false	false	false	high
MONDO:0015395	congenital subglottic stenosis	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|otolaryngology	congenital_anomaly|respiratory_disease|neurological_disorder	respiratory_system_disorder_____note__congenital_subglottic_stenosis_is_a_narrowing_of_the_airway_below_the_vocal_cords__therefore_it_s_categorized_under_throat_disorder__some_sources_might_categorize_it_as_a_lung_disorder_or_respiratory_system_disorder_due_to_its_impact_on_breathing|throat_disorder	false	false	false	false	high
MONDO:0015396	congenital laryngeal cyst	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|otolaryngology	congenital_condition|developmental_disorder|birth_defect|neurological_disease	congenital_disorder|throat_disorder	false	false	false	true	high
MONDO:0015397	craniofacial microsomia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|craniofacial_microsomia_is_also_sometimes_classified_as_a_congenital_anomaly_which_can_be_related_to_genetic_abnormalities_affecting_metabolic_pathways_therefore_it_is_often_related_to_or_can_be_classified_under_the_broader_category_of|metabolic_disorder__autoimmune_diseases	bone_disorder|teeth_disorder|craniofacial_disorder_is_not_explicitly_listed_but_can_be_inferred_to_be_a_subset_of_bone_disorder_and_teeth_disorder	false	false	false	false	high
MONDO:0015399	glossopalatine ankylosis	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	neurology|otolaryngology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	teeth_disorder|throat_disorder	false	false	false	false	medium
MONDO:0015400	frontonasal arteriovenous malformation	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	otolaryngology|pediatric|neurology	cardiovascular_disorder|neurological_disorder	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0015401	maxillary arteriovenous malformation	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	general_surgery|vascular_surgery|neurology|hematology	cardiovascular_disorder|vacular_abnormality	vascular_disorder|teeth_disorder	false	false	false	false	high
MONDO:0015402	mandibular arteriovenous malformation	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	otolaryngology|cardiology|vascular_medicine__implied_by_the_context__is_not_in_the_list_so_i_am_removing_it|neurology|genetics_and_genomics|hematology	cardiovascular_disorder|vascular_anomaly	vascular_disorder|teeth_disorder	false	false	false	false	high
MONDO:0015403	non-involuting congenital hemangioma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	dermatology|pediatric|hematology	cardiovascular_disorder|cancer|inflammatory_disease	vascular_disorder|liver_disorder	false	false	false	false	low
MONDO:0015404	rapidly involuting congenital hemangioma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	dermatology|pediatric|hematology	cardiovascular_disorder|cancer|inflammatory_disease	vascular_disorder|skin_disorder	false	false	false	true	low
MONDO:0015405	cerebrofacial arteriovenous metameric syndrome	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0015406	cerebrofacial arteriovenous metameric syndrome type 1	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	pediatrics|neurology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0015407	cerebrofacial arteriovenous metameric syndrome type 3	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	neurology|genetics_and_genomics|hematology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0015408	diffuse lymphatic malformation	cancer_or_benign_tumor|cardiovascular_disorder|immune_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	immune_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	pediatric|oncology|hematology	cancer|lymphatic_system_disorder	vascular_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0015409	isolated congenital syngnathia	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	congenital_anomaly|neurodegenerative_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0015410	nasal dorsum fistula/cyst	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis	otolaryngology|ent	nasal_dorsum_fistula_cyst__inflammatory_disease_anatomy_related	nose_disorder|nasal_dorsum_fistula_cyst_would_be_incorrect__as_this_is_a_specific_condition__so_the_best_fitting_category_for_the_general_term_nasal_dorsum_fistula_cyst_is__nose_disorder	false	false	false	false	medium
MONDO:0015411	facial cleft	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	otolaryngology|pediatric	congenital_abnormality|birth_defect|neurodevelopmental_disease	facial_cleft_is_not_a_direct_match_in_the_list_so_it_would_be_removed_leaving_only_teeth_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0015413	median cleft of the upper lip and maxilla	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|otolaryngology	congenital_disorder|craniofacial_anomaly	bone_disorder|upper_gastrointestinal_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0015414	paramedian nasal cleft	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease|hereditary_disease	other	hereditary_disease|otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|otolaryngology	craniofacial_abnormality|congenital_disorder	nose_disorder	false	false	false	false	medium
MONDO:0015416	Tessier number 5 facial cleft	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	spinal_disorder|bone_disorder|joint_disorder|facial_cleft_disorder_is_not_in_the_list_so|teeth_disorder	false	false	false	false	medium
MONDO:0015417	Tessier number 6 facial cleft	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|otolaryngology	congenital_abnormality|neurodevelopmental_disorder	jaw_disorder|face_disorder|teeth_disorder	false	false	false	false	high
MONDO:0015419	midline cervical cleft	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	otolaryngology|pediatric|neurology	neurodegenerative_disease|cleft_palate_disease	spinal_disorder|throat_disorder	false	false	false	false	medium
MONDO:0015420	cleft lip and alveolus	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	otolaryngology|pediatric	birth_defect|genetic_disorder|developmental_disorder|congenital_disorder|neurodevelopmental_disorder|craniofacial_anomaly	bone_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0015421	orofaciodigital syndrome type 12	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|teeth_disorder	false	false	false	false	very_high
MONDO:0015425	lethal recessive chondrodysplasia	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0015426	Desbuquois dysplasia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|mental_health_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0015427	paroxysmal dyskinesia	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0015428	choroidal atrophy-alopecia syndrome	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease|integumentary_system_disorder	ophthalmology|genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0015430	ring chromosome 1	chromosomal_disorder	other	chromosomal_disorder	hematology|oncology|genetics_and_genomics	cancer|neurodegenerative_disease	immune_disorder|lymphatic_disorder|chromosome_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0015431	ring chromosome 10	chromosomal_disorder|syndromic_disease	other	syndromic_disease|chromosomal_disorder	oncology|genetics_and_genomics	cancer|neurodegenerative_disease	chromosomal_disorder|genetic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0015432	ring chromosome 12	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|anemia|neurodegenerative_disease	bone_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0015433	ring chromosome 17	chromosomal_disorder	other	chromosomal_disorder	oncology|genetics_and_genomics	cancer|neurodegenerative_disease	lung_disorder|kidney_disorder	false	true	false	false	high
MONDO:0015434	ring chromosome 18	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|neurodegenerative_disease	chromosomal_disorder|kidney_disorder|chromosomal_disorder____corrected_answer___blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0015435	ring chromosome 19	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|anemia|neurodegenerative_disease	immune_disorder|chromosomal_disorder|bone_disorder|genetic_disorder	false	true	false	false	high
MONDO:0015436	ring chromosome 20	chromosomal_disorder	other	chromosomal_disorder	oncology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	spinal_disorder|kidney_disorder	false	true	false	false	high
MONDO:0015437	ring chromosome 21	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0015438	ring chromosome 22	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|neurodegenerative_disease	spinal_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0015439	ring chromosome 4	chromosomal_disorder	other	chromosomal_disorder	oncology|genetics_and_genomics	cancer|neurodegenerative_disease	bone_disorder|kidney_disorder	false	true	false	true	high
MONDO:0015440	ring chromosome 6	chromosomal_disorder	other	chromosomal_disorder	oncology|genetics_and_genomics	chromosomal_abnormalities|genetic_disorders|cancer|neoplastic_diseases	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0015441	ring chromosome 7	chromosomal_disorder	other	chromosomal_disorder	oncology|genetics_and_genomics	cancer|neurodegenerative_disease	blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0015443	chromosome 8-derived supernumerary ring/marker	chromosomal_disorder	other	chromosomal_disorder	pediatrics|oncology|genetics_and_genomics	genetic_disorder|cancer|chromosome_8_derived_supernumerary_ring_marker	blood_bone_marrow_disorder|chromosome_abnormality	false	false	false	false	high
MONDO:0015445	autosomal dominant coarctation of aorta	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|cardiology|genetics_and_genomics	autosomal_dominant_coarctation_of_aorta_has_some_overlap_characteristics_but_is_specifically_a_cardiovascular_disorder__however_more_specific_term_would_be__congenital_heart_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0015446	atypical coarctation of aorta	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|cardiology|cardiothoracic	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0015447	differentiated thyroid carcinoma	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	cancer|thyroid_carcinoma	endocrine_disorder	false	true	false	true	medium
MONDO:0015448	mitochondrial complex III deficiency	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	metabolic_disease	mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatrics|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	mitochondrial_disease|muscle_disorder	false	false	false	false	very_high
MONDO:0015449	criss-cross heart	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|cardiothoracic	cardiovascular_disorder|cardiac_abnormality	heart_disorder	false	false	false	false	high
MONDO:0015450	triatrial heart	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|cardiothoracic	triatrial_heart_is_likely_a_misspelling_of_tricuspid_atresia_which_is_related_to_cardiovascular_disorders|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0015451	univentricular heart	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|cardiology|cardiothoracic	neonatal_condition|congenital_heart_defect|cardiovascular_disorder	vascular_disorder|vessel_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0015452	Coffin-Siris syndrome	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|skeletal_disorder	false	false	false	false	high
MONDO:0015453	Cogan syndrome	immune_system_disorder|disorder_of_visual_system|otorhinolaryngologic_disease	autoimmune_disease	disorder_of_orbital_region|disorder_of_visual_system|immune_system_disorder|otorhinolaryngologic_disease	pediatric|otolaryngology|ophthalmology|rheumatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	vascular_disorder|eye_disorder|joint_disorder	false	false	false	false	high
MONDO:0015454	multiple carboxylase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|hepatology	neurodegenerative_disease|metabolic_disorder	liver_disorder	false	false	false	true	high
MONDO:0015455	gonococcal conjunctivitis	disorder_of_visual_system|infectious_disease|reproductive_system_disorder|inflammatory_disease	infectious_disease	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease|infectious_disease|reproductive_system_disorder	obstetrics_and_gynecology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0015457	corpus callosum agenesis-double urinary collecting system syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|urology|pediatric	neurodegenerative_disease	urinary_tract_disorder|brain_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0015458	intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0015459	nasopharyngeal carcinoma	cancer_or_benign_tumor|respiratory_system_disorder|digestive_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	post_infectious_disorder|digestive_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder	oncology|otolaryngology	cancer	lymphatic_disorder|throat_disorder	false	true	false	true	high
MONDO:0015461	short rib-polydactyly syndrome	musculoskeletal_system_disorder|syndromic_disease|respiratory_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|respiratory_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	congenital_abnormality|metabolic_disorder	bone_disorder|joint_disorder|skeletal_disorder_is_not_in_the_list_so_it_becomes__bone_disorder	false	false	false	false	high
MONDO:0015462	thin ribs-tubular bones-dysmorphism syndrome	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	dysmorphic_syndrome|metabolic_disorder	bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015463	craniodigital syndrome-intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|intellectual_disability_syndrome_doesn_t_have_a_direct_match_so_excluding_it	false	false	false	false	high
MONDO:0015464	craniofrontonasal dysplasia-Poland anomaly syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|breast_disorder|hereditary_disease	other	musculoskeletal_system_disorder|breast_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric|neurology	neurodegenerative_disease|mental_health_disorder|inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	bone_disorder|skull_disorder|facial_disorder	false	false	false	false	high
MONDO:0015465	craniometaphyseal dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0015466	cranio-osteoarthropathy	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0015467	craniosynostosis, Philadelphia type	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	genetic_condition|neurodevelopmental_disorder|autoimmune_diseases|congenital__anomaly|inflammatory_disease|skeletal_abnormality|connective_tissue_disease____corrected_list_using_provided_categories____metabolic_disorder	bone_disorder|brain_disorder|skull_abnormality_disorder	false	false	false	false	medium
MONDO:0015468	craniosynostosis-cataract syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric|ophthalmology	neurodegenerative_disease|metabolic_disorder	bone_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0015469	craniosynostosis	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|inflammatory_disease	bone_disorder|skull_disorder	false	false	false	false	medium
MONDO:0015471	benign focal seizures of adolescence	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	true	low
MONDO:0015473	cryptorchidism-arachnodactyly-intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|urology|pediatric	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0015474	cryptosporidiosis	infectious_disease|digestive_system_disorder	infectious_disease	digestive_system_disorder|infectious_disease	pediatric|gastroenterology	autoimmune_diseases|inflammatory_disease	liver_disorder|lower_gastrointestinal_disorder|immune_disorder	true	false	false	false	medium
MONDO:0015476	cysts and fistulae of the face and oral cavity	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	oral_cavity_suggests_ent__so_likely_otolaryngology|neurology_also_not_as_likely_as_other_two|genetics_and_genomics_is_unlikely_but_still_a_possible_match|otolaryngology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|oral_cavity	true	false	false	true	medium
MONDO:0015477	pinnae fistula or cyst	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	otolaryngology|dermatology	cyst|inflammatory_disease|allergy	skin_disorder|upper_gastrointestinal_disorder|ear_disorder	false	false	false	true	low
MONDO:0015479	submucosal cleft palate	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|otolaryngology	congenital_disorder|neurodevelopmental_disease	teeth_disorder|throat_disorder	false	false	false	true	medium
MONDO:0015480	coloboma of superior eyelid	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|ophthalmology	neurological_disease|developmental_disorder	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0015481	coloboma of inferior eyelid	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|ophthalmology	neurological_disease|ocular_condition	eye_disorder	false	false	false	false	low
MONDO:0015483	mandibulofacial dysostosis	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric|otolaryngology	genetic_disorder|metabolic_disorder	bone_disorder|teeth_disorder|joint_disorder	false	false	false	false	high
MONDO:0015484	cysticercosis	infectious_disease|digestive_system_disorder	infectious_disease	digestive_system_disorder|infectious_disease	neurology|hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0015486	keratoconus	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0015487	fatal infantile encephalocardiomyopathy	musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder|metabolic_disease	mitochondrial_disease|metabolic_disease|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	muscle_disorder|brain_disorder|heart_disorder	true	false	false	false	very_high
MONDO:0015491	immune complex mediated vasculitis	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	rheumatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0015492	anti-neutrophil cytoplasmic antibody-associated vasculitis	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	rheumatology|hematology	autoimmune_diseases|inflammatory_disease	vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0015493	lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy	metabolic_disease|hereditary_disease|integumentary_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|integumentary_system_disorder	endocrinology|cardiology|hepatology	metabolic_disorder|cardiovascular_disorder	liver_disorder|muscle_disorder|heart_disorder|endocrine_disorder	true	false	true	false	high
MONDO:0015494	isolated dystonia	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology	neurodegenerative_disease|autoimmune_diseases|adrenal_gland_disease	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0015496	macroglossia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	neonatology|pulmonology|pediatrics	neurodegenerative_disease|autoimmune_diseases	eye_disorder|throat_disorder	false	false	false	false	medium
MONDO:0015498	oromandibular-limb anomalies syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	other	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|teeth_disorder|joint_disorder	false	false	false	false	medium
MONDO:0015500	facial arteriovenous malformation	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	vascular_surgery|general_surgery|neurosurgery|dermatology|neurology|radiology	cardiovascular_disorder|vascular_disorder	skin_disorder|vascular_disorder	false	false	false	true	high
MONDO:0015514	hereditary endocrine growth disease	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	pediatric|endocrinology|genetics_and_genomics	hereditary|endocrine_growth_disease|adrenal_gland_disease|metabolic_disorder	endocrine_disorder|hereditary_disorder	false	false	false	false	high
MONDO:0015515	carnitine palmitoyltransferase II deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics|neurology|genetics_and_genomics|cardiology|hepatology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	true	high
MONDO:0015516	symbrachydactyly of hands and feet	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0015517	common variable immunodeficiency	cancer_or_benign_tumor|syndromic_disease|hematologic_disorder|hereditary_disease|immune_system_disorder	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	immunology|pediatric|genetics_and_genomics|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0015518	infantile bilateral striatal necrosis	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0015519	congenital or early infantile CACH syndrome	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	biliary_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0015520	late infantile CACH syndrome	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0015521	juvenile or adult CACH syndrome	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|endocrinology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|kidney_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0015523	epithelioid hemangioendothelioma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	hematology|oncology	cancer	vascular_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0015524	hyperplastic polyposis syndrome	syndromic_disease|cancer_or_benign_tumor|hereditary_disease|digestive_system_disorder	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|digestive_system_disorder|cancer_or_benign_tumor	oncology|genetics_and_genomics|hepatology|gastroenterology	polyposis_syndrome|cancer|neoplastic_disease|genetic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0015525	congenital pseudoarthrosis of the limbs	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0015526	cold-induced sweating syndrome	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	dermatology|neurology	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease|metabolic_disorder	skin_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0015528	congenital epulis	musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	mouth_disorder|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	dermatology|pediatric|genetics_and_genomics	neurodegenerative_disease|cancer|anemia|autoimmune_diseases|inflammatory_disease	skin_disorder|teeth_disorder	false	false	false	false	low
MONDO:0015529	paroxysmal Hemicrania	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	hematology|neurology	neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0015530	trigeminal autonomic cephalalgia	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	neurology|otolaryngology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	spinal_disorder|vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0015531	non-Langerhans cell histiocytosis	immune_system_disorder	other	immune_system_disorder	pediatric|oncology	cancer|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0015532	generalized eruptive histiocytosis	immune_system_disorder	other	immune_system_disorder	hematology|dermatology	cancer|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0015533	benign cephalic histiocytosis	immune_system_disorder	other	immune_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|cancer|inflammatory_disease	brain_disorder|blood_bone_marrow_disorder	false	false	false	true	low
MONDO:0015534	juvenile xanthogranuloma	immune_system_disorder	other	immune_system_disorder	pediatric|oncology	cancer|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0015535	xanthoma disseminatum	immune_system_disorder	other	immune_system_disorder	pediatrics|dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0015536	papular xanthoma	immune_system_disorder	other	immune_system_disorder	dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|liver_disorder	false	false	false	false	low
MONDO:0015537	necrobiotic xanthogranuloma	immune_system_disorder	other	immune_system_disorder	pathology|dermatology|oncology	neurodegenerative_disease|cancer|autoimmune_diseases|inflammatory_disease	skin_disorder|liver_disorder	false	false	false	false	low
MONDO:0015538	indeterminate dendritic cell tumor	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	medium
MONDO:0015539	progressive nodular histiocytosis	immune_system_disorder	other	immune_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0015540	hemophagocytic syndrome	syndromic_disease|immune_system_disorder	other	syndromic_disease|immune_system_disorder	hematology|pediatrics|genetics_and_genomics	anemia|metabolic_disorder|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	very_high
MONDO:0015541	hereditary hemophagocytic lymphohistiocytosis	hereditary_disease|syndromic_disease|immune_system_disorder	other	hereditary_disease|syndromic_disease|immune_system_disorder	hematology|pediatric|genetics_and_genomics	anemia|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0015542	secondary hemophagocytic lymphohistiocytosis	syndromic_disease|immune_system_disorder	other	syndromic_disease|immune_system_disorder	immunology|hematology|oncology	anemia|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0015544	acquired hemophagocytic lymphohistiocytosis associated with malignant disease	syndromic_disease|immune_system_disorder	other	syndromic_disease|immune_system_disorder	hematology|oncology	cancer|anemia|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	true	true	false	true	very_high
MONDO:0015545	macrophage activation syndrome	syndromic_disease|immune_system_disorder	other	syndromic_disease|immune_system_disorder	immunology|pulmonology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lung_disorder	false	false	false	true	high
MONDO:0015546	non-distal monosomy 10q	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|skeletal_system_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0015547	hereditary dementia	psychiatric_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0015548	Huntington disease-like syndrome	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|psychiatric_disorder|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0015550	suprabasal epidermolysis bullosa simplex	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0015552	acral dystrophic epidermolysis bullosa	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0015553	dystrophic epidermolysis bullosa, nails only	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0015554	typical urticaria pigmentosa	cancer_or_benign_tumor|hematologic_disorder|hereditary_disease|integumentary_system_disorder|inflammatory_disease|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|hereditary_disease|immune_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor|inflammatory_disease	dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	skin_disorder|liver_disorder|immune_disorder	false	false	false	true	low
MONDO:0015555	plaque-form urticaria pigmentosa	cancer_or_benign_tumor|hematologic_disorder|hereditary_disease|integumentary_system_disorder|inflammatory_disease|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|hereditary_disease|immune_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor|inflammatory_disease	dermatology|genetics_and_genomics	allergy|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0015556	nodular urticaria pigmentosa	cancer_or_benign_tumor|hematologic_disorder|hereditary_disease|integumentary_system_disorder|inflammatory_disease|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|hereditary_disease|immune_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor|inflammatory_disease	dermatology|allergy_and_immunology	allergy|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0015557	Smouldering systemic mastocytosis	cancer_or_benign_tumor|hematologic_disorder|hereditary_disease|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|hereditary_disease|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0015558	isolated bone marrow mastocytosis	cancer_or_benign_tumor|hematologic_disorder|hereditary_disease|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|hereditary_disease|immune_system_disorder|cancer_or_benign_tumor	immunology|hematology|oncology	allergy|cancer	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0015559	lymphoadenopathic mastocytosis with eosinophilia	cancer_or_benign_tumor|hematologic_disorder|hereditary_disease|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|hereditary_disease|immune_system_disorder|cancer_or_benign_tumor	hematology|allergy_and_immunology	allergy|cancer|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0015562	distal monosomy 17q	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|medical_genetics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|joint_disorder|skeletal_disorder|developmental_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0015564	Castleman disease	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	hematology|oncology	cancer|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	true	medium
MONDO:0015565	cap polyposis	hereditary_disease|digestive_system_disorder|immune_system_disorder	other	hereditary_disease|digestive_system_disorder|immune_system_disorder	oncology|genetics_and_genomics|gastroenterology	cancer|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0015566	2q24 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0015567	cataract-glaucoma syndrome	syndromic_disease|disorder_of_visual_system	other	syndromic_disease|disorder_of_visual_system	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	kidney_disorder|lower_gastrointestinal_disorder|eye_disorder	false	false	false	true	high
MONDO:0015568	isolated congenital nasal pyriform aperture stenosis	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	otolaryngology|pediatric	cardiovascular_disorder|congenital_anomaly	respiratory_disorder|nose_disorder	false	false	false	true	low
MONDO:0015569	congenital nasal pyriform aperture stenosis with holoprosencephaly	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	pediatric|neurology|genetics_and_genomics	holoprosencephaly|neurodegenerative_disease|congenital_disease|metabolic_disorder	brain_disorder|nose_disorder	false	false	false	false	very_high
MONDO:0015570	isolated congenital auditory ossicle malformation	otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	otolaryngology|pediatric|genetics_and_genomics	metabolic_disorder	ear_disorder|throat_disorder	false	false	false	false	medium
MONDO:0015571	deletion 5q35	chromosomal_disorder	other	chromosomal_disorder	hematology|genetics_and_genomics	deletion_5q35_is_a_subtype_of_alpha_thalassemia_which_is_a_form_of_anemia|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0015573	subacute cutaneous lupus erythematosus	connective_tissue_disorder|immune_system_disorder	autoimmune_disease	acute_disease|connective_tissue_disorder|immune_system_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0015574	chronic cutaneous lupus erythematosus	connective_tissue_disorder|immune_system_disorder	autoimmune_disease	connective_tissue_disorder|immune_system_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|joint_disorder	false	false	false	true	medium
MONDO:0015579	Hb Bart's hydrops fetalis	hematologic_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|hematologic_disorder	obstetrics_and_gynecology|hematology	autoimmune_diseases|metabolic_disorder	immune_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0015580	distal monosomy 7q36	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|medical_genetics	neurodegenerative_disease|anemia|metabolic_disorder	muscle_disorder|brain_disorder|joint_disorder|skeletal_disorder	false	false	false	false	very_high
MONDO:0015583	2p21 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	developmental_delay___note__the_original_list_of_categories_did_not_have_a_direct_match_for_2p21_microdeletion_syndrome__so_i_added_two_relevant_categories_that_are_commonly_associated_with_microdeletion_syndromes__if_you_would_like_to_stick_strictly_to_the_provided_category_list__the_best_fitting_category_is_brain_disorder|brain_disorder|intellectual_disability	false	false	false	false	very_high
MONDO:0015584	febrile infection-related epilepsy syndrome	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|inflammatory_disease	immune_disorder|brain_disorder|lower_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0015585	cryptogenic late-onset epileptic spasms	nervous_system_disorder	other	nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0015587	rolandic epilepsy-speech dyspraxia syndrome	nervous_system_disorder	other	nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|speech_dispraxia_syndrome_is_not_in_the_list_so_it_will_be_removed|spinal_disorder	false	false	false	true	high
MONDO:0015588	limbic encephalitis	nervous_system_disorder|inflammatory_disease	other	acute_disease|nervous_system_disorder|inflammatory_disease	neurology|psychiatry	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder	true	false	false	true	high
MONDO:0015589	paraneoplastic limbic encephalitis	nervous_system_disorder|inflammatory_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	acute_disease|nervous_system_disorder|cancer_or_benign_tumor|inflammatory_disease|syndromic_disease	neurology|oncology	cancer|autoimmune_diseases	brain_disorder|immune_disorder	false	false	false	true	high
MONDO:0015590	classic paraneoplastic limbic encephalitis	nervous_system_disorder|inflammatory_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	acute_disease|nervous_system_disorder|cancer_or_benign_tumor|inflammatory_disease|syndromic_disease	neurology|oncology	neurodegenerative_disease|cancer|autoimmune_diseases	brain_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0015592	limbic encephalitis with LGI1 antibodies	nervous_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	acute_disease|post_infectious_disorder|infectious_disease|nervous_system_disorder|inflammatory_disease	immunology|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	immune_disorder_brain_disorder	true	false	false	true	high
MONDO:0015595	posttransplant acute limbic encephalitis	nervous_system_disorder|inflammatory_disease	other	acute_disease|disease_related_to_transplantation|nervous_system_disorder|inflammatory_disease	neurology|psychiatry	inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder	false	false	false	false	high
MONDO:0015596	non-herpetic acute limbic encephalitis	nervous_system_disorder|inflammatory_disease	other	acute_disease|nervous_system_disorder|inflammatory_disease	neurology|psychiatry	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder	true	false	false	true	high
MONDO:0015597	pustulosis palmaris et plantaris	hereditary_disease|integumentary_system_disorder|inflammatory_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder|integumentary_system_disorder|inflammatory_disease	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|joint_disorder|immune_disorder	false	false	false	true	medium
MONDO:0015599	atopic keratoconjunctivitis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|allergy_and_immunology	inflammatory_disease|allergy|autoimmune_diseases	eye_disorder|skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0015600	X-linked intellectual disability, Cilliers type	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0015601	X-linked intellectual disability, van Esch type	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0015604	middle ear anomaly	otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis	other	otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis	pediatric|otolaryngology	inflammatory_disease	ear_disorder	false	false	false	false	medium
MONDO:0015605	distal monosomy 9p	endocrine_system_disorder|chromosomal_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|chromosomal_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	anemia|neurodegenerative_disease|metabolic_disorder	lymphatic_disorder|immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0015606	Xp22.3 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder|mental_health_disorder	developmental_disorder|immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0015607	partial chromosome Y deletion	chromosomal_disorder|reproductive_system_disorder	other	reproductive_system_disorder|chromosomal_disorder	genetics_and_genomics|pediatrics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0015608	acute myeloid leukemia and myelodysplastic syndromes related to radiation	immune_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|hematologic_disorder|acute_disease|connective_tissue_disorder|immune_system_disorder	oncology|hematology	cancer|anemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0015609	advanced sleep phase syndrome	hereditary_disease	other	sleep_disorder|hereditary_disease	neurology|endocrinology	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|brain_disorder	false	false	false	false	medium
MONDO:0015610	acquired aplastic anemia	hematologic_disorder	anemia	hematologic_disorder	genetics_and_genomics|hematology	anemia|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0015611	neutral lipid storage disease	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|metabolism|neonatology	neurodegenerative_disease|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0015612	Dent disease	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	renal_medicine|genetics_and_genomics|urology	anemia|autoimmune_diseases|metabolic_disorder	kidney_disorder|teeth_disorder	false	false	false	false	high
MONDO:0015613	dentin dysplasia	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	pediatric|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	bone_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0015614	dermatitis herpetiformis	immune_system_disorder|inflammatory_disease|integumentary_system_disorder	autoimmune_disease	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	allergy_and_immunology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0015622	wound myiasis	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease	dermatology|infectious_diseases	inflammatory_disease|wound_infection	nose_disorder|skin_disorder	true	false	false	true	high
MONDO:0015623	cavitary myiasis	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease	pulmonology|dermatology|otolaryngology	cancer|inflammatory_disease	nose_disorder|skin_disorder	true	false	false	false	medium
MONDO:0015624	diazoxide-sensitive diffuse hyperinsulinism	metabolic_disease|endocrine_system_disorder|hereditary_disease|digestive_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease|endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|metabolic_disease|digestive_system_disorder|disorder_of_development_or_morphogenesis	pediatric|endocrinology	adrenal_gland_disease|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0015625	diazoxide-resistant diffuse hyperinsulinism	metabolic_disease|endocrine_system_disorder|hereditary_disease|digestive_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease|endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|metabolic_disease|digestive_system_disorder|disorder_of_development_or_morphogenesis	pediatric|endocrinology	endocrine_disorder|metabolic_disorder|genetic_condition	endocrine_disorder|lower_gastrointestinal_disorder	false	false	true	false	very_high
MONDO:0015626	Charcot-Marie-Tooth disease	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0015627	multiple epiphyseal dysplasia due to collagen 9 anomaly	hereditary_disease|connective_tissue_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|connective_tissue_disorder	rheumatology|genetics_and_genomics|orthopaedic	genetic_disorder|metabolic_disorder	joint_disorder|bone_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015628	von Willebrand disease type 2A	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	cardiovascular_disorder|bleeding_disorder|genetic_disorder|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0015629	von Willebrand disease type 2B	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	anemia|cardiovascular_disorder|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0015630	von Willebrand disease type 2M	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|bleeding_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0015631	von Willebrand disease type 2N	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0015632	FASTKD2-related infantile mitochondrial encephalomyopathy	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0015634	isolated osteopoikilosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic	metabolic_disorder|osteoporosis	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	low
MONDO:0015635	porokeratotic eccrine ostial and dermal duct nevus	disorder_of_development_or_morphogenesis|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric	neurodevelopmental_disease|cancer	skin_disorder	false	false	false	false	medium
MONDO:0015636	dirofilariasis	infectious_disease	infectious_disease	infectious_disease	pulmonology|hematology|pediatric	inflammatory_disease|autoimmune_diseases	skin_disorder|lymphatic_disorder	true	false	false	true	low
MONDO:0015637	benign non-familial infantile seizures	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	metabolic_disorder|inflammatory_disease|neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0015638	benign partial epilepsy of infancy with complex partial seizures	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	low
MONDO:0015639	benign partial epilepsy with secondarily generalized seizures in infancy	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0015640	benign infantile seizures associated with mild gastroenteritis	nervous_system_disorder	other	nervous_system_disorder	gastroenterology|neurology|pediatric	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0015641	benign infantile focal epilepsy with midline spikes and wave during sleep	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	low
MONDO:0015642	benign partial infantile seizures	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	none
MONDO:0015643	photosensitive epilepsy	nervous_system_disorder|hereditary_disease	other	radiation_induced_disorder|nervous_system_disorder|hereditary_disease	neurology|pediatric	neurological_disorder	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0015644	audiogenic seizures	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	inflammatory_disease|neurodegenerative_disease|mental_health_disorder	brain_disorder|ear_disorder	false	false	false	true	medium
MONDO:0015645	eating seizures	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	upper_gastrointestinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0015646	orgasm-induced seizures	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	reproductive_system_disorder|brain_disorder	false	false	false	false	low
MONDO:0015647	thinking seizures	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|neurological_disorder	false	false	false	false	medium
MONDO:0015648	startle epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|epilepsy	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0015649	micturation-induced seizures	nervous_system_disorder	other	nervous_system_disorder	neurology|urology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0015650	epilepsy syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0015653	monogenic epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0015660	sporadic fetal brain disruption sequence	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|pediatric|obstetrics_and_gynecology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0015661	dextrocardia	hereditary_disease|syndromic_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|cardiovascular_disorder	cardiothoracic|cardiology	congenital_disorder|cardiovascular_disorder	heart_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0015663	diencephalic syndrome	syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder	neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0015664	idiopathic pulmonary artery dilatation	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	idiopathic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|pulmonology	cardiovascular_disorder|inflammatory_disease	vascular_disorder|heart_disorder|lung_disorder	false	false	false	false	medium
MONDO:0015665	scleromyxedema	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0015666	familial idiopathic dilatation of the right atrium	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	idiopathic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|cardiology|genetics_and_genomics|pediatrics	cardiovascular_disorder|familial_idiopathic_dilatation_of_the_right_atrium	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0015667	acute myeloid leukemia by FAB classification	immune_system_disorder|connective_tissue_disorder|hematologic_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|immune_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder	oncology|hematology	anemia|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0015672	diprosopus	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|autoimmune_diseases	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0015674	late infantile neuronal ceroid lipofuscinosis	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0015675	distomatosis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|liver_disorder	true	false	false	true	high
MONDO:0015677	cardiac diverticulum	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic	cardiovascular_disorder|cardiac_condition	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0015678	dysplasia of head of femur, Meyer type	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic	metabolic_disorder|inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0015681	childhood disintegrative disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|pediatric	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0015686	primary peritoneal carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|lung_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0015687	chronic eosinophilic leukemia	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder|hematologic_disorder	oncology|pulmonology|hematology	cancer|inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0015688	myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|genetics_and_genomics|hematology|immunology	cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0015689	myeloid neoplasm associated with PDGFRA rearrangement	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	anemia|cancer	blood_bone_marrow_disorder|vascular_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0015690	myeloid neoplasm associated with PDGFRB rearrangement	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	anemia|cancer	blood_bone_marrow_disorder|vascular_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0015691	hypereosinophilic syndrome	cardiovascular_disorder|immune_system_disorder|hematologic_disorder|syndromic_disease|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|immune_system_disorder|cardiovascular_disorder|syndromic_disease|hematologic_disorder	pulmonology|hematology	inflammatory_disease|autoimmune_diseases|allergy	blood_bone_marrow_disorder|vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0015692	refractory anemia with excess blasts in transformation	hematologic_disorder|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hematologic_disorder	oncology|hematology	anemia|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0015694	malignant melanoma of the mucosa	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	oncology|dermatology	cancer|malignant_melanoma_of_the_mucosa	skin_disorder	false	true	false	true	high
MONDO:0015695	combined immunodeficiency due to CRAC channel dysfunction	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	allergy_and_immunology|genetics_and_genomics|immunodeficiency_is_closely_related_to_immunology_so	metabolic_disorder|anemia|inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0015696	Good syndrome	immune_system_disorder|hematologic_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder|hematologic_disorder	oncology|pediatric|hematology	metabolic_disorder|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0015697	immunoglobulin heavy chain deficiency	immune_system_disorder	other	immune_system_disorder	genetics_and_genomics|allergy_and_immunology|pediatric|hematology	immunodeficiency|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0015698	transient hypogammaglobulinemia of infancy	immune_system_disorder|hematologic_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease|immune_system_disorder|hematologic_disorder	immunology|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	medium
MONDO:0015699	immunodeficiency due to a classical component pathway complement deficiency	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|allergy_and_immunology|rheumatology|hematology	inflammatory_disease|autoimmune_diseases|anemia	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0015700	immunodeficiency due to a late component of complement deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|allergy_and_immunology|immunology_is_not_listed__but_its_closest_equivalent_is__allergy_and_immunology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0015701	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency	immune_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	immune_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|immunology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0015702	T-B+ severe combined immunodeficiency due to CD45 deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatric|immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0015703	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|pediatric|hematology|genetics_and_genomics	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0015704	familial scaphocephaly syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	orthopaedic|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0015705	autosomal recessive centronuclear myopathy	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0015706	mosaic trisomy 1	chromosomal_disorder	other	chromosomal_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics	neurodegenerative_disease|cancer|cardiovascular_disorder|metabolic_disorder	spinal_disorder|nervous_system_disorder	false	false	false	false	medium
MONDO:0015708	immuno-osseous dysplasia	immune_system_disorder	other	immune_system_disorder	allergy_and_immunology|immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	bone_disorder|immune_disorder	false	false	false	false	high
MONDO:0015712	non-distal trisomy 10q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|anemia	bone_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0015713	idiopathic central precocious puberty	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|idiopathic_disease|reproductive_system_disorder|hereditary_disease	pediatric|endocrinology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0015714	secondary central precocious puberty	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder|hereditary_disease	pediatric|endocrinology|obstetrics_and_gynecology	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0015715	severe hemophilia B	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematogenetics_and_genomics|hematology	metabolic_disorder|inflammatory_disease|anemia	blood_bone_marrow_disorder|joint_disorder	false	false	false	true	high
MONDO:0015716	moderately severe hemophilia B	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|inflammatory_disease|anemia	blood_bone_marrow_disorder|joint_disorder	false	false	false	true	high
MONDO:0015717	mild hemophilia B	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|joint_disorder	false	false	false	true	low
MONDO:0015718	mosaic trisomy 12	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|medical_genetics	neurodegenerative_disease|intellectual_disability|developmental_disorder|genetic_disorder	bone_disorder	false	false	false	false	high
MONDO:0015719	severe hemophilia A	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|anemia	blood_bone_marrow_disorder|joint_disorder	false	false	false	true	high
MONDO:0015720	moderately severe hemophilia A	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	autoimmune_diseases|anemia|inflammatory_disease	vascular_disorder|blood_bone_marrow_disorder|joint_disorder	false	false	false	true	high
MONDO:0015721	mild hemophilia A	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	hemophilia_a|metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|joint_disorder	false	false	false	true	low
MONDO:0015722	congenital vitamin K-dependent coagulation factors deficiency	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0015723	trisomy 12p	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|anemia|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0015724	non-distal trisomy 13q	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|mental_health_disorder|inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder|joint_disorder|eye_disorder	false	false	false	false	high
MONDO:0015725	mosaic trisomy 14	chromosomal_disorder	other	chromosomal_disorder	neonatology|pediatric|genetics_and_genomics	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0015726	distal trisomy 14q	chromosomal_disorder|syndromic_disease	other	syndromic_disease|chromosomal_disorder	pediatric|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|ear_disorder|brain_disorder|kidney_disorder|joint_disorder|lower_gastrointestinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0015727	mosaic trisomy 15	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	muscle_disorder|upper_gastrointestinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0015728	distal trisomy 15q	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|developmental_disorder	false	false	false	false	high
MONDO:0015729	mosaic trisomy 16	chromosomal_disorder	other	chromosomal_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0015730	mosaic trisomy 17	chromosomal_disorder	other	chromosomal_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0015731	high anorectal malformation	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|gastroenterology	anorectal_malformation_is_a_congenital_anomaly_of_the_rectum_and_anus__typically_involving_the_rectal_pouch_being_located_above_the_pubococcygeus_muscle__levator_ani__and_not_being_able_to_open_into_the_anal_canal__this_suggests_a_developmental_issue_rather_than_a_disease_process_per_se|neurodegenerative_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0015732	intermediate anorectal malformation	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|surgery|gastroenterology	birth_defect|congenital_abnormality|cardiovascular_disorder|developmental_disorder|anorectal_malformation|metabolic_disorder|gastrointestinal_disorder|musculoskeletal_disease___corrected_list_based_on_provided_category_list____congenital_anomaly	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0015733	low anorectal malformation	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|general_surgery|obstetrics_and_gynecology|gastroenterology	anorectal_malformation|metabolic_disorder	lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0015734	rectal duplication	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|general_surgery|gastroenterology	cancer|autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0015735	severe congenital nemaline myopathy	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	pediatric|neurology|genetics_and_genomics	congenital_myopathy|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0015736	intermediate nemaline myopathy	musculoskeletal_system_disorder|nervous_system_disorder	other	nervous_system_disorder|musculoskeletal_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0015737	typical nemaline myopathy	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	pediatric|neurology|genetics_and_genomics	muscle_dystrophy|neurodegenerative_disease	spinal_disorder|muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0015738	childhood-onset nemaline myopathy	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0015739	adult-onset nemaline myopathy	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics	cardiovascular_disorder|autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0015740	trisomy 18p	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|anemia|neurodegenerative_disease	spinal_disorder|urinary_tract_disorder|brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0015741	distal trisomy 18q	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|upper_gastrointestinal_disorder|joint_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0015742	periventricular leukomalacia	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0015743	idiopathic bilateral vestibulopathy	otorhinolaryngologic_disease	other	idiopathic_disease|otorhinolaryngologic_disease	neurology|otolaryngology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	ear_disorder|vestibulopathy_is_a_disorder_related_to_the_inner_ear	false	false	false	false	medium
MONDO:0015744	distal trisomy 19q	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0015745	microcephaly-polymicrogyria-corpus callosum agenesis syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0015746	male infertility due to globozoospermia	reproductive_system_disorder	other	reproductive_system_disorder	urology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	male_infertility|reproductive_system_disorder	false	false	false	false	high
MONDO:0015748	hereditary mucosal leukokeratosis	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	cancer|inflammatory_disease	skin_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0015749	6q16 deletion syndrome	reproductive_system_disorder|disorder_of_development_or_morphogenesis|chromosomal_disorder|endocrine_system_disorder|nervous_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|chromosomal_disorder|reproductive_system_disorder|hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0015751	craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease	spinal_disorder|bone_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0015752	intellectual disability-cataracts-kyphosis syndrome	syndromic_disease	other	syndromic_disease	ophthalmology|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|kyrphosis_is_a_skeletal_disorder_so_i_will_also_add__skeletal_disease	spinal_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0015753	cap myopathy	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	orthopaedic|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|skeletal_muscle_disorder	false	false	false	false	high
MONDO:0015755	myopathy with hexagonally cross-linked tubular arrays	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics	muscle_disease|neurodegenerative_disease	muscle_disorder|myopathy	false	false	false	false	medium
MONDO:0015756	myeloid hemopathy	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|genetics_and_genomics	cancer|autoimmune_diseases|anemia	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	false	high
MONDO:0015757	lymphoid hemopathy	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|immunology|oncology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0015758	primary cutaneous T-cell lymphoma	integumentary_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|integumentary_system_disorder	dermatology|oncology	cancer|autoimmune_diseases|inflammatory_disease	skin_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	medium
MONDO:0015759	B-cell non-Hodgkin lymphoma	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	high
MONDO:0015760	T-cell non-Hodgkin lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0015761	trisomy 10p	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease|cardiovascular_disorder|neurodegenerative_disease	bone_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0015762	progressive familial intrahepatic cholestasis	endocrine_system_disorder|digestive_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|hereditary_disease|digestive_system_disorder|metabolic_disease|syndromic_disease	genetics_and_genomics|hepatology	metabolic_disorder|adrenal_gland_disease	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0015763	mosaic trisomy 2	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0015764	mosaic trisomy 20	chromosomal_disorder	other	chromosomal_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0015766	cholera	digestive_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|inflammatory_disease|digestive_system_disorder	public_health|gastroenterology|infectious_diseases	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0015767	trisomy 4p	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	limb_abnormality|developmental_delay|joint_disorder|birth_defect	false	false	false	false	high
MONDO:0015768	trisomy 5p	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	skeletal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0015769	distal trisomy 6p	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder	false	false	false	false	high
MONDO:0015770	congenital hypogonadotropic hypogonadism	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|endocrine_dysfunction	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0015771	mosaic trisomy 7	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|obstetrics_and_gynecology|pediatric	metabolic_disorder|neurodegenerative_disease|cancer	spinal_disorder|muscle_disorder|bone_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0015772	trisomy 8q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0015773	fibular dimelia-diplopodia syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0015774	thoraco-abdominal enteric duplication	digestive_system_disorder|syndromic_disease	other	digestive_system_disorder|syndromic_disease	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0015775	non-rhizomelic chondrodysplasia punctata	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|dermatology|orthopaedic|pediatric	metabolic_disorder|neurodegenerative_disease	skin_disorder|bone_disorder	false	false	false	false	medium
MONDO:0015776	rhizomelic chondrodysplasia punctata	disorder_of_visual_system|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	musculoskeletal_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease|metabolic_disease	genetics_and_genomics|dermatology|pediatric	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	joint_disorder|skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0015779	45,X/46,XY mixed gonadal dysgenesis	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	genetics_and_genomics|urology|obstetrics_and_gynecology	metabolic_disorder|sexual_health_disorder|gonadal_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0015780	dyskeratosis congenita	cancer_or_benign_tumor|syndromic_disease|integumentary_system_disorder|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|dermatology|pediatric	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|skin_disorder|bone_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0015781	facial dysmorphism-shawl scrotum-joint laxity syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|medical_genetics|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	joint_disorder|skin_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0015782	dysmorphism-cleft palate-loose skin syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|otolaryngology|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	cleft_palate_disorder|joint_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0015783	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1	endocrine_system_disorder|chromosomal_disorder|reproductive_system_disorder|syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|reproductive_system_disorder|chromosomal_disorder	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|upper_gastrointestinal_disorder|muscle_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0015784	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2	endocrine_system_disorder|chromosomal_disorder|reproductive_system_disorder|syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|reproductive_system_disorder|chromosomal_disorder	neurology|genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0015785	Prader-Willi syndrome due to translocation	endocrine_system_disorder|chromosomal_disorder|reproductive_system_disorder|syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|reproductive_system_disorder|chromosomal_disorder	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|genetic_disorder_is_not_in_the_list_but_closest_match_is_metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0015786	Prader-Willi syndrome due to imprinting mutation	endocrine_system_disorder|chromosomal_disorder|reproductive_system_disorder|syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|reproductive_system_disorder|chromosomal_disorder	genetics_and_genomics|endocrinology|gastroenterology|pediatric	metabolic_disorder|genetic_disorder	upper_gastrointestinal_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0015787	symptomatic form of hemophilia A in female carriers	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology|obstetrics_and_gynecology	anemia|metabolic_disorder	blood_bone_marrow_disorder|joint_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0015788	symptomatic form of hemophilia B in female carriers	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|joint_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0015790	central diabetes insipidus	endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder	neurology|endocrinology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0015791	peripheral precocious puberty	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	endocrinology|pediatric	autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0015792	transient congenital hypothyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|pediatric	autoimmune_diseases|metabolic_disorder	thyroid_disorder|endocrine_disorder|congenital_disorder	false	false	false	true	low
MONDO:0015793	moderate multiminicore disease with hand involvement	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|rheumatology|dermatology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0015794	antenatal multiminicore disease with arthrogryposis multiplex congenita	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|orthopaedic|pediatric|obstetrics_and_gynecology	arthrogryposis_multiplex_congenita__removed_from_consideration|metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0015795	undifferentiated embryonal sarcoma of the liver	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|hepatology|pediatric	adrenal_gland_disease|cancer	blood_bone_marrow_disorder|muscle_disorder|liver_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0015796	acute lung injury	respiratory_system_disorder|injury	other	respiratory_system_disorder|acute_disease	pulmonology|cardiothoracic	inflammatory_disease|acute_lung_injury_can_also_be_categorized_as_respiratory_disorder_which_is_not_in_the_list_but_is_often_associated_with_inflammatory_disease	lower_respiratory_injury|lung_disorder	false	false	false	false	high
MONDO:0015797	UV-sensitive syndrome	integumentary_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	true	medium
MONDO:0015798	inflammatory myofibroblastic tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|oncology|rheumatology|orthopaedic|dermatology|pediatric|hematology|pathology	inflammatory_disease|cancer	soft_tissue_disorder|muscle_disorder	false	true	false	true	medium
MONDO:0015799	Smith-McCort dysplasia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0015800	osteosclerosis-developmental delay-craniosynostosis syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	bone_disorder|developmental_delay|craniosynostosis_syndrome	false	false	false	false	high
MONDO:0015801	hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation	hematologic_disorder	other	hematologic_disorder	pulmonology|hematology|genetics_and_genomics|hepatology	metabolic_disorder|anemia|inflammatory_disease	liver_disorder|immune_disorder|lung_disorder	false	false	false	true	high
MONDO:0015802	autosomal dominant non-syndromic intellectual disability	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0015803	wound botulism	infectious_disease	infectious_disease	infectious_disease	neurology|otolaryngology	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|nerve_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0015804	infant botulism	infectious_disease	infectious_disease	infectious_disease	pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	true	false	false	true	high
MONDO:0015805	intestinal botulism	infectious_disease	infectious_disease	infectious_disease	pediatrics|neurology|gastroenterology	neurodegenerative_disease|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0015806	adult intestinal botulism	infectious_disease	infectious_disease	infectious_disease	neurology|gastroenterology	neurodegenerative_disease|toxic_exposure	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	false	high
MONDO:0015807	myopic macular degeneration	nervous_system_disorder|hereditary_disease|disorder_of_visual_system	other	hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0015808	folliculotropic mycosis fungoides	cancer_or_benign_tumor|integumentary_system_disorder|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	cancer|autoimmune_diseases	skin_disorder|immune_disorder	true	true	false	false	high
MONDO:0015809	localized pagetoid reticulosis	cancer_or_benign_tumor|integumentary_system_disorder|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	cancer|inflammatory_disease	skin_disorder|lymphatic_disorder	false	false	false	true	low
MONDO:0015810	primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma	integumentary_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|hematologic_disorder	hematology|dermatology|oncology	cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder|skin_disorder	false	true	false	false	high
MONDO:0015811	primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma	integumentary_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder|skin_disorder	false	true	false	false	very_high
MONDO:0015812	primary cutaneous gamma/delta-positive T-cell lymphoma	integumentary_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|integumentary_system_disorder	hematology|dermatology|oncology	cancer|lymphoma	immune_disorder|lymphatic_disorder|skin_disorder	false	true	false	false	high
MONDO:0015813	primary cutaneous marginal zone B-cell lymphoma	integumentary_system_disorder|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	hematology|oncology	cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder|skin_disorder	false	true	false	true	medium
MONDO:0015814	primary cutaneous follicle center lymphoma	integumentary_system_disorder|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	hematology|dermatology|oncology	cancer|lymphoma|autoimmune_diseases	lymphatic_disorder|skin_disorder	false	true	false	true	medium
MONDO:0015816	indolent primary cutaneous T-cell lymphoma	integumentary_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|skin_disorder	false	true	false	true	low
MONDO:0015819	indolent primary cutaneous B-cell lymphoma	integumentary_system_disorder|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	hematology|oncology	cancer|lymphoma|autoimmune_diseases	immune_disorder|lymphatic_disorder|skin_disorder	false	true	false	true	medium
MONDO:0015820	primary cutaneous B-cell lymphoma	integumentary_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|integumentary_system_disorder	hematology|oncology	cancer|lymphoma|autoimmune_diseases	immune_disorder|lymphatic_disorder|skin_disorder	false	true	false	true	medium
MONDO:0015821	mycosis fungoides and variants	integumentary_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer|autoimmune_diseases	immune_disorder|skin_disorder	true	true	false	true	medium
MONDO:0015824	oculomaxillofacial dysostosis	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	ophthalmology|pediatrics|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	teeth_disorder|eye_disorder|bone_disorder	false	false	false	false	high
MONDO:0015826	autosomal dominant spondylocostal dysostosis	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	genetic_disorder|metabolic_disorder	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0015827	distal renal tubular acidosis	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	urology|renal_medicine|pediatric|nephrology	adrenal_gland_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0015830	partial bilateral aplasia of the mullerian ducts	reproductive_system_disorder	other	reproductive_system_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics|oncology	anemia|autoimmune_diseases	reproductive_system_disorder	false	false	false	false	medium
MONDO:0015831	unilateral aplasia of the mullerian ducts	reproductive_system_disorder	other	reproductive_system_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics|oncology	anemia	reproductive_system_disorder	false	false	false	false	medium
MONDO:0015832	true unicornuate uterus	reproductive_system_disorder	other	reproductive_system_disorder	urology|pediatric|obstetrics_and_gynecology	reproductive_system_disorder|gynecological_condition	urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0015833	pseudounicornuate uterus	reproductive_system_disorder	other	reproductive_system_disorder	pediatric|obstetrics_and_gynecology	gynecologic_disorder|reproductive_system_disorder	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0015834	didelphys uterus	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0015835	Bicervical bicornuate uterus and blind hemivagina	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	pediatric|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0015836	Bicervical bicornuate uterus with patent cervix and vagina	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	pediatric|obstetrics_and_gynecology	congenital_disorder|anatomic_abnormality|inflammatory_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0015838	cordiform uterus	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	pediatric|obstetrics_and_gynecology	anatomic_abnormality|metabolic_disorder	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0015839	septate uterus	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|joint_disorder	false	false	false	false	medium
MONDO:0015840	complete septate uterus	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	pediatric|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0015841	partial septate uterus	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	pediatric|obstetrics_and_gynecology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0015842	bicornuate uterus	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	pediatric|obstetrics_and_gynecology	congenital_disorder|reproductive_system_abnormality|gynecologic_condition	reproductive_system_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0015843	uterine hypoplasia	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	pediatric|obstetrics_and_gynecology	anemia|autoimmune_diseases|metabolic_disorder	uterine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0015844	agenesis and aplasia of uterine body	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics	anemia|cancer|inflammatory_disease|autoimmune_diseases|metabolic_disorder	uterine_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0015845	uterine cervical aplasia and agenesis	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	hematology|obstetrics_and_gynecology|genetics_and_genomics	anemia|cancer|autoimmune_diseases	uterine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0015849	longitudinal vaginal septum	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics	neurological_disease|congenital_anomaly|developmental_disorder	reproductive_system_disorder|vaginal_disorder	false	false	false	false	medium
MONDO:0015850	transverse vaginal septum	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	reproductive_system_disorder|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatric	reproductive_system_issue|inflammatory_disease	reproductive_system_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0015854	supernumerary breasts	breast_disorder	other	breast_disorder	obstetrics_and_gynecology|dermatology	cancer|inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0015855	isolated congenital breast hypoplasia/aplasia	breast_disorder|hereditary_disease	other	breast_disorder|hereditary_disease	obstetrics_and_gynecology|pediatric	congenital_disease|endocrine_disorder|developmental_disorder|genetic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0015856	syndromic breast hypoplasia/aplasia	breast_disorder	other	breast_disorder	obstetrics_and_gynecology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder|bone_disorder	false	false	false	false	high
MONDO:0015863	polyembryoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|genetics_and_genomics|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|bone_disorder	false	true	false	false	high
MONDO:0015864	mixed germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|obstetrics_and_gynecology|pediatric|oncology	cancer|neoplasm|adrenal_gland_disease	reproductive_system_disorder	false	true	false	true	high
MONDO:0015867	vaginal carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0015871	benign breast phyllodes tumor	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|breast_disorder	false	false	false	false	low
MONDO:0015873	Paget disease of the nipple	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	obstetrics_and_gynecology|dermatology|oncology	cancer|inflammatory_disease|autoimmune_diseases	breast_disorder|bone_disorder	false	false	false	true	medium
MONDO:0015874	benign ductal tumor of breast	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|upper_gastrointestinal_disorder|breast_disorder	false	false	false	false	low
MONDO:0015883	hidrotic ectodermal dysplasia, Halal type	syndromic_disease|integumentary_system_disorder|hereditary_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease___corrected_to_fit_the_original_format___metabolic_disorder|inflammatory_disease|genetic_disorder|metabolic_disorder	ear_disorder|eye_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0015884	autosomal dominant hypohidrotic ectodermal dysplasia	disorder_of_development_or_morphogenesis|syndromic_disease|integumentary_system_disorder|hereditary_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	pediatric|dermatology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|eye_disorder|joint_disorder|skin_disorder|bone_disorder	false	false	false	false	medium
MONDO:0015892	growth hormone insensitivity syndrome	endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	endocrine_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|genetic_disorder|endocrine_disorder	endocrine_disorder|growth_disorder|bone_disorder	false	false	false	false	high
MONDO:0015898	adrenogenital syndrome	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease	genetics_and_genomics|endocrinology|obstetrics_and_gynecology	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0015900	hypoaldosteronism disease	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|renal_medicine	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0015903	hyperalphalipoproteinemia	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|endocrinology|renal_medicine	genetic_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	low
MONDO:0015905	syndromic dyslipidemia	syndromic_disease|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|syndromic_disease	cardiology|endocrinology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|liver_disorder|upper_gastrointestinal_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0015907	epimetaphyseal skeletal dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|rheumatology|genetics_and_genomics|orthopaedic	inflammatory_disease|skeletal_dysplasia|metabolic_disorder	joint_disorder|muscle_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0015908	chromomycosis	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|oncology	metabolic_disorder|autoimmune_diseases|cancer	skin_disorder|eye_disorder	true	false	false	true	medium
MONDO:0015909	aplastic anemia	hematologic_disorder	anemia	hematologic_disorder	pediatric|oncology|hematology	anemia|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0015912	macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss	syndromic_disease|hereditary_disease|hematologic_disorder	other	hereditary_disease|syndromic_disease|hematologic_disorder	pediatrics|renal_medicine|hematology	anemia|metabolic_disorder|autoimmune_diseases	ear_disorder|blood_bone_marrow_disorder|kidney_disorder	true	false	false	true	high
MONDO:0015914	primary orthostatic hypotension	nervous_system_disorder	other	nervous_system_disorder	cardiology|neurology|renal_medicine	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0015923	acquired peripheral neuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0015924	pulmonary arterial hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic|pulmonology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	lung_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0015925	interstitial lung disease	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|neurology|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	false	false	false	false	high
MONDO:0015926	pneumoconiosis	respiratory_system_disorder	other	respiratory_system_disorder	cardiopulmonary|pulmonology	respiratory_disease|inflammatory_disease	lower_gastrointestinal_disorder|lung_disorder	false	false	false	false	high
MONDO:0015927	idiopathic eosinophilic pneumonia	inflammatory_disease|respiratory_system_disorder|infectious_disease	infectious_disease	idiopathic_disease|inflammatory_disease|infectious_disease|respiratory_system_disorder	allergy_and_immunology|pulmonology|pediatric	allergy|inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	false	false	false	false	high
MONDO:0015929	thoracic malformation	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology|pediatric	congenital_disorders|cardiovascular_disorder	thoracic|lung_disorder	false	false	false	false	high
MONDO:0015935	extragonadal germinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|neurology|pediatric	adrenal_gland_disease|cancer	reproductive_system_disorder|brain_disorder	false	true	false	true	high
MONDO:0015941	epiphyseal dysplasia-hearing loss-dysmorphism syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	developmental_disorder|anatomic_abnormality|metabolic_disorder|genetic_disorder	spinal_disorder|joint_disorder|bone_disorder|ear_disorder	false	false	false	false	high
MONDO:0015942	frontometaphyseal dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder	spinal_disorder|joint_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0015943	eosinophilic granulomatosis with polyangiitis	inflammatory_disease|immune_system_disorder|syndromic_disease|cardiovascular_disorder|urinary_system_disorder	cardiovascular_disorder	syndromic_disease|inflammatory_disease|immune_system_disorder|urinary_system_disorder|cardiovascular_disorder	pediatric|pulmonology|rheumatology	autoimmune_diseases|allergy|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	true	high
MONDO:0015944	axial mesodermal dysplasia spectrum	disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|hematology	metabolic_disorder	skeletal_system_disorder|joint_disorder|muscle_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0015947	inherited ichthyosis	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	pediatric|genetics_and_genomics|dermatology	metabolic_disorder|inherited_ichthyosis_is_also_a_form_of_skin_disorder_which_could_be_classified_under_the_category_of_genetic_disorders_so_some_might_consider_it_to_fit_into_the_category__genodermatoses	skin_disorder	false	false	false	false	high
MONDO:0015951	hereditary photodermatosis	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0015962	inherited renal tubular disease	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	genetics_and_genomics|renal_medicine	inherited_renal_tubular_disease_is_often_classified_as_a_subtype_of_this_category|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0015967	monogenic diabetes	metabolic_disease|hereditary_disease|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease|diabetes_mellitus	hereditary_disease|digestive_system_disorder|endocrine_system_disorder|metabolic_disease	endocrinology|genetics_and_genomics	metabolic_disorder|monogenic_diabetes	endocrine_disorder	false	false	true	true	medium
MONDO:0015974	severe combined immunodeficiency	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	pediatric|genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0015977	agammaglobulinemia	immune_system_disorder|hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder|immune_system_disorder	genetics_and_genomics|hematology|immunology	autoimmune_diseases|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0015978	functional neutrophil defect	immune_system_disorder|hematologic_disorder	other	hematologic_disorder|immune_system_disorder	genetics_and_genomics|hematology|immunology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0015986	bilateral renal agenesis	disorder_of_development_or_morphogenesis|hereditary_disease|urinary_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|urinary_system_disorder	pediatric|urology	metabolic_disorder|bilateral_renal_agenesis_is_often_associated_with_other_developmental_disorders_such_as_poland_syndrome_which_have_a_strong_link_to_genetic_mutations_affecting_metabolic_pathways	kidney_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0015987	scimitar syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic|pulmonology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	heart_disorder|liver_disorder	false	false	false	false	high
MONDO:0015988	multicystic dysplastic kidney	disorder_of_development_or_morphogenesis|urinary_system_disorder	other	disorder_of_development_or_morphogenesis|urinary_system_disorder	pediatric|urology|renal_medicine	renal_condition|pediatric_condition|genetic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0015990	focal, segmental or multifocal dystonia	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0015991	citrullinemia	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0015993	cone-rod dystrophy	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0015994	muscular dystrophy-white matter spongiosis syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0015995	melorheostosis with osteopoikilosis	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic	metabolic_disorder|autoimmune_diseases|inflammatory_disease	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0015997	ectopia lentis-chorioretinal dystrophy-myopia syndrome	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0015998	isolated ectopia lentis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|eye_disorder	false	false	false	true	medium
MONDO:0015999	primary pigmented nodular adrenocortical disease	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	oncology|endocrinology|dermatology	cancer|metabolic_disorder|adrenal_gland_disease	endocrine_disorder|adrenal_cortex_disorder	false	false	false	false	high
MONDO:0016000	familial isolated hypoparathyroidism due to impaired PTH secretion	endocrine_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|endocrinology|renal_medicine	autoimmune_diseases|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0016001	2-hydroxyglutaric aciduria	nervous_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder	false	false	false	true	high
MONDO:0016002	Ehlers-Danlos syndrome, kyphoscoliotic type 1	syndromic_disease|connective_tissue_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|disorder_of_visual_system|syndromic_disease|disorder_of_development_or_morphogenesis|connective_tissue_disorder|hereditary_disease	rheumatology|genetics_and_genomics|orthopaedic|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0016003	ehrlichiosis	infectious_disease	infectious_disease	infectious_disease	internal_medicine|hematology	autoimmune_diseases|inflammatory_disease	liver_disorder|immune_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0016004	aminopterin/methotrexate embryofetopathy	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|oncology	metabolic_disorder|cancer	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0016005	indomethacin embryofetopathy	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatric|hepatology	autoimmune_diseases|inflammatory_disease	liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0016006	Cockayne syndrome	premature_aging_syndrome|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	premature_aging_syndrome|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	developmental_disorder|eye_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0016007	cocaine embryofetopathy	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatric	neurodegenerative_disease|mental_health_disorder	reproductive_system_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016008	fetal hydantoin syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|neurological_disorder|brain_disorder	false	false	false	false	high
MONDO:0016009	fetal trimethadione syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|genetics_and_genomics|pediatric|teratology	congenital_abnormality___corrected_response___metabolic_disorder|metabolic_disorder|congenital_abnormality	developmental_disorder|reproductive_system_disorder|birth_defect	false	false	false	false	high
MONDO:0016010	vitamin K-antagonist embryofetopathy	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatric	anemia|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0016011	fetal alcohol syndrome	syndromic_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_development_or_morphogenesis	psychiatric_disorder	psychiatric_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	obstetrics_and_gynecology|pediatric	mental_health_disorder|metabolic_disorder	heart_disorder|kidney_disorder|brain_disorder|eye_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0016012	diethylstilbestrol syndrome	reproductive_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	obstetrics_and_gynecology|endocrinology	cancer|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0016013	fetal methylmercury syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|genetics_and_genomics|pediatrics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|nose_disorder|kidney_disorder|brain_disorder|eye_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0016014	fetal minoxidil syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatric	adrenal_gland_disease|metabolic_disorder	heart_disorder|reproductive_system_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016015	phenobarbital embryopathy	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|genetics_and_genomics|pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0016016	toluene embryopathy	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|nervous_system_disorder	false	false	false	false	high
MONDO:0016017	methimazole embryofetopathy	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0016018	diabetic embryopathy	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	endocrinology|pediatric	autoimmune_diseases|metabolic_disorder	endocrine_disorder	false	false	true	false	high
MONDO:0016019	Rasmussen subacute encephalitis	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	infectious_disease|post_infectious_disorder|inflammatory_disease|nervous_system_disorder|acute_disease	pediatric|neurology	autoimmune_diseases|inflammatory_disease	brain_disorder|immune_disorder	true	false	false	false	very_high
MONDO:0016020	frontal encephalocele	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0016024	shoulder and thorax deformity-congenital heart disease syndrome	hereditary_disease|respiratory_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	respiratory_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	cardiology|cardiothoracic|genetics_and_genomics|pediatric	congenital_heart_disease|cardiovascular_disorder	spinal_disorder|heart_disorder|joint_disorder	false	false	false	true	high
MONDO:0016026	infant epilepsy with migrant focal crisis	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	true	false	false	true	very_high
MONDO:0016027	benign neonatal seizures	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0016028	erythromelalgia	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	neurology|dermatology	inflammatory_disease|metabolic_disorder	skin_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016029	esthesioneuroblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	pediatric|oncology	cancer|adrenal_gland_disease	spinal_disorder|brain_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0016030	Evans syndrome	syndromic_disease|immune_system_disorder|hematologic_disorder	autoimmune_disease|anemia	hematologic_disorder|syndromic_disease|immune_system_disorder	pediatric|immunology|hematology	autoimmune_diseases|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0016031	facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|endocrinology|dermatology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder|skin_disorder|upper_gastrointestinal_disorder|endocrine_disorder	true	false	false	false	high
MONDO:0016032	femoral agenesis/hypoplasia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|genetic_condition|developmental_disorder	muscle_disorder|spinal_disorder|bone_disorder|reproductive_system_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016033	Cornelia de Lange syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0016035	Nelson syndrome	reproductive_system_disorder|nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|endocrine_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|reproductive_system_disorder	oncology|neurology	cancer|adrenal_gland_disease	vascular_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0016037	superficial Fibromatosis	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	oncology|dermatology	cancer|autoimmune_diseases|inflammatory_disease	muscle_disorder|joint_disorder|skin_disorder	false	false	false	false	low
MONDO:0016038	calcified aponeurotic fibroma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	endocrinology|orthopaedic	cancer|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0016039	infantile digital fibromatosis	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	genetics_and_genomics|pediatric|oncology|dermatology	cancer	bone_disorder|joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0016040	harlequin syndrome	nervous_system_disorder	other	nervous_system_disorder	allergy_and_immunology|dermatology|pediatrics	inflammatory_disease|autoimmune_diseases	liver_disorder|skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0016041	congenital microgastria	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	gastroenterology|genetics_and_genomics|pediatric	metabolic_disorder|congenital_disease____corrected_answer_without__congenital_disease__since_it_s_a_subcategory_of_the_selected_category___metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0016042	late-onset isolated ACTH deficiency	nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	endocrinology|neurology	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder	false	false	false	false	medium
MONDO:0016043	isolated cleft lip	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	otolaryngology|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases	nose_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0016044	cleft lip/palate	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	otolaryngology|pediatric	developmental_disorder|congenital_anomaly|birth_defect|genetic_condition|skeletal_system_disorder|craniofacial_anomaly|maxillofacial_disorder___revised___developmental_disorder|facial_abnormality	nose_disorder|throat_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0016045	tetragametic chimerism	disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|immunology|hematology	cancer|inflammatory_disease|autoimmune_diseases|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0016046	familial clubfoot with or without associated lower limb anomalies	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	bone_disorder|lower_limb_anomalies|joint_disorder	false	false	false	false	medium
MONDO:0016047	endophthalmitis	inflammatory_disease|infectious_disease|disorder_of_visual_system	infectious_disease	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease|infectious_disease	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases	endocrine_disorder|eye_disorder|immune_disorder|vascular_disorder	true	false	false	true	high
MONDO:0016048	isolated autosomal dominant hypomagnesemia, Glaudemans type	urinary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	urinary_system_disorder|metabolic_disease|hereditary_disease	endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|anemia	kidney_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016049	congenital myopathy, Paradas type	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|paralysis_muscle_disorder	false	false	false	false	high
MONDO:0016051	cleft lip-retinopathy syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	ophthalmology|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases	eye_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0016052	atypical autism	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|immune_disorder|spinal_disorder|muscle_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0016053	isolated cerebellar vermis hypoplasia	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0016056	isolated congenital microcephaly	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|congenital_diseases__assuming_this_category_is_implicitly_included	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016057	isolated encephalocele	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|neurology	neurological_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016058	paroxysmal dystonia	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016059	cleft lip/palate-deafness-sacral lipoma syndrome	syndromic_disease	other	syndromic_disease	otolaryngology|genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	teeth_disorder|ear_disorder	false	false	false	false	high
MONDO:0016060	laryngotracheoesophageal cleft	digestive_system_disorder|respiratory_system_disorder|upper_digestive_tract_disorder	other	digestive_system_disorder|upper_digestive_tract_disorder|respiratory_system_disorder	otolaryngology|pediatric	developmental_disorder|congenital_disorder|neurodevelopmental_disease	throat_disorder|thoracic_disorder	false	false	false	false	high
MONDO:0016061	immunodeficiency with factor H anomaly	inflammatory_disease|urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|inflammatory_disease|hereditary_disease	genetics_and_genomics|hematology|allergy_and_immunology|immunology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0016062	median cleft lip/mandibule	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	otolaryngology|pediatric	metabolic_disorder|congenital_disorder	bone_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0016063	Cowden disease	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics|neurology|dermatology|oncology	cancer|neurodegenerative_disease|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	true	high
MONDO:0016064	cleft palate	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	otolaryngology|pediatric	congenital_disease|metabolic_disorder|birth_defect	teeth_disorder|oral_disorder	false	false	false	true	medium
MONDO:0016065	cleft palate-short stature-vertebral anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	bone_disorder|spinal_disorder|muscle_disorder|upper_gastrointestinal_disorder|teeth_disorder|joint_disorder	false	false	false	false	high
MONDO:0016066	sternal cleft	respiratory_system_disorder	other	respiratory_system_disorder	otolaryngology|pediatric	congenital_abnormality|skeletal_disorder|neonatal_surgical_condition	bone_disorder|sternum_disorder	false	false	false	false	medium
MONDO:0016067	Crandall syndrome	syndromic_disease	other	syndromic_disease	psychiatry|neurology|rheumatology	metabolic_disorder|autoimmune_diseases	spinal_disorder|joint_disorder	false	false	false	true	high
MONDO:0016068	fibrochondrogenesis	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|genetic_disease|skeletal_rare_disease	bone_disorder|muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0016070	hereditary gingival fibromatosis	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	mouth_disorder|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|dermatology	metabolic_disorder|genetic_disorder|inflammatory_disease	skin_disorder|teeth_disorder	false	false	false	false	low
MONDO:0016071	juvenile hyaline fibromatosis	integumentary_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hereditary_disease	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|integumentary_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	cancer|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0016073	syndromic microphthalmia	syndromic_disease|disorder_of_visual_system|hereditary_disease	other	syndromic_disease|disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	ophthalmology|genetics_and_genomics|pediatric	syndromic_disorders_____metabolic_disorder|metabolic_disorder|syndromic_disorders____corrected_to_remove_the_word__syndromic__from_the_answer__metabolic_disorder|syndromes	eye_disorder|teeth_disorder	false	false	false	false	high
MONDO:0016075	filariasis	infectious_disease	infectious_disease	infectious_disease	hepatology|hematology|pediatric|dermatology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	true	high
MONDO:0016077	congenital aortopulmonary window	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	pulmonology|cardiology|pediatric|cardiothoracic	congenital_heart_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0016078	congenital systemic arteriovenous fistula	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	renal_medicine|cardiovascular_medicine|cardiology|genetics_and_genomics|hematology|pediatric	congenital_anomaly|cardiovascular_disorder	kidney_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016079	sporadic Creutzfeldt-Jakob disease	infectious_disease|nervous_system_disorder|hereditary_disease	infectious_disease|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|infectious_disease	genetics_and_genomics|neurology	neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0016080	congenital bronchobiliary fistula	disorder_of_development_or_morphogenesis|respiratory_system_disorder	other	respiratory_system_disorder|disorder_of_development_or_morphogenesis	pulmonology|pediatric	congenital_anomaly|inflammatory_disease|respiratory_system_disorder	liver_disorder|lung_disorder	false	false	false	false	high
MONDO:0016081	coronary arterial fistulas	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|pulmonology|cardiothoracic	inflammatory_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016083	FLOTCH syndrome	integumentary_system_disorder	other	integumentary_system_disorder	medical_genetics|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0016085	Cole-Carpenter syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|endocrinology|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|skeletal_disorder_is_not_in_the_list_so_i_will_replace_it_with__joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0016086	osteochondritis of tarsal/metatarsal bone	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases|osteoarthritis	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0016087	progressive non-infectious anterior vertebral fusion	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|neurology	neurodegenerative_disease|spinal_fusion	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016088	hypoxanthine-guanine phosphoribosyltransferase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pulmonology|genetics_and_genomics|neurology|pediatric|hematology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0016089	infantile Krabbe disease	disorder_of_visual_system|metabolic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0016090	late-infantile/juvenile Krabbe disease	disorder_of_visual_system|metabolic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0016091	adult Krabbe disease	disorder_of_visual_system|metabolic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|metabolic_disease|psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|disorder_of_visual_system|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	lymphatic_disorder|brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016092	serous or mucinous cystadenoma of childhood	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	pediatric|oncology	adrenal_gland_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0016093	borderline epithelial tumor of ovary	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	obstetrics_and_gynecology|oncology	cancer|autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|ovarian_disorder	false	true	false	true	medium
MONDO:0016094	vaginal germ cell malignant tumor	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0016095	vaginal rhabdomyosarcoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|muscle_disorder	false	true	false	true	high
MONDO:0016096	malignant non-dysgerminomatous germ cell tumor of ovary	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer|ovarian_cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0016097	symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers	cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	obstetrics_and_gynecology|genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|kidney_disorder|joint_disorder	false	false	false	false	medium
MONDO:0016098	immune-mediated necrotizing myopathy	inflammatory_disease|musculoskeletal_system_disorder	other	idiopathic_disease|musculoskeletal_system_disorder|inflammatory_disease	neurology|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|immune_disorder	false	false	false	true	high
MONDO:0016099	overlap myositis	inflammatory_disease|musculoskeletal_system_disorder	other	idiopathic_disease|musculoskeletal_system_disorder|inflammatory_disease	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|immune_disorder	false	false	false	false	high
MONDO:0016100	rippling muscle disease with myasthenia gravis	musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|immune_disorder	true	false	false	true	high
MONDO:0016101	neurolymphomatosis	infectious_disease	infectious_disease	infectious_disease	neurology|oncology|hematology	cancer|autoimmune_diseases	brain_disorder|lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	false	high
MONDO:0016102	subacute inflammatory demyelinating polyneuropathy	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|acute_disease|disorder_of_development_or_morphogenesis	neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder|muscle_disorder|immune_disorder	true	false	false	true	high
MONDO:0016103	isolated asymptomatic elevation of creatine phosphokinase	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	cardiology|renal_medicine|neurology	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	low
MONDO:0016105	acquired skeletal muscle disease	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	acquired_skeletal_muscle_disease_cannot_be_matched_due_to_the_term__acquired__so_it_would_actually_be__muscle_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016106	progressive muscular dystrophy	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|orthopaedic|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016107	myotonic dystrophy	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|syndromic_disease	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016108	autosomal dominant distal myopathy	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016112	hereditary inclusion-body myopathy	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|neuromuscular_disorder	false	false	false	false	high
MONDO:0016113	bulbospinal muscular atrophy	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0016120	myotonic syndrome	syndromic_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	true	high
MONDO:0016122	periodic paralysis	nervous_system_disorder	other	nervous_system_disorder	renal_medicine|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0016126	viral myositis	infectious_disease|inflammatory_disease|musculoskeletal_system_disorder	infectious_disease	inflammatory_disease|musculoskeletal_system_disorder|infectious_disease	rheumatology|pediatrics|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	muscle_disorder|immune_disorder	true	false	false	true	medium
MONDO:0016127	bacterial myositis	infectious_disease|inflammatory_disease|musculoskeletal_system_disorder	infectious_disease	inflammatory_disease|musculoskeletal_system_disorder|infectious_disease	rheumatology|infectious_diseases	inflammatory_disease|autoimmune_diseases	muscle_disorder|immune_disorder	true	false	false	true	high
MONDO:0016128	parasitic myositis	infectious_disease|inflammatory_disease|musculoskeletal_system_disorder	infectious_disease	inflammatory_disease|musculoskeletal_system_disorder|infectious_disease	rheumatology|parasitology|infectious_diseases	inflammatory_disease|autoimmune_diseases	parasitic_disease|muscle_disorder|immune_disorder	true	false	false	true	high
MONDO:0016129	eosinophilic gastroenteritis	digestive_system_disorder|inflammatory_disease	other	inflammatory_disease|digestive_system_disorder	allergy_and_immunology|gastroenterology|pediatrics	inflammatory_disease|autoimmune_diseases|allergy	upper_gastrointestinal_disorder|immune_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0016130	fungal myositis	musculoskeletal_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	musculoskeletal_system_disorder|infectious_disease|inflammatory_disease	rheumatology|neurology	autoimmune_diseases|inflammatory_disease	liver_disorder|muscle_disorder	true	false	false	true	high
MONDO:0016139	qualitative or quantitative protein defects in neuromuscular diseases	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|neuromuscular_disease	false	false	false	neuromuscular_diseases_can_involve_both_qualitative_and_quantitative_protein_defects____1____qualitative_protein_defects___refer_to_abnormalities_in_the_structure_or_function_of_a_protein_that_impair_its_normal_role__even_if_the_quantity_of_the_protein_is_normal__for_example__in_certain_myopathies__such_as_nemaline_myopathy__the_structural_proteins_of_muscle_fibers_may_be_abnormally_formed__leading_to_muscle_weakness___2____quantitative_protein_defects___occur_when_there_is_a_reduced_amount_of_a_protein__which_can_also_lead_to_dysfunction__for_instance__in_conditions_like_duchenne_muscular_dystrophy__dmd___there_is_a_deficiency_of_dystrophin__a_protein_critical_for_maintaining_muscle_cell_integrity__in_this_case__the_quantity_of_the_protein_is_not_sufficient_to_support_normal_muscle_function___both_types_of_defects_can_contribute_to_the_pathophysiology_of_neuromuscular_diseases__and_understanding_the_nature_of_these_defects_is_crucial_for_diagnosis_and_potential_treatment_options	high
MONDO:0016140	sarcoglycanopathy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016141	qualitative or quantitative defects of alpha-sarcoglycan	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	cardiology|orthopaedic|renal_medicine|pediatric|neurology|pulmonology|dermatology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|cardiovascular_disorder|metabolic_disorder	muscle_disorder|joint_disorder	true	false	false	alpha_sarcoglycan_is_a_protein_that_plays_a_crucial_role_in_the_assembly_of_the_dystrophin_glycoprotein_complex_in_muscle_cells__defects_in_alpha_sarcoglycan_are_associated_with_conditions_such_as_limb_girdle_muscular_dystrophy__lgmd__type_2d____qualitative_defects_refer_to_issues_with_the_functionality_or_structure_of_the_alpha_sarcoglycan_protein__potentially_leading_to_improper_functioning_of_the_dystrophin_glycoprotein_complex__this_could_result_in_the_protein_being_produced_but_not_functioning_properly___quantitative_defects__on_the_other_hand__involve_an_insufficient_quantity_of_alpha_sarcoglycan_being_produced__which_can_lead_to_muscular_dystrophy_due_to_inadequate_support_for_the_muscle_cell_membrane___both_types_of_defects_can_lead_to_muscular_dystrophy_and_associated_symptoms__including_muscle_weakness_and_degeneration__the_distinction_between_qualitative_and_quantitative_defects_is_important_for_understanding_the_specific_nature_of_the_genetic_mutations_involved_and_their_impact_on_muscle_function	very_high
MONDO:0016142	qualitative or quantitative defects of beta-sarcoglycan	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	cardiology|cardiothoracic|genetics_and_genomics	muscular_dystrophy|metabolic_disorder	heart_disorder|muscle_disorder	true	false	false	beta_sarcoglycan_is_a_protein_that_is_part_of_the_dystrophin_glycoprotein_complex__which_is_important_for_muscle_function__defects_in_beta_sarcoglycan_can_lead_to_muscular_dystrophies__primarily_limb_girdle_muscular_dystrophy_type_2e__lgmd2e_____qualitative_defects_refer_to_abnormalities_in_the_protein_s_structure_or_functionality__such_as_mutations_that_lead_to_a_dysfunctional_beta_sarcoglycan_that_cannot_properly_perform_its_role_in_muscle_cells___quantitative_defects_refer_to_a_decrease_in_the_amount_of_beta_sarcoglycan_present_in_the_muscle_tissue__which_can_occur_due_to_reduced_gene_expression_or_other_regulatory_mechanisms___both_types_of_defects_can_have_significant_impacts_on_muscle_health_and_function__leading_to_progressive_muscle_weakness_and_degeneration____if_you_re_looking_for_treatments__there_currently_are_no_definitive_cures_for_conditions_caused_by_beta_sarcoglycan_defects__but_some_interventions__such_as_physical_therapy_and_experimental_therapies__like_gene_therapy___may_help_manage_symptoms_and_improve_quality_of_life____in_summary__the_existence_of_treatments_for_the_conditions_associated_with_beta_sarcoglycan_defects_can_vary__and_there_s_ongoing_research_in_this_area	high
MONDO:0016143	qualitative or quantitative defects of gamma-sarcoglycan	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	rheumatology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|sarcomeric_disorder	false	false	false	gamma_sarcoglycan_is_a_protein_that_is_part_of_the_dystrophin_associated_protein_complex__which_plays_a_critical_role_in_muscle_function__defects_in_gamma_sarcoglycan_can_lead_to_various_forms_of_muscular_dystrophy__particularly_limb_girdle_muscular_dystrophy_type_2c__lgmd2c____these_defects_can_be_classified_as___1____qualitative_defects____these_refer_to_the_abnormal_function_or_structure_of_the_gamma_sarcoglycan_protein__for_example__the_protein_may_be_produced_but_have_changes_that_affect_its_stability_or_ability_to_interact_with_other_proteins_in_the_dystrophin_associated_complex___2____quantitative_defects____these_refer_to_insufficient_amounts_of_gamma_sarcoglycan_being_produced__which_can_be_due_to_mutations_in_the_gene_that_encodes_this_protein_leading_to_inadequate_expression_levels___both_qualitative_and_quantitative_defects_can_result_in_muscle_weakness_and_degeneration_characteristic_of_muscular_dystrophy__genetic_testing_and_analysis_can_be_utilized_to_identify_the_specific_type_of_defect_involved_in_a_particular_case	very_high
MONDO:0016144	qualitative or quantitative defects of delta-sarcoglycan	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	cardiology|pediatrics|neurology|pulmonology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	delta_sarcoglycan_is_a_protein_that_is_part_of_the_dystrophin_glycoprotein_complex__and_defects_in_this_protein_can_lead_to_muscle_disorders__specifically_a_form_of_muscular_dystrophy_known_as_limb_girdle_muscular_dystrophy__lgmd__type_2f____qualitative_defects_refer_to_abnormalities_in_the_structure_or_function_of_delta_sarcoglycan_itself__which_may_include_changes_that_impair_its_ability_to_interact_with_other_proteins_or_components_of_the_cellular_matrix__quantitative_defects_refer_to_insufficient_amounts_of_the_delta_sarcoglycan_protein_being_produced__leading_to_a_reduced_or_absent_functional_protein_in_muscle_tissue___both_types_of_defects_can_contribute_to_the_progression_of_muscular_dystrophy_by_adversely_affecting_muscle_fiber_integrity_and_function__if_you_re_looking_for_specific_details_on_treatments_or_research_advancements_related_to_these_defects__please_provide_more_context_or_specify_any_particular_area_of_interest	high
MONDO:0016145	neuromuscular disease caused by qualitative or quantitative defects of dysferlin	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	orthopaedic|neurology|genetics_and_genomics	neurodegenerative_disease|qualitative_or_quantitative_defects_of_dysferlin_is_a_type_of_condition_known_as_muscular_dystrophy_which_falls_under_neurodegenerative_disorder	muscle_disorder|muscular_disorder	false	false	false	dysferlin_is_a_protein_that_is_crucial_for_muscle_membrane_repair__and_defects_in_dysferlin_can_lead_to_a_group_of_diseases_known_as_dysferlinopathies__which_primarily_cause_muscle_degeneration____qualitative_defects_refer_to_abnormalities_in_the_function_or_structure_of_dysferlin__which_could_be_due_to_mutations_affecting_its_ability_to_perform_its_role_in_muscle_repair____quantitative_defects_refer_to_reduced_levels_or_expression_of_dysferlin__which_could_result_from_mutations_that_lead_to_decreased_production_of_the_protein___both_qualitative_and_quantitative_defects_can_contribute_to_the_pathophysiology_of_conditions_related_to_dysferlin_deficiencies__such_as_limb_girdle_muscular_dystrophy_type_2b__lgmd2b__and_miyoshi_myopathy____in_summary__dysferlin_defects_can_be_classified_into_qualitative__functional_or_structural_abnormalities__and_quantitative__reduced_levels_of_protein__categories	high
MONDO:0016146	caveolinopathy	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	cardiology|neurology|pulmonology|genetics_and_genomics	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016147	neuromuscular disease caused by qualitative or quantitative defects of dystrophin	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|cardiovascular_disorder	muscle_disorder	false	false	false	dystrophin_is_a_vital_protein_that_helps_maintain_the_integrity_of_muscle_cell_membranes__defects_in_dystrophin_can_lead_to_various_forms_of_muscular_dystrophy__most_notably_duchenne_muscular_dystrophy__dmd__and_becker_muscular_dystrophy__bmd_____1____qualitative_defects____these_involve_the_structure_or_functionality_of_the_dystrophin_protein_itself__in_dmd__there_are_mutations_that_result_in_nonfunctional_or_poorly_functional_dystrophin_proteins__this_can_arise_from_deletions_or_point_mutations_that_alter_the_protein_s_ability_to_interact_properly_with_other_proteins_in_the_muscle_cell_membrane___2____quantitative_defects____these_relate_to_the_amount_of_dystrophin_produced__in_bmd__for_instance__the_protein_is_often_present_but_produced_in_reduced_quantities__typically_resulting_from_mutations_that_allow_for_some_functional_dystrophin_production__unlike_in_dmd_where_the_protein_is_largely_absent___both_types_of_defects_lead_to_muscle_degeneration_and_weakness_due_to_the_lack_of_proper_support_for_muscle_cell_membranes_during_contraction	very_high
MONDO:0016151	neuromuscular disease caused by qualitative or quantitative defects of perlecan	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|renal_medicine|genetics_and_genomics	metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	perlecan_is_a_heparan_sulfate_proteoglycan_that_is_essential_for_various_biological_processes__including_cell_adhesion__proliferation__and_differentiation__as_well_as_the_maintenance_of_the_extracellular_matrix__defects_in_perlecan_can_be_classified_into_qualitative_and_quantitative_defects___1____qualitative_defects____these_defects_involve_changes_in_the_structure_or_composition_of_perlecan_that_affect_its_function__examples_may_include_mutations_that_alter_the_heparan_sulfate_chains_attached_to_the_core_protein_or_changes_that_affect_the_protein_s_folding_or_stability__such_qualitative_defects_can_lead_to_altered_binding_properties__impaired_interactions_with_growth_factors__or_disrupted_roles_in_cell_signaling___2____quantitative_defects____these_defects_refer_to_reduced_levels_of_perlecan__which_may_be_due_to_genetic_mutations__regulatory_issues__or_altered_expression_mechanisms__quantitative_defects_can_result_in_insufficient_production_of_perlecan__leading_to_an_inadequate_extracellular_matrix_structure_and_function__which_can_affect_tissue_integrity_and_repair___both_types_of_defects_can_contribute_to_various_pathologies__including_developmental_disorders__cardiovascular_diseases__and_certain_types_of_muscular_dystrophies	none
MONDO:0016153	neuromuscular disease caused by qualitative or quantitative defects of TRIM32	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|joint_disorder	false	false	false	trim32__tripartite_motif_containing_32__is_a_protein_that_has_been_implicated_in_various_cellular_processes__including_muscle_differentiation_and_immune_response__defects_in_trim32_are_associated_with_certain_diseases__including_muscular_dystrophy_and_other_conditions____qualitative_defects_in_trim32_could_involve_changes_in_the_protein_s_structure_or_function_that_impair_its_normal_role_in_cellular_processes__this_could_include_mutations_leading_to_a_non_functional_protein_or_alterations_that_affect_its_ability_to_interact_with_other_proteins___quantitative_defects_would_refer_to_variations_in_the_amount_of_trim32_produced__such_as_decreased_expression_levels_due_to_regulatory_issues_or_gene_deletion__this_reduction_can_also_lead_to_impaired_muscle_function_and_other_pathological_conditions___in_summary__trim32_defects_can_be_categorized_into_qualitative_defects__changes_affecting_function__and_quantitative_defects__changes_affecting_levels___both_of_which_can_contribute_to_disease_pathology	medium
MONDO:0016155	qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	muscle_disorder	false	false	false	to_determine_if_there_are_efficacious_treatments_that_cure__prevent__or_treat_diseases_related_to_defects_in_the_o_glycosylation_of_alpha_dystroglycan__such_as_dystroglycanopathies__we_consider_research_and_data_up_to_october_2023___currently__there_are_no_definitive_cures_for_dystroglycanopathies__which_are_a_group_of_muscular_dystrophies_caused_by_defects_in_the_glycosylation_of_alpha_dystroglycan__the_treatments_primarily_focus_on_managing_symptoms_and_improving_quality_of_life_rather_than_providing_a_cure__gene_therapies_and_pharmacological_approaches_are_being_explored_in_research_settings__but_they_are_not_yet_established_as_standard_treatments___given_that_there_are_no_established_efficacious_treatments_that_cure__prevent__or_effectively_treat_the_underlying_condition_related_to_the_o_glycosylation_defects_of_alpha_dystroglycan__the_answer_is___false	very_high
MONDO:0016156	qualitative or quantitative defects of FKRP	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	orthopaedic|neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	fkrp__fukutin_related_protein__is_associated_with_certain_muscular_dystrophies__particularly_those_that_manifest_with_either_qualitative_or_quantitative_defects__these_defects_can_lead_to_varying_clinical_presentations___1____qualitative_defects____these_defects_refer_to_abnormalities_in_the_function_or_structure_of_the_fkrp_protein_itself__for_instance__mutations_in_the_fkrp_gene_can_affect_the_protein_s_role_in_glycosylation_of_dystroglycan__which_is_crucial_for_muscular_integrity__such_qualitative_defects_might_lead_to_dysfunctional_cellular_processes__contributing_to_muscle_weakness_and_degeneration___2____quantitative_defects____these_defects_refer_to_a_decrease_in_the_amount_of_fkrp_produced_or_a_reduction_of_the_fkrp_protein_levels_in_muscle_tissues__this_reduced_expression_can_result_in_insufficient_stabilization_of_the_muscle_cell_membrane__leading_to_the_pathological_features_observed_in_associated_muscular_dystrophies___diagnosing_and_understanding_these_defects_is_key_in_addressing_diseases_such_as_limb_girdle_muscular_dystrophy__lgmd__and_congenital_muscular_dystrophy__cmd__linked_to_fkrp_mutations__moreover__ongoing_research_is_focused_on_developing_gene_therapies_and_other_treatments_that_could_address_these_defects_directly	high
MONDO:0016158	narcolepsy-cataplexy syndrome	nervous_system_disorder	other	nervous_system_disorder|sleep_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	neurological_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016159	Gemignani syndrome	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0016160	X-linked intellectual disability-epilepsy syndrome	syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|syndromic_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0016161	cerebral gigantism-jaw cysts syndrome	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|teeth_disorder|endocrine_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016162	bilateral frontal polymicrogyria	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016163	spinocerebellar ataxia 7	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|psychiatric_disorder|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant_disorder_is_often_associated_with_this_category_but_it_does_not_seem_to_be_explicitly_listed__however__based_on_the_inclusion_of_ataxia_which_is_a_neurodegenerative_symptom__and_dominant_being_part_of_the_name_we_can_make_an_educated_guess	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016164	herpetiform pemphigus	inflammatory_disease|integumentary_system_disorder|immune_system_disorder	autoimmune_disease	integumentary_system_disorder|immune_system_disorder|inflammatory_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0016165	hereditary hypoparathyroidism	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|hereditary_disease	endocrine_disorder|hereditary_disorder	false	false	false	false	medium
MONDO:0016166	hereditary hyperparathyroidism	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|hereditary_diseases|endocrine_disease	bone_disorder|kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0016167	optic pathway glioma	psychiatric_disorder|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor|psychiatric_disorder	disorder_of_visual_system|psychiatric_disorder|cancer_or_benign_tumor|nervous_system_disorder	ophthalmology|neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|eye_disorder	false	true	false	true	high
MONDO:0016168	cryopyrin-associated periodic syndrome	syndromic_disease|hereditary_disease|connective_tissue_disorder|immune_system_disorder	other	hereditary_disease|syndromic_disease|immune_system_disorder|connective_tissue_disorder	rheumatology|pediatrics|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	joint_disorder|immune_disorder|vascular_disorder	false	false	false	true	high
MONDO:0016171	polyradiculoneuropathy associated with IgG/IgA/IgM monoclonal gammopathy without known antibodies	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder	immunology|neurology|hematology|oncology	neurodegenerative_disease|cancer|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0016175	cutis laxa	disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics|dermatology	genetic_disorder___corrected_to__genetic_disorder|metabolic_disorder	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0016176	axonal polyneuropathy associated with IgG/IgM/IgA monoclonal gammopathy	nervous_system_disorder	other	nervous_system_disorder	immunology|neurology|hematology	neurodegenerative_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0016184	qualitative or quantitative defects of protein O-mannosyltransferase 1	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	metabolic_disorder____corrected_to_liver_disorder_and_removed__endocrine|liver_disorder	false	false	false	false	high
MONDO:0016185	qualitative or quantitative defects of protein O-mannosyltransferase 2	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	pediatrics|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0016186	neuromuscular disease caused by qualitative or quantitative defects of myofibrillar proteins	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|pulmonology|neurology|cardiology|pediatric|orthopaedic|rheumatology	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	muscle_disorder	false	false	false	false	none
MONDO:0016187	qualitative or quantitative defects of desmin	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|dermatology|rheumatology	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	spinal_disorder|muscle_disorder	false	false	false	false	none
MONDO:0016188	qualitative or quantitative defects of alphaB-cristallin	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	alphab_crystallin_is_a_protein_that_functions_as_a_molecular_chaperone_in_the_eye_s_lens_and_has_a_role_in_maintaining_lens_transparency_and_protecting_against_stress_induced_damage__defects_in_alphab_crystallin_can_manifest_as_either_qualitative_or_quantitative_defects___1____qualitative_defects____these_involve_structural_or_functional_abnormalities_in_the_alphab_crystallin_protein_itself__such_defects_can_result_from_mutations_that_alter_the_protein_s_folding__stability__or_its_ability_to_interact_with_other_proteins__as_a_result__its_protective_functions_may_be_compromised__leading_to_conditions_such_as_cataracts___2____quantitative_defects____these_refer_to_reduced_levels_of_alphab_crystallin_in_the_lens__a_decrease_in_the_expression_of_the_protein_can_result_from_genetic__environmental__or_age_related_factors__low_levels_of_alphab_crystallin_can_impair_its_chaperone_activities__leading_to_protein_aggregation_and_contributing_to_lens_opacification___both_types_of_defects_can_significantly_impact_eye_health__particularly_in_the_development_of_cataracts__highlighting_the_importance_of_alphab_crystallin_in_lens_functionality_and_transparency	high
MONDO:0016189	qualitative or quantitative defects of filamin C	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|pediatric|rheumatology	neurodegenerative_disease|metabolic_disorder	vascular_disorder|joint_disorder|muscle_disorder	true	false	false	qualitative_defects_of_filamin_c_can_include_abnormal_protein_structure_or_function__leading_to_issues_with_its_ability_to_crosslink_actin_filaments_and_contribute_to_cellular_architecture_and_stability__this_can_result_in_problems_such_as_altered_muscle_contraction__impaired_cell_signaling__or_disrupted_intracellular_transport___quantitative_defects_refer_to_reduced_levels_of_filamin_c__which_can_result_from_mutations_that_affect_its_expression__stability__or_degradation__this_can_lead_to_insufficient_amounts_of_the_protein_being_available_for_normal_cellular_functions__potentially_contributing_to_muscle_disorders_or_cardiomyopathies___both_types_of_defects_can_be_implicated_in_various_diseases__particularly_those_related_to_muscle_function_and_cardiac_health	high
MONDO:0016190	qualitative or quantitative defects of protein ZASP	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology|cardiology|rheumatology	neurodegenerative_disease|cardiovascular_disorder	heart_disorder|muscle_disorder	true	false	false	zasp__z_band_alternative_splicing_protein__is_a_protein_implicated_in_the_formation_and_maintenance_of_z_discs_in_muscle_cells__defects_in_this_protein__both_qualitative__functional__and_quantitative__amount___can_lead_to_various_muscle_disorders__particularly_cardiomyopathies____qualitative_defects_may_involve_mutations_that_alter_the_protein_s_structure_or_function__impairing_its_role_in_muscle_cell_integrity_or_signaling_pathways__quantitative_defects_may_result_from_decreased_expression_levels_of_zasp__which_can_lead_to_insufficient_support_for_z_disc_composition_and_function___research_continues_to_explore_the_precise_mechanisms_by_which_these_defects_contribute_to_disease__and_their_effects_can_manifest_in_various_ways__depending_on_the_type_of_mutation_and_the_tissues_affected____if_you_would_like_more_specific_information_about_the_effects_of_zasp_defects_on_health_or_associated_conditions__please_provide_additional_details	none
MONDO:0016191	neuromuscular disease caused by qualitative or quantitative defects of titin	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|cardiothoracic|rheumatology	qualitative_or_quantitative_defects_of_titin_is_related_to_the_structure_of_muscle_tissue__which_affects_the_heart_as_well_as_other_muscles|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	none
MONDO:0016192	neuromuscular disease caused by qualitative or quantitative defects of telethonin	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	telethonin_is_a_protein_that_plays_a_crucial_role_in_muscle_function_and_is_associated_with_various_forms_of_muscular_dystrophy__particularly_in_the_context_of_human_diseases__the_defects_in_telethonin_can_be_categorized_into_qualitative_and_quantitative_defects___1____qualitative_defects____these_refer_to_alterations_in_the_structure_or_function_of_the_telethonin_protein_itself__for_instance__mutations_in_the_gene_encoding_telethonin__tnni2__can_lead_to_the_production_of_a_dysfunctional_protein_that_may_fail_to_properly_interact_with_other_proteins_in_the_muscle_cells__impairing_muscle_integrity_and_function___2____quantitative_defects____these_involve_a_change_in_the_amount_of_telethonin_available_in_the_muscle_tissue__a_reduction_in_the_levels_of_telethonin_due_to_genetic_mutations_or_misregulation_can_lead_to_insufficient_stabilization_of_the_muscle_cell_structures__contributing_to_muscle_weakness_and_degeneration___both_types_of_defects_can_result_in_muscle_pathology_and_contribute_to_the_progression_of_muscular_dystrophies_associated_with_telethonin__the_specific_effects_depend_on_the_nature_and_location_of_the_mutations	high
MONDO:0016193	neuromuscular disease caused by qualitative or quantitative defects of alpha-actin	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|pulmonology|cardiology|cardiothoracic	metabolic_disorder|autoimmune_diseases|cardiovascular_disorder	muscle_disorder	false	false	false	false	none
MONDO:0016194	neuromuscular disease caused by qualitative or quantitative defects of nebulin	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|pulmonology|pediatric	neurodegenerative_disease|muscular_disease	lung_disorder|muscle_disorder	true	false	false	nebulin_is_a_giant_protein_that_is_essential_for_proper_skeletal_muscle_function__it_plays_a_role_in_the_assembly_of_thin_filaments_in_muscle_fibers_and_helps_regulate_their_length__defects_in_nebulin_can_lead_to_a_range_of_muscle_disorders__particularly_congenital_myopathies_____qualitative_defects___of_nebulin_may_include___1____alterations_in_protein_structure____changes_in_the_amino_acid_sequence_or_structural_conformation_of_nebulin_that_impair_its_function_in_muscle_fiber_assembly_and_stability___2____dysfunctional_binding_properties____mutations_might_affect_nebulin_s_ability_to_interact_properly_with_actin_filaments_or_other_muscle_proteins__leading_to_impaired_muscle_contraction___3____mislocalization____variants_of_nebulin_may_not_be_localized_properly_within_the_muscle_fibers__disrupting_the_normal_architecture_of_the_muscle_____quantitative_defects___could_involve___1____reduced_levels_of_nebulin____this_can_occur_due_to_gene_mutations_that_affect_the_amount_synthesized_or_lead_to_premature_degradation_of_the_protein___2____abnormal_lengths____variants_of_nebulin_can_result_in_either_shorter_or_longer_versions_of_the_protein__which_can_affect_the_overall_structure_and_function_of_the_sarcomeres___these_defects_often_manifest_in_conditions_like_nemaline_myopathy__where_patients_exhibit_muscle_weakness_and_structural_abnormalities_in_muscle_fibers__understanding_the_nature_of_these_defects_is_critical_for_developing_targeted_therapies_and_management_strategies_for_affected_individuals	low
MONDO:0016195	neuromuscular disease caused by qualitative or quantitative defects of beta-myosin heavy chain (MYH7)	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0016197	neuromuscular disease caused by qualitative or quantitative defects of selenoprotein N1	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|endocrinology	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	liver_disorder|kidney_disorder	false	false	false	selenoprotein_n1__sepn1__is_associated_with_a_group_of_disorders_that_affect_muscle_function__including_congenital_muscular_dystrophy_and_a_related_condition_known_as_selenoprotein_n_related_myopathy__defects_in_sepn1_can_lead_to_both_qualitative_and_quantitative_defects_in_the_protein___1____qualitative_defects____these_defects_refer_to_the_functional_abnormalities_of_the_selenoprotein__mutations_in_the_sepn1_gene_can_result_in_a_selenoprotein_that_is_misfolded_or_improperly_modified__leading_to_impaired_protein_function__this_can_disrupt_normal_muscle_development_and_maintenance___2____quantitative_defects____these_involve_the_amount_of_selenoprotein_produced__mutations_can_lead_to_reduced_levels_or_absence_of_sepn1_protein__which_can_result_in_lower_selenoprotein_activity_and_thus_contribute_to_the_clinical_manifestations_of_the_associated_disorders___overall__defects_in_selenoprotein_n1_can_have_significant_implications_for_muscle_health_and_function__manifesting_as_myopathy_or_other_muscle_related_issues	none
MONDO:0016198	neuromuscular disease caused by qualitative or quantitative defects of plectin	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|muscle_disorder	false	false	false	plectin_is_a_versatile_cytoskeletal_protein_that_plays_a_critical_role_in_maintaining_the_structural_integrity_of_cells__defects_in_plectin_can_be_either_qualitative_or_quantitative___1____qualitative_defects____these_refer_to_mutations_in_the_plectin_gene__plec__that_lead_to_the_production_of_a_malfunctioning_or_improperly_functioning_protein__such_mutations_can_affect_the_protein_s_ability_to_interact_with_other_cytoskeletal_components_or_its_capacity_to_provide_mechanical_stability_to_cells__leading_to_various_diseases_such_as_epidermolysis_bullosa_and_myofibrillar_myopathy___2____quantitative_defects____these_involve_a_reduced_level_of_plectin_protein_due_to_deletion_mutations__splicing_errors__or_regulatory_issues_that_lower_its_expression__a_decrease_in_plectin_levels_can_disrupt_normal_cellular_functions_and_structural_integrity__contributing_to_the_pathogenesis_of_diseases___these_defects_can_lead_to_a_range_of_clinical_manifestations_depending_on_the_tissues_affected_and_the_severity_of_the_defect	none
MONDO:0016199	neuromuscular disease caused by qualitative or quantitative defects of protein SERCA1	nervous_system_disorder	other	nervous_system_disorder	renal_medicine|genetics_and_genomics|pulmonology|cardiology|hematology	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0016202	autosomal dominant rhegmatogenous retinal detachment	disorder_of_visual_system|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0016203	hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics|cardiology|endocrinology|hepatology	cardiovascular_disorder|metabolic_disorder	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0016204	idiopathic copper-associated cirrhosis	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|idiopathic_disease	hepatology|gastroenterology	liver_disease|metabolic_disorder	liver_disorder	false	false	false	false	very_high
MONDO:0016205	IRVAN syndrome	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	liver_disorder|brain_disorder	false	false	false	false	high
MONDO:0016206	idiopathic uveal effusion syndrome	inflammatory_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|idiopathic_disease|inflammatory_disease	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease	eye_disorder|immune_disorder	false	false	false	false	medium
MONDO:0016207	phacoanaphylactic uveitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	ophthalmology|allergy_and_immunology|rheumatology	autoimmune_diseases|inflammatory_disease|allergy	eye_disorder|immune_disorder	true	false	false	true	high
MONDO:0016208	solitary rectal ulcer syndrome	digestive_system_disorder	other	digestive_system_disorder	gastrointestinal____corrected_to___gastroenterology|gastroenterology	cancer|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0016209	benign familial nocturnal alternating hemiplegia of childhood	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0016210	alternating hemiplegia	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0016211	non-papillary transitional cell carcinoma of the bladder	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer|autoimmune_diseases|adrenal_gland_disease|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0016213	leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|hematology	autoimmune_diseases|anemia|inflammatory_disease	skin_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0016214	pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome	respiratory_system_disorder	other	respiratory_system_disorder	genetics_and_genomics|pulmonology|hepatology|hematology	metabolic_disorder|anemia|inflammatory_disease	liver_disorder|lung_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0016215	spastic quadriplegic cerebral palsy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|orthopaedic	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0016216	adult hepatocellular carcinoma	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	hpatology|oncology|gastroenterology	hepatic_disease|cancer	liver_disorder	false	true	false	true	very_high
MONDO:0016217	mal de Debarquement	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	pulmonology|neurology|gastroenterology	mental_health_disorder|neurodegenerative_disease	lower_gastrointestinal_disorder|digestive_system_disorder_is_not_in_the_list_but_is_related_to_upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0016218	Guillain-Barre syndrome	syndromic_disease|immune_system_disorder|nervous_system_disorder	autoimmune_disease	nervous_system_disorder|immune_system_disorder|syndromic_disease	neurology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder_spinal_disorder	false	false	false	true	high
MONDO:0016219	dysmorphism-pectus carinatum-joint laxity syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	dermatology|genetics_and_genomics|rheumatology|orthopaedic|pediatric	metabolic_disorder|joint_laxity_syndrome_is_sometimes_associated_with|autoimmune_diseases	bone_disorder|joint_disorder|skin_disorder	false	false	false	false	medium
MONDO:0016220	congenital temporomandibular joint ankylosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	inflammatory_disease|autoimmune_diseases	joint_disorder|teeth_disorder	false	false	false	false	high
MONDO:0016222	spindle cell hemangioma	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	dermatology|hematology	cancer	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0016223	infantile hemangioma of rare localization	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	dermatology|oncology|hematology|pediatric	cardiovascular_disorder|inflammatory_disease|cancer	vascular_disorder|skin_disorder	false	false	false	true	medium
MONDO:0016225	specific learning disability	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric|psychiatry	mental_health_disorder|neurodegenerative_disease	specific_learning_disability|brain_disorder	false	false	false	false	medium
MONDO:0016226	specific language disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0016227	hereditary episodic ataxia	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0016231	capillary malformation	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	dermatology|hematology|genetics_and_genomics	cardiovascular_disorder|vascular_disease	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0016236	kaposiform hemangioendothelioma	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|adrenal_gland_disease	vascular_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0016237	diffuse neonatal hemangiomatosis	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	dermatology|hematology|pediatric	inflammatory_disease|cancer|metabolic_disorder	vascular_disorder|liver_disorder	false	false	false	false	high
MONDO:0016238	solitary fibrous tumor	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	pulmonology|oncology|cardiothoracic	inflammatory_disease|cancer|autoimmune_diseases	lung_disorder	false	false	false	true	medium
MONDO:0016239	cystinosis	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	urology|renal_medicine|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0016240	hemimelia	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	hematology|genetics_and_genomics|orthopaedic	congenital_disorder|developmental_disorder|neurodegenerative_disease	bone_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016241	alternating hemiplegia of childhood	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|pediatric	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0016242	hemoglobin C disease	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	true	low
MONDO:0016243	hemoglobin E disease	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|blood_disorder	false	false	false	true	low
MONDO:0016244	atypical hemolytic-uremic syndrome	hematologic_disorder|syndromic_disease|immune_system_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder|syndromic_disease|immune_system_disorder	hematology|renal_medicine|pediatric	anemia|metabolic_disorder|autoimmune_diseases	kidney_disorder|immune_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0016248	familial ovarian cancer	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|hereditary_disease|cancer_or_benign_tumor|endocrine_system_disorder	oncology|genetics_and_genomics|obstetrics_and_gynecology	cancer	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0016249	hereditary site-specific ovarian cancer syndrome	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|hereditary_disease|cancer_or_benign_tumor|endocrine_system_disorder	oncology|genetics_and_genomics|obstetrics_and_gynecology	cancer|hereditary	reproductive_system_disorder|ovarian_cancer	false	true	false	false	high
MONDO:0016255	uterine corpus mixed epithelial and mesenchymal neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	neoplasm|cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0016256	Hennekam syndrome	cardiovascular_disorder|syndromic_disease|immune_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|immune_system_disorder	genetics_and_genomics|pediatric	cardiovascular_disorder|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	vascular_disorder|joint_disorder|lymphatic_disorder|skin_disorder|kidney_disorder	false	false	false	false	high
MONDO:0016258	uterine corpus carcinofibroma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|reproductive_system_cancer|gynecologic_cancer|ovarian_cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0016259	carcinosarcoma of the corpus uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0016260	uterine corpus rhabdomyosarcoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	muscle_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0016262	leiomyosarcoma of the corpus uteri	reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|post_infectious_disorder	oncology|obstetrics_and_gynecology	corpus_uteri_disease|cancer|gynecologic_cancer	muscle_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0016263	primitive neuroectodermal tumor of the corpus uteri	reproductive_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|neuroectodermal_tumor|cancer	reproductive_system_disorder	false	true	false	false	very_high
MONDO:0016264	autoimmune hepatitis	endocrine_system_disorder|digestive_system_disorder|inflammatory_disease|immune_system_disorder	autoimmune_disease|endocrine_system_disorder	immune_system_disorder|endocrine_system_disorder|inflammatory_disease|digestive_system_disorder	hepatology|gastroenterology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|liver_disorder	false	false	false	true	high
MONDO:0016266	squamous cell carcinoma of the corpus uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	inflammatory_disease|cancer	skin_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0016267	undifferentiated carcinoma of the corpus uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cardiovascular_disorder|metabolic_disorder|mental_health_disorder|inflammatory_disease|cancer|autoimmune_diseases|neurodegenerative_disease|anemia|allergy	upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0016268	papillary carcinoma of the corpus uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease_is_not_applicable	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0016269	high-grade neuroendocrine carcinoma of the corpus uteri	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	neurology|oncology|obstetrics_and_gynecology	neuroendocrine_carcinoma|cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0016270	low-grade neuroendocrine tumor of the corpus uteri	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|neuroendocrine_tumor	endocrine_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0016271	adenoid cystic carcinoma of the corpus uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0016272	transitional cell carcinoma of the corpus uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	kidney_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0016273	malignant germ cell tumor of corpus uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0016276	high-grade neuroendocrine carcinoma of the cervix uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	neuroendocrine_carcinoma|cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0016277	malignant mixed epithelial and mesenchymal tumor of cervix uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	metabolic_disorder|inflammatory_disease|cancer|autoimmune_diseases|adrenal_gland_disease	reproductive_system_disorder	false	true	false	false	high
MONDO:0016280	sarcoma of cervix uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	vascular_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0016281	46,XX ovotesticular disorder of sex development	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|obstetrics_and_gynecology|pediatric|endocrinology	metabolic_disorder|congenital_abnormality|genetic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0016282	rhabdomyosarcoma of the cervix uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	muscle_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0016283	leiomyosarcoma of the cervix uteri	reproductive_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|post_infectious_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|other___corrected_answer___cancer|cancer	muscle_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0016284	primitive neuroectodermal tumor of the cervix uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	neuroectodermal_tumor|cancer	brain_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0016285	papillary carcinoma of the cervix uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	cancer|reproductive_system_disorder	false	true	false	false	high
MONDO:0016289	malignant germ cell tumor of cervix uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|malignant_germ_cell_tumor_of_cervix_uteri	lymphatic_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0016290	Hernández-Aguirre Negrete syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	biliary_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0016291	craniosynostosis, Herrmann-Opitz type	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	teeth_disorder|spinal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0016292	nodular neuronal heterotopia	syndromic_disease	other	syndromic_disease	neurology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016293	congenital stationary night blindness	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|pediatric|ophthalmology	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0016294	Hirschsprung disease-type D brachydactyly syndrome	digestive_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis|digestive_system_disorder	neurology|gastroenterology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|genetic_disorders	lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0016295	neuronal ceroid lipofuscinosis	metabolic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0016296	holoprosencephaly	endocrine_system_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0016297	prelingual non-syndromic genetic hearing loss	psychiatric_disorder|nervous_system_disorder|hereditary_disease|auditory_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	genetics_and_genomics|pediatric|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder|genetic_disorder	false	false	false	false	high
MONDO:0016298	postlingual non-syndromic genetic hearing loss	psychiatric_disorder|nervous_system_disorder|hereditary_disease|auditory_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	genetics_and_genomics|pediatric|otolaryngology	genetic_hearing_loss|metabolic_disorder	ear_disorder	false	false	false	false	medium
MONDO:0016299	holoprosencephaly-caudal dysgenesis syndrome	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0016301	congenitally corrected transposition of the great arteries	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|pediatric|cardiology	congenital_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0016302	isolated congenitally uncorrected transposition of the great arteries	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	pediatric|cardiothoracic|cardiology	cardiovascular_disorder|congenital_heart_disease	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0016303	congenitally uncorrected transposition of the great arteries with cardiac malformation	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	pediatric|cardiothoracic|cardiology|genetics_and_genomics	congenital_heart_defect|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0016304	classic pantothenate kinase-associated neurodegeneration	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0016305	atypical pantothenate kinase-associated neurodegeneration	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0016306	Niemann-Pick disease type C, severe perinatal form	hereditary_disease|metabolic_disease|immune_system_disorder	metabolic_disease	metabolic_disease|immune_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0016307	Niemann-Pick disease type C, severe early infantile neurologic onset	hereditary_disease|metabolic_disease|immune_system_disorder	metabolic_disease	metabolic_disease|immune_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0016308	Niemann-Pick disease type C, late infantile neurologic onset	hereditary_disease|metabolic_disease|immune_system_disorder	metabolic_disease	metabolic_disease|immune_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|brain_disorder|muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0016309	Niemann-Pick disease type C, juvenile neurologic onset	hereditary_disease|metabolic_disease|immune_system_disorder	metabolic_disease	metabolic_disease|immune_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0016310	Niemann-Pick disease type C, adult neurologic onset	hereditary_disease|metabolic_disease|immune_system_disorder	metabolic_disease	metabolic_disease|immune_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0016311	Bockenheimer syndrome	integumentary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder	neurology|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|brain_disorder|immune_disorder	false	false	false	false	medium
MONDO:0016312	5-fluorouracil poisoning	poisoning	other	poisoning	oncology|gastroenterology|hepatology|hematology	metabolic_disorder|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0016315	mucopolysaccharidosis type 2, severe form	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|metabolic_disease|syndromic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|joint_disorder|brain_disorder|muscle_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0016316	mucopolysaccharidosis type 2, attenuated form	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|metabolic_disease|syndromic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|joint_disorder|muscle_disorder|liver_disorder	false	false	false	true	medium
MONDO:0016318	progressive multifocal leukoencephalopathy	nervous_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	nervous_system_disorder|acute_disease|infectious_disease|inflammatory_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	true	false	false	false	high
MONDO:0016319	congenital insensitivity to pain with hyperhidrosis	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	skin_disorder|neurological_disorders	false	false	false	false	high
MONDO:0016321	pulmonary interstitial glycogenosis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|genetics_and_genomics	metabolic_disorder|genetic_disorder	lung_disorder|liver_disorder	false	false	false	false	medium
MONDO:0016322	neuroendocrine cell hyperplasia of infancy	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pediatric|endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder	false	false	false	false	medium
MONDO:0016323	chronic respiratory distress with surfactant metabolism deficiency	respiratory_system_disorder|hereditary_disease	other	respiratory_system_disorder|hereditary_disease	pediatric|pulmonology	metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|lung_disorder	false	false	false	false	high
MONDO:0016330	non-familial hypertrophic cardiomyopathy	cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder	pediatric|cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0016331	infantile systemic hyalinosis	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	rheumatology|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease	joint_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0016332	hypertrophic cardiomyopathy due to intensive athletic training	cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder	pediatrics|cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0016333	familial dilated cardiomyopathy	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiothoracic|cardiology|genetics_and_genomics	familial_dilated_cardiomyopathy_seems_to_also_be_closely_related_to_metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016338	non-familial dilated cardiomyopathy	cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder	renal_medicine|pulmonology|cardiothoracic|cardiology|hematology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0016340	familial restrictive cardiomyopathy	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	pediatric|cardiothoracic|cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016342	familial isolated arrhythmogenic right ventricular dysplasia	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiology|genetics_and_genomics	familial_isolated_arrhythmogenic_right_ventricular_dysplasia_is_not_a_clear_match_for_any_category_so_the_best_fitting_categories_are_cardiovascular_disorder__genetic_disease|cardiovascular_disorder	heart_disorder|vascular_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016344	hydranencephaly	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric	inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0016345	non-familial restrictive cardiomyopathy	cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder	pulmonology|cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016346	hydrocephalus-obesity-hypogonadism syndrome	syndromic_disease	other	syndromic_disease	pediatric|endocrinology	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	endocrine_disorder|brain_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0016349	congenital hydrocephalus	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric	congenital_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0016350	hydrocephalus-blue sclerae-nephropathy syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	kidney_disorder|brain_disorder	true	false	false	false	high
MONDO:0016351	anti-HLA hyperimmunization	immune_system_disorder	other	immune_system_disorder	immunology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|allergy	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0016353	palmoplantar keratoderma-spastic paralysis syndrome	integumentary_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0016354	xeroderma pigmentosum-Cockayne syndrome complex	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|cancer|metabolic_disorder|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0016356	diffuse cutaneous systemic sclerosis	connective_tissue_disorder|integumentary_system_disorder|immune_system_disorder	autoimmune_disease	immune_system_disorder|integumentary_system_disorder|connective_tissue_disorder	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder|skin_disorder	false	false	false	true	very_high
MONDO:0016357	dysplastic cortical hyperostosis	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics|orthopaedic	endocrine_disorder|metabolic_disorder	skeletal_disorder|bone_disorder	false	false	false	false	low
MONDO:0016358	limited cutaneous systemic sclerosis	integumentary_system_disorder|connective_tissue_disorder|immune_system_disorder	autoimmune_disease	immune_system_disorder|integumentary_system_disorder|connective_tissue_disorder	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0016359	limited systemic sclerosis	connective_tissue_disorder|integumentary_system_disorder|immune_system_disorder	autoimmune_disease	immune_system_disorder|integumentary_system_disorder|connective_tissue_disorder	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder_skin_disorder	true	false	false	false	medium
MONDO:0016360	marcothrombocytopenia with mitral valve insufficiency	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|cardiology	anemia|cardiovascular_disorder|autoimmune_diseases	blood_bone_marrow_disorder|heart_disorder	false	false	false	false	high
MONDO:0016362	attenuated familial adenomatous polyposis	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	oncology|genetics_and_genomics|gastroenterology	cancer|familial_cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0016364	Joubert syndrome with ocular defect	disorder_of_visual_system|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0016365	familial primary hyperparathyroidism	endocrine_system_disorder|cancer_or_benign_tumor|hereditary_disease	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|renal_medicine|endocrinology	familial_primary_hyperparathyroidism_is_more_specifically_related_to_this_category__however_in_the_list_provided_it_would_categorize_under__metabolic_disorder|metabolic_disorder	endocrine_disorder	false	false	false	true	high
MONDO:0016366	maternal phenylketonuria	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|vascular_disorder	false	false	false	true	high
MONDO:0016367	dermatomyositis	integumentary_system_disorder|inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	other	musculoskeletal_system_disorder|idiopathic_disease|integumentary_system_disorder|connective_tissue_disorder|inflammatory_disease	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|muscle_disorder	false	false	false	true	high
MONDO:0016368	Rothmund-Thomson syndrome type 1	integumentary_system_disorder|syndromic_disease|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|hereditary_disease	cancer_or_benign_tumor	integumentary_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|pediatrics	anemia|metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|eye_disorder	false	false	false	false	high
MONDO:0016369	Rothmund-Thomson syndrome type 2	integumentary_system_disorder|disorder_of_visual_system|syndromic_disease|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|hereditary_disease	cancer_or_benign_tumor	integumentary_system_disorder|syndromic_disease|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	eye_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0016370	Marchiafava-Bignami disease	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0016371	combined hyperactive dysfunction syndrome of the cranial nerves	nervous_system_disorder	other	nervous_system_disorder	otolaryngology|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder|nose_disorder	false	false	false	false	high
MONDO:0016372	glossopharyngeal neuralgia	nervous_system_disorder	other	nervous_system_disorder	otolaryngology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|throat_disorder	false	false	false	true	high
MONDO:0016373	isolated facial myokymia	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	low
MONDO:0016374	cranial neuralgia	nervous_system_disorder	other	nervous_system_disorder	otolaryngology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0016376	confetti-like macular atrophy	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|ophthalmology|neurology	inflammatory_disease|neurodegenerative_disease	eye_disorder|macular_atrophy	false	false	false	false	medium
MONDO:0016377	Pitt-Hopkins-like syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0016378	maternal hyperthermia induced birth defects	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|obstetrics_and_gynecology|pediatric	metabolic_disorder|adrenal_gland_disease	maternal_hypertension|endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0016379	erosive pustular dermatosis of the scalp	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0016380	acquired hypertrichosis lanuginosa	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	endocrine_disorder|skin_disorder	false	false	false	false	high
MONDO:0016381	hypertrichosis lanuginosa congenita	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	congenital_disorder|skin_disease|endocrine_disorder|metabolic_disorder|genetic_disorder	endocrine_disorder|skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0016382	hereditary poikiloderma	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	hereditary_disease|skin_disorder	false	false	false	false	medium
MONDO:0016383	nephrogenic diabetes insipidus	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	renal_medicine|endocrinology|pediatric	metabolic_disorder|autoimmune_diseases	kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0016384	hypogonadotropic hypogonadism-frontoparietal alopecia syndrome	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology|neurology	endocrine_disorder|genetic_condition|developmental_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0016385	hypogonadism-mitral valve prolapse-intellectual disability syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|endocrinology|cardiology|pediatric|neurology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	endocrine_disorder|heart_disorder|intellectual_disability_is_a_brain_disorder_but_it_s_not_listed_so_i_m_assuming_you_don_t_want_that_as_a_category__however_since_intellectual_disability_does_have_a_relation_to_endocrine_issues_through_hypogonadism_i_ve_included_this_one__reproductive_system_disorder	false	false	false	false	high
MONDO:0016386	hypogonadotropic hypogonadism-retinitis pigmentosa syndrome	syndromic_disease|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	syndromic_disease|reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	genetics_and_genomics|ophthalmology|endocrinology	endocrine_disorder|genetic_disorder|neurodegenerative_disease	endocrine_disorder|eye_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0016387	mitochondrial oxidative phosphorylation disorder	mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	genetics_and_genomics|cardiology|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	high
MONDO:0016390	familial hypoparathyroidism	endocrine_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease|endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|metabolic_disease	endocrinology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0016391	neonatal diabetes mellitus	endocrine_system_disorder|metabolic_disease|digestive_system_disorder|hereditary_disease	metabolic_disease|diabetes_mellitus|endocrine_system_disorder	hereditary_disease|digestive_system_disorder|endocrine_system_disorder|metabolic_disease	endocrinology|pediatric	metabolic_disorder|autoimmune_diseases	endocrine_disorder|neonatal_disease_mellitus	false	false	true	true	high
MONDO:0016392	cerebellar hypoplasia-tapetoretinal degeneration syndrome	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0016394	sporadic infantile bilateral striatal necrosis	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0016395	foveal hypoplasia-presenile cataract syndrome	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	disorder_of_orbital_region|nervous_system_disorder|disorder_of_visual_system|hereditary_disease|psychiatric_disorder	genetics_and_genomics|ophthalmology|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0016396	pontocerebellar hypoplasia type 1	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|psychiatric_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0016407	oligomeganephronia	urinary_system_disorder	other	urinary_system_disorder	pediatric|renal_medicine|genetics_and_genomics	kidney_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0016408	permanent congenital hypothyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|pediatric	autoimmune_diseases|metabolic_disorder	thyroid_disorder|endocrine_disorder|congenital_disorder	false	false	false	true	high
MONDO:0016410	central congenital hypothyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|pediatric|neonatology	endocrine_disorder|congenital_disease|metabolic_disorder	endocrine_disorder|central_nervous_system_disorder	false	false	false	true	medium
MONDO:0016411	hypothyroidism due to deficient transcription factors involved in pituitary development or function	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	pituitary_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0016412	peripheral hypothyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|neurology	metabolic_disorder|autoimmune_diseases	peripheral_endocrine_disorder_is_a_subset_of_peripheral_disease|endocrine_disorder	false	false	false	false	medium
MONDO:0016413	congenital hypothyroidism due to maternal intake of antithyroid drugs	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|pediatric	metabolic_disorder|autoimmune_diseases	endocrine_disorder|maternal_factors	false	false	false	true	high
MONDO:0016414	hypotrichosis-intellectual disability, Lopes type	syndromic_disease	other	syndromic_disease	neurology|pediatric|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|skin_disorder	false	false	false	false	high
MONDO:0016416	diphallia	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	reproductive_system_disorder|disorder_of_development_or_morphogenesis	pediatric|obstetrics_and_gynecology|genetics_and_genomics	developmental_disorder|congenital_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder	false	false	false	false	low
MONDO:0016417	congenital ichthyosis-microcephalus-tetraplegia syndrome	syndromic_disease	other	syndromic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|skin_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0016418	multiple system atrophy, cerebellar type	nervous_system_disorder|hereditary_disease|metabolic_disease	neurodegenerative_disease|metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016419	hereditary breast carcinoma	cancer_or_benign_tumor|hereditary_disease|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics|oncology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease|cancer	hereditary_blood_bone_marrow_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0016420	familial flecked retinopathy	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	genetics_and_genomics|ophthalmology	metabolic_disorder|genetic_disease	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0016421	toxic oil syndrome	poisoning	other	poisoning	pulmonology|cardiothoracic	metabolic_disorder|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0016422	autoimmune polyendocrinopathy type 3	syndromic_disease|endocrine_system_disorder|immune_system_disorder	endocrine_system_disorder|autoimmune_disease	endocrine_system_disorder|syndromic_disease|immune_system_disorder	endocrinology|genetics_and_genomics|rheumatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	endocrine_disorder|immune_disorder	false	false	false	false	high
MONDO:0016423	autoimmune polyendocrinopathy type 4	syndromic_disease|endocrine_system_disorder|immune_system_disorder	endocrine_system_disorder|autoimmune_disease	endocrine_system_disorder|syndromic_disease|immune_system_disorder	endocrinology|genetics_and_genomics|immunology|rheumatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	endocrine_disorder|immune_disorder	false	false	false	false	high
MONDO:0016424	progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder	cardiology|pediatric|genetics_and_genomics|otolaryngology	cardiovascular_disorder|neurodegenerative_disease	ear_disorder|heart_disorder	false	false	false	false	medium
MONDO:0016425	Hughes-Stovin syndrome	syndromic_disease	other	syndromic_disease	hematology|cardiology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	heart_disorder|immune_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0016426	fusariosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|dermatology	neurodegenerative_disease|inflammatory_disease	lung_disorder|lower_gastrointestinal_disorder|other____note__fusariosis_is_a_fungal_infection_that_can_affect_the_lungs_and_gastrointestinal_tract	true	false	false	true	high
MONDO:0016429	Marburg acute multiple sclerosis	disorder_of_development_or_morphogenesis|nervous_system_disorder|immune_system_disorder	neurodegenerative_disease|autoimmune_disease	acute_disease|immune_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|pediatric	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0016430	Balo concentric sclerosis	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|dermatology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0016431	autosomal dominant Charcot-Marie-Tooth disease type 2M	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	orthopaedic|pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant	peripheral_nerve_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0016432	heart-hand syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|cardiology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease|autoimmune_diseases	heart_disorder|muscle_disorder|joint_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016433	dysmorphism-short stature-deafness-disorder of sex development syndrome	disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	developmental_disorders_are_more_commonly_associated_with_genetics_and_genomics_however_the_symptoms_described_would_also_be_found_in_developmental_disorders_which_is_actually_a_part_of_pediatrics_therefore_pediatric_should_come_first|endocrinology|pediatric|psychiatry|obstetrics_and_gynecology|genetics_and_genomics|otolaryngology	metabolic_disorder|disorder_of_sex_development|autoimmune_diseases	bone_disorder|reproductive_system_disorder|endocrine_disorder|ear_disorder	true	false	false	true	high
MONDO:0016437	late-onset focal dermal elastosis	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder	skin_disorder	false	false	false	false	low
MONDO:0016438	linear focal dermal elastosis	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	skin_condition|autoimmune_diseases|inflammatory_disease	skin_disorder	false	false	false	false	low
MONDO:0016439	elastoderma	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder	false	false	false	false	medium
MONDO:0016440	elastofibroma dorsi	cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	orthopaedic|dermatology	inflammatory_disease	muscle_disorder|joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0016441	acquired pseudoxanthoma elasticum	integumentary_system_disorder	other	integumentary_system_disorder	rheumatology|dermatology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0016442	elastoma	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	cancer|adrenal_gland_disease	skin_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0016443	papular elastorrhexis	integumentary_system_disorder	other	integumentary_system_disorder	rheumatology|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	elastorhexis_is_often_associated_with_skin|skin_disorder	false	false	false	false	low
MONDO:0016444	primary anetoderma	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0016445	familial anetoderma	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder	skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0016446	acquired cutis laxa	integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder	muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0016447	white fibrous papulosis of the neck	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|otolaryngology	autoimmune_diseases|inflammatory_disease	skin_disorder	false	false	false	false	low
MONDO:0016448	pseudoxanthoma elasticum-like papillary dermal elastolysis	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|other____there_were_3_best_fitting_categories	false	false	false	false	low
MONDO:0016449	mid-dermal elastolysis	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0016450	autoimmune hemolytic anemia, cold type	immune_system_disorder|hematologic_disorder	anemia|autoimmune_disease	hematologic_disorder|immune_system_disorder	hematology|allergy_and_immunology	anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0016451	idiopathic hypersomnia with long sleep time	other	other	idiopathic_disease|sleep_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	endocrine_disorder|brain_disorder	false	false	false	false	medium
MONDO:0016452	idiopathic hypersomnia without long sleep time	other	other	idiopathic_disease|sleep_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	endocrine_disorder|brain_disorder	false	false	false	false	medium
MONDO:0016453	foodborne botulism	infectious_disease	infectious_disease	infectious_disease	neurology|gastroenterology	neurodegenerative_disease|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0016454	Charcot-Marie-Tooth disease type 2B5	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|orthopaedic|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016455	virus-associated trichodysplasia spinulosa	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease	pediatric|genetics_and_genomics|dermatology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	skin_disorder|eye_disorder	true	false	false	false	medium
MONDO:0016456	5q14.3 microdeletion syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0016457	ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome	syndromic_disease	other	syndromic_disease	neurology|ophthalmology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|upper_gastrointestinal_disorder|eye_disorder	true	false	false	false	high
MONDO:0016458	8q12 microduplication syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0016459	2q23.1 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0016460	polyvalvular heart disease syndrome	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|hematology|pulmonology|genetics_and_genomics	cardiovascular_disorder|autoimmune_diseases	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016461	5q35 microduplication syndrome	chromosomal_disorder	other	chromosomal_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0016462	isolated agammaglobulinemia	immune_system_disorder|hematologic_disorder|hereditary_disease	other	hematologic_disorder|immune_system_disorder|hereditary_disease	allergy_and_immunology|hematology|genetics_and_genomics|immunology	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0016463	syndromic agammaglobulinemia	immune_system_disorder|hematologic_disorder|syndromic_disease|hereditary_disease	other	hematologic_disorder|syndromic_disease|immune_system_disorder|hereditary_disease	hematology|genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	immune_disorder_lymphatic_disorder	false	false	false	true	high
MONDO:0016464	insulin-resistance syndrome type B	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	cardiology|endocrinology	insulin_resistance_syndrome_type_b_does_fit_into_the_category__autoimmune_diseases__as_well_but_that_is_less_fitting_than_metabolic_disorder|metabolic_disorder	endocrine_disorder|metabolic_disorder	false	false	true	false	high
MONDO:0016466	asbestosis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiothoracic	cancer|inflammatory_disease	lung_disorder	false	false	false	false	high
MONDO:0016467	isotretinoin syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0016468	toxin-mediated infectious botulism	infectious_disease	infectious_disease	infectious_disease	neurology|pediatric|infectious_diseases	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|muscle_disorder	true	false	false	true	high
MONDO:0016469	Ehlers-Danlos syndrome, vascular-like type	syndromic_disease|hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|cardiovascular_disorder	rheumatology|genetics_and_genomics|dermatology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|joint_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016470	Ehlers-Danlos/osteogenesis imperfecta syndrome	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	orthopaedic|genetics_and_genomics|dermatology|rheumatology	genetic_disorder|connective_tissue_disease|musculoskeletal_disorder|metabolic_disorder	skin_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0016471	pachyonychia congenita	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|dermatology	anemia|neurodegenerative_disease	skin_disorder|joint_disorder	false	false	false	false	medium
MONDO:0016472	dracunculiasis	infectious_disease	infectious_disease	infectious_disease	pediatric|parasitology|infectious_disease	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0016473	familial rhabdoid tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|oncology	cancer|adrenal_gland_disease	brain_disorder|kidney_disorder	false	true	false	false	very_high
MONDO:0016474	drug-induced lupus erythematosus	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	connective_tissue_disorder|immune_system_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0016475	Beckwith-Wiedemann syndrome due to imprinting defect of 11p15	musculoskeletal_system_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	cancer|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0016476	Beckwith-Wiedemann syndrome due to CDKN1C mutation	musculoskeletal_system_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	cancer|metabolic_disorder	vascular_disorder|kidney_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0016477	Beckwith-Wiedemann syndrome due to 11p15 microdeletion	musculoskeletal_system_disorder|syndromic_disease|cancer_or_benign_tumor|chromosomal_disorder|hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|chromosomal_disorder|hereditary_disease	pediatric|genetics_and_genomics|oncology	cancer|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0016478	Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion	musculoskeletal_system_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|oncology	cancer|metabolic_disorder	ear_disorder|blood_bone_marrow_disorder|endocrine_disorder|muscle_disorder|nose_disorder|skin_disorder|joint_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|vascular_disorder|eye_disorder|kidney_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0016479	silver-Russell syndrome due to 7p11.2p13 microduplication	syndromic_disease|chromosomal_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|chromosomal_disorder|hereditary_disease	pediatric|endocrinology|genetics_and_genomics	mental_health_disorder|metabolic_disorder	developmental_disorder|endocrine_disorder|growth_disorder|bone_disorder	false	false	false	false	high
MONDO:0016480	silver-Russell syndrome due to an imprinting defect of 11p15	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|chromosomal_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|chromosomal_disorder|hereditary_disease	pediatric|genetics_and_genomics	mental_health_disorder|metabolic_disorder	growth_disorder|endocrine_disorder|bone_disorder|developmental_disorder	false	false	false	false	high
MONDO:0016481	silver-Russell syndrome due to 11p15 microduplication	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|chromosomal_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|chromosomal_disorder|hereditary_disease	endocrinology|pediatric|genetics_and_genomics	mental_health_disorder|metabolic_disorder	growth_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0016482	silver-Russell syndrome due to maternal uniparental disomy of chromosome 11	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|chromosomal_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|chromosomal_disorder|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|developmental_disorder|chromosomal_disorder|genetic_disorder	growth_disorder|endocrine_disorder|bone_disorder	false	false	false	false	high
MONDO:0016483	intracranial berry aneurysm	nervous_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	neurology|neurosurgery	cardiovascular_disorder|neurological_disorder	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016484	Usher syndrome type 2	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|ear_disorder	false	false	false	false	medium
MONDO:0016485	Usher syndrome type 3	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	neurology|otolaryngology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0016486	beta-thalassemia major	hematologic_disorder|endocrine_system_disorder|hereditary_disease	anemia|endocrine_system_disorder	hematologic_disorder|hereditary_disease|endocrine_system_disorder	hematology|pediatric|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|hereditary_disorder|genetic_disorder	false	false	false	true	very_high
MONDO:0016487	beta-thalassemia intermedia	hematologic_disorder|endocrine_system_disorder|hereditary_disease	anemia|endocrine_system_disorder	hematologic_disorder|hereditary_disease|endocrine_system_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0016489	delta-beta-thalassemia	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0016490	hemoglobin C-beta-thalassemia syndrome	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	hematology|pediatric|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0016491	hemoglobin E-beta-thalassemia syndrome	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0016496	pharyngeal-cervical-brachial variant of Guillain-Barre syndrome	nervous_system_disorder|syndromic_disease|immune_system_disorder	autoimmune_disease	nervous_system_disorder|syndromic_disease|immune_system_disorder	neurology|otolaryngology	autoimmune_diseases|inflammatory_disease	immune_disorder|throat_disorder|spinal_disorder	false	false	false	true	high
MONDO:0016497	paraparetic variant of Guillain-Barre syndrome	nervous_system_disorder|syndromic_disease|immune_system_disorder	autoimmune_disease	nervous_system_disorder|syndromic_disease|immune_system_disorder	neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|brain_disorder|immune_disorder|spinal_disorder	true	false	false	true	medium
MONDO:0016498	acute pure sensory neuropathy	nervous_system_disorder|syndromic_disease|immune_system_disorder	autoimmune_disease	nervous_system_disorder|syndromic_disease|immune_system_disorder|acute_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|nerve_muscle_disorder_is_implied_by_the_term_sensory_so_this_could_be_a_better_match__brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0016499	autoimmune autonomic ganglionopathy	nervous_system_disorder|syndromic_disease|immune_system_disorder	autoimmune_disease	nervous_system_disorder|syndromic_disease|immune_system_disorder|acute_disease	neurology|rheumatology___revised_to_match_format___neurology|autonomic_nervous_system__note__i_assume__autonomic_nervous_system__is_a_category__as_it_is_not_in_the_original_list|allergy_and_immunology|rheumatology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	autoimmune_disorder|immune_disorder|vascular_disorder	false	false	false	true	high
MONDO:0016500	acute sensory ataxic neuropathy	immune_system_disorder|nervous_system_disorder|syndromic_disease	autoimmune_disease	immune_system_disorder|nervous_system_disorder|syndromic_disease|acute_disease	neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016501	Hermansky-Pudlak syndrome with pulmonary fibrosis	hereditary_disease|integumentary_system_disorder|hematologic_disorder|syndromic_disease|respiratory_system_disorder|metabolic_disease	metabolic_disease	hematologic_disorder|hereditary_disease|integumentary_system_disorder|metabolic_disease|syndromic_disease|respiratory_system_disorder	genetics_and_genomics|pediatric|immunology|pulmonology	anemia|autoimmune_diseases|inflammatory_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder|lung_disorder	false	false	false	false	high
MONDO:0016502	Hermansky-Pudlak syndrome without pulmonary fibrosis	hereditary_disease|integumentary_system_disorder|hematologic_disorder|syndromic_disease|metabolic_disease	metabolic_disease	hematologic_disorder|hereditary_disease|integumentary_system_disorder|metabolic_disease|syndromic_disease	genetics_and_genomics|pediatric	anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0016503	congenital erosive and vesicular dermatosis	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|congenital_disorder	false	false	false	false	medium
MONDO:0016504	primary unilateral adrenal hyperplasia	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|pediatric	genetic_disorder|endocrine_disorder|metabolic_disorder|adrenal_gland_disease	endocrine_disorder	false	false	false	false	medium
MONDO:0016505	aldosterone-producing adrenal cortex adenoma	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cardiology|endocrinology|renal_medicine	cancer|metabolic_disorder|adrenal_gland_disease	vascular_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0016506	ectopic aldosterone-producing tumor	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|oncology|renal_medicine	cancer|adrenal_gland_disease	endocrine_disorder|kidney_disorder	false	true	false	true	high
MONDO:0016509	microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|ophthalmology	neurodegenerative_disease|autoimmune_diseases|cardiovascular_disorder|inflammatory_disease|metabolic_disorder	vascular_disorder|eye_disorder	false	false	false	false	high
MONDO:0016510	epibulbar lipodermoid-preauricular appendage-polythelia syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	dermatology|ophthalmology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0016511	infectious embryofetopathy	infectious_disease|disorder_of_development_or_morphogenesis	infectious_disease	disorder_of_development_or_morphogenesis|infectious_disease	obstetrics_and_gynecology|pediatric	infectious_diseases|embryofetopathy	reproductive_system_disorder|liver_disorder	true	false	false	false	high
MONDO:0016512	Kabuki syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|dermatology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	ear_disorder|joint_disorder|skin_disorder|spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0016514	epidermolysis bullosa simplex with anodontia/hypodontia	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|pediatric|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	immune_disorder|skin_disorder|teeth_disorder	false	false	false	false	high
MONDO:0016515	Kallmann syndrome-heart disease syndrome	hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	cardiology|genetics_and_genomics|endocrinology	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	heart_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0016516	Kenny-Caffey syndrome	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	upper_gastrointestinal_disorder|brain_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0016521	muscular pseudohypertrophy-hypothyroidism syndrome	endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder	orthopaedic|endocrinology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	muscle_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0016522	Kousseff syndrome	syndromic_disease	other	syndromic_disease	neurology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0016523	bronchogenic cyst	disorder_of_development_or_morphogenesis|respiratory_system_disorder	other	respiratory_system_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|pulmonology	respiratory_disease|cancer|inflammatory_disease	throat_disorder|lung_disorder	false	false	false	false	low
MONDO:0016525	familial hyperaldosteronism	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	endocrinology|cardiology|renal_medicine	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0016526	trisomy 9p	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	developmental_disorder|growth_disorder|skeletal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0016527	glycogen storage disease due to lactate dehydrogenase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|genetics_and_genomics|hepatology|pediatrics	metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016528	limb body wall complex	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	developmental_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0016529	duplication of urethra	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|urinary_system_disorder	genetics_and_genomics|pediatric|renal_medicine|urology	inflammatory_disease|congenital_anomaly	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0016530	laryngocele	respiratory_system_disorder	other	respiratory_system_disorder	head_and_neck_surgery|otolaryngology	inflammatory_disease	throat_disorder	false	false	false	false	medium
MONDO:0016531	digestive duplication	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|pediatric	cancer|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0016532	Lennox-Gastaut syndrome	nervous_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0016533	apolipoprotein A-II amyloidosis	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|cardiology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016534	infundibulo-neurohypophysitis	immune_system_disorder|endocrine_system_disorder|reproductive_system_disorder|nervous_system_disorder|inflammatory_disease	autoimmune_disease|endocrine_system_disorder	nervous_system_disorder|reproductive_system_disorder|immune_system_disorder|inflammatory_disease|endocrine_system_disorder	neurology|endocrinology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	endocrine_disorder|brain_disorder|neuro_disorder|pituitary_gland_disorder	true	false	false	false	medium
MONDO:0016535	hypohidrotic ectodermal dysplasia	integumentary_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	dermatology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	skin_disorder|teeth_disorder|ear_disorder|eye_disorder|joint_disorder	false	false	false	false	high
MONDO:0016537	lymphoproliferative syndrome	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	hematology|oncology	cancer|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	true	true	false	true	high
MONDO:0016539	atypical hypotonia-cystinuria syndrome	metabolic_disease|mitochondrial_disease|chromosomal_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|chromosomal_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	kidney_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016540	congenital secondary polycythemia	immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	other	immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	genetics_and_genomics|hematology	metabolic_disorder|cardiovascular_disorder|genetic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0016541	acquired secondary polycythemia	immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	other	immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	hematology|pulmonology|oncology	metabolic_disorder|anemia	blood_bone_marrow_disorder|bone_disorder|hematology_disorder	false	false	false	false	medium
MONDO:0016542	IL10-related early-onset inflammatory bowel disease	immune_system_disorder|connective_tissue_disorder|hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease|connective_tissue_disorder|immune_system_disorder	allergy_and_immunology|gastroenterology|rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|joint_disorder|immune_disorder	true	false	false	false	very_high
MONDO:0016543	hyperphenylalaninemia due to tetrahydrobiopterin deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	kidney_disorder|brain_disorder|metabolic_disorder	false	false	false	true	very_high
MONDO:0016544	IgG4-related mesenteritis	immune_system_disorder	autoimmune_disease	immune_system_disorder	gastroenterology|rheumatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0016545	leukoencephalopathy-palmoplantar keratoderma syndrome	hereditary_disease	other	hereditary_disease	neurology|dermatology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|brain_disorder|skin_disorder	false	false	false	false	high
MONDO:0016546	primary orthostatic tremor	nervous_system_disorder	other	nervous_system_disorder	neurology|cardiology	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0016547	Beckwith-Wiedemann syndrome due to NSD1 mutation	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cancer_or_benign_tumor|cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder|cancer_or_benign_tumor|syndromic_disease|musculoskeletal_system_disorder	neurology|obstetrics_and_gynecology|genetics_and_genomics|pediatric|psychiatry|oncology	cancer|metabolic_disorder|neurodegenerative_disease	developmental_disorder|brain_disorder|growth_disorder	false	false	false	false	high
MONDO:0016548	megacystis-megaureter syndrome	urinary_system_disorder	other	urinary_system_disorder	genetics_and_genomics|pediatric|renal_medicine|urology	congenital_abnormality|metabolic_disorder|urinary_system_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0016549	primary megaureter, adult-onset form	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|urinary_system_disorder	renal_medicine|urology	metabolic_disorder|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0016550	congenital primary megaureter, obstructed form	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|urinary_system_disorder	pediatric|urology	urogenital_disease|pediatric_condition|birth_defect|congenital_anomaly|obstructive_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0016551	congenital primary megaureter, refluxing form	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|urinary_system_disorder	pediatric|urology	metabolic_disorder|urinary_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0016552	congenital primary megaureter, nonrefluxing and unobstructed form	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|urinary_system_disorder	pediatric|urology	genetic_disorder|urinary_system_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0016553	isolated congenital hypogonadotropic hypogonadism	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|endocrine_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0016554	neonatal iodine exposure	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	obstetrics_and_gynecology|pediatric	metabolic_disorder|autoimmune_diseases	thyroid_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0016555	transient congenital hypothyroidism due to maternal factor	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|pediatric	metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0016556	transient congenital hypothyroidism due to neonatal factor	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|pediatric	congenital_hypothyroidism|metabolic_disorder	endocrine_disorder|neonatal_factor	false	false	false	true	low
MONDO:0016557	leukonychia totalis	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology|hematology	anemia|autoimmune_diseases	blood_bone_marrow_disorder|teeth_disorder	false	false	false	false	low
MONDO:0016558	familial congenital mirror movements	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	low
MONDO:0016559	glaucoma secondary to spherophakia/ectopia lentis and megalocornea	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	musculoskeletal_disorder|eye_disorder	false	false	false	true	high
MONDO:0016560	ptosis-syndactyly-learning difficulties syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|joint_disorder|eye_disorder	false	false	false	false	medium
MONDO:0016561	1q44 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0016562	progressive supranuclear palsy-pure akinesia with gait freezing syndrome	nervous_system_disorder|disorder_of_visual_system|syndromic_disease|hereditary_disease	neurodegenerative_disease	hereditary_disease|disorder_of_visual_system|syndromic_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016563	progressive supranuclear palsy-corticobasal syndrome	nervous_system_disorder|disorder_of_visual_system|syndromic_disease|hereditary_disease	neurodegenerative_disease	hereditary_disease|disorder_of_visual_system|syndromic_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0016564	progressive supranuclear palsy-progressive non-fluent aphasia syndrome	nervous_system_disorder|disorder_of_visual_system|syndromic_disease|hereditary_disease	neurodegenerative_disease	hereditary_disease|disorder_of_visual_system|syndromic_disease|nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|inflammatory_disease|mental_health_disorder|autoimmune_diseases	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016566	loiasis	infectious_disease	infectious_disease	infectious_disease	neurology|hematology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|brain_disorder|skin_disorder	true	false	false	true	medium
MONDO:0016567	locked-in syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0016568	Lowe-Kohn-Cohen syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|cardiovascular_disorder|autoimmune_diseases	kidney_disorder|liver_disorder|heart_disorder	false	false	false	false	low
MONDO:0016570	primary pulmonary lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|pulmonology|oncology	cancer|autoimmune_diseases|lymphoma	lymphatic_disorder|lung_disorder	false	true	false	false	medium
MONDO:0016571	macrocephaly-short stature-paraplegia syndrome	nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0016572	central bilateral macrogyria	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|adrenal_gland_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0016573	acute fatty liver of pregnancy	obstetric_disorder	other	obstetric_disorder|acute_disease	gastroenterology|obstetrics_and_gynecology|hepatology	metabolic_disorder|inflammatory_disease|adrenal_gland_disease	liver_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0016574	hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome	integumentary_system_disorder	other	integumentary_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	endocrine_disorder|brain_disorder|skin_disorder	false	false	false	true	high
MONDO:0016575	primary ciliary dyskinesia	respiratory_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease|respiratory_system_disorder	neurology|genetics_and_genomics|pulmonology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder|nose_disorder	false	false	false	false	high
MONDO:0016576	split hand-foot malformation	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0016577	biliary atresia with splenic malformation syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|hepatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	liver_disorder|biliary_disorder|upper_gastrointestinal_disorder	false	false	false	true	very_high
MONDO:0016580	congenital pulmonary airway malformation	respiratory_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|respiratory_system_disorder	pediatric|pulmonology	cardiovascular_disorder|congenital_disease	lung_disorder|congenital_disorder	false	false	false	false	high
MONDO:0016581	conotruncal heart malformations	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|pediatric|cardiothoracic	cardiovascular_disorder|congenital_heart_disorder	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0016582	congenital mitral malformation	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|cardiology|pediatric	cardiovascular_disorder|congenital_heart_disease	heart_disorder|congenital_heart_disorder	false	false	false	false	high
MONDO:0016583	familial intestinal malrotation-facial anomalies syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric|gastroenterology	metabolic_disorder|congenital_abnormality	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0016584	mandibuloacral dysplasia	integumentary_system_disorder|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	musculoskeletal_system_disorder|integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	orthopaedic|genetics_and_genomics|pediatric|dermatology	metabolic_disorder|genetic_disorder	teeth_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0016586	systemic mastocytosis	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	hematology|oncology	cancer|anemia|inflammatory_disease|autoimmune_diseases	immune_disorder_blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0016587	arrhythmogenic right ventricular cardiomyopathy	cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder	genetics_and_genomics|cardiology|cardiothoracic	cardiovascular_disorder|autoimmune_diseases	muscle_disorder|heart_disorder	false	false	false	true	high
MONDO:0016588	infantile mercury poisoning	poisoning	other	poisoning	neurology|pediatric	neurodegenerative_disease|mental_health_disorder	nervous_system_disorder|brain_disorder	false	false	false	true	high
MONDO:0016591	sporadic adult-onset ataxia of unknown etiology	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0016593	acquired ataxia	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0016594	superficial siderosis	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	dermatology|hematology	anemia	skin_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0016595	inhalational anthrax	infectious_disease	infectious_disease	infectious_disease	allergy_and_immunology|pulmonology	cancer|inflammatory_disease|autoimmune_diseases|infectious_disease	immune_disorder|nose_disorder|lung_disorder	true	false	false	true	very_high
MONDO:0016596	hyperphosphatasia-intellectual disability syndrome	syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|bone_disorder	false	false	false	false	high
MONDO:0016598	autosomal recessive secondary polycythemia not associated with VHL gene	musculoskeletal_system_disorder|immune_system_disorder|hematologic_disorder	other	musculoskeletal_system_disorder|immune_system_disorder|hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0016600	acute neonatal citrullinemia type I	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|acute_disease|metabolic_disease	pediatric|hepatology|genetics_and_genomics|renal_medicine	metabolic_disorder|neonatal_disease|inherited_condition	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0016601	adult-onset citrullinemia type I	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics_is_incorrect|hepatology|genetics_and_genomics|renal_medicine	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0016602	citrin deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics|endocrinology|hepatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0016603	citrullinemia type II	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0016604	dysraphism-cleft lip/palate-limb reduction defects syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder	joint_disorder|facial_disorder|limb_reducing_disorder	false	false	false	false	high
MONDO:0016605	perinatal lethal hypophosphatasia	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|obstetrics_and_gynecology	neurodegenerative_disease|metabolic_disorder	note__perinatal_lethal_hypophosphatasia_is_a_rare_genetic_disorder_affecting_bones|skeletal_disorder_is_not_in_the_list_but_bone_is_so_i_am_using_it|bone_disorder	false	false	false	false	very_high
MONDO:0016607	odontohypophosphatasia	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	pediatric|endocrinology|genetics_and_genomics|orthopaedic|osteogenesis_imperfecta_like_diseases_subcategory	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0016608	megalencephaly	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016609	inflammatory myopathy with abundant macrophages	inflammatory_disease|musculoskeletal_system_disorder	other	idiopathic_disease|inflammatory_disease|musculoskeletal_system_disorder	hematology|genetics_and_genomics|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|muscle_disorder	true	false	false	false	high
MONDO:0016610	idiopathic eosinophilic myositis	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|idiopathic_disease|inflammatory_disease	hematology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016611	lipoblastoma	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	pediatric|oncology	cancer|adrenal_gland_disease|other___corrected_answer__removed__other__as_it_was_specified_to_be_removed_if_multiple_categories_match____cancer	bone_marrow_disorder|bone_disorder	false	true	false	false	medium
MONDO:0016612	X-linked cerebellar ataxia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016613	APC-related attenuated familial adenomatous polyposis	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	gastroenterology|genetics_and_genomics|oncology	polyposis|cancer|familial_adenomatous_polyposis|gastrointestinal_disease|hereditary_cancer_predisposition	lower_gastrointestinal_disorder_upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0016614	autosomal recessive ataxia due to PEX10 deficiency	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0016615	oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|idiopathic_disease|inflammatory_disease|connective_tissue_disorder	pediatric|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder	false	false	false	true	high
MONDO:0016616	oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|idiopathic_disease|inflammatory_disease|connective_tissue_disorder	pediatric|rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder	false	false	false	true	medium
MONDO:0016617	rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|idiopathic_disease|inflammatory_disease|connective_tissue_disorder	pediatric|genetics_and_genomics|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder	true	false	false	true	medium
MONDO:0016618	rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|idiopathic_disease|inflammatory_disease|connective_tissue_disorder	pediatric|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder	false	false	false	true	medium
MONDO:0016619	autosomal recessive hypohidrotic ectodermal dysplasia	syndromic_disease|integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	dermatology|pediatric|genetics_and_genomics	metabolic_disorder|skin_disease|ectodermal_dysplasia|ectodermal_dysplasia____corrected_list_to_match_the_format___metabolic_disorder	joint_disorder|nose_disorder|skin_disorder|eye_disorder|throat_disorder|ear_disorder|muscle_disorder|bone_disorder	false	false	false	false	medium
MONDO:0016620	primary hypertrophic osteoarthropathy	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	rheumatology|orthopaedic	metabolic_disorder|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0016621	juvenile Huntington disease	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0016622	Melhem-Fahl syndrome	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	none
MONDO:0016624	hereditary anemia	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hematology|pediatrics|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	medium
MONDO:0016625	acquired deficiency anemia	hematologic_disorder	anemia	hematologic_disorder	renal_medicine|hematology|blood_disorders	metabolic_disorder|acquired_deficiency_anemia|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	medium
MONDO:0016630	isolated delta-storage pool disease	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	hepatology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder	false	false	false	false	medium
MONDO:0016638	familial hypodysfibrinogenemia	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|familial_hypodysfibrinoemia_is_a_bleeding_disorder_caused_by_deficiency_of_fibrinogen	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0016639	lower limb deficiency-hypospadias syndrome	syndromic_disease	other	syndromic_disease	urology|pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_condition	lower_limb_deficiency|reproductive_system_disorder|bone_disorder	false	false	false	false	medium
MONDO:0016641	limb transversal defect-cardiac anomaly syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiothoracic|pediatric|genetics_and_genomics|cardiology	cardiac_anomaly_syndrome|cardiovascular_disorder	heart_disorder|cardiac_anomaly|limb_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0016642	meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0016643	frontonasal dysplasia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|developmental_disorder	upper_gastrointestinal_disorder|brain_disorder|spinal_disorder|bone_disorder|nose_disorder	false	false	false	false	medium
MONDO:0016644	logopenic progressive aphasia	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	genetics_and_genomics|psychiatry|neurology	neurodegenerative_disease|mental_health_disorder|adrenal_gland_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016646	autosomal dominant optic atrophy and peripheral neuropathy	mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	metabolic_disease|nervous_system_disorder|hereditary_disease|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|mitochondrial_disease|disorder_of_visual_system	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0016648	multiple epiphyseal dysplasia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0016649	Warburg micro syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder|disorder_of_orbital_region|hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system	pediatrics|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0016650	paternal uniparental disomy of chromosome 1	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	reproductive_system_disorder	false	false	false	false	none
MONDO:0016651	maternal uniparental disomy of chromosome 1	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|genetic_disorder_____i_replaced_the_original_category_list_with_the_correct_one	reproductive_system_disorder	false	false	false	false	low
MONDO:0016652	2q31.1 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016653	2q33.1 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|developmental_disorder____note__i_ve_assumed_the_category__developmental_disorder__is_implied_as_microdeletions_often_affect_development	false	false	false	false	very_high
MONDO:0016654	ring chromosome 5	chromosomal_disorder	other	chromosomal_disorder	oncology|genetics_and_genomics	neurodegenerative_disease|cancer	kidney_disorder|liver_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0016655	6p22 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder|mental_health_disorder	vascular_disorder|brain_disorder|immune_disorder|kidney_disorder|lung_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016656	7q31 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016657	8p11.2 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	oncology|pediatric|genetics_and_genomics	neurodegenerative_disease|cancer	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0016658	8p23.1 microdeletion syndrome	syndromic_disease|chromosomal_disorder	other	chromosomal_disorder|syndromic_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|immune_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016659	8p23.1 duplication syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|medical_genetics|genetics_and_genomics	neurodegenerative_disease|genetic_disorder|developmental_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016660	autosomal recessive primary microcephaly	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016661	infantile onset panniculitis with uveitis and systemic granulomatosis	connective_tissue_disorder|syndromic_disease	other	connective_tissue_disorder|syndromic_disease	dermatology|rheumatology|pediatric	autoimmune_diseases|inflammatory_disease	eye_disorder|immune_disorder|skin_disorder	true	false	false	false	very_high
MONDO:0016662	idiopathic recurrent pericarditis	connective_tissue_disorder|syndromic_disease	other	idiopathic_disease|connective_tissue_disorder|syndromic_disease	cardiology|rheumatology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	vascular_disorder|immune_disorder|heart_disorder	false	false	false	true	medium
MONDO:0016663	overlapping connective tissue disease	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	immune_system_disorder|connective_tissue_disorder	allergy_and_immunology|rheumatology	autoimmune_diseases|inflammatory_disease|overlapping_connective_tissue_disease	joint_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0016664	drug-induced vasculitis	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	allergy_and_immunology|rheumatology	autoimmune_diseases|inflammatory_disease	vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0016666	unexplained long-lasting fever/inflammatory syndrome	connective_tissue_disorder	other	connective_tissue_disorder	infectious_disease_is_implied_but_not_in_the_list__all_of_them_could_be_relevant_except_for_cardiology__cardiothoracic__dermatology__endocrinology__ophthalmology__otolaryngology__obstetrics_and_gynecology__oncology__orthopaedic__psychiatry__pulmonology__renal_medicine__urology|rheumatology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder	true	false	false	false	high
MONDO:0016668	sickle cell-beta-thalassemia disease syndrome	hereditary_disease|syndromic_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder|syndromic_disease	pediatric|hematologie|hematology|genetics_and_genomics	metabolic_disorder|anemia	kidney_disorder|bone_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0016669	sickle cell-hemoglobin c disease syndrome	hereditary_disease|syndromic_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder|syndromic_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	kidney_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0016670	sickle cell-hemoglobin d disease syndrome	hereditary_disease|syndromic_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder|syndromic_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0016671	sickle cell-hemoglobin E disease syndrome	hereditary_disease|syndromic_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder|syndromic_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	vascular_disorder|kidney_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0016672	hereditary persistence of fetal hemoglobin-sickle cell disease syndrome	hereditary_disease|syndromic_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder|syndromic_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	joint_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0016673	localized junctional epidermolysis bullosa, non-Herlitz type	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	muscle_disorder|joint_disorder|skin_disorder	false	false	false	true	medium
MONDO:0016674	46,XY partial gonadal dysgenesis	disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	urology|endocrinology|genetics_and_genomics	metabolic_disorder|genetic_disease|developmental_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0016675	distal arthrogryposis type 10	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0016677	toxic or drug-related embryofetopathy	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatric	metabolic_disorder	liver_disorder	false	false	false	true	high
MONDO:0016680	high grade astrocytic tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|autoimmune_diseases|allergy|cancer|inflammatory_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0016681	gliosarcoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0016682	giant cell glioblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0016683	gliomatosis cerebri	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0016684	anaplastic astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0016685	low-grade astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0016686	diffuse astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0016687	protoplasmic astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0016688	fibrillary astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurooncology|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0016689	gemistocytic astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology|genetics_and_genomics	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0016690	pleomorphic xanthoastrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0016691	pilocytic astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0016692	pilomyxoid astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0016693	subependymal giant cell astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric|neurology|genetics_and_genomics	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	low
MONDO:0016695	oligodendroglioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0016696	anaplastic oligodendroglioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0016697	low grade ependymoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric|neurology	cancer|neurological_disease	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0016698	ependymoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0016699	myxopapillary ependymoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurological_disorder	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0016700	anaplastic ependymoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology|pediatric	cancer|neurological_disease|tumor	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0016702	oligoastrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0016703	anaplastic oligoastrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer|other___corrected_answer__cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0016705	angiocentric glioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0016706	chordoid glioma of the third ventricle	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	vascular_disorder|brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0016707	astroblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|genetics_and_genomics|pediatric	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0016709	anaplastic/large cell medulloblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology|pediatric	cancer|adrenal_gland_disease	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0016710	medulloblastoma with extensive nodularity	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric	cancer	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0016711	desmoplastic/nodular medulloblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric|neurology	cancer|adrenal_gland_disease	brain_disorder|neurological_disorder	false	true	false	true	high
MONDO:0016712	classic medulloblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0016713	central nervous system Ewing sarcoma/peripheral primitive neuroectodermal tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric|neurology	neurodegenerative_disease|peripheral_primitive_neuroectodermal_tumor_is_more_specifically__a_subset_of_peripheral_nervous_system_tumors|cancer	brain_disorder|spinal_disorder|peripheral_neuroectodermal_tumor_is_not_in_the_list_so__brain_disorder	false	true	false	false	very_high
MONDO:0016715	ependymoblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0016717	choroid plexus neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology|ophthalmology	cancer|neurological_cancers	brain_disorder|eye_disorder	false	true	false	false	high
MONDO:0016718	choroid plexus carcinoma	nervous_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	nervous_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	oncology|neurology	cancer	brain_disorder|eye_disorder	false	true	false	false	very_high
MONDO:0016719	microcephaly-seizures-intellectual disability-heart disease syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	brain_disorder|heart_disorder|intellectual_disability_indicates_inclusion_in_category__developmental_delay__which_is_related_to_brain_disorder_so_list_this_too	true	false	false	false	very_high
MONDO:0016722	pineoblastoma	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|adrenal_gland_disease	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0016723	pineocytoma	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurooncology|cancer|brain_cancer	brain_disorder|spinal_disorder	false	true	false	false	low
MONDO:0016724	papillary tumor of the pineal region	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|tumor	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0016727	extraventricular neurocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	medium
MONDO:0016729	mixed neuronal-glial tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer	brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0016730	gangliocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|adrenal_gland_disease	brain_disorder|spinal_disorder	false	false	false	false	low
MONDO:0016731	desmoplastic infantile astrocytoma/ganglioglioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0016733	ganglioglioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurooncology|cancer	brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0016734	anaplastic ganglioglioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0016735	papillary glioneuronal tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	low
MONDO:0016736	rosette-forming glioneuronal tumor of fourth ventricule	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0016739	yolk sac tumor of central nervous system	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|neurology	cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0016740	choriocarcinoma of the central nervous system	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology|obstetrics_and_gynecology	malignancy|cancer|central_nervous_system_disease|tumor	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0016742	mixed germ cell tumor of central nervous system	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|genetics_and_genomics|neurology|pediatric	cancer|adrenal_gland_disease	brain_disorder|spinal_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0016743	tumor of meninges	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0016745	diffuse leptomeningeal melanocytosis	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0016746	meningeal melanocytoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	oncology|neurology	neurocancer|cancer	brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0016747	primary melanoma of the central nervous system	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	oncology|neurology	cancer|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder|skin_disorder	false	true	false	false	very_high
MONDO:0016748	hemangioblastoma	cardiovascular_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	oncology|hematology|pediatric	cancer|adrenal_gland_disease	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0016749	tumor of cranial and spinal nerves	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0016750	microcephaly-cleft palate syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	teeth_disorder|brain_disorder|cleft_palate_is_actually_covered_under_throat_disorder_but_i_will_assume_that_s_the_closest_match|ear_disorder	false	false	false	false	high
MONDO:0016751	malignant perineurioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pathology	cancer|adrenal_gland_disease	soft_tissue_disorder_is_not_listed_so_use__lymphatic_disorder|muscle_disorder	false	true	false	false	high
MONDO:0016752	benign peripheral nerve sheath tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer	nerve_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0016755	neurofibroma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|genetics_and_genomics|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0016757	malignant triton tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|adrenal_gland_disease	spinal_disorder|nerve_system_disorder	false	true	false	false	very_high
MONDO:0016758	microcephaly-brain defect-spasticity-hypernatremia syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|kidney_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0016759	pontocerebellar hypoplasia type 2	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0016760	microcephaly-microcornea syndrome, Seemanova type	syndromic_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	disorder_of_visual_system|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0016761	spondyloepiphyseal dysplasia	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|genetic_disorder|inflammatory_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0016762	microcornea-corectopia-macular hypoplasia syndrome	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|pediatric|ophthalmology	ocular_disorder|eye_disease	eye_disorder|corectopia|macular_hypoplasia_syndrome	false	false	false	false	medium
MONDO:0016763	spondylometaphyseal dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	rheumatology|genetics_and_genomics|orthopaedic	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0016764	isolated anophthalmia-microphthalmia syndrome	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|pediatric|ophthalmology	eye_abnormality|genetic_condition|neurodevelopmental_disorder	eye_disorder	false	false	false	false	high
MONDO:0016765	19p13.12 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|brain_disorder|spinal_disorder|vascular_disorder|eye_disorder|immune_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016769	linear lichen planus	inflammatory_disease|integumentary_system_disorder	other	inflammatory_disease|integumentary_system_disorder	dermatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	low
MONDO:0016770	actinic lichen planus	inflammatory_disease|integumentary_system_disorder	other	inflammatory_disease|integumentary_system_disorder	oncology|hematology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	low
MONDO:0016771	annular atrophic lichen planus	inflammatory_disease|integumentary_system_disorder	other	inflammatory_disease|integumentary_system_disorder	immunology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0016772	annular lichen planus	inflammatory_disease|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease	dermatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0016773	atrophic lichen planus	inflammatory_disease|integumentary_system_disorder	other	inflammatory_disease|integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0016774	lichen planus pigmentosus	inflammatory_disease|integumentary_system_disorder	other	inflammatory_disease|integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0016775	lichen planus pemphigoides	inflammatory_disease|integumentary_system_disorder	other	inflammatory_disease|integumentary_system_disorder	dermatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0016776	frontal fibrosing alopecia	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	hair_disorder|skin_disorder	false	false	false	false	medium
MONDO:0016777	inhalational botulism	infectious_disease	infectious_disease	infectious_disease	pediatric|neurology	adrenal_gland_disease|neurodegenerative_disease	lower_gastrointestinal_disorder|muscle_disorder|lung_disorder	true	false	false	true	high
MONDO:0016778	iatrogenic botulism	iatrogenic_disease|infectious_disease	infectious_disease	iatrogenic_disease|infectious_disease	toxicology|neurology	neurodegenerative_disease	neurological_disorder__since_this_is_an_iatrogenic_botulism__it_can_be_associated_with_a_neurological_disorder|muscle_disorder	true	false	false	true	high
MONDO:0016779	multiple congenital anomalies due to 14q32.2 maternally expressed gene defect	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|obstetrics_and_gynecology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	heart_disorder|joint_disorder|spinal_disorder|eye_disorder|bone_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0016780	paternal 14q32.2 microdeletion syndrome	syndromic_disease|chromosomal_disorder	other	chromosomal_disorder|syndromic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	brain_disorder|joint_disorder|vascular_disorder|reproductive_system_disorder|upper_gastrointestinal_disorder|muscle_disorder|immune_disorder	false	false	false	false	high
MONDO:0016781	maternal 14q32.2 microdeletion syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatrics|obstetrics_and_gynecology	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	brain_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0016782	paternal 14q32.2 hypomethylation syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder	false	false	false	false	high
MONDO:0016783	maternal 14q32.2 hypermethylation syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|cancer	reproductive_system_disorder|maternal	false	false	false	false	high
MONDO:0016785	complete hydatidiform mole	reproductive_system_disorder|obstetric_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	obstetric_disorder|hereditary_disease|reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|anemia	vascular_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0016786	partial hydatidiform mole	obstetric_disorder|hereditary_disease|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	obstetric_disorder|hereditary_disease|cancer_or_benign_tumor|reproductive_system_disorder	oncology|genetics_and_genomics|obstetrics_and_gynecology	anemia|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0016787	epithelioid trophoblastic tumor	obstetric_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	obstetric_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0016789	pyruvate metabolism disorder	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|gastroenterology|genetics_and_genomics|endocrinology	metabolic_disorder|pyruvate_metabolism_disorder	metabolic_disorder|liver_disorder	false	false	false	false	high
MONDO:0016790	tricarboxylic acid cycle disorder	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0016796	mitochondrial DNA depletion syndrome, encephalomyopathic form	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	metabolic_disease	mitochondrial_disease|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0016798	ataxia neuropathy spectrum	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	true	false	false	false	high
MONDO:0016800	mitochondrial membrane transport disorder	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|cardiology|pediatrics|pulmonology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|mitochondrially_related_disorders_are_often_categorized_as_involving_the_muscle_or_neurological_systems_because_of_their_function_in_energy_production__but_this_one_specifically_mentions_mitochondrial_membrane_transport_disorder_which_would_point_more_towards_a_specific_issue_with_cellular_respiration_and_therefore_points_to_another_category___mitochondrial_disorders_would_be_categorized_under__muscle_disorder	false	false	false	false	high
MONDO:0016801	mitochondrial substrate carrier disorder	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|endocrinology|pediatrics	neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016802	mitochondrial protein import disorder	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric|endocrinology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016806	maternally-inherited mitochondrial dystonia	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric|obstetrics_and_gynecology	neurodegenerative_disease|mitochondrial_dystonia_is_not_in_the_list_so_none|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016807	pure mitochondrial myopathy	mitochondrial_disease	other	mitochondrial_disease	neurology|genetics_and_genomics	neurodegenerative_disease|mitochondrial_myopathies_are_often_classified_as_a_type_of_metabolic_disorder|metabolic_disorder	muscle_disorder	false	false	false	false	medium
MONDO:0016809	spinocerebellar ataxia with epilepsy	mitochondrial_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|mitochondrial_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0016810	autosomal recessive progressive external ophthalmoplegia	mitochondrial_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|mitochondrial_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0016811	renal tubulopathy-encephalopathy-liver failure syndrome	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease	renal_medicine|hepatology|neurology	renal_tubulopathies_and_liver_function_abnormalities|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0016812	dopa-responsive dystonia	nervous_system_disorder|metabolic_disease	metabolic_disease	metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0016814	maternally-inherited Leigh syndrome	mitochondrial_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0016817	Meier-Gorlin syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric	skeletal_rare_disease|metabolic_disorder	lymphatic_disorder|skeletal_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0016818	Mikati-Najjar-Sahli syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|cardiology	cardiovascular_disorder|autoimmune_diseases|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016819	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome	reproductive_system_disorder|disorder_of_visual_system|endocrine_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	endocrine_system_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|reproductive_system_disorder|nervous_system_disorder|syndromic_disease|endocrine_system_disorder|disorder_of_visual_system	genetics_and_genomics|endocrinology|neurology	hypogonadotropic_hypogonadism_syndrome|neurodegenerative_disease|axonal_neuropathy	endocrine_disorder|brain_disorder|muscle_disorder|eye_disorder|reproductive_system_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016820	Moyamoya disease	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|hereditary_disease	pediatrics|neurology	neurodegenerative_disease|cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016821	shoulder and girdle defects-familial intellectual disability syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016822	myalgia-eosinophilia syndrome associated with tryptophan	connective_tissue_disorder	other	connective_tissue_disorder	rheumatology|immunology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|muscle_disorder	true	false	false	true	high
MONDO:0016823	mycetoma	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease	otolaryngology|oncology|hematology|urology|dermatology|pulmonology	cancer|inflammatory_disease|metabolic_disorder	lymphatic_disorder|skin_disorder	true	false	false	true	high
MONDO:0016824	infantile myofibromatosis	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hereditary_disease	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|pediatric|oncology	cancer|neurodegenerative_disease	muscle_disorder|bone_disorder	false	false	false	true	high
MONDO:0016825	mitochondrial myopathy-lactic acidosis-deafness syndrome	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|mitochondrial_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	ear_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016826	methylmalonic aciduria and homocystinuria	metabolic_disease|nutritional_disorder|hematologic_disorder|hereditary_disease	anemia|metabolic_disease	metabolic_disease|hematologic_disorder|nutritional_disorder|hereditary_disease	genetics_and_genomics|hematology|pediatrics	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder|blood_bone_marrow_disorder|urinary_tract_disorder	false	false	false	true	very_high
MONDO:0016827	myopathy-growth delay-intellectual disability-hypospadias syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	intellectual_disability|muscle_disorder|growth_delay	false	false	false	false	high
MONDO:0016828	autosomal recessive sideroblastic anemia	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0016829	familial visceral myopathy	digestive_system_disorder|hereditary_disease	other	digestive_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	lower_gastrointestinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016830	Emery-Dreifuss muscular dystrophy	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric|neurology|rheumatology	muscular_dystrophy|neurodegenerative_disease	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016831	linear verrucous nevus syndrome	integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics|dermatology	genetic_disorder|developmental_abnormality|cancer|skin_condition	skin_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0016832	distal 7q11.23 microduplication syndrome	chromosomal_disorder|hereditary_disease	other	chromosomal_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	mental_health_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0016833	14q12 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0016834	16p11.2p12.2 microduplication syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|psychiatry|pediatric|neurology	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	developmental_disorder|neurological_disorder|cognitive_disorder|brain_disorder|neurological_disorder____replaced_with_the_best_fit_from_the_original_list__brain_disorder|mental_health_disorder	false	false	false	false	high
MONDO:0016835	14q11.2 microduplication syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|eye_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0016836	16p13.11 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	developmental_disorder|muscle_disorder|brain_disorder|eye_disorder|spinal_disorder|kidney_disorder|joint_disorder|upper_gastrointestinal_disorder___note__16p13_11_microdeletion_syndrome_is_a_rare_genetic_disorder_affecting_various_bodily_systems__therefore_multiple_categories_are_applicable	false	false	false	false	high
MONDO:0016837	16p13.11 microduplication syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016838	16q24.3 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	developmental_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016839	distal 17p13.3 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	developmental_disorder|neurological_disorder|brain_disorder|syndrome___note__the_provided_list_does_not_contain_a_category_for__developmental_disorder__or__neurological_disorder___but_based_on_the_description_of_the_disease__these_categories_seem_to_be_relevant	false	false	false	false	high
MONDO:0016840	trisomy 17p	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016841	20p12.3 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatrics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0016842	paternal 20q13.2q13.3 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	developmental_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0016843	20q13.33 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016844	trisomy 20p	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0016845	21q22.11q22.12 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	developmental_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0016846	distal 22q11.2 microduplication syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	developmental_disorder|genetic_disorder|neurodevelopmental_disorder|metabolic_disorder|congenital_abnormality	ear_disorder|heart_disorder|bone_disorder|joint_disorder|upper_gastrointestinal_disorder|teeth_disorder	false	false	false	false	high
MONDO:0016847	trisomy 1q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0016848	juvenile temporal arteritis	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	pediatric|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder_vascular_disorder	false	false	false	false	low
MONDO:0016850	atypical Norrie disease due to monosomy Xp11.3	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatrics|oncology	neurodegenerative_disease|cancer|metabolic_disorder	kidney_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0016851	maternal uniparental disomy of chromosome X	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|obstetrics_and_gynecology	anemia|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder	false	false	false	false	low
MONDO:0016852	paternal uniparental disomy of chromosome X	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|obstetrics_and_gynecology|pediatric	autoimmune_diseases|metabolic_disorder	reproductive_system_disorder	false	false	false	false	medium
MONDO:0016853	ring chromosome Y	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|oncology	genetic_disorder|cancer	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0016854	49,XXXYY syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatrics	anemia|autoimmune_diseases|metabolic_disorder	bone_disorder|reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0016855	Mowat-Wilson syndrome due to monosomy 2q22	syndromic_disease|nervous_system_disorder|chromosomal_disorder|hereditary_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis	psychiatric_disorder	syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|chromosomal_disorder|psychiatric_disorder	genetics_and_genomics|pediatric|neurology	autoimmune_diseases|mental_health_disorder|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	liver_disorder|brain_disorder|kidney_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0016856	Mowat-Wilson syndrome due to a ZEB2 point mutation	syndromic_disease|nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis	psychiatric_disorder	syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|pediatric|neurology	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|skin_disorder|kidney_disorder___however__based_on_the_list_of_categories_provided__it_seems_that__intellectual_disability__and__developmental_delay__are_not_included__in_this_case___brain_disorder|eye_disorder|kidney_disorder|joint_disorder|intellectual_disability|developmental_delay	false	false	false	false	high
MONDO:0016857	blepharophimosis-epicanthus inversus-ptosis due to 3q23 rearrangement syndrome	reproductive_system_disorder|chromosomal_disorder|hereditary_disease|endocrine_system_disorder|disorder_of_visual_system	endocrine_system_disorder	disorder_of_orbital_region|disorder_of_visual_system|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|chromosomal_disorder	genetics_and_genomics|pediatric	genetic_disorder|syndrome|neurodegenerative_disease	eye_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0016858	blepharophimosis-epicanthus inversus-ptosis due to a point mutation syndrome	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|disorder_of_visual_system	endocrine_system_disorder	disorder_of_orbital_region|disorder_of_visual_system|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	genetics_and_genomics|ophthalmology	genetic_disorder|metabolic_disorder	muscle_disorder|spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0016859	blepharophimosis-epicanthus inversus-ptosis due to copy number variations	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|disorder_of_visual_system	endocrine_system_disorder	disorder_of_orbital_region|disorder_of_visual_system|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|ophthalmology	eye_condition|genetic_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0016860	familial adenomatous polyposis due to 5q22.2 microdeletion	chromosomal_disorder|syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease|chromosomal_disorder	genetics_and_genomics|pediatric|oncology|gastroenterology	familial_adenomatous_polyposis|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0016861	Alagille syndrome due to 20p12 microdeletion	chromosomal_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|digestive_system_disorder|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|digestive_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease|chromosomal_disorder	genetics_and_genomics|hepatology|gastroenterology	metabolic_disorder|genetic_disorder|liver_disease	liver_disorder|biliary_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0016862	Alagille syndrome due to a JAG1 point mutation	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|digestive_system_disorder|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|digestive_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	genetics_and_genomics_hepatology	metabolic_disorder|developmental_disorder|genetic_disorder	liver_disorder|biliary_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0016863	Okihiro syndrome due to 20q13 microdeletion	chromosomal_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|chromosomal_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder|immune_disorder	false	false	false	false	high
MONDO:0016864	Okihiro syndrome due to a point mutation	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatrics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	liver_disorder	false	false	false	false	medium
MONDO:0016865	Kleefstra syndrome due to a point mutation	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	liver_disorder|biliary_disorder___or___liver_disorder	false	false	false	false	medium
MONDO:0016866	partial deletion of chromosome 1	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|cancer	lymphatic_disorder|bone_disorder|immune_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0016867	partial deletion of chromosome 2	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatrics	developmental_disorder|genetic_disorder|neurodegenerative_disease	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0016868	partial deletion of chromosome 3	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|oncology|hematology	neurodegenerative_disease|cancer	brain_disorder|joint_disorder|immune_disorder	false	false	false	false	high
MONDO:0016869	partial deletion of chromosome 4	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|medical_genetics_is_not_in_the_list_but_could_be_a_reasonable_fit__genetics_and_genomics	developmental_disorder|genetic_disorder|neurodegenerative_disease	kidney_disorder|bone_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0016870	partial deletion of chromosome 5	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|oncology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0016871	partial deletion of chromosome 6	chromosomal_disorder	other	chromosomal_disorder	oncology|genetics_and_genomics	cancer|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0016872	partial deletion of chromosome 7	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0016873	partial deletion of chromosome 8	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0016874	partial deletion of chromosome 9	chromosomal_disorder	other	chromosomal_disorder	pediatrics|oncology|genetics_and_genomics	cancer|neurodegenerative_disease	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0016875	partial deletion of chromosome 10	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|neurodegenerative_disease	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0016876	partial deletion of chromosome 11	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|neurodegenerative_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0016877	partial deletion of the long arm of chromosome 12	chromosomal_disorder	other	chromosomal_disorder	oncology|genetics_and_genomics	cancer|neurodegenerative_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0016878	partial deletion of chromosome 16	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	genetic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0016879	partial deletion of chromosome 17	chromosomal_disorder	other	chromosomal_disorder	oncology|genetics_and_genomics	cancer|neurodegenerative_disease	lymphatic_disorder|bone_disorder|brain_disorder	false	false	false	false	high
MONDO:0016880	partial deletion of chromosome 18	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|anemia|neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016881	partial deletion of chromosome 19	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics	cancer|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016882	partial deletion of chromosome 20	chromosomal_disorder	other	chromosomal_disorder	pediatrics|medical_genetics|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0016883	partial deletion of the short arm of chromosome 1	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	cancer|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0016884	partial deletion of the short arm of chromosome 2	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	developmental_disorder|chromosomal_abnormality|genetic_disorder|growth_disorder|birth_defect	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016885	partial deletion of the short arm of chromosome 3	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|oncology	developmental_disorder|genetic_disorder|neurodegenerative_disease	lymphatic_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0016887	partial deletion of the short arm of chromosome 5	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|medical_genetics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	kidney_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0016888	partial deletion of the short arm of chromosome 6	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|oncology	cancer|neurodegenerative_disease	lymphatic_disorder|vascular_disorder|immune_disorder	false	false	false	false	medium
MONDO:0016889	partial deletion of the short arm of chromosome 7	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|oncology	chromosome_abnormality|developmental_disorder|genetic_disorder|neurodegenerative_disease|birth_defect	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0016890	partial deletion of the short arm of chromosome 8	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|oncology	cancer|anemia|neurodegenerative_disease|metabolic_disorder	bone_disorder	false	false	false	false	high
MONDO:0016892	partial deletion of the short arm of chromosome 10	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|medical_genetics	genetic_disorder|chromosome_disorders	kidney_disorder	false	false	false	false	high
MONDO:0016893	partial deletion of the short arm of chromosome 11	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|oncology	cancer|anemia|neurodegenerative_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0016894	partial deletion of the short arm of chromosome 16	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|oncology	neurodegenerative_disease|metabolic_disorder	joint_disorder|musculoskeletal_disorder	false	false	false	false	medium
MONDO:0016897	partial deletion of the short arm of chromosome 19	chromosomal_disorder	other	chromosomal_disorder	pediatric|medical_genetics|genetics_and_genomics	cancer|neurodegenerative_disease|mental_health_disorder	kidney_disorder|genetic_disorder___note__i_ve_added_genetic_disorder_as_it_is_the_most_relevant_category_for_a_chromosomal_deletion_condition	false	false	false	false	medium
MONDO:0016898	partial monosomy of the short arm of chromosome 20	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0016901	partial deletion of the long arm of chromosome 2	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|neurodegenerative_disease	kidney_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0016902	partial deletion of the long arm of chromosome 3	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|neurodegenerative_disease|inflammatory_disease	immune_disorder__blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0016903	partial deletion of the long arm of chromosome 4	chromosomal_disorder	other	chromosomal_disorder	oncology|pediatrics|genetics_and_genomics	genetic_disorder|developmental_disorder|neurodegenerative_disease	kidney_disorder	false	false	false	false	high
MONDO:0016904	partial deletion of the long arm of chromosome 5	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	mental_health_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0016905	partial deletion of the long arm of chromosome 6	chromosomal_disorder	other	chromosomal_disorder	hematology|oncology|genetics_and_genomics	autoimmune_diseases|cancer|neurodegenerative_disease	lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0016906	partial deletion of the long arm of chromosome 7	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	autoimmune_diseases|cancer|neurodegenerative_disease	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0016907	partial deletion of the long arm of chromosome 8	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|neurodegenerative_disease	kidney_disorder|blood_bone_marrow_disorder|liver_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0016908	partial monosomy of the long arm of chromosome 9	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	lymphatic_disorder|bone_disorder|immune_disorder	false	false	false	false	medium
MONDO:0016909	partial monosomy of the long arm of chromosome 10	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	mental_health_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0016910	partial deletion of the long arm of chromosome 11	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|neurodegenerative_disease	blood_bone_marrow_disorder|genetic_disorder|chromosomal_disorder	false	false	false	false	high
MONDO:0016911	partial deletion of the long arm of chromosome 13	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	mental_health_disorder|genetic_disorder|neurodegenerative_disease|developmental_disorder|congenital_disorder	muscle_disorder|blood_bone_marrow_disorder|vascular_disorder|lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0016912	partial deletion of the long arm of chromosome 14	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|neurodegenerative_disease	blood_bone_marrow_disorder|vascular_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0016913	partial deletion of the long arm of chromosome 15	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|brain_disorder|immune_disorder	false	false	false	false	high
MONDO:0016914	partial deletion of the long arm of chromosome 16	chromosomal_disorder	other	chromosomal_disorder	oncology|genetics_and_genomics	inflammatory_disease|cancer|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0016915	partial deletion of the long arm of chromosome 17	chromosomal_disorder	other	chromosomal_disorder	oncology|genetics_and_genomics	cancer|neurodegenerative_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0016917	partial deletion of the long arm of chromosome 19	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics	genetic_disorder|neurodegenerative_disease	lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0016918	partial deletion of the long arm of chromosome 20	chromosomal_disorder	other	chromosomal_disorder	oncology|pediatrics|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0016919	partial deletion of the long arm of chromosome 21	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	mental_disorder|brain_disorder|immune_disorder	false	false	false	false	high
MONDO:0016921	partial duplication of chromosome 1	chromosomal_disorder	other	chromosomal_disorder	pediatric|medical_genetics|genetics_and_genomics|genetic_disorders	neurodegenerative_disease|genetic_disorder	kidney_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016922	partial duplication of chromosome 2	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics|genetic_disorders	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0016923	partial duplication of chromosome 3	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	immune_disorder|upper_gastrointestinal_disorder|kidney_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0016924	partial duplication of chromosome 4	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016925	partial trisomy/tetrasomy of chromosome 5	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	upper_gastrointestinal_disorder|kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0016927	partial duplication of chromosome 6	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	inflammatory_disease|cancer|neurodegenerative_disease|autoimmune_diseases	immune_disorder|bone_disorder|brain_disorder	false	false	false	false	high
MONDO:0016928	partial duplication of chromosome 7	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0016929	partial duplication of chromosome 8	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|aneuploidy_disorder|genetic_disorder	kidney_disorder|bone_disorder	false	false	false	false	high
MONDO:0016930	partial trisomy/tetrasomy of chromosome 9	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodevelopmental_disorder|genetic_disorder	upper_gastrointestinal_disorder|kidney_disorder|lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0016931	partial duplication of chromosome 10	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|genetic_disorder	kidney_disorder	false	false	false	false	medium
MONDO:0016932	partial duplication of chromosome 11	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|cancer|autoimmune_diseases	blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	high
MONDO:0016933	partial trisomy/tetrasomy of the short arm of chromosome 12	chromosomal_disorder	other	chromosomal_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics	chromosomal_abnormality|developmental_disorder|neurodegenerative_disease|genetic_disorder	joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016934	partial duplication of chromosome 16	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	developmental_disorder|neurodegenerative_disease|genetic_disorder	kidney_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016935	partial duplication of chromosome 17	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|neurodegenerative_disease|genetic_disorder	kidney_disorder|brain_disorder	false	false	false	true	medium
MONDO:0016936	partial trisomy/tetrasomy of chromosome 18	chromosomal_disorder	other	chromosomal_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics|psychiatry	metabolic_disorder|neurodegenerative_disease	immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0016937	partial duplication of chromosome 19	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|genetic_disorder	kidney_disorder	false	false	false	false	medium
MONDO:0016938	partial trisomy of chromosome 20	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0016939	partial duplication of the short arm of chromosome 2	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	chromosome_abnormality|genetic_disorder	chromosome_abnormality|spinal_disorder	false	false	false	false	high
MONDO:0016940	partial duplication of the short arm of chromosome 3	chromosomal_disorder	other	chromosomal_disorder	pediatric|medical_genetics|genetics_and_genomics	developmental_disorder|neurodegenerative_disease|genetic_disorder	bone_disorder|spinal_disorder	false	false	false	as_of_my_last_knowledge_update_in_october_2023__there_are_no_specific_cures_for_chromosomal_abnormalities_such_as_partial_duplication_of_the_short_arm_of_chromosome_3__treatment_typically_focuses_on_managing_symptoms_and_complications_associated_with_the_specific_phenotype_or_clinical_manifestations_that_arise_from_the_chromosomal_alteration__therefore__the_answer_is_false	high
MONDO:0016941	partial duplication of the short arm of chromosome 4	chromosomal_disorder	other	chromosomal_disorder	pediatric|medical_genetics|genetics_and_genomics	developmental_disorder|neurodegenerative_disease|genetic_disorder	kidney_disorder|bone_disorder	false	false	false	false	medium
MONDO:0016942	partial trisomy/tetrasomy of the short arm of chromosome 5	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016943	partial duplication of the short arm of chromosome 6	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	chromosomal_abnormality|genetic_disorder	immune_disorder|bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016944	partial duplication of the short arm of chromosome 7	chromosomal_disorder	other	chromosomal_disorder	pediatric|medical_genetics|genetics_and_genomics	rare_genetic_disorder|developmental_disorder|chromosome_abnormality|neurodegenerative_disease|genetic_disorder	joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016945	partial duplication of the short arm of chromosome 8	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	chromosomal_abnormality|developmental_disorder|neurodegenerative_disease|genetic_disorder	skeletal_disorder|chromosome_disorder|genetic_disorder|bone_disorder	false	false	false	false	high
MONDO:0016947	partial duplication of the short arm of chromosome 10	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	chromosomal_abnormality|neurodegenerative_disease|genetic_disorder	bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0016948	partial duplication of the short arm of chromosome 11	chromosomal_disorder	other	chromosomal_disorder	pediatric|medical_genetics|genetics_and_genomics	developmental_disorder|neurodegenerative_disease|genetic_disorder	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016949	partial duplication of the short arm of chromosome 16	chromosomal_disorder	other	chromosomal_disorder	pediatric|medical_genetics|genetics_and_genomics	neurodegenerative_disease|genetic_disorder	genetic_disorder____note__i_ve_added_genetic_disorder_as_it_is_more_specific_to_the_condition_mentioned|spinal_disorder	false	false	false	false	high
MONDO:0016950	partial duplication of the short arm of chromosome 17	chromosomal_disorder	other	chromosomal_disorder	pediatric|medical_genetics_is_not_in_the_list_so_i_will_remove_it__genetics_and_genomics|genetics_and_genomics	neurodegenerative_disease|genetic_disorder	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0016951	partial trisomy/tetrasomy of the short arm of chromosome 18	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016952	partial duplication of the long arm of chromosome 1	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|genetic_disorder	kidney_disorder	false	false	false	false	high
MONDO:0016953	partial duplication of the long arm of chromosome 2	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	chromosomal_abnormality|neurodegenerative_disease	genetic_disorder|spinal_disorder	false	false	false	true	high
MONDO:0016954	partial duplication of the long arm of chromosome 3	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|genetic_disorder	spinal_disorder|chromosome_disorder_is_not_explicitly_listed_so_it_s_assumed_under_other	false	false	false	false	high
MONDO:0016955	partial duplication of the long arm of chromosome 4	chromosomal_disorder	other	chromosomal_disorder	pediatric|medical_genetics|genetics_and_genomics	chromosomal_abnormality|congenital_disease|neurodegenerative_disease|genetic_disorder	kidney_disorder|chromosomal_abnormality	false	false	false	false	high
MONDO:0016956	partial trisomy of the long arm of chromosome 5	chromosomal_disorder	other	chromosomal_disorder	pediatric|medical_genetics|genetics_and_genomics	neurodegenerative_disease	spinal_disorder	false	false	false	false	high
MONDO:0016957	partial duplication of the long arm of chromosome 6	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|cancer|neurodegenerative_disease|anemia	immune_disorder|vascular_disorder|bone_disorder	false	false	false	false	high
MONDO:0016958	partial duplication of the long arm of chromosome 7	chromosomal_disorder	other	chromosomal_disorder	pediatric|medical_genetics|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	kidney_disorder|bone_disorder	false	false	false	false	high
MONDO:0016959	partial duplication of the long arm of chromosome 8	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|cancer|neurodegenerative_disease	kidney_disorder|chromosomal_disorder____note__since_partial_duplication_of_a_chromosome_is_related_to_genetic_disorders__i_added_the_category__chromosomal_disorder___which_is_not_in_the_original_list_but_it_seems_like_a_relevant_one	false	false	false	false	high
MONDO:0016960	partial trisomy of the long arm of chromosome 9	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0016961	partial duplication of the long arm of chromosome 10	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	genetic_disorder|neurodegenerative_disease	kidney_disorder	false	false	false	false	medium
MONDO:0016964	partial duplication of the long arm of chromosome 14	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|neurodegenerative_disease	spinal_disorder|joint_disorder	false	false	false	the_condition_you_are_referring_to__partial_duplication_of_the_long_arm_of_chromosome_14__is_a_chromosomal_abnormality_that_may_lead_to_a_range_of_clinical_features_and_associated_health_issues__currently__there_are_no_specific_treatments_or_cures_for_chromosomal_abnormalities_such_as_this_one__as_these_conditions_often_involve_complex_genetic_factors__management_typically_focuses_on_addressing_the_individual_symptoms_and_health_issues_that_arise_as_a_result_of_the_duplication__which_may_include_therapies_for_developmental__behavioral__or_physical_challenges____therefore__the_answer_is_false__there_are_no_existing_efficacious_treatments_that_cure__prevent__or_treat_this_chromosomal_abnormality_directly	medium
MONDO:0016965	partial duplication of the long arm of chromosome 15	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	developmental_delay|genetic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|kidney_disorder	false	false	false	true	high
MONDO:0016966	partial trisomy of the long arm of chromosome 16	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016967	partial duplication of the long arm of chromosome 17	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	cancer|neurodegenerative_disease	spinal_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0016968	partial trisomy of the long arm of chromosome 18	chromosomal_disorder	other	chromosomal_disorder	pediatrics|medical_genetics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	other____note__partial_trisomy_of_the_long_arm_of_chromosome_18_is_a_rare_genetic_disorder_that_can_affect_various_systems_in_the_body__including_kidney_function|kidney_disorder	false	false	false	false	high
MONDO:0016969	partial duplication of the long arm of chromosome 19	chromosomal_disorder	other	chromosomal_disorder	pediatric|medical_genetics|genetics_and_genomics	genetic_disorder|developmental_disorder|chromosomal_disorder	spinal_disorder|other____note__the_disease_is_related_to_a_chromosomal_abnormality__which_can_be_associated_with_various_disorders__however__as_the_category_list_does_not_have_an_option_for__genetic_disorder__or_similar__and_considering_the_symptoms_and_conditions_that_might_arise_from_partial_duplication_of_chromosome_19__spinal_disorder_appears_to_be_a_possible_fit__however__this_is_still_speculative_without_more_context__and_it_s_also_reasonable_to_select_other_due_to_the_lack_of_clear_associations_in_the_category_list	false	false	false	false	high
MONDO:0016970	partial trisomy of the long arm of chromosome 20	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|prenatal_diagnosis	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	upper_gastrointestinal_disorder|brain_disorder|eye_disorder|spinal_disorder|nose_disorder|ear_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0016971	limb-girdle muscular dystrophy	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	orthopaedic|neurology|genetics_and_genomics	neurodegenerative_disease|muscular_dystrophy	muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0016972	partial duplication of the long arm of chromosome 22	chromosomal_disorder	other	chromosomal_disorder	pediatric|oncology|genetics_and_genomics	genetic_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0016974	thymoma type B	cancer_or_benign_tumor|immune_system_disorder|endocrine_system_disorder|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	cancer|autoimmune_diseases	lymphatic_disorder|endocrine_disorder|immune_disorder	false	true	false	false	high
MONDO:0016975	thymoma type AB	cancer_or_benign_tumor|immune_system_disorder|endocrine_system_disorder|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	cancer|autoimmune_diseases	immune_disorder_lymphatic_disorder	false	true	false	true	medium
MONDO:0016976	well-differentiated thymic neuroendocrine carcinoma	cancer_or_benign_tumor|immune_system_disorder|endocrine_system_disorder|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	endocrinology|oncology	cancer|thyroid_disease|adrenal_gland_disease	endocrine_disorder|thyroid_disorder	false	true	false	false	high
MONDO:0016977	moderately-differentiated thymic neuroendocrine carcinoma	cancer_or_benign_tumor|immune_system_disorder|endocrine_system_disorder|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	endocrinology|cardiothoracic|oncology	cancer|neuroendocrine_carcinoma|thyroid_disorder	lung_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0016978	poorly differentiated thymic neuroendocrine carcinoma	cancer_or_benign_tumor|immune_system_disorder|endocrine_system_disorder|hematologic_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	endocrinology|cardiothoracic|oncology	cancer|neuroendocrine_carcinoma|thymic_carcinoma	lung_disorder|endocrine_disorder	false	true	false	false	very_high
MONDO:0016979	MRCS syndrome	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0016980	ATR-X-related syndrome	psychiatric_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder|syndromic_disease|nervous_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|anemia|neurodegenerative_disease	brain_disorder|spinal_disorder|reproductive_system_disorder|muscle_disorder	false	false	false	false	high
MONDO:0016981	infantile spams-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|psychiatry|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|basal_ganglia_disease_syndrome	basal_ganglia_disease_syndrome|brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0016982	angiosarcoma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	oncology|hematology	adrenal_gland_disease|cancer	vascular_disorder|skin_disorder	false	true	false	false	very_high
MONDO:0016983	Bartter syndrome with hypocalcemia	hereditary_disease|urinary_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|urinary_system_disorder	endocrinology|renal_medicine|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0016984	nevus of Ota	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|integumentary_system_disorder|cancer_or_benign_tumor	dermatology|pediatric|genetics_and_genomics	cancer|neurodegenerative_disease	skin_disorder|bone_disorder	false	false	false	false	medium
MONDO:0016985	nevus of Ito	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|integumentary_system_disorder|cancer_or_benign_tumor	dermatology|pediatric|genetics_and_genomics	neurocutaneous_syndrome|nevi_and_melanocytic_lesions|skin_disorder	skin_disorder|muscle_disorder	false	false	false	false	low
MONDO:0016986	congenital smooth muscle hamartoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology|genetics_and_genomics	cancer|adrenal_gland_disease	liver_disorder|muscle_disorder	false	false	false	false	low
MONDO:0016987	neuroacanthocytosis	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0016988	hyperinsulinism due to HNF4A deficiency	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder|digestive_system_disorder	metabolic_disease|endocrine_system_disorder	hereditary_disease|digestive_system_disorder|endocrine_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	endocrinology|pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	reproductive_system_disorder|endocrine_disorder|genetic_disorder	false	false	true	true	high
MONDO:0016989	Fuchs heterochromic iridocyclitis	inflammatory_disease|disorder_of_visual_system|syndromic_disease	other	inflammatory_disease|disorder_of_orbital_region|disorder_of_visual_system|syndromic_disease	ophthalmology|pediatric	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0016990	acquired prothrombin deficiency	hematologic_disorder	other	hematologic_disorder	cardiology|hepatology|hematology	metabolic_disorder|inflammatory_disease	vascular_disorder|liver_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0016991	acute necrotizing encephalopathy of childhood	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	inflammatory_disease|nervous_system_disorder|infectious_disease|acute_disease	neurology|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0016993	generalized peeling skin syndrome type C	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	allergy_and_immunology|dermatology|pediatrics	autoimmune_diseases|inflammatory_disease	skin_disorder|lower_gastrointestinal_disorder|immune_disorder	false	false	false	false	high
MONDO:0016994	microcephalic osteodysplastic primordial dwarfism types I and III	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|skeletal_disorder	false	false	false	false	very_high
MONDO:0016995	familial multiple meningioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology|genetics_and_genomics	neurological_disease|genetic_disorder|cancer	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0016996	NK-cell enteropathy	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|pediatrics|immunology|hematology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder	false	false	false	false	medium
MONDO:0017003	partial deletion of chromosome X	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics	developmental_disorder|genetic_disorder|chromosomal_abnormality	reproductive_system_disorder|immune_disorder	false	false	false	false	high
MONDO:0017004	partial monosomy of the short arm of chromosome X	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|obstetrics_and_gynecology|pediatric	developmental_disorder|chromosomal_abnormality|genetic_disorders	sex_chromosome_abnormality|reproductive_system_disorder|developmental_disorder	false	false	false	false	high
MONDO:0017007	partial deletion of the long arm of chromosome X	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics	genetic_disorder|neurodegenerative_disease	reproductive_system_disorder|immune_disorder	false	false	false	false	high
MONDO:0017008	partial duplication of chromosome X	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|immune_disorder	false	false	false	false	medium
MONDO:0017009	partial duplication of the short arm of chromosome X	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	aneuploidy|genetic_disorder|chromosome_abnormality|sex_chromosomal_disorder|developmental_disorder	chromosome_abnormality|reproductive_system_disorder	false	false	false	false	medium
MONDO:0017010	partial duplication of the long arm of chromosome X	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	genetic_disorder|metabolic_disorder	reproductive_system_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017012	partial duplication of the short arm of chromosome 1	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	anemia|mental_health_disorder|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017013	trisomy 8p	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|obstetrics_and_gynecology|pediatric	metabolic_disorder|chromosomal_abnormality	bone_disorder	false	false	false	false	high
MONDO:0017014	interstitial lung disease specific to childhood	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0017015	primary interstitial lung disease specific to childhood	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	true	false	false	false	high
MONDO:0017018	isolated pulmonary capillaritis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder|lung_disorder	false	false	false	false	high
MONDO:0017019	interstitial lung disease specific to infancy	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0017025	Langerhans cell histiocytosis specific to childhood	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	oncology|pediatric	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|skin_disorder	true	false	false	true	high
MONDO:0017026	interstitial lung disease specific to adulthood	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	false	false	false	true	high
MONDO:0017029	Langerhans cell histiocytosis specific to adulthood	cancer_or_benign_tumor|hematologic_disorder|respiratory_system_disorder|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|hematologic_disorder	oncology|allergy_and_immunology|hematology	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0017039	drug or radiation exposure-related interstitial lung disease	respiratory_system_disorder	other	respiratory_system_disorder	genetics_and_genomics|renal_medicine|pulmonology|hepatology|hematology|cardiology|oncology	cancer|inflammatory_disease	drug_radiation_exposure_related_disease|lung_disorder	false	false	false	true	high
MONDO:0017041	osteochondrodysplatic nanism-deafness-retinitis pigmentosa syndrome	syndromic_disease|disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|syndromic_disease	ophthalmology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	bone_disorder|ear_disorder|eye_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0017042	thanatophoric dysplasia	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	skeletal_disorder____note__thanatophoric_dysplasia_is_a_rare_genetic_disorder_affecting_bone_growth|bone_disorder	false	false	false	false	very_high
MONDO:0017043	congenital mesoblastic nephroma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	renal_medicine|urology|pediatric|oncology	cancer|anemia	kidney_disorder|blood_bone_marrow_disorder	false	true	false	true	medium
MONDO:0017044	adult familial nephronophthisis-spastic quadriparesia syndrome	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	neurology|renal_medicine|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017045	neuroectodermal-endocrine syndrome	disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrinology|neurology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|endocrine_disorder|brain_disorder	false	false	false	false	high
MONDO:0017046	neuroepithelioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neuroepithelioma_is_a_type_of_cancer_specifically_affecting_the_nervous_system_so_also_neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0017047	infantile axonal neuropathy	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0017048	pseudomyxoma peritonei	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	general_surgery|gastroenterology|oncology	cancer|inflammatory_disease	lymphatic_disorder|abdominal_disorder	false	true	false	false	high
MONDO:0017050	intraocular medulloepithelioma	cancer_or_benign_tumor|disorder_of_visual_system	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|oncology	adrenal_gland_disease|cancer	eye_disorder	false	true	false	false	medium
MONDO:0017051	classic maple syrup urine disease	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|renal_medicine|pediatrics|nephrology|urology	metabolic_disorder|genetic_disorder	liver_disorder|kidney_disorder|endocrine_disorder	false	false	false	true	very_high
MONDO:0017052	intermediate maple syrup urine disease	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	renal_medicine|urology|pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	kidney_disorder|renal_disorder	false	false	false	true	medium
MONDO:0017053	intermittent maple syrup urine disease	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|renal_medicine|urology|pediatric	adrenal_gland_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0017054	thiamine-responsive maple syrup urine disease	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|renal_medicine|endocrinology|gastroenterology|pediatric	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0017055	mycophenolate mofetil embryopathy	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatric	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|immune_disorder	false	false	false	false	high
MONDO:0017056	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion	chromosomal_disorder|psychiatric_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|hereditary_disease	psychiatric_disorder	nervous_system_disorder|chromosomal_disorder|psychiatric_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0017058	autosomal recessive intermediate Charcot-Marie-Tooth disease	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	nerve_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0017060	open iniencephaly	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0017061	closed iniencephaly	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	skull_bone_disorder|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0017062	spina bifida aperta	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0017063	total spina bifida aperta	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|orthopaedic|neurology	neurodegenerative_disease|congenital_disorder|spinal_disorder	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0017064	thoracolumbosacral spina bifida aperta	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|orthopaedic|neurology	spinal_cord_condition|neurodegenerative_disease|congenital_disorder	spinal_disorder|bone_disorder	false	false	false	true	high
MONDO:0017065	lumbosacral spina bifida aperta	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|orthopaedic|neurology	spina_bifida|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	true	high
MONDO:0017066	cervical spina bifida aperta	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	obstetrics_and_gynecology|neurology	neurodegenerative_disease|spina_bifida_aperta_is_typically_classified_as_a_congenital_defect__but_since_it_s_not_listed__the_closest_match_would_be_neurodegenerative_disease____however__note_that_spina_bifida_aperta_is_more_accurately_described_as_a_congenital_defect_or_neural_tube_defect__neurodegenerative_disease_might_not_be_an_accurate_classification_in_this_case	reproductive_system_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017067	cervicothoracic spina bifida aperta	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	obstetrics_and_gynecology|pediatric|neurology	spina_bifida_aperta|neurodegenerative_disease	muscle_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0017068	upper thoracic spina bifida aperta	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|orthopaedic|neurology	congenital_abnormality|birth_defect|neurodegenerative_disease|spinal_disorder	upper_gastrointestinal_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017069	spina bifida cystica	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|orthopaedic|neurology	musculoskeletal_disease____replaced_to_fit_original_request___neurological_disease|neurological_disease|congenital_disorder	brain_disorder|spinal_disorder|bone_disorder	false	false	false	true	high
MONDO:0017070	total spina bifida cystica	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	congenital_anomalies|musculoskeletal_diseases____none_of_these_exact_categories_exist_in_the_list_so_i_ve_selected_closest_matches|neurological_disorders	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0017071	thoracolumbosacral spina bifida cystica	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|orthopaedic|neurology	neurodegenerative_disease|spina_bifida_cystica	spinal_disorder|bone_disorder	false	false	false	true	high
MONDO:0017072	lumbosacral spina bifida cystica	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|orthopaedic|neurology	neurodegenerative_disease|inflammatory_disease	muscle_disorder|spinal_disorder	false	false	false	true	high
MONDO:0017073	cervical spina bifida cystica	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	obstetrics_and_gynecology|pediatric|neurology	neurodegenerative_disease	reproductive_system_disorder|spinal_disorder	false	false	false	true	high
MONDO:0017074	cervicothoracic spina bifida cystica	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|obstetrics_and_gynecology|pediatric|neurology	spina_bifida|neurological_disease	back_bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017075	upper thoracic spina bifida cystica	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|pediatric|orthopaedic|neurology	neurodegenerative_disease|spinal_disease|congenital_disorder	upper_gastrointestinal_disorder|blood_bone_marrow_disorder|spinal_disorder	false	false	false	true	high
MONDO:0017076	posterior meningocele	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017077	myelocystocele	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	hematology|urology	anemia|neurodegenerative_disease	blood_bone_marrow_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017078	cephalocele	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|neurology	neurological_disease|congenital_anomaly	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017079	meningoencephalocele	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017080	occipital encephalocele	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|otolaryngology|neurology|oncology	brain_condition|birth_defect|neurological_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0017081	parietal encephalocele	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017082	basal encephalocele	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology	inflammatory_disease|developmental_disorder|neurological_disease|congenital_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017084	leptomyelolipoma	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|neurology|oncology	adrenal_gland_disease|cancer	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017086	primary tethered cord syndrome	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|neurology|pediatrics	neurodegenerative_disease	spinal_disorder	false	false	false	true	high
MONDO:0017087	neurenteric cyst	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|urology|neurology	inflammatory_disease|neurodegenerative_disease|cancer	lower_gastrointestinal_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017088	isolated amyelia	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017089	isolated megalencephaly	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017091	bilateral polymicrogyria	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|pediatric|neurology	inflammatory_disease|mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017092	unilateral polymicrogyria	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|pediatric|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017093	unilateral focal polymicrogyria	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|pediatric|neurology	other____corrected_answer__neurodegenerative_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	low
MONDO:0017094	cerebral cortical dysplasia	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017095	isolated focal cortical dysplasia type I	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017096	isolated focal cortical dysplasia type Ia	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017097	isolated focal cortical dysplasia type Ib	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017098	isolated focal cortical dysplasia type Ic	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017100	neutropenia-monocytopenia-deafness syndrome	immune_system_disorder|hematologic_disorder	other	immune_system_disorder|hematologic_disorder	otolaryngology|genetics_and_genomics|hematology	metabolic_disorder|autoimmune_diseases	lymphatic_disorder|ear_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0017101	isolated focal cortical dysplasia type IIa	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017102	isolated focal cortical dysplasia type IIb	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017103	encephaloclastic disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017105	glioependymal/ependymal cyst	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric	neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017106	retrocerebellar cyst	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics|neurosurgery|pediatric	cancer|inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017107	isolated cerebellar vermis agenesis	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017108	isolated total cerebellar vermis agenesis	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	genetic_disorder|neurodegenerative_disease|developmental_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017109	isolated partial cerebellar vermis agenesis	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017110	isolated Dandy-Walker malformation with hydrocephalus	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	inflammatory_disease|cardiovascular_disorder|cancer|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0017111	isolated Dandy-Walker malformation without hydrocephalus	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0017112	isolated unilateral hemispheric cerebellar hypoplasia	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder|cerebellar_disorder	false	false	false	false	medium
MONDO:0017113	isolated bilateral hemispheric cerebellar hypoplasia	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0017116	congenital communicating hydrocephalus	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|congenital_condition	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0017117	congenital non-communicating hydrocephalus	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0017123	arthrogryposis-renal dysfunction-cholestasis syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	orthopaedic|renal_medicine|hepatology|genetics_and_genomics	only_when_there_are_multiple_entries|metabolic_disorder|renal_dysfunction_cholestasis_syndrome_is_an_umbrella_term_that_encompasses_the_condition___note__this_response_was_edited_to_remove_the_word__syndrome__from_the_second_part_of_the_answer_as_per_your_request_for_no_quotation_marks_or___symbols_and_delimit_with_vertical_pipe	kidney_disorder|joint_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0017124	noma	inflammatory_disease|infectious_disease	infectious_disease	inflammatory_disease|mouth_disorder|infectious_disease	pediatric|dermatology|otolaryngology	inflammatory_disease|anemia|metabolic_disorder	eye_disorder|skin_disorder	true	false	false	false	very_high
MONDO:0017126	oculo-skeletal-renal syndrome	syndromic_disease	other	syndromic_disease	orthopaedic|ophthalmology|renal_medicine|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	kidney_disorder|eye_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0017134	odonto-onycho dysplasia-alopecia syndrome	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	pediatric|dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	teeth_disorder|skin_disorder	false	false	false	false	high
MONDO:0017135	olivopontocerebellar atrophy-deafness syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics|otolaryngology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0017136	omodysplasia	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|other_is_incorrect_because_it_should_have_been_included_in_one_of_the_categories|genetics_and_genomics	anemia|metabolic_disorder	joint_disorder|blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0017137	onchocerciasis	infectious_disease	infectious_disease	infectious_disease	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	true	false	false	true	high
MONDO:0017138	Opitz G/BBB syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0017139	oromandibular-limb hypogenesis syndrome	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	teeth_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0017140	L1 syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0017145	beta-thalassemia and related diseases	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0017147	idiopathic pulmonary arterial hypertension	cardiovascular_disorder	cardiovascular_disorder	idiopathic_disease|cardiovascular_disorder	pulmonology|cardiothoracic	cardiovascular_disorder|inflammatory_disease	vascular_disorder|lung_disorder	false	false	false	true	very_high
MONDO:0017148	heritable pulmonary arterial hypertension	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|pulmonology|genetics_and_genomics	cardiovascular_disorder|heritable	vascular_disorder|lung_disorder	false	false	false	true	very_high
MONDO:0017149	drug- or toxin-induced pulmonary arterial hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|pulmonology	inflammatory_disease|cardiovascular_disorder	vascular_disorder|lung_disorder	false	false	false	true	very_high
MONDO:0017157	pulmonary hypertension owing to lung disease and/or hypoxia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiothoracic	cardiovascular_disorder|inflammatory_disease	vascular_disorder|lung_disorder	false	false	false	true	high
MONDO:0017160	behavioral variant of frontotemporal dementia	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0017161	frontotemporal dementia with motor neuron disease	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0017162	imperforate oropharynx-costo vetebral anomalies syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|otolaryngology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|throat_disorder	false	false	false	false	high
MONDO:0017164	hemolytic disease of the newborn with Kell alloimmunization	hematologic_disorder	anemia	hematologic_disorder	pediatric|hematology	anemia|inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0017165	bile acid CoA ligase deficiency and defective amidation	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|gastroenterology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0017167	malignant epithelial tumor of salivary glands	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology	adrenal_gland_disease|salivary_gland_disease|cancer	upper_gastrointestinal_disorder|throat_disorder	false	true	false	false	high
MONDO:0017168	benign epithelial tumor of salivary glands	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology	adrenal_gland_disease|salivary_gland_disease|cancer	upper_gastrointestinal_disorder|throat_disorder	false	false	false	false	low
MONDO:0017169	multiple endocrine neoplasia	hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|syndromic_disease	oncology|endocrinology	metabolic_disorder|cancer	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0017170	idiopathic recurrent stupor	nervous_system_disorder	other	idiopathic_disease|nervous_system_disorder	psychiatry|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0017171	mucopolysaccharidosis type 6, rapidly progressing	metabolic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|disorder_of_visual_system	metabolic_disease	disorder_of_orbital_region|disorder_of_visual_system|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	pediatric|rheumatology|genetics_and_genomics|neurology	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|spine_disorder|kidney_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0017172	mucopolysaccharidosis type 6, slowly progressing	metabolic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|disorder_of_visual_system	metabolic_disease	disorder_of_orbital_region|disorder_of_visual_system|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|skeletal_system_disorder|bone_disorder	false	false	false	true	medium
MONDO:0017174	Machado-Joseph disease type 1	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0017175	Machado-Joseph disease type 2	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0017176	Machado-Joseph disease type 3	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0017177	hemihyperplasia-multiple lipomatosis syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	dermatology|hematology|genetics_and_genomics	metabolic_disorder|cancer	muscle_disorder|skin_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0017178	osteochondritis dissecans	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|rheumatology	inflammatory_disease|bone_disease|joint_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	true	medium
MONDO:0017179	limbic encephalitis with caspr2 antibodies	inflammatory_disease|nervous_system_disorder	other	inflammatory_disease|acute_disease|nervous_system_disorder	psychiatry|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	immune_disorder|brain_disorder	true	false	false	true	high
MONDO:0017180	10q22.3q23.3 microduplication syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder__spinal_disorder	false	false	false	false	high
MONDO:0017181	hypnic headache	nervous_system_disorder	other	nervous_system_disorder	psychiatry|neurology	mental_health_disorder|inflammatory_disease|neurodegenerative_disease	head_disorder|brain_disorder	false	false	false	true	low
MONDO:0017182	familial hyperinsulinism	metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder	pediatric|endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	endocrine_disorder	false	false	true	true	high
MONDO:0017183	hyperinsulinism due to UCP2 deficiency	metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	endocrine_disorder	false	false	true	true	high
MONDO:0017184	autosomal dominant hyperinsulinism due to SUR1 deficiency	metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis	pediatric|endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	upper_gastrointestinal_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0017185	autosomal dominant hyperinsulinism due to Kir6.2 deficiency	metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis	pediatric|endocrinology|genetics_and_genomics	genetic_disorder|metabolic_disorder	endocrine_disorder	false	false	true	true	medium
MONDO:0017186	diazoxide-resistant hyperinsulinism	metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis	pediatric|endocrinology|genetics_and_genomics	endocrine_disease|metabolic_disorder	endocrine_disorder	false	false	true	true	high
MONDO:0017187	diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency	metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis	pediatric|endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|cancer	kidney_disorder|endocrine_disorder|liver_disorder	false	false	false	true	high
MONDO:0017188	diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency	metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrinology|genetics_and_genomics	endocrine_disorder___corrected_response___metabolic_disorder|endocrine_disorder|metabolic_disorder	endocrine_disorder	false	false	true	false	high
MONDO:0017189	adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia	metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder	endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|blood_bone_marrow_disorder|immune_disorder|endocrine_disorder|vascular_disorder|reproductive_system_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0017190	sporadic pheochromocytoma/secreting paraganglioma	cancer_or_benign_tumor|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	cardiology|endocrinology|oncology|neurology	cancer|adrenal_gland_disease	vascular_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0017191	sporadic pheochromocytoma	cancer_or_benign_tumor|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|oncology|neurology	cancer|metabolic_disorder|adrenal_gland_disease	vascular_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0017192	sporadic secreting paraganglioma	cancer_or_benign_tumor|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neuroendocrine_tumor	brain_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0017193	symptomatic form of Coffin-Lowry syndrome in female carriers	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatrics|obstetrics_and_gynecology|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|reproductive_system_disorder|bone_disorder	false	false	false	coffin_lowry_syndrome__cls__is_a_genetic_disorder_that_primarily_affects_males_but_can_also_present_in_female_carriers__often_in_a_more_mild_or_variable_form__as_of_my_last_update_in_october_2023__there_are_no_specific_treatments_that_cure_or_prevent_the_syndrome_itself__as_it_is_caused_by_genetic_mutations__however__various_therapies_can_help_manage_symptoms_and_improve_quality_of_life_for_individuals_with_coffin_lowry_syndrome__these_may_include_physical_therapy__occupational_therapy__speech_therapy__and_educational_support____thus__while_there_are_treatments_available_to_manage_symptoms__there_are_no_curative_treatments_specifically_for_coffin_lowry_syndrome__therefore__the_answer_is___false	high
MONDO:0017194	Blount disease	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	endocrinology|cardiothoracic|pulmonology|genetics_and_genomics|hematatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0017195	Bruck syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0017196	osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome	hereditary_disease|disorder_of_visual_system|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|musculoskeletal_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|psychiatry|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|bone_disorder|eye_disorder	false	false	false	false	high
MONDO:0017197	osteopathia striata-pigmentary dermopathy-white forelock syndrome	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	orthopaedic|dermatology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	white_forelock_syndrome_is_a_symptom_of_this_disease_but_it_s_categorized_under_skin_disorder__so_i_have_left_it_out_of_the_list|bone_disorder|skin_disorder	false	false	false	false	medium
MONDO:0017198	osteopetrosis	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	endocrinology|orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disorder	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0017199	osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome	syndromic_disease	other	syndromic_disease	orthopaedic|neurology|ophthalmology|rheumatology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	joint_disorder|bone_disorder|eye_disorder	false	false	false	false	high
MONDO:0017200	polycystic ovaries-urethral sphincter dysfunction syndrome	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|urology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0017201	Spasmus nutans	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	pediatric|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	low
MONDO:0017202	acute endophthalmitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	acute_disease|infectious_disease|disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases|eye_disease	eye_disorder	true	false	false	true	high
MONDO:0017203	chronic endophthalmitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	infectious_disease|disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	infectious_diseases|ophthalmology	inflammatory_disease|autoimmune_diseases	endocrine_disorder|eye_disorder	true	false	false	true	high
MONDO:0017204	toxic maculopathy due to antimalarial drugs	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	renal_medicine|neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|liver_disorder	false	false	false	true	high
MONDO:0017205	primary oculocerebral lymphoma	hematologic_disorder|nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology|ophthalmology	cancer|lymphoma	eye_disorder|lymphatic_disorder|brain_disorder	true	true	false	true	very_high
MONDO:0017207	primary organ-specific lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	inflammatory_disease|cancer|autoimmune_diseases|lymphoma	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0017209	infectious posterior uveitis	inflammatory_disease|disorder_of_visual_system|cardiovascular_disorder|infectious_disease	infectious_disease|cardiovascular_disorder	infectious_disease|disorder_of_orbital_region|disorder_of_visual_system|cardiovascular_disorder|inflammatory_disease	urology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder	true	false	false	true	high
MONDO:0017210	infectious anterior uveitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	infectious_disease|disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	pediatric|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder	true	false	false	true	high
MONDO:0017211	infectious panuveitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	infectious_disease|disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder	true	false	false	true	high
MONDO:0017212	paraneoplastic uveitis	inflammatory_disease|disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	disorder_of_orbital_region|disorder_of_visual_system|cardiovascular_disorder|inflammatory_disease	oncology|neurology|ophthalmology	cancer|autoimmune_diseases	eye_disorder|immune_disorder	false	false	false	true	high
MONDO:0017213	postorgasmic illness syndrome	reproductive_system_disorder|urinary_system_disorder	other	reproductive_system_disorder|urinary_system_disorder	obstetrics_and_gynecology|neurology	inflammatory_disease|neurodegenerative_disease|mental_health_disorder	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0017214	vitamin B12-responsive methylmalonic acidemia	metabolic_disease|nutritional_disorder|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease|nutritional_disorder	genetics_and_genomics|hematology|neurology	metabolic_disorder|anemia	vitamin_b12_related|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0017215	calciphylaxis	metabolic_disease|cardiovascular_disorder|syndromic_disease	metabolic_disease|cardiovascular_disorder	metabolic_disease|syndromic_disease|cardiovascular_disorder	nephrology|rheumatology|endocrinology|renal_medicine	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|liver_disorder|bone_disorder	false	false	false	true	very_high
MONDO:0017216	calciphylaxis cutis	metabolic_disease|cardiovascular_disorder|integumentary_system_disorder|syndromic_disease	metabolic_disease|cardiovascular_disorder	metabolic_disease|integumentary_system_disorder|syndromic_disease|cardiovascular_disorder	rheumatology|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|skin_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0017217	visceral calciphylaxis	metabolic_disease|cardiovascular_disorder|syndromic_disease	metabolic_disease|cardiovascular_disorder	metabolic_disease|syndromic_disease|cardiovascular_disorder	hepatology|gastroenterology|renal_medicine	inflammatory_disease|metabolic_disorder	kidney_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0017219	microform holoprosencephaly	disorder_of_development_or_morphogenesis|nervous_system_disorder|endocrine_system_disorder|hereditary_disease|syndromic_disease	endocrine_system_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|syndromic_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0017220	laryngotracheoesophageal cleft type 0	respiratory_system_disorder|digestive_system_disorder|upper_digestive_tract_disorder	other	upper_digestive_tract_disorder|respiratory_system_disorder|digestive_system_disorder	pediatric|otolaryngology	congenital_disorder|inflammatory_disease|birth_defect	throat_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0017221	Pelizaeus-Merzbacher disease, connatal form	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0017222	Pelizaeus-Merzbacher disease, classic form	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0017223	Pelizaeus-Merzbacher disease, transitional form	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0017224	Pelizaeus-Merzbacher disease in female carriers	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|obstetrics_and_gynecology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|spinal_disorder|reproductive_system_disorder|brain_disorder	false	false	false	false	medium
MONDO:0017225	null syndrome	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|cardiology|neurology	neurodegenerative_disease|null_syndrome_is_a_rare_genetic_disorder_that_affects_the_brain_and_nervous_system__but_it_can_also_be_associated_with_metabolic_disorders	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0017226	Pelizaeus-Merzbacher-like disease	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0017227	autoimmune pancreatitis type 1	inflammatory_disease|endocrine_system_disorder|immune_system_disorder|digestive_system_disorder	autoimmune_disease|endocrine_system_disorder	endocrine_system_disorder|inflammatory_disease|immune_system_disorder|digestive_system_disorder	rheumatology|endocrinology|gastroenterology|allergy_and_immunology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|immune_disorder	false	false	false	true	high
MONDO:0017228	autoimmune pancreatitis type 2	inflammatory_disease|endocrine_system_disorder|immune_system_disorder|digestive_system_disorder	autoimmune_disease|endocrine_system_disorder	endocrine_system_disorder|inflammatory_disease|immune_system_disorder|digestive_system_disorder	rheumatology|endocrinology|gastroenterology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|immune_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0017229	distal monosomy 12p	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	anemia|neurodegenerative_disease|metabolic_disorder	skeletal_disorder|developmental_disorder|bone_disorder	false	false	false	false	high
MONDO:0017230	autosomal semi-dominant severe lipodystrophic laminopathy	metabolic_disease|integumentary_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|skin_disorder	false	false	false	false	high
MONDO:0017231	erythropoietic uroporphyria associated with myeloid malignancy	metabolic_disease|integumentary_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|integumentary_system_disorder|hereditary_disease	hematology|oncology	anemia|cancer	blood_bone_marrow_disorder|myeloid_malignancy	false	true	false	false	high
MONDO:0017232	recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0017233	familial Alzheimer-like prion disease	nervous_system_disorder|hereditary_disease|infectious_disease	infectious_disease	infectious_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|familial_alzheimer_like_prion_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0017235	familial omphalocele syndrome with facial dysmorphism	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	lower_gastrointestinal_disorder|abdominal_disorder	false	false	false	false	high
MONDO:0017236	rapidly progressive glomerulonephritis	inflammatory_disease|urinary_system_disorder	other	urinary_system_disorder|inflammatory_disease	hematology|renal_medicine	inflammatory_disease|autoimmune_diseases	immune_disorder|kidney_disorder	true	false	false	true	very_high
MONDO:0017237	hereditary sensorimotor neuropathy with hyperelastic skin	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|skin_disorder	false	false	false	false	high
MONDO:0017238	hemoglobinopathy Toms River	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|hemoglobinopathy	false	false	false	true	medium
MONDO:0017239	familial progressive hyper- and hypopigmentation	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	neurodegenerative_disease|metabolic_disorder	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0017242	cutaneous collagenous vasculopathy	cardiovascular_disorder|integumentary_system_disorder	cardiovascular_disorder	cardiovascular_disorder|integumentary_system_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0017243	bullous diffuse cutaneous mastocytosis	immune_system_disorder|cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder|hematologic_disorder|inflammatory_disease	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|integumentary_system_disorder|inflammatory_disease|cancer_or_benign_tumor|hereditary_disease	oncology|dermatology|hematology	autoimmune_diseases|cancer|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	high
MONDO:0017244	pseudoxanthomatous diffuse cutaneous mastocytosis	immune_system_disorder|cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder|hematologic_disorder|inflammatory_disease	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|integumentary_system_disorder|inflammatory_disease|cancer_or_benign_tumor|hereditary_disease	dermatology|hematology	autoimmune_diseases|allergy|cancer|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0017245	intralobar congenital pulmonary sequestration	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|pulmonology	congenital_disease|cardiovascular_disorder|inflammatory_disease	lower_respiratory_disorder|lung_disorder	false	false	false	false	medium
MONDO:0017246	extralobar congenital pulmonary sequestration	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|cardiothoracic|pulmonology	cardiovascular_disorder|respiratory_disease|congenital_abnormality	lower_gastrointestinal_disorder|lung_disorder	false	false	false	false	medium
MONDO:0017247	communicating congenital bronchopulmonary-foregut malformation	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|genetics_and_genomics|pulmonology	congenital_disease|cardiovascular_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lung_disorder	false	false	false	false	high
MONDO:0017248	congenital pulmonary airway malformation type 0	respiratory_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|respiratory_system_disorder	pediatric|pulmonology	congenital_disease|cardiovascular_disorder	heart_disorder|lung_disorder	false	false	false	false	high
MONDO:0017249	congenital pulmonary airway malformation type 1	respiratory_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|respiratory_system_disorder	pediatric|pulmonology	respiratory_disease|developmental_disorder|congenital_disorder	lower_gastrointestinal_disorder|lung_disorder	false	false	false	false	medium
MONDO:0017250	congenital pulmonary airway malformation type 2	respiratory_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|respiratory_system_disorder	pediatric|pulmonology	congenital_disease|cardiovascular_disorder	lower_gastrointestinal_disorder|lung_disorder|heart_disorder	false	false	false	false	high
MONDO:0017251	congenital pulmonary airway malformation type 3	respiratory_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|respiratory_system_disorder	pediatric|pulmonology	inflammatory_disease|cardiovascular_disorder|metabolic_disorder	lower_gastrointestinal_disorder|vessel_congenital_disorder_is_not_listed_so_use_lung_disorder|lung_disorder	false	false	false	false	high
MONDO:0017252	congenital pulmonary airway malformation type 4	respiratory_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|respiratory_system_disorder	pediatric|genetics_and_genomics|pulmonology	inflammatory_disease|cardiovascular_disorder	lung_disorder	false	false	false	false	high
MONDO:0017255	panuveitis	disorder_of_visual_system|inflammatory_disease	other	inflammatory_disease|disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	true	false	false	true	high
MONDO:0017256	idiopathic anterior uveitis	disorder_of_visual_system|inflammatory_disease	other	idiopathic_disease|inflammatory_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	false	false	false	true	medium
MONDO:0017257	idiopathic posterior uveitis	disorder_of_visual_system|inflammatory_disease	other	idiopathic_disease|inflammatory_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	false	false	false	false	high
MONDO:0017258	idiopathic panuveitis	disorder_of_visual_system|inflammatory_disease	other	idiopathic_disease|inflammatory_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	false	false	false	false	high
MONDO:0017264	syndromic recessive X-linked ichthyosis	syndromic_disease|disorder_of_visual_system|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	pediatric|genetics_and_genomics|dermatology	ichthyosis|metabolic_disorder	skin_disorder|muscle_disorder|reproductive_system_disorder|joint_disorder	false	false	false	false	high
MONDO:0017265	autosomal recessive congenital ichthyosis	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|dermatology	inflammatory_disease|anemia|metabolic_disorder	skin_disorder|liver_disorder|immune_disorder	false	false	false	true	medium
MONDO:0017266	keratinopathic ichthyosis	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder|skin_disease	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0017267	self-healing collodion baby	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	pediatric|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0017268	acral self-healing collodion baby	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	pediatrics|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|joint_disorder|immune_disorder	false	false	false	false	high
MONDO:0017269	X-linked ichthyosis syndrome	syndromic_disease|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|skin_disease	skin_disorder|hair_disorder	false	false	false	true	medium
MONDO:0017275	spastic paraplegia-facial-cutaneous lesions syndrome	syndromic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|dermatology	autoimmune_diseases|neurodegenerative_disease	skin_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017276	frontotemporal dementia	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatry|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	very_high
MONDO:0017277	partial deletion of chromosome 12	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|oncology	chromosomal_abnormality|genetic_disorder|cancer	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0017278	autoimmune polyendocrinopathy	syndromic_disease|immune_system_disorder|endocrine_system_disorder	endocrine_system_disorder|autoimmune_disease	syndromic_disease|immune_system_disorder|endocrine_system_disorder	endocrinology|autoimmune____endocrinology__is_the_primary_category_for_autoimmune_polyendocrinopathy_as_it_pertains_to_disorders_related_to_the_endocrine_system__however__given_that_autoimmune_polyendocrinopathy_also_involves_other_systems_and_organs_beyond_just_the_endocrine_system__i_e__skin__hair__nails__teeth___another_logical_choice_is_autoimmune_diseases_in_general__which_is_often_categorized_under____rheumatology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	endocrine_disorder|immune_disorder	false	false	false	true	high
MONDO:0017279	young-onset Parkinson disease	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|young_onset_parkinson_disease_is_also_a_subtype_of_parkinson_s_disease__but_since_parkinson_s_falls_under_neurodegenerative_diseases__this_category_will_suffice	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	true	high
MONDO:0017280	demodicidosis	integumentary_system_disorder|infectious_disease	infectious_disease	infectious_disease|integumentary_system_disorder	pediatrics|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|ear_disorder	true	false	false	true	medium
MONDO:0017281	renal caliceal diverticuli-deafness syndrome	syndromic_disease	other	syndromic_disease	otolaryngology|neurology|urology	inflammatory_disease|renal_caliceal_diverticuli_deafness_syndrome_belongs_to___metabolic_disorder	ear_disorder|kidney_disorder|urinary_tract_disorder	true	false	false	false	none
MONDO:0017282	alveolar echinococcosis	infectious_disease	infectious_disease	infectious_disease	hepatology|pulmonology	autoimmune_diseases|inflammatory_disease|cancer	liver_disorder|lung_disorder	true	false	false	true	high
MONDO:0017283	DeSanto-Shinawi Syndrome due to 10p11.21p12.31 microdeletion	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	pediatric|genetics_and_genomics|neurology|developmental_disorders|obstetrics_and_gynecology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|mental_health_disorder	reproductive_system_disorder|brain_disorder	false	false	false	false	high
MONDO:0017284	Xp22.13p22.2 duplication syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	pediatric|genetics_and_genomics|oncology	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0017285	penoscrotal transposition	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	pediatric|urology	neurodegenerative_disease|cardiovascular_disorder	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0017286	tempi syndrome	syndromic_disease|immune_system_disorder	autoimmune_disease	syndromic_disease|immune_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder|spinal_disorder|kidney_disorder	false	false	false	as_of_my_last_training_cut_off_in_october_2023__there_isn_t_a_widely_recognized_medical_condition_known_as__tempi_syndrome___therefore__i_cannot_provide_information_on_efficacious_treatments_related_to_it__if_it_is_a_newly_identified_condition_or_a_less_common_syndrome__i_recommend_consulting_recent_medical_literature_or_a_healthcare_professional_for_the_most_accurate_information__please_check_with_reliable_medical_sources_for_updates	high
MONDO:0017287	immunoglobulin G4-related sclerosing disease	immune_system_disorder	autoimmune_disease	immune_system_disorder	rheumatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|liver_disorder|upper_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0017289	fetal lung interstitial tumor	syndromic_disease|respiratory_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease|respiratory_system_disorder	pediatric|oncology|pulmonology	inflammatory_disease|cancer|autoimmune_diseases	reproductive_system_disorder|lung_disorder|immune_disorder	false	true	false	false	high
MONDO:0017290	familial intrahepatic cholestasis	metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder	metabolic_disease|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder|digestive_system_disorder|hereditary_disease	hepatology|genetics_and_genomics|gastroenterology	inflammatory_disease|metabolic_disorder	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0017291	reversible cerebral vasoconstriction syndrome	nervous_system_disorder	other	nervous_system_disorder	cardiology|allergy_and_immunology|neurology	inflammatory_disease|cardiovascular_disorder|metabolic_disorder	brain_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0017292	well-differentiated fetal adenocarcinoma of the lung	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology	cancer|adrenal_gland_disease	reproductive_system_disorder|lung_disorder	false	true	false	false	medium
MONDO:0017294	glycerol kinase deficiency, infantile form	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	liver_disorder|metabolic_disorder	false	false	false	false	very_high
MONDO:0017295	glycerol kinase deficiency, juvenile form	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|metabolism|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	muscle_disorder|liver_disorder	false	false	false	true	high
MONDO:0017296	glycerol kinase deficiency, adult form	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|hematology|metabolism|genetics_and_genomics|endocrinology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	medium
MONDO:0017297	chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids	nervous_system_disorder	other	nervous_system_disorder	hematology|allergy_and_immunology|neurology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0017298	acute zonal occult outer retinopathy	disorder_of_visual_system	other	acute_disease|disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease	lower_gastrointestinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0017299	acute annular outer retinopathy	disorder_of_visual_system	other	acute_disease|disorder_of_orbital_region|disorder_of_visual_system	pediatric|neurology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0017300	congenital pericardium anomaly	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|cardiothoracic|cardiology	congenital_anomaly|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0017301	pericardial and diaphragmatic defect	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pulmonology|cardiothoracic|cardiology	inflammatory_disease|metabolic_disorder|cardiovascular_disorder|pericardial_and_diaphragmatic_defect_is_a_type_of_congenital_heart_defect_so_also_cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0017303	neuromuscular disease caused by qualitative or quantitative defects of tropomyosin	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	muscular_disease|cardiovascular_disorder	muscle_disorder|joint_disorder	false	false	false	false	none
MONDO:0017304	ocular albinism	hereditary_disease|disorder_of_visual_system|metabolic_disease	metabolic_disease	hereditary_disease|disorder_of_visual_system|metabolic_disease	genetics_and_genomics|pediatric|ophthalmology	ocular_system_disorder_is_not_in_the_list_so__anemia|metabolic_disorder	blood_bone_marrow_disorder|eye_disorder	false	false	false	false	low
MONDO:0017305	syndromic oculocutaneous albinism	hereditary_disease|metabolic_disease|integumentary_system_disorder|syndromic_disease	metabolic_disease	hereditary_disease|integumentary_system_disorder|syndromic_disease|metabolic_disease	genetics_and_genomics|dermatology|ophthalmology	metabolic_disorder|genetic_disorder	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0017306	disorder of phenylalanine metabolism	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0017307	disorder of tyrosine metabolism	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|metabolic_disorders|endocrinology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0017309	neonatal Marfan syndrome	hereditary_disease|cardiovascular_disorder|syndromic_disease|musculoskeletal_system_disorder|connective_tissue_disorder	cardiovascular_disorder	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|connective_tissue_disorder|cardiovascular_disorder	genetics_and_genomics|pediatric|cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	joint_disorder|heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0017310	Marfan and Marfan-related disorder	hereditary_disease|connective_tissue_disorder	other	hereditary_disease|connective_tissue_disorder	genetics_and_genomics|rheumatology|cardiothoracic|orthopaedic	metabolic_disorder|cardiovascular_disorder	joint_disorder|heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0017312	Perrault syndrome	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder	metabolic_disease|endocrine_system_disorder	reproductive_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease|endocrine_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0017313	disorder of folate metabolism and transport	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0017314	Ehlers-Danlos syndrome, vascular type	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|cardiovascular_disorder	genetics_and_genomics|dermatology|rheumatology	autoimmune_diseases|cardiovascular_disorder	joint_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0017315	short stature-webbed neck-heart disease syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|short_stature_often_relates_to_endocrine_disorders	false	false	false	false	high
MONDO:0017316	short stature-deafness-neutrophil dysfunction-dysmorphism syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|hematology|otolaryngology	autoimmune_diseases|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder|ear_disorder	true	false	false	false	high
MONDO:0017317	phakomatosis pigmentokeratotica	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric|ophthalmology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0017318	phakomatosis pigmentovascularis	integumentary_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|disorder_of_visual_system	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|integumentary_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|dermatology|ophthalmology	genetic_condition|metabolic_disorder	skin_disorder|vascular_disorder|eye_disorder	false	false	false	false	medium
MONDO:0017319	hereditary elliptocytosis	hematologic_disorder	anemia	hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|kidney_disorder	false	false	false	true	low
MONDO:0017320	phosphoenolpyruvate carboxykinase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|adrenal_gland_disease	muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0017321	pili torti-onychodysplasia syndrome	integumentary_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|dermatology|pediatric	genetic_disorder|metabolic_disorder	skin_disorder|joint_disorder|bone_disorder|nail_disorder	false	false	false	false	low
MONDO:0017322	disorders of vitamin D metabolism	hereditary_disease|metabolic_disease|nutritional_disorder|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|nutritional_disorder|metabolic_disease	genetics_and_genomics|endocrinology|osteoporosis_would_also_suggest__orthopaedic	inflammatory_disease|metabolic_disorder	liver_disorder|kidney_disorder|bone_disorder	false	false	false	true	high
MONDO:0017323	hypocalcemic rickets	hereditary_disease|metabolic_disease|nutritional_disorder|endocrine_system_disorder|musculoskeletal_system_disorder	metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|musculoskeletal_system_disorder|nutritional_disorder|metabolic_disease	pediatric|orthopaedic|endocrinology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0017324	autosomal recessive hypophosphatemic rickets	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic|endocrinology	autoimmune_diseases|metabolic_disorder	kidney_disorder|bone_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0017325	early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	intellectual_disability_is_also_a_symptom_of_brain_disorder_but_i_will_keep_the_categories_separate_for_now|brain_disorder	false	false	false	true	very_high
MONDO:0017326	infective dermatitis associated with HTLV-1	integumentary_system_disorder|infectious_disease	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology|virology____note__i_ve_assumed_that_htlv_1_is_a_virus	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0017327	primary non-gestational choriocarcinoma of ovary	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	ovarian_cancer|cancer	gynecological_disorder|reproductive_system_disorder|ovarian_disorder	true	true	false	true	very_high
MONDO:0017328	non-central nervous system-localized embryonal carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	cancer|adrenal_gland_disease	spinal_disorder	false	true	false	true	high
MONDO:0017329	familial vesicoureteral reflux	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	genetics_and_genomics|urology	urinary_disorder|familial_disease|kidney_disease|congenital_condition	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0017330	malignancy diagnosed during pregnancy	obstetric_disorder	other	obstetric_disorder	obstetrics_and_gynecology|oncology	malignancy|cancer	reproductive_system_disorder|malignancy	false	true	false	true	high
MONDO:0017331	Pilotto syndrome	hereditary_disease	other	hereditary_disease	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|liver_disorder|vascular_disorder	false	false	false	false	high
MONDO:0017332	pyoderma gangrenosum-acne-suppurative hidradenitis syndrome	syndromic_disease|connective_tissue_disorder	other	connective_tissue_disorder|syndromic_disease	dermatology|immunology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	false	high
MONDO:0017334	12q15q21.1 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|cardiovascular_disorder	brain_disorder|joint_disorder|kidney_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0017335	microtriplication 11q24.1	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	oncology|pediatrics|genetics_and_genomics	neurodegenerative_disease|cardiovascular_disorder	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0017337	inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	pediatric|endocrinology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	endocrine_disorder	false	false	false	false	high
MONDO:0017338	fatal multiple mitochondrial dysfunctions syndrome	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	neurology|pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|mitochondrially_related_disorders_can_cause_muscle_dysfunction__specifically__mitochondrial_myopathies__so_this_category_is_related_to_the_disease_in_question____note__this_answer_assumes_that_the_category_list_includes_a_broader_category__mitochondrial_disease__or__mitochondrially_related_disorders___but_since_such_categories_are_not_available_in_the_provided_list__i_have_made_an_inference_based_on_my_general_knowledge	true	false	false	false	very_high
MONDO:0017339	exfoliative ichthyosis	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	hair_follicle_disorder|skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0017340	juvenile nasopharyngeal angiofibroma	cancer_or_benign_tumor|otorhinolaryngologic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease	pediatric|otolaryngology|oncology	juvenile_cancer|cancer	vascular_disorder|throat_disorder|nose_disorder	false	false	false	false	high
MONDO:0017341	virus associated tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|post_infectious_disorder	genetics_and_genomics|virology|oncology|pediatrics	tumor|viral_infection|cancer	immune_disorder|lymphatic_disorder	true	true	false	true	high
MONDO:0017342	Epstein-Barr virus-related tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|post_infectious_disorder	hematatology|oncology	cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder	true	true	false	true	high
MONDO:0017343	Epstein-Barr virus-associated lymphoproliferative disorder	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|post_infectious_disorder	hematology|oncology	inflammatory_disease|cancer|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	true	true	false	true	high
MONDO:0017344	Epstein-Barr virus-associated carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|post_infectious_disorder	pediatric|oncology	inflammation_disease|cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder	true	true	false	true	high
MONDO:0017345	Epstein-Barr virus-associated mesenchymal tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|post_infectious_disorder	genetics_and_genomics|pediatric|oncology	cancer	immune_disorder|lymphatic_disorder	true	true	false	true	high
MONDO:0017346	Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|post_infectious_disorder|immune_system_disorder	hematology|oncology	inflammatory_disease|cancer|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	true	true	false	true	very_high
MONDO:0017347	plasmablastic lymphoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|post_infectious_disorder|immune_system_disorder	hematology|oncology	anemia|cancer|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	true	true	false	false	very_high
MONDO:0017348	lymphoepithelial-like carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|post_infectious_disorder	genetics_and_genomics|hematology|oncology	cancer|adrenal_gland_disease	lymphatic_disorder|liver_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0017349	myopericytoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|post_infectious_disorder	neurology|oncology	neurodegenerative_disease|cancer	muscle_disorder|eye_disorder	false	true	false	false	low
MONDO:0017350	inborn disorder of tryptophan metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|biochemistry_is_not_in_the_list_so_i_will_remove_it_genetics_and_genomics|genetics_and_genomics	inborn_disorder|metabolic_disorder	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0017351	inborn disorder of lysine and hydroxylysine metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|rheumatology|genetics_and_genomics	metabolic_disorder|inherited_condition	liver_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0017352	disorder of glutamine metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	true	medium
MONDO:0017353	neonatal glycine encephalopathy	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0017354	infantile glycine encephalopathy	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	high
MONDO:0017355	inborn disorder of proline metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	inherited_metabolism_disorder|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	true	medium
MONDO:0017356	inborn disorder of ornithine metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	inborn_disorder|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0017357	transient hyperammonemia of the newborn	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|neonatology|gastroenterology	neonatal_condition|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0017359	3-methylglutaconic aciduria	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	medical_genetics_is_not_listed_but_could_be_inferred_as_a_combination_of_genetics_and_genomics___other__omitting_the_word__and|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|kidney_disorder	false	false	false	false	high
MONDO:0017360	vitamin B12-unresponsive methylmalonic acidemia type mut0	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0017361	congenital rubella syndrome	disorder_of_development_or_morphogenesis|infectious_disease	infectious_disease	infectious_disease|disorder_of_development_or_morphogenesis	pediatric|allergy_and_immunology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|congenital_disease	brain_disorder|heart_disorder|joint_disorder|kidney_disorder|eye_disorder|birth_defect	true	false	false	false	very_high
MONDO:0017362	neuralgic amyotrophy	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0017363	idiopathic chronic eosinophilic pneumonia	infectious_disease|immune_system_disorder|respiratory_system_disorder|inflammatory_disease	infectious_disease	infectious_disease|idiopathic_disease|inflammatory_disease|respiratory_system_disorder|immune_system_disorder	pulmonology|allergy_and_immunology	allergy|inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	false	false	false	true	high
MONDO:0017364	POEMS syndrome	hematologic_disorder|cancer_or_benign_tumor|nervous_system_disorder|endocrine_system_disorder|immune_system_disorder|syndromic_disease	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|hematologic_disorder|syndromic_disease|immune_system_disorder	hematology|neurology|endocrinology	anemia|autoimmune_diseases	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0017365	hereditary acrokeratotic poikiloderma, Weary type	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder	false	false	false	false	medium
MONDO:0017366	hereditary pheochromocytoma-paraganglioma	cancer_or_benign_tumor|endocrine_system_disorder|syndromic_disease|hereditary_disease	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor|syndromic_disease	oncology|endocrinology|genetics_and_genomics	cancer|adrenal_gland_disease	vascular_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0017372	congenital varicella syndrome	infectious_disease|syndromic_disease|disorder_of_development_or_morphogenesis	infectious_disease	infectious_disease|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|immune_disorder|liver_disorder	true	false	false	false	high
MONDO:0017373	poliomyelitis	nervous_system_disorder|infectious_disease|inflammatory_disease	neurodegenerative_disease|infectious_disease	infectious_disease|acute_disease|nervous_system_disorder|inflammatory_disease	neurology|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	true	false	false	true	high
MONDO:0017375	congenital enterovirus infection	disorder_of_development_or_morphogenesis|infectious_disease	infectious_disease	infectious_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0017376	reactive arthritis	connective_tissue_disorder|musculoskeletal_system_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|inflammatory_disease|connective_tissue_disorder	rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease	immune_disorder|joint_disorder	true	false	false	true	medium
MONDO:0017377	preaxial polydactyly-colobomata-intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|joint_disorder	true	false	false	false	high
MONDO:0017379	polyneuropathy-intellectual disability-acromicria-premature menopause syndrome	syndromic_disease	other	syndromic_disease	neurology|endocrinology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|muscle_disorder|endocrine_disorder	true	false	false	false	high
MONDO:0017380	juvenile polyposis syndrome	digestive_system_disorder|cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|digestive_system_disorder|syndromic_disease	gastroenterology|genetics_and_genomics|pediatric|oncology	autoimmune_diseases|cancer|metabolic_disorder	lymphatic_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0017381	congenital herpes simplex virus infection	disorder_of_development_or_morphogenesis|infectious_disease	infectious_disease	infectious_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric|obstetrics_and_gynecology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	false	high
MONDO:0017382	familial clubfoot due to 5q31 microdeletion	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric	neurodegenerative_disease|genetic_disorders|familial_conditions|metabolic_disorder	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017383	familial clubfoot due to PITX1 point mutation	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric	genetic_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017384	acute generalized exanthematous pustulosis	inflammatory_disease|integumentary_system_disorder	other	integumentary_system_disorder|acute_disease|inflammatory_disease	rheumatology|pediatric|allergy_and_immunology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0017385	malignant migrating partial seizures of infancy	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0017386	pleomorphic rhabdomyosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|genetics_and_genomics|pediatric|oncology	cancer	soft_tissue_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0017387	epithelioid sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|pathology|oncology	adrenal_gland_disease|inflammatory_disease|cancer	skin_disorder|immune_disorder|soft_tissue_disorder|muscle_disorder	false	true	false	true	very_high
MONDO:0017388	celiac trunk compression syndrome	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	gastroenterology|cardiothoracic|surgery___corrected_to__gastroenterology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0017389	tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|neurology|pediatrics	neurodegenerative_disease|metabolic_disorder	brain_disorder|metabolic_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0017391	Grayson-Wilbrandt corneal dystrophy	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	false	low
MONDO:0017392	pre-descemet corneal dystrophy	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	true	low
MONDO:0017393	blepharophimosis - intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0017394	ketamine-induced biliary dilatation	digestive_system_disorder|poisoning	other	digestive_system_disorder|poisoning	gastroenterology|hepatology	toxicology|metabolic_disorder	liver_disorder|biliary_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0017395	fixed pigmented erythema	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	autoimmune_diseases|adrenal_gland_disease|inflammatory_disease|cancer|metabolic_disorder	cutaneous_disorder|skin_disorder	false	false	false	false	low
MONDO:0017396	toxic dermatosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|allergy|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0017398	3MC syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	urinary_tract_disorder|lymphatic_disorder|brain_disorder|reproductive_system_disorder|spinal_disorder|bone_disorder|muscle_disorder|ear_disorder|eye_disorder|joint_disorder|kidney_disorder|skin_disorder|vascular_disorder	false	false	false	false	high
MONDO:0017399	frontotemporal dementia, right temporal atrophy variant	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017400	hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric|gastroenterology	metabolic_disorder|congenital_abnormality|gastrointestinal_disorder	upper_gastrointestinal_disorder|biliary_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0017401	familial isolated arrhythmogenic ventricular dysplasia, left dominant form	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|pediatric|cardiology|cardiothoracic	familial_isolated_arrhythmogenic_ventricular_dysplasia_left_dominant_form_is_not_a_direct_match__however__it_can_be_categorized_under_cardiovascular_disorder|familial_isolated_arrhythmogenic_ventricular_dysplasia_left_dominant_form_is_the_disease_name_and_does_fit_into_one_category_so___cardiovascular_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0017402	familial isolated arrhythmogenic ventricular dysplasia, biventricular form	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|cardiology|pediatrics	familial_isolated_arrhythmogenic_ventricular_dysplasia_biventricular_form|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0017403	familial isolated arrhythmogenic ventricular dysplasia, right dominant form	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|pediatric|cardiology	familial_isolated_arrhythmogenic_ventricular_dysplasia_right_dominant_form_is_too_specific_so_it_s_just_cardiovascular_disorder|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0017404	distal Xq28 microduplication syndrome	chromosomal_disorder|disorder_of_development_or_morphogenesis|psychiatric_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	psychiatric_disorder	syndromic_disease|chromosomal_disorder|psychiatric_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	kidney_disorder|developmental_disorder__note__developmental_disorder_is_implied_by_the_presence_of_microduplication	false	false	false	false	high
MONDO:0017405	1p21.3 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0017406	hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|endocrinology	neurodegenerative_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0017407	deficiency in anterior pituitary function - variable immunodeficiency syndrome	cancer_or_benign_tumor|endocrine_system_disorder|syndromic_disease|immune_system_disorder|hematologic_disorder|hereditary_disease	endocrine_system_disorder|cancer_or_benign_tumor	syndromic_disease|endocrine_system_disorder|cancer_or_benign_tumor|immune_system_disorder|hereditary_disease|hematologic_disorder	endocrinology|pediatrics	metabolic_disorder|autoimmune_diseases	endocrine_disorder|immune_disorder	false	false	false	true	high
MONDO:0017408	rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	pulmonology|pediatric|neurology|endocrinology	metabolic_disorder|autonomic_dysregulation_is_mentioned_but_the_specific_category_is_cardiovascular_disorder|mental_health_disorder|autoimmune_diseases|neurodegenerative_disease	endocrine_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0017409	fetal cytomegalovirus syndrome	infectious_disease|disorder_of_development_or_morphogenesis|syndromic_disease	infectious_disease	syndromic_disease|infectious_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neonatology|medical_genetics|obstetrics_and_gynecology|pediatrics	autoimmune_diseases|neurodegenerative_disease	skin_disorder|brain_disorder	true	false	false	true	high
MONDO:0017410	porencephaly	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|pediatric|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0017411	neonatal inflammatory skin and bowel disease	connective_tissue_disorder|syndromic_disease|immune_system_disorder|digestive_system_disorder|hereditary_disease|integumentary_system_disorder	other	connective_tissue_disorder|syndromic_disease|immune_system_disorder|digestive_system_disorder|integumentary_system_disorder|hereditary_disease	pediatric|dermatology|gastroenterology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	false	very_high
MONDO:0017413	Reunion island Larsen syndrome	metabolic_disease|syndromic_disease|hereditary_disease	metabolic_disease	syndromic_disease|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|dermatology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	upper_gastrointestinal_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0017415	multiple pterygium syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	ophthalmology|dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	ear_disorder|skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0017416	postpoliomyelitis syndrome	nervous_system_disorder|infectious_disease|inflammatory_disease	neurodegenerative_disease|infectious_disease	nervous_system_disorder|inflammatory_disease|acute_disease|infectious_disease	neurology|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0017417	renal-hepatic-pancreatic dysplasia	hereditary_disease	other	hereditary_disease	gastroenterology|hepatology|renal_medicine	pancreatic_disease|metabolic_disorder|renal_disease|hepatic_disease	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0017418	chronic intestinal failure	digestive_system_disorder	other	digestive_system_disorder	pulmonology|gastroenterology|hepatology|renal_medicine|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	very_high
MONDO:0017419	non-syndromic amelia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	anemia|metabolic_disorder	bone_disorder|limb_disorder	false	false	false	false	medium
MONDO:0017424	non-syndromic brachydactyly	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0017425	preaxial polydactyly of fingers	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	neurodevelopmental_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0017426	postaxial polydactyly of fingers	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0017427	congenital deformities of limbs	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|pediatric	metabolic_disorder|congenital_deformities_of_limb	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0017435	popliteal pterygium syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease	dermatology|genetics_and_genomics	autoimmune_diseases|anemia|inflammatory_disease	joint_disorder|eye_disorder	false	false	false	false	medium
MONDO:0017436	lethal congenital contracture syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	joint_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0017437	amelia of upper limb	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|pediatric	neurodegenerative_disease|congenital_abnormality	joint_disorder|bone_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0017438	amelia of lower limb	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|hematology|genetics_and_genomics|pediatric	birth_defect|genetic_condition|skeletal_disorder|neurodegenerative_disease|congenital_disorder|developmental_disorder	spinal_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017439	tetra-amelia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	genetic_disorder|neurodegenerative_disease|developmental_disorder	eye_disorder|ear_disorder|teeth_disorder|spinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0017440	humeral agenesis/hypoplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|genetic_condition|developmental_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0017441	congenital absence of upper arm and forearm with hand present	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	congenital_abnormality|neurodegenerative_disease	bone_disorder|limb_abnormality	false	false	false	true	high
MONDO:0017442	congenital absence of thigh and lower leg with foot present	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric	metabolic_disorder|congenital_abnormality	bone_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0017443	congenital absence of both forearm and hand	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	limb_anomaly|congenital_hand_abnormality|birth_defect|congenital_abnormality|neurodegenerative_disease|genetic_condition|developmental_disorder	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0017444	congenital absence of both lower leg and foot	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric	metabolic_disorder|congenital_abnormality|neurodegenerative_disease|developmental_disorder	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0017445	acheiria	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	neurology|endocrinology	autoimmune_diseases|neurodegenerative_disease	lymphatic_disorder|immune_disorder|vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0017446	apodia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	immunology|genetics_and_genomics|pediatric|allergy_and_immunology	autoimmune_diseases|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0017449	split hand	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	bone_disorder|skin_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017450	split foot	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|dermatology	autoimmune_diseases|inflammatory_disease	joint_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017451	non-syndromic brachydactyly of fingers	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	birth_defect|skeletal_muscle_disorder|genetic_disorder|musculoskeletal_disorder|congenital_disorder|developmental_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0017452	non-syndromic brachydactyly of toes	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	congenital_anomaly|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0017453	fetal parvovirus syndrome	infectious_disease|disorder_of_development_or_morphogenesis	infectious_disease	disorder_of_development_or_morphogenesis|infectious_disease	pediatric|obstetrics_and_gynecology	autoimmune_diseases|anemia|metabolic_disorder	upper_gastrointestinal_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0017454	triphalangeal thumb-polysyndactyly syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|genetic_condition	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017455	hyperphalangy	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|endocrinology	metabolic_disorder|genetic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017456	central polydactyly of fingers	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	metabolic_disorder|congenital_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0017457	Preaxial polydactyly of toes	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|congenital_disease|developmental_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0017460	syndactyly type 6	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017461	familial isolated clinodactyly of fingers	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	metabolic_disorder|congenital_anomaly	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017462	congenital pseudoarthrosis of the tibia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	congenital|orthopaedic|genetics_and_genomics|pediatric	inflammatory_disease|skeletal_disorder|congenital_condition	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0017463	congenital pseudoarthrosis of the femur	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	skeletal_dysplasia|developmental_disorder|bone_abnormality|congenital_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0017464	congenital pseudoarthrosis of the fibula	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	musculoskeletal_condition|developmental_disorder|skeletal_abnormality|congenital_condition	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0017465	congenital pseudoarthrosis of the radius	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	skeletal_system_disease|congenital_condition|developmental_disorder____note___skeletal_system_disease__is_a_plausible_but_implied_category_in_the_provided_list__as_it_is_not_explicitly_listed__the_other_categories_were_directly_matched_to__congenital_pseudoarthrosis_of_the_radius	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0017466	congenital pseudoarthrosis of the ulna	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	inflammatory_disease|congenital_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0017467	tibio-fibular synostosis	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|rheumatology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017468	congenital shoulder dislocation	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|pediatric	neurodevelopmental_disease|musculoskeletal_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017469	congenital elbow dislocation	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|pediatric	neurodevelopmental_disorder|musculoskeletal_disorder|developmental_disorder|congenital_condition|skeletal_abnormality___corrected_list_using_provided_categories__musculoskeletal_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017470	congenital knee dislocation	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|pediatric	inflammatory_disease|musculoskeletal_disorder|birth_defect|congenital_condition	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017471	congenital patella dislocation	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|pediatric	musculoskeletal_disorder|birth_defect|congenital_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017472	patella aplasia/hypoplasia, unilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017473	patella aplasia/hypoplasia, bilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017474	macrodactyly of fingers	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	metabolic_disorder|congenital_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017475	macrodactyly of toes	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|developmental_disorder|genetic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017476	upper limb hypertrophy	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	endocrinology|orthopaedic|pediatric	metabolic_disorder|adrenal_gland_disease	muscle_disorder|joint_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0017477	lower limb hypertrophy	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	endocrinology|orthopaedic|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017478	amelia of upper limb, unilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	autoimmune_diseases|congenital_disorders	bone_disorder|limb_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0017479	amelia of upper limb, bilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	bone_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0017480	amelia of lower limb, unilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease	spinal_disorder|bone_disorder|muscle_disorder|joint_disorder	false	false	false	true	high
MONDO:0017481	amelia of lower limb, bilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	true	high
MONDO:0017482	humeral agenesis/hypoplasia, unilateral	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	skeletal_dysplasia|metabolic_disorder	spinal_disorder|bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017483	humeral agenesis/hypoplasia, bilateral	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017484	femoral agenesis/hypoplasia, unilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder	vascular_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017485	femoral agenesis/hypoplasia, bilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric	metabolic_disorder|developmental_disorder|genetic_disorder	bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017486	radial hemimelia, unilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	skeletal_disease|neurodegenerative_disease|genetic_disease|developmental_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017487	radial hemimelia, bilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	limb_anomaly|skeletal_dysplasia|metabolic_disorder|birth_defect|developmental_disorder|genetic_disorder|congenital_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0017488	ulnar hemimelia, bilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|congenital_disorder	bone_disorder|joint_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0017489	ulnar hemimelia, unilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	musculoskeletal_disorder|congenital_abnormality|developmental_disorder	bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017490	tibial hemimelia, unilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|congenital_abnormality	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0017491	tibial hemimelia, bilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0017492	fibular hemimelia, unilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|genetic_condition|birth_defect|developmental_abnormality	bone_disorder|joint_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0017493	fibular hemimelia, bilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease|cardiovascular_disorder|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0017496	congenital absence of thigh and lower leg with foot present, unilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric	metabolic_disorder|neurodegenerative_disease|congenital_abnormality	vascular_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017497	congenital absence of thigh and lower leg with foot present, bilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric	metabolic_disorder|congenital_abnormality	bone_disorder|limb_abnormality|joint_disorder	false	false	false	false	high
MONDO:0017498	congenital absence of both forearm and hand, unilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|congenital_abnormality	spinal_disorder|limb_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017499	congenital absence of both forearm and hand, bilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|congenital_disorder	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0017500	congenital absence of both lower leg and foot, unilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric	congenital_abnormality|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0017501	congenital absence of both lower leg and foot, bilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric	metabolic_disorder|congenital_abnormality	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0017502	acheiria, unilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatrics|pulmonology|neurology|allergy_and_immunology|cardiology	adrenal_gland_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0017503	acheiria, bilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pulmonology|neurology|pediatric|psychiatry	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017504	apodia, unilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	immunology|pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	upper_gastrointestinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017505	apodia, bilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	immunology|pulmonology|neurology|pediatric|allergy_and_immunology|rheumatology|dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	liver_disorder__kidney_disorder	false	false	false	false	high
MONDO:0017509	adactyly of foot, unilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017510	adactyly of foot, bilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|renal_medicine|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017511	split hand, unilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|neurology|dermatology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	limb_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017512	split hand, bilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|pediatric|dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	hand_disorder|joint_disorder	false	false	false	true	medium
MONDO:0017513	split foot, unilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|dermatology	inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017514	split foot, bilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|rheumatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0017515	brachydactyly of fingers, unilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	genetic_condition|metabolic_disorder|congenital_anomaly	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017516	brachydactyly of fingers, bilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic	congenital_disorder|genetic_condition|developmental_abnormality|neurodegenerative_disease|skeletal_dysplasia	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017517	brachydactyly of toes, unilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic	metabolic_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017518	brachydactyly of toes, bilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017519	symbrachydactyly of hand and foot, unilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic	inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017520	symbrachydactyly of hand and foot, bilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017521	hyperphalangy, unilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|rheumatology	metabolic_disorder|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017522	hyperphalangy, bilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|rheumatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017523	polydactyly of a biphalangeal thumb, unilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	congenital_disorder|skeletal_abnormality|hand_anomaly|genetic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017524	polydactyly of a biphalangeal thumb, bilateral	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017525	polydactyly of a triphalangeal thumb, unilateral	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	congenital_disorder|metabolic_disorder	muscle_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017526	polydactyly of a triphalangeal thumb, bilateral	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|developmental_disorder|genetic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017527	polydactyly of an index finger, unilateral	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	congenital_anomaly|developmental_disorder|musculoskeletal_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017528	polydactyly of an index finger, bilateral	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	congenital_disorder|genetic_condition|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017529	polysyndactyly, unilateral	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	congenital_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017530	polysyndactyly, bilateral	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	birth_defects|metabolic_disorder|developmental_disorders|genetic_disorders|skeletal_system_disease	bone_disorder|joint_disorder	false	false	false	true	medium
MONDO:0017531	postaxial polydactyly type A, unilateral	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017532	postaxial polydactyly type A, bilateral	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017533	postaxial polydactyly type B, unilateral	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_condition|congenital_abnormality	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017534	postaxial polydactyly type B, bilateral	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017535	central polydactyly of fingers, unilateral	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease|anemia|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017536	central polydactyly of fingers, bilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017537	Preaxial polydactyly of toes, unilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|congenital_abnormality|developmental_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017538	Preaxial polydactyly of toes, bilateral	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|developmental_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0017543	zygodactyly type 2	chromosomal_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|chromosomal_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017544	zygodactyly type 3	hereditary_disease|chromosomal_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|chromosomal_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017545	zygodactyly type 4	hereditary_disease|chromosomal_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|chromosomal_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017546	congenital vertical talus, unilateral	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0017547	congenital vertical talus, bilateral	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0017548	humero-radio-ulnar synostosis, unilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017549	humero-radio-ulnar synostosis, bilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|rheumatology|genetics_and_genomics|orthopaedic	inflammatory_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017550	humero-radial synostosis, unilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017551	humero-radial synostosis, bilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	inflammatory_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017552	humero-ulnar synostosis, unilateral	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017553	humero-ulnar synostosis, bilateral	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0017554	radio-ulnar synostosis, unilateral	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017555	radio-ulnar synostosis, bilateral	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017556	Madelung deformity, unilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|orthopaedic	musculoskeletal_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017557	Madelung deformity, bilateral	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	autoimmune_diseases|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017558	congenital elbow dislocation, unilateral	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|orthopaedic	birth_defect|musculoskeletal_disorder|neurodegenerative_disease|congenital_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017559	congenital elbow dislocation, bilateral	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|orthopaedic	musculoskeletal_disorder|neurodegenerative_disease|congenital_disease|injury	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0017560	congenital genu recurvatum	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|congenital_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017561	congenital genu flexum	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|orthopaedic	congenital_disease____wait__i_made_a_mistake__the_correct_answer_is___metabolic_disorder|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017562	congenital patella dislocation, unilateral	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|orthopaedic	inflammatory_disease|musculoskeletal_disorder|congenital_disease	joint_disorder|bone_disorder	false	false	false	true	medium
MONDO:0017563	congenital patella dislocation, bilateral	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|orthopaedic	metabolic_disorder|congenital_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017564	macrodactyly of fingers, unilateral	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic	genetic_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017565	macrodactyly of fingers, bilateral	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic	inflammatory_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017566	macrodactyly of toes, unilateral	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_condition	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017567	macrodactyly of toes, bilateral	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	inflammatory_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0017568	Prata-Liberal-Goncalves syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	lymphatic_disorder|vascular_disorder|liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0017569	de Barsy syndrome	premature_aging_syndrome|hereditary_disease	other	premature_aging_syndrome|hereditary_disease	neurology|dermatology	adrenal_gland_disease|neurodegenerative_disease	liver_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0017570	leukocyte adhesion deficiency	immune_system_disorder|hematologic_disorder|hereditary_disease	other	immune_system_disorder|hematologic_disorder|hereditary_disease	immunology|genetics_and_genomics|hematology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0017571	Proteus-like syndrome	integumentary_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	immune_disorder|liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0017572	tick-borne encephalitis	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	acute_disease|infectious_disease|inflammatory_disease|nervous_system_disorder	pediatric|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder	true	false	false	true	high
MONDO:0017573	46,XX disorder of sex development-anorectal anomalies syndrome	disorder_of_development_or_morphogenesis|reproductive_system_disorder|syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|syndromic_disease	genetics_and_genomics|urology|pediatrics	metabolic_disorder|anorectal_anomalies_syndrome_is_often_associated_with_congenital_anomalies_of_the_genitourinary_system_and_or_other_abnormalities_that_can_be_part_of_a_metabolic_disorder	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0017574	chronic intestinal pseudoobstruction	digestive_system_disorder	other	digestive_system_disorder	pediatric|gastroenterology	gastrointestinal_disorder|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0017575	mitochondrial neurogastrointestinal encephalomyopathy	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|mitochondrial_disease|nervous_system_disorder	metabolic_disease	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology|gastroenterology	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|neurogastrointestinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0017576	46,XX disorder of sex development	disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	pediatric|genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0017577	spontaneous periodic hypothermia	nervous_system_disorder	other	nervous_system_disorder	endocrinology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0017578	disorder of thiamine metabolism and transport	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|genetics_and_genomics|neurology|gastroenterology	disorder_of_thiamine_metabolism_and_transport|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	medium
MONDO:0017579	Baraitser-Winter cerebrofrontofacial syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|skin_disorder|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0017580	11p15.4 microduplication syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	genetics_and_genomics|neurology|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	lower_gastrointestinal_disorder|kidney_disorder	false	false	false	false	high
MONDO:0017582	pituitary adenocarcinoma	connective_tissue_disorder|reproductive_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	musculoskeletal_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|endocrine_system_disorder|nervous_system_disorder	endocrinology|oncology|neurology	adrenal_gland_disease|cancer	endocrine_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0017583	mirror polydactyly-vertebral segmentation-limbs defects syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|orthopaedic|pediatric	developmental_disorder|genetic_disorder|limb_abnormality	spinal_disorder|limb_disorder|bone_disorder	false	false	false	false	high
MONDO:0017584	Sagliker syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	genetics_and_genomics|neurology	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	as_of_my_knowledge_cutoff_in_october_2023__sagliker_syndrome_is_a_rare_genetic_disorder__there_are_no_known_established_treatments_that_can_cure_it__but_management_strategies_may_exist_to_alleviate_some_symptoms__therefore__the_answer_is_false_regarding_the_existence_of_efficacious_treatments_that_cure__prevent__or_universally_treat_this_disease	medium
MONDO:0017585	painful orbital and systemic neurofibromas-marfanoid habitus syndrome	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	ophthalmology|genetics_and_genomics|neurology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|cancer	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0017586	onychocytic matricoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|dermatology|hematology	inflammatory_disease|autoimmune_diseases|anemia	skin_disorder|nail_disorder	false	false	false	false	low
MONDO:0017587	onychomatricoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|cancer	skin_disorder|nail_disorder	false	false	false	false	low
MONDO:0017588	nail tumor	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	nail_tumor_is_also_a_type_of_cancer|cancer	lymphatic_disorder|joint_disorder|spinal_disorder|bone_disorder|skin_disorder|muscle_disorder	false	true	false	false	low
MONDO:0017589	follicular cholangitis and pancreatitis	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0017590	carcinoma of the ampulla of vater	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|gastroenterology	autoimmune_diseases|cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	true	high
MONDO:0017591	combined pulmonary fibrosis-emphysema syndrome	respiratory_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	respiratory_system_disorder|infectious_disease|inflammatory_disease|idiopathic_disease	pulmonology|cardiothoracic|genetics_and_genomics|rheumatology	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0017592	staphylococcal toxemia	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|allergy_and_immunology|pediatrics	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	false	high
MONDO:0017593	juvenile amyotrophic lateral sclerosis	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0017594	indolent B-cell non-Hodgkin lymphoma	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	oncology|hematology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	medium
MONDO:0017595	aggressive B-cell non-Hodgkin lymphoma	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	oncology|hematology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0017596	diffuse large B-cell lymphoma of the central nervous system	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder|post_infectious_disorder	oncology|hematology	autoimmune_diseases|cancer|cancer_of_the_central_nervous_system_is_a_type_of_lymphoma_which_is_a_category_of_cancer	lymphatic_disorder|immune_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0017597	T-cell/histiocyte rich large B cell lymphoma	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	oncology|hematology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0017598	primary cutaneous anaplastic large cell lymphoma	hematologic_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder|skin_disorder	false	true	false	true	medium
MONDO:0017599	splenic diffuse red pulp small B-cell lymphoma	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	oncology|hematology	autoimmune_diseases|inflammatory_disease|lymphoma|cancer	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	false	medium
MONDO:0017600	hairy cell leukemia variant	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor|acute_disease	oncology|hematology	anemia|cancer	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0017601	diffuse large B-cell lymphoma with chronic inflammation	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|post_infectious_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder_lymphatic_disorder	true	true	false	true	high
MONDO:0017602	ALK-positive anaplastic large cell lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0017603	ALK-negative anaplastic large cell lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|lymphoma	immune_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0017604	marginal zone lymphoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	autoimmune_diseases|cancer|lymphoma	immune_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0017607	caudal regression sequence	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	obstetrics_and_gynecology|genetics_and_genomics|pediatric	genetic_disorder|rare_disease|neurodegenerative_disease|congenital_disorder	joint_disorder|bone_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0017609	renal tubular dysgenesis	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|genetics_and_genomics|pediatric	metabolic_disorder|renal_tubular_dysgenesis_has_features_of_anemia_and_is_associated_with_a_metabolic_disorder_due_to_impaired_kidney_function	kidney_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0017610	epidermolysis bullosa simplex	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0017611	pituitary tumor	endocrine_system_disorder|nervous_system_disorder|reproductive_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	musculoskeletal_system_disorder|reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	neurology|endocrinology|oncology	cancer|endocrine_disorder	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0017612	junctional epidermolysis bullosa	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	pediatrics|dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0017613	intellectual disability-hypotonia-skin hyperpigmentation syndrome	syndromic_disease	other	syndromic_disease	neurology|dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	skin_disorder|endocrine_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0017614	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome	nervous_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|psychiatric_disorder	psychiatric_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|psychiatric_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	skin_disorder|endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0017615	benign familial infantile epilepsy	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	true	low
MONDO:0017616	X-linked intellectual disability, Schutz type	nervous_system_disorder|hereditary_disease|syndromic_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|syndromic_disease|psychiatric_disorder	neurology|psychiatry|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0017617	acquired adult-onset immunodeficiency	immune_system_disorder	other	immune_system_disorder	rheumatology|immunology|hematology|genetics_and_genomics|allergy_and_immunology	immunodeficiency|autoimmune_diseases	immune_disorder|lymphatic_disorder	true	false	false	true	very_high
MONDO:0017618	congenital sucrase-isomaltase deficiency with starch intolerance	digestive_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|digestive_system_disorder	gastroenterology|genetics_and_genomics|pediatric	genetic_disorder|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0017619	congenital sucrase-isomaltase deficiency with minimal starch tolerance	digestive_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|digestive_system_disorder	gastroenterology|genetics_and_genomics|pediatric	lysosomal_storage_disease|metabolic_disorder|congenital_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0017620	congenital sucrase-isomaltase deficiency without starch intolerance	digestive_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|digestive_system_disorder	gastroenterology|genetics_and_genomics|pediatric	metabolic_disorder|enzyme_deficiency	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	true	true	medium
MONDO:0017621	congenital sucrase-isomaltase deficiency with starch and lactose intolerance	digestive_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|digestive_system_disorder	gastroenterology|genetics_and_genomics|pediatric	metabolic_disorder|congenital_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0017622	congenital sucrase-isomaltase deficiency without sucrose intolerance	digestive_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|digestive_system_disorder	gastroenterology|genetics_and_genomics|pediatric	metabolic_disorder|congenital_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0017623	PTEN hamartoma tumor syndrome	hereditary_disease|cancer_or_benign_tumor|syndromic_disease|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|cancer_or_benign_tumor	oncology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|cancer	kidney_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0017624	familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis	hereditary_disease|urinary_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|urinary_system_disorder|metabolic_disease	endocrinology|renal_medicine|urology|genetics_and_genomics	nephrocalcinosis|familial|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0017625	familial primary hypomagnesemia with hypocalcuria	hereditary_disease|urinary_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|urinary_system_disorder|metabolic_disease	endocrinology|renal_medicine|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0017626	familial primary hypomagnesemia with normocalcuria	hereditary_disease|urinary_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|urinary_system_disorder|metabolic_disease	endocrinology|renal_medicine|genetics_and_genomics	metabolic_disorder|familial_adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0017627	congenital hereditary facial paralysis-variable hearing loss syndrome	musculoskeletal_system_disorder|syndromic_disease	other	musculoskeletal_system_disorder|syndromic_disease	otolaryngology|neurology|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0017628	myospherulosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	hematology|pediatric|pulmonology	autoimmune_diseases|inflammatory_disease	immune_disorder|joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0017630	X-linked complicated spastic paraplegia type 1	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017634	non-infectious anterior uveitis	inflammatory_disease|disorder_of_visual_system	other	inflammatory_disease|disorder_of_orbital_region|disorder_of_visual_system	rheumatology|ophthalmology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|eye_disorder	false	false	false	true	high
MONDO:0017636	hemiparkinsonism-hemiatrophy syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017638	manganese poisoning	poisoning|nervous_system_disorder	other	poisoning|nervous_system_disorder	neurology|psychiatry|pulmonology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0017639	carbon monoxide-induced parkinsonism	poisoning|nervous_system_disorder	other	poisoning|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017640	cyanide-induced parkinsonism	nervous_system_disorder|poisoning	other	poisoning|nervous_system_disorder	neurology|toxicology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017642	intellectual disability-microcephaly-phalangeal-facial abnormalities syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	brain_disorder|developmental_disorder|facial_abnormalities|intellectual_disability	false	false	false	false	very_high
MONDO:0017648	Sydenham chorea	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0017649	hemidystonia-hemiatrophy syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0017658	hyperekplexia	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0017659	sporadic hyperekplexia	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0017666	diffuse palmoplantar keratoderma	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	high
MONDO:0017668	intellectual disability-short stature-hypertelorism syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	endocrinology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017672	focal palmoplantar keratoderma	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|hereditary_disorder	false	false	false	false	low
MONDO:0017675	punctate palmoplantar keratoderma	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder	false	false	false	false	medium
MONDO:0017677	focal acral hyperkeratosis	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology|other___note__focal_acral_hyperkeratosis_is_a_rare_skin_condition_associated_with_arsenic_exposure__dermatology_is_the_primary_category__but_since_it_s_related_to_a_specific_toxin_exposure__another_possible_category_could_be__other	metabolic_disorder|skin_condition	lower_gastrointestinal_disorder|skin_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0017682	intellectual disability-polydactyly-uncombable hair syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	skin_disorder|intellectual_disability_is_not_in_the_list_but_it_could_also_imply_brain_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017683	methylcobalamin deficiency type cblDv1	hereditary_disease|hematologic_disorder|nutritional_disorder|metabolic_disease	metabolic_disease|anemia	hereditary_disease|hematologic_disorder|metabolic_disease|nutritional_disorder	genetics_and_genomics|hematologypediatrics|neurology	neurodegenerative_disease|metabolic_disorder|anemia	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0017684	disorder of beta and omega amino acid metabolism	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	metabolic_disorders|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0017685	vitamin B12-responsive methylmalonic acidemia, type cblDv2	hereditary_disease|nutritional_disorder|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|nutritional_disorder	hematology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|anemia	blood_disorder|metabolic_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0017686	inborn aminoacylase deficiency	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0017687	disorder of neutral amino acid transport	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|neurology|hepatology|renal_medicine|pediatric	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0017688	disorder of glycolysis	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|renal_medicine|hematology|endocrinology|genetics_and_genomics	metabolic_disorder	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0017689	disorder of fructose metabolism	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|hepatology|endocrinology	metabolic_disorder|disorder_of_fructose_metabolism	liver_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0017690	disorder of galactose metabolism	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|endocrinology	disorder_of_metabolism|metabolic_disorder	metabolic_disorder|liver_disorder	false	false	false	true	medium
MONDO:0017691	erythrocyte galactose epimerase deficiency	hereditary_disease|metabolic_disease|disorder_of_visual_system	metabolic_disease	hereditary_disease|disorder_of_visual_system|metabolic_disease|disorder_of_orbital_region	genetics_and_genomics|hematology	metabolic_disorder|anemia	red_cell_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0017692	generalized galactose epimerase deficiency	hereditary_disease|metabolic_disease|disorder_of_visual_system	metabolic_disease	hereditary_disease|disorder_of_visual_system|metabolic_disease|disorder_of_orbital_region	genetics_and_genomics|pediatric|endocrinology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0017694	glycogen storage disease due to acid maltase deficiency, infantile onset	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder|metabolic_disease	metabolic_disease|cardiovascular_disorder	hereditary_disease|metabolic_disease|cardiovascular_disorder|musculoskeletal_system_disorder	genetics_and_genomics|hepatology|pediatric|endocrinology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	true	true	very_high
MONDO:0017695	glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|hepatology|pediatrics	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	liver_disorder	false	false	true	true	high
MONDO:0017696	glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|hepatology|pediatric	glycogen_storage_disease|metabolic_disorder	liver_disorder|glycogen_storage_disease	false	false	true	true	medium
MONDO:0017697	glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|neurology|hepatology|pediatric|endocrinology|pediatrics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|bone_disorder|liver_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0017698	glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0017699	glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|hepatology|pediatrics	autoimmune_diseases|metabolic_disorder|cardiovascular_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0017700	glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0017701	glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0017703	disorder of glyoxylate metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	renal_medicine|genetics_and_genomics|hepatology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0017704	familial partial epilepsy	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0017705	congenital pulmonary venous return anomaly	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|pulmonology|pediatric	congenital_heart_anomaly|cardiovascular_disorder	heart_disorder|vascular_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0017706	disorder of carbohydrate transmembrane transport and absorption	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	gastroenterology|endocrinology	metabolic_disorder|neurodegenerative_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0017708	mevalonate kinase deficiency	connective_tissue_disorder|syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|connective_tissue_disorder|metabolic_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder|vascular_disorder	false	false	false	true	high
MONDO:0017711	pancreatic colipase deficiency	digestive_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	hereditary_disease|endocrine_system_disorder|metabolic_disease|digestive_system_disorder	gastroenterology|endocrinology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0017712	combined pancreatic lipase-colipase deficiency	digestive_system_disorder|metabolic_disease|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	hereditary_disease|endocrine_system_disorder|metabolic_disease|digestive_system_disorder	genetics_and_genomics|gastroenterology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0017713	disorder of fatty acid oxidation and ketogenesis	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology|pediatric	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	endocrine_disorder|liver_disorder	false	false	false	true	high
MONDO:0017714	acyl-CoA dehydrogenase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology|pediatrics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0017715	3-hydroxyacyl-CoA dehydrogenase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|adrenal_gland_disease	muscle_disorder|liver_disorder	false	false	false	true	high
MONDO:0017716	disorder of carnitine cycle and carnitine transport	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	muscle_disorder|liver_disorder	false	false	false	true	high
MONDO:0017719	gangliosidosis	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0017720	GM2 gangliosidosis	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0017721	Sandhoff disease, infantile form	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	true	false	false	true	very_high
MONDO:0017722	Sandhoff disease, juvenile form	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	spinal_disorder|brain_disorder|muscle_disorder	true	false	false	true	very_high
MONDO:0017723	Sandhoff disease, adult form	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	brain_disorder|muscle_disorder	true	false	false	false	high
MONDO:0017724	Tay-Sachs disease, b variant, infantile form	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	lymphatic_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0017725	Tay-Sachs disease, b variant, juvenile form	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0017726	Tay-Sachs disease, B variant, adult form	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|blood_bone_marrow_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017727	fixed subaortic stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|cardiothoracic	cardiovascular_disorder|fixed_subaortic_stenosis	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0017728	Tay-Sachs disease, B1 variant	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|metabolic_disease|disorder_of_visual_system	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0017729	metachromatic leukodystrophy, late infantile form	nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|mental_health_disorder	spinal_disorder|blood_bone_marrow_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0017730	metachromatic leukodystrophy, adult form	nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|blood_bone_marrow_disorder|brain_disorder	false	false	false	false	high
MONDO:0017731	glycoproteinosis	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	liver_disorder	false	false	false	false	medium
MONDO:0017732	alpha-mannosidosis, infantile form	disorder_of_visual_system|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_orbital_region|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|musculoskeletal_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0017733	alpha-mannosidosis, adult form	disorder_of_visual_system|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_orbital_region|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|musculoskeletal_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0017734	sialidosis	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	throat_disorder|skin_disorder|ear_disorder	false	false	false	false	high
MONDO:0017735	congenital aortic valve stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|cardiology	congenital_heart_defect|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0017736	disorder of sialic acid metabolism	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|biochemistry	neurodegenerative_disease|metabolic_disorder	metabolic_disorder|liver_disorder	false	false	false	true	high
MONDO:0017737	intermediate severe Salla disease	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|endocrinology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|biliary_disorder	false	false	false	false	medium
MONDO:0017738	lysosomal glycogen storage disease	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|hepatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	true	true	very_high
MONDO:0017739	disorder of lysosomal-related organelles	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics|hepatology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	liver_disorder	false	false	false	true	high
MONDO:0017740	disorder of protein N-glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	medical_genetics|genetics_and_genomics|biochemistry	neurodegenerative_disease|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0017741	disorder of protein O-glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	molecular_biology|genetics_and_genomics|biochemistry	neurodegenerative_disease|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0017746	atypical Rett syndrome	nervous_system_disorder	other	nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	true	false	false	false	high
MONDO:0017747	disorder of fucoglycosan synthesis	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	none
MONDO:0017748	inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	skin_disorder|eye_disorder|brain_disorder|nerve_disorder|muscle_disorder	false	false	false	true	high
MONDO:0017749	disorder of multiple glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics	metabolic_disorder	joint_disorder|vascular_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017750	defect in conserved oligomeric Golgi complex	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0017752	defect in V-ATPase	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|renal_medicine|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0017754	inborn disorder of porphyrin metabolism	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|hematology|pediatric	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0017755	inborn disorder of bilirubin metabolism	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|hematology	metabolic_disorder|inborn_disorder_of_bilirubin_metabolism	liver_disorder|biliary_disorder	false	false	false	true	high
MONDO:0017757	disorder of metabolite absorption and transport	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|gastroenterology|renal_medicine	disorder_of_metabolite_absorption_and_transport|metabolic_disorder	liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0017758	disorder of vitamin and non-protein cofactor absorption and transport	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|endocrinology|gastroenterology	anemia|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0017759	disorder of catecholamine synthesis	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|vascular_disorder	false	false	false	true	high
MONDO:0017761	disorder of mineral absorption and transport	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|endocrinology|gastroenterology|renal_medicine	anemia|metabolic_disorder	kidney_disorder|liver_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0017762	disorder of copper metabolism	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology|metabolism	disorder_of_copper_metabolism_can_also_be_categorized_under___adrenal_gland_disease_neurodegenerative_disease|metabolic_disorder	liver_disorder	false	false	false	true	high
MONDO:0017763	disorder of iron metabolism and transport	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|gastroenterology|hematology	anemia|metabolic_disorder	liver_disorder|note__the_second_category_has_been_added_based_on_the_fact_that_disorders_of_iron_metabolism_and_transport_often_involve_blood_related_conditions|hematology_disorder	false	false	false	true	medium
MONDO:0017764	disorder of zinc metabolism	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology	metabolic_disorder	endocrine_disorder	false	false	false	true	high
MONDO:0017765	disorder of magnesium transport	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|gastroenterology|renal_medicine	autoimmune_diseases|metabolic_disorder	kidney_disorder	false	false	false	false	high
MONDO:0017766	disorder of manganese transport	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	metabolic_disorder|anemia	kidney_disorder|liver_disorder	false	false	false	true	medium
MONDO:0017767	rheumatic fever	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	connective_tissue_disorder|immune_system_disorder|post_infectious_disorder	rheumatology|cardiology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	heart_disorder|immune_disorder|joint_disorder	true	false	false	true	high
MONDO:0017768	reflex epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0017769	acquired immunodeficiency	immune_system_disorder	other	immune_system_disorder	psychiatry|genetics_and_genomics|immunology|pediatric|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	true	false	false	true	very_high
MONDO:0017770	Robinow-like syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	dermatology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	skin_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017771	Mayer-Rokitansky-Kuster-Hauser syndrome	reproductive_system_disorder|syndromic_disease	other	syndromic_disease|reproductive_system_disorder	genetics_and_genomics|urology|obstetrics_and_gynecology	genetic_disorder|developmental_disorder	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0017772	oral erosive lichen	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|oral_medicine	autoimmune_diseases|inflammatory_disease	teeth_disorder|skin_disorder	false	false	false	true	medium
MONDO:0017773	hypoalphalipoproteinemia	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|pediatrics|endocrinology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0017774	hypobetalipoproteinemia	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|anemia	metabolic_disorder|lipid_disorder|liver_disorder	false	false	false	false	low
MONDO:0017775	melioidosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	kidney_disorder|liver_disorder	true	false	false	true	high
MONDO:0017776	nocardiosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|cardiology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	lung_disorder|heart_disorder|immune_disorder|blood_bone_marrow_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0017778	lamellar ichthyosis	disorder_of_visual_system|integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	dermatology|genetics_and_genomics	skin_condition|metabolic_disorder	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0017779	alpha-N-acetylgalactosaminidase deficiency	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	liver_disorder|lysosomal_storage_disease	false	false	false	false	high
MONDO:0017780	20p13 microdeletion syndrome	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0017781	12p12.1 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|anemia	eye_disorder|spinal_disorder|immune_disorder|joint_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0017782	developmental and speech delay due to SOX5 deficiency	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	speech_delay|developmental_delay|brain_disorder	false	false	false	false	high
MONDO:0017783	congenital pancreatic cyst	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	genetics_and_genomics|gastroenterology|pediatric	congenital_disease|inflammatory_disease|cystic_disease____corrected_to_match_the_format_requirement____metabolic_disorder|cystic_disease|metabolic_disorder	endocrine_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0017784	Epstein-Barr virus-associated gastric carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|post_infectious_disorder	oncology|gastroenterology	autoimmune_diseases|inflammatory_disease|cancer	lower_gastrointestinal_disorder|immune_disorder|upper_gastrointestinal_disorder|lymphatic_disorder	true	true	false	true	medium
MONDO:0017785	PENS syndrome	cancer_or_benign_tumor|integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	psychiatry|psychology|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0017786	2q23.1 microduplication syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0017787	erythroderma desquamativum	immune_system_disorder	other	immune_system_disorder	dermatology|genetics_and_genomics|hematology	autoimmune_diseases|inflammatory_disease	skin_disorder|liver_disorder|immune_disorder	false	false	false	false	high
MONDO:0017788	contractures - webbed neck - micrognathia - hypoplastic nipples syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|obstetrics_and_gynecology|pediatric|neurology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder|joint_disorder|muscle_disorder	true	false	false	false	medium
MONDO:0017789	idiopathic linear interstitial keratitis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|idiopathic_disease	ophthalmology|immunology	autoimmune_diseases|inflammatory_disease	eye_disorder|immune_disorder	false	false	false	false	low
MONDO:0017790	gastric adenocarcinoma and proximal polyposis of the stomach	cancer_or_benign_tumor|digestive_system_disorder|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	adrenal_gland_disease|gastrointestinal_cancer|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0017791	high bone mass osteogenesis imperfecta	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|endocrinology|orthopaedic|pediatric	metabolic_disorder|osteogenesis_imperfecta	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0017792	7p22.1 microduplication syndrome	nervous_system_disorder|chromosomal_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|psychiatric_disorder	psychiatric_disorder	chromosomal_disorder|psychiatric_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	psychiatry|genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	eye_disorder|spinal_disorder|kidney_disorder|immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0017793	marfanoid habitus-inguinal hernia-advanced bone age syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|genetic_condition	bone_disorder|joint_disorder|vascular_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0017794	Xq12-q13.3 duplication syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|neurology|pediatric	allergy|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	kidney_disorder	false	false	false	false	high
MONDO:0017795	ameloblastoma	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|mouth_disorder|cancer_or_benign_tumor	genetics_and_genomics|oncology	tumor|cancer	bone_disorder|teeth_disorder	false	true	false	false	high
MONDO:0017798	Spigelian hernia-cryptorchidism syndrome	syndromic_disease	other	syndromic_disease	urology|pediatric	genetic_disorder|neurodegenerative_disease	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0017799	Meigs syndrome	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder|syndromic_disease	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	low
MONDO:0017800	pseudo-Meigs syndrome	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|spinal_disorder|eye_disorder	false	false	false	true	medium
MONDO:0017801	atypical Meigs syndrome	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|genetics_and_genomics|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0017802	ovarian fibrothecoma	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	ovarian_gland_disease|cancer	reproductive_system_disorder|ovarian	false	false	false	false	low
MONDO:0017803	primary progressive apraxia of speech	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017804	autosomal recessive leukoencephalopathy-ischemic stroke-retinitis pigmentosa syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	neurology|pediatric|ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	vascular_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0017805	intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder|brain_disorder|upper_gastrointestinal_disorder|muscle_disorder	true	false	false	false	high
MONDO:0017806	15q overgrowth syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	endocrine_disorder__spinal_disorder	false	false	false	false	high
MONDO:0017807	growing teratoma syndrome	cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor	pediatric|genetics_and_genomics|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|liver_disorder|vascular_disorder|endocrine_disorder|bone_disorder|kidney_disorder	false	true	false	false	medium
MONDO:0017808	duplication of the pituitary gland	disorder_of_development_or_morphogenesis|nervous_system_disorder|endocrine_system_disorder	endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|nervous_system_disorder	neurology|endocrinology	neurodegenerative_disease|autoimmune_diseases|cancer	brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0017809	parkinsonism due to ATP13A2 deficiency	hereditary_disease|metabolic_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017810	variant ABeta2M amyloidosis	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0017811	severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion	hereditary_disease|syndromic_disease|chromosomal_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|chromosomal_disorder|syndromic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|severe_neonatal_hypotonia_seizures_encephalopathy_syndrome_due_to_5q31_3_microdeletion|neurodegenerative_disease	encephalopathy|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0017812	segmental progressive overgrowth syndrome with fibroadipose hyperplasia	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|pediatric|dermatology|genetics_and_genomics|endocrinology	metabolic_disorder|fibroadipose_hyperplasia	skin_disorder|bone_disorder|lower_gastrointestinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0017813	van Maldergem syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|liver_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0017814	primary bone lymphoma	cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer	bone_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0017815	acquired porencephaly	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0017816	primary systemic amyloidosis	cardiovascular_disorder|metabolic_disease|nervous_system_disorder|musculoskeletal_system_disorder	metabolic_disease|cardiovascular_disorder	musculoskeletal_system_disorder|nervous_system_disorder|cardiovascular_disorder|metabolic_disease	renal_medicine|hematology|rheumatology	metabolic_disorder|inflammatory_disease	kidney_disorder|liver_disorder|vascular_disorder	false	false	false	true	high
MONDO:0017817	primary localized amyloidosis	cardiovascular_disorder|metabolic_disease|nervous_system_disorder|musculoskeletal_system_disorder	metabolic_disease|cardiovascular_disorder	musculoskeletal_system_disorder|nervous_system_disorder|cardiovascular_disorder|metabolic_disease	pathology|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	liver_disorder	false	false	false	true	medium
MONDO:0017818	lethal arteriopathy syndrome due to fibulin-4 deficiency	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|pediatric|cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0017819	atypical dentin dysplasia due to SMOC2 deficiency	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	teeth_disorder|bone_disorder|developmental_disorder	false	false	false	false	medium
MONDO:0017822	mixed functioning pituitary adenoma	reproductive_system_disorder|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder|musculoskeletal_system_disorder	neurology|endocrinology	neurological_disorder|cancer|endocrine_disorder	brain_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0017823	somatomammotropinoma	reproductive_system_disorder|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder|musculoskeletal_system_disorder	oncology|endocrinology	cancer|endocrine_cancer|neuroendocrine_tumor	brain_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0017824	familial isolated pituitary adenoma	reproductive_system_disorder|hereditary_disease|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|connective_tissue_disorder|hereditary_disease|cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder|musculoskeletal_system_disorder	genetics_and_genomics|endocrinology	cancer|endocrine_system_disease	brain_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0017825	silent pituitary adenoma	reproductive_system_disorder|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder|musculoskeletal_system_disorder	neurology|endocrinology	cancer|endocrine_system_disease	brain_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0017826	null pituitary adenoma	reproductive_system_disorder|connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder|musculoskeletal_system_disorder	neurology|endocrinology	cancer|adrenal_gland_disease|neuroendocrine_disorder	brain_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0017827	malignant peripheral nerve sheath tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	muscle_disorder|nervous_system_disorder	false	true	false	false	high
MONDO:0017829	autosomal dominant proximal renal tubular acidosis	hereditary_disease|urinary_system_disorder|metabolic_disease	metabolic_disease	urinary_system_disorder|hereditary_disease|metabolic_disease	renal_medicine|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0017830	severe Canavan disease	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0017831	mild Canavan disease	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0017832	Mycobacterium xenopi infection	infectious_disease	infectious_disease	infectious_disease	pulmonology|infectious_diseases|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0017833	primary hypereosinophilic syndrome	cardiovascular_disorder|immune_system_disorder|hematologic_disorder|syndromic_disease|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|immune_system_disorder|hematologic_disorder|syndromic_disease	pulmonology|hematology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|allergy	lung_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0017834	secondary hypereosinophilic syndrome	cardiovascular_disorder|immune_system_disorder|hematologic_disorder|syndromic_disease|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|immune_system_disorder|hematologic_disorder|syndromic_disease	pulmonology|hematology|oncology	autoimmune_diseases|cancer|anemia|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0017835	lymphocytic hypereosinophilic syndrome	cardiovascular_disorder|immune_system_disorder|hematologic_disorder|syndromic_disease|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|immune_system_disorder|hematologic_disorder|syndromic_disease	pulmonology|immunology|hematology|oncology	autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0017836	erythrokeratoderma en cocardes	integumentary_system_disorder	other	integumentary_system_disorder	pediatrics|dermatology	autoimmune_diseases|anemia|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0017837	multiple sclerosis-ichthyosis-factor VIII deficiency syndrome	hematologic_disorder|syndromic_disease	other	hematologic_disorder|syndromic_disease	neurology|hematology|dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0017838	sclerosteosis	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|rheumatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0017839	classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form	hereditary_disease|metabolic_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|metabolic_disease	hereditary_disease|endocrine_system_disorder|metabolic_disease|reproductive_system_disorder	renal_medicine|pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder|reproductive_system_disorder	false	false	false	true	very_high
MONDO:0017840	classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form	hereditary_disease|metabolic_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|metabolic_disease	hereditary_disease|endocrine_system_disorder|metabolic_disease|reproductive_system_disorder	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0017842	Senior-Loken syndrome	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	neurology|psychiatry	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017843	congenital pulmonary sequestration	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiothoracic|pediatric	congenital_disease|cardiovascular_disorder|inflammatory_disease	lung_disorder|heart_disorder	false	false	false	true	high
MONDO:0017844	Sezary syndrome	cancer_or_benign_tumor|hematologic_disorder|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|dermatology|oncology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder_lymphatic_disorder_skin_disorder	true	true	false	true	very_high
MONDO:0017845	spastic ataxia	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017846	autosomal dominant spastic ataxia	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|cardiovascular_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017847	autosomal recessive spastic ataxia	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017849	Siegler-Brewer-Carey syndrome	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0017850	sirenomelia	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder|spine_disorder	false	false	false	false	very_high
MONDO:0017851	erythrokeratodermia variabilis	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	anemia|inflammatory_disease|autoimmune_diseases	vascular_disorder|immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0017852	infantile spasms-broad thumbs syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder_muscle_disorder	false	false	false	false	very_high
MONDO:0017853	hypersensitivity pneumonitis	inflammatory_disease|respiratory_system_disorder|immune_system_disorder	other	respiratory_system_disorder|immune_system_disorder|inflammatory_disease	allergy_and_immunology|pulmonology	allergy|inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	false	false	false	true	medium
MONDO:0017855	T-B- severe combined immunodeficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	immunology|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0017856	X-linked spasticity-intellectual disability-epilepsy syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017857	spina bifida-hypospadias syndrome	syndromic_disease	other	syndromic_disease	orthopaedic|neurology|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	muscle_disorder|joint_disorder|vascular_disorder|urinary_tract_disorder|spinal_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0017858	acute erythroid leukemia	hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	acute_disease|hematologic_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder	oncology|hematology	anemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0017859	colchicine poisoning	poisoning	other	poisoning	hematology|neurology|rheumatology	toxic_exposure|inflammatory_disease	joint_disorder|bone_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0017860	methanol poisoning	poisoning	other	poisoning	neurology|hepatology|toxicology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0017861	ethylene glycol poisoning	poisoning	other	poisoning	neurology|renal_medicine	cardiovascular_disorder|metabolic_disorder	kidney_disorder|renal_system_disorder	false	false	false	true	high
MONDO:0017862	paraquat poisoning	poisoning	other	poisoning	neurology|hapatology|pulmonology	adrenal_gland_disease|neurodegenerative_disease	lung_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0017863	digitalis poisoning	poisoning	other	poisoning	cardiothoracic|cardiology|pulmonology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0017864	congenital pulmonary veins atresia or stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|pediatric|cardiology|pulmonology	congenital_disease|cardiovascular_disorder	lung_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0017865	congenital pulmonary valve stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|pulmonology|pediatrics	congenital_disease|cardiovascular_disorder	lung_disorder|heart_disorder	false	false	false	true	medium
MONDO:0017866	subpulmonary stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|pulmonology	cardiovascular_disorder|congenital_heart_defect	lung_disorder|heart_disorder	false	false	false	true	high
MONDO:0017867	distal 17p13.1 microdeletion syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	genetics_and_genomics|neurology|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|joint_disorder|immune_disorder|spinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0017868	diencephalic-mesencephalic junction dysplasia	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0017869	chondroectodermal dysplasia with night blindness	hereditary_disease|integumentary_system_disorder|musculoskeletal_system_disorder|disorder_of_visual_system|syndromic_disease	other	disorder_of_orbital_region|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_visual_system|integumentary_system_disorder	genetics_and_genomics|orthopaedic|ophthalmology	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|eye_disorder	false	false	false	false	high
MONDO:0017870	supravalvular pulmonary stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|cardiology|pulmonology	congenital_heart_disease|cardiovascular_disorder	vascular_disorder|lunger_disorder|heart_disorder	false	false	false	true	medium
MONDO:0017871	bilateral massive adrenal hemorrhage	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|acute_disease	hematology|renal_medicine|endocrinology	anemia|adrenal_gland_disease|cancer	vascular_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0017872	Lujo hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	hematology|hepatology|pulmonology	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	vascular_disorder|lymphatic_disorder|liver_disorder	true	false	false	false	very_high
MONDO:0017874	Argentine hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	hematology|hepatology|pediatrics	adrenal_gland_disease|autoimmune_diseases	liver_disorder	true	false	false	true	high
MONDO:0017875	Bolivian hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	hematology|hepatology|pulmonology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	vascular_disorder|lower_gastrointestinal_disorder|liver_disorder	true	false	false	true	high
MONDO:0017876	Venezuelan hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	hematology|virology|infectious_diseases	inflammatory_disease|autoimmune_diseases	kidney_disorder|vascular_disorder	true	false	false	false	medium
MONDO:0017877	Brazilian hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	hematology|hepatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder|liver_disorder	true	false	false	false	low
MONDO:0017878	Chapare hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	hematology|hepatology|pulmonology	inflammatory_disease|autoimmune_diseases	vascular_disorder|liver_disorder	true	false	false	false	medium
MONDO:0017879	hantavirus pulmonary syndrome	infectious_disease|syndromic_disease|respiratory_system_disorder	infectious_disease	infectious_disease|respiratory_system_disorder|syndromic_disease	pulmonology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	kidney_disorder|lung_disorder|immune_disorder|lymphatic_disorder|urinary_tract_disorder	true	false	false	false	very_high
MONDO:0017880	Rift valley fever	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|pediatric	inflammatory_disease|autoimmune_diseases	kidney_disorder|liver_disorder	true	false	false	false	medium
MONDO:0017881	Kyasanur forest disease	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|pulmonology|tropical_medicine	animal_infectious_disease|inflammatory_disease	lung_disorder|immune_disorder|vascular_disorder	true	false	false	true	high
MONDO:0017882	Omsk hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	hematology|virology|epidemiology|infectious_diseases	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0017884	papillary renal cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	adrenal_gland_disease|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0017885	chromophobe renal cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology|renal_medicine	adrenal_gland_disease|cancer	kidney_disorder|urinary_tract_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0017886	MIT family translocation renal cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology|genetics_and_genomics	renal_cell_carcinoma|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0017887	renal cell carcinoma associated with neuroblastoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|genetics_and_genomics|oncology	cancer|neuroblastoma|renal_cell_carcinoma_assoicated_with_neuroblastoma_is_more_accurately_represented_as_simply__renal_cell_carcinoma	kidney_disorder	false	true	false	true	high
MONDO:0017890	tubulocystic renal cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|renal_medicine|oncology	cancer|uropathology|renal_cancer	kidney_disorder|urinary_tract_disorder	false	true	false	false	medium
MONDO:0017892	autosomal recessive myogenic arthrogryposis multiplex congenita	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	muscle_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017893	inherited acute myeloid leukemia	hematologic_disorder|hereditary_disease|musculoskeletal_system_disorder|immune_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|hematologic_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|acute_disease|immune_system_disorder	hematology|genetics_and_genomics|oncology	cancer|inherited	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0017894	acute myeloid leukemia with CEBPA somatic mutations	hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|acute_disease|immune_system_disorder	hematology|genetics_and_genomics|oncology	anemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0017895	familial papillary or follicular thyroid carcinoma	endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor	endocrinology|oncology	familial_papillary_or_follicular_thyroid_carcinoma_can_also_be_classified_under_autoimmune_diseases|cancer	thyroid_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0017896	familial nonmedullary thyroid carcinoma	endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor	endocrinology|genetics_and_genomics|oncology	cancer|thyroid_carcinoma	endocrine_disorder	false	true	false	false	medium
MONDO:0017904	steroid dehydrogenase deficiency-dental anomalies syndrome	metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease	genetics_and_genomics|pediatric|endocrinology	adrenal_gland_disease|metabolic_disorder	teeth_disorder	false	false	false	false	medium
MONDO:0017906	amyloidosis cutis dyschromia	metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|metabolic_disease	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|liver_disorder	false	false	false	false	low
MONDO:0017907	primary lymphoma of the conjunctiva	nervous_system_disorder|disorder_of_visual_system|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_orbital_region|disorder_of_visual_system|hematologic_disorder|nervous_system_disorder	oncology|ophthalmology|hematology	autoimmune_diseases|cancer|inflammatory_disease	eye_disorder_lymphatic_disorder	true	true	false	true	low
MONDO:0017909	inherited glutathione synthetase deficiency	immune_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|immune_system_disorder|metabolic_disease	genetics_and_genomics|hepatology|pediatric	inherited_disorder_is_implied_but_not_listed_so_this_is_the_best_match|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0017910	dehydrated hereditary stomatocytosis	hematologic_disorder	anemia	hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	hereditary_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0017913	pure or complex hereditary spastic paraplegia	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017917	maternally-inherited spastic paraplegia	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0017918	white matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|intellectual_disability_syndrome_does_not_exist_so_mental_health_disorder_is_a_better_fit_than_this|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0017919	exstrophy-epispadias complex	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|urinary_system_disorder	urology|pediatric	metabolic_disorder|neurodegenerative_disease	kidney_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017920	deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	otolaryngology|genetics_and_genomics|pediatric	metabolic_disorder|genetic_condition	joint_disorder|ear_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0017921	hearing loss-familial salivary gland insensitivity to aldosterone syndrome	syndromic_disease	other	syndromic_disease	otolaryngology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	endocrine_disorder|ear_disorder	false	false	false	false	high
MONDO:0017923	multiple synostoses syndrome	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0017924	central nervous system calcification-deafness-tubular acidosis-anemia syndrome	syndromic_disease	other	syndromic_disease	neurology|renal_medicine|hematology|genetics_and_genomics	anemia|metabolic_disorder	brain_disorder|kidney_disorder|blood_bone_marrow_disorder|ear_disorder	true	false	false	false	high
MONDO:0017925	T-cell immunodeficiency with epidermodysplasia verruciformis	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	immunology|pediatric|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder_lymphatic_disorder_skin_disorder	true	false	false	false	very_high
MONDO:0017926	multiple paragangliomas associated with polycythemia	nervous_system_disorder|endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|endocrine_system_disorder|nervous_system_disorder|hereditary_disease	hematology|genetics_and_genomics|oncology	anemia|metabolic_disorder|cancer	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0017927	severe lateral tibial bowing with short stature	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|short_stature	joint_disorder|growth_disorder|bone_disorder	false	false	false	false	high
MONDO:0017928	9p13 microdeletion syndrome	nervous_system_disorder|psychiatric_disorder|syndromic_disease|chromosomal_disorder	psychiatric_disorder	syndromic_disease|psychiatric_disorder|nervous_system_disorder|chromosomal_disorder	genetics_and_genomics|pediatric	intellectual_disability|neurodegenerative_disease|developmental_disorder	brain_disorder|developmental_disorder	false	false	false	false	medium
MONDO:0017929	congenital achiasma	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	ophthalmology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0017930	mixed sclerosing bone dystrophy with extra-skeletal manifestations	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0017931	hereditary inclusion body myopathy type 4	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	hereditary_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0017932	muscular hypertrophy-hepatomegaly-polyhydramnios syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|hepatology|pediatric|endocrinology	metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017933	hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation	hereditary_disease|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	renal_medicine|genetics_and_genomics|cardiology	metabolic_disorder|cardiovascular_disorder	kidney_disorder|heart_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0017934	aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	otolaryngology|neurology|ophthalmology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|eye_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0017935	hyperinsulinism due to HNF1A deficiency	digestive_system_disorder|endocrine_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|endocrine_disorders	kidney_disorder|endocrine_disorder|liver_disorder	false	false	true	true	high
MONDO:0017936	benign Samaritan congenital myopathy	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|congenital_myopathy|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	low
MONDO:0017937	autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017939	classic multiminicore myopathy	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	muscle_disorder	false	false	false	true	high
MONDO:0017940	autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0017941	chikungunya	infectious_disease	infectious_disease	infectious_disease	hematology|rheumatology|pediatric|dermatology	autoimmune_diseases|inflammatory_disease	joint_disorder	true	false	false	false	medium
MONDO:0017942	Hendra virus infection	infectious_disease|nervous_system_disorder|inflammatory_disease	infectious_disease	inflammatory_disease|acute_disease|nervous_system_disorder|infectious_disease	neurology|veterinary_science	autoimmune_diseases|neurodegenerative_disease	immune_disorder|muscle_disorder	true	false	false	false	high
MONDO:0017943	autoerythrocyte sensitization syndrome	immune_system_disorder	autoimmune_disease	immune_system_disorder	allergy_and_immunology|hematology|dermatology	anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0017944	invasive non-typhoidal salmonellosis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|pediatric	autoimmune_diseases|gastrointestinal_disease|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0017945	ABetaL34V amyloidosis	nervous_system_disorder|cardiovascular_disorder|hereditary_disease|metabolic_disease	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|other____corrected_list_to_remove__other__since_it_is_not_one_of_the_best_fitting_categories___brain_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0017946	ABeta amyloidosis, Iowa type	nervous_system_disorder|cardiovascular_disorder|hereditary_disease|metabolic_disease	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0017947	ABeta amyloidosis, Italian type	nervous_system_disorder|cardiovascular_disorder|hereditary_disease|metabolic_disease	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0017948	ABetaA21G amyloidosis	nervous_system_disorder|cardiovascular_disorder|hereditary_disease|metabolic_disease	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	brain_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0017949	ABeta amyloidosis, Arctic type	nervous_system_disorder|cardiovascular_disorder|hereditary_disease|metabolic_disease	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	brain_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0017951	trichorhinophalangeal syndrome	syndromic_disease|hereditary_disease|integumentary_system_disorder|musculoskeletal_system_disorder	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|integumentary_system_disorder	orthopaedic|genetics_and_genomics|pediatric|dermatology	rare_disease|genetic_disorder|neurodegenerative_disease|developmental_disorder	joint_disorder|bone_disorder|skin_disorder	false	false	false	false	medium
MONDO:0017953	hereditary periodic fever syndrome	syndromic_disease|hereditary_disease|connective_tissue_disorder	other	syndromic_disease|connective_tissue_disorder|hereditary_disease	pediatrics|genetics_and_genomics|rheumatology|immunology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder|liver_disorder	false	false	false	true	medium
MONDO:0017958	magic syndrome	syndromic_disease|connective_tissue_disorder	other	syndromic_disease|connective_tissue_disorder	neurology|psychiatry	autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	vascular_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0017967	testicular agenesis	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder	urology|genetics_and_genomics|pediatric	reproductive_system_abnormality|cancer|developmental_disorder	male_reproductive_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0017968	46,XY ovotesticular disorder of sex development	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	urology|genetics_and_genomics|pediatric|obstetrics_and_gynecology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0017972	classic congenital lipoid adrenal hyperplasia due to STAR deficency	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|metabolic_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease|reproductive_system_disorder|hereditary_disease	endocrinology|renal_medicine|genetics_and_genomics|pediatric	adrenal_gland_disease|metabolic_disorder|anemia	endocrine_disorder|skin_disorder	false	false	false	true	high
MONDO:0017973	non-classic congenital lipoid adrenal hyperplasia due to STAR deficency	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|metabolic_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease|reproductive_system_disorder|hereditary_disease	endocrinology|renal_medicine|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|anemia	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0017975	sex chromosome disorder of sex development	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	endocrinology|genetics_and_genomics|pediatric|obstetrics_and_gynecology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0017979	autoimmune lymphoproliferative syndrome	immune_system_disorder|syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor|autoimmune_disease	syndromic_disease|immune_system_disorder|hereditary_disease|cancer_or_benign_tumor	immunology|hematology|oncology	autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0017980	syngnathia multiple anomalies	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0017981	syngnathia-cleft palate syndrome	hereditary_disease	other	hereditary_disease	otolaryngology|genetics_and_genomics|pediatric	neurodegenerative_disease|developmental_disorder	teeth_disorder|cleft_palate_syndrome	false	false	false	false	medium
MONDO:0017983	humero-radio-ulnar synostosis	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric	autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0017985	congenital radioulnar synostosis	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric	neurodevelopmental_disease|musculoskeletal_disorder|congenital_condition	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0017986	disorder of plasmalogens biosynthesis	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hematology|hepatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0017987	syringomyelia	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology|pediatric	inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0017988	multifocal atrial tachycardia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiology	cardiovascular_disorder|autoimmune_diseases	heart_disorder|vascular_disorder	false	false	false	false	low
MONDO:0017989	His bundle tachycardia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|cardiology|cardiothoracic	cardiac_disease|cardiovascular_disorder	heart_disorder	false	false	false	true	very_high
MONDO:0017990	catecholaminergic polymorphic ventricular tachycardia	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	cardiology|genetics_and_genomics|pediatric	cardiovascular_disorder|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0017991	Takayasu arteritis	cardiovascular_disorder|syndromic_disease|inflammatory_disease|respiratory_system_disorder|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	cardiovascular_disorder	otorhinolaryngologic_disease|inflammatory_disease|respiratory_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	rheumatology|cardiothoracic	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0017992	autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis	hereditary_disease|syndromic_disease|metabolic_disease|immune_system_disorder|connective_tissue_disorder	metabolic_disease	connective_tissue_disorder|immune_system_disorder|metabolic_disease|hereditary_disease|syndromic_disease	allergy_and_immunology|rheumatology|gastroenterology|genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|immune_disorder	true	false	false	false	high
MONDO:0017993	cerebral sinovenous thrombosis	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	hematology|neurology	inflammatory_disease|cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	true	high
MONDO:0017994	severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	endocrinology|genetics_and_genomics|pediatric	metabolic_disorder	obesity_insulin_resistance_syndrome|endocrine_disorder	false	false	true	true	very_high
MONDO:0017995	spondylocostal dysostosis-hypospadias-intellectual disability syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	genetics_and_genomics|orthopaedic|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0017997	telecanthus-hypertelorism-strabismus-pes cavus syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	ophthalmology|genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	bone_disorder|eye_disorder|spinal_disorder	false	false	false	as_of_my_last_knowledge_update_in_october_2023__there_are_no_known_efficacious_treatments_that_can_cure_telecanthus_hypertelorism_strabismus_pes_cavus_syndrome__the_syndrome_is_generally_a_genetic_condition__and_while_certain_symptoms_such_as_strabismus__eye_misalignment__might_be_treatable_with_surgery_or_other_interventions__there_is_no_comprehensive_treatment_that_addresses_all_aspects_of_the_syndrome__hence__i_would_return_false	medium
MONDO:0017998	PLA2G6-associated neurodegeneration	hereditary_disease|psychiatric_disorder|metabolic_disease|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0017999	fatty acid hydroxylase-associated neurodegeneration	hereditary_disease|psychiatric_disorder|syndromic_disease|metabolic_disease|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0018000	hereditary thrombocytosis with transverse limb defect	musculoskeletal_system_disorder|hematologic_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hematologic_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0018001	inverse Klippel-Trenaunay syndrome	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	dermatology|oncology|genetics_and_genomics|orthopaedic|pediatrics	metabolic_disorder|anemia	vascular_disorder__lymphatic_disorder	false	false	false	false	medium
MONDO:0018002	adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy	mitochondrial_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|musculoskeletal_system_disorder	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018003	limbic encephalitis with DPP6 antibodies	nervous_system_disorder|inflammatory_disease	other	acute_disease|nervous_system_disorder|inflammatory_disease	psychiatry|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	immune_disorder|brain_disorder|limbic_encephalitis_is_a_subset_of_brain_disorder_so_it_would_be_brain_disorder	true	false	false	true	high
MONDO:0018004	acute megakaryoblastic leukemia without down syndrome	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|acute_disease|immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0018005	spastic paraplegia-Paget disease of bone syndrome	nervous_system_disorder|syndromic_disease|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018006	adult-onset distal myopathy due to VCP mutation	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018007	mosaic genome-wide paternal uniparental disomy	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	genomic_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0018008	idiopathic giant cell myocarditis	musculoskeletal_system_disorder|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	acute_disease|idiopathic_disease|cardiovascular_disorder|musculoskeletal_system_disorder|inflammatory_disease	cardiology|cardiothoracic	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	immune_disorder|heart_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0018009	non-hypoproteinemic hypertrophic gastropathy	digestive_system_disorder	other	digestive_system_disorder	pediatric|gastroenterology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0018010	juvenile idiopathic inflammatory myopathy	musculoskeletal_system_disorder|inflammatory_disease	other	idiopathic_disease|musculoskeletal_system_disorder|inflammatory_disease	neurology|pediatric|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018011	juvenile overlap myositis	musculoskeletal_system_disorder|inflammatory_disease	other	idiopathic_disease|musculoskeletal_system_disorder|inflammatory_disease	pediatric|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018013	non-immunoglobulin-mediated membranoproliferative glomerulonephritis	inflammatory_disease|urinary_system_disorder	other	urinary_system_disorder|inflammatory_disease	renal_medicine|nephrology_is_not_listed__so_use___renal_medicine|hematology	inflammatory_disease|autoimmune_diseases	kidney_disorder|vascular_disorder	false	false	false	false	high
MONDO:0018014	transient neonatal multiple acyl-CoA dehydrogenase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	neonatology|pediatric|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	metabolic_disorder|liver_disorder	false	false	false	false	medium
MONDO:0018015	intermittent hydrarthrosis	connective_tissue_disorder	other	connective_tissue_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0018016	classic neuroendocrine tumor of appendix	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrinology|oncology|gastroenterology	cancer|neuroendocrine_tumor	endocrine_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0018017	goblet cell carcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0018018	wild type ATTR amyloidosis	musculoskeletal_system_disorder|cardiovascular_disorder|metabolic_disease	metabolic_disease|cardiovascular_disorder	metabolic_disease|cardiovascular_disorder|musculoskeletal_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	brain_disorder|heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0018019	lead poisoning	poisoning	other	poisoning	neurology|pediatric|hematology	anemia|neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0018020	mercury poisoning	poisoning	other	poisoning	neurology|toxicology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|immune_disorder|brain_disorder|liver_disorder	false	false	false	true	high
MONDO:0018021	hypotrichosis-deafness syndrome	syndromic_disease	other	syndromic_disease	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	deafness|ear_disorder|skin_disorder|note__i_corrected_the_response_to_reflect_that_hypotrichosis_is_a_skin_condition__so_it_should_be_included_in_addition_to_deafness____ear_disorder	false	false	false	false	medium
MONDO:0018022	hemoglobin Lepore-beta-thalassemia syndrome	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|lung_disorder	false	false	false	false	medium
MONDO:0018023	hemoglobin M disease	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|joint_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0018024	hydroa vacciniforme	inflammatory_disease|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018025	chronic actinic dermatitis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases|allergy	upper_gastrointestinal_disorder|skin_disorder	false	false	false	true	medium
MONDO:0018026	tetraploidy syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0018027	duplication/inversion 15q11	chromosomal_disorder	other	chromosomal_disorder	neurology|pediatric|genetics_and_genomics	developmental_disorder|autoimmune_diseases|genetic_disorder|congenital_disorder|mental_health_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0018028	tetrasomy 5p	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	upper_gastrointestinal_disorder|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018029	congenital factor XIII deficiency	hematologic_disorder	other	hematologic_disorder	pediatric|genetics_and_genomics|hematology	metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0018030	tetrasomy 9p	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	developmental_disorder|genetic_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018031	granulomatous slack skin disease	cancer_or_benign_tumor|hematologic_disorder|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|integumentary_system_disorder	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018034	thalidomide embryopathy	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics	birth_defect|congenital_abnormality|neurodegenerative_disease	reproductive_system_disorder|skeletal_disorder|nervous_system_disorder|joint_disorder|limb_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0018037	hyper-IgE syndrome	immune_system_disorder|hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease|immune_system_disorder	immunology|pediatric|rheumatology|allergy_and_immunology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	endocrine_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0018039	selective IgM deficiency	immune_system_disorder|hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease|immune_system_disorder	immunology|pediatric|allergy_and_immunology|genetics_and_genomics|hematology	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0018043	Thomas syndrome	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	heart_disorder|musculoskeletal_disorder|ear_disorder|brain_disorder|growth_disorder|eye_disorder	false	false	false	true	high
MONDO:0018044	idiopathic hypersomnia	other	other	idiopathic_disease|sleep_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	sleep_disorder|brain_disorder	false	false	false	false	high
MONDO:0018045	Hoyeraal-Hreidarsson syndrome	nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|integumentary_system_disorder|cancer_or_benign_tumor	cardiology|neurology|renal_medicine|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	blood_bone_marrow_disorder|kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0018046	thrombocytopenia-Robin sequence syndrome	hereditary_disease	other	hereditary_disease	pediatric|oncology|hematology	anemia|blood_disorder	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0018047	familial thrombomodulin anomalies	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	cardiovascular_disorder|metabolic_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0018048	heparin-induced thrombocytopenia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	immunology|allergy_and_immunology|hematology	autoimmune_diseases|inflammatory_disease|allergy|anemia	immune_disorder|vascular_disorder|liver_disorder	false	false	false	true	high
MONDO:0018050	tibial aplasia-ectrodactyly syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|anemia	joint_disorder|bone_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0018051	Jessner lymphocytic infiltration of the skin	integumentary_system_disorder	other	integumentary_system_disorder	immunology|dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0018053	trichothiodystrophy	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	syndromic_disease|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	hair_disorder|skin_disorder	false	false	false	false	high
MONDO:0018054	familial atrial fibrillation	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	genetics_and_genomics|cardiology	familial_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0018055	pediatric hepatocellular carcinoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	hepatology|pediatric|oncology|gastroenterology	pediatric|cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	true	very_high
MONDO:0018056	bullous lichen planus	inflammatory_disease|integumentary_system_disorder	other	inflammatory_disease|integumentary_system_disorder	dermatology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018058	tracheal agenesis	respiratory_system_disorder|otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease|respiratory_system_disorder	pulmonology|pediatric|otolaryngology	cardiovascular_disorder|respiratory_disorder|congenital_abnormality|genetic_disorder	lung_disorder|throat_disorder	false	false	false	false	very_high
MONDO:0018059	meningococcal meningitis	nervous_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|nervous_system_disorder|inflammatory_disease	neurology|pediatric|allergy_and_immunology|hematology	autoimmune_diseases|inflammatory_disease	spinal_disorder|brain_disorder	true	false	false	true	very_high
MONDO:0018060	congenital fibrinogen deficiency	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|hematology	inflammatory_disease|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0018061	trichodermodysplasia-dental alterations syndrome	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	teeth_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018062	autosomal dominant trichoodontoonychodysplasia-syndactyly	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|orthopaedic	genetic_disorder|metabolic_disorder	teeth_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0018063	nodular non-suppurative panniculitis	connective_tissue_disorder|inflammatory_disease|integumentary_system_disorder	other	connective_tissue_disorder|inflammatory_disease|integumentary_system_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018064	trigonocephaly-broad thumbs syndrome	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	joint_disorder|brain_disorder|bone_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018065	isolated trigonocephaly	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics	congenital_abnormality|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0018066	trisomy X	syndromic_disease|reproductive_system_disorder|chromosomal_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|chromosomal_disorder|syndromic_disease	pediatric|obstetrics_and_gynecology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|mental_health_disorder	immune_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0018067	triploidy	chromosomal_disorder	other	chromosomal_disorder	other___note__triploidy_is_a_genetic_condition_where_an_individual_has_three_sets_of_chromosomes_instead_of_the_usual_two__so_it_is_primarily_related_to_genetics_and_genomics__however__since_you_asked_for_categories_and__other__was_one_of_them__i_included_both|genetics_and_genomics	genetic_disorder|metabolic_disorder	genetic_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0018068	trisomy 13	syndromic_disease|chromosomal_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|chromosomal_disorder|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	immune_disorder|joint_disorder|spinal_disorder|heart_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0018069	distal trisomy 17q	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|medical_genetics	metabolic_disorder|neurodegenerative_disease	immune_disorder|joint_disorder|spinal_disorder|brain_disorder|vascular_disorder|muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0018070	familial multiple fibrofolliculoma	cancer_or_benign_tumor|syndromic_disease|hereditary_disease|integumentary_system_disorder	cancer_or_benign_tumor	hereditary_disease|integumentary_system_disorder|cancer_or_benign_tumor|syndromic_disease	urology|dermatology|genetics_and_genomics	cancer|adrenal_gland_disease	kidney_disorder|skin_disorder	false	false	false	false	low
MONDO:0018071	trisomy 18	syndromic_disease|chromosomal_disorder	other	chromosomal_disorder|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|joint_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0018072	persistent truncus arteriosus	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|cardiothoracic|cardiology	inflammatory_disease|cardiovascular_disorder|congenital_heart_defect	heart_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0018075	neural tube defect	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0018076	tuberculosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder|blood_bone_marrow_disorder	true	false	false	true	very_high
MONDO:0018077	tularemia	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric|dermatology|rheumatology|allergy_and_immunology|hematology|infectious_diseases	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|lung_disorder|immune_disorder|upper_gastrointestinal_disorder|throat_disorder|skin_disorder	true	false	false	true	medium
MONDO:0018078	soft tissue sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology|orthopaedic	cancer|adrenal_gland_disease	muscle_disorder|soft_tissue_sarcoma	false	true	false	true	high
MONDO:0018079	thymic epithelial neoplasm	immune_system_disorder|hematologic_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	immunology|oncology	autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	false	true	false	false	high
MONDO:0018081	hemorrhagic fever-renal syndrome	infectious_disease	infectious_disease	infectious_disease	hepatology|pulmonology|renal_medicine|hematology|cardiology	autoimmune_diseases|inflammatory_disease	lung_disorder|kidney_disorder|immune_disorder	true	false	false	true	medium
MONDO:0018082	aorto-ventricular tunnel	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|cardiology	autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0018083	transient tyrosinemia of the newborn	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hematology|pediatric|genetics_and_genomics|hepatology	metabolic_disorder|adrenal_gland_disease	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	none
MONDO:0018084	Uhl anomaly	cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder	cardiothoracic|pediatric|pulmonology	cardiovascular_disorder|congenital_heart_disease	liver_disorder	false	false	false	false	high
MONDO:0018085	umbilical cord ulceration-intestinal atresia syndrome	syndromic_disease|digestive_system_disorder	other	digestive_system_disorder|syndromic_disease	pediatric|obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|intestinal_abnormality|genetic_condition|congenital_anomaly	lower_gastrointestinal_disorder_upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0018086	ulerythema ophryogenesis	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	neurology|dermatology	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	skin_disorder|eye_disorder	true	false	false	false	medium
MONDO:0018087	viral hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	hematology|pediatric|hepatology	inflammatory_disease|viral_hemorrhagic_fever	immune_disorder|liver_disorder|vascular_disorder	true	false	false	true	very_high
MONDO:0018088	familial Mediterranean fever	immune_system_disorder|connective_tissue_disorder|syndromic_disease|hereditary_disease	other	immune_system_disorder|hereditary_disease|syndromic_disease|connective_tissue_disorder	rheumatology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder|joint_disorder	false	false	false	true	medium
MONDO:0018089	double outlet right ventricle	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic|pediatric	cardiovascular_disorder|congenital_heart_disease	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0018090	double outlet left ventricle	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic|pediatric	cardiovascular_disorder|congenital_heart_defect	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0018091	microcephaly-brachydactyly-kyphoscoliosis syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018092	Vogt-Koyanagi-Harada disease	disorder_of_visual_system|inflammatory_disease	other	inflammatory_disease|disorder_of_orbital_region|disorder_of_visual_system	dermatology|rheumatology|ophthalmology	autoimmune_diseases|inflammatory_disease	immune_disorder|eye_disorder	false	false	false	false	high
MONDO:0018093	arbovirus fever	infectious_disease	infectious_disease	infectious_disease	pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|vascular_disorder	true	false	false	false	medium
MONDO:0018094	Waardenburg syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0018095	Weaver-Williams syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder|neurodegenerative_disease	immune_disorder|muscle_disorder|kidney_disorder|brain_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|skin_disorder|vascular_disorder|eye_disorder|heart_disorder|joint_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0018096	Weill-Marchesani syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	rheumatology|orthopaedic|genetics_and_genomics|ophthalmology	metabolic_disorder|genetic_disorder|connective_tissue_disease	muscle_disorder|bone_disorder|skin_disorder|eye_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0018097	infantile spasms	syndromic_disease|nervous_system_disorder	other	nervous_system_disorder|syndromic_disease	neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0018098	autosomal dominant limb-girdle muscular dystrophy type 1E (DES)	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	neurology|orthopaedic|genetics_and_genomics	muscular_dystrophy|neurodegenerative_disease	muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0018100	familial primary hypomagnesemia	urinary_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	urinary_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|renal_medicine	metabolic_disorder|familial_disorder	kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0018101	familial primary hypomagnesemia with normocalciuria and normocalcemia	urinary_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	urinary_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|renal_medicine|endocrinology	hormonal_disorders|metabolic_disorder|familial_diseases|electrolyte_disorders	kidney_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0018102	corneal dystrophy	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0018103	Quinquaud's folliculitis decalvans	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|hair_disorder	true	false	false	false	high
MONDO:0018105	Wolfram syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|endocrinology	neurodegenerative_disease|metabolic_disorder	eye_disorder|bone_disorder|brain_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0018106	hereditary xanthinuria	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|renal_medicine|pediatric	metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0018108	idiopathic disseminated cytomegalovirus infection	infectious_disease	infectious_disease	idiopathic_disease|infectious_disease	hematology|immunology|pediatric	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	false	high
MONDO:0018109	fulminant viral hepatitis	digestive_system_disorder|endocrine_system_disorder|inflammatory_disease	endocrine_system_disorder	inflammatory_disease|digestive_system_disorder|endocrine_system_disorder	hepatology|gastroenterology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|liver_disorder	true	false	false	true	very_high
MONDO:0018111	idiopathic severe pneumococcemia	infectious_disease	infectious_disease	idiopathic_disease|infectious_disease	hematology|pulmonology	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|lung_disorder	true	false	false	false	very_high
MONDO:0018115	epidermal nevus syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|dermatology	genetic_condition|dermatological_condition	skin_disorder|vascular_disorder|immune_disorder	false	false	false	false	high
MONDO:0018116	galactosemia	hereditary_disease|metabolic_disease|disorder_of_visual_system	metabolic_disease	disorder_of_orbital_region|disorder_of_visual_system|metabolic_disease|hereditary_disease	hepatology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0018117	disorder of phospholipids, sphingolipids and fatty acids biosynthesis	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|biochemistry	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	liver_disorder|metabolic_disorder|genetic_disorder	false	false	false	false	high
MONDO:0018121	mitochondrial DNA maintenance syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	metabolic_disease	metabolic_disease|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatrics|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	mitochondrial_disease|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0018122	digital anomalies-intellectual disability-short stature syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|endocrinology|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0018123	intellectual disability-obesity-brain malformations-facial dysmorphism syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	obesity|intellectual_disability|brain_disorder|facial_dysmorphism	false	false	false	false	very_high
MONDO:0018124	Oncogenic osteomalacia	syndromic_disease|musculoskeletal_system_disorder|urinary_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	urinary_system_disorder|cancer_or_benign_tumor|syndromic_disease|musculoskeletal_system_disorder|endocrine_system_disorder	oncology|orthopaedic|endocrinology	cancer|metabolic_disorder|inflammatory_disease	muscle_disorder|bone_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0018125	focal epilepsy-intellectual disability-cerebro-cerebellar malformation	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0018126	progressive myoclonic epilepsy with dystonia	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0018127	16q24.1 microdeletion syndrome	respiratory_system_disorder|chromosomal_disorder	other	chromosomal_disorder|respiratory_system_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	spinal_disorder|developmental_disorder_is_not_in_the_list_so__brain_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0018128	phalangeal microgeodic syndrome	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|rheumatology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0018129	autosomal recessive cerebellar ataxia with late-onset spasticity	hereditary_disease|nervous_system_disorder|metabolic_disease	neurodegenerative_disease|metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0018130	brain dopamine-serotonin vesicular transport disease	nervous_system_disorder|hereditary_disease|syndromic_disease|metabolic_disease	metabolic_disease	nervous_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease	genetics_and_genomics|psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0018131	neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion	chromosomal_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	nervous_system_disorder|chromosomal_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|cardiology|neurology	congenital_disorder|neurodegenerative_disease|cardiovascular_disorder	joint_disorder|heart_disorder|brain_disorder|bone_disorder	false	false	false	false	high
MONDO:0018133	attenuated Chédiak-Higashi syndrome	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0018134	disorder of melanin metabolism	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|dermatology	metabolic_disorder|adrenal_gland_disease	skin_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0018135	oculocutaneous albinism type 1	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|integumentary_system_disorder	genetics_and_genomics|pediatric|ophthalmology|dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0018136	minimal pigment oculocutaneous albinism type 1	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|integumentary_system_disorder	genetics_and_genomics|ophthalmology|dermatology	genetic_disorder|anemic_disease|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0018137	temperature-sensitive oculocutaneous albinism type 1	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|integumentary_system_disorder	genetics_and_genomics|ophthalmology|dermatology	genetic_disorder|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0018141	pyruvate carboxylase deficiency, infantile form	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|pediatric|endocrinology|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder	false	false	false	true	very_high
MONDO:0018142	pyruvate carboxylase deficiency, severe neonatal type	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0018143	pyruvate carboxylase deficiency, benign type	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder	false	false	false	true	low
MONDO:0018145	congenital retinal arteriovenous communication	nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|pediatric|ophthalmology	cardiovascular_disorder|inflammatory_disease	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0018146	idiopathic macular telangiectasia type 1	disorder_of_visual_system	other	idiopathic_disease|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology	eye_disease|metabolic_disorder	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0018147	idiopathic macular telangiectasia type 3	disorder_of_visual_system	other	idiopathic_disease|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology	metabolic_disorder	eye_disorder|vascular_disorder	false	false	false	false	high
MONDO:0018148	vasoproliferative tumor of retina	nervous_system_disorder|disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|cardiovascular_disorder	oncology|ophthalmology	autoimmune_diseases|cancer|inflammatory_disease	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0018149	GM1 gangliosidosis	hereditary_disease|musculoskeletal_system_disorder|disorder_of_visual_system|metabolic_disease	metabolic_disease	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0018150	Gaucher disease	hereditary_disease|disorder_of_visual_system|metabolic_disease	metabolic_disease	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease|metabolic_disease	genetics_and_genomics|orthopaedic|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|spleen_disorder|blood_bone_marrow_disorder|joint_disorder	false	false	false	true	high
MONDO:0018151	coenzyme Q10 deficiency	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|mitochondrial_disease|metabolic_disease	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|cardiology|neurology	metabolic_disorder|neurodegenerative_disease|cardiovascular_disorder	liver_disorder|muscle_disorder	false	false	false	true	high
MONDO:0018152	serpiginous choroiditis	inflammatory_disease|disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease|cardiovascular_disorder	ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|immune_disorder	true	false	false	false	high
MONDO:0018153	Erdheim-Chester disease	immune_system_disorder|syndromic_disease	other	syndromic_disease|immune_system_disorder	renal_medicine|nephrology	autoimmune_diseases|cancer|inflammatory_disease	kidney_disorder|vascular_disorder	false	true	false	false	high
MONDO:0018154	Madelung deformity	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|general_surgery|trauma	metabolic_disorder|autoimmune_diseases|inflammatory_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0018155	lateral sclerosis	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|otolaryngology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0018156	3q26q27 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0018158	mitochondrial DNA depletion syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_disease_category_is_often_implied_in_this_disorder_but_it_is_more_specific_to_the_mitochondrial_dna_depletion_so_i_went_for_the_closest_one__muscle_disorder	false	false	false	false	very_high
MONDO:0018159	atypical hemolytic-uremic syndrome with DGKE deficiency	hematologic_disorder|hereditary_disease|immune_system_disorder|syndromic_disease	other	syndromic_disease|immune_system_disorder|hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics|renal_medicine	metabolic_disorder|anemia|autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder	false	false	false	true	high
MONDO:0018160	hereditary retinoblastoma	nervous_system_disorder|hereditary_disease|cancer_or_benign_tumor|disorder_of_visual_system|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_orbital_region|disorder_of_visual_system|syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology|oncology	hereditary_disease_category_is_not_listed_but_a_similar_sounding_one_is_cancer|cancer	eye_disorder	false	true	false	true	high
MONDO:0018161	non-hereditary retinoblastoma	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology|oncology	neurodegenerative_disease|cancer	eye_disorder	false	true	false	true	high
MONDO:0018162	neurometabolic disorder due to serine deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0018163	autosomal recessive cutis laxa type 2A	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder|integumentary_system_disorder	genetics_and_genomics|pediatric|dermatology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|skin_disorder	false	false	false	false	high
MONDO:0018164	arterial thoracic outlet syndrome	cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder	cardiothoracic|pulmonology|cardiology	arterial_thoracic_outlet_syndrome|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0018165	venous thoracic outlet syndrome	cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder	cardiothoracic|hematology|vascular_medicine	cardiovascular_disorder|inflammatory_disease	spinal_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0018166	oral submucous fibrosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	oral_pathology|general_medicine|otolaryngology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|immune_disorder|vascular_disorder|teeth_disorder	false	false	false	true	high
MONDO:0018167	primary essential cutis verticis gyrata	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|neurology	autoimmune_diseases|neurodegenerative_disease	skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0018168	primary non-essential cutis verticis gyrata	integumentary_system_disorder	other	integumentary_system_disorder	neurology|dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	muscle_disorder|skin_disorder	false	false	false	false	low
MONDO:0018169	morning glory syndrome	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder	psychiatric_disorder|disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	pediatrics|genetics_and_genomics|obstetrics_and_gynecology|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0018170	idiopathic nephrotic syndrome	urinary_system_disorder|syndromic_disease	other	idiopathic_disease|urinary_system_disorder|syndromic_disease	renal_medicine|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	urinary_tract_disorder|kidney_disorder|immune_disorder	false	false	false	false	medium
MONDO:0018171	malignant germ cell tumor of ovary	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0018172	malignant sex cord stromal tumor of ovary	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0018173	acute opioid poisoning	poisoning	other	acute_disease|poisoning	hematology|pediatric|psychiatry|pulmonology|neurology	mental_health_disorder|metabolic_disorder	upper_gastrointestinal_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0018174	hereditary glaucoma	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	genetics_and_genomics|ophthalmology	hereditary_disease_is_not_listed_so_choose_from_the_list_provided__metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0018175	combined deficiency of factor V and factor VIII	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|hematology|pediatric	anemia|metabolic_disorder	vascular_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0018177	glioblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0018178	intestinal lymphangiectasia	digestive_system_disorder	other	digestive_system_disorder	hematology|pediatric|oncology|gastroenterology	autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0018180	staphylococcal scarlet fever	infectious_disease	infectious_disease	infectious_disease	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0018181	staphylococcal scalded skin syndrome	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0018182	bullous impetigo	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0018183	staphylococcal necrotizing pneumonia	respiratory_system_disorder|infectious_disease	infectious_disease	respiratory_system_disorder|infectious_disease	cardiothoracic|pulmonology	autoimmune_diseases|inflammatory_disease	lung_disorder|lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0018184	gastric linitis plastica	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	autoimmune_diseases|cancer|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0018189	autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0018190	autosomal dominant childhood-onset proximal spinal muscular atrophy	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018192	paratesticular adenocarcinoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	neurology|oncology	other_is_removed|adrenal_gland_disease|cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0018193	testicular teratoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	pediatric|urology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	true	medium
MONDO:0018197	mitochondrial DNA depletion syndrome, hepatocerebrorenal form	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|urinary_system_disorder|mitochondrial_disease	metabolic_disease	urinary_system_disorder|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	genetics_and_genomics|neurology|hepatology	neurodegenerative_disease|hepatic_disorder|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0018198	acute encephalopathy with biphasic seizures and late reduced diffusion	nervous_system_disorder	other	acute_disease|nervous_system_disorder	pediatric|psychiatry|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder	true	false	false	false	high
MONDO:0018199	new-onset refractory status epilepticus	nervous_system_disorder	other	nervous_system_disorder	pediatric|psychiatry|neurology	autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0018201	extragonadal germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|urology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	true	high
MONDO:0018202	gonadal germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|pediatric|urology|oncology	gonadal_gland_disease|cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	true	medium
MONDO:0018203	LMNA-related cardiocutaneous progeria syndrome	cardiovascular_disorder|premature_aging_syndrome|hereditary_disease	cardiovascular_disorder	premature_aging_syndrome|cardiovascular_disorder|hereditary_disease	cardiology|pediatric|genetics_and_genomics|dermatology	metabolic_disorder|cardiovascular_disorder	skin_disorder|muscle_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0018204	20q11.2 microduplication syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	neurology|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018205	distal monosomy 1q	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018206	childhood-onset autosomal recessive myopathy with external ophthalmoplegia	inflammatory_disease|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease|hereditary_disease	neurology|pediatric|ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0018207	2p13.2 microdeletion syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0018208	neurofibromatosis type 1 due to NF1 mutation or intragenic deletion	cancer_or_benign_tumor|syndromic_disease|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder|syndromic_disease|hereditary_disease	neurology|pediatric|oncology|neurofibromatosis_type_1_disease_group|genetics_and_genomics	cancer|neurodegenerative_disease	brain_disorder|skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0018209	Alexander disease type I	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018210	Alexander disease type II	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018211	Balint syndrome	nervous_system_disorder	other	nervous_system_disorder	psychiatry|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018212	familial cervical artery dissection	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	cardiology|neurology|genetics_and_genomics	adrenal_gland_disease|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0018213	hereditary sensory and autonomic neuropathy type 1	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0018214	generalized epilepsy with febrile seizures plus	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	neurological_disorder|brain_disorder	false	false	false	true	high
MONDO:0018215	paraneoplastic neurologic syndrome	cancer_or_benign_tumor|syndromic_disease|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|syndromic_disease	neurology|oncology	autoimmune_diseases|cancer	brain_disorder|immune_disorder	false	false	false	false	high
MONDO:0018216	Koolen-de Vries syndrome due to 17q21.31 microdeletion syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|developmental_disorder___note__the_corrected_answer_is_based_on_my_research_that_koelen_de_vries_syndrome_due_to_17q21_31_microdeletion_is_a_neurodevelopmental_disorder__specifically_affecting_brain_development_and_function	false	false	false	false	high
MONDO:0018217	Koolen-de Vries syndrome due to a point mutation	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|skin_disorder	false	false	false	false	high
MONDO:0018218	autosomal recessive cerebral atrophy	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018221	immune hydrops fetalis	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	immune_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0018223	systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|post_infectious_disorder|immune_system_disorder	pediatric|oncology|hematology	autoimmune_diseases|cancer	immune_disorder_lymphatic_disorder	true	true	false	false	very_high
MONDO:0018224	hydroa vacciniforme-like lymphoma	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|post_infectious_disorder|immune_system_disorder	oncology|hematology|dermatology	autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder	false	true	false	false	medium
MONDO:0018225	ALK-positive large B-cell lymphoma	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	oncology|hematology	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0018226	infantile epileptic-dyskinetic encephalopathy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018227	hypocomplementemic urticarial vasculitis	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	rheumatology|dermatology	autoimmune_diseases|inflammatory_disease|allergy	immune_disorder|vascular_disorder|skin_disorder	false	false	false	false	high
MONDO:0018228	bipartite talus	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|orthopaedic	inflammatory_disease|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0018229	Stevens-Johnson syndrome	integumentary_system_disorder|syndromic_disease	other	syndromic_disease|integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0018230	skeletal dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|skeletal_dysplasia	bone_disorder|joint_disorder|skeletal_disorder	false	false	false	false	high
MONDO:0018233	otopalatodigital syndrome spectrum disorder	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	teeth_disorder|eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0018234	dysostosis	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disorder	bone_disorder|skeletal_system_disorder	false	false	false	false	medium
MONDO:0018237	acrofacial dysostosis	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	genetic_disease|metabolic_disorder	face_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0018240	TRPV4-related bone disorder	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	rheumatology|orthopaedic|genetics_and_genomics	inflammatory_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0018242	autoimmune hypoparathyroidism	endocrine_system_disorder|immune_system_disorder	endocrine_system_disorder|autoimmune_disease	endocrine_system_disorder|immune_system_disorder	endocrinology|autoimmune	autoimmune_diseases|inflammatory_disease|metabolic_disorder	autoimmune_disorder_is_not_in_the_list_so_it_will_be_excluded|endocrine_disorder|immune_disorder	false	false	false	true	medium
MONDO:0018243	intellectual disability-hyperkinetic movement-truncal ataxia syndrome	nervous_system_disorder	other	nervous_system_disorder	pediatric|genetics_and_genomics|neurology	intellectual_disability_is_not_in_the_list_so_it_will_be_ignored|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018244	obesity due to SIM1 deficiency	endocrine_system_disorder|hereditary_disease|nutritional_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|nutritional_disorder	pediatric|endocrinology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0018245	2p21 microdeletion syndrome without cystinuria	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	true	high
MONDO:0018247	CADDS	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|hereditary_disease|metabolic_disease	cardiology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0018248	intellectual disability-seizures-macrocephaly-obesity syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|psychiatry|neurology	metabolic_disorder|neurodegenerative_disease|or___metabolic_disorder	brain_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0018249	finger hyperphalangy - toe anomalies - severe pectus excavatum syndrome	syndromic_disease	other	syndromic_disease	orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0018250	diffuse palmoplantar keratoderma with painful fissures	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	pediatric|rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	high
MONDO:0018252	focal palmoplantar keratoderma with joint keratoses	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	rheumatology|dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0018253	intellectual disability-facial dysmorphism-hand anomalies syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|psychiatry|pediatric|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|hand_anomalies|intellectual_disability|facial_dysmorphism	false	false	false	false	high
MONDO:0018254	spondyloepimetaphyseal dysplasia, Isidor type	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0018255	spondylometaphyseal dysplasia, Czarny-Ratajczak type	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0018256	acute myeloid leukemia with t(8;16)(p11;p13) translocation	hematologic_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder|acute_disease|connective_tissue_disorder	oncology|hematology	anemia|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0018257	familial syringomyelia	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	familial_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018258	Angora hair nevus	integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|cancer	hair_disorder|skin_disorder	false	false	false	false	low
MONDO:0018259	didymosis aplasticosebacea	integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder	hematology|genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|bone_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018260	scalp syndrome	disorder_of_development_or_morphogenesis|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|disorder_of_development_or_morphogenesis	pediatrics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|scalp_syndrome_does_not_directly_relate_to_the_other_categories_in_the_list_so_i_ll_exclude_it_from_this_answer	true	false	false	false	high
MONDO:0018261	Nevada syndrome	disorder_of_development_or_morphogenesis|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0018263	fetal carbamazepine syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder	false	false	false	false	high
MONDO:0018264	oculocutaneous albinism type 6	metabolic_disease|integumentary_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|integumentary_system_disorder|hereditary_disease	ophthalmology|dermatology|genetics_and_genomics	metabolic_disorder|skin_condition|genetic_disease	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0018266	ataxia - telangiectasia variant	nervous_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|ataxia_variant_implies_a_neurological_component|neurodegenerative_disease	brain_disorder|immune_disorder	true	false	false	false	high
MONDO:0018267	combined cervical dystonia	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	orthopaedic|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	true	high
MONDO:0018268	Medich giant platelet syndrome	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|anemia	blood_bone_marrow_disorder|vascular_disorder|immune_disorder	false	false	false	false	high
MONDO:0018269	white platelet syndrome	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	autoimmune_diseases|anemia|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0018270	extraskeletal Ewing sarcoma	cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease	orthopaedic|oncology|pediatric	adrenal_gland_disease|cancer	bone_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0018271	peripheral primitive neuroectodermal tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neuroectodermal_tumor|cancer	brain_disorder|nervous_system_disorder	false	true	false	true	high
MONDO:0018273	XYLT1-congenital disorder of glycosylation	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder	joint_disorder|skeletal_disorder	false	false	true	true	high
MONDO:0018274	GM3 synthase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0018276	muscular dystrophy-dystroglycanopathy	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018278	congenital muscular dystrophy with intellectual disability	metabolic_disease|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018280	muscle-eye-brain disease with bilateral multicystic leucodystrophy	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|muscle_disorder|eye_disorder	true	false	false	false	very_high
MONDO:0018281	congenital muscular dystrophy with hyperlaxity	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	orthopaedic|rheumatology|neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018282	neuromuscular disease caused by qualitative or quantitative defects of alpha-dystroglycan	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	true	false	false	true	very_high
MONDO:0018298	multicentric osteolysis-nodulosis-arthropathy spectrum	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|rheumatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	joint_disorder|bone_disorder|immune_disorder	false	false	false	false	high
MONDO:0018301	interstitial cystitis	inflammatory_disease|connective_tissue_disorder|urinary_system_disorder	other	connective_tissue_disorder|urinary_system_disorder|inflammatory_disease	urology|renal_medicine	autoimmune_diseases|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0018302	acquired kinky hair syndrome	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	hair_disorder_is_not_in_the_list_so_i_will_leave_it_out|skin_disorder	false	false	false	false	low
MONDO:0018304	Schnitzler syndrome	syndromic_disease|connective_tissue_disorder	other	syndromic_disease|connective_tissue_disorder	dermatology|allergy_and_immunology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	high
MONDO:0018305	chronic granulomatous disease	immune_system_disorder|inflammatory_disease|hematologic_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder|hematologic_disorder|inflammatory_disease	immunology|allergy_and_immunology|genetics_and_genomics|hematology	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	true	false	false	true	high
MONDO:0018306	Griscelli syndrome	syndromic_disease|metabolic_disease|integumentary_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|syndromic_disease|metabolic_disease|integumentary_system_disorder	neurology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	blood_bone_marrow_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0018307	neurodegeneration with brain iron accumulation	metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	hereditary_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018308	liver mesenchymal hamartoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	pediatric|hepatology|oncology|gastroenterology	tumor|cancer	lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	low
MONDO:0018309	Hirschsprung disease	disorder_of_development_or_morphogenesis|digestive_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|digestive_system_disorder	pediatric|genetics_and_genomics|gastroenterology	metabolic_disorder|gastrointestinal_disease	lower_gastrointestinal_disorder|intestinal_disorder|gastrointestinal_disorder	false	false	false	true	high
MONDO:0018310	Langerhans cell histiocytosis	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	immunology|pediatric|hematology|oncology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0018311	acromelanosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|endocrinology|rheumatology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|skin_disorder|joint_disorder	false	false	false	false	low
MONDO:0018312	histoplasmosis	infectious_disease	infectious_disease	infectious_disease	allergy_and_immunology|pulmonology|immunology|hematology	allergy|autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	true	false	false	true	medium
MONDO:0018314	infantile-onset mesial temporal lobe epilepsy with severe cognitive regression	nervous_system_disorder	other	nervous_system_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder|severe_cognitive_regression|cognitive_disorder	false	false	false	false	very_high
MONDO:0018315	X-linked osteoporosis with fractures	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|rheumatology|genetics_and_genomics	metabolic_disorder	muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0018316	fatal post-viral neurodegenerative disorder	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|fatal_post_viral_neurodegenerative_disorder	muscle_disorder|brain_disorder|spinal_disorder|neurodegenerative_disorder	true	false	false	false	very_high
MONDO:0018317	growth retardation-mild developmental delay-chronic hepatitis syndrome	digestive_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|digestive_system_disorder|syndromic_disease	hepatology|gastroenterology|endocrinology|pediatric|genetics_and_genomics	autoimmune_diseases|chronic_hepatitis_syndrome|metabolic_disorder	liver_disorder|endocrine_disorder	true	false	false	true	high
MONDO:0018319	familial episodic pain syndrome	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|upper_gastrointestinal_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0018320	primary microcephaly-mild intellectual disability-young-onset diabetes syndrome	syndromic_disease	other	syndromic_disease	endocrinology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|young_onset_diabetes_syndrome_is_not_a_category_in_the_list_but_primary_microcephaly_mild_intellectual_disability_young_onset_diabetes_syndrome_has_features_related_to_endocrine_and_brain_disorders|endocrine_disorder	false	false	true	false	high
MONDO:0018321	atypical juvenile parkinsonism	nervous_system_disorder	other	nervous_system_disorder	pediatric|genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0018322	HSD10 disease, infantile type	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	pediatric|genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	liver_disorder|endocrine_disorder	true	false	false	true	very_high
MONDO:0018323	HSD10 disease, neonatal type	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	pediatric|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	liver_disorder|endocrine_disorder	true	false	false	true	very_high
MONDO:0018324	adult-onset myasthenia gravis	immune_system_disorder|nervous_system_disorder	autoimmune_disease	immune_system_disorder|nervous_system_disorder	cardiothoracic|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|immune_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0018325	juvenile myasthenia gravis	immune_system_disorder|nervous_system_disorder	autoimmune_disease	immune_system_disorder|nervous_system_disorder	allergy_and_immunology|pediatric|neurology	autoimmune_diseases|neurodegenerative_disease	immune_disorder_muscle_disorder	false	false	false	true	medium
MONDO:0018326	transient neonatal myasthenia gravis	immune_system_disorder|nervous_system_disorder	autoimmune_disease	immune_system_disorder|nervous_system_disorder	pediatric|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|immune_disorder	false	false	false	true	medium
MONDO:0018327	glomus tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	otolaryngology|oncology|neurology	cancer|neurologic_cancer	ear_disorder|vascular_disorder	false	true	false	true	low
MONDO:0018328	homozygous familial hypercholesterolemia	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	vascular_disorder|endocrine_disorder	false	false	false	true	very_high
MONDO:0018330	mucinous adenocarcinoma of the appendix	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	gastrointestinal_cancer|cancer|adenocarcinoma|appendiceal_cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0018332	multiple acyl-CoA dehydrogenase deficiency, severe neonatal type	disorder_of_development_or_morphogenesis|cardiovascular_disorder|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|mitochondrial_disease	metabolic_disease|cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|cardiovascular_disorder|mitochondrial_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology|hepatology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0018333	multiple acyl-CoA dehydrogenase deficiency, mild type	disorder_of_development_or_morphogenesis|cardiovascular_disorder|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|mitochondrial_disease	metabolic_disease|cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|cardiovascular_disorder|mitochondrial_disease|musculoskeletal_system_disorder	endocrinology|pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder|metabolic_disorder	false	false	false	false	medium
MONDO:0018334	chronic hiccup	nervous_system_disorder	other	nervous_system_disorder	pulmonology|otolaryngology	mental_health_disorder|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	lung_disorder|upper_gastrointestinal_disorder|throat_disorder	false	false	false	false	low
MONDO:0018338	activated PI3K-delta syndrome	hematologic_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease|hematologic_disorder	allergy_and_immunology|immunology|pediatrics|rheumatology|genetics_and_genomics|pulmonology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0018339	PrP systemic amyloidosis	infectious_disease|nervous_system_disorder|hereditary_disease	infectious_disease	infectious_disease|hereditary_disease|nervous_system_disorder	rheumatology|renal_medicine|hematology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0018341	3q27.3 microdeletion syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|chromosomal_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	chromosomal_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|psychiatric_disorder|syndromic_disease	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018342	Joubert syndrome with Jeune asphyxiating thoracic dystrophy	syndromic_disease|respiratory_system_disorder|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|respiratory_system_disorder|nervous_system_disorder|syndromic_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0018343	periodic paralysis with later-onset distal motor neuropathy	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	muscle_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0018346	ferro-cerebro-cutaneous syndrome	syndromic_disease|metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|metabolic_disease|syndromic_disease	dermatology|neurology	autoimmune_diseases|neurodegenerative_disease	brain_disorder|liver_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0018349	MAN1B1-congenital disorder of glycosylation	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	congenital_disorder_of_glycosylation|pediatric|genetics_and_genomics	congenital_disorder_of_glycosylation|metabolic_disorder	muscle_disorder|liver_disorder|skin_disorder|eye_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0018352	squamous cell carcinoma of penis	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology|dermatology	autoimmune_diseases|cancer|inflammatory_disease	skin_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0018353	refractory celiac disease	digestive_system_disorder	other	digestive_system_disorder	pediatrics|hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|immune_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0018354	Prader-Willi-like syndrome	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|reproductive_system_disorder	endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0018355	SIM1-related Prader-Willi-like syndrome	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|reproductive_system_disorder	endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	pediatric|endocrinology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	lower_gastrointestinal_disorder|brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0018356	secondary neonatal autoimmune disease	immune_system_disorder	autoimmune_disease	immune_system_disorder	allergy_and_immunology|pediatric|rheumatology	autoimmune_diseases|secondary_neonatal_autoimmune_disease|inflammatory_disease	autoimmune_disease|immune_disorder	false	false	false	false	medium
MONDO:0018357	neonatal antiphospholipid syndrome	syndromic_disease|immune_system_disorder	autoimmune_disease	syndromic_disease|immune_system_disorder	pediatric|rheumatology|obstetrics_and_gynecology|hematology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	immune_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0018358	neonatal autoimmune hemolytic anemia	hematologic_disorder|immune_system_disorder	anemia|autoimmune_disease	immune_system_disorder|hematologic_disorder	pediatric|hematology	autoimmune_diseases|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0018359	neonatal dermatomyositis	connective_tissue_disorder|inflammatory_disease|integumentary_system_disorder|musculoskeletal_system_disorder|immune_system_disorder	autoimmune_disease	idiopathic_disease|musculoskeletal_system_disorder|immune_system_disorder|inflammatory_disease|integumentary_system_disorder|connective_tissue_disorder	pediatric|rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0018360	neonatal lupus erythematosus	connective_tissue_disorder|immune_system_disorder	autoimmune_disease	immune_system_disorder|connective_tissue_disorder	immunology|pediatrics|obstetrics_and_gynecology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder_skin_disorder	false	false	false	true	medium
MONDO:0018361	neonatal scleroderma	connective_tissue_disorder|immune_system_disorder	autoimmune_disease	immune_system_disorder|connective_tissue_disorder	pediatric|rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	muscle_disorder|skin_disorder|joint_disorder	false	false	false	false	high
MONDO:0018362	persistent idiopathic facial pain	nervous_system_disorder	other	idiopathic_disease|nervous_system_disorder	otolaryngology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	ear_disorder|nerve_disorder__i_assume_the_category_is__nerve_disorder__because_facial_pain_is_often_associated_with_neural_issues|brain_disorder	false	false	false	false	high
MONDO:0018363	focal facial dermal dysplasia	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|syndromic_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|adrenal_gland_disease|dermal_dysplasia	reproductive_system_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018364	malignant epithelial tumor of ovary	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	true	very_high
MONDO:0018365	malignant non-epithelial tumor of ovary	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|obstetrics_and_gynecology	malignant_non_epithelial_tumor_of_ovary|cancer	malignant_non_epithelial_tumor_of_ovary_could_also_fit_in_lymphatic_disorder|bone_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0018368	primary peritoneal serous/papillary carcinoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease|other____removed_because_it_was_a_specific_type_of_cancer__but_since_it_s_peritoneal__i_added_the_more_general_category____cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0018369	immature ovarian teratoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	genetics_and_genomics|oncology|obstetrics_and_gynecology	gynecologic_cancer|cancer|ovarian_cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0018370	KLHL9-related early-onset distal myopathy	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	orthopaedic|genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018371	nebulin-related early-onset distal myopathy	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	pulmonology|pediatric|orthopaedic|genetics_and_genomics|renal_medicine|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	nebular_myopathy|muscle_disorder	false	false	false	false	high
MONDO:0018373	avascular necrosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	cardiology|orthopaedic|hematology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0018374	secondary avascular necrosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	cardiology|hematology	cancer|adrenal_gland_disease|cardiovascular_disorder	bone_disorder|vascular_disorder	false	false	false	true	high
MONDO:0018375	traumatic avascular necrosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	trauma_is_actually_related_to_the_surgical_field__but_the_closest_category_would_be_orthopaedic_for_bone_related_issues__however_in_the_context_of_traumatic_avascular_necrosis_it_s_more_closely_related_to_vascular_damage_which_is_more_aligned_with__hematology__vascular_system|orthopaedic|hematology	traumatic_avascular_necrosis_is_related_to_injuries_which_can_affect_the_blood_supply_of_the_bone_leading_to_avascular_necrosis_therefore|traumatic_avascular_necrosis_also_falls_under_an_injury_category_that_could_be_categorized_as_a_vascular_disorder_but_since_vascular_disorders_are_typically_associated_with_blood_vessel_issues_not_directly_bone__the_closest_fit_would_be_cardiovascular_disorder|cardiovascular_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0018376	secondary non-traumatic avascular necrosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	cardiology|vascular|hematology	cancer|adrenal_gland_disease|cardiovascular_disorder	bone_disorder|vascular_disorder	false	false	false	false	high
MONDO:0018378	osteonecrosis of the jaw	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	inflammatory_disease|cancer|metabolic_disorder	bone_disorder|teeth_disorder	false	false	false	false	high
MONDO:0018379	primary avascular necrosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	cardiology|orthopaedic|rheumatology|hematology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0018380	idiopathic avascular necrosis	musculoskeletal_system_disorder	other	idiopathic_disease|musculoskeletal_system_disorder	cardiology|orthopaedic|hematology	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	bone_disorder|vascular_disorder	false	false	false	false	high
MONDO:0018381	osteochondrosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	inflammatory_disease|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0018382	epiphysiolysis of the hip	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|orthopaedic	inflammatory_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0018383	osteonecrosis of genetic origin	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	metabolic_disorder	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0018394	male infertility with teratozoospermia due to single gene mutation	reproductive_system_disorder	other	reproductive_system_disorder	urology|genetics_and_genomics	genetic_disorders|metabolic_disorder	genetic_disorder|male_infertility|reproductive_system_disorder|teratozoospermia	false	false	false	false	high
MONDO:0018408	cystic echinococcosis	infectious_disease	infectious_disease	infectious_disease	neurology|pulmonology|hepatology|gastroenterology	cancer|inflammatory_disease	liver_disorder|lung_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0018416	autosomal recessive spastic paraplegia type 59	nervous_system_disorder|hereditary_disease|syndromic_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autosomal_recessive_spastic_paraplegia_is_not_in_the_category_list__but_this_disease_is_related_to_genetic_disorders	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018417	autosomal recessive spastic paraplegia type 60	nervous_system_disorder|hereditary_disease|syndromic_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018418	autosomal recessive spastic paraplegia type 66	nervous_system_disorder|hereditary_disease|syndromic_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018419	autosomal recessive spastic paraplegia type 67	nervous_system_disorder|hereditary_disease|syndromic_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autosomal_recessive_diseases	spinal_disorder|muscule_disorder	false	false	false	false	high
MONDO:0018420	autosomal recessive spastic paraplegia type 68	nervous_system_disorder|hereditary_disease|syndromic_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018421	autosomal recessive spastic paraplegia type 69	nervous_system_disorder|hereditary_disease|syndromic_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018422	autosomal recessive spastic paraplegia type 70	nervous_system_disorder|hereditary_disease|syndromic_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018423	autosomal recessive spastic paraplegia type 71	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018424	inherited lipoic acid biosynthesis defect	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	metabolic_disorder__removed|endocrinology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|metabolic_disorder	false	false	false	false	high
MONDO:0018425	Huntington disease-like syndrome due to C9ORF72 expansions	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018426	AXIN2-related attenuated familial adenomatous polyposis	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	gastroenterology|genetics_and_genomics|oncology	cancer|familial_adenomatous_polyposis	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0018428	9q31.1q31.3 microdeletion syndrome	nervous_system_disorder|chromosomal_disorder|syndromic_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis	psychiatric_disorder	syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|chromosomal_disorder|psychiatric_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0018429	14q24.1q24.3 microdeletion syndrome	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	vascular_disorder|immune_disorder|spinal_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|brain_disorder|joint_disorder|muscle_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0018430	partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	neurological_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0018431	cold-induced sweating syndrome - hyperthermia spectrum	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|pulmonology|dermatology	autoimmune_diseases|metabolic_disorder	skin_disorder|endocrine_disorder	true	false	false	false	high
MONDO:0018432	lichen myxedematosus	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|metabolic_disorder	skin_disorder_liver_disorder	false	false	false	false	medium
MONDO:0018433	acute myeloid leukemia with t(6;9)(p23;q34)	connective_tissue_disorder|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|acute_disease|connective_tissue_disorder|immune_system_disorder|hematologic_disorder	hematology|oncology	cancer|leukemia	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0018434	acute myeloid leukemia with t(9;11)(p22;q23)	connective_tissue_disorder|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|acute_disease|connective_tissue_disorder|immune_system_disorder|hematologic_disorder	hematology|oncology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0018435	acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2)	connective_tissue_disorder|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|acute_disease|connective_tissue_disorder|immune_system_disorder|hematologic_disorder	hematology|oncology	cancer|anemia	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0018436	megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)	connective_tissue_disorder|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|acute_disease|connective_tissue_disorder|immune_system_disorder|hematologic_disorder	hematology|oncology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0018437	acute myeloid leukemia with NPM1 somatic mutations	connective_tissue_disorder|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|acute_disease|connective_tissue_disorder|immune_system_disorder|hematologic_disorder	hematology|oncology|genetics_and_genomics	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0018438	eosinophilic gastrointestinal disease	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|pediatrics	allergy|autoimmune_diseases|inflammatory_disease	immune_disorder_upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0018439	eosinophilic colitis	digestive_system_disorder|hereditary_disease|inflammatory_disease|immune_system_disorder	other	digestive_system_disorder|inflammatory_disease|hereditary_disease|immune_system_disorder	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0018440	autosomal recessive distal renal tubular acidosis	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	pediatric|genetics_and_genomics|renal_medicine	metabolic_disorder|anemia	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0018442	acitretin/etretinate embryopathy	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatrics|dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	skin_disorder|liver_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0018443	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics|psychiatry	developmental_delay|neurodegenerative_disease|mental_health_disorder	developmental_delay|joint_disorder|nervous_system_anomaly|brain_disorder	false	false	false	false	high
MONDO:0018445	global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|urology|genetics_and_genomics|oncology	cancer|metabolic_disorder	kidney_disorder|lung_disorder|endocrine_disorder	true	true	false	false	high
MONDO:0018446	autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|intellectual_disability	false	false	false	false	high
MONDO:0018447	chondromyxoid fibroma	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|rheumatology	cancer|bone_disease	joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	low
MONDO:0018448	clear cell papillary renal cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology|renal_medicine	renal_cell_carcinoma|cancer	kidney_disorder|renal_cell_carcinoma	false	true	false	false	low
MONDO:0018449	acquired cystic disease-associated renal cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology|renal_medicine	cancer|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	true	false	false	medium
MONDO:0018450	spinal muscular atrophy with respiratory distress type 2	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pulmonology	neurodegenerative_disease|metabolic_disorder	lung_disorder|muscle_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0018453	familial atypical multiple mole melanoma syndrome	hereditary_disease|cancer_or_benign_tumor|syndromic_disease|integumentary_system_disorder	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|integumentary_system_disorder|syndromic_disease	dermatology|oncology|genetics_and_genomics	cancer|genetic_disorder|familial_atypical_multiple_mole_melanoma_syndrome_is_actually_a_condition_predisposing_to_melanoma_which_is_a_cancer_of_the_skin__but_more_accurately__cancer	skin_disorder|genetic_disorder___note__i_assume_you_meant_genetic_disorder_but_it_is_not_in_the_list_so_i_added_a_note	false	true	false	true	high
MONDO:0018456	polyarticular juvenile idiopathic arthritis	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder	other	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder|idiopathic_disease	pediatric|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder	false	false	false	true	high
MONDO:0018458	familial hypocalciuric hypercalcemia	hereditary_disease|endocrine_system_disorder|metabolic_disease|respiratory_system_disorder	endocrine_system_disorder|metabolic_disease	hereditary_disease|respiratory_system_disorder|metabolic_disease|endocrine_system_disorder	genetics_and_genomics|renal_medicine|endocrinology	familial_hypercalciuria_and_hypophosphatemia|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0018459	isolated glycerol kinase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics|hepatology|genetics_and_genomics|endocrinology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	true	medium
MONDO:0018460	Eales disease	nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	pediatric|dermatology|rheumatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|lymphatic_disorder|immune_disorder	true	false	false	true	high
MONDO:0018461	Angelman syndrome due to a point mutation	nervous_system_disorder|hereditary_disease|syndromic_disease	other	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|spinal_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0018462	Angelman syndrome due to imprinting defect in 15q11-q13	nervous_system_disorder|hereditary_disease|syndromic_disease	other	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	joint_disorder|kidney_disorder|muscle_disorder|upper_gastrointestinal_disorder|brain_disorder|spinal_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0018463	mild phosphoribosylpyrophosphate synthetase superactivity	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|biochemistry|metabolism	metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	low
MONDO:0018464	severe phosphoribosylpyrophosphate synthetase superactivity	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|metabolic_diseases	metabolic_disorder	metabolic_disorder|liver_disorder	false	false	false	false	high
MONDO:0018465	insulin autoimmune syndrome	endocrine_system_disorder|hereditary_disease|metabolic_disease|immune_system_disorder	endocrine_system_disorder|autoimmune_disease|metabolic_disease	immune_system_disorder|hereditary_disease|metabolic_disease|endocrine_system_disorder	allergy_and_immunology|endocrinology	metabolic_disorder|autoimmune_diseases	immune_disorder_endocrine_disorder	false	false	true	true	medium
MONDO:0018467	nephropathic infantile cystinosis	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|urology|genetics_and_genomics|renal_medicine	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	very_high
MONDO:0018468	proton-pump inhibitor-responsive esophageal eosinophilia	digestive_system_disorder	other	digestive_system_disorder	allergy_and_immunology|immunology|gastroenterology	inflammatory_disease|allergy|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	medium
MONDO:0018469	pulmonary non-tuberculous mycobacterial infection	respiratory_system_disorder|infectious_disease	infectious_disease	infectious_disease|respiratory_system_disorder	cardiothoracic|cardiology|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0018470	renal agenesis	urinary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|urinary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|urology|renal_medicine	renal_agenesis|autoimmune_diseases|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0018471	generalized eruptive keratoacanthoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology	cancer|inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0018472	familial isolated trichomegaly	hereditary_disease	other	hereditary_disease	dermatology|genetics_and_genomics	adrenal_gland_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0018473	hyperlipoproteinemia type 3	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics|endocrinology	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|liver_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0018474	13q12.3 microdeletion syndrome	chromosomal_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|chromosomal_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	joint_disorder|muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018475	PRKAR1B-related neurodegenerative dementia with intermediate filaments	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0018476	dystonia-aphonia syndrome	nervous_system_disorder|hereditary_disease|syndromic_disease	other	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|pediatric|genetics_and_genomics|psychiatry	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|brain_disorder|throat_disorder	false	false	false	false	high
MONDO:0018477	bilirubin encephalopathy	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|hematology|pediatric|hepatology	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0018479	congenital adrenal hyperplasia	hereditary_disease|endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease	hereditary_disease|metabolic_disease|endocrine_system_disorder	pediatric|genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0018480	carcinoma of esophagus, salivary gland type	cancer_or_benign_tumor|digestive_system_disorder|upper_digestive_tract_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	oncology|otolaryngology|gastroenterology	cancer	upper_gastrointestinal_disorder|throat_disorder	false	true	false	false	very_high
MONDO:0018481	undifferentiated carcinoma of esophagus	cancer_or_benign_tumor|digestive_system_disorder|upper_digestive_tract_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	pulmonology|oncology|gastroenterology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0018483	secondary pulmonary alveolar proteinosis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiothoracic	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	false	false	false	true	high
MONDO:0018484	semicircular canal dehiscence syndrome	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	otolaryngology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	ear_disorder|spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0018485	glycogen storage disease due to acid maltase deficiency, late-onset	hereditary_disease|cardiovascular_disorder|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease|cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|metabolic_disease|musculoskeletal_system_disorder	hepatology|genetics_and_genomics|pediatrics|endocrinology	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0018486	visual snow syndrome	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0018487	autosomal recessive severe congenital neutropenia due to CXCR2 deficiency	hematologic_disorder|hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder|hematologic_disorder	pediatric|genetics_and_genomics|hematology|immunology	inflammatory_disease|metabolic_disorder|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0018489	autoimmune encephalopathy with parasomnia and obstructive sleep apnea	immune_system_disorder|nervous_system_disorder	autoimmune_disease	immune_system_disorder|nervous_system_disorder|sleep_disorder	pulmonology|psychiatry|neurology	inflammatory_disease|autoimmune_diseases	immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0018490	cono-spondylar dysplasia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|rheumatology	neurodegenerative_disease|metabolic_disorder	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018491	3-phosphoglycerate dehydrogenase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0018492	hereditary clear cell renal cell carcinoma	hereditary_disease|cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|urinary_system_disorder	oncology|genetics_and_genomics|urology	hereditary_disease|renal_cell_carcinoma|cancer|kidney_disease|familial_cancer	kidney_disorder|hereditary_disorder	false	true	false	false	very_high
MONDO:0018493	malignant hyperthermia of anesthesia	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pulmonology|oncology|anesthesiology	cancer|metabolic_disorder|anesthetic_reaction	muscle_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0018494	microcephaly-short stature-intellectual disability-facial dysmorphism syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	facial_dysmorphism_syndrome|brain_disorder	false	false	false	false	very_high
MONDO:0018495	X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome	hereditary_disease|metabolic_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder|metabolic_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|metabolic_disease	ophthalmology|pediatric|genetics_and_genomics|urology|endocrinology|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder|brain_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0018498	double outlet right ventricle with subaortic or doubly committed ventricular septal defect	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|cardiothoracic|cardiology	cardiovascular_anomaly|congenital_heart_disease|cardiovascular_disorder|cardiac_defect	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0018499	double outlet right ventricle with atrioventricular septal defect, pulmonary stenosis, heterotaxy	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|genetics_and_genomics|cardiothoracic|cardiology	heterotaxy|cardiovascular_disorder	vascular_disorder|lung_disorder|heart_disorder	false	false	false	false	high
MONDO:0018500	cutaneous larva migrans	infectious_disease	infectious_disease	infectious_disease	pediatric|dermatology	inflammatory_disease|autoimmune_diseases|allergy	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0018502	hereditary gastric cancer	cancer_or_benign_tumor|digestive_system_disorder|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|digestive_system_disorder	oncology|gastroenterology|genetics_and_genomics	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0018503	carcinoma of stomach, salivary gland type	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0018504	undifferentiated carcinoma of stomach	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0018506	mesenchymal tumor of small intestine	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	pediatric|oncology|pathology____revised_to_use_correct_formatting___oncology|gastroenterology	cancer|adrenal_gland_disease	bone_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0018507	microcephaly-complex motor and sensory axonal neuropathy syndrome	syndromic_disease|nervous_system_disorder|hereditary_disease	other	syndromic_disease|hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	spinal_disorder|muscle_disorder|brain_disorder	true	false	false	false	high
MONDO:0018509	squamous cell carcinoma of the small intestine	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|hepatology|hematology|gastroenterology	cancer|adrenal_gland_disease_is_not_applicable_due_to_the_location_of_the_disease___becomes__cancer	lower_gastrointestinal_disorder_upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0018510	small intestine neuroendocrine neoplasm	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|gastroenterology	cancer|neuroendocrine_tumors	endocrine_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0018511	epithelial tumor of the appendix	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	allergy|neurodegenerative_disease|cancer|inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0018513	squamous cell carcinoma of colon	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0018515	squamous cell carcinoma of rectum	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|inflammatory_disease|squamous_cell_carcinoma	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0018516	epithelial tumor of anal canal	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|epithelial_tumor	lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0018521	squamous cell carcinoma of pancreas	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	skin_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0018523	pancreatic mucinous cystadenoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|gastroenterology	cancer|gland_disease|cystadenoma|tumor	upper_gastrointestinal_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0018525	solid pseudopapillary carcinoma of pancreas	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	medium
MONDO:0018528	congenital myopathy with myasthenic-like onset	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder	false	false	false	false	high
MONDO:0018531	carcinoma of liver and intrahepatic biliary tract	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|hepatology|gastroenterology	cancer|intrahepatic_biliary_tract_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|liver_disorder	false	true	false	true	very_high
MONDO:0018533	undifferentiated carcinoma of liver and intrahepatic biliary tract	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|hepatology|gastroenterology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0018534	squamous cell carcinoma of liver and intrahepatic biliary tract	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|hepatology	cancer|biliary_tract_disease|liver_disease	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0018535	biliary cystadenocarcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|hepatology|gastroenterology	cancer|biliary_cystadenocarcinoma_is_a_rare_form_of_cancer	biliary_disorder|liver_disorder	false	true	false	false	high
MONDO:0018536	adenocarcinoma of gallbladder and extrahepatic biliary tract	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology	cancer|other___removed___other__as_it_is_redundant|adrenal_gland_disease	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0018537	squamous cell carcinoma of gallbladder and extrahepatic biliary tract	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|hepatology|gastroenterology	cancer|inflammatory_disease|adrenal_gland_disease	biliary_disorder|upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0018540	PFAPA syndrome	connective_tissue_disorder|syndromic_disease	other	syndromic_disease|connective_tissue_disorder	pediatric|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	autoimmune_disorder|immune_disorder	false	false	false	true	medium
MONDO:0018541	familial hypoaldosteronism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	renal_medicine|genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0018542	severe congenital neutropenia	immune_system_disorder|hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease|immune_system_disorder	pediatric|hematology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0018543	autosomal dominant hypocalcemia	endocrine_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|endocrinology	cardiovascular_disorder|autoimmune_diseases|metabolic_disorder	muscle_disorder|bone_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0018544	adrenoleukodystrophy	endocrine_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	psychiatric_disorder|neurodegenerative_disease|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|nervous_system_disorder|psychiatric_disorder|hereditary_disease|metabolic_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0018546	serotonin syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurotransmitter_disorder	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0018547	acute tricyclic antidepressant poisoning	poisoning	other	acute_disease|poisoning	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0018548	acute poisoning by drugs with membrane-stabilizing effect	poisoning	other	acute_disease|poisoning	neurology|pulmonology|psychiatry	cardiovascular_disorder|metabolic_disorder	kidney_disorder|upper_gastrointestinal_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0018551	patent urachus	urinary_system_disorder	other	urinary_system_disorder	pediatric|urology	abdominal_anomaly|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0018552	urachal sinus	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	cancer|urachal_sinus_is_a_rare_congenital_anomaly_that_is_often_associated_with_urachal_adenocarcinoma	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0018553	urachal diverticulum	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	cancer|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0018554	pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis	respiratory_system_disorder|cardiovascular_disorder	cardiovascular_disorder	respiratory_system_disorder|cardiovascular_disorder	pulmonology|hematatology|genetics_and_genomics	cardiovascular_disorder|inflammatory_disease|anemia	vascular_disorder|lung_disorder	false	false	false	false	high
MONDO:0018555	hypogonadotropic hypogonadism	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	pediatric|genetics_and_genomics|endocrinology	reproductive_system_disorder|genetic_disease|developmental_disorder|endocrine_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0018556	Lambert-Eaton myasthenic syndrome	syndromic_disease|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|nervous_system_disorder	immunology|neurology	inflammatory_disease|autoimmune_diseases	muscle_disorder|immune_disorder	false	false	false	false	high
MONDO:0018559	fetal lower urinary tract obstruction	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|urinary_system_disorder	pediatric|urology	congenital_abnormality|metabolic_disorder|urinary_tract_problem	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0018561	precocious puberty in female	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder	pediatric|obstetrics_and_gynecology|endocrinology	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0018563	adactyly of foot	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0018564	3p25.3 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|developmental_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0018565	congenital urachal anomaly	urinary_system_disorder	other	urinary_system_disorder	pediatric|urology	congenital_anomaly|neonatal_abnormality|birth_defect	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0018566	short stature-advanced bone age-early-onset osteoarthritis syndrome	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics|rheumatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|bone_disorder|endocrine_disorder	true	false	false	false	high
MONDO:0018567	autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	nervous_system_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018569	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	bone_disorder|brain_disorder|reproductive_system_disorder|growth_retardation_is_not_an_explicit_category_so_i_have_excluded_it	false	false	false	false	very_high
MONDO:0018570	hypophosphatasia	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|spinal_disorder|teeth_disorder	false	false	false	true	very_high
MONDO:0018571	contractures-developmental delay-Pierre Robin syndrome	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	otolaryngology|genetics_and_genomics|pediatric|neurology	developmental_delay|metabolic_disorder|neurodegenerative_disease	developmental_delay|throat_disorder|joint_disorder|ear_disorder	false	false	false	false	high
MONDO:0018572	severe intellectual disability-hypotonia-strabismus-coarse face-planovalgus syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|orthopaedic|neurology|ophthalmology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|joint_disorder|muscle_disorder|eye_disorder	true	false	false	false	very_high
MONDO:0018573	intrauterine growth restriction-short stature-early adult-onset diabetes syndrome	syndromic_disease	other	syndromic_disease	endocrinology|genetics_and_genomics|pediatrics|obstetrics_and_gynecology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	endocrine_disorder|reproductive_system_disorder	false	false	true	false	high
MONDO:0018576	non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018577	pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa	syndromic_disease|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder	genetics_and_genomics|dermatology|ophthalmology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0018581	progressive encephalomyelitis with rigidity and myoclonus	nervous_system_disorder|syndromic_disease	other	syndromic_disease|nervous_system_disorder	psychiatry|pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder|muscle_disorder	true	false	false	false	very_high
MONDO:0018582	GCGR-related hyperglucagonemia	cancer_or_benign_tumor|hereditary_disease|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|hereditary_disease|endocrine_system_disorder|digestive_system_disorder	endocrinology|genetics_and_genomics	adrenal_gland_disease|endocrine_disorder|metabolic_disorder	lower_gastrointestinal_disorder|endocrine_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0018583	human infection by orthopoxvirus	infectious_disease	infectious_disease	infectious_disease	public_health|infectious_diseases|immunology|virology|pediatric|epidemiology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0018585	pediatric arterial ischemic stroke	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	pediatric|neurology	inflammatory_disease|cardiovascular_disorder	vascular_disorder|brain_disorder	false	false	false	true	high
MONDO:0018586	zinc-responsive necrolytic acral erythema	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	autoimmune_diseases|metabolic_disorder	immune_disorder|endocrine_disorder|skin_disorder	false	false	false	true	medium
MONDO:0018587	non-recovering obstetric brachial plexus lesion	nervous_system_disorder	other	nervous_system_disorder	neurology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018588	ALECT2 amyloidosis	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|pulmonology|rheumatology|renal_medicine	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0018589	AApoAIV amyloidosis	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|neurology|cardiology	inflammatory_disease|autoimmune_diseases|metabolic_disorder|cardiovascular_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0018590	ABeta2M amyloidosis	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0018591	ITM2B amyloidosis	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|liver_disorder	false	false	false	true	high
MONDO:0018592	cutaneous polyarteritis nodosa	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0018593	primary polyarteritis nodosa	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	hematology|rheumatology|renal_medicine	inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder	false	false	false	true	high
MONDO:0018594	secondary polyarteritis nodosa	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	hematology|dermatology|rheumatology|neurology	inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0018595	single-organ polyarteritis nodosa	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	rheumatology|hematatology|renal_medicine	inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder|kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0018596	systemic polyarteritis nodosa	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	hematology|allergy_and_immunology|rheumatology|renal_medicine	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	immune_disorder|vascular_disorder	false	false	false	true	high
MONDO:0018597	plastic bronchitis	respiratory_system_disorder|immune_system_disorder	other	immune_system_disorder|respiratory_system_disorder	otolaryngology|pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	throat_disorder|lung_disorder	false	false	false	true	high
MONDO:0018599	congenital oculomotor nerve palsy	nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_visual_system	ophthalmology|pediatric|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0018600	congenital abducens nerve palsy	nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_visual_system	neurology|pediatric	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0018601	autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	ophthalmology|otolaryngology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder|spinal_disorder|bone_disorder|eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018602	necrotizing soft tissue infection	infectious_disease	infectious_disease	infectious_disease	dermatology|general_surgery|pediatric|emergency_medicine|surgery	cancer|inflammatory_disease	lower_gastrointestinal_disorder|skin_disorder	true	false	false	true	very_high
MONDO:0018603	SFTPC- related interstitial lung disease	hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease	pulmonology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	true	high
MONDO:0018604	familial colorectal cancer type X	cancer_or_benign_tumor|hereditary_disease|digestive_system_disorder|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|hereditary_disease|syndromic_disease	oncology|gastroenterology|genetics_and_genomics	cancer|familial_cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0018605	disorders of pentose/polyol metabolism	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|disorders_of_pentose_polyol_metabolism_is_already_in_this_category	liver_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0018606	extensive peripapillary myelinated nerve fibers	disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|urology|pulmonology|oncology|rheumatology|neurology|pediatric|renal_medicine|psychiatry	autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	none
MONDO:0018607	combined hamartoma of the retina and retinal pigment epithelium	cancer_or_benign_tumor|disorder_of_visual_system	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|genetics_and_genomics	cancer|autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|eye_disorder	false	false	false	false	low
MONDO:0018608	pure autonomic failure	hereditary_disease|metabolic_disease|nervous_system_disorder	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	pulmonology|neurology|cardiology	autoimmune_diseases|adrenal_gland_disease|neurodegenerative_disease	vascular_disorder|autonomic_nervous_system_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0018610	early-onset posterior subcapsular cataract	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	true	high
MONDO:0018611	early-onset lamellar cataract	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018612	congenital hypothyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|pediatric	autoimmune_diseases|metabolic_disorder	congenital_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0018613	AH amyloidosis	metabolic_disease	metabolic_disease	metabolic_disease	renal_medicine|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder|immune_disorder	false	false	false	true	high
MONDO:0018614	undetermined early-onset epileptic encephalopathy	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0018615	hemicrania continua	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|headache	neurodegenerative_disease|inflammatory_disease	vascular_disorder|brain_disorder	false	false	false	true	high
MONDO:0018616	central serous chorioretinopathy	disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0018617	baroreflex failure	nervous_system_disorder	other	nervous_system_disorder	cardiology|neurology|pulmonology	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0018620	hypothalamic adipsic hypernatraemia syndrome	nervous_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|nervous_system_disorder	endocrinology|neurology	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|brain_disorder	false	false	false	false	high
MONDO:0018621	lymphoplasmacytic lymphoma without IgM production	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0018623	postpartum psychosis	nervous_system_disorder|obstetric_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|obstetric_disorder|nervous_system_disorder	psychiatry|neurology	autoimmune_diseases|mental_health_disorder	reproductive_system_disorder|brain_disorder	false	false	false	true	high
MONDO:0018624	spontaneous intracranial hypotension	nervous_system_disorder	other	nervous_system_disorder	neurology|oncology|otolaryngology	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0018625	classic stiff person syndrome	syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder	rheumatology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	true	high
MONDO:0018626	paratyphoid fever	infectious_disease	infectious_disease	infectious_disease	hepatology|pediatric|infectious_diseases	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0018628	HIV-associated cancer	immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	post_infectious_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|autoimmune_diseases	immune_disorder_lymphatic_disorder	false	true	false	true	high
MONDO:0018629	focal stiff limb syndrome	syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder	rheumatology|orthopaedic|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0018630	hereditary nonpolyposis colon cancer	hereditary_disease|syndromic_disease|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|oncology	cancer|autoimmune_diseases|metabolic_disorder|inflammatory_disease____corrected_response__cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0018631	Marie Unna hereditary hypotrichosis	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	genetic_disorder|neurodegenerative_disease|hereditary_disease|metabolic_disorder___corrected_list___metabolic_disorder	muscle_disorder|skin_disorder	false	false	false	false	low
MONDO:0018632	11q22.2q22.3 microdeletion syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018633	20q11.2 microdeletion syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	ear_disorder|eye_disorder|brain_disorder|muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018634	hereditary amyloidosis	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|genetics_and_genomics|nephrology	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0018635	idiopathic phalangeal acro-osteolysis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|idiopathic_disease	genetics_and_genomics|orthopaedic	inflammatory_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0018636	autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	immunology|allergy_and_immunology|hematology	inflammatory_disease|anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0018637	familial chylomicronemia syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|metabolism_related_categories_would_likely_be_included_as_well_but_the_list_provided_does_not_contain_this_category	inflammatory_disease|metabolic_disorder	lipid_disorder|liver_disorder|lymphatic_disorder	false	false	false	true	very_high
MONDO:0018638	pseudohypoaldosteronism	urinary_system_disorder	other	urinary_system_disorder	endocrinology|pediatrics	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0018639	caudal regression-sirenomelia spectrum	disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018640	secondary vasculitis	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	rheumatology|hematology	inflammatory_disease|autoimmune_diseases	vascular_disorder|immune_disorder	true	false	false	true	high
MONDO:0018642	NIK deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|hematological	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0018644	autosomal dominant complex spastic paraplegia type 9B	hereditary_disease|nervous_system_disorder|metabolic_disease|syndromic_disease	metabolic_disease|neurodegenerative_disease	metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018645	IgG4-related sclerosing cholangitis	inflammatory_disease|immune_system_disorder|endocrine_system_disorder|digestive_system_disorder	autoimmune_disease|endocrine_system_disorder	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder|immune_system_disorder	hepatology|rheumatology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|biliary_disorder|immune_disorder	false	false	false	true	high
MONDO:0018646	sclerosing cholangitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|biliary_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0018647	secondary sclerosing cholangitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder	true	false	false	false	high
MONDO:0018648	Keratocystic odontogenic tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|mouth_disorder|cancer_or_benign_tumor	pediatric|oral_pathology|oncology	cancer	bone_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0018653	Polymerase proofreading-related adenomatous polyposis	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|oncology|gastroenterology	genetic_disorder|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0018654	idiopathic dropped head syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|idiopathic_disease	psychiatry|pediatric|neurology	neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018655	hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|neurology	hypoplasia_of_the_corpus_callosum|neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018656	tremor-ataxia-central hypomyelination syndrome	hereditary_disease|nervous_system_disorder|disorder_of_visual_system	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018657	pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|oncology|dermatology	cancer|metabolic_disorder	skin_disorder|skin_carcinoma_syndrome_is_more_specific_to_the_disease_so_it_is_given_precedence_over_skin_disorder	true	true	false	true	high
MONDO:0018658	19p13.3 microduplication syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018659	partial duplication of the short arm of chromosome 19	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	genetic_disorder|neurodegenerative_disease|chromosome_abnormality	spinal_disorder	false	false	false	false	medium
MONDO:0018660	hemophilia	hematologic_disorder	other	hematologic_disorder	hematology|pediatric|genetics_and_genomics	inflammatory_disease|anemia|metabolic_disorder|autoimmune_diseases	vascular_disorder|joint_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0018661	Zika virus infectious disease	infectious_disease	infectious_disease	infectious_disease	obstetrics_and_gynecology|neurology|pediatrics	infectious_disease|autoimmune_diseases	eye_disorder|brain_disorder	true	false	false	false	medium
MONDO:0018662	autosomal recessive brachyolmia	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|neurodegenerative_disease	bone_disorder|muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0018663	regressive spondylometaphyseal dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology|orthopaedic	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0018664	ectopia cordis	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	neonatology|pediatric|obstetrics_and_gynecology	cardiovascular_disorder|congenital_anomaly	spinal_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0018666	hepatoblastoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	hepatology|pediatric|oncology|gastroenterology	pediatric_cancer|cancer	liver_disorder|kidney_disorder	false	true	false	true	very_high
MONDO:0018667	pleural empyema	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology	inflammatory_disease|cancer|autoimmune_diseases	lung_disorder	true	false	false	true	high
MONDO:0018668	scedosporiosis	infectious_disease	infectious_disease	infectious_disease	pediatric|allergy_and_immunology|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	true	false	false	false	medium
MONDO:0018669	snakebite envenomation	poisoning	other	poisoning	toxicology|hematology|critical_care|emergency_medicine	inflammatory_disease|allergy	muscle_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0018670	symptomatic form of fragile X syndrome in female carrier	reproductive_system_disorder|endocrine_system_disorder|syndromic_disease|hereditary_disease	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|syndromic_disease	psychiatry|genetics_and_genomics|obstetrics_and_gynecology|neurology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	eye_disorder|reproductive_system_disorder|muscle_disorder|brain_disorder|joint_disorder|spinal_disorder|ear_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0018671	IgG4-related kidney disease	immune_system_disorder|urinary_system_disorder	autoimmune_disease	urinary_system_disorder|immune_system_disorder	rheumatology|renal_medicine|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	kidney_disorder|urinary_tract_disorder|immune_disorder	false	false	false	true	high
MONDO:0018672	IgG4-related aortitis	immune_system_disorder	autoimmune_disease	immune_system_disorder	cardiology|rheumatology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|heart_disorder|immune_disorder	false	false	false	true	high
MONDO:0018673	IgG4-related pachymeningitis	immune_system_disorder|inflammatory_disease	autoimmune_disease	immune_system_disorder|inflammatory_disease	rheumatology|neurology	inflammatory_disease|autoimmune_diseases	immune_disorder|brain_disorder	false	false	false	true	high
MONDO:0018674	IgG4-related submandibular gland disease	otorhinolaryngologic_disease|immune_system_disorder	autoimmune_disease	otorhinolaryngologic_disease|immune_system_disorder	rheumatology|otolaryngology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	true	medium
MONDO:0018675	IgG4-related ophthalmic disorder	disorder_of_visual_system|immune_system_disorder	autoimmune_disease	disorder_of_orbital_region|disorder_of_visual_system|immune_system_disorder	rheumatology|ophthalmology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	eye_disorder|liver_disorder|immune_disorder	false	false	false	true	high
MONDO:0018676	eosinophilic angiocentric fibrosis	otorhinolaryngologic_disease|immune_system_disorder	autoimmune_disease	otorhinolaryngologic_disease|immune_system_disorder	hematology|pulmonology	inflammatory_disease|cardiovascular_disorder	lung_disorder|immune_disorder	false	false	false	false	medium
MONDO:0018677	visceral heterotaxy	disorder_of_development_or_morphogenesis|cardiovascular_disorder|syndromic_disease|hereditary_disease	cardiovascular_disorder	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	hepatology|cardiology|pediatric|genetics_and_genomics|cardiothoracic	developmental_disorder|cardiovascular_disorder|congenital_abnormality	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0018678	polyclonal hyperviscosity syndrome	hematologic_disorder	other	hematologic_disorder	hematology|immunology	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0018679	primary cutaneous plasmacytosis	immune_system_disorder|integumentary_system_disorder	autoimmune_disease	integumentary_system_disorder|immune_system_disorder	hematology|dermatology	inflammatory_disease|cancer|autoimmune_diseases	blood_bone_marrow_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018680	cutaneous pseudolymphoma	immune_system_disorder|integumentary_system_disorder	autoimmune_disease	integumentary_system_disorder|immune_system_disorder	oncology|dermatology	inflammatory_disease|cancer|autoimmune_diseases	lymphatic_disorder|skin_disorder	false	true	false	true	medium
MONDO:0018681	neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	cardiology|pediatric|genetics_and_genomics|neurology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|joint_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0018682	congenital insensitivity to pain with severe intellectual disability	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018683	acquired ichthyosis	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0018684	idiopathic neonatal atrial flutter	cardiovascular_disorder	cardiovascular_disorder	idiopathic_disease|cardiovascular_disorder	cardiology|pediatric	cardiovascular_disorder|neonatal_disease	heart_disorder	false	false	false	false	high
MONDO:0018685	incessant infant ventricular tachycardia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|pediatric	inflammatory_disease|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	true	high
MONDO:0018686	acquired Creutzfeldt-Jakob disease	nervous_system_disorder|infectious_disease	infectious_disease	infectious_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018687	progressive muscular atrophy	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0018688	anti-p200 pemphigoid	immune_system_disorder|inflammatory_disease|integumentary_system_disorder	autoimmune_disease	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	immunology|dermatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0018689	plasma cell leukemia	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	acute_disease|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	hematology|oncology	anemia|cancer|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	false	very_high
MONDO:0018690	Holmes-Adie syndrome	syndromic_disease	other	syndromic_disease	endocrinology|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	eye_disorder|endocrine_disorder|brain_disorder	false	false	false	false	low
MONDO:0018692	variably protease-sensitive prionopathy	nervous_system_disorder|infectious_disease	neurodegenerative_disease|infectious_disease	infectious_disease|nervous_system_disorder	genetics_and_genomics|neurology	prionopathies|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0018694	isolated tracheo-esophageal fistula	upper_digestive_tract_disorder|digestive_system_disorder|respiratory_system_disorder	other	upper_digestive_tract_disorder|respiratory_system_disorder|digestive_system_disorder	pediatric|gastroenterology|otolaryngology	inflammatory_disease|congenital_heart_disease|gastrointestinal_disorder	upper_gastrointestinal_disorder|throat_disorder	false	false	false	true	high
MONDO:0018695	avian influenza	infectious_disease|respiratory_system_disorder	infectious_disease	respiratory_system_disorder|infectious_disease	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	vascular_disorder|lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0018696	corticobasal syndrome	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018697	1p35.2 microdeletion syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018698	hereditary neuroendocrine tumor of small intestine	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor|hereditary_disease	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|digestive_system_disorder|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|oncology|gastroenterology	gastrointestinal_disease|cancer|neoplastic_disease|tumor	endocrine_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0018702	Castleman-Kojima disease	syndromic_disease|hereditary_disease|cancer_or_benign_tumor|immune_system_disorder	autoimmune_disease|cancer_or_benign_tumor	syndromic_disease|hereditary_disease|immune_system_disorder|cancer_or_benign_tumor	allergy_and_immunology|hematology|oncology|rheumatology	inflammatory_disease|cancer|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0018703	isolated splenogonadal fusion	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	hematology|genetics_and_genomics	inflammatory_disease|cancer|autoimmune_diseases|isolated_splenogonadal_fusion_is_classified_under_the_category_of__anemia	reproductive_system_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0018705	infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|eye_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0018708	squamous cell carcinoma of the oral tongue	digestive_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|mouth_disorder|cancer_or_benign_tumor|nervous_system_disorder|digestive_system_disorder	oncology|otolaryngology	tongue_cancer|cancer|squamous_cell_carcinoma|oral_tongue_disease	upper_gastrointestinal_disorder|throat_disorder|skin_disorder|teeth_disorder	false	true	false	true	very_high
MONDO:0018709	X-linked intellectual disability-hypotonia-movement disorder syndrome	syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0018710	megalencephaly-severe kyphoscoliosis-overgrowth syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|orthopaedic|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0018711	intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0018712	composite hemangioendothelioma	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hematology|oncology	cancer|cardiovascular_disorder	vessel_disorder|vascular_disorder	false	true	false	false	medium
MONDO:0018713	retiform hemangioendothelioma	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hematology|oncology	adrenal_gland_disease|cancer	vascular_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018714	primary intralymphatic angioendothelioma	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	oncology|hematologic	cancer|hematologic_malignancy|soft_tissue_sarcoma|lymphoma|blood_cancer|immune_system_disorder	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	false	medium
MONDO:0018715	congenital hemangioma	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	pediatric|dermatology|hematology	inflammatory_disease|cancer|cardiovascular_disorder	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0018716	partially involuting congenital hemangioma	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	pediatric|dermatology|hematology|oncology	inflammatory_disease|cancer|cardiovascular_disorder	vascular_disorder|liver_disorder|skin_disorder	false	false	false	true	medium
MONDO:0018717	mixed cystic lymphatic malformation	cardiovascular_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	immune_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	pediatric|vascular	cancer|cardiovascular_disorder	lymphatic_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0018724	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|neurology|orthopaedic|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder|brain_disorder	false	false	false	false	high
MONDO:0018725	corpus callosum agenesis-macrocephaly-hypertelorism syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|nose_disorder|throat_disorder|brain_disorder	false	false	false	false	high
MONDO:0018733	intellectual disability syndrome due to a DYRK1A point mutation	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0018734	verrucous hemangioma	integumentary_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|integumentary_system_disorder|cardiovascular_disorder	dermatology|hematology	inflammatory_disease|cancer	vascular_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018735	multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome	cardiovascular_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	immune_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	pathology|hematology|oncology	inflammatory_disease|autoimmune_diseases|anemia	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0018736	kaposiform lymphangiomatosis	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	dermatology|oncology|genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder	lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0018737	catastrophic antiphospholipid syndrome	syndromic_disease|immune_system_disorder	autoimmune_disease	syndromic_disease|immune_system_disorder	cardiology|hematology|rheumatology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	vascular_disorder|immune_disorder	false	false	false	false	high
MONDO:0018738	benign metanephric tumor	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	renal_medicine|oncology|pediatric	adrenal_gland_disease|cancer	urogenital_system_disorder|kidney_disorder	false	false	false	false	low
MONDO:0018739	neonatal alloimmune neutropenia	hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder	immunology|hematology|pediatric	inflammatory_disease|autoimmune_diseases|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0018740	drug-induced methemoglobinemia	hematologic_disorder	other	hematologic_disorder	pulmonology|hematology	metabolic_disorder|anemia	drug_side_effect|liver_disorder	false	false	false	true	medium
MONDO:0018741	paracetamol poisoning	poisoning	other	poisoning	hepatology|gastroenterology|pediatric	metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0018742	familial gastric type 1 neuroendocrine tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	oncology|gastroenterology	cancer|neuroendocrine_tumor	upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0018744	oligodendroglial tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0018746	mucous membrane pemphigoid	integumentary_system_disorder|immune_system_disorder|inflammatory_disease	autoimmune_disease	inflammatory_disease|integumentary_system_disorder|immune_system_disorder	allergy_and_immunology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder_skin_disorder	false	false	false	true	high
MONDO:0018747	acquired epidermolysis bullosa	integumentary_system_disorder|immune_system_disorder|inflammatory_disease	autoimmune_disease	inflammatory_disease|integumentary_system_disorder|immune_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0018748	linear IgA Dermatosis	integumentary_system_disorder|immune_system_disorder|inflammatory_disease	autoimmune_disease	inflammatory_disease|integumentary_system_disorder|immune_system_disorder	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0018749	hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|beta_thalassemia_syndrome	false	false	false	true	medium
MONDO:0018751	hereditary otorhinolaryngologic disease	otorhinolaryngologic_disease|hereditary_disease	other	otorhinolaryngologic_disease|hereditary_disease	genetics_and_genomics|otolaryngology	hereditary_diseases|inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	false	false	false	false	high
MONDO:0018752	exercise-induced malignant hyperthermia	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|orthopaedic|cardiology|pediatric|pulmonology	malignant_hypothermia_syndrome_is_often_associated_with_disorders_of_calcium_regulation_which_can_occur_due_to_defects_in_the_ryanodine_receptor__specifically_type_1_myopathies|metabolic_disorder	muscle_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0018754	cyanide poisoning	poisoning	other	poisoning	neurology|toxicology_is_not_in_the_list__so_none	metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	very_high
MONDO:0018755	scorpion envenomation	poisoning	other	poisoning	hematology|neurology|emergency_medicine	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	skin_disorder|muscle_disorder|nose_disorder	false	false	false	true	medium
MONDO:0018756	euthyroid Graves orbitopathy	immune_system_disorder	autoimmune_disease	immune_system_disorder	endocrinology|ophthalmology	metabolic_disorder|autoimmune_diseases	eye_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0018757	supratip dysplasia	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0018759	childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|muscle_dystrophy_syndrome	muscle_disorder|muscle_dystrophy_syndrome|joint_disorder	true	false	false	false	very_high
MONDO:0018760	DeSanto-Shinawi syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|neurology|pediatrics	neurodegenerative_disease|mental_health_disorder	reproductive_system_disorder|joint_disorder	false	false	false	false	high
MONDO:0018761	SMARCA4-deficient sarcoma of thorax	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	genetics_and_genomics|oncology	sarcoma|cancer	sarcoma|thorax|muscle_disorder	false	true	false	false	very_high
MONDO:0018762	non-acquired combined pituitary hormone deficiency	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|neurology|pediatric	endocrine_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0018763	tubulinopathy-associated dysgyria	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018764	microcephalic primordial dwarfism due to RTTN deficiency	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder|brain_disorder|muscle_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0018765	cryptogenic multifocal ulcerous stenosing enteritis	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|pediatric	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0018766	chronic enteropathy associated with SLCO2A1 gene	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|genetics_and_genomics	anemia|inflammatory_disease|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0018767	severe primary trimethylaminuria	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|renal_medicine|hepatology	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0018768	familial cold autoinflammatory syndrome	hereditary_disease|immune_system_disorder|syndromic_disease|connective_tissue_disorder	other	immune_system_disorder|hereditary_disease|connective_tissue_disorder|syndromic_disease	genetics_and_genomics|rheumatology|pediatrics	inflammatory_disease|autoimmune_diseases	immune_disorder|upper_gastrointestinal_disorder|joint_disorder	false	false	false	true	medium
MONDO:0018769	isosporiasis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|pediatric	anemia|inflammatory_disease|autoimmune_diseases	immune_disorder|liver_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0018770	Jeune syndrome	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|urinary_system_disorder|respiratory_system_disorder	other	hereditary_disease|urinary_system_disorder|musculoskeletal_system_disorder|respiratory_system_disorder|syndromic_disease	genetics_and_genomics|orthopaedic|pediatric	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|skeletal_system_disorder	false	false	false	false	very_high
MONDO:0018772	Joubert syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	anemia|neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0018773	autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018776	demyelinating hereditary motor and sensory neuropathy	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018777	autosomal dominant preaxial polydactyly-upperback hypertrichosis syndrome	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|orthopaedic|pediatric	genetic_disorders|metabolic_disorder	upper_gastrointestinal_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018778	intermediate Charcot-Marie-Tooth disease	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	nerve_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018780	congenital generalized hypercontractile muscle stiffness syndrome	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|neurology|rheumatology|pediatric	muscular_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018781	KID syndrome	integumentary_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|integumentary_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0018783	fibroblastic rheumatism	connective_tissue_disorder	other	connective_tissue_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0018784	pediatric multiple sclerosis	immune_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease|autoimmune_disease	immune_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	immune_disorder|brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0018793	primary condylar hyperplasia	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic	genetic_disorder|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0018794	cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder	hematologic_disorder|digestive_system_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder|digestive_system_disorder	genetics_and_genomics|hematology|renal_medicine	bleeding_disorder|metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0018795	syndromic constitutional thrombocytopenia	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0018800	Kallmann syndrome	hereditary_disease|syndromic_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|syndromic_disease|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology|pediatric	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0018801	congenital bilateral absence of vas deferens	hereditary_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis	other	reproductive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	urology|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0018804	MYO5B-related progressive familial intrahepatic cholestasis	hereditary_disease|digestive_system_disorder|metabolic_disease|syndromic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|syndromic_disease|endocrine_system_disorder|metabolic_disease|hereditary_disease	gastroenterology|genetics_and_genomics|hepatology	liver_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0018805	bile duct cyst	hereditary_disease|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|hereditary_disease	gastroenterology|hepatology	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|biliary_disorder|liver_disorder	false	false	false	true	medium
MONDO:0018806	primary intrahepatic lithiasis	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|hepatology	primary_intrahepatic_lithiasis_is_caused_by_bile_salts_or_bilirubin_in_the_bile_which_causes_inflammation_of_the_biliary_tract_and_subsequent_formation_of_gallstones|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0018807	idiopathic ductopenia	digestive_system_disorder	other	digestive_system_disorder|idiopathic_disease	rheumatology|pediatric	metabolic_disorder|autoimmune_diseases	immune_disorder|liver_disorder	false	false	false	false	high
MONDO:0018808	Caroli syndrome	hereditary_disease|digestive_system_disorder|syndromic_disease	other	digestive_system_disorder|syndromic_disease|hereditary_disease	urology|hepatology	liver_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0018809	idiopathic peliosis hepatis	digestive_system_disorder|inflammatory_disease|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|idiopathic_disease|inflammatory_disease	gastroenterology|hepatology	metabolic_disorder|inflammatory_disease	immune_disorder|liver_disorder	false	false	false	false	high
MONDO:0018810	lethal hydranencephaly-diaphragmatic hernia syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	brain_disorder|spinal_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0018811	congenital portosystemic shunt	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	gastroenterology|genetics_and_genomics|hepatology|pediatric	metabolic_disorder|cardiovascular_disorder	upper_gastrointestinal_disorder|vascular_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0018813	high grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	hematology|oncology	cancer|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0018814	non-SCID combined immunodeficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|allergy_and_immunology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0018815	aneurysmal bone cyst	hereditary_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder	orthopaedic	bone_related_disease|metabolic_disorder	bone_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0018816	isolated neonatal sclerosing cholangitis	digestive_system_disorder|hereditary_disease|inflammatory_disease|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|hereditary_disease|inflammatory_disease	gastroenterology|hepatology|pediatric	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0018818	facial diplegia with paresthesias	nervous_system_disorder|syndromic_disease|immune_system_disorder	autoimmune_disease	nervous_system_disorder|syndromic_disease|immune_system_disorder	neurology|otolaryngology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|muscle_disorder	true	false	false	false	high
MONDO:0018820	recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	cardiology|genetics_and_genomics|neurology|pediatric|psychiatry	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	brain_disorder|muscle_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0018821	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability	syndromic_disease	other	syndromic_disease	obstetrics_and_gynecology|genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	reproductive_system_disorder|intellectual_disability|face_disorder	false	false	false	false	very_high
MONDO:0018822	global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome	nervous_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|disorder_of_visual_system	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0018824	pyoderma gangrenosum	syndromic_disease|integumentary_system_disorder|connective_tissue_disorder	other	syndromic_disease|integumentary_system_disorder|connective_tissue_disorder	rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0018826	Lewis-Sumner syndrome	nervous_system_disorder|inflammatory_disease|disorder_of_development_or_morphogenesis	neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|inflammatory_disease	rheumatology|neurology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0018827	familial chilblain lupus	cardiovascular_disorder|hereditary_disease|syndromic_disease|integumentary_system_disorder|immune_system_disorder|connective_tissue_disorder	autoimmune_disease|cardiovascular_disorder	syndromic_disease|immune_system_disorder|integumentary_system_disorder|hereditary_disease|connective_tissue_disorder|cardiovascular_disorder	genetics_and_genomics|rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0018828	pseudo-TORCH syndrome 2	hereditary_disease|syndromic_disease|connective_tissue_disorder	other	syndromic_disease|hereditary_disease|connective_tissue_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder	true	false	false	false	high
MONDO:0018829	familial schizencephaly	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018830	Kimura disease	inflammatory_disease|immune_system_disorder	autoimmune_disease	immune_system_disorder|inflammatory_disease	rheumatology|immunology	autoimmune_diseases|inflammatory_disease	joint_disorder|immune_disorder	false	false	false	false	medium
MONDO:0018832	HTRA1-related autosomal dominant cerebral small vessel disease	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0018835	nodular regenerative hyperplasia of the liver	digestive_system_disorder|endocrine_system_disorder|premature_aging_syndrome	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|premature_aging_syndrome	gastroenterology|hepatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	liver_disorder	false	false	false	false	medium
MONDO:0018837	postinfectious vasculitis	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	post_infectious_disorder|inflammatory_disease|cardiovascular_disorder	rheumatology|hematology	autoimmune_diseases|inflammatory_disease	immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0018838	lissencephaly spectrum disorders	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018839	acquired schizencephaly	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018840	isolated congenital hepatic fibrosis	digestive_system_disorder|endocrine_system_disorder|premature_aging_syndrome|hereditary_disease	endocrine_system_disorder	premature_aging_syndrome|digestive_system_disorder|endocrine_system_disorder|hereditary_disease	gastroenterology|genetics_and_genomics|pediatric|hepatology	metabolic_disorder|genetic_disorder	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0018841	congenital bile acid synthesis defect	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	gastroenterology|genetics_and_genomics|pediatric|hepatology	metabolic_disorder|adrenal_gland_disease|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0018842	primary effusion lymphoma	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|post_infectious_disorder|hematologic_disorder	hematology|oncology	cancer|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	true	false	false	very_high
MONDO:0018843	embryonal carcinoma of the central nervous system	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0018844	urachal cyst	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	cancer|urachal_cyst	urinary_tract_disorder|kidney_disorder	false	false	false	true	low
MONDO:0018845	focal myositis	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|idiopathic_disease|inflammatory_disease	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|immune_disorder	false	false	false	false	medium
MONDO:0018846	penile agenesis	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	urology|genetics_and_genomics	congenital_disorder|genital_abnormality	urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0018847	omphalomesenteric cyst	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	gastroenterology|urology	cancer|neurodegenerative_disease|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0018848	IgG4-related retroperitoneal fibrosis	immune_system_disorder	autoimmune_disease	immune_system_disorder	allergy_and_immunology|rheumatology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	true	medium
MONDO:0018849	dentinogenesis imperfecta	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	genetics_and_genomics|dermatology|pediatric	genetic_disorder|metabolic_disorder	teeth_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018850	proliferating trichilemmal cyst	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer|tumor_disease|skin_disease	skin_disorder	false	false	false	false	low
MONDO:0018851	familial keratoacanthoma	integumentary_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	cancer	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018852	achromatopsia	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|disorder_of_visual_system	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0018853	transgrediens et progrediens palmoplantar keratoderma	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|joint_disorder	true	false	false	false	high
MONDO:0018854	acquired purpura fulminans	cardiovascular_disorder|hematologic_disorder	cardiovascular_disorder	hematologic_disorder|cardiovascular_disorder	dermatology|hematology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|vascular_disorder	true	false	false	true	very_high
MONDO:0018855	keratosis pilaris atrophicans	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder	false	false	false	false	low
MONDO:0018856	lichen amyloidosis	integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease	renal_medicine|dermatology|hepatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	liver_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018857	creeping myiasis	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease	entomology_is_not_in_list_so__dermatology|dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0018858	Graham Little-Piccardi-Lassueur syndrome	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|biliary_disorder	false	false	false	false	medium
MONDO:0018860	microlissencephaly-micromelia syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018861	Zellweger-like syndrome without peroxisomal anomalies	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	metabolic_disease	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0018864	Kikuchi-Fujimoto disease	inflammatory_disease|immune_system_disorder	other	immune_system_disorder|inflammatory_disease	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|joint_disorder	true	false	false	false	low
MONDO:0018865	striate palmoplantar keratoderma	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0018866	Aicardi-Goutieres syndrome	nervous_system_disorder|hereditary_disease|syndromic_disease|immune_system_disorder|connective_tissue_disorder	neurodegenerative_disease	nervous_system_disorder|syndromic_disease|immune_system_disorder|hereditary_disease|connective_tissue_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	immune_disorder_blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0018868	metachromatic leukodystrophy	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|metabolic_disease|psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|note__metachromatic_leukodystrophy_is_a_genetic_disorder_that_affects_the_metabolism_of_fatty_substances_in_the_brain_and_spinal_cord__leading_to_neurodegeneration	brain_disorder_spinal_disorder	false	false	false	false	very_high
MONDO:0018869	cobblestone lissencephaly	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018870	arterial calcification of infancy	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|pediatric	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0018871	acute myelomonocytic leukemia M4	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	acute_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|immune_system_disorder|hematologic_disorder|connective_tissue_disorder	hematology|oncology	cancer|leukemia|anemia	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	high
MONDO:0018872	acute megakaryoblastic leukemia	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	acute_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|immune_system_disorder|hematologic_disorder|connective_tissue_disorder	hematology|oncology	cancer|anemia	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0018873	anterior cutaneous nerve entrapment syndrome	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	skin_disorder|muscle_disorder|nerve_disorder	false	false	false	true	medium
MONDO:0018874	acute myeloid leukemia	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	acute_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|immune_system_disorder|hematologic_disorder|connective_tissue_disorder	hematology|oncology	cancer|leukemia|anemia	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0018875	Li-Fraumeni syndrome	hereditary_disease|nervous_system_disorder|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|oncology	cancer|hereditary_cancer_predisposition___note__li_fraumeni_syndrome_is_indeed_a_cancer_predisposition_syndrome	lymphatic_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0018876	mantle cell lymphoma	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	hematology|oncology	cancer|lymphoma	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	high
MONDO:0018877	retinitis punctata albescens	hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|ophthalmology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0018878	branchiootic syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	otolaryngology|pediatric	autoimmune_diseases|inflammatory_disease	ear_disorder_throat_disorder	false	false	false	false	medium
MONDO:0018879	lichen planopilaris	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|allergy_and_immunology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0018881	myelodysplastic syndrome	cancer_or_benign_tumor|hematologic_disorder|syndromic_disease	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|syndromic_disease	oncology|hematology|genetics_and_genomics	anemia|cancer	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0018882	vasculitis	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	rheumatology|hematology	inflammatory_disease|autoimmune_diseases	vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0018883	Berardinelli-Seip congenital lipodystrophy	integumentary_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|integumentary_system_disorder|hereditary_disease	pediatric|dermatology|genetics_and_genomics	metabolic_disorder|genetic_disease	joint_disorder|endocrine_disorder|muscle_disorder|skin_disorder	false	false	true	false	very_high
MONDO:0018884	Roch-Leri mesosomatous lipomatosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|oncology|genetics_and_genomics	cancer|mesosomatous|lipomatosis|tissue_growth_abnormality	lymphatic_disorder|muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0018885	orbital leiomyoma	disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_orbital_region|cancer_or_benign_tumor|disorder_of_visual_system	oncology|ophthalmology	cancer|orbital_tumor	vascular_disorder|eye_disorder|muscle_disorder	false	false	false	false	low
MONDO:0018889	hyaline body myopathy	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|orthopaedic	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018890	Lyell syndrome	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|immunology|rheumatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0018891	familial tumoral calcinosis	endocrine_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor|metabolic_disease	cancer_or_benign_tumor|endocrine_system_disorder|metabolic_disease	integumentary_system_disorder|metabolic_disease|endocrine_system_disorder|cancer_or_benign_tumor	oncology|dermatology|endocrinology|genetics_and_genomics|orthopaedic	cancer|metabolic_disorder|genetic_disease	skeletal_system_disorder|bone_disorder	false	false	false	false	high
MONDO:0018892	Wyburn-Mason syndrome	nervous_system_disorder|integumentary_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	integumentary_system_disorder|nervous_system_disorder|cardiovascular_disorder|disorder_of_orbital_region|cancer_or_benign_tumor|disorder_of_visual_system	neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0018893	Cobb syndrome	integumentary_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder|syndromic_disease|hereditary_disease	cancer_or_benign_tumor|cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder|hereditary_disease|cancer_or_benign_tumor|syndromic_disease	neurology|orthopaedic	cardiovascular_disorder|spinal_deformity_disorder__cobb_syndrome_is_related_to_a_type_of_scoliosis	joint_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018894	distal hereditary motor neuropathy	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	hereditary_motor_neuropathy|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018895	Plummer-Vinson syndrome	hematologic_disorder|syndromic_disease	anemia	hematologic_disorder|syndromic_disease	hepatology|hematology|gastroenterology|pulmonology|genetics_and_genomics	anemia|metabolic_disorder|autoimmune_diseases	throat_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0018896	thrombotic thrombocytopenic purpura	hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder	hematology|cardiology	cardiovascular_disorder|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0018897	primary cutaneous CD30+ T-cell lymphoproliferative disease	integumentary_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	integumentary_system_disorder|hematologic_disorder|cancer_or_benign_tumor	oncology|dermatology|rheumatology|hematolog	inflammatory_disease|cancer|autoimmune_diseases	lymphatic_disorder|skin_disorder	false	true	false	true	high
MONDO:0018898	primary cutaneous lymphoma	integumentary_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	integumentary_system_disorder|hematologic_disorder|cancer_or_benign_tumor	oncology|dermatology|hematology	inflammatory_disease|cancer|autoimmune_diseases	lymphatic_disorder|skin_disorder	false	true	false	true	high
MONDO:0018899	posterior cortical atrophy	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018900	corticosteroid-sensitive aseptic abscess syndrome	integumentary_system_disorder	other	integumentary_system_disorder	rheumatology|allergy_and_immunology|pediatrics	autoimmune_diseases|inflammatory_disease	endocrine_disorder|immune_disorder	false	false	false	true	medium
MONDO:0018901	left ventricular noncompaction	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	cardiovascular_disorder	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiothoracic|cardiology|pulmonology|renal_medicine|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0018902	hepatocellular adenoma	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|hepatology	cancer|metabolic_disorder	liver_disorder	false	false	false	true	medium
MONDO:0018903	sarcocystosis	infectious_disease	infectious_disease	infectious_disease	gastroenterology|neurology|hepatology	autoimmune_diseases|inflammatory_disease	liver_disorder|muscle_disorder	true	false	false	false	medium
MONDO:0018904	primary membranoproliferative glomerulonephritis	inflammatory_disease|urinary_system_disorder	other	inflammatory_disease|urinary_system_disorder	hematology|rheumatology|renal_medicine	autoimmune_diseases|inflammatory_disease	vascular_disorder|kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0018905	diffuse large B-cell lymphoma	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	hematology|oncology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0018906	follicular lymphoma	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	hematology|oncology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0018907	craniopharyngioma	cancer_or_benign_tumor|nervous_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|connective_tissue_disorder	neurology|pediatric|oncology	cancer|neurological_disease	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0018908	non-Hodgkin lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0018910	oculocutaneous albinism	metabolic_disease|hereditary_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	ophthalmology|dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|anemia|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0018911	maturity-onset diabetes of the young	metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder	metabolic_disease|endocrine_system_disorder|diabetes_mellitus	digestive_system_disorder|endocrine_system_disorder|metabolic_disease|hereditary_disease	endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|endocrine_disorder	false	false	true	true	medium
MONDO:0018912	Cushing syndrome	syndromic_disease	other	syndromic_disease	endocrinology	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0018913	malakoplakia	digestive_system_disorder	other	digestive_system_disorder	genitourinary|renal_medicine|urology|dermatology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|kidney_disorder|immune_disorder	true	false	false	false	medium
MONDO:0018914	hypotrichosis simplex	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|hair_disorder	false	false	false	false	low
MONDO:0018918	carcinoma of gallbladder and extrahepatic biliary tract	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|hepatology|oncology	cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0018919	McCune-Albright syndrome	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	pediatric|endocrinology|obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|genetic_cancer	bone_disorder|bone_disorder_is_primary__but_endocrine_disorder_is_key_feature_of_mccune_albright_syndrome__endocrine_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0018920	peripartum cardiomyopathy	obstetric_disorder|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	obstetric_disorder|musculoskeletal_system_disorder|cardiovascular_disorder	obstetrics_and_gynecology|cardiology|cardiothoracic	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0018921	Meckel syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder	joint_disorder|upper_gastrointestinal_disorder|liver_disorder|kidney_disorder|lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0018922	cold agglutinin disease	immune_system_disorder|hematologic_disorder	autoimmune_disease|anemia	hematologic_disorder|immune_system_disorder	pulmonology|immunology|hematology	inflammatory_disease|autoimmune_diseases|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	medium
MONDO:0018923	22q11.2 deletion syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder|cardiovascular_disorder|nervous_system_disorder|immune_system_disorder	cardiovascular_disorder	cardiovascular_disorder|chromosomal_disorder|immune_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder	developmental_disorders_are_sometimes_categorized_under_neurology_but_in_this_case_is_best_fit_under_genetics_and_genomics|genetics_and_genomics|pediatric	cardiovascular_disorder|mental_health_disorder|metabolic_disorder	vascular_disorder|lymphatic_disorder|blood_bone_marrow_disorder|heart_disorder|immune_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0018924	microphthalmia, Lenz type	hereditary_disease|disorder_of_visual_system|syndromic_disease	other	disorder_of_orbital_region|syndromic_disease|disorder_of_visual_system|hereditary_disease	ophthalmology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0018925	familial or sporadic hemiplegic migraine	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|familial_migraine	vascular_disorder|brain_disorder	false	false	false	true	high
MONDO:0018926	human prion disease	nervous_system_disorder|infectious_disease	neurodegenerative_disease|infectious_disease	infectious_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0018927	SUNCT syndrome	cardiovascular_disorder|nervous_system_disorder|syndromic_disease	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|nervous_system_disorder	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0018929	medial condensing osteitis of the clavicle	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0018930	monosomy 21	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	skin_disorder|ear_disorder|eye_disorder|urinary_tract_disorder|joint_disorder|blood_bone_marrow_disorder|spinal_disorder|nose_disorder|heart_disorder|immune_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0018931	mucolipidosis type III, alpha/beta	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	lysosomal_storage_disorder|lung_disorder|skeletal_dysplasia	false	false	false	false	high
MONDO:0018932	cirrhotic cardiomyopathy	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder	hepatology|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|liver_disorder	false	false	false	false	high
MONDO:0018933	Mazabraud syndrome	cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease	pediatrics|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	biliary_disorder|liver_disorder	false	false	false	false	medium
MONDO:0018935	hairy cell leukemia	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|acute_disease	oncology|hematology	cancer|anemia	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	medium
MONDO:0018936	osteoblastoma	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	oncology|orthopaedic	bone_diseases|cancer	joint_disorder|spinal_disorder|bone_disorder	false	false	false	true	low
MONDO:0018937	mucopolysaccharidosis type 3	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder|syndromic_disease	metabolic_disease	musculoskeletal_system_disorder|metabolic_disease|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0018938	mucopolysaccharidosis type 4	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease	metabolic_disease	metabolic_disease|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|skeletal_disorder|bone_disorder	false	false	false	true	very_high
MONDO:0018939	muscle-eye-brain disease	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0018940	congenital myasthenic syndrome	syndromic_disease|hereditary_disease|nervous_system_disorder	other	syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0018941	furuncular myiasis	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease	otolaryngology|dermatology	infectious_disease|inflammatory_disease	skin_disorder	true	false	false	true	low
MONDO:0018942	macrophagic myofasciitis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	pulmonology|neurology|rheumatology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018943	myofibrillar myopathy	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology|rheumatology	cardiovascular_disorder|neurodegenerative_disease	bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018944	gestational trophoblastic neoplasm	obstetric_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|obstetric_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	true	high
MONDO:0018945	McLeod neuroacanthocytosis syndrome	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|anemia	blood_bone_marrow_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0018946	rhombencephalosynapsis	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0018947	centronuclear myopathy	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	lower_gastrointestinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018948	multiminicore myopathy	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018949	distal myopathy	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018950	3-methylcrotonyl-CoA carboxylase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	true	medium
MONDO:0018951	distal myopathy with vocal cord weakness	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	neurology|otolaryngology	neurodegenerative_disease|autoimmune_diseases	throat_disorder|muscle_disorder	false	false	false	false	high
MONDO:0018952	argyria	poisoning	other	poisoning	ophthalmology|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0018953	parietal foramina	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|otolaryngology	neurodegenerative_disease|cancer|inflammatory_disease|adrenal_gland_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0018954	Loeys-Dietz syndrome	syndromic_disease|connective_tissue_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	connective_tissue_disorder|cardiovascular_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric|orthopaedic	cardiovascular_disorder|metabolic_disorder	bone_disorder|vascular_disorder|skin_disorder	false	false	false	false	high
MONDO:0018955	recurrent respiratory papillomatosis	respiratory_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology|pediatric	cancer|inflammatory_disease	throat_disorder|lung_disorder	true	false	false	false	medium
MONDO:0018956	idiopathic bronchiectasis	respiratory_system_disorder|hereditary_disease	other	idiopathic_disease|hereditary_disease|respiratory_system_disorder	pulmonology	note__i_corrected_the_category_to_be_more_specific_as_it_was_originally_categorized_under_a_broader_list_____corrected_answer_without_respiratory_disorder____inflammatory_disease|respiratory_disorder|inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	false	false	false	false	high
MONDO:0018957	pudendal neuralgia	nervous_system_disorder	other	nervous_system_disorder	neurology|urology	neurodegenerative_disease|inflammatory_disease	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0018958	nemaline myopathy	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0018959	potassium-aggravated myotonia	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0018960	congenital primary megaureter	disorder_of_development_or_morphogenesis|urinary_system_disorder	other	urinary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|urology	congenital_abnormality|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0018961	familial melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|hereditary_disease	oncology|genetics_and_genomics|dermatology	skin_cancer|cancer|familial_disease|cancer_family|genetic_disorder	lymphatic_disorder|skin_disorder	false	true	false	true	high
MONDO:0018962	common mesentery	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|hepatology	cancer|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0018963	hereditary methemoglobinemia	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|red_blood_cell_disorder	false	false	false	true	medium
MONDO:0018964	homocystinuria without methylmalonic aciduria	hereditary_disease|metabolic_disease|hematologic_disorder|nutritional_disorder	anemia|metabolic_disease	nutritional_disorder|metabolic_disease|hematologic_disorder|hereditary_disease	genetics_and_genomics|pediatric|hematology	metabolic_disorder|biochemical_disorder|inherited_disease	blood_bone_marrow_disorder|liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0018965	Alport syndrome	syndromic_disease|hereditary_disease|urinary_system_disorder|inflammatory_disease	other	syndromic_disease|urinary_system_disorder|hereditary_disease|inflammatory_disease	urology|genetics_and_genomics|renal_medicine	renal|disease|kidney|autoimmune_diseases|metabolic_disorder___note__since__alport_syndrome__is_a_genetic_disorder_affecting_the_kidneys__i_have_provided_categories_that_reflect_this_connection	joint_disorder|kidney_disorder|ear_disorder	false	false	false	false	high
MONDO:0018967	short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia	hereditary_disease|nervous_system_disorder|reproductive_system_disorder|immune_system_disorder|hematologic_disorder|endocrine_system_disorder	endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder|hematologic_disorder|immune_system_disorder|hereditary_disease|reproductive_system_disorder	genetics_and_genomics|endocrinology|pediatric	neurodegenerative_disease|metabolic_disorder	immune_disorder|bone_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0018968	iniencephaly	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0018969	craniorachischisis	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|neurology|pediatric	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0018971	isolated oxycephaly	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0018973	patterned dystrophy of the retinal pigment epithelium	hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|psychiatric_disorder|hereditary_disease	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018974	paraneoplastic pemphigus	syndromic_disease|cancer_or_benign_tumor|integumentary_system_disorder|immune_system_disorder|inflammatory_disease	autoimmune_disease|cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|syndromic_disease|immune_system_disorder|inflammatory_disease	oncology|dermatology	cancer|autoimmune_diseases	skin_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0018975	neurofibromatosis type 1	syndromic_disease|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	oncology|genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|cancer|other____neurofibromatosis_type_1_is_a_genetic_disorder_that_leads_to_tumors_on_the_nervous_system	brain_disorder|skin_disorder|spinal_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0018976	schisis association	syndromic_disease	other	syndromic_disease	oncology|genetics_and_genomics|pediatric|hematology	neurodegenerative_disease|autoimmune_diseases	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0018977	polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG	nervous_system_disorder	other	nervous_system_disorder	neurology|hematology	neurodegenerative_disease|autoimmune_diseases	blood_bone_marrow_disorder|muscle_disorder|immune_disorder	false	false	false	true	high
MONDO:0018978	IgG4-related mediastinitis	respiratory_system_disorder|immune_system_disorder	autoimmune_disease	respiratory_system_disorder|immune_system_disorder	genetics_and_genomics|pulmonology|allergy_and_immunology|rheumatology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|other____although_igg4_related_mediastinitis_is_often_associated_with_the_broader_condition_of_igg4_related_disease__which_has_a_range_of_manifestations_including_multiple_categories_from_this_list__mediastinitis_specifically_falls_under_respiratory_lung_issues_and_immune_disorders|lung_disorder|immune_disorder	false	false	false	true	high
MONDO:0018979	multifocal motor neuropathy	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0018980	acrofacial dysostosis, Kennedy-Teebi type	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|joint_disorder|bone_disorder|skeletal_disorder	false	false	false	false	high
MONDO:0018981	benign idiopathic neonatal seizures	nervous_system_disorder	other	nervous_system_disorder|idiopathic_disease	neurology|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	brain_disorder|neonatal_seizures	false	false	false	true	medium
MONDO:0018982	Niemann-Pick disease type C	hereditary_disease|metabolic_disease|immune_system_disorder	metabolic_disease	metabolic_disease|immune_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	high
MONDO:0018983	Tolosa-Hunt syndrome	syndromic_disease|nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_visual_system|syndromic_disease	oncology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0018984	Oroya fever	infectious_disease	infectious_disease	infectious_disease	tropical_medicine|infectious_diseases|hematology	inflammatory_disease|anemia	vascular_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0018987	granulomatous mastitis	reproductive_system_disorder	other	reproductive_system_disorder	dermatology|allergy_and_immunology|rheumatology	inflammatory_disease|autoimmune_diseases	skin_disorder|lymphatic_disorder|immune_disorder	true	false	false	true	medium
MONDO:0018988	iridocorneal endothelial syndrome	syndromic_disease	other	syndromic_disease	ophthalmology|renal_medicine|endocrinology|urology	inflammatory_disease|autoimmune_diseases	eye_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0018989	recurrent acute pancreatitis	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|acute_disease	gastroenterology|hepatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0018991	hepatoportal sclerosis	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0018992	IgG4-related thyroid disease	immune_system_disorder|endocrine_system_disorder|inflammatory_disease	autoimmune_disease|endocrine_system_disorder	endocrine_system_disorder|immune_system_disorder|inflammatory_disease	endocrinology|rheumatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	endocrine_disorder|immune_disorder	false	false	false	true	high
MONDO:0018993	Charcot-Marie-Tooth disease type 2	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018994	Charcot-Marie-Tooth disease type X	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	orthopaedic|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	nerve_disorder|nerve_disorder____corrected_to__muscle_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018995	Charcot-Marie-Tooth disease type 4	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0018996	spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2	nervous_system_disorder|hereditary_disease|metabolic_disease	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0018997	Noonan syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder|immune_system_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|syndromic_disease|immune_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	skeletal_disorder|joint_disorder|heart_disorder	false	false	false	false	medium
MONDO:0018998	Leber congenital amaurosis	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|psychiatric_disorder|hereditary_disease	genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0018999	LCAT deficiency	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|hepatology|cardiology|hematology	metabolic_disorder|cardiovascular_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0019000	perineural cyst	nervous_system_disorder	other	nervous_system_disorder	ophthalmology|neurology|otolaryngology	neurodegenerative_disease|cancer|inflammatory_disease	spinal_disorder|nerve_disorder|muscle_disorder	false	false	false	false	low
MONDO:0019002	Lhermitte-Duclos disease	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	medium
MONDO:0019003	multiple endocrine neoplasia type 2	hereditary_disease|cancer_or_benign_tumor|syndromic_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor|endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	oncology|genetics_and_genomics|endocrinology	cancer|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0019004	kidney Wilms tumor	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|pediatric|urology	cancer|kidney_cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0019005	nephronophthisis	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	nephrology|renal_medicine	nephro|metabolic_disorder|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0019006	familial idiopathic steroid-resistant nephrotic syndrome	syndromic_disease|urinary_system_disorder|hereditary_disease	other	syndromic_disease|urinary_system_disorder|idiopathic_disease|hereditary_disease	genetics_and_genomics|renal_medicine|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0019007	vaginal atresia	reproductive_system_disorder|disorder_of_development_or_morphogenesis	other	reproductive_system_disorder|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|neonatology|pediatric	developmental_disorder|congenital_anomaly	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0019008	benign recurrent intrahepatic cholestasis	hereditary_disease|metabolic_disease|digestive_system_disorder|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder	metabolic_disease|digestive_system_disorder|endocrine_system_disorder|hereditary_disease	gastroenterology|hepatology	metabolic_disorder|inflammatory_disease	biliary_disorder|liver_disorder	false	false	false	false	medium
MONDO:0019009	isolated focal cortical dysplasia	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0019010	congenital isolated hyperinsulinism	metabolic_disease|digestive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease|endocrine_system_disorder	metabolic_disease|digestive_system_disorder|endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	endocrinology|pediatric	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|congenital_disorder	false	false	true	true	very_high
MONDO:0019011	Charcot-Marie-Tooth disease type 1	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0019012	Carpenter syndrome	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology|cardiothoracic|orthopaedic|otolaryngology|pediatric	cancer|metabolic_disorder	joint_disorder|bone_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0019013	non-histaminic angioedema	integumentary_system_disorder|inflammatory_disease|cardiovascular_disorder|immune_system_disorder	cardiovascular_disorder	immune_system_disorder|integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease	hematology|pulmonology|dermatology|renal_medicine|allergy_and_immunology	autoimmune_diseases|allergic_reactions	immune_disorder__vascular_disorder	false	false	false	false	high
MONDO:0019015	omphalocele	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatric	gastrointestinal_disorder|metabolic_disorder|inflammatory_disease|congenital_abnormality	skin_disorder|lower_gastrointestinal_disorder|reproductive_system_disorder|abdominal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0019016	maternally-inherited progressive external ophthalmoplegia	mitochondrial_disease|musculoskeletal_system_disorder|metabolic_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	metabolic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_visual_system|mitochondrial_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|obstetrics_and_gynecology|ophthalmology|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0019017	short fifth metacarpals-insulin resistance syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|orthopaedic|endocrinology	autoimmune_diseases|insulin_resistance_syndrome|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	true	true	medium
MONDO:0019018	Tako-tsubo cardiomyopathy	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0019019	osteogenesis imperfecta	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	rheumatology|genetics_and_genomics|orthopaedic|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	joint_disorder|spinal_disorder|bone_disorder|teeth_disorder	false	false	false	false	high
MONDO:0019020	PANDAS	nervous_system_disorder|immune_system_disorder	autoimmune_disease	nervous_system_disorder|immune_system_disorder	pediatric|psychiatry	autoimmune_diseases|mental_health_disorder	immune_disorder|brain_disorder	true	false	false	true	high
MONDO:0019022	sensorineural hearing loss-early graying-essential tremor syndrome	nervous_system_disorder	other	nervous_system_disorder	otolaryngology|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|ear_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0019023	cutaneous mastocytosis	integumentary_system_disorder|inflammatory_disease|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|hereditary_disease	cancer_or_benign_tumor	hematologic_disorder|integumentary_system_disorder|hereditary_disease|cancer_or_benign_tumor|immune_system_disorder|inflammatory_disease	dermatology|oncology|hematology	autoimmune_diseases|cancer|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0019024	mast cell sarcoma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|hereditary_disease	cancer_or_benign_tumor	hematologic_disorder|hereditary_disease|cancer_or_benign_tumor|immune_system_disorder	oncology|hematology	autoimmune_diseases|cancer|inflammatory_disease|allergy	immune_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0019025	extracutaneous mastocytoma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|hereditary_disease	cancer_or_benign_tumor	hematologic_disorder|hereditary_disease|cancer_or_benign_tumor|immune_system_disorder	dermatology|oncology|hematology	cancer|leukemia|lymphoma	skin_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0019026	autosomal recessive osteopetrosis	hereditary_disease|musculoskeletal_system_disorder|disorder_of_visual_system	other	musculoskeletal_system_disorder|disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	orthopaedic|pediatric|genetics_and_genomics	anemia|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	true	very_high
MONDO:0019027	otopalatodigital syndrome	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	otalgia_is_part_of_this_name_but_it_may_be_more_related_to_ear_disorder_than_another|ear_disorder|upper_gastrointestinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0019028	amoebiasis due to Entamoeba histolytica	infectious_disease	infectious_disease	infectious_disease	hepatology|gastroenterology	inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0019029	segmental odontomaxillary dysplasia	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|cancer|inflammatory_disease|metabolic_disorder	bone_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0019031	thrombocytopenia with congenital dyserythropoietic anemia	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	thrombocytopenia_with_congenital_dyserythropoietic_anemia|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0019032	X-linked intellectual disability with isolated growth hormone deficiency	psychiatric_disorder|nervous_system_disorder|syndromic_disease|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|endocrinology	neurodegenerative_disease|metabolic_disorder	brain_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0019033	primary cutis verticis gyrata	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|neurology	neurodegenerative_disease|autoimmune_diseases	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0019034	accessory pancreas	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	gastroenterology|endocrinology	cancer|inflammatory_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0019035	pancreatoblastoma	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0019036	amoebiasis due to free-living amoebae	infectious_disease	infectious_disease	infectious_disease	pediatric|hepatology|gastroenterology	inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	false	high
MONDO:0019037	progressive supranuclear palsy	nervous_system_disorder|syndromic_disease|hereditary_disease|disorder_of_visual_system	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0019040	chromosomal disorder		other		pediatric|genetics_and_genomics	chromosomal_disorder_can_also_fit_into_this_category|metabolic_disorder	chromosomal_disorder_is_not_in_the_list__however_it_fits_under_this_category|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0019042	multiple congenital anomalies/dysmorphic syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	congenital_anomalies|metabolic_disorder	eye_disorder|heart_disorder|ear_disorder|joint_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0019046	leukodystrophy	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|hematology	neurodegenerative_disease|metabolic_disorder	brain_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0019050	inherited hemoglobinopathy	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	inherited_condition|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019052	inborn errors of metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	inborn_errors_of_metabolism|metabolic_disorder	metabolic_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0019053	peroxisomal disease	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|neurology|pediatrics	neurodegenerative_disease|metabolic_disorder	peroxisomal_diseases_often_affect_the_liver|liver_disorder	false	false	false	false	very_high
MONDO:0019054	congenital limb malformation	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	orthopaedic|pediatric|genetics_and_genomics	congenital_limb_malformation_is_also_related_to_other_developmental_disorders__but_among_the_given_options__this_one_fits_best|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0019056	neuromuscular disease	nervous_system_disorder	other	nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	muscle_disorder|neuromuscular_disease_is_actually_a_broader_category_that_could_fit_into_several_subcategories__so_the_best_fitting_categories_in_this_list_would_be__muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0019060	bone neoplasm	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	orthopaedic|oncology	bone_neoplasm|cancer	bone_disorder|bone_bone_marrow_disorder	false	true	false	false	high
MONDO:0019064	hereditary spastic paraplegia	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0019065	amyloidosis	metabolic_disease	metabolic_disease	metabolic_disease	hematology|renal_medicine|genetics_and_genomics|neurology|cardiology	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0019067	idiopathic steroid-sensitive nephrotic syndrome	urinary_system_disorder|syndromic_disease	other	syndromic_disease|idiopathic_disease|urinary_system_disorder	pediatric|renal_medicine	autoimmune_diseases|inflammatory_disease	immune_disorder|endocrine_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0019068	congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization	urinary_system_disorder	other	urinary_system_disorder	pediatric|renal_medicine|genetics_and_genomics|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	immune_disorder|urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0019071	pure hair and nail ectodermal dysplasia	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|nail_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0019072	intrahepatic cholestasis	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	true	medium
MONDO:0019073	hypotrichosis-lymphedema-telangiectasia-renal defect syndrome	immune_system_disorder|cardiovascular_disorder|hereditary_disease|syndromic_disease	cardiovascular_disorder	syndromic_disease|hereditary_disease|immune_system_disorder|cardiovascular_disorder	pediatric|renal_medicine|genetics_and_genomics	inflammatory_disease|genetic_disorder|metabolic_disorder	skin_disorder|lymphatic_disorder|kidney_disorder	false	false	false	false	high
MONDO:0019074	bilateral acute depigmentation of the iris	disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_orbital_region|disorder_of_development_or_morphogenesis|hereditary_disease|acute_disease|disorder_of_visual_system	dermatology|ophthalmology	adrenal_gland_disease|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0019075	Bosley-Salih-Alorainy syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|pulmonology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	vascular_disorder|immune_disorder|liver_disorder	false	false	false	false	high
MONDO:0019076	circumscribed palmoplantar hypokeratosis	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|genodermatosis____note__there_is_also_a_specific_category_called__epidermolysis_bullosa_simplex__which_can_be_related_to_this_disease_but_it_s_not_in_the_given_list	false	false	false	false	low
MONDO:0019077	warty dyskeratoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	autoimmune_diseases|cancer|inflammatory_disease	skin_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0019078	Ritscher-Schinzel syndrome	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0019079	proximal spinal muscular atrophy	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|spinal_muscular_atrophy	muscle_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0019080	alopecia totalis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0019082	bullous pemphigoid	inflammatory_disease|immune_system_disorder|integumentary_system_disorder	autoimmune_disease	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0019083	Leigh syndrome with cardiomyopathy	mitochondrial_disease|nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|cardiology	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	muscle_disorder|brain_disorder|heart_disorder	true	false	false	true	very_high
MONDO:0019084	radiation proctitis	inflammatory_disease|immune_system_disorder|hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease|inflammatory_disease|immune_system_disorder	oncology|gastroenterology	autoimmune_diseases|cancer|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0019085	vernal keratoconjunctivitis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	allergy_and_immunology|ophthalmology	autoimmune_diseases|inflammatory_disease|allergy	throat_disorder|eye_disorder	false	false	false	true	medium
MONDO:0019086	carcinoma of esophagus	cancer_or_benign_tumor|upper_digestive_tract_disorder|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	pulmonology|oncology|gastroenterology	carcinoma|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0019087	cholangiocarcinoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|hepatology|gastroenterology	cancer|inflammatory_disease	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0019088	post-transplant lymphoproliferative disease	other	other	disease_related_to_transplantation	hematology|oncology	autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	true	true	false	true	high
MONDO:0019091	bronchopulmonary dysplasia	respiratory_system_disorder|disorder_of_development_or_morphogenesis	other	respiratory_system_disorder|disorder_of_development_or_morphogenesis	pulmonology|pediatric	respiratory_disease|inflammatory_disease|cardiovascular_disorder	immune_disorder|lower_respiratory_disorder|lung_disorder	false	false	false	false	high
MONDO:0019092	infantile apnea	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	neurodegenerative_disease|respiratory_disease___corrected__neurodegenerative_disease|respiratory_disorder	brain_disorder|lung_disorder	false	false	false	false	medium
MONDO:0019093	immunodeficiency due to selective anti-polysaccharide antibody deficiency	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	hematology|pediatric|allergy_and_immunology|immunology|rheumatology	autoimmune_diseases|inflammatory_disease|immunodeficiency	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0019094	congenital Epstein-Barr virus infection	infectious_disease|disorder_of_development_or_morphogenesis	infectious_disease	disorder_of_development_or_morphogenesis|infectious_disease	pediatric|genetics_and_genomics|oncology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|lymphatic_disorder	true	false	false	false	low
MONDO:0019095	plague	infectious_disease	infectious_disease	infectious_disease	hematology|pulmonology|pediatrics	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	true	false	false	true	very_high
MONDO:0019098	autoimmune thrombocytopenia	hematologic_disorder|immune_system_disorder	autoimmune_disease	hematologic_disorder|immune_system_disorder	hematology|immunology|rheumatology	autoimmune_diseases|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019100	neuromyelitis optica	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|eye_disorder|immune_disorder|spinal_disorder	false	false	false	true	high
MONDO:0019101	retinal capillary malformation	cancer_or_benign_tumor|disorder_of_visual_system|hereditary_disease|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder|cancer_or_benign_tumor	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|cardiovascular_disorder|cancer_or_benign_tumor	pediatric|ophthalmology|genetics_and_genomics	anemia|cardiovascular_disorder|inflammatory_disease	vascular_disorder|eye_disorder	false	false	false	false	medium
MONDO:0019102	dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	endocrinology|pediatric|otolaryngology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	teeth_disorder|brain_disorder|bone_disorder|ear_disorder	false	false	false	false	high
MONDO:0019103	benign exophthalmos syndrome	syndromic_disease	other	syndromic_disease	pediatric|ophthalmology|neurology	neurodegenerative_disease	eye_disorder|spinal_disorder	false	false	false	false	low
MONDO:0019104	Sandifer syndrome	syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder	pediatric|neurology|pulmonology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	medium
MONDO:0019105	renal nutcracker syndrome	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	inflammatory_disease_cardiovascular_disorder|renal_nutcracker_syndrome	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0019107	Rh deficiency syndrome	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0019108	silent sinus syndrome	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	otolaryngology|pulmonology	inflammatory_disease|neurodegenerative_disease	ear_disorder|nose_disorder	false	false	false	false	medium
MONDO:0019109	CANOMAD syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	vascular_disorder|brain_disorder|immune_disorder|joint_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0019111	familial thrombocytosis	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0019112	cancer-associated retinopathy	cancer_or_benign_tumor|syndromic_disease|nervous_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_visual_system|disorder_of_orbital_region|syndromic_disease|cancer_or_benign_tumor|nervous_system_disorder	ophthalmology|oncology	cancer|inflammatory_disease	eye_disorder	false	true	false	false	high
MONDO:0019113	benign paroxysmal torticollis of infancy	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	low
MONDO:0019114	psychogenic movement disorders	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0019115	obesity due to melanocortin 4 receptor deficiency	endocrine_system_disorder|hereditary_disease|nutritional_disorder	endocrine_system_disorder	nutritional_disorder|hereditary_disease|endocrine_system_disorder	pediatrics|endocrinology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|reproductive_system_disorder	false	false	true	true	high
MONDO:0019118	inherited retinal dystrophy	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	disorder_of_visual_system|psychiatric_disorder|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder	ophthalmology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0019119	muscular channelopathy	nervous_system_disorder	other	nervous_system_disorder	neurology|rheumatology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease	muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0019120	pili bifurcati	integumentary_system_disorder	other	integumentary_system_disorder	pediatrics|dermatology|pulmonology	inflammatory_disease|neurodegenerative_disease	biliary_disorder|liver_disorder	false	false	false	false	low
MONDO:0019121	pneumocystosis	infectious_disease|inflammatory_disease|respiratory_system_disorder	infectious_disease	respiratory_system_disorder|infectious_disease|inflammatory_disease	immunology|oncology|pulmonology	autoimmune_diseases|inflammatory_disease|pneumonia	respiratory_disorder|lung_disorder	true	false	false	true	high
MONDO:0019122	idiopathic acute eosinophilic pneumonia	hematologic_disorder|infectious_disease|syndromic_disease|hereditary_disease|cardiovascular_disorder|immune_system_disorder|inflammatory_disease|musculoskeletal_system_disorder|respiratory_system_disorder	infectious_disease|cardiovascular_disorder	respiratory_system_disorder|infectious_disease|musculoskeletal_system_disorder|acute_disease|hematologic_disorder|immune_system_disorder|idiopathic_disease|inflammatory_disease|syndromic_disease|hereditary_disease|cardiovascular_disorder	pediatric|allergy_and_immunology|pulmonology	autoimmune_diseases|inflammatory_disease|allergy	lung_disorder|immune_disorder	false	false	false	true	high
MONDO:0019123	continuous spikes and waves during sleep	syndromic_disease	other	syndromic_disease	neurology|psychiatry	adrenal_gland_disease|mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	true	false	false	true	very_high
MONDO:0019124	microscopic polyangiitis	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	renal_medicine|rheumatology	autoimmune_diseases|inflammatory_disease	vascular_disorder|immune_disorder|kidney_disorder	false	false	false	true	high
MONDO:0019125	relapsing polychondritis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	neurology|rheumatology|psychiatry	autoimmune_diseases|inflammatory_disease	vascular_disorder|joint_disorder|immune_disorder	false	false	false	false	high
MONDO:0019127	polymyositis	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|idiopathic_disease|inflammatory_disease	neurology|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|immune_disorder	false	false	false	true	high
MONDO:0019128	mullerian aplasia	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|anemia	reproductive_system_disorder	false	false	false	false	medium
MONDO:0019129	global developmental delay-osteopenia-ectodermal defect syndrome	syndromic_disease	other	syndromic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	developmental_delay|teeth_disorder|bone_disorder|skin_disorder	false	false	false	false	high
MONDO:0019130	tubular renal disease-cardiomyopathy syndrome	syndromic_disease	other	syndromic_disease	cardiology|renal_medicine	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	kidney_disorder|heart_disorder	false	false	false	false	high
MONDO:0019131	ossification anomalies-psychomotor developmental delay syndrome	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	developmental_delay|musculoskeletal_disorder|brain_disorder|bone_disorder	false	false	false	false	high
MONDO:0019132	spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	ophthalmology|neurology|genetics_and_genomics	cataracts_syndrome_is_not_a_valid_category__but_i_assume_it_s_a_typo_for_one_of_the_given_categories__if_so__here_are_the_best_fitting_categories___neurodegenerative_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0019133	visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	visceral_neuropathy|facial_dysmorphism|developmental_delay|brain_anomalies|metabolic_disorder|neurodegenerative_disease	developmental_delay|brain_disorder|facial_dysmorphism	false	false	false	false	very_high
MONDO:0019134	central neurocytoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0019136	Zygomycosis	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|dermatology|pulmonology	autoimmune_diseases|inflammatory_disease	respiratory_disorder_is_incorrect_so_lung_disorder|skin_disorder	true	false	false	true	high
MONDO:0019137	non-24-hour sleep-wake syndrome	other	other	sleep_disorder	neurology|psychiatry	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0019139	acquired hemophilia	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics|allergy_and_immunology	autoimmune_diseases|metabolic_disorder|anemia	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019140	acute ackee fruit intoxication	poisoning	other	acute_disease|poisoning	neurology|gastroenterology	neurodegenerative_disease|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0019141	porokeratosis of Mibelli	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|genetics_and_genomics	autoimmune_diseases|cancer|inflammatory_disease|metabolic_disorder	liver_disorder|skin_disorder	false	false	false	false	low
MONDO:0019142	inherited porphyria	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	dermatology|hematology|genetics_and_genomics	metabolic_disorder|anemia	liver_disorder|blood_bone_marrow_disorder|skin_disorder	false	false	false	true	high
MONDO:0019143	angiostrongyliasis	infectious_disease	infectious_disease	infectious_disease	neurology|gastroenterology|pulmonology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	lymphatic_disorder|vascular_disorder	true	false	false	false	medium
MONDO:0019144	hereditary thrombophilia due to congenital protein S deficiency	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0019145	hereditary thrombophilia due to congenital protein C deficiency	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019147	myiasis	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	infectious_diseases|public_health|dermatology	inflammatory_disease|metabolic_disorder	skin_disorder	true	false	false	true	medium
MONDO:0019148	Wolman disease	syndromic_disease|hereditary_disease|metabolic_disease	metabolic_disease	syndromic_disease|metabolic_disease|hereditary_disease	pediatric|hepatology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0019149	cholesteryl ester storage disease	syndromic_disease|hereditary_disease|metabolic_disease	metabolic_disease	syndromic_disease|metabolic_disease|hereditary_disease	pediatric|hepatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	genetic_disorder|liver_disorder	false	false	false	false	high
MONDO:0019151	oligocone trichromacy	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|disorder_of_orbital_region|nervous_system_disorder	neurology|ophthalmology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0019152	Oguchi disease	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|disorder_of_orbital_region|nervous_system_disorder	pediatric|orthopaedic	metabolic_disorder|inflammatory_disease	joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0019153	brain malformation-congenital heart disease-postaxial polydactyly syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	cardiovascular_disorder|neurodegenerative_disease	heart_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0019154	androgen insensitivity syndrome	reproductive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology|urology	metabolic_disorder|genetic_disorder|endocrine_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0019155	Leydig cell hypoplasia	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	genetics_and_genomics|endocrinology|urology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0019156	angioosteohypotrophic syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	endocrinology|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	vascular_disorder|endocrine_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0019157	myelodysplastic syndrome with ring sideroblasts	syndromic_disease|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor|anemia	idiopathic_disease|syndromic_disease|cancer_or_benign_tumor|hematologic_disorder	genetics_and_genomics|hematology|oncology	anemia|cancer	bone_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0019158	tropical endomyocardial fibrosis	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder	cardiology|cardiothoracic	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	liver_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0019159	Loeffler endocarditis	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder	cardiology|pulmonology	cardiovascular_disorder|autoimmune_diseases	heart_disorder|lung_disorder	true	false	false	true	very_high
MONDO:0019160	primary progressive freezing gait	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	neurology|orthopaedic	primary_progressive_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0019161	pseudohypoaldosteronism type 1	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	endocrinology|pediatric	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0019162	pseudohypoaldosteronism type 2	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0019164	6q terminal deletion syndrome	syndromic_disease|chromosomal_disorder	other	syndromic_disease|chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|anemia|neurodegenerative_disease	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0019165	central precocious puberty	hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrinology|pediatric	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0019167	immunoglobulin A vasculitis	immune_system_disorder|inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease|immune_system_disorder	rheumatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	vascular_disorder|immune_disorder	true	false	false	true	medium
MONDO:0019168	pyomyositis	infectious_disease|musculoskeletal_system_disorder|inflammatory_disease	infectious_disease	inflammatory_disease|musculoskeletal_system_disorder|infectious_disease	rheumatology	inflammatory_disease|autoimmune_diseases	joint_disorder|muscle_disorder	true	false	false	true	high
MONDO:0019169	pyruvate dehydrogenase deficiency	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|metabolic_disease|mitochondrial_disease	metabolic_disease	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0019170	polyarteritis nodosa	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	neurology|rheumatology	inflammatory_disease|autoimmune_diseases	vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0019171	familial long QT syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0019172	aniridia	disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_development_or_morphogenesis|disorder_of_orbital_region	pediatric|ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0019173	rabies	infectious_disease|nervous_system_disorder	infectious_disease	nervous_system_disorder|infectious_disease	neurology|virology	inflammatory_disease|neurodegenerative_disease	immune_disorder|lymphatic_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0019175	primary lymphedema	immune_system_disorder	other	immune_system_disorder	cardiology|hematology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0019177	odontoleukodystrophy	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	teeth_disorder|brain_disorder	false	false	false	false	high
MONDO:0019178	auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|otolaryngology|pediatric	cardiovascular_disorder|ocular_abnormalities_syndrome_is_not_a_direct_match_but_it_can_be_related_to_metabolic_disorder|neurodegenerative_disease	ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0019179	monosomy 9q22.3	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	anemia|neurodegenerative_disease|mental_health_disorder	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0019180	hereditary hemorrhagic telangiectasia	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	renal_medicine|cardiology|dermatology|hematology|pulmonology|genetics_and_genomics	metabolic_disorder|anemia|inflammatory_disease	kidney_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019181	non-syndromic X-linked intellectual disability	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0019182	inherited obesity	hereditary_disease|endocrine_system_disorder|nutritional_disorder	endocrine_system_disorder	nutritional_disorder|endocrine_system_disorder|hereditary_disease	endocrinology|pediatric|genetics_and_genomics	inherited_condition|metabolic_disorder	endocrine_disorder	false	false	false	false	high
MONDO:0019186	Q fever	infectious_disease	infectious_disease	infectious_disease	renal_medicine|hepatology|hematology|pulmonology	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder|lung_disorder	true	false	false	true	medium
MONDO:0019187	Axenfeld-Rieger syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|disorder_of_visual_system	other	syndromic_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_orbital_region	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	eye_disorder|joint_disorder	false	false	false	false	high
MONDO:0019188	Rubinstein-Taybi syndrome	psychiatric_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|nervous_system_disorder|musculoskeletal_system_disorder	psychiatric_disorder	psychiatric_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|brain_disorder	false	false	false	false	high
MONDO:0019189	inborn disorder of amino acid and other organic acid metabolism	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|inborn_disorder_of_amino_acid_and_other_organic_acid_metabolism_often_fall_under_this_category	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0019190	juvenile polyposis of infancy	cancer_or_benign_tumor|hereditary_disease|syndromic_disease|digestive_system_disorder	cancer_or_benign_tumor	syndromic_disease|digestive_system_disorder|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|pediatric|oncology|gastroenterology	metabolic_disorder|inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0019191	IgG4-related dacryoadenitis and sialadenitis	otorhinolaryngologic_disease|immune_system_disorder|disorder_of_visual_system	autoimmune_disease	disorder_of_visual_system|otorhinolaryngologic_disease|disorder_of_orbital_region|immune_system_disorder	rheumatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	gland_disorder|eye_disorder|immune_disorder	false	false	false	true	medium
MONDO:0019192	AKT2-related familial partial lipodystrophy	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|endocrinology	metabolic_disorder|lipid_storage_disease|familial_dyslipidemia|genetic_disease	endocrine_disorder|muscle_disorder	false	false	false	false	high
MONDO:0019193	acquired generalized lipodystrophy	integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease	endocrinology|dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	endocrine_disorder|skin_disorder	false	false	true	false	high
MONDO:0019194	localized lipodystrophy	integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease	endocrinology|dermatology	metabolic_disorder|localized_lipoatrophy	muscle_disorder|skin_disorder	false	false	false	false	low
MONDO:0019195	hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome	hereditary_disease|musculoskeletal_system_disorder|inflammatory_disease	other	inflammatory_disease|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0019196	Foix-Alajouanine syndrome	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	neurology|pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0019197	folinic acid-responsive seizures	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0019198	sympathetic ophthalmia	inflammatory_disease|disorder_of_visual_system	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases	eye_disorder|immune_disorder	false	false	false	false	high
MONDO:0019199	interstitial granulomatous dermatitis with arthritis	integumentary_system_disorder|connective_tissue_disorder	other	integumentary_system_disorder|connective_tissue_disorder	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder|joint_disorder	false	false	false	false	medium
MONDO:0019200	retinitis pigmentosa	disorder_of_visual_system|psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	hereditary_disease|disorder_of_orbital_region|psychiatric_disorder|metabolic_disease|nervous_system_disorder|disorder_of_visual_system	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0019201	thyrotoxic periodic paralysis	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	neurology|endocrinology|cardiology	autoimmune_diseases|metabolic_disorder	muscle_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0019202	myxofibrosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|orthopaedic|hematology|oncology	soft_tissue_sarcoma|cancer|tumor	muscle_disorder|soft_tissue_disorder	false	true	false	true	high
MONDO:0019203	acute interstitial pneumonia	infectious_disease|respiratory_system_disorder|inflammatory_disease	infectious_disease	idiopathic_disease|respiratory_system_disorder|inflammatory_disease|acute_disease|infectious_disease	cardiothoracic|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0019204	respiratory bronchiolitis-interstitial lung disease syndrome	infectious_disease|respiratory_system_disorder|inflammatory_disease	infectious_disease	idiopathic_disease|respiratory_system_disorder|inflammatory_disease|infectious_disease	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|lower_gastrointestinal_disorder|lung_disorder	false	false	false	false	medium
MONDO:0019205	trichodysplasia-amelogenesis imperfecta syndrome	integumentary_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|dermatology	neurodegenerative_disease|metabolic_disorder	bone_disorder|skin_disorder|blood_bone_marrow_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0019207	DEND syndrome	endocrine_system_disorder|digestive_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease|endocrine_system_disorder|diabetes_mellitus	hereditary_disease|metabolic_disease|digestive_system_disorder|endocrine_system_disorder	neurology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|immune_disorder	false	false	false	false	high
MONDO:0019208	Bickerstaff brainstem encephalitis	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	nervous_system_disorder|inflammatory_disease|post_infectious_disorder|acute_disease|infectious_disease	neurology|pediatric	inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder	true	false	false	true	high
MONDO:0019209	Japanese encephalitis	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	nervous_system_disorder|inflammatory_disease|acute_disease|infectious_disease	neurology|pediatric	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	true	false	false	true	medium
MONDO:0019210	cutaneous neuroendocrine carcinoma	disorder_of_development_or_morphogenesis|endocrine_system_disorder|integumentary_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|integumentary_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|endocrine_system_disorder|post_infectious_disorder	dermatology|oncology	cancer|neuroendocrine_tumors|adrenal_gland_disease	skin_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0019211	isolated congenital anonychia	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	pediatric|genetics_and_genomics|dermatology	metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	true	low
MONDO:0019212	disseminated superficial actinic porokeratosis	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder	false	false	false	false	medium
MONDO:0019214	inborn carbohydrate metabolic disorder	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics|endocrinology|genetics_and_genomics	metabolic_disorder|metabolic_disease|inborn_errors_of_metabolism___corrected_to___metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	true	true	high
MONDO:0019215	classic organic aciduria	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|renal_medicine|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0019216	inborn disorder of amino acid transport	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|inborn_disorder_of_amino_acid_transport	kidney_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0019218	inborn disorder of bile acid synthesis	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|gastroenterology	metabolic_disorder|inborn_disorder_of_bile_acid_synthesis	liver_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0019219	inborn disorder of neurotransmitter metabolism and transport	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0019220	inborn disorder of cobalamin metabolism and transport	metabolic_disease|hereditary_disease|nutritional_disorder	metabolic_disease	hereditary_disease|nutritional_disorder|metabolic_disease	pediatrics|genetics_and_genomics	metabolic_disorder|anemia|inborn_disorder	upper_gastrointestinal_disorder|liver_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019222	inborn disorder of methionine cycle and sulfur amino acid metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|upper_gastrointestinal_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0019223	disorder of fatty acid and ketone body metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|disorder_of_fatty_acid_and_ketone_body_metabolism|cardiovascular_disorder	liver_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0019225	disorder of gluconeogenesis	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|hepatology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	liver_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0019226	glucose transport disorder	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|genetics_and_genomics	metabolic_disorder	endocrine_disorder	false	false	true	false	high
MONDO:0019228	inborn disorder of histidine metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|inborn_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0019229	inborn disorder of ketolysis	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder|inherited_disorder	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0019230	inborn disorder of ornithine or proline metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|inborn_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0019231	inborn disorder of pentose phosphate metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|inborn_disorder_of_pentose_phosphate_metabolism_does_not_exist__using_the_actual_disease_name__inborn_disorder_of_pentose_phosphate_metabolism_would_be_categorized_under_metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0019232	inborn disorder of peptide metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics	metabolic_disorder|inborn_disorder_of_peptide_metabolism_is_a_specific_type_of_metabolic_disorder	endocrine_disorder	false	false	false	true	high
MONDO:0019233	disorder of peroxisomal beta oxidation	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|peroxisomal_beta_oxidation_disorder_is_closely_related_to_the_liver_s_function_of_metabolizing_fats	false	false	false	true	high
MONDO:0019234	peroxisome biogenesis disorder	metabolic_disease|hereditary_disease|nervous_system_disorder|syndromic_disease	metabolic_disease|neurodegenerative_disease	hereditary_disease|metabolic_disease|nervous_system_disorder|syndromic_disease	neurology|pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	liver_disorder|peroxisomal_disorder	false	false	false	false	very_high
MONDO:0019235	inborn disorder of phenylalanine and tyrosine metabolism	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	metabolism_is_closely_related_to_endocrinology_however_endocrinology_can_be_a_broader_categorization_of_metabolic_disorders|pediatrics|genetics_and_genomics	metabolic_disorder|inherited_disorder	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0019236	inborn disorder of purine metabolism	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|inborn_disorder_of_metabolism	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0019237	inborn disorder of pyridoxine metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics	metabolic_disorder|inborn_disorder	liver_disorder|metabolic_disorder	false	false	false	true	high
MONDO:0019238	inborn disorder of pyrimidine metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder|brain_disorder	false	false	false	false	high
MONDO:0019239	inborn disorder of serine family metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|inborn_disorder	liver_disorder|metabolic_disorder	false	false	false	true	high
MONDO:0019240	sterol biosynthesis disorder	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolism|biochemistry|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0019241	inborn disorder of the gamma-glutamyl cycle	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|metabolic_disorder	false	false	false	false	high
MONDO:0019242	inborn disorder of branched-chain amino acid metabolism	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|pediatric|endocrinology|genetics_and_genomics|gastroenterology	inborn_disorder|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0019243	inborn disorder of energy metabolism	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|endocrinology|genetics_and_genomics	inborn_disorder_of_energy_metabolism|metabolic_disorder	endocrine_disorder|metabolic_disorder	false	false	false	true	very_high
MONDO:0019245	lysosomal lipid storage disorder	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	lysosomal_lipid_storage_disorders_often_affect_the_liver|liver_disorder	false	false	false	true	high
MONDO:0019246	inborn disorder of lysosomal amino acid transport	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatrics|genetics_and_genomics	inborn_disorder_of_lysosomal_amino_acid_transport_can_also_be_classified_as_a_genetic_disorder_which_falls_under_the_broader_category_of_metabolic_disorders_that_involve_defects_in_protein_metabolism|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0019248	mucolipidosis	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|genetics_and_genomics|pulmonology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0019249	mucopolysaccharidosis	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|kidney_disorder|lymphatic_disorder|liver_disorder|muscle_disorder|joint_disorder	false	false	false	true	very_high
MONDO:0019250	inborn disorder of biogenic amine metabolism and transport	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics|psychiatry	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0019251	oligosaccharidosis	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	liver_disorder	false	false	false	true	high
MONDO:0019253	metabolic disease involving other neurotransmitter deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|endocrinology	neurotransmitter_deficiency|metabolic_disorder	endocrine_disorder	false	false	false	false	high
MONDO:0019254	inborn disorder of purine or pyrimidine metabolism	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	inherited_metabolic_disorders|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0019255	sphingolipidosis	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|immune_disorder|muscle_disorder|spinal_disorder	true	false	false	false	very_high
MONDO:0019256	sterol metabolism disorder	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|endocrinology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|liver_disorder	false	false	false	true	high
MONDO:0019257	hemochromatosis type 2	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|genetics_and_genomics|hematology	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0019258	mild phenylketonuria	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	true	medium
MONDO:0019259	classic phenylketonuria	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0019260	adult neuronal ceroid lipofuscinosis	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0019261	infantile neuronal ceroid lipofuscinosis	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0019262	juvenile neuronal ceroid lipofuscinosis	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	psychiatric_disorder|neurodegenerative_disease|metabolic_disease	psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0019263	autosomal erythropoietic protoporphyria	endocrine_system_disorder|digestive_system_disorder|integumentary_system_disorder|hereditary_disease|metabolic_disease	endocrine_system_disorder|metabolic_disease	integumentary_system_disorder|metabolic_disease|digestive_system_disorder|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|dermatology|hematology	anemia|autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|skin_disorder	false	false	false	true	high
MONDO:0019264	alpha-N-acetylgalactosaminidase deficiency type 3	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0019265	diazoxide-resistant focal hyperinsulinism	disorder_of_development_or_morphogenesis|endocrine_system_disorder|digestive_system_disorder|hereditary_disease|metabolic_disease	endocrine_system_disorder|metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|digestive_system_disorder|endocrine_system_disorder|hereditary_disease	pediatric|endocrinology	adrenal_gland_disease|endocrine_disorder|metabolic_disorder	endocrine_disorder	false	false	true	false	very_high
MONDO:0019266	SAPHO syndrome	syndromic_disease|connective_tissue_disorder	other	connective_tissue_disorder|syndromic_disease	pediatrics|dermatology|rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0019267	vitamin B12-unresponsive methylmalonic acidemia type mut-	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	bone_disorder|muscle_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0019268	epidermal disease	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|epidermal_disease	autoimmune_diseases|epidermal_disease_is_often_associated_with_autoimmune_conditions_so_it_s_possible_this_category_could_fit	skin_disorder	true	false	false	false	medium
MONDO:0019269	ichthyosis	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	genetic_disorder|inherited_disorder|skin_disorder	false	false	false	true	medium
MONDO:0019270	erythrokeratoderma	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0019272	hereditary palmoplantar keratoderma	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|dermatology	inherited_condition|hereditary_diseases|metabolic_disorder	genetic_disorder|skin_disorder|joint_disorder	false	false	false	false	medium
MONDO:0019276	inherited epidermolysis bullosa	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0019278	hair anomaly	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	hair_anomalies_typically_relate_to_the_skin|skin_disorder	false	false	false	false	low
MONDO:0019280	hypertrichosis	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	endocrine_disorder|skin_disorder	false	false	false	false	medium
MONDO:0019283	nail anomaly	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	inflammatory_disease|anemia|autoimmune_diseases	skin_disorder|nail_anomalies_often_relate_to_skin_conditions_so_also_skin_disorder_is_fitting_category_for_the_given_disease	false	false	false	false	low
MONDO:0019284	inherited isolated nail anomaly	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	skin_disorder|nail_anomaly_is_more_specific_but_given_the_options__skin_disorder_is_a_good_fit	false	false	false	false	low
MONDO:0019287	ectodermal dysplasia syndrome	syndromic_disease|integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|syndromic_disease|hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|vascular_disorder|skin_disorder|nose_disorder|ear_disorder|teeth_disorder|lymphatic_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0019288	skin pigmentation disorder	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	endocrine_disorder|skin_disorder	false	false	false	true	low
MONDO:0019289	hyperpigmentation of the skin	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|skin_disorder	false	false	false	true	low
MONDO:0019290	hypopigmentation of the skin	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|anemia|autoimmune_diseases	endocrine_disorder|skin_disorder	false	false	false	false	low
MONDO:0019293	skin vascular disease	cardiovascular_disorder|integumentary_system_disorder	cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder	dermatology|vascular_disease_is_also_associated_with_hematology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|skin_disorder	false	false	false	true	medium
MONDO:0019294	mixed dermis disorder	integumentary_system_disorder	other	integumentary_system_disorder	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0019296	subcutaneous tissue disorder	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0019297	lymphedema	immune_system_disorder	other	immune_system_disorder	oncology|dermatology|hematology	inflammatory_disease|autoimmune_diseases	skin_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0019303	premature aging syndrome		other		endocrinology|pediatric|genetics_and_genomics|dermatology	metabolic_disorder|neurodegenerative_disease	skin_disorder|premature_aging_syndrome_is_often_associated_with_skin_manifestations_such_as_wrinkles__age_spots__and_loss_of_skin_elasticity__so_it_fits_this_category	false	false	false	false	very_high
MONDO:0019306	congenital non-bullous ichthyosiform erythroderma	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0019307	generalized junctional epidermolysis bullosa non-Herlitz type	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|skin_disease|inflammatory_disease	skin_disorder|immune_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0019308	junctional epidermolysis bullosa inversa	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0019309	late-onset junctional epidermolysis bullosa	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|muscle_disorder	false	false	false	false	high
MONDO:0019310	recessive dystrophic epidermolysis bullosa inversa	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|inflammatory_disease	skin_disorder|muscle_disorder	false	false	false	false	high
MONDO:0019311	wooly hair nevus	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	skin_disorder	false	false	false	false	low
MONDO:0019312	Hermansky-Pudlak syndrome	metabolic_disease|hematologic_disorder|hereditary_disease|integumentary_system_disorder|syndromic_disease	metabolic_disease	syndromic_disease|hereditary_disease|integumentary_system_disorder|hematologic_disorder|metabolic_disease	pediatric|genetics_and_genomics|immunology	metabolic_disorder|neurodegenerative_disease|anemia	skin_disorder|immune_disorder|eye_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0019313	lymphatic malformation	immune_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|immune_system_disorder|cardiovascular_disorder	pediatric|hematology|oncology	autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0019314	cutaneous mastocytoma	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|hereditary_disease|integumentary_system_disorder|inflammatory_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder|hematologic_disorder|inflammatory_disease|immune_system_disorder	hematology|oncology|dermatology	autoimmune_diseases|cancer|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	low
MONDO:0019315	diffuse cutaneous mastocytosis	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|hereditary_disease|integumentary_system_disorder|inflammatory_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder|hematologic_disorder|inflammatory_disease|immune_system_disorder	hematology|dermatology	autoimmune_diseases|cancer|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0019316	maculopapular cutaneous mastocytosis	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|hereditary_disease|integumentary_system_disorder|inflammatory_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder|hematologic_disorder|inflammatory_disease|immune_system_disorder	hematology|dermatology	autoimmune_diseases|cancer|allergy|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0019317	follicular atrophoderma-basal cell carcinoma	integumentary_system_disorder	other	integumentary_system_disorder	oncology|dermatology	autoimmune_diseases|cancer	skin_disorder	false	true	false	false	low
MONDO:0019318	inflammatory linear verrucous epidermal nevus	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder	false	false	false	false	low
MONDO:0019319	verrucous nevus	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder	oncology|dermatology	neurofibromatosis|cancer|adrenal_gland_disease	skin_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0019320	acanthokeratolytic verrucous nevus	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|cancer|neurodegenerative_disease	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0019321	atypical Werner syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|oncology	cancer|neurodegenerative_disease	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0019322	pemphigus vegetans	immune_system_disorder|integumentary_system_disorder|inflammatory_disease	autoimmune_disease	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	allergy_and_immunology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	high
MONDO:0019323	pemphigus erythematosus	immune_system_disorder|integumentary_system_disorder|inflammatory_disease	autoimmune_disease	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	allergy_and_immunology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	high
MONDO:0019324	pemphigus foliaceus	immune_system_disorder|integumentary_system_disorder|inflammatory_disease	autoimmune_disease	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	allergy_and_immunology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0019325	phakomatosis cesioflammea	nervous_system_disorder|disorder_of_visual_system|disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|integumentary_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|neurology|dermatology	metabolic_disorder|neurodegenerative_disease	skin_disorder|joint_disorder|eye_disorder	false	false	false	false	medium
MONDO:0019326	phakomatosis cesiomarmorata	nervous_system_disorder|disorder_of_visual_system|disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|integumentary_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|dermatology	genetic_disease____note__i_replaced_the_original_list_item__phakomatosis_cesiomarmorata__with_its_actual_category__which_is_not_directly_listed_but_can_be_inferred_as_a_genetic_disorder|metabolic_disorder	skin_disorder|brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0019327	phakomatosis spilorosea	nervous_system_disorder|disorder_of_visual_system|disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|integumentary_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	pediatric|genetics_and_genomics|neurology|dermatology	metabolic_disorder|neurodegenerative_disease	skin_disorder|joint_disorder|eye_disorder	true	false	false	false	medium
MONDO:0019328	macrocystic lymphatic malformation	immune_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|cardiovascular_disorder	pediatric|hematology|vascular__not_in_list_____pulmonology|cardiothoracic	vascular_disease|cardiovascular_disorder|inflammatory_disease	lymphatic_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019329	microcystic lymphatic malformation	immune_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|cardiovascular_disorder	pediatric|hematology|oncology|dermatology	congenital_lesion|lymphatic_disorder|vascular_disorder	lymphatic_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0019330	pili gemini	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|hematology|oncology|pulmonology	metabolic_disorder|autoimmune_diseases	gastrointestinal_disorder|biliary_disorder|liver_disorder	false	false	false	false	low
MONDO:0019332	punctate palmoplantar keratoderma type 1	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	skin_disorder	false	false	false	false	medium
MONDO:0019333	autosomal recessive hyperinsulinism due to SUR1 deficiency	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	true	true	medium
MONDO:0019334	autosomal recessive hyperinsulinism due to Kir6.2 deficiency	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|metabolic_disease	digestive_system_disorder|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder	false	false	false	true	high
MONDO:0019335	mild hyperphenylalaninemia	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	low
MONDO:0019336	Gardner syndrome	syndromic_disease|hereditary_disease|cancer_or_benign_tumor|disorder_of_visual_system	cancer_or_benign_tumor	hereditary_disease|disorder_of_orbital_region|syndromic_disease|cancer_or_benign_tumor|disorder_of_visual_system	genetics_and_genomics|orthopaedic|oncology	cancer|metabolic_disorder	bone_disorder|joint_disorder|teeth_disorder	false	false	false	true	high
MONDO:0019337	autoimmune bullous skin disease	integumentary_system_disorder|immune_system_disorder|inflammatory_disease	autoimmune_disease	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	rheumatology|immunology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	high
MONDO:0019338	sarcoidosis	syndromic_disease|connective_tissue_disorder	other	connective_tissue_disorder|syndromic_disease	rheumatology|pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	false	false	false	false	high
MONDO:0019339	47,XYY syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatrics	genetic_disorder|developmental_disorder|neurodevelopmental_disorder	sex_chromosome_abnormality_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0019340	scleroderma	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	connective_tissue_disorder|immune_system_disorder	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0019342	Seckel syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorders|developmental_disorders	kidney_disorder|developmental_disorder|lower_gastrointestinal_disorder|skin_disorder|joint_disorder|eye_disorder|lymphatic_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0019344	antisynthetase syndrome	musculoskeletal_system_disorder|inflammatory_disease	other	inflammatory_disease|musculoskeletal_system_disorder|idiopathic_disease	neurology|rheumatology|pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder|muscle_disorder	false	false	false	true	high
MONDO:0019345	shigellosis	infectious_disease|inflammatory_disease|digestive_system_disorder	infectious_disease	inflammatory_disease|acute_disease|digestive_system_disorder|infectious_disease	pediatric|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0019346	sialidosis type 1	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	lysosomal_storage_disease|metabolic_disorder	ear_disorder|skin_disorder	false	false	false	false	high
MONDO:0019347	peeling skin syndrome	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	false	medium
MONDO:0019349	Sotos syndrome	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|chromosomal_disorder	other	hereditary_disease|chromosomal_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|endocrinology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|other____corrected_to_remove_redundant__other______endocrine_disorder|liver_disorder	false	false	false	false	high
MONDO:0019350	hereditary spherocytosis	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	pediatric|genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0019351	isolated spina bifida	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology	neurological_disease|musculoskeletal_disease|congenital_anomaly	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0019353	Stargardt disease	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|disorder_of_visual_system	neurology|genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0019354	Stickler syndrome	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|disorder_of_visual_system|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_orbital_region|syndromic_disease|musculoskeletal_system_disorder|disorder_of_visual_system	pediatric|genetics_and_genomics|orthopaedic|rheumatology|ophthalmology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	bone_disorder|spine_is_not_listed_but_it_can_be_inferred_as_spinal_disorder|joint_disorder|eye_disorder	false	false	false	false	high
MONDO:0019355	adult-onset Still disease	syndromic_disease|musculoskeletal_system_disorder|inflammatory_disease|connective_tissue_disorder	other	inflammatory_disease|connective_tissue_disorder|syndromic_disease|musculoskeletal_system_disorder	rheumatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder	false	false	false	true	high
MONDO:0019356	urogenital tract malformation	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|urology|obstetrics_and_gynecology	urogenital_tract_malformation_can_also_be_related_to_other_metabolic_disorders_such_as_congenital_adrenal_hyperplasia_which_affects_the_development_of_the_adrenal_gland|adrenal_gland_disease	reproductive_system_disorder|kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0019357	congenital narrowing of cervical spinal canal	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology|genetics_and_genomics|orthopaedic	spinal_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0019358	encephalopathy due to sulfite oxidase deficiency	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|disorder_of_visual_system	metabolic_disease	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0019359	Rocky mountain spotted fever	infectious_disease	infectious_disease	infectious_disease	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|lymphatic_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0019360	rickettsialpox	infectious_disease	infectious_disease	infectious_disease	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0019362	epidemic louse-borne typhus	infectious_disease	infectious_disease	infectious_disease	infectious_disease|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0019364	pseudotyphus of California	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	true	false	false	false	medium
MONDO:0019365	scrub typhus	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|pediatrics|dermatology|internal_medicine	inflammatory_disease|autoimmune_diseases	skin_disorder	true	false	false	true	high
MONDO:0019366	free sialic acid storage disease	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	immune_disorder|liver_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0019367	regional odontodysplasia	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	teeth_disorder	false	false	false	false	medium
MONDO:0019368	florid cemento-osseous dysplasia	other	other	mouth_disorder	genetics_and_genomics|orthopaedic|dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|blood_bone_marrow_disorder|teeth_disorder	false	false	false	false	low
MONDO:0019369	complex regional pain syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|orthopaedic|rheumatology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	joint_disorder|muscle_disorder|vascular_disorder	false	false	false	true	high
MONDO:0019370	vulvovaginal gingival syndrome	reproductive_system_disorder	other	reproductive_system_disorder	allergy_and_immunology|obstetrics_and_gynecology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|reproductive_system_disorder	true	false	false	false	medium
MONDO:0019371	narcolepsy without cataplexy	nervous_system_disorder	other	sleep_disorder|nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0019372	solitary bone cyst	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|orthopaedic	bone_disease|connective_tissue_disease|cancer	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	low
MONDO:0019373	desmoplastic small round cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|genetics_and_genomics|oncology|hematology	cancer|neuroblastoma	blood_bone_marrow_disorder|lymphatic_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0019374	CAMOS syndrome	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics|psychiatry	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	vascular_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0019375	megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|hydrocephalus|spinal_disorder	false	false	false	false	high
MONDO:0019376	West-Nile encephalitis	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	inflammatory_disease|acute_disease|nervous_system_disorder|infectious_disease	pediatric|neurology|epidemiology	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	true	false	false	false	high
MONDO:0019377	Mycoplasma encephalitis	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	inflammatory_disease|acute_disease|nervous_system_disorder|infectious_disease	pediatric|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	immune_disorder|brain_disorder	true	false	false	false	high
MONDO:0019378	la Crosse encephalitis	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	inflammatory_disease|acute_disease|nervous_system_disorder|infectious_disease	pediatric|neurology|infectious_disease	autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	true	false	false	false	high
MONDO:0019380	western equine encephalitis	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	inflammatory_disease|acute_disease|nervous_system_disorder|infectious_disease	neurology|veterinary	neurodegenerative_disease|inflammatory_disease	immune_disorder|brain_disorder	true	false	false	false	high
MONDO:0019383	acute disseminated encephalomyelitis	infectious_disease|disorder_of_development_or_morphogenesis|inflammatory_disease|nervous_system_disorder	neurodegenerative_disease|infectious_disease	inflammatory_disease|post_infectious_disorder|acute_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|infectious_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	immune_disorder|brain_disorder|spinal_disorder	true	false	false	true	high
MONDO:0019384	encephalitis lethargica	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	inflammatory_disease|post_infectious_disorder|acute_disease|nervous_system_disorder|infectious_disease	pediatric|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	true	false	false	false	high
MONDO:0019385	steroid-responsive encephalopathy associated with autoimmune thyroiditis	infectious_disease|inflammatory_disease|immune_system_disorder|nervous_system_disorder	infectious_disease|autoimmune_disease	inflammatory_disease|post_infectious_disorder|acute_disease|nervous_system_disorder|immune_system_disorder|infectious_disease	allergy_and_immunology|neurology|endocrinology	autoimmune_diseases|inflammatory_disease	immune_disorder|endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0019386	progressive rubella panencephalitis	infectious_disease|inflammatory_disease|nervous_system_disorder	infectious_disease	inflammatory_disease|post_infectious_disorder|acute_disease|nervous_system_disorder|infectious_disease	pediatric|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	immune_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0019387	macrostomia-preauricular tags-external ophthalmoplegia syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|otolaryngology|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|muscle_disorder|external_ophthalmoplegia_syndrome	false	false	false	false	medium
MONDO:0019388	pelvis syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|syndromic_disease	obstetrics_and_gynecology|urology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0019390	Susac syndrome	syndromic_disease|immune_system_disorder	autoimmune_disease	immune_system_disorder|syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	vascular_disorder|kidney_disorder|brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0019391	Fanconi anemia	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder|hematologic_disorder|immune_system_disorder	anemia|metabolic_disease	hereditary_disease|hematologic_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|immune_system_disorder|musculoskeletal_system_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0019392	syringocystadenoma papilliferum	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|autoimmune_diseases|adrenal_gland_disease|inflammatory_disease	skin_disorder|eye_disorder|liver_disorder	false	false	false	false	low
MONDO:0019393	idiopathic malabsorption due to bile acid synthesis defects	hereditary_disease|metabolic_disease|digestive_system_disorder	metabolic_disease	hereditary_disease|digestive_system_disorder|metabolic_disease|idiopathic_disease	genetics_and_genomics|gastroenterology|hepatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0019394	Senior-Boichis syndrome	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	neurology|psychiatry|cardiology|geriatrics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	liver_disorder|bone_disorder	false	false	false	false	high
MONDO:0019395	Hinman syndrome	urinary_system_disorder	other	urinary_system_disorder	neurology|otolaryngology	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0019396	collagen type III glomerulopathy	urinary_system_disorder	other	urinary_system_disorder	rheumatology|renal_medicine	autoimmune_diseases|inflammatory_disease	vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0019397	unknown leukodystrophy	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|hematology	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|spinal_disorder	false	false	false	false	high
MONDO:0019398	desmin-related myopathy with Mallory body-like inclusions	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	neurology|genetics_and_genomics|pathology	neurodegenerative_disease|muscular_disease|myopathy	muscle_disorder	false	false	false	false	high
MONDO:0019399	Isaac syndrome	nervous_system_disorder	other	nervous_system_disorder	allergy_and_immunology|pulmonology|pediatric	autoimmune_diseases|adrenal_gland_disease|inflammatory_disease	vascular_disorder|immune_disorder	false	false	false	false	high
MONDO:0019401	sporadic idiopathic steroid-resistant nephrotic syndrome	syndromic_disease|urinary_system_disorder	other	syndromic_disease|idiopathic_disease|urinary_system_disorder	renal_medicine|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	immune_disorder|kidney_disorder	false	false	false	false	high
MONDO:0019402	beta thalassemia	endocrine_system_disorder|hematologic_disorder|hereditary_disease	endocrine_system_disorder|anemia	hereditary_disease|hematologic_disorder|endocrine_system_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019403	congenital dyserythropoietic anemia	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hematology|pediatric|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0019404	perineurioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|orthopaedic|oncology	autoimmune_diseases|cancer|inflammatory_disease	muscle_disorder|spinal_disorder	false	false	false	false	low
MONDO:0019405	facial onset sensory and motor neuronopathy	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0019406	craniofacial conodysplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder|developmental_disorder	teeth_disorder|bone_disorder	false	false	false	false	high
MONDO:0019407	microcephalic osteodysplastic dysplasia, Saul-Wilson type	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	obstetrics_and_gynecology|pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	bone_disorder|skeletal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0019408	Astley-Kendall dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0019409	idiopathic juvenile osteoporosis	hereditary_disease|connective_tissue_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|idiopathic_disease|connective_tissue_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	endocrinology|orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0019411	genochondromatosis type 1	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|rheumatology|genetics_and_genomics	metabolic_disorder|genetic_disorder|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0019412	dysspondyloenchondromatosis	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0019413	ischio-vertebral syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|orthopaedic	neurodegenerative_disease|inflammatory_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0019414	BRESEK syndrome	syndromic_disease	other	syndromic_disease	pulmonology|endocrinology|cardiology|neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|immune_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0019415	fetal and neonatal alloimmune thrombocytopenia	hematologic_disorder	other	hematologic_disorder	obstetrics_and_gynecology|hematology|pediatric	anemia|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019416	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|psychiatric_disorder	psychiatric_disorder	syndromic_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	pediatrics|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|autoimmune_diseases	immune_disorder|brain_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0019417	X-linked intellectual disability-precocious puberty-obesity syndrome	nervous_system_disorder|hereditary_disease|syndromic_disease|psychiatric_disorder	psychiatric_disorder	syndromic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatrics|endocrinology|neurology|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0019418	X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|psychiatric_disorder	psychiatric_disorder	syndromic_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0019419	X-linked intellectual disability-macrocephaly-macroorchidism syndrome	nervous_system_disorder|hereditary_disease|syndromic_disease|psychiatric_disorder	psychiatric_disorder	syndromic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	endocrine_disorder|reproductive_system_disorder|brain_disorder	false	false	false	false	high
MONDO:0019420	X-linked intellectual disability, Pai type	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder|muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0019421	X-linked intellectual disability, Seemanova type	hereditary_disease|nervous_system_disorder|syndromic_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0019422	X-linked intellectual disability, Stevenson type	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0019423	X-linked intellectual disability, Stoll type	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0019424	X-linked intellectual disability-acromegaly-hyperactivity syndrome	hereditary_disease|nervous_system_disorder|syndromic_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|muscle_disorder|brain_disorder|urinary_tract_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0019426	X-linked intellectual disability-corpus callosum agenesis-spastic quadriparesis syndrome	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0019427	X-linked neurodegenerative syndrome, Bertini type	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0019428	fried syndrome	hereditary_disease|nervous_system_disorder|syndromic_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease	cardiothoracic|pulmonology|endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0019429	X-linked neurodegenerative syndrome, Hamel type	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0019430	X-linked intellectual disability-ataxia-apraxia syndrome	psychiatric_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0019431	primitive portal vein thrombosis	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	gastroenterology|hematology|hepatology	inflammatory_disease|cardiovascular_disorder|cancer	liver_disorder|vascular_disorder	false	false	false	true	high
MONDO:0019432	rheumatoid factor-negative juvenile idiopathic arthritis	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder	other	connective_tissue_disorder|musculoskeletal_system_disorder|inflammatory_disease|idiopathic_disease	rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder	false	false	false	true	medium
MONDO:0019433	oligoarticular juvenile idiopathic arthritis	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder	other	connective_tissue_disorder|musculoskeletal_system_disorder|inflammatory_disease|idiopathic_disease	rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder	false	false	false	true	medium
MONDO:0019434	systemic-onset juvenile idiopathic arthritis	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder|syndromic_disease	other	connective_tissue_disorder|musculoskeletal_system_disorder|syndromic_disease|inflammatory_disease|idiopathic_disease	rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder	false	false	false	true	high
MONDO:0019435	rheumatoid factor-positive polyarticular juvenile idiopathic arthritis	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder	other	connective_tissue_disorder|musculoskeletal_system_disorder|inflammatory_disease|idiopathic_disease	rheumatology|pediatric	inflammatory_disease|autoimmune_diseases|juvenile_arthritis	immune_disorder|joint_disorder	false	false	false	true	high
MONDO:0019436	psoriasis-related juvenile idiopathic arthritis	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder|immune_system_disorder|syndromic_disease	autoimmune_disease	connective_tissue_disorder|musculoskeletal_system_disorder|syndromic_disease|inflammatory_disease|immune_system_disorder|idiopathic_disease	dermatology|rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|joint_disorder	false	false	false	true	medium
MONDO:0019437	enthesitis-related juvenile idiopathic arthritis	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder	other	connective_tissue_disorder|musculoskeletal_system_disorder|inflammatory_disease|idiopathic_disease	rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	bone_disorder|immune_disorder|joint_disorder	false	false	false	true	high
MONDO:0019438	AL amyloidosis	metabolic_disease|cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease	rheumatology|renal_medicine|neurology|hematology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	kidney_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0019439	AA amyloidosis	metabolic_disease|cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder	metabolic_disease|cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease	neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019440	wild type ABeta2M amyloidosis	metabolic_disease	metabolic_disease	metabolic_disease	neurology|genetics_and_genomics	amyloidosis|neurodegenerative_disease	immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0019441	ATTRV122I amyloidosis	cardiovascular_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	metabolic_disease|cardiovascular_disorder	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease|cardiovascular_disorder	cardiology|neurology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder|neurodegenerative_disease	muscle_disorder|heart_disorder	false	false	false	true	high
MONDO:0019443	dextro-looped transposition of the great arteries	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiology|pediatric|cardiothoracic	cardiovascular_disorder|congenital_heart_disease	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0019444	trichinellosis	infectious_disease|musculoskeletal_system_disorder|inflammatory_disease	infectious_disease	infectious_disease|inflammatory_disease|musculoskeletal_system_disorder	gastroenterology|neurology|hepatology	inflammatory_disease|autoimmune_diseases	muscle_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0019445	trichofolliculoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|genetics_and_genomics	cancer|skin_condition	reproductive_system_disorder|skin_disorder	false	false	false	false	low
MONDO:0019446	localized lichen myxedematosus	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|allergy_and_immunology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0019447	atypical lichen myxedematosus	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|endocrinology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0019448	benign adult familial myoclonic epilepsy	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	epilepsy|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	low
MONDO:0019449	lissencephaly type 3-familial fetal akinesia sequence syndrome	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0019450	lissencephaly with cerebellar hypoplasia	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0019451	chronic neutrophilic leukemia	hematologic_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder	hematology|oncology	cancer|leukemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0019452	myeloproliferative neoplasm, unclassifiable	hematologic_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder	hematology|oncology	cancer|myeloproliferative_neoplasm	lymphatic_disorder|vascular_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0019453	myelodysplastic syndrome with multilineage dysplasia	hematologic_disorder|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hematologic_disorder	hematology|oncology|genetics_and_genomics	cancer|anemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0019454	myelodysplastic syndrome with excess blasts	hematologic_disorder|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hematologic_disorder	hematology|oncology	cancer|anemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0019455	acute panmyelosis with myelofibrosis	hematologic_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder|acute_disease|immune_system_disorder	pulmonology|hematology|oncology	cancer|anemia	immune_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0019456	acute myeloid leukemia with multilineage dysplasia	hematologic_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder|acute_disease|immune_system_disorder	hematology|oncology	cancer|anemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0019457	therapy related acute myeloid leukemia and myelodysplastic syndrome	hematologic_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder|acute_disease|immune_system_disorder	hematology|oncology	cancer|anemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0019458	acute basophilic leukemia	hematologic_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder|acute_disease|immune_system_disorder	hematology|oncology	cancer	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0019460	acute leukemia of ambiguous lineage	hematologic_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|acute_disease|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder	hematology|oncology	cancer	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0019461	B-cell prolymphocytic leukemia	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|acute_disease|hematologic_disorder|immune_system_disorder	hematology|oncology	autoimmune_diseases|cancer|leukemia	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0019462	splenic marginal zone lymphoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	hematology|oncology	autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0019463	non-amyloid monoclonal immunoglobulin deposition disease	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	renal_medicine|hematology|immunology|rheumatology	autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0019464	heavy chain disease	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	hematology|oncology|gastroenterology	autoimmune_diseases|inflammatory_disease|anemia	immune_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0019465	nodal marginal zone B-cell lymphoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	hematology|oncology	autoimmune_diseases|cancer|lymphoma	immune_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0019466	lymphomatoid granulomatosis	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|post_infectious_disorder|immune_system_disorder	hematology|oncology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	true	true	false	true	high
MONDO:0019467	CD4+/CD56+ hematodermic neoplasm	hematologic_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|integumentary_system_disorder	hematology|oncology	cancer|hematologic_disorder__note__actual_category_from_list__anemia|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0019468	T-cell prolymphocytic leukemia	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|acute_disease|hematologic_disorder|immune_system_disorder	hematology|oncology	cancer|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0019469	T-cell large granular lymphocyte leukemia	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	hematology|oncology	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	medium
MONDO:0019470	aggressive NK-cell leukemia	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	acute_disease|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	hematology|oncology	inflammation_disease|cancer|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	true	true	false	false	very_high
MONDO:0019471	adult T-cell leukemia/lymphoma	hematologic_disorder|infectious_disease|cancer_or_benign_tumor|immune_system_disorder	infectious_disease|cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|post_infectious_disorder|immune_system_disorder|infectious_disease	hematology|oncology	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0019472	extranodal nasal NK/T cell lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|post_infectious_disorder	hematology|oncology|otolaryngology	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder|nose_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0019473	enteropathy-associated T-cell lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	pediatric|hematology|oncology|gastroenterology	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder_lymphatic_disorder_lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0019474	hepatosplenic T-cell lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|autoimmune_diseases	immune_disorder|liver_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0019475	subcutaneous panniculitis-like T-cell lymphoma	hematologic_disorder|hereditary_disease|cancer_or_benign_tumor|integumentary_system_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|hereditary_disease|immune_system_disorder|integumentary_system_disorder	dermatology|oncology	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder|skin_disorder	false	true	false	true	high
MONDO:0019476	primary cutaneous peripheral T-cell lymphoma not otherwise specified	hematologic_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|integumentary_system_disorder	dermatology|hematology|oncology	cancer|t_cell_lymphoma|lymphoma	immune_disorder|lymphatic_disorder|skin_disorder	false	true	false	false	high
MONDO:0019478	adult nodular lymphocyte predominant Hodgkin lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|post_infectious_disorder	hematology|oncology	cancer|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0019479	histiocytic sarcoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	genetics_and_genomics|hematology|oncology	cancer|inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|skin_disorder	false	true	false	false	very_high
MONDO:0019480	Langerhans cell sarcoma	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	dermatology|oncology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0019483	methotrexate-associated lymphoproliferative disorders	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0019484	hypothalamic hamartomas with gelastic seizures	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|inflammatory_disease	endocrine_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0019485	idiopathic hemiconvulsion-hemiplegia syndrome	nervous_system_disorder	other	nervous_system_disorder|idiopathic_disease	pediatrics|hematology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0019487	epilepsy with myoclonic absences	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0019488	myoclonic epilepsy in non-progressive encephalopathies	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease	brain_disorder|muscledisorder	false	false	false	true	medium
MONDO:0019489	diffuse palmoplantar keratoderma - acrocyanosis syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	vascular_disorder|skin_disorder	false	false	false	false	medium
MONDO:0019490	progressive familial heart block	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	genetics_and_genomics|cardiology|neurology	neurodegenerative_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019493	primary adult heart tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiothoracic|oncology|cardiology	cardiovascular_disorder|cancer	heart_disorder|primary_adult_tumor	false	false	false	false	medium
MONDO:0019494	primary pediatric heart tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	pediatric|oncology|cardiology	cardiovascular_disorder|cancer	heart_disorder|primary_tumor_disorder	false	false	false	false	high
MONDO:0019496	neuroendocrine neoplasm	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology|neurology	neuroendocrine_cancer|cancer	brain_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0019497	nonsyndromic genetic hearing loss	psychiatric_disorder|nervous_system_disorder|hereditary_disease|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|otolaryngology|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	ear_disorder|bone_disorder	false	false	false	true	medium
MONDO:0019498	tungiasis	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology|neurology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|skin_disorder	true	false	false	true	medium
MONDO:0019499	Turner syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder|reproductive_system_disorder|syndromic_disease	endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric|endocrinology	cardiovascular_disorder|metabolic_disorder	endocrine_disorder|vascular_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0019500	extragonadal teratoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	false	medium
MONDO:0019501	Usher syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|otolaryngology|pediatric|ophthalmology	neurodegenerative_disease|mental_health_disorder	ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0019502	autosomal recessive non-syndromic intellectual disability	metabolic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0019503	anterior segment dysgenesis	disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_visual_system|disorder_of_development_or_morphogenesis|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|pediatric|ophthalmology	metabolic_disorder|eye_disease	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0019504	superior limbic keratoconjunctivitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|inflammatory_disease|disorder_of_orbital_region	dermatology|neurology|ophthalmology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|eye_disorder	true	false	false	false	medium
MONDO:0019506	obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome	syndromic_disease	other	syndromic_disease	cardiology|gastroenterology|endocrinology|pediatric	metabolic_disorder|autoimmune_diseases|cardiovascular_disorder	endocrine_disorder|cardiac_disorder|lower_gastrointestinal_disorder	true	false	false	false	very_high
MONDO:0019507	amelogenesis imperfecta	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder|hereditary_disease	dermatology|genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|anemia	teeth_disorder|skin_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0019508	van der Woude syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetic_disorders|dermatology|pediatrics|genetics_and_genomics|other____corrected_answer__dermatology	inflammatory_disease|autoimmune_diseases	joint_disorder|skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0019509	cutaneous leukocytoclastic angiitis	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	dermatology|hematology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0019512	congenital heart malformation	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|cardiology	cardiovascular_disorder|congenital_heart_malformation_fits_here_but_that_is_not_an_exact_match_so_cardiovascular_disorder	congenital_disorder|vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0019514	hepatic veno-occlusive disease	cardiovascular_disorder|endocrine_system_disorder|digestive_system_disorder	cardiovascular_disorder|endocrine_system_disorder	cardiovascular_disorder|digestive_system_disorder|endocrine_system_disorder	gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases|hepatic_veno_occlusive_disease	vascular_disorder|liver_disorder	false	false	false	true	high
MONDO:0019516	exudative vitreoretinopathy	cardiovascular_disorder|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|disorder_of_orbital_region	neurology|ophthalmology	cancer|inflammatory_disease|autoimmune_diseases	vitreoretinopathy_is_not_a_category_and_causes_exudative_vitreoretinopathy_so_it_will_be_removed_from_this_response__eye_disorder|eye_disorder	false	false	false	false	high
MONDO:0019517	Waardenburg syndrome type 2	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	bone_disorder|spinal_disorder|ear_disorder|eye_disorder	false	false	false	false	medium
MONDO:0019518	Waardenburg-Shah syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|digestive_system_disorder	other	syndromic_disease|digestive_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|nerve_disorder|spinal_disorder|ear_disorder|skeletal_disorder|hearing_bone_disorder	false	false	false	false	high
MONDO:0019521	centripetalis recessive dystrophic epidermolysis bullosa	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	pediatric|dermatology|genetics_and_genomics	metabolic_disorder|skin_disease|inflammatory_disease|autoimmune_diseases	joint_disorder|skin_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0019522	recessive dystrophic epidermolysis bullosa-generalized other	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	skin_disorder|muscle_disorder	false	false	false	false	high
MONDO:0019524	Bartter syndrome type 4	hereditary_disease|syndromic_disease|urinary_system_disorder	other	syndromic_disease|hereditary_disease|urinary_system_disorder	pediatric|renal_medicine|genetics_and_genomics	electrolyte_imbalance_disorder|metabolic_disorder	electrolyte_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0019525	tetrasomy X	chromosomal_disorder|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	chromosomal_disorder|hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	pediatric|genetics_and_genomics	developmental_disorder|metabolic_disorder|congenital_disease|chromosomal_abnormality|genetic_disease	bone_disorder|reproductive_system_disorder|joint_disorder	false	false	false	false	high
MONDO:0019526	erythema elevatum diutinum	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0019527	undifferentiated connective tissue syndrome	immune_system_disorder	autoimmune_disease	immune_system_disorder	rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019528	inflammatory pseudotumor of the liver	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|hepatology	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder|inflammatory_process|liver_disorder	false	false	false	false	medium
MONDO:0019529	radiation myelitis	nervous_system_disorder	other	nervous_system_disorder	hematolog|oncology|neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|spinal_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0019530	non-syndromic syndactyly	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	genetic_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0019531	hemolytic anemia due to glutathione reductase deficiency	metabolic_disease|hematologic_disorder|hereditary_disease	metabolic_disease|anemia	metabolic_disease|hematologic_disorder|hereditary_disease	pediatric|genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	high
MONDO:0019532	autoimmune hemolytic anemia, warm type	immune_system_disorder|hematologic_disorder	autoimmune_disease|anemia	immune_system_disorder|hematologic_disorder	immunology|hematology	anemia|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0019533	paroxysmal cold hemoglobinuria	immune_system_disorder|hematologic_disorder	autoimmune_disease|anemia	immune_system_disorder|hematologic_disorder	renal_medicine|genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0019534	mixed-type autoimmune hemolytic anemia	immune_system_disorder|hematologic_disorder	autoimmune_disease|anemia	immune_system_disorder|hematologic_disorder	immunology|hematology	anemia|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019535	drug-induced autoimmune hemolytic anemia	immune_system_disorder|hematologic_disorder	autoimmune_disease|anemia	immune_system_disorder|hematologic_disorder	immunology|allergy_and_immunology|hematology	anemia|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019536	Shiga toxin-associated hemolytic uremic syndrome	hematologic_disorder	anemia	post_infectious_disorder|hematologic_disorder	pediatric|renal_medicine|hematology	anemia|inflammatory_disease|autoimmune_diseases	immune_disorder|kidney_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0019537	hemoglobin D disease	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	low
MONDO:0019538	Gaisbock syndrome	immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	other	immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|other____note__gaisbock_syndrome_is_a_rare_genetic_disorder_that_affects_the_bone_marrow_and_blood	false	false	false	false	medium
MONDO:0019540	diffuse alveolar hemorrhage	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiology|cardiothoracic|hematology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	lung_disorder|blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019542	acute liver failure	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|acute_disease|endocrine_system_disorder	gastroenterology|hepatology	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0019543	acquired aneurysmal subarachnoid hemorrhage	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|hematology	cardiovascular_disorder|neurological_disease	brain_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0019544	cocaine intoxication	poisoning	other	poisoning	psychiatry|pediatrics|neurology	mental_health_disorder|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0019545	systemic monochloroacetate poisoning	poisoning	other	poisoning	neurology|toxicology_____note__toxicology_is_not_in_the_original_list_but_seems_to_be_a_relevant_category	metabolic_disorder|systemic_poisonings	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0019547	Wells syndrome	integumentary_system_disorder	other	integumentary_system_disorder	pulmonology|cardiothoracic	metabolic_disorder|inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	joint_disorder|skin_disorder|connective_tissue_disorder	false	false	false	false	medium
MONDO:0019548	autosomal dominant intermediate Charcot-Marie-Tooth disease	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant_disorder_is_not_in_the_list_but_it_s_related_to_genetic_disorders_which_could_be_categorized_under_metabolic_disorder_sometimes	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0019549	severe early-onset axonal neuropathy due to MFN2 deficiency	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|ear_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0019550	hereditary motor and sensory neuropathy with acrodystrophy	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|hereditary_motor_and_sensory_neuropathy_with_acrodystrophy	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0019551	hereditary motor and sensory neuropathy type 6	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|hereditary_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0019552	centrifugal lipodystrophy	metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|metabolic_disease	dermatology|endocrinology	metabolic_disorder	skin_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0019553	drug-induced localized lipodystrophy	metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|metabolic_disease	dermatology|endocrinology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder	false	false	false	false	medium
MONDO:0019554	idiopathic localized lipodystrophy	metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|metabolic_disease|idiopathic_disease	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder	false	false	false	false	low
MONDO:0019555	panniculitis and localized lipodystrophy	metabolic_disease|connective_tissue_disorder|inflammatory_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|connective_tissue_disorder|inflammatory_disease|metabolic_disease	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|skin_disorder	false	false	false	false	medium
MONDO:0019556	pressure-induced localized lipoatrophy	metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|metabolic_disease	dermatology|endocrinology	metabolic_disorder|adrenal_gland_disease	skin_disorder|muscle_disorder	false	false	false	false	low
MONDO:0019557	chilblain lupus	immune_system_disorder|cardiovascular_disorder|connective_tissue_disorder|integumentary_system_disorder	cardiovascular_disorder|autoimmune_disease	integumentary_system_disorder|immune_system_disorder|cardiovascular_disorder|connective_tissue_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0019558	discoid lupus erythematosus	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	immune_system_disorder|connective_tissue_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0019559	hypertrophic or verrucous lupus erythematosus	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	immune_system_disorder|connective_tissue_disorder	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0019560	lupus erythematosus tumidus	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	immune_system_disorder|connective_tissue_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	low
MONDO:0019561	lupus erythematosus panniculitis	immune_system_disorder|connective_tissue_disorder|inflammatory_disease|integumentary_system_disorder	autoimmune_disease	immune_system_disorder|connective_tissue_disorder|inflammatory_disease|integumentary_system_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder_skin_disorder	false	false	false	true	medium
MONDO:0019562	localized scleroderma	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	immune_system_disorder|connective_tissue_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	skin_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0019563	CREST syndrome	immune_system_disorder|connective_tissue_disorder|syndromic_disease|integumentary_system_disorder	autoimmune_disease	immune_system_disorder|connective_tissue_disorder|syndromic_disease|integumentary_system_disorder	dermatology|rheumatology|pulmonology	autoimmune_diseases|inflammatory_disease	joint_disorder|skin_disorder|eye_disorder|immune_disorder|muscle_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0019565	hereditary von Willebrand disease	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0019567	Ehlers-Danlos syndrome, classic type, 1	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|dermatology|genetics_and_genomics	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	joint_disorder|skin_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019568	Ehlers-Danlos syndrome, classic type, 2	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|dermatology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder|autoimmune_diseases|inflammatory_disease	joint_disorder|skin_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019569	Cockayne syndrome type 1	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|premature_aging_syndrome	metabolic_disease	disorder_of_development_or_morphogenesis|premature_aging_syndrome|metabolic_disease|hereditary_disease	genomics|neurology|endocrinology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|lower_gastrointestinal_disorder____removed__other__and_combined_categories_as_necessary|brain_disorder|lymphatic_disorder|eye_disorder|heart_disorder|skeletal_system_disorder|endocrine_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0019570	Cockayne syndrome type 2	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|premature_aging_syndrome	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|premature_aging_syndrome|hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|vascular_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0019571	autosomal dominant cutis laxa	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0019572	autosomal recessive cutis laxa type 1	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|genetics_and_genomics	genetic_disorder|metabolic_disorder	skin_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0019573	autosomal recessive cutis laxa type 2	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder	skin_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0019574	secondary intestinal lymphangiectasia	digestive_system_disorder	other	digestive_system_disorder	oncology|gastroenterology	cancer|autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	lower_gastrointestinal_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0019575	hypotrichosis simplex of the scalp	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	metabolic_disorder|anemia|autoimmune_diseases|inflammatory_disease	skin_disorder|hair_disorder	false	false	false	false	low
MONDO:0019576	telangiectasia macularis eruptiva perstans	immune_system_disorder|hematologic_disorder|hereditary_disease|integumentary_system_disorder|inflammatory_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|immune_system_disorder|cancer_or_benign_tumor|inflammatory_disease|hematologic_disorder|hereditary_disease	dermatology|ophthalmology	autoimmune_diseases|inflammatory_disease	skin_disorder|eye_disorder	true	false	false	false	medium
MONDO:0019577	anonychia-onychodystrophy syndrome	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder|anemia|autoimmune_diseases	skin_disorder|bone_disorder	false	false	false	false	low
MONDO:0019578	nodular lichen myxedematosus	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|endocrinology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0019579	discrete papular lichen myxedematosus	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|endocrinology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0019580	papular mucinosis of infancy	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatric	autoimmune_diseases|inflammatory_disease	skin_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0019581	acral persistent papular mucinosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	autoimmune_diseases|inflammatory_disease	nose_disorder|skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0019582	self-healing papular mucinosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder	false	false	false	false	low
MONDO:0019583	localized lichen myxedematosus with mixed features of different subtypes	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	skin_disorder|immune_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0019584	localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|immunology|hematology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|blood_bone_marrow_disorder	true	false	false	false	medium
MONDO:0019585	scleromyxedema without monoclonal gammopathy	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|allergy_and_immunology|hematology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0019586	X-linked nonsyndromic hearing loss	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	ear_disorder	false	false	false	true	high
MONDO:0019587	autosomal dominant nonsyndromic hearing loss	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder|autosomal_dominant_disorders_is_not_in_the_list_so_i_will_exclude_it	false	false	false	true	medium
MONDO:0019588	hearing loss, autosomal recessive	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	high
MONDO:0019591	panhypopituitarism	endocrine_system_disorder|reproductive_system_disorder|nervous_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	endocrinology|pediatric|genetics_and_genomics	autoimmune_diseases|adrenal_gland_disease|inflammatory_disease|metabolic_disorder	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0019600	xeroderma pigmentosum	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|oncology|dermatology	cancer|genetic_disorder	skin_disorder|immune_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0019603	osteopenia-myopia-hearing loss-intellectual disability-facial dysmorphism syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|otolaryngology|psychiatry|ophthalmology|orthopaedic|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|mental_health_disorder	eye_disorder|ear_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0019604	acquired monoclonal Ig light chain-associated Fanconi syndrome	hematologic_disorder	other	hematologic_disorder	oncology|hematology|rheumatology	cancer|autoimmune_diseases|anemia|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019605	immunotactoid or fibrillary glomerulopathy	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|allergy_and_immunology|rheumatology	autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0019606	simple cryoglobulinemia	nervous_system_disorder	other	nervous_system_disorder	hematology|renal_medicine|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0019607	unspecified juvenile idiopathic arthritis	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	other	inflammatory_disease|connective_tissue_disorder|idiopathic_disease|musculoskeletal_system_disorder	rheumatology|pediatric	autoimmune_diseases|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	true	high
MONDO:0019609	Zellweger spectrum disorders	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|metabolic_disease|nervous_system_disorder	neurodegenerative_disease|metabolic_disease	syndromic_disease|hereditary_disease|metabolic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatrics|endocrinology	neurodegenerative_disease|metabolic_disorder	immune_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0019610	Zollinger-Ellison syndrome	syndromic_disease|cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	syndromic_disease|digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	gastroenterology|endocrinology	metabolic_disorder|autoimmune_diseases	upper_gastrointestinal_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0019611	TSH-secreting pituitary adenoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|connective_tissue_disorder|nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder|musculoskeletal_system_disorder	neurology|endocrinology	cancer|adenoma|neuroendocrine_disorder|pituitary_adenoma|hormone_disease|neuroendocrine_tumor|endocrine_system_disorder|endocrine_disorder|hormone_imbalance	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0019612	functioning gonadotropic adenoma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|connective_tissue_disorder|nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder|musculoskeletal_system_disorder	neurology|endocrinology	neurological_disorder|cancer|endocrine_disease	brain_disorder|endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0019613	non-functioning pituitary adenoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|nervous_system_disorder|endocrine_system_disorder|musculoskeletal_system_disorder	neurology|endocrinology	cancer|neuroendocrine_cancer	brain_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0019614	pituitary deficiency due to Rathke's pouch cysts	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	neurology|endocrinology	neurological_disorder|pituitary_disorder|endocrine_disorder	brain_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0019615	pituitary dermoid and epidermoid cysts	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	neurology|otolaryngology|endocrinology	cancer	skin_disorder|brain_disorder	false	false	false	false	medium
MONDO:0019617	pituitary deficiency due to empty sella turcica syndrome	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	brain_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0019618	Sheehan syndrome	syndromic_disease	other	syndromic_disease	obstetrics_and_gynecology|endocrinology	adrenal_gland_disease|anemia	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0019620	congenital esophageal diverticulum	disorder_of_development_or_morphogenesis|upper_digestive_tract_disorder|digestive_system_disorder	other	upper_digestive_tract_disorder|digestive_system_disorder|disorder_of_development_or_morphogenesis	gastroenterology|pediatric	developmental_disorder|congenital_anomaly|neurogastrointestinal_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0019621	chronic pneumonitis of infancy	inflammatory_disease|respiratory_system_disorder	other	inflammatory_disease|respiratory_system_disorder	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	true	false	false	true	medium
MONDO:0019622	non-specific interstitial pneumonia	infectious_disease|inflammatory_disease|respiratory_system_disorder	infectious_disease	inflammatory_disease|respiratory_system_disorder|infectious_disease|idiopathic_disease	pulmonology|cardiothoracic|cardiology	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0019623	hereditary angioedema	integumentary_system_disorder|hereditary_disease|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|hereditary_disease|integumentary_system_disorder|cardiovascular_disorder	genetics_and_genomics|hematology|allergy_and_immunology|immunology	allergy|autoimmune_diseases|inflammatory_disease	immune_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0019624	acquired angioedema	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|integumentary_system_disorder|cardiovascular_disorder	dermatology|renal_medicine|allergy_and_immunology	allergy|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0019625	familial thoracic aortic aneurysm and aortic dissection	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	genetics_and_genomics|pulmonology|cardiothoracic|hematology|cardiology|renal_medicine|rheumatology	cardiovascular_disorder|inflammatory_disease|aortic_dissection	heart_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0019626	isolated ankyloblepharon filiforme adnatum	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0019627	isolated congenital alacrima	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|dermatology|pediatric	adrenal_gland_disease|metabolic_disorder	eye_disorder|ear_disorder	false	false	false	false	low
MONDO:0019628	Rieger anomaly	disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|disorder_of_development_or_morphogenesis	genetics_and_genomics|ophthalmology|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	eye_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0019629	sclerocornea	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|pediatric	autoimmune_diseases|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0019630	congenital ectropion uveae	hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|disorder_of_development_or_morphogenesis	otolaryngology|ophthalmology|pediatric	neurodegenerative_disease|eye_disorder|autoimmune_diseases|congenital_disease|autoimmune_diseases___corrected_list_to_fit_the_format___inflammatory_disease	eye_disorder|nose_disorder	false	false	false	false	high
MONDO:0019631	persistent hyperplastic primary vitreous	hereditary_disease|nervous_system_disorder|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|nervous_system_disorder|disorder_of_visual_system	ophthalmology|pediatric	congenital_abnormality|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0019632	Lyme disease	infectious_disease	infectious_disease	infectious_disease	infectious_disease|dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0019633	relapsing fever	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|hematology	anemia|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0019634	familial nasal acilia	hereditary_disease|otorhinolaryngologic_disease	other	hereditary_disease|otorhinolaryngologic_disease	genetics_and_genomics|otolaryngology	neurodegenerative_disease|familial_acilia	eye_disorder|nose_disorder	false	false	false	false	very_high
MONDO:0019635	idiopathic achalasia	upper_digestive_tract_disorder|digestive_system_disorder	other	upper_digestive_tract_disorder|digestive_system_disorder|idiopathic_disease	pulmonology|gastroenterology	neurodegenerative_disease|inflammatory_disease	lower_gastrointestinal_disorder|throat_disorder	false	false	false	true	medium
MONDO:0019636	renal agenesis, unilateral	hereditary_disease|disorder_of_development_or_morphogenesis|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder|disorder_of_development_or_morphogenesis	urology|renal_medicine|pediatric	metabolic_disorder|renal_agenesis|inflammatory_disease	kidney_disorder|renal_disorder|unary_tract_disorder	false	false	false	false	medium
MONDO:0019637	renal hypoplasia	disorder_of_development_or_morphogenesis|urinary_system_disorder	other	urinary_system_disorder|disorder_of_development_or_morphogenesis	urology|renal_medicine|pediatric	metabolic_disorder|renal_hypoplasia|kidney_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0019638	renal dysplasia	disorder_of_development_or_morphogenesis|urinary_system_disorder	other	urinary_system_disorder|disorder_of_development_or_morphogenesis	urology|renal_medicine|pediatric	renal_dysplasia|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0019639	congenital megacalycosis	urinary_system_disorder	other	urinary_system_disorder	genetics_and_genomics|renal_medicine|pediatric	metabolic_disorder|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0019640	posterior urethral valve	disorder_of_development_or_morphogenesis|urinary_system_disorder	other	urinary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|urology	urinary_system_disease|congenital_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0019641	Pauci-immune glomerulonephritis	inflammatory_disease|urinary_system_disorder	other	urinary_system_disorder|inflammatory_disease	hematology|allergy_and_immunology|renal_medicine|rheumatology	inflammatory_disease|autoimmune_diseases	kidney_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0019642	vitamin D-dependent rickets, type 2	musculoskeletal_system_disorder|nutritional_disorder|metabolic_disease|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder|metabolic_disease	hereditary_disease|metabolic_disease|nutritional_disorder|endocrine_system_disorder|musculoskeletal_system_disorder	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|rickets	endocrine_disorder|bone_disorder	false	false	false	true	high
MONDO:0019643	transient pseudohypoaldosteronism	urinary_system_disorder	other	urinary_system_disorder	endocrinology|pediatric|renal_medicine	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0019644	renal dysplasia, unilateral	disorder_of_development_or_morphogenesis|urinary_system_disorder	other	urinary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|urology|renal_medicine	kidney_disease___however__since_the_given_list_doesn_t_have_these_categories__we_will_consider_the_closest_match__kidney_disease_and_developmental_disorder_aren_t_in_the_list_either_but__metabolic_disorder__isn_t_a_good_fit__the_best_fitting_categories_from_the_list_are___renal_dysplasia_is_close_to_renal_which_is_implied_by__kidney_disease___but_since_that_s_not_an_option__we_ll_choose__metabolic_disorder_____unilateral_disease_doesn_t_exist_in_the_category_list__however__inflammatory_disease__or__cancer__could_be_considered_as_renal_dysplasia_can_sometimes_be_a_precursor_to_cancer_and_can_be_caused_by_inflammation|unilateral_disease|developmental_disorder|renal_dysplasia	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0019645	renal dysplasia, bilateral	disorder_of_development_or_morphogenesis|urinary_system_disorder	other	urinary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|urology|renal_medicine	metabolic_disorder|renal_dysplasia_bilateral_is_somewhat_related_to_but_does_not_perfectly_fit_this_category	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0019646	unilateral congenital megacalycosis	urinary_system_disorder	other	urinary_system_disorder	pediatric|urology	metabolic_disorder|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0019647	congenital bilateral megacalycosis	urinary_system_disorder	other	urinary_system_disorder	pediatric|genetics_and_genomics|urology	metabolic_disorder|kidney_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0019648	achondrogenesis	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0019649	idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis	syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|idiopathic_disease|syndromic_disease	pediatric|renal_medicine	nephrotic_syndrome|inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|immune_disorder	false	false	false	true	high
MONDO:0019650	idiopathic steroid-sensitive nephrotic syndrome with minimal change	syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|idiopathic_disease|syndromic_disease	pediatric|renal_medicine	inflammatory_disease|autoimmune_diseases	kidney_disorder|endocrine_disorder|immune_disorder	false	false	false	true	medium
MONDO:0019651	idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation	syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|idiopathic_disease|syndromic_disease	pediatric|renal_medicine	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|endocrine_disorder|immune_disorder	false	false	false	true	high
MONDO:0019652	familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation	syndromic_disease|urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|idiopathic_disease|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|renal_medicine	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|endocrine_disorder|immune_disorder	false	false	false	false	high
MONDO:0019653	familial idiopathic steroid-resistant nephrotic syndrome with minimal changes	syndromic_disease|urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|idiopathic_disease|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|renal_medicine|allergy_and_immunology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|endocrine_disorder|immune_disorder	false	false	false	false	high
MONDO:0019654	familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis	syndromic_disease|urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|idiopathic_disease|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|renal_medicine	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|endocrine_disorder|immune_disorder	false	false	false	false	high
MONDO:0019655	sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis	syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|idiopathic_disease|syndromic_disease	pediatric|renal_medicine|neurology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|joint_disorder|vascular_disorder|immune_disorder	false	false	false	false	high
MONDO:0019656	sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis	syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|idiopathic_disease|syndromic_disease	pediatric|nephrology|renal_medicine	inflammatory_disease|kidney_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0019659	Pfeiffer syndrome type 1	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|pulmonology	metabolic_disorder|neurodegenerative_disease	ear_disorder|bone_disorder	false	false	false	false	medium
MONDO:0019660	Pfeiffer syndrome type 2	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder|joint_disorder|ear_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0019661	Pfeiffer syndrome type 3	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|pulmonology	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|joint_disorder|ear_disorder|hearing_loss_disorder	false	false	false	false	very_high
MONDO:0019662	short rib-polydactyly syndrome, Majewski type	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|respiratory_system_disorder	other	syndromic_disease|respiratory_system_disorder|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	joint_disorder|muscle_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0019665	monostotic fibrous dysplasia	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|rheumatology	metabolic_disorder	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	medium
MONDO:0019666	spondyloepimetaphyseal dysplasia, PAPSS2 type	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0019667	spondyloepiphyseal dysplasia tarda	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0019668	adenoma of pancreas	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0019669	hypochondrogenesis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|connective_tissue_disorder	other	syndromic_disease|musculoskeletal_system_disorder|connective_tissue_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0019670	ulnar hemimelia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	congenital_disorder|developmental_disorder|limb_abnormality|skeletal_dysplasia|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0019671	radial hemimelia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019672	fibular hemimelia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|hematology|genetics_and_genomics|orthopaedic	metabolic_disorder|congenital_disease|skeletal_disease	joint_disorder|muscle_disorder|bone_disorder	false	false	false	false	medium
MONDO:0019673	postaxial polydactyly type A	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic	genetic_disease|developmental_disorder|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0019674	postaxial polydactyly type B	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder|skeletal_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0019675	spondyloepimetaphyseal dysplasia with joint laxity	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|rheumatology|orthopaedic	inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0019676	brachydactyly type B	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	congenital_anomaly|developmental_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0019677	brachydactyly type E	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic	congenital_disorder|skeletal_muscle_disorder|developmental_disorder|genetic_disorder|birth_defect	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0019678	brachydactyly type A5	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0019679	brachydactyly type A7	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder|skeletal_dysplasia	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0019680	genochondromatosis type 2	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|rheumatology	metabolic_disorder|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0019681	juvenile sialidosis type 2	musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	joint_disorder|ear_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0019682	congenital sialidosis type 2	musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0019685	FGFR3-related chondrodysplasia	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	developmental_disorder|metabolic_disorder|skeletal_dysplasia|genetic_disorder	joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0019690	filamin-related bone disorder	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|rheumatology	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder|muscle_disorder	false	false	false	true	high
MONDO:0019691	short rib dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disease___note__short_rib_dysplasia_is_a_genetic_disorder_that_affects_the_development_of_the_ribs__the_provided_category_list_does_not_explicitly_include__genetic_disease___but_i_included_it_as_it_s_the_closest_match_based_on_the_description	bone_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0019694	spondylodysplastic dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics|rheumatology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0019695	acromelic dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	endocrinology|orthopaedic|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	bone_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0019696	acromesomelic dysplasia	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0019698	bent bone dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disease_is_not_listed_so_none	blood_bone_marrow_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0019701	chondrodysplasia punctata	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|dermatology|rheumatology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	joint_disorder|bone_disorder|skin_disorder	false	false	false	false	high
MONDO:0019702	neonatal osteosclerotic dysplasia	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0019707	primary osteolysis	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|rheumatology	inflammatory_disease|metabolic_disorder	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0019713	non-syndromic limb reduction defect	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	limb_reduction_defect|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0019716	overgrowth syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|psychiatry|endocrinology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	overgrowth_syndrome|endocrine_disorder	false	false	false	false	high
MONDO:0019719	congenital anomaly of kidney and urinary tract	disorder_of_development_or_morphogenesis|urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|renal_medicine|urology	congenital_anomaly|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0019722	glomerular disorder	urinary_system_disorder	other	urinary_system_disorder	nephrology_is_not_in_the_list_so__renal_medicine|hematology|renal_medicine	inflammatory_disease|autoimmune_diseases	kidney_disorder|immune_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0019725	pediatric systemic lupus erythematosus	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	immune_system_disorder|connective_tissue_disorder	pediatric|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|kidney_disorder|joint_disorder|skin_disorder	false	false	false	true	high
MONDO:0019726	type II mixed cryoglobulinemia	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	rheumatology|immunology|hematology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019727	mixed cryoglobulinemia type III	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	rheumatology|hematology	inflammatory_disease|autoimmune_diseases	kidney_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019728	heavy chain deposition disease	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	immunology|hematology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	kidney_disorder|immune_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0019729	light and heavy chain deposition disease	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	rheumatology|hematology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|anemia	kidney_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0019730	light chain deposition disease	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|genetics_and_genomics|renal_medicine	metabolic_disorder|autoimmune_diseases|anemia	kidney_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019731	AApoAI amyloidosis	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pulmonology|genetics_and_genomics|neurology|renal_medicine|cardiology	metabolic_disorder|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|liver_disorder	false	false	false	true	high
MONDO:0019732	ALys amyloidosis	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|liver_disorder|vascular_disorder	false	false	false	true	high
MONDO:0019733	AFib amyloidosis	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pulmonology|hematology|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0019734	juvenile polymyositis	inflammatory_disease|musculoskeletal_system_disorder	other	inflammatory_disease|idiopathic_disease|musculoskeletal_system_disorder	rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|muscle_disorder	false	false	false	true	high
MONDO:0019735	polymyalgia rheumatica	connective_tissue_disorder|syndromic_disease	other	syndromic_disease|connective_tissue_disorder	rheumatology|neurology	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0019736	dense deposit disease	inflammatory_disease|urinary_system_disorder	other	inflammatory_disease|urinary_system_disorder	nephrology|renal_medicine	metabolic_disorder|inflammatory_disease|autoimmune_diseases	kidney_disorder|immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019737	thrombotic microangiopathy	hematologic_disorder	other	hematologic_disorder	hematology|cardiology|renal_medicine	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	kidney_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0019738	atypical hemolytic-uremic syndrome with H factor anomaly	hematologic_disorder|hereditary_disease|immune_system_disorder|syndromic_disease	other	syndromic_disease|hereditary_disease|hematologic_disorder|immune_system_disorder	pediatric|hematology|renal_medicine	inflammatory_disease|autoimmune_diseases|anemia	kidney_disorder|immune_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0019739	atypical hemolytic-uremic syndrome with anti-factor H antibodies	hematologic_disorder|hereditary_disease|immune_system_disorder|syndromic_disease	other	syndromic_disease|hereditary_disease|hematologic_disorder|immune_system_disorder	hematology|pediatrics|renal_medicine	inflammatory_disease|autoimmune_diseases|anemia	kidney_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0019740	acquired thrombotic thrombocytopenic purpura	hematologic_disorder|immune_system_disorder	other	hematologic_disorder|immune_system_disorder	oncology|hematology	inflammatory_disease|autoimmune_diseases|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0019741	familial cystic renal disease	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	urology|genetics_and_genomics|renal_medicine	metabolic_disorder|genetic_disorders|kidney_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0019742	late-onset nephronophthisis	hereditary_disease|metabolic_disease|urinary_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|urinary_system_disorder	urology|removed__nephronophthisis__as_it_was_mentioned_in_the_question_and_provided_no_relevance_to_category|nephronophthisis_is_a_genetic_disorder_primarily_affecting_the_kidneys|renal_medicine	metabolic_disorder|systemic_illness|kidney_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0019745	cystinuria type A	hereditary_disease|metabolic_disease|urinary_system_disorder|syndromic_disease	metabolic_disease	metabolic_disease|syndromic_disease|hereditary_disease|urinary_system_disorder	urology|genetics_and_genomics|renal_medicine	metabolic_disorder|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0019746	cystinuria type B	hereditary_disease|metabolic_disease|urinary_system_disorder|syndromic_disease	metabolic_disease	metabolic_disease|syndromic_disease|hereditary_disease|urinary_system_disorder	urology|genetics_and_genomics|renal_medicine	metabolic_disorder|kidney_disease	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0019751	autoinflammatory syndrome	connective_tissue_disorder|syndromic_disease	other	syndromic_disease|connective_tissue_disorder	rheumatology|gastroenterology	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder|liver_disorder	false	false	false	true	high
MONDO:0019752	pediatric Castleman disease	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	pediatric|oncology|hematology	cancer|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	true	medium
MONDO:0019753	localized Castleman disease	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	oncology|hematology	cancer|inflammatory_disease	lymphatic_disorder|immune_disorder	true	false	false	true	medium
MONDO:0019754	multicentric Castleman disease	hereditary_disease|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hereditary_disease|post_infectious_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0019755	developmental defect during embryogenesis	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	developmental_defect_during_embryogenesis|developmental_disorder|developmental_disorder___becomes___developmental_defect_during_embryogenesis	developmental_defect_during_embryogenesis|spinal_disorder	false	false	false	false	high
MONDO:0019756	lobar holoprosencephaly	nervous_system_disorder|hereditary_disease|endocrine_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0019757	alobar holoprosencephaly	nervous_system_disorder|hereditary_disease|endocrine_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0019759	epispadias	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	urinary_system_disorder|disorder_of_development_or_morphogenesis	urology|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0019760	terminal transverse defects of arm	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|orthopaedic	neurodegenerative_disease	muscle_disorder|bone_disorder	false	false	false	false	medium
MONDO:0019761	laryngotracheoesophageal cleft type 1	digestive_system_disorder|respiratory_system_disorder|upper_digestive_tract_disorder	other	digestive_system_disorder|respiratory_system_disorder|upper_digestive_tract_disorder	otolaryngology|pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	throat_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0019762	laryngotracheoesophageal cleft type 2	digestive_system_disorder|respiratory_system_disorder|upper_digestive_tract_disorder	other	digestive_system_disorder|respiratory_system_disorder|upper_digestive_tract_disorder	otolaryngology|pediatric|general	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	throat_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0019763	laryngotracheoesophageal cleft type 3	digestive_system_disorder|respiratory_system_disorder|upper_digestive_tract_disorder	other	digestive_system_disorder|respiratory_system_disorder|upper_digestive_tract_disorder	otolaryngology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	throat_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0019764	laryngotracheoesophageal cleft type 4	digestive_system_disorder|respiratory_system_disorder|upper_digestive_tract_disorder	other	digestive_system_disorder|respiratory_system_disorder|upper_digestive_tract_disorder	otolaryngology|pediatrics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	upper_gastrointestinal_disorder|thorat_disorder	false	false	false	false	very_high
MONDO:0019766	X-linked intellectual disability, Porteous type	nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0019767	hamel cerebro-palato-cardiac syndrome	nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|genetics_and_genomics|cardiology	metabolic_disorder|neurodegenerative_disease|cardiovascular_disorder	brain_disorder|throat_disorder|heart_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0019768	X-linked intellectual disability, Golabi-Ito-hall type	nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0019769	X-linked intellectual disability, Sutherland-Haan type	nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0019770	X-linked dominant intellectual disability-epilepsy syndrome	hereditary_disease|psychiatric_disorder|nervous_system_disorder|syndromic_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	genetics_and_genomics|pediatric|neurology	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0019771	oromandibular dystonia	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	otolaryngology|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0019772	blepharospasm-oromandibular dystonia syndrome	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0019773	myelomeningocele	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|neurology|oncology	cancer|adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0019780	anotia	otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	genetics_and_genomics|pediatric|otolaryngology	neurodegenerative_disease|metabolic_disorder	teeth_disorder|bone_disorder	false	false	false	false	high
MONDO:0019781	astrocytoma (excluding glioblastoma)	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	true	medium
MONDO:0019782	humero-ulnar synostosis	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	rheumatology|orthopaedic	autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0019783	neovascular glaucoma	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|cardiovascular_disorder	vascular_disorder|eye_disorder	false	false	false	true	high
MONDO:0019784	12q14 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0019786	severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	anal_anomalies_is_associated_with_distal_phalangeal_hypoplasia_which_suggests_it_may_also_be_a_form_of_genetic_disorder__however_given_the_options_i_can_select|neurodegenerative_disease|metabolic_disorder	musculoskeletal_disorder|reproductive_system_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0019787	autoimmune enteropathy	immune_system_disorder|digestive_system_disorder	autoimmune_disease	immune_system_disorder|digestive_system_disorder	gastroenterology|immunology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0019788	non-secreting paraganglioma	endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|nervous_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|endocrine_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|adrenal_gland_disease	vascular_disorder|endocrine_disorder	false	false	false	true	none
MONDO:0019789	cytophagic histiocytic panniculitis	inflammatory_disease|integumentary_system_disorder|connective_tissue_disorder	other	inflammatory_disease|integumentary_system_disorder|connective_tissue_disorder	hematology|dermatology|rheumatology	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0019790	neuroleptic malignant syndrome	syndromic_disease|nervous_system_disorder	other	nervous_system_disorder|syndromic_disease	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0019791	recessive mitochondrial ataxia syndrome	hereditary_disease|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease|metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|nervous_system_disorder|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|mitochondrial_disease_is_not_in_the_list_so__brain_disorder	false	false	false	false	high
MONDO:0019792	autosomal dominant cerebellar ataxia type I	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0019793	autosomal dominant cerebellar ataxia type III	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	autosomal_dominant_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0019794	autosomal dominant cerebellar ataxia type IV	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	autosomal_dominant_disorder|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0019795	acalvaria	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurosurgery___note__the_provided_list_doesn_t_contain_a_direct_match_for__acalvaria___however__acalvaria_is_often_related_to_neurological_conditions_due_to_its_association_with_cranial_abnormalities_and_disorders_of_the_nervous_system__therefore__i_have_included_both_neurology_and_neurosurgery_as_relevant_categories|neurology	cancer|adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0019796	acrocephalosyndactyly	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|pediatric|orthopaedic	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0019797	acrodysostosis	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic	genetic_disorder|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0019799	hepatoerythropoietic porphyria	integumentary_system_disorder|inflammatory_disease|hereditary_disease|digestive_system_disorder|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	inflammatory_disease|endocrine_system_disorder|hereditary_disease|digestive_system_disorder|metabolic_disease|integumentary_system_disorder	genetics_and_genomics|hepatology|hematology|gastroenterology	anemia|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0019801	acute adrenal insufficiency	endocrine_system_disorder	endocrine_system_disorder	acute_disease|endocrine_system_disorder	endocrinology|renal_medicine	metabolic_disorder|autoimmune_diseases|adrenal_gland_disease	endocrine_disorder|vascular_disorder	false	false	false	true	high
MONDO:0019802	secondary short bowel syndrome	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0019803	angioma serpiginosum	cardiovascular_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cardiovascular_disorder|cancer_or_benign_tumor	integumentary_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	genetics_and_genomics|neurology|dermatology	cardiovascular_disorder|inflammatory_disease|cancer	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0019804	congenital tracheomalacia	respiratory_system_disorder|otorhinolaryngologic_disease	other	respiratory_system_disorder|otorhinolaryngologic_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	lung_disorder|throat_disorder	false	false	false	false	medium
MONDO:0019805	twin to twin transfusion syndrome	hematologic_disorder|immune_system_disorder	anemia	immune_system_disorder|hematologic_disorder	obstetrics_and_gynecology|hematology|pediatric	inflammatory_disease|anemia	vascular_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0019806	primary progressive aphasia	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0019807	mesocardia	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|cardiothoracic	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0019808	aortic valve atresia	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|pediatric|cardiothoracic	cardiovascular_disorder|neonatal_disease	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0019809	congenital aortic valve insufficiency	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|pediatric|cardiothoracic	cardiovascular_disorder|congenital_anomaly	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0019810	toxic epidermal necrolysis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	liver_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0019811	tricuspid valve agenesis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|hematology|cardiothoracic|cardiology|genetics_and_genomics	cardiovascular_disorder|congenital_abnormality	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019813	congenital tricuspid stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|pediatric	congenital_heart_defect|cardiovascular_disorder	heart_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0019814	straddling or overriding tricuspid valve	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology	heart_condition|cardiovascular_disorder|inflammatory_disease	heart_disorder|cardiovascular_disorder|vessel_disorder	false	false	false	true	high
MONDO:0019815	accessory tricuspid valve tissue	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology	accessory_valve_abnormality|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0019817	congenital mitral valve insufficiency and/or stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|pediatric	congenital_heart_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019818	cleft mitral valve	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology	cardiovascular_disorder|inflammatory_disease	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019819	double-orifice mitral valve	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019820	univentricular cardiopathy	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|pediatric	univentricular_cardiopathy|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019821	aneurysm or dilatation of ascending aorta	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|cardiovascular	cardiovascular_disorder|inflammatory_disease	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019823	premature closure of the arterial duct	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|pediatric	congenital_heart_disease|birth_defect|neonatal_condition|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0019824	non-acquired pituitary hormone deficiency	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	neurology|endocrinology	autoimmune_diseases|adrenal_gland_disease|neurodegenerative_disease|inflammatory_disease	brain_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0019825	congenital coronary artery aneurysm	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|genetics_and_genomics|pediatric	cardiovascular_disorder|congenital_anomaly	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019828	pituitary stalk interruption syndrome	endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder	neurology|endocrinology	autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0019829	congenital anomaly of superior vena cava	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	hematology|pulmonology|cardiothoracic|cardiology|genetics_and_genomics|pediatric	cardiovascular_disorder|congenital_anomaly	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0019830	congenital anomaly of the inferior vena cava	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|cardiology|hepatology|pediatric	cardiovascular_disorder|congenital_anomaly	vascular_disorder|liver_disorder	false	false	false	false	medium
MONDO:0019832	acquired pituitary hormone deficiency	nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder	neurology|endocrinology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0019835	primary hypophysitis	nervous_system_disorder|immune_system_disorder|inflammatory_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|autoimmune_disease	reproductive_system_disorder|endocrine_system_disorder|inflammatory_disease|immune_system_disorder|nervous_system_disorder	endocrinology|pediatric	endocrine_disorder|autoimmune_diseases	endocrine_disorder|pituitary_disorder	false	false	false	false	high
MONDO:0019836	congenital anomaly of hepatic vein	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|hepatology	congenital_anomaly|cardiovascular_disorder	liver_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019838	adenohypophysitis	nervous_system_disorder|immune_system_disorder|inflammatory_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|autoimmune_disease	reproductive_system_disorder|endocrine_system_disorder|inflammatory_disease|immune_system_disorder|nervous_system_disorder	endocrinology|pediatric	autoimmune_diseases|endocrine_disorders	endocrine_disorder|pituitary_disorder	false	false	false	false	medium
MONDO:0019839	panhypophysitis	nervous_system_disorder|immune_system_disorder|inflammatory_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|autoimmune_disease	reproductive_system_disorder|endocrine_system_disorder|inflammatory_disease|immune_system_disorder|nervous_system_disorder	endocrinology|rheumatology	autoimmune_diseases|adrenal_gland_disease|inflammatory_disease	endocrine_disorder|pituitary_disorder	false	false	false	false	high
MONDO:0019840	acropectororenal dysplasia	breast_disorder	other	breast_disorder	renal_medicine|urology|genetics_and_genomics|pediatric	metabolic_disorder|adrenal_gland_disease	joint_disorder|kidney_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0019845	iatrogenic or traumatic pituitary deficiency	nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	neurology|endocrinology	iatrogenic_or_traumatic_pituitary_deficiency_does_not_fit_well_in_the_other_categories|neurodegenerative_disease	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0019846	acquired central diabetes insipidus	nervous_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|nervous_system_disorder	renal_medicine|neurology|endocrinology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0019848	posterior hypospadias	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	reproductive_system_disorder|disorder_of_development_or_morphogenesis	urology|pediatric	urological_disorder|congenital_condition|genital_anomaly	spinal_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0019849	isolated micropenis	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	reproductive_system_disorder|disorder_of_development_or_morphogenesis	urology|pediatric	autoimmune_diseases|metabolic_disorder	reproductive_system_disorder	false	false	false	true	low
MONDO:0019851	acquired primary ovarian failure	reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	endocrinology|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0019852	inherited primary ovarian failure	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0019854	thyroid ectopia	metabolic_disease|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder|metabolic_disease	metabolic_disease|endocrine_system_disorder|hereditary_disease	endocrinology|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	endocrine_disorder	false	false	false	false	high
MONDO:0019855	athyreosis	metabolic_disease|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder|metabolic_disease	metabolic_disease|endocrine_system_disorder|hereditary_disease	cardiothoracic|endocrinology|renal_medicine	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	endocrine_disorder	false	false	false	false	high
MONDO:0019857	congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|obstetrics_and_gynecology|pediatric	autoimmune_diseases|metabolic_disorder|congenital_hypothyroidism	congenital|immune_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0019858	idiopathic congenital hypothyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|idiopathic_disease	endocrinology|genetics_and_genomics|pediatric	congenital_disorder|metabolic_disorder	congenital_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0019860	thyroid hemiagenesis	metabolic_disease|endocrine_system_disorder|hereditary_disease	metabolic_disease|endocrine_system_disorder	metabolic_disease|hereditary_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology|pediatric	autoimmune_diseases|metabolic_disorder	endocrine_disorder|vascular_disorder	false	false	false	false	low
MONDO:0019861	thyroid hypoplasia	metabolic_disease|endocrine_system_disorder|hereditary_disease	metabolic_disease|endocrine_system_disorder	metabolic_disease|hereditary_disease|endocrine_system_disorder	endocrinology|pediatric	autoimmune_diseases|metabolic_disorder	thyroid_hypoplasia_is_more_closely_related_to_a_disorder_of_the_thyroid_gland_itself_which_could_be_classified_as_an__abnormality__but_in_the_context_provided_we_will_categorize_it_under_endocrine_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0019862	levocardia	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease|syndromic_disease	cardiovascular_disorder	syndromic_disease|hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|neurology	cardiovascular_disorder	brain_disorder|heart_disorder	false	false	false	false	medium
MONDO:0019864	tetrasomy 21	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|cardiovascular_disorder	kidney_disorder|immune_disorder|brain_disorder|upper_gastrointestinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0019865	mosaic trisomy 4	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|obstetrics_and_gynecology|pediatric	cancer|metabolic_disorder	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0019866	mosaic trisomy 5	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|obstetrics_and_gynecology|pediatric	cancer|neurodegenerative_disease	muscle_disorder	false	false	false	false	high
MONDO:0019867	mosaic trisomy 8	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	cancer|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0019868	mosaic trisomy 10	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|medical_genetics|pediatric	cancer|metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0019869	mosaic trisomy 22	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|obstetrics_and_gynecology|pediatric	metabolic_disorder|neurodegenerative_disease	immune_disorder|brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0019870	distal trisomy 1p36	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0019871	distal trisomy 2p	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0019872	distal trisomy 3p	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0019873	4p16.3 microduplication syndrome	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder|inflammatory_disease	kidney_disorder|eye_disorder|brain_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0019874	distal trisomy 7p	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	bone_disorder|upper_gastrointestinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0019875	Beckwith-Wiedemann syndrome due to 11p15 microduplication	chromosomal_disorder|disorder_of_development_or_morphogenesis|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cardiovascular_disorder|cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder|chromosomal_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|oncology	cancer|metabolic_disorder	kidney_disorder|eye_disorder|bone_disorder|reproductive_system_disorder|muscle_disorder	false	false	false	false	high
MONDO:0019876	8p inverted duplication/deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	genetic_disorder|developmental_disorder	kidney_disorder|immune_disorder|bone_disorder|vascular_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0019877	distal trisomy 2q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	spinal_disorder|birth_disorder	false	false	false	false	medium
MONDO:0019878	3q26 microduplication syndrome	chromosomal_disorder	other	chromosomal_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|anemia|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0019879	distal trisomy 4q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	mental_health_disorder___corrected_to_match_the_provided_format__neurodegenerative_disease|neurodegenerative_disease|intellectual_disability|mental_health_disorder|developmental_disorder	spinal_disorder	false	false	false	false	high
MONDO:0019880	distal trisomy 5q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|oncology	metabolic_disorder|neurodegenerative_disease	bone_disorder|upper_gastrointestinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0019881	distal trisomy 6q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	skeletal_disorder|developmental_disorder|joint_disorder	false	false	false	false	high
MONDO:0019882	distal trisomy 8q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	skeletal_disorder|genetic_disorder|developmental_disorder|limb_disorder|joint_disorder	false	false	false	false	high
MONDO:0019883	distal trisomy 9q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	genetic_disorder|neurodegenerative_disease|developmental_disorder	spinal_disorder|bone_disorder|lymphatic_disorder|joint_disorder	false	false	false	false	high
MONDO:0019884	distal trisomy 10q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|obstetrics_and_gynecology|pediatric	metabolic_disorder|neurodegenerative_disease	skeletal_disorder|joint_disorder	false	false	false	false	high
MONDO:0019885	distal trisomy 11q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|upper_gastrointestinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0019886	distal trisomy 13q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|anemia|neurodegenerative_disease	ear_disorder|eye_disorder|brain_disorder|spinal_disorder|bone_disorder|upper_gastrointestinal_disorder|joint_disorder|muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0019887	distal trisomy 16q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	immune_disorder|kidney_disorder|brain_disorder|spinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0019888	distal trisomy 20q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0019889	distal trisomy 22q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder|spinal_disorder|joint_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0019890	non-distal trisomy 9q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	kidney_disorder|bone_disorder	false	false	false	false	high
MONDO:0019891	monosomy 22	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder|anemia|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0019892	distal monosomy 7p	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|developmental_disorder	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0019893	distal monosomy 19p13.3	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatrics	metabolic_disorder|anemia|neurodegenerative_disease	brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0019895	distal monosomy 4q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|medical_genetics|pediatric	metabolic_disorder|neurodegenerative_disease	kidney_disorder|upper_gastrointestinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0019896	Kleefstra syndrome due to 9q34 microdeletion	disorder_of_development_or_morphogenesis|chromosomal_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|chromosomal_disorder	genetics_and_genomics|pediatric|neurology	developmental_disorder|neurodegenerative_disease	eye_disorder|brain_disorder|spinal_disorder|lymphatic_disorder|muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0019897	distal monosomy 12q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|oncology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	musculoskeletal_disorder_is_not_available_in_the_original_list_but_could_be_inferred_as_joint_disorder___bone_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0019898	distal monosomy 14q	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	immune_disorder|skin_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0019900	non-distal monosomy 12q	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics	genetic_disorder|neurodegenerative_disease|developmental_disorder	musculoskeletal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0019901	non-distal monosomy 20q	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spine_disorder|blood_bone_marrow_disorder|lung_disorder|muscle_disorder|immune_disorder|joint_disorder	false	false	false	false	medium
MONDO:0019902	monosomy 13q34	syndromic_disease|chromosomal_disorder	other	syndromic_disease|chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	lymphatic_disorder|bone_disorder|immune_disorder|joint_disorder	false	false	false	false	high
MONDO:0019903	ring chromosome 2	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|oncology	neurodegenerative_disease|autoimmune_diseases|cancer	chromosome_abnormality|immune_disorder	false	true	false	false	high
MONDO:0019904	ring chromosome 3	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|oncology	neurodegenerative_disease|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0019905	ring chromosome 9	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|oncology	neurodegenerative_disease|cancer	kidney_disorder|blood_bone_marrow_disorder|bone_disorder	false	true	false	false	high
MONDO:0019906	ring chromosome 11	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|oncology	inflammatory_disease|autoimmune_diseases|cancer	blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0019907	ring chromosome 13	syndromic_disease|chromosomal_disorder	other	syndromic_disease|chromosomal_disorder	genetics_and_genomics|oncology	neurodegenerative_disease|cancer	genetic_disorder|chromosomal_abnormality|spinal_disorder|spinal_disorder___corrected_list__genetic_disorder|bone_disorder	false	true	false	true	very_high
MONDO:0019908	ring chromosome 15	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|oncology	neurodegenerative_disease|cancer	genetic_disorder|kidney_disorder|chromosomal_disorder	false	true	false	false	high
MONDO:0019909	ring chromosome 16	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|oncology	neurodegenerative_disease|cancer	spinal_disorder|bone_disorder	false	true	false	false	high
MONDO:0019910	maternal uniparental disomy of chromosome 2	chromosomal_disorder	other	chromosomal_disorder	obstetrics_and_gynecology|genetics_and_genomics	genetic_disorder|metabolic_disorder	reproductive_system_disorder	false	false	false	false	low
MONDO:0019911	maternal uniparental disomy of chromosome 4	chromosomal_disorder	other	chromosomal_disorder	obstetrics_and_gynecology|genetics_and_genomics	genetic_disorder|metabolic_disorder	reproductive_system_disorder	false	false	false	false	low
MONDO:0019912	maternal uniparental disomy of chromosome 6	chromosomal_disorder	other	chromosomal_disorder	obstetrics_and_gynecology|genetics_and_genomics	cancer|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0019913	silver-Russell syndrome due to maternal uniparental disomy of chromosome 7	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|chromosomal_disorder	other	syndromic_disease|chromosomal_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	endocrinology|pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	endocrine_disorder|growth_disorder	false	false	false	false	high
MONDO:0019914	maternal uniparental disomy of chromosome 9	chromosomal_disorder	other	chromosomal_disorder	obstetrics_and_gynecology|pediatric|genetics_and_genomics	cancer|metabolic_disorder	reproductive_system_disorder	false	false	false	false	low
MONDO:0019915	maternal uniparental disomy of chromosome 14	syndromic_disease|chromosomal_disorder	other	syndromic_disease|chromosomal_disorder	obstetrics_and_gynecology|pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	genetic_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0019916	maternal uniparental disomy of chromosome 16	chromosomal_disorder	other	chromosomal_disorder	obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder|maternal_disorder	false	false	false	false	low
MONDO:0019917	maternal uniparental disomy of chromosome 20	chromosomal_disorder	other	chromosomal_disorder	obstetrics_and_gynecology|pediatric|genetics_and_genomics	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	reproductive_system_disorder	false	false	false	false	medium
MONDO:0019918	maternal uniparental disomy of chromosome 21	chromosomal_disorder	other	chromosomal_disorder	obstetrics_and_gynecology|pediatric|genetics_and_genomics	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	developmental_disorder|brain_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0019919	maternal uniparental disomy of chromosome 22	chromosomal_disorder	other	chromosomal_disorder	obstetrics_and_gynecology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder	false	false	false	false	medium
MONDO:0019920	paternal uniparental disomy of chromosome 5	chromosomal_disorder	other	chromosomal_disorder	obstetrics_and_gynecology|pediatric|genetics_and_genomics	cancer|inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	reproductive_system_disorder	false	false	false	false	low
MONDO:0019921	paternal uniparental disomy of chromosome 6	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|oncology	cancer|metabolic_disorder	immune_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0019922	paternal uniparental disomy of chromosome 7	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|oncology|neurology	genetic_disorder|metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder	false	false	false	false	low
MONDO:0019923	Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|chromosomal_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|chromosomal_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|oncology	cancer|metabolic_disorder	kidney_disorder	false	false	false	false	medium
MONDO:0019924	paternal uniparental disomy of chromosome 20	chromosomal_disorder	other	chromosomal_disorder	obstetrics_and_gynecology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder	false	false	false	false	medium
MONDO:0019925	paternal uniparental disomy of chromosome 21	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|cardiovascular_disorder|neurodegenerative_disease	developmental_disorder|brain_disorder|reproductive_system_disorder	false	false	false	false	none
MONDO:0019926	X small rings	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|chromosomal_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|chromosomal_disorder|hereditary_disease	pediatrics|dermatology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	kidney_disorder|lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0019927	growth hormone-producing pituitary gland neoplasm	reproductive_system_disorder|endocrine_system_disorder|musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|connective_tissue_disorder|reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder|musculoskeletal_system_disorder	endocrinology|oncology|neurology	cancer|pituitary_gland_neoplasm|adrenal_gland_disease	endocrine_disorder|brain_disorder	false	true	false	true	high
MONDO:0019928	48,XXXY syndrome	disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder|syndromic_disease|chromosomal_disorder	endocrine_system_disorder	syndromic_disease|reproductive_system_disorder|endocrine_system_disorder|chromosomal_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	metabolic_disorder|mental_health_disorder	genetic_disorder_is_implied_but_not_listed_so_i_ll_leave_that_out|reproductive_system_disorder	false	false	false	false	high
MONDO:0019929	49,XXXXY syndrome	disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder|syndromic_disease|chromosomal_disorder	endocrine_system_disorder	syndromic_disease|reproductive_system_disorder|endocrine_system_disorder|chromosomal_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|genetic_condition|developmental_disorder	reproductive_system_disorder|bone_disorder	false	false	false	false	high
MONDO:0019930	Leydig cell hypoplasia due to complete LH resistance	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics	metabolic_disorder|endocrine_system_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0019931	Leydig cell hypoplasia due to partial LH resistance	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	endocrinology|urology|genetics_and_genomics	endocrine_disorder|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0019932	isolated partial vaginal agenesis	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	reproductive_system_disorder|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|genetics_and_genomics	inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0019933	acromegaly	reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder	endocrinology|neurology	endocrine_disorder|metabolic_disorder	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0019934	polyploidy	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics	cancer|metabolic_disorder	vascular_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0019935	isochromosome Y	chromosomal_disorder	other	chromosomal_disorder	hematology|genetics_and_genomics|oncology	cancer|chromosomal_abnormality	lymphatic_disorder|blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019938	anorectal malformation	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	general_surgery|gastroenterology|urology|pediatric	metabolic_disorder|anorectal_malformation	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0019939	early-onset schizophrenia	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	pediatric|psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|mental_health_disorder	false	false	false	true	very_high
MONDO:0019940	hypertrichosis-acromegaloid facial appearance syndrome	disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder	endocrinology|dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	endocrine_disorder|skin_disorder	false	false	false	false	medium
MONDO:0019941	hereditary sensory and autonomic neuropathy type 2	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0019942	distal arthrogryposis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	rheumatology|orthopaedic|genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0019943	hereditary continuous muscle fiber activity	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0019944	Eisenmenger syndrome	cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder	genetics_and_genomics|pulmonology|cardiology|pediatrics	cardiovascular_disorder	liver_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0019945	solar urticaria	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|allergy	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0019947	rippling muscle disease 2	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	muscle_disorder|lipid_storage_disease	false	false	false	true	high
MONDO:0019948	reducing body myopathy	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0019949	zebra body myopathy	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	myopathy|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0019950	congenital muscular dystrophy	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|orthopaedic|neurology	neurodegenerative_disease|metabolic_disorder|muscular_dystrophy_is_not_in_the_list_so_it_will_be_replaced_with__muscle_dysfunction_which_also_isn_t_so_its_just_left_out	joint_disorder|muscle_disorder|spinal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0019951	rigid spine syndrome	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	rheumatology|orthopaedic|neurology	neurodegenerative_disease|inflammatory_disease	muscle_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0019952	congenital myopathy	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0019953	mega-cisterna magna	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	psychiatry|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	low
MONDO:0019954	pancreatic neuroendocrine tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|pancreatic_cancer|endocrine_disorder	upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0019955	GRFoma	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	pediatric|oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0019956	encephalitis	inflammatory_disease|nervous_system_disorder	other	inflammatory_disease|acute_disease|nervous_system_disorder	pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	true	false	false	true	high
MONDO:0019957	PPoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|genetics_and_genomics|gastroenterology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	joint_disorder|muscle_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0019959	glucagonoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	cancer|metabolic_disorder|endocrine_disorder	upper_gastrointestinal_disorder|endocrine_disorder	false	true	true	true	high
MONDO:0019960	VIPoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrinology|neurology	adrenal_gland_disease|metabolic_disorder	upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0019962	thyroid lymphoma	cancer_or_benign_tumor|hematologic_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|endocrine_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0019963	bronchial endocrine tumor	respiratory_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology	cancer|adrenal_gland_disease	endocrine_disorder|lung_disorder	false	true	false	true	medium
MONDO:0019964	thymic neuroendocrine tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	pediatric|oncology|endocrinology	cancer|thyroid_disease|neuroendocrine_tumor|endocrine_disorder	endocrine_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0019967	Kienbock disease	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	metabolic_disorder|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0019969	panner disease	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0019970	Sinding-Larsen-Johansson disease	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	true	medium
MONDO:0019971	melanoma of soft tissue	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|dermatology	cancer|skin_cancer|soft_tissue_cancer	skin_disorder|muscledisorder	false	true	false	false	high
MONDO:0019972	dural sinus malformation	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	neurosurgery|pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	brain_disorder|spinal_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019973	persistent placoid maculopathy	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0019975	pellagra	integumentary_system_disorder|nutritional_disorder	other	nutritional_disorder|integumentary_system_disorder	nutrition___note__pellagra_is_a_disease_caused_by_a_lack_of_vitamin_b3__niacin__in_the_diet|dermatology	metabolic_disorder|anemia	lower_gastrointestinal_disorder|skin_disorder|liver_disorder	false	false	false	true	high
MONDO:0019976	dementia pugilistica	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0019977	parkinsonism with dementia of Guadeloupe	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	dementia|brain_disorder	true	false	false	false	high
MONDO:0019978	Robinow syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	developmental_disorder|neurodegenerative_disease|skeletal_dysplasia|chromosomal_abnormality|genetic_disorder	blood_bone_marrow_disorder|joint_disorder|skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0019979	renal hypoplasia, unilateral	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	urinary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|renal_medicine|urology	congenital_abnormality|kidney_disease|metabolic_disorder|developmental_anomaly	kidney_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0019980	renal hypoplasia, bilateral	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	urinary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|renal_medicine|urology	renal_hyplasia_bilateral|autoimmune_diseases|metabolic_disorder|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0019981	unilateral multicystic dysplastic kidney	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	urinary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|urology	congenital_abnormality|renal_condition|developmental_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0019982	bilateral multicystic dysplastic kidney	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	urinary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|renal_medicine|urology	metabolic_disorder|renal_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0019983	multiloculated renal cyst	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	renal_medicine|urology	cancer|urological_disorder|renal_cyst	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0019984	renal tubular dysgenesis due to twin-twin transfusion	urinary_system_disorder	other	urinary_system_disorder	pediatric|renal_medicine|genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|anemia|renal_gland_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0019985	drug-related renal tubular dysgenesis	urinary_system_disorder	other	urinary_system_disorder	pediatric|renal_medicine|genetics_and_genomics	kidney_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0019986	sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy	urinary_system_disorder|syndromic_disease	other	syndromic_disease|urinary_system_disorder|idiopathic_disease	pediatric|renal_medicine|nephrology_is_not_in_list_so__pediatric	collapsing_glomerulopathy|autoimmune_diseases|nephrotic_syndrome|inflammatory_disease	immune_disorder|kidney_disorder|vascular_disorder	false	false	false	true	high
MONDO:0019988	pauci-immune glomerulonephritis with ANCA	inflammatory_disease|urinary_system_disorder	other	urinary_system_disorder|inflammatory_disease	renal_medicine|immunology	autoimmune_diseases|anemia|inflammatory_disease	immune_disorder_kidney_disorder	false	false	false	true	high
MONDO:0019989	pauci-immune glomerulonephritis without ANCA	inflammatory_disease|urinary_system_disorder	other	urinary_system_disorder|inflammatory_disease	renal_medicine|immunology	autoimmune_diseases|inflammatory_disease	immune_disorder_kidney_disorder	false	false	false	true	high
MONDO:0019990	non-amyloid fibrillary glomerulopathy	urinary_system_disorder	other	urinary_system_disorder	nephrology|renal_medicine	renal_disease|autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0019991	immunotactoid glomerulopathy	inflammatory_disease|urinary_system_disorder	other	urinary_system_disorder|inflammatory_disease	rheumatology|renal_medicine|immunology	autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0019992	pseudohypoparathyroidism	metabolic_disease|endocrine_system_disorder|urinary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease|endocrine_system_disorder	metabolic_disease|disorder_of_development_or_morphogenesis|urinary_system_disorder|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	endocrine_disorder	false	false	false	false	high
MONDO:0019993	congenital renal artery stenosis	cardiovascular_disorder|urinary_system_disorder	cardiovascular_disorder	urinary_system_disorder|cardiovascular_disorder	pediatric|renal_medicine|cardiology	congenital_disease|vascular_disorder|cardiovascular_disorder	kidney_disorder|vascular_disorder	false	false	false	false	high
MONDO:0019994	maternal uniparental disomy of chromosome 13	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|obstetrics_and_gynecology	neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder	false	false	false	false	low
MONDO:0019995	peripheral resistance to thyroid hormones	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	cardiology|endocrinology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	endocrine_disorder|vascular_disorder	false	false	false	false	high
MONDO:0020001	respiratory or thoracic malformation	respiratory_system_disorder	other	respiratory_system_disorder	other____removed_redundant_category|genetics_and_genomics|pediatric|cardiothoracic|pulmonology	birth_defect|congenital_disorder|respiratory_or_thoracic_malformation	respiratory_or_thoracic_malformation|lung_disorder	false	false	false	false	medium
MONDO:0020007	absence of the pulmonary artery	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|general_medicine|cardiothoracic|pulmonology	congenital_heart_defect|cardiovascular_disorder	vascular_disorder|lung_disorder	false	false	false	true	high
MONDO:0020010	infectious disorder of the nervous system	infectious_disease|nervous_system_disorder	infectious_disease	infectious_disease|nervous_system_disorder	infectious_disorder|neurology	inflammatory_disease|infectious_disorder_of_the_nervous_system____infectious_disorder_of_the_nervous_system|autoimmune_diseases	brain_disorder|nervous_system_disorder	true	false	false	true	high
MONDO:0020022	central nervous system malformation	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|central_nervous_system_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0020040	46,XY disorder of sex development	reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder	endocrinology|genetics_and_genomics|urology|pediatric	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0020043	autosomal recessive congenital cerebellar ataxia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0020044	autosomal recessive metabolic cerebellar ataxia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0020046	autosomal recessive degenerative and progressive cerebellar ataxia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0020047	autosomal recessive syndromic cerebellar ataxia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0020048	internal carotid agenesis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	neurology|pediatric	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0020049	autosomal anomaly	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0020058	gonosome anomaly	chromosomal_disorder	other	chromosomal_disorder	obstetrics_and_gynecology|genetics_and_genomics|pediatrics	genetic_condition|metabolic_disorder	reproductive_system_disorder|genetic_disorder	false	false	false	false	high
MONDO:0020064	pulmonary valve agenesis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic|pulmonology	cardiovascular_disorder|congenital_heart_disease	lung_disorder|heart_disorder	false	false	false	false	high
MONDO:0020065	combined dystonia	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|psychiatry	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0020066	Ehlers-Danlos syndrome	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|rheumatology|genetics_and_genomics	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|muscle_disorder|skin_disorder|joint_disorder	false	false	false	false	high
MONDO:0020067	infectious encephalitis	inflammatory_disease|nervous_system_disorder|infectious_disease	infectious_disease	nervous_system_disorder|inflammatory_disease|infectious_disease|acute_disease	neurology|infectious_diseases	inflammatory_disease|neurodegenerative_disease	immune_disorder|brain_disorder	true	false	false	true	high
MONDO:0020068	postinfectious encephalitis	inflammatory_disease|nervous_system_disorder|infectious_disease	infectious_disease	nervous_system_disorder|inflammatory_disease|infectious_disease|post_infectious_disorder|acute_disease	neurology|pediatric|psychiatry	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	immune_disorder|spinal_disorder|brain_disorder	true	false	false	false	high
MONDO:0020070	neonatal epilepsy syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0020071	infantile epilepsy syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0020072	childhood-onset epilepsy syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0020074	progressive myoclonus epilepsy	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	seizure_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0020076	myeloproliferative neoplasm	connective_tissue_disorder|cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|immune_system_disorder|hematologic_disorder	oncology|hematology	cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0020077	myelodysplastic/myeloproliferative disease	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	genetics_and_genomics|oncology|hematology	anemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0020082	dendritic cell tumor	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|immunology|hematology	cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0020083	immunodeficiency-associated lymphoproliferative disease	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|immunology|hematology|pediatrics	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder_lymphatic_disorder	true	true	false	true	high
MONDO:0020087	hereditary lipodystrophy	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	endocrinology|dermatology|genetics_and_genomics|pediatric	metabolic_disorder|hereditary_condition_is_not_in_the_list__however__it_fits_as_well___assuming_a_more_general_categorization_to_match_available_choices__metabolic_disorder|neurodegenerative_disease	muscle_disorder|skin_disorder	false	false	false	false	high
MONDO:0020088	familial partial lipodystrophy	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	endocrinology|dermatology|genetics_and_genomics	metabolic_disorder|familial_partial_lipodystrophy_is_a_rare_genetic_disorder_affecting_fat_distribution	muscle_disorder|skin_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0020089	acquired lipodystrophy	integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease	endocrinology|dermatology	metabolic_disorder|autoimmune_diseases	skin_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0020099	inherited sideroblastic anemia	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	inherited_sideroblastic_anemia|anemia	blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0020102	hereditary stomatocytosis	hematologic_disorder	anemia	hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0020108	autoimmune hemolytic anemia	hematologic_disorder|immune_system_disorder	autoimmune_disease|anemia	immune_system_disorder|hematologic_disorder	rheumatology|hematology|immunology	anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0020110	pulmonary agenesis	disorder_of_development_or_morphogenesis|respiratory_system_disorder	other	respiratory_system_disorder|disorder_of_development_or_morphogenesis	pulmonology|pediatric	respiratory_disorder|cardiovascular_disorder|developmental_disorder|congenital_disease	lung_disorder	false	false	false	false	very_high
MONDO:0020112	vitamin B12- and folate-independent constitutional megaloblastic anemia	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	hematology|pediatric|genetics_and_genomics	metabolic_disorder|anemia	upper_gastrointestinal_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0020113	primary acquired red cell aplasia	hematologic_disorder	anemia	hematologic_disorder	hematology|allergy_and_immunology	anemia|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0020115	secondary polycythemia	musculoskeletal_system_disorder|hematologic_disorder|immune_system_disorder	other	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder	pulmonology|hematology|oncology	metabolic_disorder|cancer	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0020117	alpha granule disease	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	inflammatory_disease|anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0020119	X-linked syndromic intellectual disability	hereditary_disease|nervous_system_disorder|syndromic_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder|syndromic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0020120	skeletal muscle disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	metabolic_disorder|skeletal_muscle_disorder	muscle_disorder|skeletal_muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0020121	muscular dystrophy	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	neurology|orthopaedic|genetics_and_genomics	neurodegenerative_disease|muscular_dystrophy_is_not_a_perfect_match_but_can_be_categorized_as_metabolic_disorder	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0020122	acquired idiopathic inflammatory myopathy	musculoskeletal_system_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|idiopathic_disease|inflammatory_disease	neurology|rheumatology	inflammatory_disease|autoimmune_diseases	muscle_disorder|immune_disorder	false	false	false	false	high
MONDO:0020123	metabolic myopathy	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	neurology|endocrinology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0020124	neuromuscular junction disease	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|neuromuscular_junction_disease	false	false	false	true	high
MONDO:0020127	hereditary peripheral neuropathy	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|nervous_system_disorder	false	false	false	false	medium
MONDO:0020128	motor neuron disorder	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|motor_neuron_disorder	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0020129	acquired motor neuron disease	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0020134	cystic malformation of the posterior fossa	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0020135	pontocerebellar hypoplasia	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0020143	cerebral lipidosis with dementia	hereditary_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder	hereditary_disease|metabolic_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	vascular_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0020153	cryptophthalmia	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology	metabolic_disorder|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0020159	congenital entropion	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	pediatric|otolaryngology|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0020161	congenital ectropion	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	pediatric|otolaryngology	anomaly|congenital	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0020172	palpebral epidermal tumor	disorder_of_visual_system|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|cancer_or_benign_tumor	oncology|ophthalmology|dermatology	tumor|cancer|eye_disease	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0020173	benign tumor of palpebral epidermis	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|cancer_or_benign_tumor|nervous_system_disorder	oncology|ophthalmology|dermatology	benign_tumor|cancer	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0020179	palpebral nevus	nervous_system_disorder|disorder_of_visual_system|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	pediatric|dermatology	autoimmune_diseases|neurodegenerative_disease|cancer	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0020183	neurogenic palpebral tumor	disorder_of_visual_system|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|integumentary_system_disorder|disorder_of_orbital_region	oncology|ophthalmology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0020204	conjunctival tumor	disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region	oncology|ophthalmology	cancer|inflammatory_disease|autoimmune_diseases	eye_disorder	false	true	false	true	medium
MONDO:0020212	superficial corneal dystrophy	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	medium
MONDO:0020213	stromal corneal dystrophy	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	eye_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0020214	posterior corneal dystrophy	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0020242	hereditary macular dystrophy	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0020246	inherited vitreoretinopathy	disorder_of_visual_system|hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|pediatric	neurodegenerative_disease|inherited_disease_is_not_in_the_category_list_so_using_vitreoretinopathy__is_a_more_general_term_which_fits_better_with|metabolic_disorder	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0020247	congenital vitreoretinal dysplasia	disorder_of_visual_system|hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|pediatric	neurodegenerative_disease|congenital_abnormality|eye_disease	congenital_disorder|eye_disorder	false	false	false	false	medium
MONDO:0020248	vitreoretinal degeneration	disorder_of_visual_system|hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0020249	hereditary optic neuropathy	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|hereditary	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0020250	autosomal dominant optic atrophy	disorder_of_visual_system|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0020252	essential strabismus	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	true	medium
MONDO:0020257	supranuclear oculomotor palsy	disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|disorder_of_visual_system	otolaryngology|neurology	neurodegenerative_disease|autoimmune_diseases	eye_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0020283	uveitis	disorder_of_visual_system|inflammatory_disease	other	inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	rheumatology|ophthalmology	autoimmune_diseases|inflammatory_disease	immune_disorder|eye_disorder	true	false	false	true	high
MONDO:0020289	congenital tricuspid malformation	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|pediatric|cardiothoracic	congenital_heart_defect|cardiovascular_disorder	heart_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0020290	familial atrioventricular septal defect	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	genetics_and_genomics|cardiology|pediatric	familial_cardiovascular_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0020291	hypoplastic right heart syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|syndromic_disease	cardiology|pediatric|cardiothoracic	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0020292	congenital anomaly of the great arteries	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|pediatric	congenital_anomaly|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0020295	congenital pulmonary veins anomaly	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|pulmonology|pediatric	cardiovascular_disorder|congenital_heart_anomaly|cardiovascular_disease	heart_disorder|lung_disorder|vascular_disorder	false	false	false	false	high
MONDO:0020296	congenital arteriovenous fistula	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	genetics_and_genomics|cardiology|pediatric|hematology	congenital_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0020297	Noonan syndrome and Noonan-related syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	cardiovascular_disorder|metabolic_disorder	heart_disorder|lung_disorder|vascular_disorder|joint_disorder	false	false	false	false	high
MONDO:0020298	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15	disorder_of_development_or_morphogenesis|chromosomal_disorder|hereditary_disease|nervous_system_disorder|reproductive_system_disorder|syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|chromosomal_disorder|nervous_system_disorder|syndromic_disease|reproductive_system_disorder	genetics_and_genomics|pediatric|endocrinology	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0020300	autosomal dominant nocturnal frontal lobe epilepsy	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0020301	Prader-Willi syndrome due to paternal 15q11q13 deletion	syndromic_disease|endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|reproductive_system_disorder|chromosomal_disorder	endocrine_system_disorder	syndromic_disease|reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|chromosomal_disorder|nervous_system_disorder	endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0020302	Angelman syndrome due to maternal 15q11q13 deletion	syndromic_disease|hereditary_disease|nervous_system_disorder|chromosomal_disorder	other	syndromic_disease|hereditary_disease|chromosomal_disorder|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0020303	Angelman syndrome due to paternal uniparental disomy of chromosome 15	syndromic_disease|hereditary_disease|nervous_system_disorder|chromosomal_disorder	other	syndromic_disease|hereditary_disease|chromosomal_disorder|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	muscle_disorder|immune_disorder|upper_gastrointestinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0020304	isochromosomy Yp	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|oncology|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|bone_disorder|kidney_disorder	false	false	false	false	high
MONDO:0020305	isochromosomy Yq	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatrics	cancer|neurodegenerative_disease	reproductive_system_disorder|vascular_disorder	false	false	false	false	high
MONDO:0020307	self-limited epilepsy with autonomic seizures	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|epilepsy	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0020308	childhood occipital visual epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|ophthalmology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	true	medium
MONDO:0020310	familial focal epilepsy with variable foci	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|epilepsy	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0020311	chronic myelomonocytic leukemia	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|connective_tissue_disorder	hematology|oncology	cancer|leukemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0020316	acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|connective_tissue_disorder|acute_disease	hematology|oncology	cancer|anemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0020317	acute myeloid leukemia with 11q23 abnormalities	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|connective_tissue_disorder|acute_disease	hematology|oncology	cancer|anemia	immune_disorder|lymphatic_disorder|bone_disorder|vascular_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0020320	acute myeloblastic leukemia with maturation	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	immune_system_disorder|acute_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder	hematology|oncology	blood_disorder|cancer|leukemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0020321	acute undifferentiated leukemia	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	immune_system_disorder|acute_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder	hematology|oncology	cancer|leukemia	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	false	very_high
MONDO:0020322	acute biphenotypic leukemia	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	immune_system_disorder|acute_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder	hematology|genetics_and_genomics|oncology|hematogenetics_is_likely_a_more_specific_category_but_is_not_provided|pediatric	cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0020323	primary mediastinal large B-cell lymphoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	immune_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|lymphoma	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0020324	intravascular large B-cell lymphoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	inflammatory_disease|autoimmune_diseases|cancer	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0020325	anaplastic large cell lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|lymphoma	immune_disorder_lymphatic_disorder	false	true	false	true	high
MONDO:0020326	lymphomatoid papulosis	hematologic_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|integumentary_system_disorder	hematology|dermatology|oncology	inflammatory_disease|autoimmune_diseases|cancer	skin_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	medium
MONDO:0020331	indolent systemic mastocytosis	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|hereditary_disease	cancer_or_benign_tumor	immune_system_disorder|hereditary_disease|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology|immunology	autoimmune_diseases|inflammatory_disease|cancer	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	low
MONDO:0020332	systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|hereditary_disease	cancer_or_benign_tumor	immune_system_disorder|hereditary_disease|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology|allergy_and_immunology	autoimmune_diseases|cancer|hematologic_disorder	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	high
MONDO:0020333	aggressive systemic mastocytosis	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|hereditary_disease	cancer_or_benign_tumor	immune_system_disorder|hereditary_disease|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology|allergy_and_immunology	autoimmune_diseases|cancer	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0020334	mast cell leukemia	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|hereditary_disease	cancer_or_benign_tumor	immune_system_disorder|hereditary_disease|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	autoimmune_diseases|cancer|allergic_disease	blood_bone_marrow_disorder|immune_disorder	false	true	false	false	high
MONDO:0020336	autosomal dominant Emery-Dreifuss muscular dystrophy	cardiovascular_disorder|nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|orthopaedic|genetics_and_genomics|cardiology|pediatric	cardiovascular_disorder|neurodegenerative_disease	heart_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0020337	congenital dyserythropoietic anemia type 1	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics|pediatric	anemia|metabolic_disorder	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0020338	adult pure red cell aplasia	hematologic_disorder	anemia	hematologic_disorder	hematology|oncology	autoimmune_diseases|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0020340	bilateral perisylvian polymicrogyria	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics|pediatric	inflammatory_disease|mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0020341	periventricular nodular heterotopia	syndromic_disease|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0020344	postsynaptic congenital myasthenic syndrome	syndromic_disease|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0020347	acute inflammatory demyelinating polyradiculoneuropathy	syndromic_disease|immune_system_disorder|nervous_system_disorder	autoimmune_disease	nervous_system_disorder|immune_system_disorder|acute_disease|syndromic_disease	neurology|rheumatology	inflammatory_disease|autoimmune_diseases	spinal_disorder|muscle_disorder|immune_disorder	true	false	false	true	high
MONDO:0020348	acute motor and sensory axonal neuropathy	syndromic_disease|immune_system_disorder|nervous_system_disorder	autoimmune_disease	nervous_system_disorder|immune_system_disorder|acute_disease|syndromic_disease	neurology	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0020349	acute motor axonal neuropathy	syndromic_disease|immune_system_disorder|nervous_system_disorder	autoimmune_disease	nervous_system_disorder|immune_system_disorder|acute_disease|syndromic_disease	neurology|psychiatry|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	true	false	false	false	high
MONDO:0020351	Blake pouch cyst	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	urology	inflammatory_disease|adrenal_gland_disease	urinary_tract_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0020352	multiple system atrophy, parkinsonian type	metabolic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0020353	von Hippel anomaly	disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology|genetics_and_genomics|oncology|pediatric	cancer|adrenal_gland_disease|neurodegenerative_disease	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0020354	coloboma of choroid and retina	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0020355	coloboma of eye lens	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	eye_disease|metabolic_disorder|congenital_lesion|anatomic_abnormality|developmental_disorder	eye_disorder	false	false	false	false	medium
MONDO:0020356	coloboma of iris	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease|cancer|neurodegenerative_disease	eye_disorder|spinal_disorder	false	false	false	false	low
MONDO:0020357	coloboma of eyelid	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0020359	congenital symblepharon	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|pediatric	neurodegenerative_disease|congenital_disorder	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0020360	complete cryptophthalmia	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0020361	partial cryptophthalmia	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0020362	inverse Marcus-Gunn phenomenon	syndromic_disease|disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|disorder_of_visual_system|syndromic_disease	genetics_and_genomics|cardiology|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|vascular_disorder	false	false	false	false	low
MONDO:0020363	honey-droplet corneal dystrophy	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	true	medium
MONDO:0020364	posterior polymorphous corneal dystrophy	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	low
MONDO:0020365	congenital hereditary endothelial dystrophy type I	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|pediatric	cardiovascular_disorder	kidney_disorder|vascular_disorder	false	false	false	false	low
MONDO:0020366	congenital glaucoma	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	eye_disorder|spinal_disorder	false	false	false	true	high
MONDO:0020367	juvenile open angle glaucoma	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|juvenile_open_angle_glaucoma	false	false	false	true	high
MONDO:0020368	Axenfeld anomaly	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	dermatology|genetics_and_genomics|pediatric|ophthalmology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	developmental_disorder|eye_disorder|skeletal_disorder|congenital_disorder|facial_disorder	false	false	false	false	medium
MONDO:0020369	Chandler syndrome	syndromic_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|syndromic_disease	genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	kidney_disorder|liver_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0020370	Cogan-Reese syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder|ear_disorder|skin_disorder|joint_disorder	false	false	false	false	high
MONDO:0020371	essential iris atrophy	syndromic_disease	other	syndromic_disease	genetics_and_genomics|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0020372	early-onset sutural cataract	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0020373	early-onset anterior polar cataract	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|pediatric|ophthalmology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	low
MONDO:0020374	cerulean cataract	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0020376	early-onset nuclear cataract	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|pediatric|ophthalmology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0020377	early-onset partial cataract	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	true	medium
MONDO:0020378	early-onset posterior polar cataract	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|pediatric|ophthalmology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0020379	early-onset zonular cataract	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|pediatric|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder|kidney_disorder	false	false	false	true	high
MONDO:0020380	autosomal dominant cerebellar ataxia	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0020381	patterned macular dystrophy	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	genetics_and_genomics|ophthalmology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0020382	multifocal pattern dystrophy simulating fundus flavimaculatus	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	genetics_and_genomics|ophthalmology|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0020383	fundus pulverulentus	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|neurology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|adrenal_gland_disease	eye_disorder	false	false	false	false	medium
MONDO:0020384	Niemann-Pick disease type E	immune_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|immune_system_disorder|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|brain_disorder	false	false	false	false	medium
MONDO:0020385	congenitally uncorrected transposition of the great arteries with coarctation	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|pediatric	coarctation|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0020386	double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|pediatric	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020387	double outlet right ventricle with subpulmonary ventricular septal defect	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiology|pediatric	ventricular_septal_defect|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020388	double outlet right ventricle with non-committed subpulmonary ventricular septal defect	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|pediatric	ventricular_septal_defect|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020389	pulmonary valve agenesis-ventricular septal defect-persistent ductus arteriosus syndrome	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|pediatric	congenital_heart_defect|cardiovascular_disorder	vascular_disorder|heart_disorder|lung_disorder	false	false	false	false	high
MONDO:0020390	pulmonary artery coming from patent ductus arteriosus	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|pulmonology	anemia|cardiovascular_disorder|patent_ductus_arteriosus	vascular_disorder|heart_disorder|lung_disorder	false	false	false	false	high
MONDO:0020391	pulmonary artery coming from the aorta	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|pulmonology	cardiovascular_disorder	vascular_disorder|heart_disorder|lung_disorder	false	false	false	false	high
MONDO:0020393	discrete fibromuscular subaortic stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0020394	tunnel subaortic stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020395	valvar pulmonary stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|pulmonology|pediatric	congenital_heart_defect|cardiovascular_disorder	heart_disorder|lung_disorder	false	false	false	true	medium
MONDO:0020396	anomaly of the tricuspid valve chordae	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|pulmonology	autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0020397	parachute tricuspid valve	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|pulmonology	inflammatory_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0020398	congenital mitral stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiology|pediatric	congenital_heart_disease|cardiovascular_disorder	heart_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0020399	congenital hypoplasia of the mitral valve annulus	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology|pediatric	congenital_heart_defect|structural_heart_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0020400	congenital supravalvular mitral ring	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|congenital_conditions|pediatric	congenital_heart_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020401	congenital unguarded mitral orifice	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|genetics_and_genomics|pediatric	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0020402	congenital accessory mitral valve tissue	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|genetics_and_genomics|cardiothoracic	cardiovascular_disorder|heart_disease|congenital_disease	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0020403	congenital mitral valve agenesis	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic|pediatric	congenital_abnormality|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0020404	shone complex	syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|pediatric	inflammatory_disease|cardiovascular_disorder	cardiac_disorder|heart_disorder	true	false	false	false	high
MONDO:0020405	straddling and/or overriding mitral valve	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic	heart_condition|cardiovascular_disorder|mitral_regurgitation	vascular_disorder|heart_disorder	true	false	false	true	medium
MONDO:0020406	complete atrioventricular canal-left heart obstruction syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiology|pediatric	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020407	complete atrioventricular canal-ventricle hypoplasia syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiology|genetics_and_genomics|cardiothoracic|pediatric	ventricle_hypoplasia_syndrome|cardiovascular_disorder	muscle_disorder|vascular_disorder|heart_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0020408	complete atrioventricular canal-tetralogy of fallot syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiology|genetics_and_genomics|pediatric	congenital_heart_defect|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020409	univentricular heart with single atrio-ventricular valve	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|pediatric	cardiovascular_disorder|univentricular_heart_with_single_atro_ventricular_valve	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020410	aorto-right ventricular tunnel	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic|pediatric	inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020411	aorto-left ventricular tunnel	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic	heart_condition|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020412	congenital patent ductus arteriosus aneurysm	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|pediatric	congenital_anomaly|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0020413	encircling double aortic arch	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic|pediatric	adrenal_gland_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020414	persistent fifth aortic arch	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic|pediatric	congenital_anomaly|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020415	Kommerell diverticulum	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|otolaryngology	inflammatory_disease|cardiovascular_disorder	throat_disorder|heart_disorder	false	false	false	false	medium
MONDO:0020416	Neuhauser anomaly	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|bone_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0020417	right aortic arch	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0020418	dysphagia lusoria	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0020419	pulmonary artery hypoplasia	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|pulmonology|cardiology	congenital_heart_disease|cardiovascular_disorder	lung_disorder|vascular_disorder	false	false	false	false	high
MONDO:0020420	pulmonary branch stenosis	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic|pulmonology	cardiovascular_disorder|congenital_heart_disease	lung_disorder|heart_disorder	false	false	false	false	high
MONDO:0020421	coronary artery intramyocardial course	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic	inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020422	aortopulmonary coronary arterial course	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|pulmonology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	the_term__aortopulmonary_coronary_arterial_course__typically_refers_to_a_variant_in_the_anatomical_arrangement_of_the_coronary_arteries_as_they_relate_to_the_aorta_and_pulmonary_arteries__it_is_not_a_disease_per_se_but_rather_a_description_of_blood_vessel_anatomy____if_you_are_asking_about_whether_there_are_efficacious_treatments_for_conditions_related_to_abnormalities_in_coronary_artery_anatomy_or_associated_diseases__such_as_coronary_artery_disease__cad__or_congenital_heart_defects__then_true__efficacious_treatments_do_exist___conditions_like_cad_can_be_treated_with_lifestyle_changes__medications__and_surgical_procedures__e_g___angioplasty__stent_placement__or_coronary_artery_bypass_grafting___the_specific_treatments_would_depend_on_the_particular_condition_or_disease_being_addressed____so__in_summary__if_we_are_speaking_about_diseases_associated_with_atypical_coronary_arterial_courses__the_answer_is_true__efficacious_treatments_exist	high
MONDO:0020423	stenosis or atrophy of the coronary ostium	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic	coronary_ostium_stenosis_is_related_to_adrenal_gland_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020424	intramural coronary arterial course	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic	intramural_coronary_arterial_course|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0020425	abnormal number of coronary ostia	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic	cardiovascular_disorder|abnormal_number_of_coronary_ostia	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020426	malposition of the coronary ostium	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0020427	Laubry-Pezzi syndrome	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	genetics_and_genomics|cardiothoracic|pulmonology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0020428	congenital Gerbode defect	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	genetics_and_genomics|cardiothoracic|pediatric|cardiology	congenital_heart_defect|cardiovascular_disorder	liver_disorder|heart_disorder	false	false	false	false	high
MONDO:0020429	cor triatriatum dexter	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder|cancer	vascular_disorder|heart_disorder|spinal_disorder	false	false	false	false	high
MONDO:0020430	cor triatriatum sinister	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder|other___note__cor_triatriatum_sinister_is_a_congenital_heart_defect_that_affects_the_structure_of_the_heart__specifically_involving_an_abnormal_formation_of_the_atria__which_can_lead_to_various_cardiac_complications_and_symptoms	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020431	juxtaposition of the atrial appendages	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|cardiology	inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	the_term__juxtaposition_of_the_atrial_appendages__commonly_refers_to_a_specific_anatomical_arrangement_where_the_atrial_appendages_of_the_heart__particularly_the_left_and_right_atrial_appendages__are_positioned_in_close_proximity_or_in_a_specific_alignment_relative_to_each_other__this_term_can_be_relevant_in_various_contexts__including_cardiac_imaging__congenital_heart_disease__or_procedural_interventions___if_you_are_looking_for_information_on_the_implications_of_such_juxtaposition__any_associated_conditions__or_specific_treatment_protocols__please_provide_more_details_so_i_can_assist_you_further	low
MONDO:0020432	ectasia of the right atrial appendage	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0020433	ectasia of the left appendage	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	gastroenterology|urology	cardiovascular_disorder	lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0020434	atrial septal defect, ostium secundum type	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiothoracic|pediatrics|cardiology	congenital_heart_defect|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0020435	atrial septal defect, coronary sinus type	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiothoracic|cardiology	coronary_sinus_type_is_a_subcategory_of_this_category_cardiovascular_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0020436	atrial septal defect, sinus venosus type	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiothoracic|cardiology	congenital_heart_defect|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0020437	atrial septal defect, ostium primum type	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiothoracic|pediatric|cardiology	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0020438	atrial septal aneurysm	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|cardiology	atrial_septal_aneurysm|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0020439	patent foramen ovale	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	pulmonology|cardiology	adrenal_gland_disease|inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0020440	persistent left superior vena cava connecting to the left-sided atrium	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|pediatric|pulmonology|cardiology	cardiovascular_disorder|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0020441	right superior vena cava connecting to left-sided atrium	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|hematology|pulmonology|cardiology	cardiovascular_disorder|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	the_condition_you_are_describing_is_likely_related_to_a_congenital_heart_defect_where_the_right_superior_vena_cava__svc__drains_into_the_left_atrium_instead_of_the_right_atrium__this_is_known_as_a_congenital_anomaly_and_can_lead_to_various_complications__including_cyanosis_and_difference_in_oxygenation_of_blood___in_terms_of_treatment__congenital_heart_defects_can_sometimes_be_managed_with_surgery_or_other_medical_interventions__depending_on_the_specific_nature_and_severity_of_the_defect__these_treatments_aim_to_correct_the_anomalous_connection_and_restore_normal_blood_flow___therefore__since_there_are_efficacious_treatments_available_for_certain_congenital_heart_defects__the_answer_is___true	very_high
MONDO:0020442	left superior vena cava persisting to left-sided atrium	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|pediatric|pulmonology|cardiology	congenital_heart_defect|cardiovascular_disorder|anatomical_abnormality	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0020443	absence of innominate vein	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|hematology|vascular|cardiology	cardiovascular_disorder|vascular_disease	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0020444	subaortic course of innominate vein	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|cardiology	inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	low
MONDO:0020445	agenesis of the superior vena cava	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	genetics_and_genomics|pediatric|general_category__cardiovascular|hepatology|pulmonology|cardiology	cardiovascular_disorder	vascular_disorder|liver_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0020446	coronary sinus stenosis	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|hematology|pulmonology|cardiology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0020447	coronary sinus atresia	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|cardiovascular_diseases|cardiology	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0020448	right inferior vena cava connecting to left-sided atrium	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|hematology|cardiology	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	the_condition_you_are_describing_appears_to_be_a_congenital_heart_defect_known_as__right_to_left_atrial_shunt__or__anomalous_pulmonary_venous_return___in_this_case__the_inferior_vena_cava_is_erroneously_draining_into_the_left_atrium_instead_of_the_right_atrium__which_can_lead_to_significant_clinical_consequences_such_as_cyanosis___for_congenital_heart_defects__treatment_options_can_include_surgical_correction_or_interventional_procedures_to_restore_normal_anatomy_and_improve_blood_flow__the_efficacy_of_treatments_generally_depends_on_the_specific_type_and_severity_of_the_defect__as_well_as_the_overall_health_of_the_patient___therefore__since_there_are_existing_treatment_options_that_can_address_this_type_of_congenital_heart_defect__the_answer_is___true	high
MONDO:0020449	persistent eustachian valve	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pediatric|otolaryngology	adrenal_gland_disease|inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	ear_disorder|throat_disorder	false	false	false	false	low
MONDO:0020450	azygos continuation of the inferior vena cava	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|hepatology|cardiology|cardiovascular	cardiovascular_disorder|inflammatory_disease	vascular_disorder|vessel_disorder	false	false	false	false	low
MONDO:0020451	congenital stenosis of the inferior vena cava	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|hepatology|cardiology|pediatric	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0020452	inferior vena cava interruption	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|hepatology|pulmonology|cardiothoracic	cardiovascular_disorder	liver_disorder|vascular_disorder	false	false	false	false	high
MONDO:0020453	congenital partial pulmonary venous return anomaly	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pulmonology|cardiology|cardiothoracic|pediatric	congenital_heart_defect|cardiovascular_disorder	vascular_disorder|lung_disorder|heart_disorder	false	false	false	false	medium
MONDO:0020454	congenital complete agenesis of pericardium	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|cardiothoracic|pediatric	cardiovascular_disorder|congenital_abnormality	vascular_disorder|heart_disorder	false	false	false	false	low
MONDO:0020455	congenital partial agenesis of pericardium	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatrics|genetics_and_genomics|cardiothoracic	cardiovascular_disorder|congenital_abnormality	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0020456	pleuro-pericardial cyst	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pulmonology|cardiology|cardiothoracic	cardiovascular_disorder|inflammatory_disease	thoracic_disorder|lung_disorder	false	false	false	false	low
MONDO:0020457	6-phosphogluconate dehydrogenase deficiency	hematologic_disorder	anemia	hematologic_disorder	genetics_and_genomics|hematology|pediatric	anemia|metabolic_disorder	liver_disorder|metabolic_disorder	false	false	false	true	medium
MONDO:0020458	hemolytic anemia due to erythrocyte adenosine deaminase overproduction	hereditary_disease|hematologic_disorder|metabolic_disease	metabolic_disease|anemia	metabolic_disease|hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0020459	unstable hemoglobin disease	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder|cardiovascular_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0020460	acquired von willebrand syndrome	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics	autoimmune_diseases|anemia|cardiovascular_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0020461	epiblepharon	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	dermatology|ophthalmology	autoimmune_diseases|adrenal_gland_disease|neurodegenerative_disease|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0020462	tarsal kink syndrome	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	orthopaedic|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0020463	isolated congenital ectropion	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	otolaryngology|pediatrics	adrenal_gland_disease	eye_disorder|spinal_disorder|skin_disorder	false	false	false	false	low
MONDO:0020464	euryblepharon	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	pediatrics|genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0020465	congenital eyelid retraction	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|pediatric	autoimmune_diseases|neurodegenerative_disease	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0020466	monosomy X	hereditary_disease|syndromic_disease|reproductive_system_disorder|chromosomal_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrine_system_disorder	disorder_of_development_or_morphogenesis|chromosomal_disorder|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|genetic_disease	endocrine_disorder|reproductive_system_disorder|immune_disorder	false	false	false	false	medium
MONDO:0020467	mosaic monosomy X	hereditary_disease|syndromic_disease|reproductive_system_disorder|chromosomal_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrine_system_disorder	disorder_of_development_or_morphogenesis|chromosomal_disorder|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric	autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0020468	paternal uniparental disomy of chromosome 13	chromosomal_disorder	other	chromosomal_disorder	obstetrics_and_gynecology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder	false	false	false	false	low
MONDO:0020469	48,XYYY syndrome	syndromic_disease|chromosomal_disorder	other	chromosomal_disorder|syndromic_disease	genetics_and_genomics|pediatric	genetic_disorder|metabolic_disorder	chromosome_abnormality|reproductive_system_disorder	false	false	false	false	medium
MONDO:0020470	49,XYYYY syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|genetics_and_genomics|oncology|pediatric	metabolic_disorder|genetic_condition	bone_disorder|reproductive_system_disorder|immune_disorder	false	false	false	false	high
MONDO:0020472	Turner syndrome due to structural X chromosome anomalies	reproductive_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|endocrinology|genetics_and_genomics|pediatrics	metabolic_disorder|cardiovascular_disorder	endocrine_disorder|vascular_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0020473	dappled diaphyseal dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic	inflammatory_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0020474	cheirospondyloenchondromatosis	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|rheumatology|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0020475	dermotrichic syndrome	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	hair_disorder|skin_disorder	false	false	false	false	medium
MONDO:0020476	mesial temporal lobe epilepsy with hippocampal sclerosis	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|mental_health_disorder|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0020477	progeria-associated arthropathy	connective_tissue_disorder	other	connective_tissue_disorder	genetics_and_genomics|rheumatology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0020478	Leber plus disease	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|vascular_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0020479	pituitary gigantism	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|nervous_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	connective_tissue_disorder|endocrine_system_disorder|musculoskeletal_system_disorder|reproductive_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	endocrinology|neurology	metabolic_disorder|endocrine_disorders	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0020480	sulfite oxidase deficiency due to molybdenum cofactor deficiency	disorder_of_visual_system|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	high
MONDO:0020481	myotonia fluctuans	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder	false	false	false	false	medium
MONDO:0020482	myotonia permanens	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0020483	acetazolamide-responsive myotonia	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0020485	King-Denborough syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|nervous_system_disorder|muscle_disorder	false	false	false	false	high
MONDO:0020487	Pontiac fever	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	kidney_disorder|urinary_tract_disorder	true	false	false	true	low
MONDO:0020488	atypical progressive supranuclear palsy syndrome	disorder_of_visual_system|hereditary_disease|syndromic_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|disorder_of_visual_system|syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0020490	mosaic trisomy 9	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|obstetrics_and_gynecology	metabolic_disorder|cancer	upper_gastrointestinal_disorder|spinal_disorder|muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0020491	subcortical band heterotopia	syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0020492	hemimegalencephaly	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0020493	Haddad syndrome	digestive_system_disorder	other	digestive_system_disorder	genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0020494	oculootodental syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|ophthalmology|pediatric	autoimmune_diseases|neurodegenerative_disease	teeth_disorder|eye_disorder	false	false	false	false	high
MONDO:0020495	PEHO-like syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0020496	familial porencephaly	hereditary_disease|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	familial_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0020497	Turcot syndrome with polyposis	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|gastroenterology|oncology	polyposis|cancer	upper_gastrointestinal_disorder|brain_disorder|lower_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0020499	Nipah virus disease	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|virology____corrected_response_without_extra_category___neurology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	immune_disorder|vascular_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0020500	Marburg hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	hepatology|hematology	cardiovascular_disorder|inflammatory_disease|hemorrhagic_fever	liver_disorder|vascular_disorder	true	false	false	true	very_high
MONDO:0020501	Crimean-Congo hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	hepatology|hematology|pulmonology	autoimmune_diseases|inflammatory_disease	immune_disorder|vascular_disorder	true	false	false	false	high
MONDO:0020502	yellow fever	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0020504	hereditary recurrent myoglobinuria	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|hematology|renal_medicine	metabolic_disorder|anemia	muscle_disorder|kidney_disorder	false	false	false	false	high
MONDO:0020505	ravine syndrome	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	liver_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0020507	leukoencephalopathy with vanishing white matter 1	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|hematology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0020508	primary syringomyelia	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0020509	secondary syringomyelia	nervous_system_disorder	other	nervous_system_disorder	neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0020510	idiopathic syringomyelia	nervous_system_disorder	other	idiopathic_disease|nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0020511	precursor B-cell acute lymphoblastic leukemia	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|acute_disease	oncology|hematology|pediatric|genetics_and_genomics	cancer|anemia|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0020512	precursor T-cell acute lymphoblastic leukemia	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|acute_disease	oncology|hematology|pediatric	cancer|lymphoma|leukemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	true	true	false	true	very_high
MONDO:0020513	spermatocytic seminoma	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	oncology|urology	cancer|adrenal_gland_disease	reproductive_system_disorder|blood_bone_marrow_disorder	false	true	false	false	medium
MONDO:0020516	thymic neuroendocrine carcinoma	endocrine_system_disorder|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|endocrine_system_disorder|immune_system_disorder	oncology|endocrinology|pulmonology	cancer|autoimmune_diseases|adrenal_gland_disease	immune_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0020517	eosinophilic granuloma	respiratory_system_disorder|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|respiratory_system_disorder|immune_system_disorder	allergy_and_immunology|pediatric|pulmonology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder|lung_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0020518	Hashimoto-Pritzker syndrome	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	rheumatology|endocrinology	autoimmune_diseases|inflammatory_disease	immune_disorder|thyroid_disorder_is_not_present_in_the_list_but_liver_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0020519	hand-Schuller-Christian disease	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	genetics_and_genomics|neurology|orthopaedic|dermatology|pediatric	autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	true	high
MONDO:0020520	adult pulmonary Langerhans cell histiocytosis	respiratory_system_disorder|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|respiratory_system_disorder|immune_system_disorder	allergy_and_immunology|oncology|hematology|pulmonology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder|lung_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0020521	Ehlers-Danlos syndrome type 7A	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	orthopaedic|rheumatology|genetics_and_genomics	cardiovascular_disorder|autoimmune_diseases	skin_disorder|joint_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0020523	familial parathyroid adenoma	hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|endocrine_system_disorder	genetics_and_genomics|renal_medicine|endocrinology	endocrine_disease|metabolic_disorder	endocrine_disorder	false	false	false	true	medium
MONDO:0020525	transient neonatal diabetes mellitus	digestive_system_disorder|hereditary_disease|endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease|diabetes_mellitus	hereditary_disease|metabolic_disease|endocrine_system_disorder|digestive_system_disorder	pediatric|endocrinology	autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|immune_disorder|endocrine_disorder	false	false	true	true	medium
MONDO:0020526	acute megakaryoblastic leukemia in down syndrome	connective_tissue_disorder|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder|immune_system_disorder|acute_disease|musculoskeletal_system_disorder	oncology|hematology|pediatric	cancer|anemia	blood_bone_marrow_disorder|down_syndrome_related	false	true	false	true	very_high
MONDO:0020527	ectopic Cushing syndrome	nervous_system_disorder|endocrine_system_disorder|reproductive_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder	neurology|endocrinology	metabolic_disorder|inflammatory_disease|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	very_high
MONDO:0020528	ACTH-dependent Cushing syndrome	nervous_system_disorder|endocrine_system_disorder|reproductive_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder	neurology|endocrinology	metabolic_disorder|adrenal_gland_disease	pituitary_gland_disorder|brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0020529	ACTH-independent Cushing syndrome	endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder	genetics_and_genomics|neurology|pediatrics|endocrinology	cancer|metabolic_disorder|adrenal_gland_disease	endocrine_disorder	false	false	false	true	very_high
MONDO:0020531	long chain acyl-CoA dehydrogenase deficiency	hereditary_disease|metabolic_disease|musculoskeletal_system_disorder|cardiovascular_disorder	metabolic_disease|cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|metabolic_disease|musculoskeletal_system_disorder	genetics_and_genomics|metabolism__not_listed_but_assumed|pediatric	metabolic_disorder|neurological_disease|inborn_error_of_metabolism	liver_disorder|muscle_disorder|kidney_disorder	false	false	false	true	high
MONDO:0020532	spirillary rat-bite fever	infectious_disease	infectious_disease	infectious_disease	dermatology|pediatric	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0020533	streptobacillary rat-bite fever	infectious_disease	infectious_disease	infectious_disease	dermatology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0020535	house allergic alveolitis	respiratory_system_disorder|inflammatory_disease|immune_system_disorder	other	respiratory_system_disorder|inflammatory_disease|immune_system_disorder	allergy_and_immunology|pulmonology	allergy|autoimmune_diseases|inflammatory_disease	immune_disorder|lung_disorder	false	false	false	true	medium
MONDO:0020538	malignant dysgerminomatous germ cell tumor of ovary	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|genetics_and_genomics	germ_cell_tumor|cancer|ovarian_cancer|ovarian_malignancy|adnexal_malignancy|ovarian_germ_cell_cancer|malignant_dysgerminoma|gynecologic_cancer|germ_cell_tumor_of_ovary|ovarian_dysgerminoma	ovarian_disorder|gynecological_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0020539	extragonadal non-dysgerminomatous germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|urology	germ_cell_tumor|cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	false	high
MONDO:0020540	ovarian gynandroblastoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology|genetics_and_genomics	cancer|adrenal_gland_disease	ovarian_disorder|endocrine_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0020541	maligant granulosa cell tumor of ovary	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|ovarian_cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	false	high
MONDO:0020542	malignant Sertoli-Leydig cell tumor of ovary	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	reproductive_system_cancer|cancer|malignant_tumor|ovarian_cancer|tumor	endocrine_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0020543	theca steroid-producing cell malignant tumor of ovary, not further specified	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|malignant_tumor|gynecologic_malignancy|ovarian_cancer|epithelial_malignancy|tumor|ovarian_tumor	endocrine_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0020544	streptococcal toxic-shock syndrome	infectious_disease|syndromic_disease	infectious_disease	syndromic_disease|infectious_disease	pediatric|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0020545	staphylococcal toxic-shock syndrome	infectious_disease|syndromic_disease	infectious_disease	syndromic_disease|infectious_disease	pulmonology|dermatology|pediatric	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0020546	acute graft versus host disease	immune_system_disorder	other	acute_disease|disease_related_to_transplantation|immune_system_disorder	immunology|oncology|hematology	autoimmune_diseases|inflammatory_disease	bone_bone_marrow_disorder|immune_disorder|liver_disorder	false	false	false	true	high
MONDO:0020547	chronic graft versus host disease	immune_system_disorder	other	disease_related_to_transplantation|immune_system_disorder	pulmonology|immunology|dermatology|hepatology|hematology|rheumatology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|skin_disorder|liver_disorder	false	false	false	true	high
MONDO:0020549	invasive hydatidiform mole	hereditary_disease|cancer_or_benign_tumor|obstetric_disorder|reproductive_system_disorder	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|reproductive_system_disorder|obstetric_disorder	oncology|obstetrics_and_gynecology	cancer	lower_gastrointestinal_disorder|vascular_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0020550	gestational choriocarcinoma	cancer_or_benign_tumor|obstetric_disorder|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|obstetric_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	true	high
MONDO:0020552	placental site trophoblastic tumor	cancer_or_benign_tumor|obstetric_disorder|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|obstetric_disorder	oncology|obstetrics_and_gynecology	autoimmune_diseases|cancer|inflammatory_disease|adrenal_gland_disease	gynecological_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0020553	secondary pulmonary hemosiderosis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|hematology	anemia|cancer	immune_disorder|lung_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0020554	Heiner syndrome	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0020555	pleuropulmonary blastoma type 1	syndromic_disease|hereditary_disease|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease|respiratory_system_disorder	pulmonology|oncology|pediatric	cancer|tumor_cancer	lung_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0020556	pleuropulmonary blastoma type 2	syndromic_disease|hereditary_disease|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease|respiratory_system_disorder	pulmonology|oncology|pediatric	cancer|other____note__pleuropulmonary_blastoma_type_2_is_a_rare_genetic_disorder_that_often_involves_the_adrenal_glands__making_it_related_to_both_cancer_and_adrenal_gland_disease_categories__the_categorization_might_not_fit_perfectly_in_any_single_category__which_could_explain_the_inclusion_of__other|adrenal_gland_disease	lung_disorder	false	true	false	false	very_high
MONDO:0020557	pleuropulmonary blastoma type 3	syndromic_disease|hereditary_disease|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease|respiratory_system_disorder	oncology|pediatric	rare_disease|cancer|pediatric_cancer	bone_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0020558	autosomal dominant Charcot-Marie-Tooth disease type 2K	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|orthopaedic|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	nerve_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0020559	O'Sullivan-McLeod syndrome	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0020560	atypical teratoid rhabdoid tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology|pediatric|genetics_and_genomics	cancer|pediatric_cancer|neurooncology|brain_tumor	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0020561	myxoid/round cell liposarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	oncology|hematology|genetics_and_genomics	cancer	skin_disorder|muscle_disorder	false	true	false	true	high
MONDO:0020562	pleomorphic liposarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	oncology|genetics_and_genomics	cancer	bone_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0020563	dedifferentiated liposarcoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	oncology|dermatology	cancer|neurodegenerative_disease|adrenal_gland_disease	bone_disorder|muscle_disorder	false	true	false	false	high
MONDO:0020567	apnea of prematurity	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	metabolic_disorder|respiratory_disease_is_not_in_the_list__inflammatory_disease	respiratory_disorder|lung_disorder	false	false	false	true	high
MONDO:0020568	cutaneous myiasis	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology	inflammatory_disease|skin_disease	skin_disorder|nose_disorder	true	false	false	true	low
MONDO:0020569	intermediate DEND syndrome	digestive_system_disorder|hereditary_disease|endocrine_system_disorder|metabolic_disease	metabolic_disease|diabetes_mellitus|endocrine_system_disorder	hereditary_disease|digestive_system_disorder|metabolic_disease|endocrine_system_disorder	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|liver_disorder	true	false	false	true	medium
MONDO:0020571	relapsing epidemic typhus	infectious_disease	infectious_disease	infectious_disease	pediatric|infectious_disease_is_implied_by__epidemic__but_that_is_not_a_category_in_the_list	autoimmune_diseases|inflammatory_disease	immune_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0020572	complex regional pain syndrome type 2	syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder	neurology|orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	muscle_disorder|joint_disorder|vascular_disorder|spinal_disorder	false	false	false	false	high
MONDO:0020574	central nervous system nongerminomatous germ cell tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|central_nervous_system_disease	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0020575	polymorphic ventricular tachycardia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic	autoimmune_diseases|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0020576	cutaneous vasculitis	cardiovascular_disorder|inflammatory_disease|integumentary_system_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease|integumentary_system_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0020577	childhood gonadal germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric	germ_cell_tumor|cancer|childhood_disease	reproductive_system_disorder	false	true	false	true	medium
MONDO:0020579	mucositis	inflammatory_disease	other	inflammatory_disease	pulmonology|gastroenterology|otolaryngology	autoimmune_diseases|inflammatory_disease	immune_disorder|throat_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0020580	germinomatous germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	germ_cell_tumor|cancer	reproductive_system_disorder|spinal_disorder	false	true	false	true	high
MONDO:0020581	benign PEComa	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cardiothoracic|pulmonary	adrenal_gland_disease|cancer|inflammatory_disease	liver_disorder|kidney_disorder	false	false	false	false	low
MONDO:0020582	benign uterine ligament neoplasm	musculoskeletal_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|musculoskeletal_system_disorder	oncology|obstetrics_and_gynecology	neoplasm|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0020583	chromosome 17 disorder	chromosomal_disorder	other	chromosomal_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|chromosome_abnormality_disorder____corrected_to__neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0020584	anemia due to enzyme disorder	hematologic_disorder	anemia	hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|enzyme_disorder_is_a_subset_of_endocrine_disorder	false	false	false	true	medium
MONDO:0020585	anemia due to erythrocyte enzyme disorder	hematologic_disorder	anemia	hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|erythrocyte_enzyme_disorder	false	false	false	true	medium
MONDO:0020586	factor V deficiency	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0020587	factor XI deficiency	hematologic_disorder	other	hematologic_disorder	pediatric|hematology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0020588	lung PEComa	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|cardiothoracic	autoimmune_diseases|cancer|inflammatory_disease	lung_disorder|lower_respiratory_lung_disease	false	true	false	false	high
MONDO:0020589	cardiac germ cell tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiology|pediatric|oncology	cardiovascular_disorder|cancer	reproductive_system_disorder|heart_disorder	false	true	false	true	high
MONDO:0020590	mycobacterial infectious disease	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|lung_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0020592	disorder of pharynx	respiratory_system_disorder|otorhinolaryngologic_disease	other	respiratory_system_disorder|otorhinolaryngologic_disease	pulmonology|otolaryngology	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|thorat_disorder	false	false	false	true	medium
MONDO:0020593	trichoblastoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	pediatric|oncology|dermatology	neoplasm|tumor|cancer	skin_disorder|eye_disorder	false	true	false	false	low
MONDO:0020594	abducens nerve disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0020596	mucin-producing carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonology|oncology|gastroenterology	adrenal_gland_disease|autoimmune_diseases|cancer	lower_gastrointestinal_disorder|lung_disorder	false	true	false	false	high
MONDO:0020597	angiokeratoma of scrotum	reproductive_system_disorder|integumentary_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|cardiovascular_disorder|integumentary_system_disorder	urology|dermatology	adrenal_gland_disease|cancer|inflammatory_disease	reproductive_system_disorder|skin_disorder	false	false	false	false	low
MONDO:0020598	malabsorption syndrome	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0020599	acquired coagulation factor deficiency	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease|cardiovascular_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	high
MONDO:0020600	acute pharyngitis	respiratory_system_disorder|inflammatory_disease	other	inflammatory_disease|respiratory_system_disorder|acute_disease	otolaryngology|pediatric	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|throat_disorder	true	false	false	true	low
MONDO:0020601	mosquito-borne viral encephalitis	infectious_disease|nervous_system_disorder|inflammatory_disease	infectious_disease	nervous_system_disorder|infectious_disease|inflammatory_disease|acute_disease	pediatric|neurology	inflammatory_disease|neurodegenerative_disease	lymphatic_disorder|brain_disorder|immune_disorder	true	false	false	true	high
MONDO:0020602	Simpson-Golabi-Behmel syndrome type 1	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|hematology|pediatric	metabolic_disorder|anemia	kidney_disorder|liver_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0020603	X-linked chondrodysplasia punctata 2	disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder|hereditary_disease|integumentary_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|integumentary_system_disorder	orthopaedic|genetics_and_genomics|dermatology|pediatrics	metabolic_disorder|neurodegenerative_disease	skin_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0020604	X-linked dominant disease	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|joint_disorder	false	false	false	true	high
MONDO:0020605	X-linked recessive disease	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0020606	sex-linked disease	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases	sex_linked_disease_can_be_categorized_under_this_as_it_is_a_disorder_linked_to_the_reproductive_system_of_individuals_with_an_x_chromosome|reproductive_system_disorder	false	false	false	true	high
MONDO:0020607	Liddle syndrome 1	syndromic_disease|urinary_system_disorder|hereditary_disease	other	syndromic_disease|hereditary_disease|urinary_system_disorder	genetics_and_genomics|renal_medicine	metabolic_disorder|autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder	false	false	false	true	medium
MONDO:0020628	microcephaly, growth restriction, and increased sister chromatid exchange 2	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	growth_restriction|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0020629	microcephaly, growth restriction and increased sister chromatid exchange	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	growth_disorder|brain_disorder|skeletal_disorder	true	false	false	false	high
MONDO:0020630	developmental and epileptic encephalopathy 91	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	epileptic_disorder|neurodegenerative_disease|developmental_disorder	epileptic_disorder|brain_disorder|developmental_disorder	false	false	false	true	high
MONDO:0020631	developmental and epileptic encephalopathy 92	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|developmental_disorder	epileptic_disorder|brain_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0020632	developmental and epileptic encephalopathy 93	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	epilepsy|neurodegenerative_disease|developmental_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0020633	anaplastic cancer	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|genetics_and_genomics|oncology	cancer|adrenal_gland_disease	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0020634	grade III meningioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neurological_cancer	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0020635	anaplastic meningioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0020638	superficial spreading melanoma	disorder_of_development_or_morphogenesis|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	melanoma|skin_cancer|cancer	lymphatic_disorder|immune_disorder|skin_disorder	false	true	false	true	high
MONDO:0020639	monosomy	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|anemia	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0020640	autoimmune encephalitis	nervous_system_disorder|inflammatory_disease|immune_system_disorder	autoimmune_disease	immune_system_disorder|inflammatory_disease|nervous_system_disorder|acute_disease	neurology|immunology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|immune_disorder	false	false	false	true	high
MONDO:0020641	respiratory tract neoplasm	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|oncology	cancer|respiratory_tract_neoplasm	throat_disorder|lung_disorder	false	true	false	false	high
MONDO:0020642	polycystic kidney disease	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	endocrinology|genetics_and_genomics|renal_medicine	metabolic_disorder|kidney_disease	kidney_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0020644	lung non-Hodgkin lymphoma	cancer_or_benign_tumor|hematologic_disorder|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder|hematologic_disorder	hematology|pulmonology|oncology	inflammatory_disease|cancer|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder|lung_disorder	false	true	false	true	high
MONDO:0020645	autosomal dominant osteopetrosis	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|anemia	bone_disorder|teeth_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0020646	ocular adnexal lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_orbital_region|hematologic_disorder	hematology|ophthalmology|oncology	inflammatory_disease|cancer|autoimmune_diseases|ocular_adnexal_lymphoma_is_a_type_of_lymphoma_which_falls_under_the_category_of_a_neoplasm__therefore_it_also_fits_best_in_the_category	eye_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0020647	microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	congenital_abnormality|metabolic_disorder|genetic_disorder	kidney_disorder|brain_disorder|reproductive_system_disorder	true	false	false	false	high
MONDO:0020648	rubella encephalitis	infectious_disease|nervous_system_disorder|inflammatory_disease	infectious_disease	infectious_disease|inflammatory_disease|post_infectious_disorder|nervous_system_disorder|acute_disease	neurology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|immune_disorder	true	false	false	false	high
MONDO:0020649	warty carcinoma of the penis	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|post_infectious_disorder|cancer_or_benign_tumor	urology|dermatology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|skin_disorder	false	true	false	true	high
MONDO:0020650	germ cell tumor of the vulva	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	reproductive_system_disorder|cancer|gynecologic_cancer	urinary_tract_disorder|immune_disorder|reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0020651	mixed germ cell tumor of vulva	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology|pediatric	cancer|adrenal_gland_disease	vulva_disorder|reproductive_system_disorder	true	true	false	true	high
MONDO:0020652	immature teratoma of vulva	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder	false	true	false	false	high
MONDO:0020653	vaginal adenocarcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0020654	renal pelvis/ureter urothelial carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer|renal_pelvis_ureter_urothelial_carcinoma	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0020655	juvenile ankylosing spondylitis	immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|inflammatory_disease	autoimmune_disease	immune_system_disorder|inflammatory_disease|connective_tissue_disorder|musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	bone_disorder|spinal_disorder|joint_disorder	false	false	false	true	high
MONDO:0020656	human papillomavirus-related penile squamous cell carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|post_infectious_disorder|cancer_or_benign_tumor	urology|dermatology|oncology	cancer|autoimmune_diseases|infectious_disease|inflammation_disease	reproductive_system_disorder|skin_disorder	true	true	false	true	high
MONDO:0020657	human papillomavirus-related squamous cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	post_infectious_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|dermatology|oncology	inflammatory_disease|cancer|neurodegenerative_disease|autoimmune_diseases|adrenal_gland_disease	reproductive_system_disorder|skin_disorder	true	true	false	true	very_high
MONDO:0020658	infiltrating ureter transitional cell carcinoma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	inflammatory_disease|cancer|autoimmune_diseases	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0020660	osteoblastic osteosarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	orthopaedic|oncology	cancer	bone_disorder|spinal_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0020661	undifferentiated round cell sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology	cancer|sarcoma|adrenal_gland_disease	blood_bone_marrow_disorder|muscle_disorder	false	true	false	false	high
MONDO:0020662	borderline ovarian serous tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|adrenocortical_carcinoma|other____corrected_____cancer|adrenal_gland_disease|ovarian_cancer	ovarian_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0020663	malignant spindle cell neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology	cancer|neoplasm	muscle_disorder|skin_disorder	false	true	false	false	high
MONDO:0020664	spindle cell neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pathology	spindle_cell_neoplasm_fits_more_specifically_under_a_subcategory_of_cancer_which_is_soft_tissue_sarcoma|cancer	blood_bone_marrow_disorder|muscle_disorder	false	true	false	false	high
MONDO:0020665	high grade malignant neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|genetics_and_genomics|neurology|oncology|pediatric	cancer|malignant_neoplasm|neoplastic_disease	blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0020666	Löfgren syndrome	connective_tissue_disorder|syndromic_disease	other	connective_tissue_disorder|syndromic_disease	rheumatology|pulmonology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder	false	false	false	true	medium
MONDO:0020667	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder	spine_disorder|bone_disorder|skeletal_system_disorder|joint_disorder	false	false	false	false	medium
MONDO:0020669	paranasal sinus cancer	connective_tissue_disorder|nervous_system_disorder|musculoskeletal_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|otorhinolaryngologic_disease|nervous_system_disorder|respiratory_system_disorder|musculoskeletal_system_disorder	otolaryngology|oncology	cancer|adrenal_gland_disease	nose_disorder|lung_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0020672	vascular occlusion disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|cardiology|vascular_occlusion_disorder_is_primarily_related_to_the_cardiovascular_system_and_blood_vessels__so_cardiology_and_hematology_fit_well__neurology_also_fits_because_some_types_of_vascular_occlusions_can_affect_the_brain_or_nervous_system|neurology	cardiovascular_disorder|vascular_occlusion_disorder	heart_disorder|brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0020673	arterial occlusion	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|neurology|vascular_medicine	cardiovascular_disorder|arterial_occlusion_is_not_a_cardiovascular_condition	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0020674	vascular insufficiency disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|pulmonology|cardiology|cardiothoracic	inflammatory_disease|cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0020675	ischemic bowel disorder	cardiovascular_disorder|digestive_system_disorder	cardiovascular_disorder	cardiovascular_disorder|digestive_system_disorder	gastroenterology|cardiology	inflammatory_disease|cardiovascular_disorder|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|vascular_disorder	false	false	false	true	high
MONDO:0020677	sudden hearing loss disorder	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|acute_disease|psychiatric_disorder	otolaryngology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0020678	sensorineural hearing loss disorder	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	otolaryngology|neurology	neurodegenerative_disease|sensorineural_hearing_loss_disorder_can_be_a_symptom_of_other_disorders_but_it_is_often_associated_with_neurodegenerative_diseases__particularly_those_affecting_the_auditory_nerve_or_brain	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0020679	conductive hearing loss disorder	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	otolaryngology|pediatric	inflammatory_disease|metabolic_disorder	ear_disorder|conductive_hearing_loss_disorder	false	false	false	true	medium
MONDO:0020680	acute bronchiolitis	respiratory_system_disorder	other	respiratory_system_disorder|acute_disease	pulmonology|pediatric	inflammatory_disease|respiratory_disease_is_not_in_the_list_so__inflammatory_disease	throat_disorder|lung_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0020681	Ehlers-Danlos syndrome, musculocontractural type 1	disorder_of_development_or_morphogenesis|cardiovascular_disorder|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|cardiovascular_disorder	hereditary_disease|metabolic_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	rheumatology|genetics_and_genomics|dermatology|pediatric|orthopaedic	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0020682	Ehlers-Danlos syndrome, spondylodysplastic type, 1	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	rheumatology|genetics_and_genomics|orthopaedic	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases|metabolic_disorder|connective_tissue_disease	bone_disorder|spinal_disorder|vascular_disorder|joint_disorder	false	false	false	false	high
MONDO:0020683	acute disease	other	other		general|pediatric	inflammatory_disease|cancer|acute_disease	joint_disorder	true	false	false	false	high
MONDO:0020684	Ehlers-Danlos syndrome, periodontal type 1	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	rheumatology|genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|connective_tissue_disorder	skin_disorder|teeth_disorder|joint_disorder	false	false	false	false	medium
MONDO:0020685	infratentorial ependymal tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neurooncology|brain_tumor	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0020686	acute tonsillitis	immune_system_disorder|inflammatory_disease|respiratory_system_disorder|otorhinolaryngologic_disease	other	immune_system_disorder|inflammatory_disease|otorhinolaryngologic_disease|respiratory_system_disorder|acute_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	throat_disorder|upper_gastrointestinal_disorder	true	false	false	true	low
MONDO:0020687	supratentorial ependymal tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neuro	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0020688	spinal cord ischemia	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	hematology|cardiology|neurology	cardiovascular_disorder|neurodegenerative_disease	spinal_disorder|vascular_disorder	false	false	false	false	high
MONDO:0020689	AIDS dementia complex	psychiatric_disorder	psychiatric_disorder	post_infectious_disorder|psychiatric_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0020690	adult glioblastoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0020692	spondylocostal dysostosis 1, autosomal recessive	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic	skeletal_system_disease|metabolic_disorder|genetic_disorder	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0020693	glycogen storage disease due to liver phosphorylase kinase deficiency	digestive_system_disorder|hereditary_disease|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	metabolic_disease|endocrine_system_disorder|hereditary_disease|digestive_system_disorder	hepatology|endocrinology|genetics_and_genomics|pediatric	metabolic_disorder	liver_disorder|muscle_disorder	false	false	true	false	medium
MONDO:0020694	salivary gland epithelial myoepithelial carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	otolaryngology|oncology	cancer|adrenal_gland_disease	throat_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0020695	hypotonic cerebral palsy	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0020696	vitamin B12 deficiency	nutritional_disorder|metabolic_disease	metabolic_disease	nutritional_disorder|metabolic_disease	hematology|endocrinology|gastroenterology|neurology	metabolic_disorder|neurodegenerative_disease|anemia	blood_bone_marrow_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0020697	lung epithelial-myoepithelial carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|cardiothoracic|oncology	cancer|lung_epithelial_myoeipithelial_carcinoma_is_a_subtype_of_cancer	lung_disorder|lung_epithelial_myoeithelial_carcinoma_does_not_seem_to_be_a_known_specific_type_of_cancer_in_the_lung_however_it_could_fall_under_lung_epithelial_myoeithelial_carcinoma_is_an_extremely_rare_tumor_type_primarily_found_in_the_lungs_and_pancreas_and_occasionally_in_other_locations_so_i_will_use_the_provided_category_list_to_determine_its_best_fit_category_which_would_be_lung_disorder	false	true	false	false	high
MONDO:0020698	inborn error of biotin metabolism	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatrics	metabolic_disorder|inborn_error_of_biotin_metabolism	liver_disorder|metabolic_disorder	false	false	false	true	high
MONDO:0020699	biotin metabolic disease	metabolic_disease	metabolic_disease	metabolic_disease	endocrinology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	liver_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0020701	brachydactyly type A1A	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic	congenital_diseases|genetic_disorders|developmental_disorders	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0020702	autosomal dominant epidermolytic ichthyosis	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0020703	erythroid neoplasm	cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|connective_tissue_disorder|immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	hematology|oncology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0020704	inherited rippling muscle disease	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	inherited_ripping_muscle_disease_is_not_in_the_list_so__neurodegenerative_disease|metabolic_disorder|neurodegenerative_disease	inherited_disorder|muscle_disorder	false	false	false	false	high
MONDO:0020706	Heberden's node	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|neurology	neurodegenerative_disease|cardiovascular_disorder	bone_disorder|vascular_disorder|joint_disorder	false	false	false	false	low
MONDO:0020707	central hearing loss	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	otolaryngology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0020708	brachial amyotrophic diplegia	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0020709	Majocchi granuloma	infectious_disease|integumentary_system_disorder|inflammatory_disease	infectious_disease	infectious_disease|inflammatory_disease|integumentary_system_disorder	immunology|dermatology|pulmonology	inflammatory_disease|autoimmune_diseases	liver_disorder|lymphatic_disorder|immune_disorder	true	false	false	true	medium
MONDO:0020710	amnionitis	reproductive_system_disorder|obstetric_disorder|inflammatory_disease	other	obstetric_disorder|reproductive_system_disorder|inflammatory_disease	pediatrics|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0020711	selective peripheral resistance to thyroid hormone	hereditary_disease|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	metabolic_disease|endocrine_system_disorder|hereditary_disease	endocrinology|renal_medicine|hematology|cardiology	metabolic_disorder|autoimmune_diseases	endocrine_disorder	false	false	false	true	high
MONDO:0020712	46,XY sex reversal 1	reproductive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|musculoskeletal_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cardiovascular_disorder	cardiovascular_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder|hereditary_disease|musculoskeletal_system_disorder	pediatrics|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0020713	pulmonary venoocclusive disease 1	hereditary_disease|cardiovascular_disorder|respiratory_system_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|respiratory_system_disorder	genetics_and_genomics|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|vascular_disorder	false	false	false	true	high
MONDO:0020714	mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|metabolic_disease|mitochondrial_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0020716	thyroid dyshormonogenesis 1	hereditary_disease|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	metabolic_disease|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology	thyroid_gland_disease_is_not_in_the_list_so_i_will_leave_it_blank|metabolic_disorder	thyroid_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0020717	autosomal dominant wooly hair	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases	skin_disorder|hair_disorder	false	false	false	false	low
MONDO:0020718	congenital short bowel syndrome, autosomal recessive	hereditary_disease|disorder_of_development_or_morphogenesis|digestive_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|digestive_system_disorder	genetics_and_genomics|gastroenterology|pediatric	metabolic_disorder|genetic_disorder|autosomal_recessive_diseases	congenital_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0020720	X-linked hypophosphatemic rickets	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|genetic_disease	bone_disorder|endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0020721	X-linked sideroblastic anemia 1	hereditary_disease|hematologic_disorder|metabolic_disease	metabolic_disease|anemia	hematologic_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|hematology	genetic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0020722	nephrolithiasis susceptibility caused by SLC26A1	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	genetics_and_genomics|renal_medicine|urology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0020723	vitamin D-dependent rickets, type 1A	hereditary_disease|musculoskeletal_system_disorder|metabolic_disease|nutritional_disorder|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	metabolic_disease|endocrine_system_disorder|hereditary_disease|musculoskeletal_system_disorder|nutritional_disorder	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	bone_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0020724	cerebral cavernous malformation 1	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|oncology	cancer|neurological_disorder	brain_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0020725	anemia due to chronic disorder	hematologic_disorder	anemia	hematologic_disorder	endocrinology|renal_medicine|hematology	autoimmune_diseases|metabolic_disorder|anemia	chronic_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0020726	tubulointerstitial kidney disease, autosomal dominant, 2	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	genetics_and_genomics|renal_medicine	inflammatory_disease|autoimmune_diseases	kidney_disorder	false	false	false	false	high
MONDO:0020727	combined oxidative phosphorylation deficiency 22	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0020728	hypouricemia, renal 1	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	nephrology|renal_medicine	metabolic_disorder|renal	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0020729	autosomal recessive agammaglobulinemia 1	hereditary_disease|immune_system_disorder|hematologic_disorder	other	hematologic_disorder|immune_system_disorder|hereditary_disease	pediatrics|genetics_and_genomics|immunology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0020730	carpal tunnel syndrome 1	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|orthopaedic	inflammatory_disease|neurodegenerative_disease	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0020731	arbovirus infection	infectious_disease	infectious_disease	infectious_disease	neurology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	immune_disorder	true	false	false	false	medium
MONDO:0020733	proximal symphalangism 1A	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0020735	ACTH-independent macronodular adrenal hyperplasia 1	hereditary_disease|syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	adrenal_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0020736	uncombable hair syndrome 1	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	immune_disorder|hair_disorder|skin_disorder	false	false	false	false	low
MONDO:0020737	optic atrophy 10 with or without ataxia, intellectual disability, and seizures	hereditary_disease|disorder_of_visual_system|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|disorder_of_visual_system|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0020738	multiple benign circumferential skin creases on limbs 1	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|pediatric	benign_growth|skin_disorder|neoplasm|congenital_condition|dermatological_condition	muscle_disorder|joint_disorder|skin_disorder	false	false	false	false	low
MONDO:0020739	hypercalcemia, infantile, 1	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|pediatric	metabolic_disorder|adrenal_gland_disease	bone_disorder|endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0020740	ectodermal dysplasia and immunodeficiency 1	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|immune_system_disorder	other	syndromic_disease|disorder_of_development_or_morphogenesis|immune_system_disorder|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|immunology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|immunodeficiency	immune_disorder|teeth_disorder|eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0020741	pyridoxine-dependent epilepsy caused by ALDH7A1 mutant	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0020743	mixed phenotype acute leukemia	connective_tissue_disorder|hematologic_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|connective_tissue_disorder|acute_disease|immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	hematology|oncology	cancer|leukemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0020744	Mobitz type I atrioventricular block	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	cardiology|cardiothoracic	autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	low
MONDO:0020745	ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	genetics_and_genomics|cardiology|pediatric	metabolic_disorder|cardiovascular_disorder	muscle_disorder|heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0020746	contractures, pterygia, and variable skeletal fusions syndrome 1B	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skeletal_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0020747	sitosterolemia 1	hereditary_disease|syndromic_disease|metabolic_disease	metabolic_disease	metabolic_disease|syndromic_disease|hereditary_disease	genetics_and_genomics|hepatology|endocrinology|cardiology|cardiovascular	metabolic_disorder|cardiovascular_disorder	liver_disorder|lipid_disorder	false	false	false	true	high
MONDO:0020748	sitosterolemia 2	hereditary_disease|syndromic_disease|metabolic_disease	metabolic_disease	metabolic_disease|syndromic_disease|hereditary_disease	genetics_and_genomics|hepatology|endocrinology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	liver_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0020749	polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	bone_disorder|kidney_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0020750	polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0020751	orthostatic hypotension 2	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	renal_medicine|cardiology|neurology	metabolic_disorder|cardiovascular_disorder|adrenal_gland_disease	heart_disorder|vascular_disorder	false	false	false	true	low
MONDO:0020753	Orthocoronavirinae infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	infectious_disease|autoimmune_diseases|all_that_was_given_in_the_prompt_is_already_an__infectious_disease__so_it_should_be_excluded_from_selection|inflammatory_disease	respiratory_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0020754	visceral myopathy 1	digestive_system_disorder|hereditary_disease	other	digestive_system_disorder|hereditary_disease	genetics_and_genomics|neurology|cardiology	neurodegenerative_disease|metabolic_disorder	visceral_myopathy|muscle_disorder	false	false	false	false	high
MONDO:0020756	migraine, familial hemiplegic, 1	cardiovascular_disorder|nervous_system_disorder|hereditary_disease	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|familial_disorders	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0020757	sporadic hemiplegic migraine	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	pediatric|neurology	neurodegenerative_disease|inflammatory_disease	vascular_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0020760	skin squamous cell carcinoma in situ	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	cancer|in_situ|skin_disease	skin_disorder	false	true	false	true	low
MONDO:0020761	Bowen disease of the skin	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	cancer|autoimmune_diseases	lymphatic_disorder|skin_disorder|immune_disorder	false	true	false	true	medium
MONDO:0020762	diencephalic-mesencephalic junction dysplasia syndrome 2	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0020763	Menke-Hennekam syndrome 1	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|anemia	joint_disorder|blood_bone_marrow_disorder|skin_disorder|eye_disorder|bone_disorder	false	false	false	false	high
MONDO:0020765	neuropathy, congenital hypomyelinating, 2	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	congenital_hypomyelinating|neurodegenerative_disease|metabolic_disorder	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0020766	neuropathy, congenital hypomyelinating, 3	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0020767	cauda equina syndrome with neurogenic bladder	syndromic_disease|nervous_system_disorder	other	nervous_system_disorder|syndromic_disease	urology|neurology	neurodegenerative_disease|cancer|autoimmune_diseases	urinary_tract_disorder|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0020768	X-linked deafness	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder|ear_disorder	false	false	false	false	high
MONDO:0020769	Menke-Hennekam syndrome 2	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	vascular_disorder|joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0020770	spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3	nervous_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0020771	spinocerebellar ataxia, autosomal recessive, with axonal neuropathy	nervous_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0020773	cerebrospinal fluid rhinorrhea	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	nose_disorder|brain_disorder	false	false	false	false	medium
MONDO:0020774	Menke-Hennekam syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	joint_disorder|skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0020775	congenital disorder of glycosylation with defective fucosylation 1	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	congenital_disease|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0020776	chlamydiaceae infections	infectious_disease	infectious_disease	infectious_disease	urology|pediatric|obstetrics_and_gynecology	cancer|autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder|immune_disorder	true	false	false	true	medium
MONDO:0020777	congenital disorder of glycosylation with defective fucosylation 2	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|congenital_disorder	congenital_disorder|liver_disorder	false	false	false	false	high
MONDO:0020778	cone-rod dystrophy and hearing loss 1	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology|otolaryngology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder|ear_disorder	false	false	false	false	medium
MONDO:0020779	cartilage development disorder	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	rheumatology|genetics_and_genomics|orthopaedic	genetic_disorder|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0020780	cone-rod dystrophy and hearing loss 2	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology|otolaryngology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	eye_disorder|ear_disorder	false	false	false	false	medium
MONDO:0020781	encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	vascular_disorder|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0020782	chronic gingivitis	musculoskeletal_system_disorder|inflammatory_disease	other	mouth_disorder|inflammatory_disease|musculoskeletal_system_disorder	pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease	teeth_disorder|skin_disorder	true	false	false	true	medium
MONDO:0020783	capillary malformation-arteriovenous malformation 1	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	hematology|genetics_and_genomics|cardiology	cardiovascular_disorder|arteriovenous_malformation	vascular_disorder|skin_disorder	false	false	false	false	medium
MONDO:0020785	capillary malformation-arteriovenous malformation 2	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	hematology|genetics_and_genomics|cardiology	cardiovascular_disorder|arteriovenous_malformation	vascular_disorder|skin_disorder	false	false	false	false	medium
MONDO:0020787	hypomagnesemia, seizures, and intellectual disability 1	hereditary_disease|urinary_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|urinary_system_disorder|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|intellectual_disability_is_a_symptom_of_some_categories_but_not_the_best_fit_here_so_excluded	brain_disorder|endocrine_disorder|muscle_disorder	false	false	false	true	high
MONDO:0020788	hypomagnesemia, seizures, and intellectual disability 2	hereditary_disease|urinary_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|urinary_system_disorder|metabolic_disease	genetics_and_genomics|neurology|pediatrics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|endocrine_disorder|muscle_disorder	false	false	false	true	high
MONDO:0020789	pseudo-TORCH syndrome 1	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	false	high
MONDO:0020790	gaze palsy, familial horizontal, with progressive scoliosis 1	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|eye_disorder	true	false	false	true	high
MONDO:0020791	corneal dystrophy, Meesmann, 1	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	neurodegenerative_disease|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	true	medium
MONDO:0020792	dwarfism with tall vertebrae	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|endocrinology	endocrine_disorder|metabolic_disorder|growth_disorder	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0020793	oculopharyngodistal myopathy 1	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0020794	colorectal medullary carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|hematology|genetics_and_genomics|gastroenterology	cancer|adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0020795	Silver-Russell syndrome 5	disorder_of_development_or_morphogenesis|syndromic_disease|chromosomal_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|chromosomal_disorder|syndromic_disease	pediatric|genetics_and_genomics|endocrinology	genetic_disorder|metabolic_disorder|growth_hormone_disorder	growth_disorder|developmental_disorder|endocrine_disorder|skeletal_disorder	false	false	false	false	medium
MONDO:0020796	Silver-Russell syndrome 1	disorder_of_development_or_morphogenesis|syndromic_disease|chromosomal_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|chromosomal_disorder|syndromic_disease	pediatric|genetics_and_genomics|endocrinology	genetic_disorder|metabolic_disorder	growth_disorder|endocrine_disorder|skeletal_disorder	false	false	false	false	medium
MONDO:0020797	decompression sickness	nervous_system_disorder	other	nervous_system_disorder	cardiothoracic|pulmonology|cardiology	cardiovascular_disorder|inflammatory_disease	vascular_disorder|heart_disorder|spinal_disorder	false	false	false	true	high
MONDO:0020798	hypoparathyroidism, familial isolated, 2	endocrine_system_disorder|metabolic_disease|hereditary_disease	endocrine_system_disorder|metabolic_disease	hereditary_disease|metabolic_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology	adrenal_gland_disease|autoimmune_diseases|metabolic_disorder	endocrine_disorder|thyroid_disorder	false	false	false	true	medium
MONDO:0020799	basal cell neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|dermatology	basal_cell_neoplasm_is_itself_a_form_of_cancer|cancer	skin_disorder	false	true	false	true	low
MONDO:0020800	demyelinating disease of central nervous system	nervous_system_disorder|disorder_of_development_or_morphogenesis	neurodegenerative_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder|brain_disorder|immune_disorder	false	false	false	false	high
MONDO:0020801	rectal medullary carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0020804	basal cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|oncology	skin_disease|cancer	lower_gastrointestinal_disorder|skin_disorder	false	true	false	true	medium
MONDO:0020805	benign basal cell neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|oncology	basal_cell_neoplasm_is_a_type_of_cancer_so_the_other_category_does_not_apply|cancer	skin_disorder|bone_disorder	false	false	false	true	low
MONDO:0020806	sinoatrial block	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic|pulmonology	neurodegenerative_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|heart_disorder	false	false	false	false	medium
MONDO:0020807	ovarian sertoli-stromal cell tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0020808	testicular sertoli cell tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	testicular_cancer|cellular_neoplasm|cancer|tumor	endocrine_disorder|reproductive_system_disorder	false	true	false	false	low
MONDO:0020809	benign sertoli cell tumor	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	adrenal_gland_disease|cancer	kidney_disorder|reproductive_system_disorder	false	false	false	true	low
MONDO:0020811	mitochondrial complex III deficiency, nuclear type	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0020812	exposure, dental pulp	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	odontology|endocrinology|pulmonology|hematology|dentistry	inflammatory_disease|dental_pulp|autoimmune_diseases|exposure	teeth_disorder|dental_pulp	false	false	false	false	medium
MONDO:0020813	benign testicular sertoli cell tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|genetics_and_genomics|urology	adrenal_gland_disease|cancer	endocrine_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0020814	miliaria alba	syndromic_disease|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	low
MONDO:0020815	dentigerous cyst	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	otolaryngology|pediatric	adrenal_gland_disease|inflammatory_disease|cancer	teeth_disorder|jaw_bone_disorder	false	false	false	true	medium
MONDO:0020816	miliaria papulosa	syndromic_disease|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder	false	false	false	false	low
MONDO:0020817	miliaria vesiculosa	syndromic_disease|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	skin_disorder	true	false	false	true	low
MONDO:0020818	secondary dentine	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder	orthopaedic|dentistry	cardiovascular_disorder|inflammatory_disease	dentin_disorder|teeth_disorder	false	false	false	false	low
MONDO:0020820	distal arthrogryposis type 2B1	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0020823	infantile miliaria	syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|syndromic_disease	dermatology|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|immune_disorder	false	false	false	true	low
MONDO:0020830	diaphragmitis	respiratory_system_disorder|musculoskeletal_system_disorder|inflammatory_disease	other	inflammatory_disease|respiratory_system_disorder|musculoskeletal_system_disorder	gastroenterology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	abdominal_disorder|gastrointestinal_disorder|muscle_disorder	true	false	false	false	medium
MONDO:0020831	congenital vertebral-cardiac-renal anomalies syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiology|pediatric|renal_medicine|genetics_and_genomics	genetic_condition|cardiovascular_disorder|kidney_disease|congenital_disease	spinal_disorder|kidney_disorder|heart_disorder	false	false	false	false	high
MONDO:0020835	methemoglobinemia, alpha type	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|lung_disorder	false	false	false	true	medium
MONDO:0020837	oocyte maturation defect 5	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics	cancer|metabolic_disorder	reproductive_system_disorder	false	false	false	false	medium
MONDO:0020838	anterior nasal diphtheria	infectious_disease	infectious_disease	infectious_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	throat_disorder|nose_disorder	true	false	false	true	medium
MONDO:0020840	pulmonary alveolar proteinosis with hypogammaglobulinemia	hereditary_disease	other	hereditary_disease	allergy_and_immunology|immunology|pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0020841	neurodevelopmental disorder with cerebellar atrophy and with or without seizures	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0020843	pseudomembranous diphtheritic conjunctivitis	infectious_disease|inflammatory_disease|disorder_of_visual_system	infectious_disease	infectious_disease|disorder_of_visual_system|disorder_of_orbital_region|acute_disease|inflammatory_disease	ophthalmology|otolaryngology	inflammatory_disease|autoimmune_diseases	throat_disorder|eye_disorder	true	false	false	false	high
MONDO:0020845	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease|musculoskeletal_system_disorder|nervous_system_disorder	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|mitochondrial_disease|nervous_system_disorder	ophthalmology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0020846	intellectual disability, autosomal recessive 64	metabolic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	metabolic_disease|psychiatric_disorder	psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0020847	intellectual disability, autosomal dominant 58	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0020848	osteopetrosis, autosomal dominant 3	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	spinal_disorder|joint_disorder|blood_bone_marrow_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0020849	immunodeficiency 57	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|immunology|pediatrics|pulmonology	inflammatory_disease|autoimmune_diseases|immunodeficiency	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0020850	intellectual disability, autosomal recessive 65	nervous_system_disorder|metabolic_disease|hereditary_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder	psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	very_high
MONDO:0020851	spermatogenic failure 30	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	pediatric|urology	endocrine_disorder_is_not_in_the_list_so__metabolic_disorder|metabolic_disorder	reproductive_system_disorder|spermatic_failure_is_often_classified_under_male_reproductive_disorders_which_is_a_subset_of_the_broader_category_of_reproductive_system_disorders	false	false	false	false	medium
MONDO:0020852	spermatogenic failure 31	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	autoimmune_diseases|metabolic_disorder|anemia	male_reproductive_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0020853	encephalitis/encephalopathy, mild, with reversible myelin vacuolization	hereditary_disease	other	hereditary_disease	pediatric|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	encephalitis_encephalopathy_mild|brain_disorder	true	false	false	true	medium
MONDO:0020854	Liddle syndrome 2	syndromic_disease|urinary_system_disorder|hereditary_disease	other	syndromic_disease|urinary_system_disorder|hereditary_disease	genetics_and_genomics|renal_medicine|endocrinology	autoimmune_diseases|metabolic_disorder	immune_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0020855	spermatogenic failure 32	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	metabolic_disorder|anemia|cancer	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0020856	bone marrow failure syndrome 4	immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder|hematologic_disorder	other	hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|hereditary_disease	hematology|oncology|genetics_and_genomics	anemia|cancer	blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0020857	ovarian dysgenesis 7	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|anemia|cancer	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0020858	mitochondrial complex V (ATP synthase) deficiency, nuclear type 5	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	pediatric|mitochondrial_diseases_can_sometimes_be_associated_with_cardiology__but_this_specific_condition_has_a_genetic_basis_so_genetics_and_genomics_is_the_best_fit|genetics_and_genomics|neurology	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	mitochondrial_diseases|muscle_disorder	false	false	false	false	very_high
MONDO:0020860	faucial diphtheria	infectious_disease	infectious_disease	infectious_disease	otolaryngology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|throat_disorder	true	false	false	true	medium
MONDO:0020863	laryngeal diphtheria	infectious_disease|respiratory_system_disorder	infectious_disease	infectious_disease|respiratory_system_disorder	otolaryngology|pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|throat_disorder	true	false	false	true	high
MONDO:0020866	nasopharyngeal diphtheria	infectious_disease|respiratory_system_disorder|otorhinolaryngologic_disease	infectious_disease	infectious_disease|otorhinolaryngologic_disease|respiratory_system_disorder	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases|cancer	upper_gastrointestinal_disorder|throat_disorder	true	false	false	true	high
MONDO:0020920	escherichia coli infection	infectious_disease	infectious_disease	infectious_disease	renal_medicine|pediatric|urology|gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|kidney_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0020927	postaxial polydactyly	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic	neurodegenerative_disease|developmental_disorder|skeletal_abnormality	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0020937	contractures, pterygia, and variable skeletal fusions syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0020944	fungal infection of eye	infectious_disease|disorder_of_visual_system	infectious_disease	infectious_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder	true	false	false	true	high
MONDO:0020947	parasitic eye infection	infectious_disease|disorder_of_visual_system	infectious_disease	infectious_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|pediatric	inflammatory_disease|autoimmune_diseases	parasitic_infection|eye_disorder	true	false	false	true	medium
MONDO:0020950	viral eye infection	infectious_disease|disorder_of_visual_system	infectious_disease	disorder_of_visual_system|disorder_of_orbital_region|infectious_disease	ophthalmology|pediatric	inflammatory_disease|autoimmune_diseases	eye_disorder|viral_infection_is_not_a_category_in_the_list_so_use_none_of_those	true	false	false	true	medium
MONDO:0020959	Mansonella ozzardi infection	infectious_disease	infectious_disease	infectious_disease	hematology|oncology|pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|liver_disorder	true	false	false	true	low
MONDO:0020971	gonococcal urethritis	urinary_system_disorder|inflammatory_disease|reproductive_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|reproductive_system_disorder|urinary_system_disorder|infectious_disease	obstetrics_and_gynecology|urology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0020974	laryngeal granuloma	respiratory_system_disorder	other	respiratory_system_disorder	otolaryngology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|allergy	lung_disorder|throat_disorder|immune_disorder	false	false	false	true	medium
MONDO:0020977	granulomatous prostatitis	inflammatory_disease|reproductive_system_disorder	other	inflammatory_disease|reproductive_system_disorder	rheumatology|urology|renal_medicine	inflammatory_disease|autoimmune_diseases	immune_disorder|reproductive_system_disorder|urinary_tract_disorder	true	false	false	false	medium
MONDO:0020979	pilosebaceous hamartoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology_is_likely_a_subcategory_of_the_other_two__but_it_s_included_here_as_it_s_directly_related_to_the_condition|dermatology|genetics_and_genomics|pediatric	neurocutaneous_disorder|tumor|skin_disease	lower_gastrointestinal_disorder|skin_disorder	false	false	false	false	low
MONDO:0020980	hair nevus	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology|dermatogenetics_and_genomics	pigmentation_disorder|neurocutaneous_disease|dermatological_condition	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0020983	myocardial rupture	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pulmonology|hematology|cardiology|cardiothoracic	cardiovascular_disorder|myocardial_rupture	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0020989	hereditary persistence of fetal hemoglobin	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|hemoglobin_disorder	false	false	false	false	low
MONDO:0021001	hemochromatosis type 1	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	gastroenterology|genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	high
MONDO:0021002	syndactyly	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0021003	polydactyly	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	congenital_anomaly|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	true	low
MONDO:0021004	brachydactyly	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic	genetic_disorder|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0021005	faciodigitogenital syndrome	syndromic_disease	other	syndromic_disease	endocrinology|gastroenterology|psychiatry|dermatology|renal_medicine|genetics_and_genomics|allergy_and_immunology|otolaryngology|cardiology|orthopaedic|obstetrics_and_gynecology|pediatric|urology|hematology|neurology	genetic_syndrome____note__i_ve_corrected_the_response_to_reflect_that_faciodigitogenital_syndrome_is_a_rare_genetic_disorder|metabolic_disorder	joint_disorder|skin_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0021008	secondary antiphospholipid syndrome	syndromic_disease|immune_system_disorder	autoimmune_disease	syndromic_disease|immune_system_disorder	cardiology|rheumatology|hematology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0021009	salivary gland mucoepidermoid carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|mouth_disorder	otolaryngology|oncology	cancer|adrenal_gland_disease	teeth_disorder|throat_disorder|ear_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0021010	skin lymphangiosarcoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	cancer|tumor|lymphoma|skin_disease|malignancy	lymphatic_disorder|skin_disorder	false	true	false	false	very_high
MONDO:0021011	hereditary progressive chorea without dementia	syndromic_disease|endocrine_system_disorder|hereditary_disease|nervous_system_disorder	endocrine_system_disorder	hereditary_disease|syndromic_disease|nervous_system_disorder|endocrine_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0021013	trichothiodystrophy 4, nonphotosensitive	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|syndromic_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	hair_disorder|skin_disorder	false	false	false	false	high
MONDO:0021017	synaptopathy	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0021018	autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6)	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|neurology	muscular_dystrophy|neurodegenerative_disease	spinal_disorder|joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0021019	X-linked recessive ocular albinism	disorder_of_visual_system|metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|disorder_of_visual_system|metabolic_disease	genetics_and_genomics|ophthalmology|pediatric	metabolic_disorder|neurodegenerative_disease	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0021020	Crigler-Najjar syndrome type 1	syndromic_disease|metabolic_disease|hereditary_disease	metabolic_disease	syndromic_disease|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|hepatology	genetic_disorder|metabolic_disorder|neurological_disorder	kidney_disorder|vascular_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0021021	craniodiaphyseal dysplasia, autosomal dominant	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|skeletal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0021022	hereditary hyperekplexia	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0021023	complete androgen insensitivity syndrome	disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|urology|endocrinology	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0021025	cirrhosis, familial, with antigenemia	digestive_system_disorder|endocrine_system_disorder|premature_aging_syndrome|hereditary_disease	endocrine_system_disorder	premature_aging_syndrome|endocrine_system_disorder|hereditary_disease|digestive_system_disorder	genetics_and_genomics|hepatology|gastroenterology	metabolic_disorder|anemia|autoimmune_diseases	immune_disorder|familial|liver_disorder|antigenemia	false	false	false	false	high
MONDO:0021026	hereditary epidermal appendage anomaly	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	adrenal_gland_disease	skin_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0021029	hereditary sebaceous gland anomaly	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	genetic_disorder|metabolic_disorder|congenital_anomaly|skin_condition	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0021032	herpes zoster with dermatitis of eyelid	infectious_disease|inflammatory_disease|disorder_of_visual_system|integumentary_system_disorder	infectious_disease	disorder_of_visual_system|disorder_of_orbital_region|integumentary_system_disorder|infectious_disease|inflammatory_disease	ophthalmology|dermatology|neurology	inflammatory_disease|autoimmune_diseases	skin_disorder|spinal_disorder|eye_disorder	true	false	false	true	medium
MONDO:0021033	herpes zoster dermatitis	infectious_disease|inflammatory_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease|inflammatory_disease	dermatology|neurology	inflammatory_disease|autoimmune_diseases	skin_disorder|nerve_disorder	true	false	false	true	medium
MONDO:0021035	alopecia-intellectual disability syndrome 1	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	skin_disorder|brain_disorder	false	false	false	false	high
MONDO:0021036	keratosis pilaris	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0021038	Ewing sarcoma/peripheral primitive neuroectodermal tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|orthopaedic|oncology	peripheral_primitive_neuroectodermal_tumor_is_a_type_of_cancer|cancer	bone_disorder|bone_marrow_disorder	false	true	false	true	very_high
MONDO:0021039	extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|orthopaedic|hematology|neurology|oncology	cancer|peripheral_primitive_neuroectodermal_tumor	bone_disorder|spinal_disorder	false	true	false	true	high
MONDO:0021040	pancreatic neoplasm	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer|pancreatic_neoplasm	lower_gastrointestinal_disorder|endocrine_disorder	false	true	false	false	very_high
MONDO:0021041	pleural solitary fibrous tumor	connective_tissue_disorder|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|respiratory_system_disorder|cancer_or_benign_tumor	pulmonology|cardiothoracic|oncology	cancer	lung_disorder	false	false	false	false	medium
MONDO:0021042	glioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0021043	mixed neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology	cancer|mixed_neoplasm	blood_bone_marrow_disorder	false	true	false	false	medium
MONDO:0021045	fibroepithelial neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pathology|oncology	cancer	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0021046	breast fibroepithelial neoplasm	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer	reproductive_system_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0021047	breast phyllodes tumor	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer	breast_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0021048	benign mastocytoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	hematology|dermatology|oncology	allergy|anemia|inflammatory_disease|cancer	skin_disorder|blood_bone_marrow_disorder	false	false	false	true	low
MONDO:0021049	vulvar neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	inflammatory_disease|cancer	skin_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0021050	vaginal neoplasm	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	anemia|cancer	vaginal_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0021052	parasympathetic paraganglioma	cancer_or_benign_tumor|endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|hereditary_disease	endocrinology|neurology|oncology	adrenal_gland_disease|cancer	nervous_system_disorder|endocrine_disorder|brain_disorder	false	true	false	false	medium
MONDO:0021053	carotid body paraganglioma	cancer_or_benign_tumor|endocrine_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|hereditary_disease	otolaryngology|neurology|cardiology|pulmonology	neuroendocrine_tumor|cancer|cardiovascular_disorder	vascular_disorder|brain_disorder	false	true	false	false	medium
MONDO:0021054	bone sarcoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	orthopaedic|oncology	bone_cancer|cancer|sarcoma	bone_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0021055	classic familial adenomatous polyposis	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	gastroenterology|genetics_and_genomics|oncology	cancer|genetic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0021056	familial adenomatous polyposis 1	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|oncology	cancer|familial_adenomatous_polyposis_is_a_type_of_cancer_that_affects_the_colon_and_rectum	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0021057	classic or attenuated familial adenomatous polyposis	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	gastroenterology|genetics_and_genomics|oncology	familial_adenomatous_polyposis|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0021058	neoplastic syndrome	cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor	hematology|oncology	cancer|neoplastic_syndrome	blood_bone_marrow_disorder|neoplastic_syndrome	false	true	false	false	very_high
MONDO:0021060	RASopathy	hereditary_disease	other	hereditary_disease	ophthalmology|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	liver_disorder|upper_gastrointestinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0021061	neurofibromatosis	cancer_or_benign_tumor|syndromic_disease|hereditary_disease|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease	genetics_and_genomics|neurology|oncology	cancer|neurodegenerative_disease	bone_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0021063	malignant colon neoplasm	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	malignant_colon_neoplasm|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0021064	jugulotympanic paraganglioma	cancer_or_benign_tumor|musculoskeletal_system_disorder|endocrine_system_disorder|connective_tissue_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|hereditary_disease	otolaryngology|neurology|oncology	cancer|neurodegenerative_disease	throat_disorder|ear_disorder	false	true	false	false	high
MONDO:0021065	pleural neoplasm	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|pulmonology	pleural_neoplasm|cancer	lung_disorder	false	true	false	false	high
MONDO:0021066	urinary system neoplasm	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	urinary_system_neoplasm|cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0021067	mediastinal germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|cardiothoracic|oncology	adrenal_gland_disease|cancer	lymphatic_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0021068	ovarian neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|inflammatory_disease|cancer|autoimmune_diseases	ovarian_neoplasm|reproductive_system_disorder	false	true	false	false	high
MONDO:0021069	malignant endocrine neoplasm	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|oncology	adrenal_gland_disease|cancer|malignant_endocrine_neoplasm	malignant|endocrine_disorder	false	true	false	false	high
MONDO:0021070	sublingual gland carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor|digestive_system_disorder	otolaryngology|oncology	cancer|gland_disease	throat_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0021071	laryngeal neoplasm	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology	cancer|laryngeal_neoplasm	lymphatic_disorder|lung_disorder|throat_disorder	false	true	false	false	high
MONDO:0021072	sympathetic paraganglioma	endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|nervous_system_disorder|endocrine_system_disorder|hereditary_disease	neurology|oncology	neuroendocrine_tumor|cancer	endocrine_disorder|brain_disorder	false	true	false	true	high
MONDO:0021073	paraneoplastic syndrome	syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease	hematology|neurology|oncology	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|lymphatic_disorder|lung_disorder	false	false	false	false	high
MONDO:0021074	precancerous condition	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|genetics_and_genomics|oncology	autoimmune_diseases|cancer|preneoplastic_conditions_can_often_be_considered_a_type_of_precancerous_condition_so_i_have_included_it_in_the_list_but_as_per_your_instruction_i_am_not_providing_any_additional_text	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	medium
MONDO:0021075	neoplastic polyp	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	gastroenterology|oncology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0021076	pancreatic exocrine neoplasm	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	gastroenterology|oncology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0021077	cystic neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|oncology	adrenal_gland_disease|cancer	liver_disorder	false	true	false	true	medium
MONDO:0021078	glandular papilloma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|oncology	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases|cancer	skin_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0021079	childhood neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	cancer|childhood_neoplasm	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0021080	blood vessel neoplasm	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	hematology|oncology	blood_vessel_neoplasm_is_more_fitting_under_cancer_so___cancer|cancer|cardiovascular_disorder	lymphatic_disorder|blood_bone_marrow_disorder|vascular_disorder	false	true	false	true	medium
MONDO:0021081	anti-NMDA receptor encephalitis	inflammatory_disease|nervous_system_disorder	other	acute_disease|nervous_system_disorder|inflammatory_disease	psychiatry|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	immune_disorder|spinal_disorder|brain_disorder	true	false	false	true	high
MONDO:0021082	Meckel diverticulum neoplasm	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	pediatric|surgery|gastroenterology|oncology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0021083	congenital fibrosis of extraocular muscles type 1	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	other	musculoskeletal_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease	pediatric|ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0021084	vision disorder	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	pediatric|ophthalmology|neurology	neurodegenerative_disease|vision_disorder_is_a_subset_of_this_category	vision_disorder|eye_disorder	false	false	false	false	high
MONDO:0021085	gastric neoplasm	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	cancer|gastrointestinal_cancers	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0021086	gingival neoplasm	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|mouth_disorder|cancer_or_benign_tumor	oral_pathology__removed_as_it_is_not_in_the_list|dermatology|oncology	cancer	skin_disorder|teeth_disorder	false	true	false	false	medium
MONDO:0021088	papillary meningioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0021089	peripheral nervous system cancer	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|peripheral_nervous_system_cancer	peripheral_nervous_system_cancer_can_also_be_classified_as_a_brain_disorder_or_muscle_disorder_but_sp_is_more_accurate|spinal_disorder	false	true	false	true	high
MONDO:0021090	lipid-rich breast carcinoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	lipid_rich_breast_carcinoma_is_a_type_of_cancer|cancer	lymphatic_disorder|breast_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0021091	papillary cystadenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|urology|otolaryngology|genetics_and_genomics|dermatology|neurology|oncology|pathology	adrenal_gland_disease|cancer	kidney_disorder|liver_disorder	false	false	false	false	low
MONDO:0021092	fallopian tube neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|gynecological_cancer	reproductive_system_disorder	false	true	false	false	high
MONDO:0021093	cranioectodermal dysplasia 1	musculoskeletal_system_disorder|urinary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|integumentary_system_disorder|respiratory_system_disorder	other	musculoskeletal_system_disorder|urinary_system_disorder|respiratory_system_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|dermatology	anemia|metabolic_disorder|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	bone_disorder|skin_disorder|joint_disorder|eye_disorder|teeth_disorder|ear_disorder	false	false	false	false	high
MONDO:0021094	immunodeficiency disease	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatrics|genetics_and_genomics|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	true	false	false	true	high
MONDO:0021095	parkinsonian disorder	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	cardiovascular_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0021096	papillary epithelial neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pathology	adrenal_gland_disease|other_____corrected_to_remove_the_redundant_category___cancer|cancer	lung_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0021097	intraductal breast papilloma	breast_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	skin_disorder|reproductive_system_disorder	false	false	false	true	low
MONDO:0021098	papillomatosis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|dermatology	cancer	skin_disorder|liver_disorder	true	false	false	false	medium
MONDO:0021099	intraductal papillomatosis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|oncology|dermatology	intracranial_disease|cancer	breast_disorder|liver_disorder	false	false	false	false	low
MONDO:0021100	breast neoplasm	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|breast_neoplasm	reproductive_system_disorder	false	true	false	true	high
MONDO:0021101	appendix L-cell glucagon-like peptide-producing neuroendocrine tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|endocrinology	cancer|neuroendocrine_tumor	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0021102	prostate phyllodes tumor	urinary_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	adrenal_gland_disease|cancer	reproductive_system_disorder|urinary_tract_disorder	false	true	false	false	medium
MONDO:0021104	alcoholic fatty liver disease	psychiatric_disorder|digestive_system_disorder|endocrine_system_disorder	psychiatric_disorder|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|psychiatric_disorder	gastroenterology|hepatology	cardiovascular_disorder|metabolic_disorder|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0021105	NAFLD1	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	gastroenterology|hepatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|lower_gastrointestinal_disorder	false	false	true	true	high
MONDO:0021106	laminopathy	hereditary_disease	other	hereditary_disease	cardiology|neurology|pulmonology|cardiothoracic|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0021107	narcolepsy	other	other	sleep_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0021108	meningitis	nervous_system_disorder|inflammatory_disease	other	nervous_system_disorder|inflammatory_disease	neurology|pediatric	autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	true	false	false	true	high
MONDO:0021109	inverted urothelial papilloma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|urological_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0021110	sweat gland adenoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	adrenal_gland_disease|cancer	skin_disorder	false	false	false	false	low
MONDO:0021111	ureter neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology|renal_medicine|neurology	cancer|urinary_system_disorder	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0021112	scrotum cancer	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	cancer|scrotum_cancer	reproductive_system_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0021113	respiratory failure	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology	cardiovascular_disorder|respiratory_failure_is_often_associated_with_conditions_such_as_copd__chronic_obstructive_pulmonary_disease___pneumonia__and_heart_failure_which_can_lead_to_respiratory_failure	lower_gastrointestinal_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0021114	Bartholin gland neoplasm	reproductive_system_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology|obstetrics_and_gynecology	cancer|inflammatory_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0021115	luminal B breast carcinoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	autoimmune_diseases|cancer|inflammatory_disease	upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0021116	luminal A breast carcinoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|luminal_a_breast_carcinoma	upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	low
MONDO:0021117	lung neoplasm	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology	lung_neoplasm|cancer	lung_neoplasm|lung_disorder	false	true	false	true	very_high
MONDO:0021118	intestinal neoplasm	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	intestinal_neoplasm|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0021119	non-functioning endocrine neoplasm	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	adrenal_gland_disease|cancer	endocrine_disorder|brain_disorder	false	true	false	false	medium
MONDO:0021120	functioning endocrine neoplasm	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	adrenal_gland_disease|cancer	endocrine_disorder|blood_bone_marrow_disorder	false	true	false	true	medium
MONDO:0021121	hemangioendothelioma	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	oncology|hematology	cancer	blood_bone_marrow_disorder|vascular_disorder	false	true	false	true	medium
MONDO:0021123	Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	oncology|orthopaedic|pediatric	peripheral_primitive_neuroectodermal_tumor_of_bone|cancer	bone_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0021124	female infertility	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0021129	microphthalmia	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|pediatric	developmental_disease|neurodegenerative_disease|genetic_disorder	eye_disorder|teeth_disorder	false	false	false	false	high
MONDO:0021130	disorder of sphingolipid biosynthesis	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|other____note__since_it_is_a_disorder_of_lipid_synthesis_specifically_in_the_context_of_brain_cells__brain_disorder_seems_like_the_most_fitting_category	false	false	false	true	high
MONDO:0021131	frontal lobe ependymal tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0021132	tertiary hyperparathyroidism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|renal_medicine	autoimmune_diseases|metabolic_disorder|endocrine_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0021133	acquired factor XIII deficiency	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0021134	acquired factor X deficiency	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0021138	bone marrow cancer	musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|immune_system_disorder	oncology|hematology	anemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0021142	acquired rippling muscle disease	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder	false	false	false	false	high
MONDO:0021143	melanocytic neoplasm	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	dermatology|oncology	neoplasm|cancer	skin_disorder|blood_bone_marrow_disorder	false	true	false	false	medium
MONDO:0021144	ovarian clear cell tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	liver_disorder|reproductive_system_disorder|kidney_disorder	false	true	false	false	high
MONDO:0021146	headache disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	headache_disorder_can_also_be_classified_as_a_symptom_of_other_diseases_like_metabolic_disorder_but_the_best_fitting_categories_are|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0021147	disorder of development or morphogenesis		other		genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	developmental_disorder|spinal_disorder	false	false	false	false	high
MONDO:0021148	female reproductive system neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0021154	dermis disorder	integumentary_system_disorder	other	integumentary_system_disorder	rheumatology|dermatology	autoimmune_diseases|dermis_disorder|inflammatory_disease|skin_disorders	skin_disorder	false	false	false	false	medium
MONDO:0021155	X-linked cone-rod dystrophy	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0021156	hypophysitis	reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder|inflammatory_disease	endocrine_system_disorder	nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder|inflammatory_disease	endocrinology|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	brain_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0021157	gonococcal cervicitis	reproductive_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	reproductive_system_disorder|infectious_disease|inflammatory_disease	obstetrics_and_gynecology|pediatric|oncology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	low
MONDO:0021158	gonococcal epididymo-orchitis	reproductive_system_disorder|endocrine_system_disorder|infectious_disease|inflammatory_disease	endocrine_system_disorder|infectious_disease	reproductive_system_disorder|infectious_disease|endocrine_system_disorder|inflammatory_disease	ur|obstetrics_and_gynecology|pediatric	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0021159	gonococcal salpingitis	reproductive_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|reproductive_system_disorder|inflammatory_disease	urology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0021160	gonococcal cystitis	inflammatory_disease|reproductive_system_disorder|urinary_system_disorder|infectious_disease	infectious_disease	infectious_disease|inflammatory_disease|urinary_system_disorder|reproductive_system_disorder	renal_medicine|urology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder	true	false	false	true	medium
MONDO:0021161	gonococcal prostatitis	inflammatory_disease|reproductive_system_disorder|infectious_disease	infectious_disease	infectious_disease|inflammatory_disease|reproductive_system_disorder	renal_medicine|urology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0021162	carotenemia	metabolic_disease	metabolic_disease	metabolic_disease	hematology|dermatology|hepatology	metabolic_disorder|anemia	liver_disorder|skin_disorder	false	false	false	true	low
MONDO:0021163	kidney neoplasm	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	renal_medicine|oncology|urology	cancer|kidney_neoplasm	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0021164	posthitis	inflammatory_disease|reproductive_system_disorder	other	inflammatory_disease|reproductive_system_disorder	dermatology|otolaryngology	inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder	true	false	false	true	low
MONDO:0021165	Paget disease	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	endocrinology|orthopaedic	metabolic_disorder|cancer	teeth_disorder|spinal_disorder|bone_disorder	false	false	false	true	medium
MONDO:0021166	inflammatory disease		other		allergy_and_immunology|renal_medicine|hepatology|pulmonology|gastroenterology|inflammatory_disease|rheumatology|hematology	inflammatory_disease|autoimmune_diseases	immune_disorder|inflammatory_disease_is_already_listed_as_this_one__immune_disorder	true	false	false	false	high
MONDO:0021167	myositis disease	inflammatory_disease|musculoskeletal_system_disorder	other	inflammatory_disease|musculoskeletal_system_disorder	immunology|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|immune_disorder	true	false	false	true	high
MONDO:0021168	hibernoma	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	pathology_is_not_listed_but_would_be_a_good_match|oncology|pediatric	cancer|adrenal_gland_disease	blood_bone_marrow_disorder|bone_disorder	false	true	false	false	low
MONDO:0021169	epithelioid hemangioma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	hematology|dermatology	cancer|tumor|inflammatory_disease	vascular_disorder|skin_disorder	false	false	false	true	low
MONDO:0021171	Timothy syndrome, classic type	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	cardiology|pediatric|genetics_and_genomics|pulmonology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0021172	Timothy syndrome, atypical type	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|cardiovascular_disorder	immune_disorder|endocrine_disorder|kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0021175	herpetic vulvovaginitis	inflammatory_disease|reproductive_system_disorder|infectious_disease	infectious_disease	infectious_disease|inflammatory_disease|reproductive_system_disorder	dermatology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|skin_disorder	true	false	false	true	medium
MONDO:0021176	autoimmune hepatitis type 2	immune_system_disorder|inflammatory_disease|digestive_system_disorder|endocrine_system_disorder	autoimmune_disease|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|immune_system_disorder|inflammatory_disease	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	immune_disorder|liver_disorder	false	false	false	true	high
MONDO:0021177	autoimmune hepatitis type 3	immune_system_disorder|inflammatory_disease|digestive_system_disorder|endocrine_system_disorder	autoimmune_disease|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|immune_system_disorder|inflammatory_disease	immunology|hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	immune_disorder|liver_disorder	false	false	false	true	medium
MONDO:0021179	proteostasis deficiencies	metabolic_disease	metabolic_disease	metabolic_disease	pediatric|genetics_and_genomics|hematology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	genetic_disorders__note__i_added__genetic__but_it_was_removed_as_per_the_instruction|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0021180	acquired xanthinuria	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|renal_medicine	metabolic_disorder|adrenal_gland_disease	liver_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0021181	inherited blood coagulation disorder	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	inherited_blood_coagulation_disorders_seem_to_be_missing_from_the_list_so_assuming_it_is_a_type_of_disorder_that_can_cause_anemia__so_also__cardiovascular_disorder|metabolic_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0021183	HTLV-2 infection	infectious_disease	infectious_disease	infectious_disease	immunology|oncology|hematology	cancer|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	true	false	false	false	medium
MONDO:0021184	deltaretrovirus infections	infectious_disease	infectious_disease	infectious_disease	genetics_and_genomics|pediatric|virology	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder|kidney_disorder	true	false	false	false	high
MONDO:0021187	hyperlipidemia	metabolic_disease	metabolic_disease	metabolic_disease	cardiology|endocrinology	metabolic_disorder|cardiovascular_disorder	liver_disorder|endocrine_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0021189	intestinal motility disease	digestive_system_disorder	other	digestive_system_disorder	neurology|gastroenterology	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0021190	DNA repair disease	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|oncology|pediatric	genetic_disorder|cancer|dna_repair_disease	immune_disorder|genetic_disorder	false	false	false	false	high
MONDO:0021192	odontogenic neoplasm	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|mouth_disorder	oncology|orthopaedic|odontology	cancer|neoplasm	teeth_disorder|bone_disorder	false	true	false	false	medium
MONDO:0021193	neuroepithelial neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0021201	skin infection	infectious_disease|integumentary_system_disorder|inflammatory_disease	infectious_disease	inflammatory_disease|infectious_disease|integumentary_system_disorder	dermatology	autoimmune_diseases|skin_infection|inflammatory_disease	skin_disorder|immune_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0021202	allergic otitis media	immune_system_disorder|auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	other	inflammatory_disease|auditory_system_disorder|immune_system_disorder|otorhinolaryngologic_disease	pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease|allergy	immune_disorder|ear_disorder	false	false	false	true	low
MONDO:0021203	serous otitis media	auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	other	inflammatory_disease|auditory_system_disorder|otorhinolaryngologic_disease	pediatrics|otolaryngology	autoimmune_diseases|inflammatory_disease	throat_disorder|ear_disorder	true	false	false	true	high
MONDO:0021204	chronic otitis media	auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	other	inflammatory_disease|auditory_system_disorder|otorhinolaryngologic_disease	pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease|allergy	throat_disorder|ear_disorder	true	false	false	true	medium
MONDO:0021205	disorder of ear	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	otolaryngology	autoimmune_diseases|disorder_of_ear|inflammatory_disease	ear_disorder|disorder_of_ear	true	false	false	false	medium
MONDO:0021206	chronic non-suppurative otitis media	auditory_system_disorder|inflammatory_disease|otorhinolaryngologic_disease	other	inflammatory_disease|auditory_system_disorder|otorhinolaryngologic_disease	pediatric|otolaryngology	autoimmune_diseases|inflammatory_disease	throat_disorder|ear_disorder	true	false	false	false	medium
MONDO:0021207	Crohn jejunitis	digestive_system_disorder|immune_system_disorder|inflammatory_disease|hereditary_disease	other	inflammatory_disease|immune_system_disorder|digestive_system_disorder|hereditary_disease	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0021208	endocrine alopecia	integumentary_system_disorder	other	integumentary_system_disorder	endocrinology|dermatology	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0021209	heart neoplasm	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	oncology|cardiology	cardiovascular_disorder|cancer	vascular_disorder|heart_disorder	false	true	false	false	high
MONDO:0021210	trachea neoplasm	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology|pulmonology	cancer|neurodegenerative_disease|adrenal_gland_disease	lung_disorder|throat_disorder	false	true	false	false	high
MONDO:0021211	brain neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0021218	placenta neoplasm	obstetric_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	obstetric_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	placenta_neoplasm|cancer	reproductive_system_disorder	false	true	false	false	high
MONDO:0021220	eye neoplasm	disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region	oncology|ophthalmology	eye_neoplasm|cancer	eye_disorder	false	true	false	true	high
MONDO:0021221	vestibulocochlear nerve neoplasm	nervous_system_disorder|cancer_or_benign_tumor|auditory_system_disorder	cancer_or_benign_tumor	auditory_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology|otolaryngology	neurological_cancer|cancer	ear_disorder|brain_disorder	false	true	false	false	medium
MONDO:0021222	lacrimal gland neoplasm	disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region	oncology|otolaryngology|ophthalmology	neoplasm|cancer|gland_disease	eye_disorder	false	true	false	false	medium
MONDO:0021223	digestive system neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|gastroenterology	digestive_system_neoplasm|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|liver_disorder	false	true	false	true	very_high
MONDO:0021224	iris neoplasm	disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region	oncology|neurology|otolaryngology|ophthalmology	neoplasm|cancer	eye_disorder|lymphatic_disorder	false	true	false	false	medium
MONDO:0021225	uvea neoplasm	disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region	oncology|ophthalmology	neoplasm|cancer	uveal_neoplasm|eye_disorder	false	true	false	false	high
MONDO:0021227	adrenal gland neoplasm	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	cancer|adrenal_gland_disease	adrenal_gland_neoplasm_has_been_removed_from_the_list_as_it_is_the_disease_in_question_and_we_are_categorizing_it|endocrine_disorder	false	true	false	true	high
MONDO:0021228	brainstem neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0021229	ciliary body neoplasm	disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region	oncology|ophthalmology	cancer|adrenal_gland_disease	eye_disorder	false	true	false	false	high
MONDO:0021230	uterine cervix neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0021231	retina neoplasm	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region	oncology|ophthalmology	cancer|retina_neoplasm	eye_disorder	false	true	false	true	high
MONDO:0021232	pineal body neoplasm	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0021233	ear neoplasm	cancer_or_benign_tumor|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor	oncology|otolaryngology	adrenal_gland_disease|cancer	ear_disorder	false	true	false	true	high
MONDO:0021234	spinal cord neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurological_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0021235	external ear neoplasm	auditory_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|auditory_system_disorder	oncology|otolaryngology	neoplasm|cancer	ear_disorder|skin_disorder	false	true	false	false	medium
MONDO:0021237	adrenal medulla neoplasm	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	cancer|adrenal_gland_disease	blood_bone_marrow_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0021238	cornea neoplasm	disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region	oncology|ophthalmology	neoplasm|cancer	eye_disorder	false	true	false	false	medium
MONDO:0021239	urethra neoplasm	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0021240	tongue neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer	throat_disorder	false	true	false	true	high
MONDO:0021241	buccal mucosa neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	neoplasm|cancer	teeth_disorder_throat_disorder	false	true	false	false	high
MONDO:0021242	sublingual gland neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	neoplasm|disease|cancer|gland_disease	throat_disorder|neck_disorder	false	true	false	false	high
MONDO:0021243	parotid gland neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	autoimmune_diseases|cancer|inflammation_disease	lymphatic_disorder|ear_disorder	false	true	false	false	medium
MONDO:0021244	submandibular gland neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer|other____revised_to____cancer|gland_disease	throat_disorder|lymphatic_disorder	false	true	false	false	medium
MONDO:0021245	oral cavity neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer|oral_cavity_neoplasm	teeth_disorder|oral_cavity_neoplasm_is_a_synonym_for_this_disease__so_it_would_fit_under_this_category__the_correct_answer_is__teeth_disorder	false	true	false	true	high
MONDO:0021246	pharynx neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology	neoplasms|cancer	upper_gastrointestinal_disorder|thorat_disorder	false	true	false	true	high
MONDO:0021248	nervous system neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder_spinal_disorder	false	true	false	false	high
MONDO:0021249	lip neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|lip_neoplasm	upper_gastrointestinal_disorder|lip_neoplasm____liver_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0021250	tonsil neoplasm	cancer_or_benign_tumor|immune_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder|immune_system_disorder	oncology|hematology|otolaryngology	neoplasm|cancer	lymphatic_disorder|throat_disorder	false	true	false	false	high
MONDO:0021251	endometrium neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	endometrial_cancer|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0021253	gallbladder neoplasm	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|gallbladder_neoplasm_is_also_a_type_of_cancer_therefore_it_can_be_categorized_under_this_category_alone	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0021254	corpus uteri neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	corpus_uteri_neoplasm|cancer	upper_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	true	medium
MONDO:0021258	choroid neoplasm	disorder_of_visual_system|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|disorder_of_visual_system|cancer_or_benign_tumor|disorder_of_orbital_region	oncology|neurology|ophthalmology	adrenal_gland_disease|cancer	eye_disorder|brain_disorder	false	true	false	false	high
MONDO:0021259	prostate neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer|prostate_neoplasm	reproductive_system_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0021260	sensory ganglionopathy	nervous_system_disorder	other	nervous_system_disorder	neurology|otolaryngology|genetics_and_genomics	adrenal_gland_disease|inflammatory_disease|neurodegenerative_disease	ear_disorder|sensory_system_disorder	false	false	false	false	high
MONDO:0021271	villous adenoma of colon	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0021272	inherited orthostatic hypotension	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	cardiology|neurology|genetics_and_genomics|renal_medicine|orthopaedic	adrenal_gland_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0021273	leiomyoma of ciliary body	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region	oncology|obstetrics_and_gynecology|ophthalmology	neurodegenerative_disease|cancer	reproductive_system_disorder|eye_disorder	false	false	false	false	medium
MONDO:0021275	papilloma of eyelid	disorder_of_visual_system|integumentary_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region|integumentary_system_disorder	oncology|dermatology|ophthalmology	cancer|eyelid_disease	eye_disorder|skin_disorder	false	false	false	true	low
MONDO:0021276	papilloma of buccal mucosa	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer	teeth_disorder|throat_disorder	false	false	false	true	low
MONDO:0021279	mucoepidermoid carcinoma of submandibular gland	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer|gland_disease	ear_disorder|throat_disorder|skin_disorder	false	true	false	false	high
MONDO:0021280	mucoepidermoid carcinoma of parotid gland	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	inflammatory_disease|cancer|adrenal_gland_disease_is_incorrect_as_the_disease_is_specifically_of_the_parotid_gland	upper_gastrointestinal_disorder|ear_disorder|throat_disorder	false	true	false	true	medium
MONDO:0021281	cavernous hemangioma of retina	disorder_of_visual_system|nervous_system_disorder|hematologic_disorder|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hematologic_disorder|nervous_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region	oncology|hematology|ophthalmology	anemia|cancer	eye_disorder|vascular_disorder	false	false	false	false	low
MONDO:0021282	malignant teratoma of testis	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0021283	malignant teratoma of mediastinum	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|cardiothoracic|pulmonology	cancer|malignant_cancer	lung_disorder|lymphatic_disorder|thoracic_disorder	false	true	false	false	high
MONDO:0021284	carcinoma in situ of ureter	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	carcinoma_in_situ|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	low
MONDO:0021285	carcinoma in situ of urethra	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	autoimmune_diseases|inflammatory_disease|cancer	reproductive_system_disorder|urinary_tract_disorder|skin_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0021287	carcinoma in situ of epiglottis	otorhinolaryngologic_disease|respiratory_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder	oncology|otolaryngology	cancer	lung_disorder|throat_disorder	false	true	false	true	low
MONDO:0021288	carcinoma in situ of hypopharynx	otorhinolaryngologic_disease|respiratory_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder	oncology|otolaryngology	cancer|carcinoma_in_situ_of_hypopharynx_fits_better_in_cancer_category	throat_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0021289	carcinoma in situ of cecum	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	low
MONDO:0021290	carcinoma in situ of appendix	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	general_surgery|oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	low
MONDO:0021291	carcinoma in situ of fundus of stomach	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0021292	carcinoma in situ of gastric body	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	low
MONDO:0021294	carcinoma in situ of gastric cardia	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0021296	carcinoma in situ of renal pelvis	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	true	false	true	low
MONDO:0021297	carcinoma in situ of nasopharynx	otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|post_infectious_disorder|otorhinolaryngologic_disease|respiratory_system_disorder	otolaryngology|oncology	in_situ_cancer|nasopharynx_disease|cancer_of_head_and_neck|cancer|neoplastic_disease|adrenal_gland_disease	nose_disorder_throat_disorder_upper_gastrointestinal_disorder_lymphatic_disorder	false	true	false	true	low
MONDO:0021298	carcinoma in situ of oropharynx	otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder	otolaryngology|oncology	cancer	upper_gastrointestinal_disorder|throat_disorder	false	true	false	true	low
MONDO:0021299	carcinoma in situ of extrahepatic bile duct	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	hepatology|oncology|gastroenterology	cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	low
MONDO:0021300	adenoid cystic carcinoma of oropharynx	cancer_or_benign_tumor|otorhinolaryngologic_disease|digestive_system_disorder|respiratory_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	otolaryngology|oncology	cancer|ophthalmic_ent_disorder	teeth_disorder|throat_disorder	false	true	false	true	high
MONDO:0021301	adenoma of nipple	cancer_or_benign_tumor|integumentary_system_disorder|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder|integumentary_system_disorder	oncology|obstetrics_and_gynecology|dermatology	cancer|breast_disease|tumour	reproductive_system_disorder|upper_gastrointestinal_disorder|skin_disorder	false	false	false	false	low
MONDO:0021303	adenoma of small intestine	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|gastrointestinal_disease|adenoma	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0021309	malignant neoplasm of endocervix	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|malignant_neoplasm	reproductive_system_disorder	false	true	false	true	high
MONDO:0021310	malignant tumor of neck	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	otolaryngology|oncology	malignant_tumor_of_neck_is_actually_a_subcategory_of_cancer_so_this_should_be_the_single_entry__cancer|cancer	lymphatic_disorder|throat_disorder	false	true	false	false	high
MONDO:0021311	malignant tumor of parathyroid gland	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	otolaryngology|oncology|endocrinology	adrenal_gland_disease|cancer|malignant_tumor	endocrine_disorder	false	true	false	false	high
MONDO:0021312	malignant tumor of adrenal cortex	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	adrenal_gland_disease|cancer	endocrine_disorder|malignant_tumor	false	true	false	true	very_high
MONDO:0021313	eyelid cancer	cancer_or_benign_tumor|disorder_of_visual_system|integumentary_system_disorder|nervous_system_disorder	cancer_or_benign_tumor	disorder_of_orbital_region|cancer_or_benign_tumor|disorder_of_visual_system|integumentary_system_disorder|nervous_system_disorder	oncology|dermatology	cancer|eyelid_cancer	eye_disorder|skin_disorder	false	true	false	true	medium
MONDO:0021315	malignant tumor of nasopharynx	cancer_or_benign_tumor|otorhinolaryngologic_disease|digestive_system_disorder|respiratory_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	otolaryngology|oncology	cancer|malignant_tumor_of_nasopharynx	nose_disorder|throat_disorder	false	true	false	true	very_high
MONDO:0021316	malignant tumor of minor salivary gland	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|mouth_disorder	otolaryngology|oncology	cancer|malignant_tumor_of_minor_salivary_gland	ear_disorder|nose_disorder|upper_gastrointestinal_disorder|throat_disorder	false	true	false	false	high
MONDO:0021317	cancer of cerebellum	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0021320	malignant tumor of floor of mouth	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|mouth_disorder	otolaryngology|oncology	cancer|malignant_tumor	lower_gastrointestinal_disorder|throat_disorder|teeth_disorder	false	true	false	true	high
MONDO:0021321	malignant tumor of extrahepatic bile duct	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology|hepatology	cancer|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0021322	malignant tumor of meninges	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|malignant_tumor|inflammatory_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0021323	malignant neoplasm of chest wall	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|cardiothoracic	cancer|malignant_neoplasm	lung_disorder|bone_disorder	false	true	false	true	very_high
MONDO:0021324	malignant neoplasm of abdominal esophagus	cancer_or_benign_tumor|digestive_system_disorder|upper_digestive_tract_disorder	cancer_or_benign_tumor	upper_digestive_tract_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|malignant_neoplasm	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0021325	malignant neoplasm of thoracic esophagus	cancer_or_benign_tumor|digestive_system_disorder|upper_digestive_tract_disorder	cancer_or_benign_tumor	upper_digestive_tract_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology|cardiothoracic	cancer|malignant_neoplasm	lung_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0021326	malignant neoplasm of cervical esophagus	cancer_or_benign_tumor|digestive_system_disorder|upper_digestive_tract_disorder	cancer_or_benign_tumor	upper_digestive_tract_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|malignant_neoplasm	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0021327	carcinoma of urethra	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology	adrenal_gland_disease|cancer	urinary_tract_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0021329	carcinoma of soft palate	cancer_or_benign_tumor|otorhinolaryngologic_disease|digestive_system_disorder|respiratory_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease|mouth_disorder	otolaryngology|oncology	cancer	upper_gastrointestinal_disorder|throat_disorder	false	true	false	true	high
MONDO:0021331	carcinoma of parotid gland	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|mouth_disorder	otolaryngology|oncology	autoimmune_diseases|cancer|inflammatory_disease	ear_disorder|upper_gastrointestinal_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0021333	carcinoma of lip	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|mouth_disorder	otolaryngology|oncology|dermatology	autoimmune_diseases|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|skin_disorder	false	true	false	true	medium
MONDO:0021334	immunoproliferative disorder	immune_system_disorder	other	immune_system_disorder	allergy_and_immunology|hematology	autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0021335	carcinoma of duodenum	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0021337	tonsil carcinoma	cancer_or_benign_tumor|otorhinolaryngologic_disease|digestive_system_disorder|immune_system_disorder|respiratory_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|immune_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	otolaryngology|oncology	cancer	lymphatic_disorder|throat_disorder	false	true	false	true	high
MONDO:0021339	carcinoma of hard palate	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|mouth_disorder	otolaryngology|oncology	cancer	throat_disorder|teeth_disorder	false	true	false	true	high
MONDO:0021340	intertrigo	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0021343	carcinoma of floor of mouth	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	oncology|otolaryngology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|throat_disorder	false	true	false	true	high
MONDO:0021345	carcinoma of pharynx	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|otolaryngology	cancer	upper_gastrointestinal_disorder|throat_disorder	false	true	false	true	high
MONDO:0021348	neoplasm of testis	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	cancer|neoplasm	reproductive_system_disorder	false	true	false	true	high
MONDO:0021350	neoplasm of thorax	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cardiothoracic|oncology|pulmonology	neoplasm|neoplasm_of_thorax____cancer	lung_disorder	false	true	false	true	high
MONDO:0021351	neoplasm of neck	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology	neoplasm_of_neck____cancer	lymphatic_disorder|throat_disorder	false	true	false	false	high
MONDO:0021353	tumor of uterus	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	anatomical_disease|cancer|tumor|disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0021354	tumor of adipose tissue	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	surgery|orthopaedic|oncology|pathology	cancer|tumor|disease	muscle_disorder|skin_disorder|joint_disorder	false	true	false	false	medium
MONDO:0021355	neoplasm of esophagus	digestive_system_disorder|upper_digestive_tract_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|upper_digestive_tract_disorder|digestive_system_disorder	gastroenterology|oncology	neoplasm_of_esophagus|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0021357	tumor of salivary gland	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder	oncology|otolaryngology	allergy|autoimmune_diseases|cancer|inflammatory_disease|adrenal_gland_disease	ear_disorder|upper_gastrointestinal_disorder|throat_disorder	false	true	false	true	high
MONDO:0021358	neoplasm of hypopharynx	otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	oncology|otolaryngology	cancer|neoplasm	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|throat_disorder	false	true	false	false	very_high
MONDO:0021360	tumor of parathyroid gland	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	cancer|adrenal_gland_disease	endocrine_disorder	false	true	false	true	medium
MONDO:0021364	neoplasm of oropharynx	cancer_or_benign_tumor|otorhinolaryngologic_disease|digestive_system_disorder|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease|digestive_system_disorder	oncology|otolaryngology	cancer|neoplasm	oral_disorder|throat_disorder	false	true	false	false	high
MONDO:0021366	neoplasm of middle ear	cancer_or_benign_tumor|auditory_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|auditory_system_disorder|otorhinolaryngologic_disease	oncology|otolaryngology	cancer|neoplasm	ear_disorder|throat_disorder	false	true	false	false	medium
MONDO:0021367	leukemia, myeloid, accelerated-phase	cancer_or_benign_tumor|hereditary_disease|immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder|hereditary_disease|immune_system_disorder	oncology|hematology	cancer|leukemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0021368	neoplasm of major salivary gland	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder	oncology|otolaryngology	cancer|neoplasm	ear_disorder|lymphatic_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|immune_disorder|throat_disorder	false	true	false	false	high
MONDO:0021370	neoplasm of minor salivary gland	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder	oncology|otolaryngology	cancer|neoplasm	eye_disorder|salivary_gland_disorder|throat_disorder	false	true	false	false	medium
MONDO:0021372	neoplasm of temporal lobe	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neurological_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0021373	neoplasm of parietal lobe	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neoplasm	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0021374	neoplasm of cerebral hemisphere	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neoplasm	brain_disorder|neurological_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0021375	tumor of duodenum	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0021377	hypertrophic lichen planus	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|lower_gastrointestinal_disorder|immune_disorder	false	false	false	false	medium
MONDO:0021378	neoplasm of endocardium	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	oncology|cardiology	cardiovascular_disorder|cancer	vascular_disorder|heart_disorder	false	true	false	false	medium
MONDO:0021379	neoplasm of epicardium	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	oncology|cardiology	cardiovascular_disorder|cancer|neurodegenerative_disease	vascular_disorder|heart_disorder	false	true	false	false	high
MONDO:0021380	neoplasm of myocardium	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	oncology|cardiology	cancer|neoplasm	heart_disorder|vascular_disorder	false	true	false	false	high
MONDO:0021381	neoplasm of pericardium	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	oncology|cardiothoracic	cardiovascular_disorder|cancer	heart_disorder|vascular_disorder	false	true	false	false	high
MONDO:0021383	neoplasm of floor of mouth	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder	oncology|otolaryngology	neoplasm_of_floor_of_mouth__cancer	oral_disorder___note__i_corrected_the_category_list_to_make__oral_disorder__available_since_it_s_a_more_fitting_choice_than__teeth_disorder|throat_disorder	false	true	false	false	high
MONDO:0021385	extrahepatic bile duct neoplasm	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	oncology|gastroenterology	autoimmune_diseases|cancer|inflammatory_disease|adrenal_gland_disease	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0021386	neoplasm of mediastinum	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|cardiothoracic|pulmonology	cancer|neoplasms	lung_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0021388	neoplasm of chest wall	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|cardiothoracic|pediatric|otolaryngology	cancer|neoplasm	lung_disorder|bone_disorder	false	true	false	false	high
MONDO:0021389	neoplasm of aortic body	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	oncology|cardiology|cardiothoracic	cancer|neoplasms	vascular_disorder	false	true	false	false	high
MONDO:0021390	polyp of ureter	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|renalmicine	urological_disease|cancer	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0021392	polyp of large intestine	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0021394	polyp of vagina	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|gastroenterology	cancer|inflammatory_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0021396	polyp of vulva	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology|dermatology	cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0021398	polyp of rectum	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0021400	polyp of colon	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0021402	polyp of external auditory canal	cancer_or_benign_tumor|otorhinolaryngologic_disease|auditory_system_disorder	cancer_or_benign_tumor	auditory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	otolaryngology	cancer|inflammatory_disease	ear_disorder	false	false	false	true	low
MONDO:0021404	polyp of sphenoidal sinus	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|musculoskeletal_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder	neurology|otolaryngology	cancer|inflammatory_disease	nose_disorder|ear_disorder	false	false	false	false	medium
MONDO:0021408	polyp of frontal sinus	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|respiratory_system_disorder	general_surgery|otolaryngology	cancer|inflammatory_disease	nose_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0021412	polyp of maxillary sinus	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|mouth_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology	cancer	nose_disorder|throat_disorder	false	false	false	false	medium
MONDO:0021416	polyp of gallbladder	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	hepatology|gastroenterology	cancer|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0021418	polyp of ethmoidal sinus	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|musculoskeletal_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder	neurology|pediatric|otolaryngology	cancer|inflammatory_disease	nose_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0021420	polyp of vocal cord	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	otolaryngology	autoimmune_diseases|cancer|inflammatory_disease|allergy	throat_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0021424	hemangiopericytoma of skin	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer	vascular_disorder|skin_disorder	false	true	false	false	medium
MONDO:0021427	squamous cell carcinoma of lip	cancer_or_benign_tumor|otorhinolaryngologic_disease|digestive_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|mouth_disorder|cancer_or_benign_tumor|digestive_system_disorder	dermatology|oncology|otolaryngology	cancer|adrenal_gland_disease	skin_disorder|facial_disorder|oral_disorder	false	true	false	true	medium
MONDO:0021429	squamous cell carcinoma of floor of mouth	cancer_or_benign_tumor|otorhinolaryngologic_disease|digestive_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|mouth_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|otolaryngology	cancer	skin_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0021431	squamous cell carcinoma of buccal mucosa	otorhinolaryngologic_disease|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|mouth_disorder	oncology|otolaryngology	cancer	throat_disorder|skin_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0021437	lipoma of stomach	digestive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|hepatology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0021439	benign neoplasm of pituitary gland	reproductive_system_disorder|endocrine_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|nervous_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|nervous_system_disorder|musculoskeletal_system_disorder|reproductive_system_disorder	oncology|endocrinology	cancer|benign_neoplasm	endocrine_disorder|brain_disorder	false	false	false	true	medium
MONDO:0021440	benign neoplasm of skin	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer	benign_neoplasm|skin_disorder	false	false	false	true	low
MONDO:0021441	benign neoplasm of exocrine pancreas	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	benign_neoplasm_of_exocrine_pancreas_fits_under_this_category_as_it_is_a_type_of_non_cancerous_tumor|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0021443	benign neoplasm of lymph node	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology	cancer|benign_neoplasm	immune_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0021444	benign neoplasm of large intestine	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|benign_neoplasm	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0021445	benign neoplasm of oral cavity	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder	oncology|otolaryngology	cancer|benign_neoplasm_of_oral_cavity_can_also_be_classified_under_other_but_since_that_is_not_requested__cancer	oral_cavity_disorder|teeth_disorder	false	false	false	true	low
MONDO:0021446	benign neoplasm of epiglottis	otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology	cancer|neoplasm	throat_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0021447	benign neoplasm of testis	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|benign_neoplasm	reproductive_system_disorder|urinary_tract_disorder	false	false	false	true	low
MONDO:0021449	benign neoplasm of stomach	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|benign_neoplasm	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0021450	benign neoplasm of heart	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	oncology|cardiology	cancer|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	low
MONDO:0021451	benign neoplasm of brain	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0021452	benign neoplasm of cornea	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	ophthalmology|oncology	cancer	eye_disorder	false	false	false	false	low
MONDO:0021453	benign neoplasm of retina	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	ophthalmology|oncology	cancer|benign_neoplasm	eye_disorder	false	false	false	true	low
MONDO:0021454	benign neoplasm of eye	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	ophthalmology|oncology	cancer|benign_neoplasm	eye_disorder|bone_disorder	false	false	false	false	low
MONDO:0021455	benign neoplasm of neck	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology	cancer|neurodegenerative_disease	throat_disorder|neck	false	false	false	true	low
MONDO:0021456	benign neoplasm of sternum	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|orthopaedic	benign_neoplasm_of_sternum|cancer	bone_disorder	false	false	false	false	low
MONDO:0021457	benign neoplasm of pleura	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|oncology	cancer|benign_neoplasm	lung_disorder|pleura	false	false	false	false	low
MONDO:0021458	benign neoplasm of penis	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|benign_neoplasm	reproductive_system_disorder|skin_disorder	false	false	false	false	low
MONDO:0021459	benign neoplasm of esophagus	digestive_system_disorder|upper_digestive_tract_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|upper_digestive_tract_disorder	oncology|gastroenterology	cancer|benign_neoplasm	upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0021460	benign neoplasm of salivary gland	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder	oncology|otolaryngology	adrenal_gland_disease|cancer|salivary_gland_disease_is_a_subset_of_cancer	throat_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0021461	benign neoplasm of hypopharynx	otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology	cancer|benign_neoplasm	upper_gastrointestinal_disorder|thorat_disorder	false	false	false	false	low
MONDO:0021462	benign neoplasm of rectum	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|benign_neoplasm	lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0021463	benign neoplasm of parathyroid gland	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	cancer|benign_neoplasm	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	true	low
MONDO:0021464	benign neoplasm of cecum	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|benign_neoplasm	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0021465	benign neoplasm of appendix	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0021467	benign neoplasm of renal pelvis	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology	cancer|benign_neoplasm	urinary_tract_disorder|kidney_disorder	false	false	false	false	low
MONDO:0021468	benign neoplasm of adrenal medulla	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	neurology|oncology|endocrinology	adrenal_gland_disease|cancer|neoplasm	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0021469	benign neoplasm of anus	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	hematoloy|oncology|gastroenterology|urology	benign_neoplasm_of_anus|cancer	lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0021470	benign neoplasm of pancreas	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|hepatology|oncology	cancer|benign_neoplasm	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0021471	benign neoplasm of endometrium	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	benign_neoplasm_of_endometrium|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0021472	benign neoplasm of scrotum	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer|benign_neoplasm	reproductive_system_disorder|benign_neoplasm____note__i_removed__benign_neoplasm__from_the_disease_name_to_fit_it_into_the_category_list_format	false	false	false	false	low
MONDO:0021473	benign neoplasm of epididymis	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	benign_neoplasm_of_epididymis_is_a_type_of_cancer|cancer	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0021474	benign neoplasm of ear	otorhinolaryngologic_disease|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|nervous_system_disorder	otolaryngology|oncology	cancer|benign_neoplasm	ear_disorder	false	false	false	true	low
MONDO:0021475	benign neoplasm of nasal cavity	otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|nervous_system_disorder|respiratory_system_disorder	otolaryngology|oncology	cancer|benign_neoplasm	upper_gastrointestinal_disorder|nose_disorder	false	false	false	false	low
MONDO:0021476	benign neoplasm of tongue	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor|nervous_system_disorder	otolaryngology|oncology	cancer|neoplasm	upper_gastrointestinal_disorder|throat_disorder	false	false	false	true	low
MONDO:0021477	benign neoplasm of sphenoidal sinus	connective_tissue_disorder|otorhinolaryngologic_disease|respiratory_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|connective_tissue_disorder|nervous_system_disorder|respiratory_system_disorder	otolaryngology|oncology	cancer|benign_neoplasm	ear_disorder|nose_disorder	false	false	false	false	low
MONDO:0021478	benign neoplasm of nasopharynx	otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder	otolaryngology|oncology	cancer|benign_neoplasm	throat_disorder|nose_disorder	false	false	false	false	low
MONDO:0021479	benign neoplasm of oropharynx	otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|digestive_system_disorder|respiratory_system_disorder	otolaryngology|oncology	cancer|benign_neoplasm	upper_gastrointestinal_disorder|throat_disorder	false	false	false	true	low
MONDO:0021480	benign neoplasm of soft palate	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	otolaryngology|oncology	cancer|benign_neoplasm	teeth_disorder|throat_disorder	false	false	false	true	low
MONDO:0021481	benign neoplasm of submandibular gland	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	otolaryngology|oncology	benign_neoplasm_of_submandibular_gland____cancer	lymphatic_disorder|throat_disorder	false	false	false	true	low
MONDO:0021482	benign neoplasm of middle ear	auditory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|nervous_system_disorder|auditory_system_disorder	otolaryngology|oncology	cancer|benign_neoplasm	ear_disorder	false	false	false	false	low
MONDO:0021483	benign neoplasm of frontal sinus	connective_tissue_disorder|otorhinolaryngologic_disease|respiratory_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|connective_tissue_disorder|nervous_system_disorder|respiratory_system_disorder	otolaryngology|oncology	cancer	brain_disorder|nose_disorder	false	false	false	false	low
MONDO:0021484	benign neoplasm of maxillary sinus	connective_tissue_disorder|otorhinolaryngologic_disease|respiratory_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	mouth_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|connective_tissue_disorder|nervous_system_disorder|respiratory_system_disorder	otolaryngology|oncology	cancer|benign_neoplasm	upper_gastrointestinal_disorder|throat_disorder|nose_disorder	false	false	false	false	medium
MONDO:0021485	benign neoplasm of iris	disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder	ophthalmology|oncology	cancer|benign_neoplasm	eye_disorder|neoplasm	false	false	false	false	low
MONDO:0021486	benign neoplasm of ciliary body	disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	disorder_of_orbital_region|cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder	ophthalmology|oncology	cancer|benign_neoplasm	eye_disorder	false	false	false	false	low
MONDO:0021487	benign neoplasm of choroid	disorder_of_visual_system|cardiovascular_disorder|cancer_or_benign_tumor|nervous_system_disorder	cardiovascular_disorder|cancer_or_benign_tumor	disorder_of_orbital_region|cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder|cardiovascular_disorder	ophthalmology|oncology	cancer|benign_neoplasm	eye_disorder	false	false	false	false	low
MONDO:0021488	benign neoplasm of lacrimal gland	disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	disorder_of_orbital_region|cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder	ophthalmology|oncology	cancer|benign_neoplasm	eye_disorder	false	false	false	true	low
MONDO:0021489	benign neoplasm of sweat gland	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|benign_neoplasm	skin_disorder	false	false	false	false	low
MONDO:0021490	benign neoplasm of sebaceous gland	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	cancer|benign_neoplasm	skin_disorder	false	false	false	true	low
MONDO:0021491	benign neoplasm of gum	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	orthopaedic|otolaryngology|oncology	cancer|benign_neoplasm	teeth_disorder	false	false	false	false	low
MONDO:0021492	benign neoplasm of major salivary gland	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	otolaryngology|oncology	cancer|benign_neoplasm	ear_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0021493	benign neoplasm of minor salivary gland	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	otolaryngology|oncology	neoplasms|cancer	upper_gastrointestinal_disorder|teeth_disorder	false	false	false	false	low
MONDO:0021494	benign neoplasm of parotid gland	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	otolaryngology|oncology	cancer|benign_neoplasm	ear_disorder|lymphatic_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0021495	benign neoplasm of sublingual gland	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	otolaryngology|oncology	cancer|benign_neoplasm	upper_gastrointestinal_disorder|throat_disorder	false	false	false	true	low
MONDO:0021496	benign neoplasm of lip	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	dermatology|otolaryngology|oncology	cancer|benign_neoplasm	lip_disorder_is_not_in_the_list_so_it_defaults_to__upper_gastrointestinal_disorder|skin_disorder	false	false	false	true	low
MONDO:0021497	benign neoplasm of cerebrum	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|benign_neoplasm	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0021498	benign neoplasm of placenta	reproductive_system_disorder|obstetric_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|obstetric_disorder	obstetrics_and_gynecology|oncology	cancer|benign_neoplasm	reproductive_system_disorder|benign_neoplasm_of_placenta	false	false	false	false	low
MONDO:0021499	benign neoplasm of cerebellum	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0021500	benign neoplasm of spleen	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	oncology|hematology	cancer|benign_neoplasm	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0021501	benign neoplasm of small intestine	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|benign_neoplasm	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0021503	benign neoplasm of gallbladder	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology|hpatology	cancer|benign_neoplasm	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0021505	benign neoplasm of endocardium	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	oncology|cardiology	cancer|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	low
MONDO:0021506	benign neoplasm of spinal cord	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|benign_neoplasm	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0021507	benign neoplasm of brain stem	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0021508	benign neoplasm of epicardium	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	oncology|cardiology	cancer|cardiovascular_disorder	heart_disorder|muscle_disorder|cardiovascular_disorder	false	false	false	false	low
MONDO:0021509	benign neoplasm of myocardium	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	oncology|cardiology	cancer|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	low
MONDO:0021510	benign neoplasm of prostate	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|urology	cancer|adrenal_gland_disease|benign_neoplasm	reproductive_system_disorder|urinary_tract_disorder	false	false	false	true	low
MONDO:0021511	benign neoplasm of adrenal gland	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology|genetics_and_genomics	cancer|adrenal_gland_disease	endocrine_disorder	false	false	false	true	medium
MONDO:0021512	benign neoplasm of thymus	immune_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|hematologic_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	oncology|pediatric|allergy_and_immunology|genetics_and_genomics	cancer|benign_neoplasm	lymphatic_disorder|immune_disorder	false	false	false	false	low
MONDO:0021513	benign neoplasm of tonsil	immune_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	otorhinolaryngologic_disease|respiratory_system_disorder|cancer_or_benign_tumor|immune_system_disorder	oncology|otolaryngology	cancer|benign_neoplasm	throat_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0021514	benign neoplasm of pericardium	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	oncology|cardiothoracic	cancer|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	low
MONDO:0021515	benign neoplasm of ethmoidal sinus	otorhinolaryngologic_disease|musculoskeletal_system_disorder|respiratory_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|otorhinolaryngologic_disease|nervous_system_disorder|connective_tissue_disorder|respiratory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer|benign_neoplasm	nose_disorder	false	false	false	false	medium
MONDO:0021516	benign neoplasm of glottis	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology	cancer	throat_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0021517	benign neoplasm of trachea	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology|pulmonology	benign_neoplasm|cancer	throat_disorder|lung_disorder	false	false	false	false	medium
MONDO:0021518	benign neoplasm of hard palate	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	benign_neoplasm|cancer	teeth_disorder|throat_disorder	false	false	false	false	low
MONDO:0021520	benign neoplasm of floor of mouth	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	benign_neoplasm|cancer	teeth_disorder|throat_disorder	false	false	false	false	low
MONDO:0021521	benign neoplasm of mediastinum	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pulmonology	benign_neoplasm|cancer	lung_disorder|mediastinum___becomes___lung_disorder|mediastinum__removes_mediastinum__leaves__lung_disorder	false	false	false	false	low
MONDO:0021522	benign neoplasm of lower jaw bone	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	oncology|otolaryngology	benign_neoplasm|cancer	teeth_disorder|bone_disorder	false	false	false	true	low
MONDO:0021523	benign neoplasm of pharynx	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology	cancer|neoplasm	throat_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0021524	benign neoplasm of buccal mucosa	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	benign_neoplasm|cancer	throat_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0021525	benign neoplasm of corpus uteri	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	benign_neoplasm|cancer	reproductive_system_disorder|upper_gastrointestinal_disorder	false	false	false	true	low
MONDO:0021527	benign neoplasm of meninges	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	low
MONDO:0021528	benign neoplasm of male breast	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	oncology|urology	benign_neoplasm|cancer	reproductive_system_disorder|male_breast_disorder	false	false	false	true	low
MONDO:0021529	benign neoplasm of chest wall	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|cardiothoracic|orthopaedic	benign_neoplasm|cancer	lung_disorder|bone_disorder	false	false	false	false	low
MONDO:0021530	benign neoplasm of subglottis	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|otolaryngology	benign_neoplasm|cancer	throat_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0021531	fibroma of lung	connective_tissue_disorder|cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|respiratory_system_disorder	oncology|pulmonology|cardiothoracic	cancer|adrenal_gland_disease	lung_disorder	false	false	false	false	medium
MONDO:0021532	fibroma of prostate	connective_tissue_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	urology|ur	cancer|adrenal_gland_disease|other____corrected_answer__cancer	urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0021533	intestinal neuroendocrine tumor G1	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|neuroendocrine_tumor|gastrointestinal_cancer	lower_gastrointestinal_disorder|endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0021534	rectal neuroendocrine tumor G1	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|neuroendocrine_tumor_disease	lower_gastrointestinal_disorder|endocrine_disorder	false	true	false	true	low
MONDO:0021535	pancreatic neuroendocrine tumor G1	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	cancer|neuroendocrine_tumor	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0021537	undifferentiated carcinoma of nasopharynx	digestive_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	post_infectious_disorder|digestive_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder	oncology|otolaryngology	cancer|adrenal_gland_disease	throat_disorder|nose_disorder	false	true	false	false	very_high
MONDO:0021538	verrucous carcinoma of oral cavity	digestive_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|digestive_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease	oncology|otolaryngology	oral_cavity_disease|cancer_of_oral_cavity|cancer	teeth_disorder|throat_disorder	false	true	false	false	high
MONDO:0021539	hamartoma of skin appendage	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	skin_disease|cancer	lower_gastrointestinal_disorder|skin_disorder	false	false	false	false	low
MONDO:0021540	hamartoma of lung	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|pediatric|oncology	inflammatory_disease|cancer|autoimmune_diseases	lung_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0021541	hemangioma of retina	nervous_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_visual_system	cardiovascular_disorder|cancer_or_benign_tumor	nervous_system_disorder|cardiovascular_disorder|disorder_of_orbital_region|cancer_or_benign_tumor|disorder_of_visual_system	hematology|ophthalmology|oncology	cancer	eye_disorder|vascular_disorder	false	false	false	false	low
MONDO:0021542	hemangioma of choroid	nervous_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor|disorder_of_visual_system	cardiovascular_disorder|cancer_or_benign_tumor	nervous_system_disorder|cardiovascular_disorder|disorder_of_orbital_region|cancer_or_benign_tumor|disorder_of_visual_system	hematology|ophthalmology|oncology	inflammatory_disease|cancer	eye_disorder|vascular_disorder	false	false	false	true	low
MONDO:0021543	hemangioma of gingiva	cardiovascular_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	mouth_disorder|musculoskeletal_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	dermatology|hematology|oncology	inflammatory_disease|cancer	teeth_disorder|vascular_disorder|skin_disorder	false	false	false	true	low
MONDO:0021545	myomatous neoplasm	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	muscle_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0021546	ependymal tumor of spinal cord	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0021547	amelogenesis imperfecta type 3B	hereditary_disease|musculoskeletal_system_disorder	other	mouth_disorder|hereditary_disease|musculoskeletal_system_disorder	dermatology|genetics_and_genomics|hematology	metabolic_disorder|anemia	teeth_disorder|blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0021548	total early-onset cataract	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|pediatric|neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	true	high
MONDO:0021553	transverse myelitis	nervous_system_disorder|inflammatory_disease	other	inflammatory_disease|nervous_system_disorder	neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0021559	non-autoimmune hemolytic anemia	hematologic_disorder	anemia	hematologic_disorder	hematology|genetics_and_genomics	anemia|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0021562	omphalitis	inflammatory_disease	other	inflammatory_disease	pediatrics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0021568	renal tubule disorder	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	metabolic_disorder|renal_tubule_disorders_often_relate_to_kidney_function__which_is_closely_tied_to_the_metabolic_processes_of_the_body	kidney_disorder|urinary_tract_disorder|renal_tubule_disorder	false	false	false	false	high
MONDO:0021569	Emery-Dreifuss muscular dystrophy 2, autosomal dominant	nervous_system_disorder|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|cardiovascular_disorder	orthopaedic|genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0021573	oocyte maturation defect 2	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|genetic_disorders	reproductive_system_disorder|other____revision____reproductive_system_disorder	false	false	false	false	high
MONDO:0021574	oocyte maturation defect 3	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder	reproductive_system_disorder	false	false	false	false	high
MONDO:0021575	oocyte maturation defect 4	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder	false	false	false	false	medium
MONDO:0021576	fallopian tube endometrioid tumor	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	ovarian_cancer|cancer|endometrial_cancer|gynecologic_malignancy	reproductive_system_disorder|gynecological_disorder	false	true	false	false	high
MONDO:0021577	malignant mediastinal neural neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pulmonology|neurology|oncology	neural_neoplasm|cancer	lung_disorder|neural_disorder	false	true	false	false	high
MONDO:0021578	sternal neoplasm	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	cardiothoracic|oncology	cancer|sternal_neoplasm	bone_disorder	false	true	false	false	high
MONDO:0021579	neoplasm of femur	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	orthopaedic|oncology	cancer|neoplasm	bone_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0021580	neoplasm of jaw	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	mouth_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	otolaryngology|oncology	neoplasm_of_jaw____cancer	teeth_disorder|jaw__note__jaw_is_a_synonym_for_teeth_disorder_but_since_it_s_the_primary_location_of_the_neoplasm__i_ve_included_it|bone_disorder	false	true	false	false	high
MONDO:0021581	connective tissue neoplasm	cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	rheumatology|oncology	autoimmune_diseases|inflammatory_disease|cancer	joint_disorder|immune_disorder	false	true	false	false	medium
MONDO:0021582	lentigo	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology|oncology	cancer|skin_condition	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0021583	melanocytic skin neoplasm	cancer_or_benign_tumor|integumentary_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	neoplastic_disease|cancer	skin_disorder|blood_bone_marrow_disorder	false	true	false	false	medium
MONDO:0021588	eyelid sebaceous gland carcinoma	nervous_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor	nervous_system_disorder|integumentary_system_disorder|disorder_of_orbital_region|cancer_or_benign_tumor|disorder_of_visual_system	dermatology|oncology	cancer|adrenal_gland_disease	skin_disorder|eye_disorder	false	true	false	true	high
MONDO:0021605	benign eyelid neoplasm	integumentary_system_disorder|nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|integumentary_system_disorder|cancer_or_benign_tumor	ophthalmology|dermatology|oncology	cancer|benign_neoplasm_is_a_type_of_non_cancerous_tumor	eye_disorder|skin_disorder	false	false	false	true	low
MONDO:0021607	eyelid seborrheic keratosis	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	disorder_of_development_or_morphogenesis|disorder_of_orbital_region|disorder_of_visual_system|integumentary_system_disorder|hereditary_disease	ophthalmology|dermatology	cancer|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0021627	eyelid capillary hemangioma	integumentary_system_disorder|nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	disorder_of_orbital_region|cardiovascular_disorder|disorder_of_visual_system|integumentary_system_disorder|cancer_or_benign_tumor|nervous_system_disorder	ophthalmology|dermatology	cancer|inflammatory_disease|cardiovascular_disorder	vascular_disorder|skin_disorder|eyelid_disorder	false	false	false	true	low
MONDO:0021629	uterine ligament neoplasm	musculoskeletal_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	uterine_ligament_neoplasm_is_best_categorized_as_cancer_since_it_refers_to_the_abnormal_growth_of_cells_in_the_uterus_ligaments|cancer	reproductive_system_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0021630	lipoma of face	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	dermatology|otolaryngology	cancer|inflammatory_disease	skin_disorder|muscle_disorder	false	false	false	false	low
MONDO:0021631	brain astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0021632	primary brain neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0021633	cerebral astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0021634	epithelial skin neoplasm	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|epithelial_skin_neoplasm_can_also_be_classified_under____neoplastic_disease_tumor_malignant_tumor_skin_cancer	epithelial_skinned_neoplasm_is_a_specific_type_of_skin_disorder_so_it_fits_under_this_category|skin_disorder	false	true	false	true	medium
MONDO:0021635	neurocristopathy	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0021636	astrocytic tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurological_cancer|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0021637	low grade glioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	true	medium
MONDO:0021638	low grade astrocytic tumor	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	true	medium
MONDO:0021639	grade II glioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	true	medium
MONDO:0021640	grade III glioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0021641	Bunyaviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	renal_medicine|hematology	autoimmune_diseases|inflammatory_disease	immune_disorder|kidney_disorder	true	false	false	true	medium
MONDO:0021642	vulval varices	reproductive_system_disorder|cardiovascular_disorder	cardiovascular_disorder	reproductive_system_disorder|cardiovascular_disorder	hematology|obstetrics_and_gynecology	inflammatory_disease|cardiovascular_disorder	vascular_disorder|liver_disorder	false	false	false	false	low
MONDO:0021643	mesenteric varices	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hepatology|gastroenterology|hematology	inflammatory_disease|cardiovascular_disorder	lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0021644	esophageal varices without bleeding	upper_digestive_tract_disorder|digestive_system_disorder|cardiovascular_disorder	cardiovascular_disorder	upper_digestive_tract_disorder|cardiovascular_disorder|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|cardiovascular_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	medium
MONDO:0021645	esophageal varices with bleeding	upper_digestive_tract_disorder|digestive_system_disorder|cardiovascular_disorder	cardiovascular_disorder	upper_digestive_tract_disorder|cardiovascular_disorder|digestive_system_disorder	hepatology|gastroenterology|hematology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|liver_disorder	true	false	false	true	very_high
MONDO:0021650	uterine corpus neuroendocrine neoplasm	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0021651	synpolydactyly	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic	neurodegenerative_disease|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0021652	diffuse type adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|gastroenterology|pulmonology	adrenal_gland_disease|cancer|autoimmune_diseases	upper_gastrointestinal_disorder|lung_disorder	false	true	false	false	high
MONDO:0021653	cutaneous focal mucinosis	integumentary_system_disorder	other	integumentary_system_disorder	pediatrics|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|lymphatic_disorder	false	false	false	false	none
MONDO:0021654	diffuse cutaneous mucinosis	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|dermatology	inflammatory_disease|metabolic_disorder|cancer|autoimmune_diseases	skin_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0021655	secondary catabolic mucinosis of skin	integumentary_system_disorder	other	integumentary_system_disorder	pathology|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0021656	nongerminomatous germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology|genetics_and_genomics	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0021657	ovarian sex cord-stromal tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	inflammatory_disease|ovarian_cancer|adrenal_gland_disease|cancer	reproductive_system_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0021658	vascular ectasia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|vascular	vascular_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0021659	combined carcinoid and adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatrics|endocrinology|gastroenterology|hepatology|neurology	adrenal_gland_disease|cancer|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0021660	deep seated dermatophytosis	integumentary_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|integumentary_system_disorder|inflammatory_disease	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0021661	coronary atherosclerosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|pulmonology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0021662	bile duct neoplasm	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|gastroenterology|hepatology	inflammatory_disease|neoplastic|adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	very_high
MONDO:0021663	sarcomatoid squamous cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|dermatology|pulmonology	adrenal_gland_disease|other_is_not_needed_as_the_correct_answer_is_cancer_but_sarcomatoid_squamous_cell_carcinoma_can_also_be_associated_with_the_adrenal_gland__so_i_will_include_this_category_as_well|cancer	lung_disorder|skin_disorder	false	true	false	false	high
MONDO:0021666	ear infection	infectious_disease|otorhinolaryngologic_disease|inflammatory_disease	infectious_disease	infectious_disease|inflammatory_disease|otorhinolaryngologic_disease	pediatric|otolaryngology	inflammatory_disease|all_allergy|autoimmune_diseases	throat_disorder|ear_disorder	true	false	false	true	medium
MONDO:0021667	neuralgia	nervous_system_disorder	other	nervous_system_disorder	pain_management|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0021669	post-infectious disorder	other	other		psychiatry|pediatric|neurology	mental_health_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder	true	false	false	false	high
MONDO:0021670	post-infectious syndrome	syndromic_disease	other	post_infectious_disorder|syndromic_disease	pediatric|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder	true	false	false	false	high
MONDO:0021673	post-bacterial disorder	other	other	post_infectious_disorder	pediatric	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|liver_disorder	true	false	false	false	medium
MONDO:0021674	post-viral disorder	other	other	post_infectious_disorder	pediatric|allergy_and_immunology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	immune_disorder	true	false	false	false	medium
MONDO:0021677	post-infectious neuralgia	nervous_system_disorder	other	nervous_system_disorder|post_infectious_disorder	neurology|psychiatry	inflammatory_disease|autoimmune_diseases	nerve_disorder|immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0021678	gram-negative bacterial infections	infectious_disease	infectious_disease	infectious_disease	pediatric|rheumatology|renal_medicine|infectious_disease_is_not_in_the_list_so__pediatric|pulmonology|hematology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|urinary_tract_disorder	true	false	false	true	very_high
MONDO:0021679	gram-positive bacterial infections	infectious_disease	infectious_disease	infectious_disease	pediatric|urology|oncology|otolaryngology|rheumatology|cardiology|renal_medicine|hepatology|dermatology|pulmonology|hematology|cardiothoracic|hematatology	gram_positive_bacterial_infections_is_not_a_category_in_the_list__so_this_response_is_to_inform_that_a_better_match_would_be__inflammatory_disease__which_is_associated_with_gram_positive_bacterial_infections|inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|urinary_tract_disorder|bone_disorder|skin_disorder|joint_disorder	true	false	false	true	high
MONDO:0021680	streptococcal infection	infectious_disease	infectious_disease	infectious_disease	otolaryngology|rheumatology|allergy_and_immunology|hematology|pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder_throat_disorder	true	false	false	true	medium
MONDO:0021681	sexually transmitted disease	infectious_disease|reproductive_system_disorder	infectious_disease	reproductive_system_disorder|infectious_disease	obstetrics_and_gynecology|urology	sexually_transmitted_disease_does_not_exist_in_the_category_list_so_i_ll_remove_it_from_the_output____autoimmune_diseases|inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|sexually_transmitted_disease	true	false	false	true	high
MONDO:0021682	viral sexually transmitted disease	infectious_disease|reproductive_system_disorder	infectious_disease	reproductive_system_disorder|infectious_disease	obstetrics_and_gynecology|urology|dermatology	inflammatory_disease|sexually_transmitted_disease|autoimmune_diseases	reproductive_system_disorder|skin_disorder	true	false	false	true	high
MONDO:0021697	chlamydia infectious disease	reproductive_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease	obstetrics_and_gynecology|pediatric	inflammatory_disease|autoimmune_diseases|infectious_disease	reproductive_system_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0021698	alcohol-related disorders	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0021699	alcohol-induced disorders	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	hepatology|neurology|psychiatry	mental_health_disorder|addiction	liver_disorder	false	false	false	true	high
MONDO:0021702	alcohol amnestic disorder	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	metabolic_disorder|mental_health_disorder	brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0021718	polyneuritis	inflammatory_disease|nervous_system_disorder	other	inflammatory_disease|nervous_system_disorder	neurology	inflammatory_disease|autoimmune_diseases	nerve_disorder|muscle_disorder	true	false	false	true	high
MONDO:0021722	vulvodynia	reproductive_system_disorder|nervous_system_disorder	other	reproductive_system_disorder|nervous_system_disorder	obstetrics_and_gynecology|urology	autoimmune_diseases|inflammatory_disease	skin_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0021723	vaginismus	reproductive_system_disorder	other	reproductive_system_disorder	psychiatry|obstetrics_and_gynecology|urology	mental_health_disorder	muscle_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0021726	abdominal cystic lymphangioma	cardiovascular_disorder|immune_system_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	genetics_and_genomics|gastroenterology|hepatology|oncology|pediatric|hematology	cancer|inflammatory_disease	lymphatic_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0021727	aberrant subclavian artery	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	vascular|cardiothoracic	cardiovascular_disorder	vascular_disorder|joint_disorder	false	false	false	false	low
MONDO:0021736	proctosigmoiditis	digestive_system_disorder|inflammatory_disease|hereditary_disease|immune_system_disorder	other	immune_system_disorder|inflammatory_disease|digestive_system_disorder|hereditary_disease	gastroenterology|hematology	cancer|autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0021739	prurigo	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|allergy	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0021742	puerperal infection	infectious_disease|obstetric_disorder	infectious_disease	infectious_disease|obstetric_disorder	obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	immune_disorder|reproductive_system_disorder	true	false	false	true	high
MONDO:0021745	psychosocial short stature	nervous_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|nervous_system_disorder	endocrinology|pediatric	mental_health_disorder|metabolic_disorder	endocrine_disorder|psychosocial_short_stature_is_often_associated_with_growth_hormone_deficiency_which_falls_under_endocrine_disorder	false	false	false	false	medium
MONDO:0021746	pyelocystitis	inflammatory_disease|urinary_system_disorder	other	inflammatory_disease|urinary_system_disorder	urology|renal_medicine	autoimmune_diseases|inflammatory_disease	kidney_disorder|urinary_tract_disorder	true	false	false	false	medium
MONDO:0021747	Acanthamoeba infectious disease	infectious_disease	infectious_disease	infectious_disease	neurology|pediatrics|ophthalmology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	eye_disorder|skin_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0021750	pyonephrosis	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	autoimmune_diseases|cancer|inflammatory_disease	kidney_disorder|urinary_tract_disorder	true	false	false	true	high
MONDO:0021752	Achard-Thiers syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|endocrinology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	metabolic_disorder|endocrine_disorder|growth_disorder	false	false	true	false	high
MONDO:0021758	acquired agranulocytosis	hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder	hematology|immunology	anemia|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0021759	acquired fructose intolerance	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	gastroenterology|endocrinology|hepatology	adrenal_gland_disease|metabolic_disorder	kidney_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0021761	acral dysostosis dyserythropoiesis syndrome	syndromic_disease	other	syndromic_disease	hematology|orthopaedic|genetics_and_genomics	anemia|inflammatory_disease|metabolic_disorder	joint_disorder|bone_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0021762	acrocoxomesomelic dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	upper_gastrointestinal_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0021764	acrofacial dysostosis Preis type	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	genetic_disease_is_not_in_the_list_so__metabolic_disorder|autoimmune_diseases|metabolic_disorder	facial_disorder|skeletal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0021765	radiculitis	inflammatory_disease|nervous_system_disorder	other	inflammatory_disease|nervous_system_disorder	neurology|orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0021777	acute rheumatic heart disease	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder|acute_disease	rheumatology|cardiology|pediatric	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	heart_disorder|joint_disorder	true	false	false	false	high
MONDO:0021783	streptococcal sore throat	inflammatory_disease|infectious_disease|respiratory_system_disorder	infectious_disease	infectious_disease|respiratory_system_disorder|inflammatory_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|throat_disorder	true	false	false	true	medium
MONDO:0021804	silicotuberculosis	respiratory_system_disorder|infectious_disease	infectious_disease	infectious_disease|respiratory_system_disorder	orthopaedic|pulmonology|occupational_medicine	inflammatory_disease|autoimmune_diseases|cancer	lung_disorder|bone_disorder	true	false	false	false	high
MONDO:0021805	acromesomelic dysplasia, Campailla Martinelli type	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder|genetic_disorder___corrected_answer_to_fit_the_original_format_request__metabolic_disorder	skeletal_disorder___corrected_list_to_fit_the_format___bone_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0021808	acute cholinergic dysautonomia	nervous_system_disorder	other	acute_disease|nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0021809	primary dysautonomia	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0021811	acute mountain sickness	respiratory_system_disorder	other	acute_disease|respiratory_system_disorder	pulmonology	inflammatory_disease|metabolic_disorder|cardiovascular_disorder	lung_disorder|vascular_disorder	false	false	false	true	low
MONDO:0021812	adnexal spiradenoma/cylindroma of a sweat gland	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	adrenal_gland_disease|cancer	skin_disorder	false	false	false	false	low
MONDO:0021824	adult progressive spinal muscular atrophy, Aran Duchenne type	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0021826	aerobic Actinomyces infection	infectious_disease	infectious_disease	infectious_disease	microbiology|pulmonology	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|lung_disorder|bone_disorder	true	false	false	false	low
MONDO:0021829	agnathia-microstomia-synotia	syndromic_disease	other	syndromic_disease	otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|congenital_anomaly	ear_disorder|teeth_disorder	false	false	false	false	high
MONDO:0021834	Akaba Hayasaka syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	psychiatry|neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|kidney_disorder|vascular_disorder	false	false	false	false	high
MONDO:0021836	Aksu von Stockhausen syndrome	syndromic_disease	other	syndromic_disease	neurology|rheumatology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	joint_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0021838	Al Gazali Khidr Prem Chandran syndrome	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease|connective_tissue_disorder	neurodegenerative_disease|cancer_or_benign_tumor	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_orbital_region|disorder_of_visual_system|musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	lymphatic_disorder|reproductive_system_disorder|joint_disorder|eye_disorder|spinal_disorder|teeth_disorder|brain_disorder|muscle_disorder|urinary_tract_disorder|lung_disorder|throat_disorder|skin_disorder|nose_disorder|liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0021839	spirochaetales infections	infectious_disease	infectious_disease	infectious_disease	hepatology|urology|cardiology|neurology|hematology|rheumatology|ophthalmology|otolaryngology|pediatric|gastroenterology|dermatology|pulmonology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder|vascular_disorder	true	false	false	true	high
MONDO:0021845	Aloi Tomasini Isaia syndrome	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	other	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	joint_disorder|upper_gastrointestinal_disorder|bone_disorder|liver_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0021851	alopecia universalis onychodystrophy vitiligo	immune_system_disorder|integumentary_system_disorder|inflammatory_disease	autoimmune_disease	immune_system_disorder|integumentary_system_disorder|inflammatory_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0021856	Alsing syndrome	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	neurology|genetics_and_genomics	alsing_syndrome|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0021879	small cell variant anaplastic large cell lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|lung_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0021895	temporomandibular joint dysfunction syndrome	syndromic_disease|musculoskeletal_system_disorder	other	syndromic_disease|musculoskeletal_system_disorder	neurology|rheumatology|orthopaedic	musculoskeletal_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|teeth_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0021896	anterior spinal artery stroke	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	neurology|cardiology	cardiovascular_disorder|inflammatory_disease|neurodegenerative_disease	vascular_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0021902	aortopulmonary window	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology|pulmonology	cardiovascular_disorder|anomaly	lung_disorder|heart_disorder	false	false	false	false	high
MONDO:0021905	Apert-like polydactyly syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|orthopaedic	congenital_dysmorphism|metabolic_disorder	joint_disorder|teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0021907	aplasia cutis autosomal recessive	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology|hematology	anemia|metabolic_disorder	skin_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0021908	aplasia cutis congenita dominant	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology|pediatric|hematology	anemia|metabolic_disorder	skin_disorder|blood_bone_marrow_disorder	false	false	false	true	low
MONDO:0021913	aquagenic pruritus	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatrics	allergy|autoimmune_diseases|inflammatory_disease	skin_disorder	false	false	false	false	medium
MONDO:0021915	arakawa syndrome 2	hereditary_disease|syndromic_disease|metabolic_disease	metabolic_disease	hereditary_disease|syndromic_disease|metabolic_disease	genetics_and_genomics|neurology|pediatric	autoimmune_diseases|metabolic_disorder|anemia|inflammatory_disease|neurodegenerative_disease	liver_disorder|immune_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0021918	arena syndrome	syndromic_disease	other	syndromic_disease	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	lymphatic_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0021921	Arnold stickler bourne syndrome	urinary_system_disorder|syndromic_disease|disorder_of_visual_system|musculoskeletal_system_disorder	other	urinary_system_disorder|musculoskeletal_system_disorder|syndromic_disease|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|pediatrics|orthopaedic	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0021923	Arroyo Garcia Cimadevilla syndrome	hereditary_disease|upper_digestive_tract_disorder|digestive_system_disorder|reproductive_system_disorder	other	digestive_system_disorder|hereditary_disease|upper_digestive_tract_disorder|reproductive_system_disorder	genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0021925	tracheobronchitis	respiratory_system_disorder|inflammatory_disease	other	inflammatory_disease|respiratory_system_disorder	pulmonology|otolaryngology	autoimmune_diseases|inflammatory_disease	throat_disorder|lung_disorder	true	false	false	true	medium
MONDO:0021929	traumatic myositis ossificans	inflammatory_disease|musculoskeletal_system_disorder	other	inflammatory_disease|musculoskeletal_system_disorder	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	muscle_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0021932	infection by Trypanosoma gambiense	inflammatory_disease|integumentary_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|integumentary_system_disorder|infectious_disease	neurology|parasitology_is_not_in_the_list_so__hematology|hematology	autoimmune_diseases|infection|inflammatory_disease	vascular_disorder|brain_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0021935	aspergillus niger infection	infectious_disease	infectious_disease	infectious_disease	pulmonology|allergy_and_immunology|hematology	cancer|allergy|inflammatory_disease	liver_disorder|lower_gastrointestinal_disorder|lung_disorder	true	false	false	true	medium
MONDO:0021941	infection by Trypanosoma rhodesiense	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|tropical_medicine|hematology	autoimmune_diseases|anemia|inflammatory_disease	vascular_disorder|immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0021943	tuberculoma	infectious_disease	infectious_disease	infectious_disease	oncology|pulmonology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder|lung_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0021944	auditory neuropathy	auditory_system_disorder|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	neurology|otolaryngology	auditory_neuropathy|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0021945	hearing disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	neurology|otolaryngology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0021948	cutaneous tuberculosis	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	other____note__the_category__other__is_included_because_cutaneous_tuberculosis_is_a_manifestation_of_the_disease_that_presents_through_the_skin__which_does_not_fit_neatly_into_dermatology_alone|dermatology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder|skin_disorder	true	false	false	true	medium
MONDO:0021950	autoimmune oophoritis	inflammatory_disease|immune_system_disorder|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|autoimmune_disease	endocrine_system_disorder|inflammatory_disease|immune_system_disorder|reproductive_system_disorder	allergy_and_immunology|obstetrics_and_gynecology|urology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0021952	progestogen hypersensitivity	immune_system_disorder	other	immune_system_disorder	dermatology|obstetrics_and_gynecology	inflammatory_disease|allergy|autoimmune_diseases	immune_disorder|skin_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0021953	tuberculous fibrosis of lung	respiratory_system_disorder|infectious_disease	infectious_disease	respiratory_system_disorder|infectious_disease	pulmonology|cardiothoracic	inflammatory_disease|autoimmune_diseases	vascular_disorder|immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0021957	autosomal recessive nonsyndromic congenital nuclear cataract	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0021960	ureteritis	inflammatory_disease|urinary_system_disorder	other	inflammatory_disease|urinary_system_disorder	urology|renal_medicine	inflammatory_disease|autoimmune_diseases	kidney_disorder|urinary_tract_disorder	true	false	false	false	medium
MONDO:0021962	baetz-greenwalt syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|hematology|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0021964	bagatelle Cassidy syndrome	disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	joint_disorder|blood_bone_marrow_disorder	false	false	false	false	none
MONDO:0021966	baker Vinters syndrome	nervous_system_disorder|syndromic_disease	other	syndromic_disease|nervous_system_disorder	dermatology|ophthalmology	autoimmune_diseases|neurodegenerative_disease	biliary_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0021977	basaloid follicular hamartoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|genetics_and_genomics|oncology|pediatric	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0021979	Basaran Yilmaz syndrome	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0021994	Berk-Tabatznik syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiology|genetics_and_genomics|cardiothoracic	cancer|adrenal_gland_disease|autoimmune_diseases|metabolic_disorder	kidney_disorder|bone_disorder	false	false	false	false	high
MONDO:0022007	water intoxication	poisoning	other	poisoning	nephrology|renal_medicine	metabolic_disorder|water_intoxication_can_also_be_related_to_neurological_disorders_but_the_primary_cause_is_due_to_imbalance_of_electrolytes_in_body_which_makes_it_a_metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0022011	bobble-head doll syndrome	syndromic_disease	other	syndromic_disease	pediatric|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0022013	Boerhaave syndrome	syndromic_disease	other	syndromic_disease	pulmonology|gastroenterology|cardiothoracic	inflammatory_disease|cardiovascular_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0022020	Boudhina Yedes Khiari syndrome	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|immune_disorder|vascular_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0022022	bowenoid papulosis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|post_infectious_disorder	oncology|dermatology	autoimmune_diseases|inflammatory_disease|cancer	reproductive_system_disorder|skin_disorder	true	true	false	false	medium
MONDO:0022025	boylan dew greco syndrome	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0022034	lentivirus infection	infectious_disease	infectious_disease	infectious_disease	pulmonology|immunology|pediatric	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|vascular_disorder	true	false	false	false	medium
MONDO:0022037	large-cell immunoblastic lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	inflammation_disease|autoimmune_diseases|cancer	immune_disorder_lymphatic_disorder	true	true	false	true	high
MONDO:0022055	Calabro syndrome	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0022057	calcifying epithelial odontogenic tumor	cancer_or_benign_tumor|integumentary_system_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder|mouth_disorder|musculoskeletal_system_disorder	oncology|orthopaedic|pediatric|pathology	cancer|odontogenic_tumor	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0022060	calloso-genital dysplasia	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease	obstetrics_and_gynecology|urology	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	reproductive_system_disorder|skin_disorder	false	false	false	false	medium
MONDO:0022067	Cantu Sanchez-Corona Fragoso syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	skin_disorder|hair_disorder_is_not_an_option_so_i_will_remove_it_from_consideration__liver_disorder|bone_disorder	false	false	false	false	high
MONDO:0022070	Cantu Sanchez-Corona Hernandez syndrome	syndromic_disease	other	syndromic_disease	neurology|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0022071	carbon baby syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	liver_disorder	false	false	false	false	low
MONDO:0022089	Carnevale hernandez castillo syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	liver_disorder	false	false	false	false	high
MONDO:0022094	Cartwright Nelson Fryns syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder|developmental_disorder___note__since_the_original_list_of_categories_did_not_include__genetic_disorder__or__developmental_disorder___i_couldn_t_use_them_directly__however__cartwright_nelson_fryns_syndrome_is_a_known_genetic_condition_and_developmental_disorder__so_i_included_those_as_relevant_subcategories	skeletal_disorder|joint_disorder	false	false	false	false	high
MONDO:0022096	pyogenic granuloma	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	pediatric|dermatology	cancer|inflammatory_disease|allergy	vascular_disorder|skin_disorder	false	false	false	true	low
MONDO:0022098	catamenial pneumothorax	respiratory_system_disorder	other	respiratory_system_disorder	obstetrics_and_gynecology|pulmonology	cancer|inflammatory_disease|cardiovascular_disorder	lung_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0022103	chronic prostatitis	reproductive_system_disorder|inflammatory_disease	other	inflammatory_disease|reproductive_system_disorder	urology|renal_medicine	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder|reproductive_system_disorder	true	false	false	false	medium
MONDO:0022113	central centrifugal cicatricial alopecia	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	hair_related_disorders__this_is_a_match__although_it_is_not_on_the_list|skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0022140	Charles bonnet syndrome	syndromic_disease	other	syndromic_disease	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0022151	Chitty Hall Webb syndrome	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	cardiovascular_disorder|autoimmune_diseases|neurodegenerative_disease	nose_disorder|vascular_disorder|muscle_disorder|spinal_disorder|throat_disorder|brain_disorder	false	false	false	false	high
MONDO:0022171	chromhidrosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|endocrinology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|skin_disorder	false	false	false	false	low
MONDO:0022173	chromosome 11q trisomy	chromosomal_disorder	other	chromosomal_disorder	oncology|pediatric|genetics_and_genomics	cancer|genetic_disorder|metabolic_disorder	blood_bone_marrow_disorder|genetic_disorder____note__i_have_to_assume_that__genetic_disorder__is_implied_in_the_list_since_chromosome_11q_trisomy_is_a_genetic_condition	false	false	false	false	high
MONDO:0022174	chromosome 12p deletion	chromosomal_disorder	other	chromosomal_disorder	oncology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	chromosome_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0022177	chromosome 13q trisomy	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology|obstetrics_and_gynecology	metabolic_disorder|neurodegenerative_disease	developmental_disorder|developmental_disorder____corrected_answer__brain_disorder|brain_disorder	false	false	false	false	high
MONDO:0022178	chromosome 13q-mosaicism	chromosomal_disorder	other	chromosomal_disorder	oncology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	chromosome_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0022180	chromosome 16 trisomy	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|neurodegenerative_disease	intellectual_disability|spinal_disorder|brain_disorder|joint_disorder___corrected_list_without__intellectual_disability__which_isn_t_part_of_the_original_category_list____brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0022196	chronic erosive gastritis	digestive_system_disorder|inflammatory_disease	other	digestive_system_disorder|inflammatory_disease	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0022205	pustular psoriasis	inflammatory_disease|integumentary_system_disorder|immune_system_disorder|hereditary_disease	other	integumentary_system_disorder|immune_system_disorder|hereditary_disease|inflammatory_disease	dermatology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	high
MONDO:0022208	crystal arthropathy	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|joint_disorder	false	false	false	true	medium
MONDO:0022220	Parinaud syndrome	syndromic_disease	other	syndromic_disease	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder|brain_disorder	true	false	false	false	medium
MONDO:0022236	colpocephaly	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0022293	vascular disorder of penis	reproductive_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|reproductive_system_disorder	hematology|cardiology|urology	cardiovascular_disorder|vascular_disorder	urinary_tract_disorder|reproductive_system_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0022308	corticobasal degeneration disorder	nervous_system_disorder|syndromic_disease	neurodegenerative_disease	syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0022311	cote katsantoni syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|liver_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0022316	hair defect with photosensitivity and intellectual disability syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	neurology|genetics_and_genomics|dermatology	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	hair_disorder|skin_disorder	true	false	false	true	high
MONDO:0022321	2-methylacetoacetyl CoA thiolase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	metabolic_disorders__implied__but_not_listed|pediatrics|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	liver_disorder|metabolic_disorder	false	false	false	false	high
MONDO:0022323	2-hydroxyethyl methacrylate sensitization	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	other	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	allergy_and_immunology|dermatology	allergy|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0022330	4-hydroxyphenylacetic aciduria	metabolic_disease|digestive_system_disorder|hereditary_disease	metabolic_disease	digestive_system_disorder|metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|renal_medicine	metabolic_disorder|adrenal_gland_disease	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0022333	5-nucleotidase syndrome	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatrics|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0022337	AIDS dysmorphic syndrome	syndromic_disease	other	syndromic_disease	psychiatry|pediatric|genetics_and_genomics	mental_health_disorder|autoimmune_diseases|neurodegenerative_disease	immune_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0022338	ALK+ histiocytosis	immune_system_disorder	other	immune_system_disorder	hematology|oncology|genetics_and_genomics|pulmonology	autoimmune_diseases|inflammatory_disease|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0022349	congenital absence of septum pellucidum	syndromic_disease|disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder|nervous_system_disorder|hereditary_disease	endocrine_system_disorder	syndromic_disease|reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|congenital_anomaly	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0022357	congenital acardia	cardiovascular_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	genetics_and_genomics|pediatric|obstetrics_and_gynecology	congenital_disease__note__congenital_acardia_is_a_condition_characterized_by_the_absence_of_a_heartbeat_in_an_infant__thus_relating_to_cardiovascular_systems|cardiovascular_disorder	heart_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0022380	acute lymphoblastic leukemia congenital sporadic aniridia	syndromic_disease	other	acute_disease|syndromic_disease	hematology|genetics_and_genomics|pediatric|oncology	congenital_disorder|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0022394	cervical intraepithelial neoplasia	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0022398	aglossia and situs inversus	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|surgical	inflammatory_disease|metabolic_disorder	spinal_disorder|skeletal_system_disorder	false	false	false	false	high
MONDO:0022401	agyria pachygyria polymicrogyria	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|polymicrogyria_is_a_type_of_brain_malformation_that_is_often_associated_with_neurodevelopmental_disorders__so_polymicrogyria_would_be_categorized_under_neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0022402	agyria-pachygyria type 1	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0022403	Ahumada Del Castillo syndrome	syndromic_disease	other	syndromic_disease	pediatrics|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	vascular_disorder|liver_disorder	false	false	false	false	high
MONDO:0022410	retinal ciliopathy	hereditary_disease|disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0022417	alopecia congenita keratosis palmoplantaris	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	hair_disorder|immune_disorder|skin_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0022424	alpha-mannosidosis type 1	hereditary_disease|disorder_of_visual_system|metabolic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0022428	aluminosis	syndromic_disease	other	syndromic_disease	occupational_health|allergy_and_immunology	inflammatory_disease|adrenal_gland_disease|anemia|autoimmune_diseases	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0022430	persistent fetal circulation syndrome	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|obstetrics_and_gynecology|pulmonology|pediatric	metabolic_disorder|inflammatory_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0022432	alves Castelo dos Santos syndrome	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	integumentary_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|cancer	immune_disorder|bone_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0022435	Mauriac syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	immune_disorder|joint_disorder|muscle_disorder	false	false	true	false	high
MONDO:0022444	amyloidosis bronchopulmonary	metabolic_disease	metabolic_disease	metabolic_disease	cardiothoracic|cardiology|pulmonology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0022453	angiomyomatous hamartoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|genetics_and_genomics|oncology|pediatric	adrenal_gland_disease|cancer	vascular_disorder|liver_disorder	false	false	false	false	low
MONDO:0022454	angiosarcoma of the scalp	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer	vascular_disorder|skin_disorder	false	true	false	false	high
MONDO:0022456	ankle defects short stature	syndromic_disease	other	syndromic_disease	orthopaedic|genetics_and_genomics|endocrinology|pediatric	short_stature_is_a_characteristic_of_growth_hormone_deficiency_which_is_also_a_component_of_some_metabolic_disorders|metabolic_disorder	joint_disorder|bone_disorder|short_stature	false	false	false	false	low
MONDO:0022457	ankyloblepharon filiforme imperforate anus	syndromic_disease	other	syndromic_disease	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	eye_disorder|lower_gastrointestinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0022458	annular constricting bands	syndromic_disease	other	syndromic_disease	pulmonology|cardiology|dermatology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	spinal_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0022461	anophthalmia cleft palate micrognathia	syndromic_disease	other	syndromic_disease	otolaryngology|genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorders	eye_disorder|spinal_disorder|teeth_disorder|muscle_disorder	false	false	false	false	high
MONDO:0022462	anophthalmia esophageal atresia cryptorchidism	syndromic_disease	other	syndromic_disease	urology|genetics_and_genomics|pediatric	neurodegenerative_disease|developmental_disorder|genitourinary_system_disorder	eye_disorder|reproductive_system_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0022465	anotia facial palsy cardiac defect	syndromic_disease	other	syndromic_disease	cardiology|neurology|pediatric	cardiac_defect|autoimmune_diseases|cardiovascular_disorder	ear_disorder_heart_disorder___note__anotia_is_a_rare_congenital_condition_characterized_by_underdevelopment_of_the_ear__while_facial_palsy_can_be_caused_by_a_variety_of_conditions_affecting_the_nerves_controlling_facial_movements__cardiac_defect_refers_to_an_abnormality_in_the_structure_or_function_of_the_heart	true	false	false	true	very_high
MONDO:0022468	antigen-peptide-transporter 2 deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	renal_medicine|genetics_and_genomics|allergy_and_immunology|pediatrics	metabolic_disorder|genetic_disorder	immune_disorder|liver_disorder	false	false	false	false	high
MONDO:0022470	aortic dissection lentiginosis	syndromic_disease	other	syndromic_disease	cardiology|genetics_and_genomics	cardiovascular_disorder	heart_disorder_vascular_disorder	false	false	false	false	high
MONDO:0022471	childhood aortic valve stenosis	syndromic_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|syndromic_disease	cardiothoracic|cardiology|pediatric	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0022481	APO A-i deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	cardiology|lipidology_is_not_an_option_so_i_will_leave_it_off_the_answer|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	vascular_disorder|liver_disorder	false	false	false	false	high
MONDO:0022496	arthrogryposis IUGR thoracic dystrophy	syndromic_disease	other	syndromic_disease	genetics_and_genomics|orthopaedic|pediatrics|pulmonology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0022500	arthrogryposis multiplex congenita CNS calcification	syndromic_disease	other	syndromic_disease	orthopaedic|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0022504	arthrogryposis spinal muscular atrophy	syndromic_disease	other	syndromic_disease	orthopaedic|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0022509	asternia	syndromic_disease	other	syndromic_disease	hematology|hepatology|genetics_and_genomics	neurodegenerative_disease	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0022510	atlanto-axial fusion	syndromic_disease	other	syndromic_disease	orthopaedic|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	true	high
MONDO:0022513	atrophoderma of Pierini and Pasini	syndromic_disease|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|adrenal_gland_disease	lymphatic_disorder|skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0022518	autoimmune inner ear disease	immune_system_disorder|auditory_system_disorder|otorhinolaryngologic_disease	autoimmune_disease	immune_system_disorder|otorhinolaryngologic_disease|auditory_system_disorder	otolaryngology|rheumatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	ear_disorder|immune_disorder	false	false	false	true	high
MONDO:0022519	autoimmune myocarditis	cardiovascular_disorder|musculoskeletal_system_disorder|immune_system_disorder|inflammatory_disease	cardiovascular_disorder|autoimmune_disease	immune_system_disorder|cardiovascular_disorder|inflammatory_disease|musculoskeletal_system_disorder	rheumatology|cardiology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	heart_disorder|immune_disorder	false	false	false	true	high
MONDO:0022529	BK-virus nephropathy	infectious_disease|urinary_system_disorder	infectious_disease	urinary_system_disorder|infectious_disease	renal_medicine|urology	inflammatory_disease|autoimmune_diseases	kidney_disorder|immune_disorder	true	false	false	true	high
MONDO:0022535	autonomic facial cephalgia	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	otolaryngology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0022538	leukoplakia of gingiva	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|mouth_disorder	hematology|oncology	cancer|inflammatory_disease	teeth_disorder|gum_disorder|oral_disorder___became___teeth_disorder|oral_disorder|mouth_disorder	false	false	false	false	medium
MONDO:0022545	Barnicoat Baraitser syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|dermatology|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	joint_disorder|bone_disorder|skeletal_rack_disorder	false	false	false	false	high
MONDO:0022551	Basedow's coma	syndromic_disease	other	syndromic_disease	endocrinology|neurology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0022552	Bazopoulou Kyrkanidou syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	skeletal_dysplasia|bone_disorder	false	false	false	false	very_high
MONDO:0022553	BD syndrome	syndromic_disease	other	syndromic_disease	neurology|psychiatry	autoimmune_diseases|mental_health_disorder	joint_disorder|lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder|brain_disorder	false	false	false	true	high
MONDO:0022555	Beardwell syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics	inflammatory_disease|adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0022557	Behrens Baumann dust syndrome	disorder_of_visual_system|syndromic_disease|nervous_system_disorder|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|nervous_system_disorder|syndromic_disease|disorder_of_visual_system	pulmonology|allergy_and_immunology	inflammatory_disease|allergy|autoimmune_diseases	respiratory_disorder|immune_disorder|lung_disorder	false	false	false	true	high
MONDO:0022559	benign angiitis of the central nervous system	nervous_system_disorder|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|nervous_system_disorder|cardiovascular_disorder	neurology|pediatrics	inflammatory_disease|autoimmune_diseases	vascular_disorder|brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0022560	benign metastasizing leiomyoma	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder|muscle_disorder	false	true	false	false	low
MONDO:0022567	bhaskar jagannathan syndrome	disorder_of_visual_system|syndromic_disease|hereditary_disease	other	hereditary_disease|disorder_of_orbital_region|syndromic_disease|disorder_of_visual_system	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0022568	bidirectional tachycardia	syndromic_disease	other	syndromic_disease	pediatric|renal_medicine|pulmonology|cardiothoracic|cardiology	autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0022572	bilateral renal agenesis dominant type	disorder_of_development_or_morphogenesis|urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|urology	adrenal_gland_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0022573	biliary atresia intrahepatic non syndromic form	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	pediatric|hepatology|gastroenterology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder|biliary_disorder	false	false	false	false	high
MONDO:0022574	biliary atresia intrahepatic syndromic form	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	pediatric_hepatology	inflammatory_disease|metabolic_disorder	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0022576	bilirubin induced brain injury in the newborn	syndromic_disease	other	syndromic_disease	pediatric|neurology|neonatology|hepatology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|anemia	liver_disorder|brain_disorder	false	false	false	true	high
MONDO:0022578	childhood bladder carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	pediatric|oncology|urology	cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0022580	blepharo naso facial syndrome van Maldergem type	syndromic_disease	other	syndromic_disease	genetics_and_genomics|dermatology|otolaryngology|pediatric|ophthalmology	inflammatory_disease|autoimmune_diseases	nose_disorder|eye_disorder	false	false	false	false	high
MONDO:0022586	bone dysplasia Moore type	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|genetic_disorder	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0022587	bone dysplasia corpus callosum agenesis	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|pediatric|neurology|orthopaedic	metabolic_disorder|neurodegenerative_disease	bone_disorder|brain_disorder	false	false	false	false	medium
MONDO:0022598	brachydactyly absence of distal phalanges	syndromic_disease	other	syndromic_disease	genetics_and_genomics|orthopaedic	neurodegenerative_disease|congenital_disorder	bone_disorder|joint_disorder|teeth_disorder	false	false	false	false	low
MONDO:0022599	brachydactyly anonychia	syndromic_disease	other	syndromic_disease	genetics_and_genomics|orthopaedic	autoimmune_diseases|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0022602	brachydactyly small stature face anomalies	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0022603	brachydactyly tibial hypoplasia	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|orthopaedic	developmental_disorder|musculoskeletal_disease|congenital_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0022606	branchial arch disease	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	otolaryngology|pediatric	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	upper_gastrointestinal_disorder|throat_disorder	false	false	false	false	high
MONDO:0022607	extraovarian Brenner tumor of the vagina	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0022608	brittle bone syndrome lethal type	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	skeletal_dysplasia___corrected_list_based_on_the_original_request_for_only_a_single_category_____metabolic_disorder|metabolic_disorder|genetic_disorder	bone_disorder|blood_bone_marrow_disorder	true	false	false	false	very_high
MONDO:0022609	bronchial adenomas/carcinoids childhood	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology|pulmonology	cancer|adrenal_gland_disease	childhood|lung_disorder	false	true	false	true	medium
MONDO:0022610	bronchiectasis oligospermia	syndromic_disease	other	syndromic_disease	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|lung_disorder	false	false	false	false	medium
MONDO:0022611	Brunoni syndrome	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	syndromic_disease|hereditary_disease|integumentary_system_disorder	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0022612	Brunsting-Perry syndrome	syndromic_disease	other	syndromic_disease	neurology|dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	liver_disorder|upper_gastrointestinal_disorder|brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0022613	bruyn scheltens syndrome	syndromic_disease	other	syndromic_disease	neurology|rheumatology	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0022615	burn goodship syndrome	syndromic_disease	other	syndromic_disease	burn|dermatology	inflammatory_disease|adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0022618	burning mouth syndrome type 3	syndromic_disease	other	syndromic_disease|mouth_disorder	otolaryngology|neurology|dentistry|oral_medicine	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|teeth_disorder	false	false	false	false	high
MONDO:0022622	congenital disorder of glycosylation syndrome type 4	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|congenital_disease	liver_disorder	false	false	true	false	high
MONDO:0022623	CDK4 linked melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	oncology|dermatology|genetics_and_genomics	cancer|adrenal_gland_disease|autoimmune_diseases	skin_disorder|lymphatic_disorder|muscle_disorder	false	true	false	true	high
MONDO:0022633	camptodactyly joint contractures and facial skeletal dysplasia	syndromic_disease	other	syndromic_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	bone_disorder|facial_skeletal_dysplasia|joint_disorder	false	false	false	false	medium
MONDO:0022634	camptodactyly vertebral fusion	syndromic_disease	other	syndromic_disease	orthopaedic|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0022636	candida glabrata infection	infectious_disease	infectious_disease	infectious_disease	pediatrics|infectious_diseases|dermatology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|skin_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0022639	Cantu Sanchez-Corona Garcia-Cruz syndrome	syndromic_disease	other	syndromic_disease	neurology|dermatology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	liver_disorder|skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0022642	childhood carcinoid tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	pediatric|oncology	cancer	endocrine_disorder|lung_disorder	false	true	false	true	medium
MONDO:0022643	carcinoma of the vocal tract	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology	cancer|adrenal_gland_disease	throat_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0022644	cardiac hydatid cysts with intracavitary expansion	syndromic_disease	other	syndromic_disease	cardiology|cardiothoracic	cardiovascular_disorder|cancer|inflammatory_disease	heart_disorder|liver_disorder	true	false	false	false	high
MONDO:0022645	cardioencephalomyopathy	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	heart_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0022646	cardiofacial syndrome short limbs	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|orthopaedic	cardiovascular_disorder|metabolic_disorder	heart_disorder|short_limbs_is_more_specific_to_bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0022647	cardiomelic syndrome stratton Koehler type	syndromic_disease	other	syndromic_disease	renal_medicine|genetics_and_genomics|cardiology|cardiothoracic|pulmonology	cardiovascular_disorder|metabolic_disorder|autoimmune_diseases	heart_disorder|liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0022648	cardiomyopathy and deafness due to tRNA lysine gene mutation	syndromic_disease	other	syndromic_disease	otolaryngology|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder	ear_disorder|heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0022650	cardiomyopathy diabetes deafness	syndromic_disease	other	syndromic_disease	endocrinology|neurology|cardiology	cardiovascular_disorder|metabolic_disorder	endocrine_disorder|heart_disorder|ear_disorder	false	false	true	false	high
MONDO:0022653	cardiomyopathy due to anthracyclines	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder	oncology|cardiology	cancer|cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0022654	cardiomyopathy hypogonadism collagenoma syndrome	syndromic_disease	other	syndromic_disease	endocrinology|genetics_and_genomics|rheumatology|cardiology|pulmonology	cardiovascular_disorder|metabolic_disorder	endocrine_disorder|heart_disorder|muscle_disorder	false	false	false	false	none
MONDO:0022655	cardiomyopathy hypogonadism metabolic anomalies	hereditary_disease|syndromic_disease|metabolic_disease	metabolic_disease	syndromic_disease|hereditary_disease|metabolic_disease	endocrinology|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder	endocrine_disorder|heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0022656	cardiomyopathy spherocytosis	syndromic_disease	other	syndromic_disease	hematoloy|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0022662	carpo tarsal osteolysis recessive	syndromic_disease	other	syndromic_disease	genetics_and_genomics|rheumatology|orthopaedic	metabolic_disorder|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0022666	cassavism	poisoning	other	poisoning	gastroenterology|pediatric	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0022672	autosomal dominant cataract	syndromic_disease|hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|syndromic_disease|disorder_of_orbital_region	pediatric|ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	medium
MONDO:0022673	autosomal dominant non-nuclear cataract	syndromic_disease|hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|syndromic_disease|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	true	medium
MONDO:0022675	cataract skeletal anomalies	syndromic_disease	other	syndromic_disease	orthopaedic|ophthalmology|genetics_and_genomics	adrenal_gland_disease|skeletal_anomalies|metabolic_disorder|neurodegenerative_disease	skeletal_anomalies|eye_disorder	false	false	false	false	high
MONDO:0022682	cennamo gangemi syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|liver_disorder|kidney_disorder	false	false	false	as_of_my_last_update_in_october_2023__there_are_no_known_efficacious_treatments_that_cure__prevent__or_specifically_treat_cennamo_gangemi_syndrome__this_is_a_rare_genetic_disorder__and_management_typically_focuses_on_addressing_the_symptoms_associated_with_the_condition_rather_than_offering_a_definitive_cure__therefore__i_would_return_false	high
MONDO:0022685	cerebellar agenesis	syndromic_disease	other	syndromic_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0022687	cerebellar degeneration	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	neurology|genetics_and_genomics	cerebellar_degeneration|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0022691	cerebello-olivary atrophy	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0022693	cerebral calcification cerebellar hypoplasia	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0022694	cerebral calcifications opalescent teeth phosphaturia	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder|teeth_disorder|liver_disorder	true	true	false	true	medium
MONDO:0022697	athetoid cerebral palsy	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0022699	cerebral palsy spastic hemiplegic	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	spastic_hemiplegic_is_not_a_category_in_the_list|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0022700	cerebral palsy spastic monoplegic	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology|pediatric	cerebral_palisy_spastic_monoplegic|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0022712	oculo digital syndrome	syndromic_disease	other	syndromic_disease	ophthalmology|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0022714	chester porphyria	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	metabolic_disease|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder|anemia	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0022715	Chiari malformation type 3	hereditary_disease	other	hereditary_disease	neurology|pediatric	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0022716	Chiari malformation type 4	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	cardiovascular_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0022723	chondrodysplasia	syndromic_disease	other	syndromic_disease	genetics_and_genomics|orthopaedic|rheumatology|pediatric	metabolic_disorder|genetic_disorders	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0022729	chondrodysplasia punctata with steroid sulfatase deficiency	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|dermatology	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0022733	choreoacanthocytosis amyotrophic	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0022734	chorioretinopathy dominant form microcephaly	syndromic_disease	other	syndromic_disease	genetics_and_genomics|ophthalmology|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0022735	choroid plexus cyst	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder|eye_disorder	false	false	false	false	low
MONDO:0022736	occupational lung disease	respiratory_system_disorder	other	respiratory_system_disorder|occupational_disorder	pulmonology|occupational_medicine	inflammatory_disease|occupational_lung_disease	occupational_lung_disease_is_already_a_lung_disease|lung_disorder	false	false	false	true	high
MONDO:0022737	choroideremia hypopituitarism	nervous_system_disorder|cardiovascular_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	cardiovascular_disorder|psychiatric_disorder	disorder_of_orbital_region|cardiovascular_disorder|disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|endocrinology|ophthalmology	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|eye_disorder	false	false	false	false	high
MONDO:0022739	Christian Demyer Franken syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|endocrinology|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0022740	Christian Johnson angenieta syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|geneticsofgenetics_and_genomics	metabolic_disorder|neurodegenerative_disease	biliary_disorder|liver_disorder	false	false	false	false	none
MONDO:0022742	occupational asthma	respiratory_system_disorder	other	respiratory_system_disorder|occupational_disorder	pulmonology|occupational_safety_and_health_is_part_of_a_broader_field_that_intersects_with_the_specialty_of_occupational_medicine__which_in_turn_is_closely_related_to_pulmonology	allergy|inflammatory_disease	occupational_asthma_was_removed_from_the_list_for_this_example__but_it_would_fit_into_these_categories_as_well|lung_disorder|immune_disorder	false	false	false	true	medium
MONDO:0022745	mixed dust pneumoconiosis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|respiratory	inflammatory_disease|cancer	lower_gastrointestinal_disorder|lung_disorder	false	false	false	true	high
MONDO:0022746	chromosome 13p duplication	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|oncology|pediatric	neurodegenerative_disease|developmental_disorder|genetic_disorder|chromosomal_disorder	lymphatic_disorder|blood_bone_marrow_disorder|chromosome_abnormalities	false	false	false	false	high
MONDO:0022749	non-neoplastic nevus	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	skin_condition|inflammatory_disease|autoimmune_diseases	skin_disorder|dermatological_condition	false	false	false	true	low
MONDO:0022752	chromosome 16p13.3 deletion syndrome	nervous_system_disorder|chromosomal_disorder|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|psychiatric_disorder	psychiatric_disorder	chromosomal_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|immune_disorder	false	false	false	false	high
MONDO:0022754	chromosome 17p deletion	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|oncology|hematology	neurodegenerative_disease|cancer	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0022755	chromosome 18 mosaic monosomy	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|anemia	blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	high
MONDO:0022756	chromosome 1q deletion	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder|developmental_disorder	false	false	false	false	high
MONDO:0022757	chromosome 20 trisomy	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|obstetrics_and_gynecology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|joint_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0022758	chromosome 22, monosome mosaic	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0022759	trisomy 22	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	lymphatic_disorder|brain_disorder|joint_disorder|spinal_disorder|vascular_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0022760	chromosome 22q deletion	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	immune_disorder|blood_bone_marrow_disorder|brain_disorder	false	false	false	false	high
MONDO:0022761	chromosome 3 duplication syndrome	chromosomal_disorder|syndromic_disease	other	chromosomal_disorder|syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	muscle_disorder|immune_disorder|lymphatic_disorder|joint_disorder|lower_gastrointestinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0022762	chromosome 4 short arm deletion	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	spinal_disorder|chromosome_abnormality	false	false	false	false	high
MONDO:0022765	chronic demyelinizing neuropathy with IgM monoclonal	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|immunology|hematology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|immune_disorder|lymphatic_disorder|brain_disorder	false	false	false	true	high
MONDO:0022768	chronic polyradiculoneuritis	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|neurological_disorder	true	false	false	false	high
MONDO:0022769	ciliary dyskinesia-bronchiectasis	syndromic_disease	other	syndromic_disease	pediatric|pulmonology	bronchiectasis_is_a_respiratory_condition__so_the_best_fitting_categories_are___inflammatory_disease|autoimmune_diseases	respiratory_system_disorder|lung_disorder	true	false	false	false	high
MONDO:0022770	circumscribed cutaneous aplasia of the vertex	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|dermatology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	bone_bone_marrow_disorder|skin_disorder	false	false	false	true	low
MONDO:0022771	circumscribed disseminated keratosis Jadassohn lew type	syndromic_disease	other	syndromic_disease	genetics_and_genomics|dermatology	cancer|inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0022772	classic Kaposi sarcoma	cardiovascular_disorder|cancer_or_benign_tumor|infectious_disease	cardiovascular_disorder|cancer_or_benign_tumor|infectious_disease	post_infectious_disorder|cancer_or_benign_tumor|cardiovascular_disorder|infectious_disease	oncology|dermatology|hematology	cancer|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|skin_disorder	true	true	false	true	medium
MONDO:0022775	cleft lip and palate malrotation cardiopathy	syndromic_disease	other	syndromic_disease	cardiology|pediatric|cardiothoracic	cardiovascular_disorder|autoimmune_diseases|metabolic_disorder	teeth_disorder|heart_disorder|throat_disorder	false	false	false	false	high
MONDO:0022776	cleft lip and/or palate with mucous cysts of lower	syndromic_disease	other	syndromic_disease	otolaryngology|pediatric	cancer|anemia|inflammatory_disease|autoimmune_diseases	teeth_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0022777	cleft lip palate dysmorphism kumar type	syndromic_disease	other	syndromic_disease	otolaryngology|genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|teeth_disorder|nose_disorder|lymphatic_disorder|joint_disorder|throat_disorder|lower_gastrointestinal_disorder|ear_disorder|upper_gastrointestinal_disorder|vascular_disorder|skin_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0022778	cleft lip palate intellectual disability corneal opacity	syndromic_disease	other	syndromic_disease	genetics_and_genomics|ophthalmology|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	throat_disorder|upper_gastrointestinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0022779	cleft lip palate oligodontia syndactyly pili torti	syndromic_disease	other	syndromic_disease	otolaryngology|genetics_and_genomics|pediatric	congenital_anomaly|genetic_condition|metabolic_disorder	teeth_disorder|joint_disorder	false	false	false	false	high
MONDO:0022780	cleft lip palate pituitary deficiency	syndromic_disease	other	syndromic_disease	otolaryngology|endocrinology|pediatric	metabolic_disorder|pituitary_deficiency_is_likely_related_to_an_endocrine_disorder_but_the_category_provided_doesn_t_specifically_match_that_so_it_s_placed_in_metabolic_disorders_for_lack_of_a_better_fit	throat_disorder|brain_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0022781	cleft lip palate-tetraphocomelia	syndromic_disease	other	syndromic_disease	genetics_and_genomics|otolaryngology|pediatric	other____however__it_is_worth_noting_that_cleft_lip_palate_tetraphocomelia_appears_to_be_a_congenital_disorder_related_to_cleft_lip_palate_and_tetraphocomelia_which_would_categorize_under__other|metabolic_disorder	teeth_disorder|cleft_lip_palate_disorder|bone_disorder|ear_disorder	false	false	false	false	high
MONDO:0022782	cleft lower lip cleft lateral canthi chorioretinal	syndromic_disease	other	syndromic_disease	otolaryngology|pediatric	skin_condition|congenital_abnormality|eye_disease|metabolic_disorder	teeth_disorder|eye_disorder	false	false	false	false	medium
MONDO:0022785	cleft palate cardiac defect ectrodactyly	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	cardiovascular_disorder|congenital_abnormality|genetic_disorder	teeth_disorder|heart_disorder|ectrodactyly	false	false	false	false	high
MONDO:0022786	cleft palate colobomata radial synostosis deafness	syndromic_disease	other	syndromic_disease	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|craniofacial_anomaly____corrected_to_fit_the_original_format_____metabolic_disorder|developmental_disorder|birth_defect|congenital_abnormality|genetic_disorder	teeth_disorder|bone_disorder|ear_disorder	false	false	false	false	high
MONDO:0022787	cleft palate heart disease polydactyly absent tibia	syndromic_disease	other	syndromic_disease	cardiology|orthopaedic|pediatric	cardiovascular_disorder|cleft_palate_is_not_in_the_category_list_but_since_cleft_palate_heart_disease_is_paired_together_it_suggests_a_connection__so_also_cardiovascular_disorder	absent_tibia_is_implied_to_be_a_limb_disorder_but_that_category_isn_t_provided__however__the_list_of_categories_does_contain__bone_disorder|teeth_disorder|joint_disorder|heart_disorder|bone_disorder	false	false	false	false	high
MONDO:0022790	cleft tongue	syndromic_disease	other	syndromic_disease	otolaryngology|pediatric	neurodegenerative_disease|inflammatory_disease	teeth_disorder|throat_disorder	false	false	false	false	medium
MONDO:0022791	coarse face hypotonia constipation	syndromic_disease	other	syndromic_disease	neurology|gastroenterology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	lower_gastrointestinal_disorder|muscle_disorder	false	false	false	based_on_the_symptoms_you_ve_mentioned___coarse_face__hypotonia__reduced_muscle_tone___and_constipation___these_could_be_indicative_of_a_variety_of_conditions__however__without_a_specific_diagnosis__it_is_challenging_to_determine_if_there_are_efficacious_treatments_that_cure__prevent__or_treat_the_disease___if_you_are_referring_to_a_specific_condition_such_as_a_genetic_syndrome__e_g___prader_willi_syndrome__which_may_present_with_hypotonia_and_constipation_among_other_symptoms___then_there_are_treatments_available_that_can_help_manage_symptoms_but_may_not_cure_the_underlying_condition___in_general__for_the_symptoms_of_hypotonia_and_constipation__there_are_various_therapies__such_as_physical_therapy_for_hypotonia__and_lifestyle_management_strategies__such_as_dietary_changes_and_medications_for_constipation__that_may_help_alleviate_symptoms___since_treatment_efficacy_can_vary_widely_depending_on_the_specific_condition__a_definitive_answer_cannot_be_provided_without_knowing_the_exact_diagnosis___thus__the_safe_answer_is___false	medium
MONDO:0022792	coccygodynia	musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder	neurology|orthopaedic|urology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|muscle_disorder	false	false	false	false	low
MONDO:0022795	deficiency of coenzyme q cytochrome c reductase	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	cardiology|genetics_and_genomics|hematology|pulmonology	metabolic_disorder|cardiovascular_disorder|neurodegenerative_disease	mitochondrial_disease|liver_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0022798	Cohen Lockood Wyborney syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|adrenal_gland_disease|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0022799	cold urticaria	inflammatory_disease|integumentary_system_disorder	other	inflammatory_disease|integumentary_system_disorder	allergy_and_immunology|dermatology	allergy|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0022800	type 2 collagenopathy	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder	other	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|connective_tissue_disorder	genetics_and_genomics|rheumatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0022802	Collins-Sakati syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0022803	coloboma porencephaly hydronephrosis	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|neurology|urology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	eye_disorder|kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0022804	colobomata unilobar lung heart defect	syndromic_disease	other	syndromic_disease	pulmonology|cardiothoracic|pediatric|cardiology	cardiovascular_disorder|lung_heart_defect	heart_disorder|lung_disorder	false	false	false	false	high
MONDO:0022805	colonic malakoplakia	syndromic_disease	other	syndromic_disease	hematology|gastroenterology|hepatology	cancer|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	false	medium
MONDO:0022809	Colver Steer Godman syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|neurology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0022810	Combarros Calleja Leno syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|liver_disorder|eye_disorder|brain_disorder|joint_disorder	false	false	false	false	medium
MONDO:0022812	complement receptor deficiency	syndromic_disease|hereditary_disease|immune_system_disorder	other	hereditary_disease|syndromic_disease|immune_system_disorder	genetics_and_genomics|immunology|hematology	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0022815	congenital absence of the sternocleidomastoid muscle	syndromic_disease	other	syndromic_disease	pediatric|orthopaedic	neurodegenerative_disease|musculoskeletal_disorder|congenital_abnormality	spinal_disorder|muscle_disorder	false	false	false	false	low
MONDO:0022817	congenital amputation	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|orthopaedic	congenital_amputation_is_a_type_of_birth_defect_which_can_be_caused_by_metabolic_disorders_during_pregnancy|metabolic_disorder	spinal_disorder|congenital_amputation_is_related_to_birth_defects_which_can_also_affect_the_limbs_so_another_category_is_bone_disorder	false	false	false	false	medium
MONDO:0022818	congenital aneurysms of the great vessels	syndromic_disease	other	syndromic_disease	genetics_and_genomics|hematology|cardiothoracic|pediatric|cardiology	congenital_heart_defect|cardiovascular_disorder|congenital_abnormality	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0022820	congenital articular rigidity	syndromic_disease	other	syndromic_disease	rheumatology|pediatric|neurology|orthopaedic	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0022821	congenital benign spinal muscular atrophy dominant	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0022822	congenital cardiovascular shunt	syndromic_disease	other	syndromic_disease	pediatric|cardiology	cardiovascular_disorder|congenital_condition	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0022823	congenital contractures	syndromic_disease	other	syndromic_disease	pediatric|orthopaedic	metabolic_disorder|congenital_contractures_is_a_type_of_condition_that_can_be_related_to_a_metabolic_disorder_because_it_involves_abnormalities_in_the_musculoskeletal_system_that_may_have_a_genetic_component_and_can_result_from_an_underlying_metabolic_issue	muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0022824	congenital craniosynostosis maternal hyperthyroiditis	syndromic_disease	other	syndromic_disease	endocrinology|obstetrics_and_gynecology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	endocrine_disorder|bone_disorder	false	false	false	true	medium
MONDO:0022825	congenital cystic eye	syndromic_disease	other	syndromic_disease	pediatric|ophthalmology|genetics_and_genomics	eye_disease|congenital_condition|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0022826	congenital cystic eye multiple ocular and intracranial anomalies	syndromic_disease	other	syndromic_disease	pediatric|ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	eye_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0022831	congenital heart disease ptosis hypodontia craniostosis	syndromic_disease	other	syndromic_disease	pediatric|cardiology	cardiovascular_disorder|congenital_heart_disease	spinal_disorder|eye_disorder|heart_disorder|teeth_disorder|bone_disorder|vascular_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0022832	congenital heart disease radio ulnar synostosis intellectual disability	syndromic_disease	other	syndromic_disease	pediatric|cardiology|genetics_and_genomics	cardiovascular_disorder|intellectual_disability_is_related_to_a_neurological_condition_but_it_can_also_be_associated_with_other_conditions_such_as_genetic_disorders_that_may_have_cardiovascular_manifestations	heart_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0022839	congenital human immunodeficiency virus	infectious_disease|reproductive_system_disorder	infectious_disease	infectious_disease|reproductive_system_disorder	pediatric|allergy_and_immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	true	false	false	true	very_high
MONDO:0022841	congenital hypotrichosis milia	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	skin_disorder|congenital_disorder	false	false	false	false	low
MONDO:0022843	congenital mumps	syndromic_disease|infectious_disease	infectious_disease	infectious_disease|syndromic_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	immune_disorder|ear_disorder|joint_disorder	true	false	false	false	high
MONDO:0022846	congenital nonhemolytic jaundice	hereditary_disease	other	hereditary_disease	pediatric|hepatology|genetics_and_genomics	congenital_nonhemolytic_jaundice_can_also_be_classified_as_a_metabolic_disorder|metabolic_disorder	liver_disorder|biliary_disorder	false	false	false	false	medium
MONDO:0022849	congenital stenosis of cervical medullary canal	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|cardiovascular_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0022851	Dennis-Fairhurst-Moore syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	vascular_disorder|bone_disorder|liver_disorder|joint_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0022854	congenital unilateral pulmonary hypoplasia	syndromic_disease	other	syndromic_disease	pulmonology|pediatric	respiratory_disease_is_not_listed_so_i_will_remove_it_and_return__cardiovascular_disorder|cardiovascular_disorder	heart_disorder|lung_disorder	false	false	false	false	high
MONDO:0022855	congenital vagal hyperreflexivity	syndromic_disease	other	syndromic_disease	pediatrics|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	vascular_disorder|brain_disorder|heart_disorder	false	false	false	false	medium
MONDO:0022859	cor biloculare	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	ophthalmology|cardiology|cardiothoracic	neurodegenerative_disease|cardiovascular_disorder	heart_disorder|eye_disorder	false	false	false	false	high
MONDO:0022862	Cormier Rustin Munnich syndrome	syndromic_disease	other	syndromic_disease	pediatrics|genetics_and_genomics|pulmonology	neurodegenerative_disease|metabolic_disorder	liver_disorder|genetic_disorder____based_on_my_research_cormier_rustin_munnich_syndrome_is_a_rare_genetic_disorder_affecting_the_liver	false	false	false	false	high
MONDO:0022863	corneal crystals myopathy neuropathy	syndromic_disease	other	syndromic_disease	genetics_and_genomics|ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	muscle_disorder|neuropathy_is_not_in_the_list_so_this_will_be_omitted|eye_disorder	false	false	false	false	none
MONDO:0022865	corneal dystrophy ichthyosis microcephaly intellectual disability	syndromic_disease	other	syndromic_disease	genetics_and_genomics|ophthalmology|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	intellectual_disability|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0022866	corneal dystrophy pigmentary anomaly malabsorption	syndromic_disease	other	syndromic_disease	genetics_and_genomics|ophthalmology	metabolic_disorder|malabsorption__neurodegenerative_disease|corneal_dystrophy_pigmentary_anomaly	eye_disorder	false	false	false	false	low
MONDO:0022871	corpus callosum agenesis of blepharophimosis robin type	syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|autoimmune_diseases|mental_health_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0022872	corpus callosum dysgenesis X-linked recessive	syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0022873	corpus callosum dysgenesis cleft spasm	syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0022874	corpus callosum dysgenesis hypopituitarism	syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder	genetics_and_genomics|neurology|endocrinology	neurodegenerative_disease|mental_health_disorder	brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0022875	cortada Koussef Matsumoto syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	adrenal_gland_disease|autoimmune_diseases	immune_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0022876	Cortes Lacassie syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	adrenal_gland_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	endocrine_disorder|liver_disorder	false	false	false	false	high
MONDO:0022883	craniofacial and skeletal defects	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|craniofacial_and_skeletal_defects	bone_disorder|teeth_disorder	false	false	false	false	high
MONDO:0022884	craniofacial dysostosis arthrogryposis progeroid appearance	syndromic_disease	other	syndromic_disease	genetics_and_genomics|orthopaedic|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|teeth_disorder	false	false	false	false	high
MONDO:0022887	craniofrontonasal syndrome Teebi type	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	craniofacial_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0022888	craniostenosis cataract	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology	metabolic_disorder|inflammatory_disease	bone_disorder|eye_disorder	false	false	false	false	medium
MONDO:0022889	craniostenosis with congenital heart disease intellectual disability	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|cardiology|pediatric	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	intellectual_disability|heart_disorder|bone_disorder	false	false	false	true	very_high
MONDO:0022890	craniosynostosis Fontaine type	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	bone_disorder|spinal_disorder|skull_bone_disorder	false	false	false	false	high
MONDO:0022891	craniosynostosis Maroteaux Fonfria type	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|skull_bone_disorder	false	false	false	false	high
MONDO:0022892	craniosynostosis alopecia brain defect	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|brain_defect	bone_disorder|brain_disorder|spinal_disorder|craniosynostosis	false	false	false	false	high
MONDO:0022893	craniosynostosis arthrogryposis cleft palate	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	otolaryngology|orthopaedic|pediatric	neurodegenerative_disease|birth_defect|congenital_disorder|skeletal_dysplasia	bone_disorder|joint_disorder|cleft_palate_is_actually_a_congenital_anomaly_so_i_will_remove_it_from_the_list_to_provide_an_accurate_answer__bone_disorder	false	false	false	false	high
MONDO:0022894	craniosynostosis autosomal dominant	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	bone_disorder|spinal_disorder|skull_disorder	false	false	false	false	high
MONDO:0022895	craniosynostosis cleft lip palate arthrogryposis	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|otolaryngology|orthopaedic|pediatric	genetic_condition|neurodegenerative_disease|developmental_disorder|congenital_abnormality|skeletal_disorder	bone_disorder|facial_disorder|joint_disorder	false	false	false	false	high
MONDO:0022896	craniosynostosis contractures cleft	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	otolaryngology|orthopaedic|pediatric	neurodegenerative_disease|craniosynostosis_contractures_cleft	teeth_disorder|bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0022897	craniosynostosis exostoses nevus epibulbar dermoid	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|ophthalmology|orthopaedic|dermatology	neurodegenerative_disease|inflammatory_disease	bone_disorder|eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0022898	craniosynostosis intellectual disability heart defects	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	neurology|cardiology|pediatric	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	heart_disorder|bone_disorder|brain_disorder	false	false	false	false	high
MONDO:0022899	crawfurd syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0022901	Crohn disease of the esophagus	upper_digestive_tract_disorder|inflammatory_disease|immune_system_disorder|digestive_system_disorder|hereditary_disease	other	inflammatory_disease|digestive_system_disorder|hereditary_disease|upper_digestive_tract_disorder|immune_system_disorder	gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder_upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0022904	cryofibrinogenemia	immune_system_disorder	autoimmune_disease	immune_system_disorder	hematology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	false	medium
MONDO:0022907	cutaneous sclerosis	integumentary_system_disorder	other	integumentary_system_disorder	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|muscle_disorder	false	false	false	false	high
MONDO:0022908	cutis gyratum acanthosis nigricans craniosynostosis	syndromic_disease	other	syndromic_disease	dermatology|genetics_and_genomics	neurodegenerative_disease|craniosynostosis___in_craniosynostosis___adrenal_gland_disease	skin_disorder|craniosynostosis	false	false	false	false	high
MONDO:0022909	cutis laxa osteoporosis	syndromic_disease	other	syndromic_disease	rheumatology|endocrinology|dermatology|genetics_and_genomics	osteoporosis|cutis_laxa|metabolic_disorder	skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0022912	cutis verticis gyrata mental deficiency	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|skin_disorder	false	false	false	false	low
MONDO:0022919	cytokine receptor deficiency	immune_system_disorder	other	immune_system_disorder	immunology|allergy_and_immunology|pediatric|genetics_and_genomics	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0022930	Dandy-Walker malformation with nasopharyngeal teratoma and diaphragmatic hernia	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	oncology|otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|congenital_disorder|cancer	spine_disorder|brain_disorder|throat_disorder	false	false	false	false	high
MONDO:0022932	Davenport-Donlan syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0022934	Davis Lafer syndrome	syndromic_disease	other	syndromic_disease	pediatric|allergy_and_immunology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	joint_disorder|upper_gastrointestinal_disorder|immune_disorder	false	false	false	false	medium
MONDO:0022936	de Hauwere Leroy adriaenssens syndrome	syndromic_disease	other	syndromic_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|bone_disorder|immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0022937	deafness conductive stapedial ear malformation facial palsy	syndromic_disease	other	syndromic_disease	otolaryngology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	stapedial|ear_disorder	false	false	false	false	high
MONDO:0022938	deafness goiter stippled epiphyses	syndromic_disease	other	syndromic_disease	otolaryngology|pediatric|genetics_and_genomics	endocrine_disorder|congenital_disorder|metabolic_disorder	endocrine_disorder|ear_disorder	false	false	false	false	medium
MONDO:0022941	deafness hypospadias metacarpal and metatarsal syndrome	syndromic_disease	other	syndromic_disease	otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	joint_disorder|bone_disorder|ear_disorder	false	false	false	false	medium
MONDO:0022942	deafness mesenteric diverticula of small bowel neuropathy	syndromic_disease	other	syndromic_disease	otolaryngology|neurology|gastroenterology	neurodegenerative_disease|autoimmune_diseases	lower_gastrointestinal_disorder|neuropathy|ear_disorder	false	false	false	false	low
MONDO:0022945	deafness peripheral neuropathy arterial disease	syndromic_disease	other	syndromic_disease	otolaryngology|neurology|peripheral_neuropathy_is_more_closely_associated_with_neurology__whereas_deafness_is_a_symptom_related_to_otolaryngology__arterial_disease_is_more_commonly_associated_with_cardiology|cardiology	arterial_disease|cardiovascular_disorder|peripheral_neuropathy|deafness	vascular_disorder|ear_disorder	false	false	false	false	medium
MONDO:0022946	deafness progressive cataract autosomal dominant	syndromic_disease	other	syndromic_disease	ophthalmology|otolaryngology|genetics_and_genomics	autosomal_dominant|neurodegenerative_disease|metabolic_disorder	autosomal_dominant|eye_disorder|ear_disorder	false	false	false	true	medium
MONDO:0022948	Deal Barratt Dillon syndrome	urinary_system_disorder|syndromic_disease	other	urinary_system_disorder|syndromic_disease	pediatrics|genetics_and_genomics|cardiothoracic	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0022949	defective apolipoprotein b-100	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder	liver_disorder|heart_disorder	false	false	false	false	high
MONDO:0022960	dermatocardioskeletal syndrome boronne type	syndromic_disease	other	syndromic_disease	dermatology|orthopaedic|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder|autoimmune_diseases	skin_disorder|bone_disorder|skeletal_disorder|heart_disorder	false	false	false	false	high
MONDO:0022963	desmoplastic infantile astrocytoma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology|pediatric	tumor|cancer|neurological_disease	brain_disorder|spinal_disorder	false	true	false	true	low
MONDO:0022965	desmoplastic infantile ganglioglioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology|pediatric	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0022968	dextrocardia with situs inversus	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|cardiology|cardiothoracic	congenital_heart_disease|cardiovascular_disorder	heart_disorder	false	false	false	false	medium
MONDO:0022971	diabetes persistent mullerian ducts	syndromic_disease	other	syndromic_disease	endocrinology|urology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0022972	diabetic mastopathy	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	endocrinology|obstetrics_and_gynecology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0022975	diaphragmatic agenesis radial aplasia omphalocele	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|cardiothoracic|obstetrics_and_gynecology	cardiovascular_disorder|congenital_abnormality|genetic_disorder	abdominal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0022977	diaphragmatic hernia exomphalos corpus callosum agenesis	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics	neurodevelopmental_disease|congenital_abnormality|metabolic_disorder	abdominal_disorder|spinal_disorder	false	false	false	false	high
MONDO:0022978	diaphragmatic hernia upper limb defects	syndromic_disease	other	syndromic_disease	general_surgery|pediatric|cardiothoracic	inflammatory_disease|autoimmune_diseases|cancer	abdominal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0022981	die Smulders droog van dijk syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	bone_disorder|immune_disorder|liver_disorder	false	false	false	false	high
MONDO:0022983	Dieterich disease	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	gastroenterology|hepatology	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0022985	diffuse cavernous hemangioma of the rectum	digestive_system_disorder|cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|hematology|gastroenterology	inflammatory_disease|cancer	vascular_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0022986	diffuse idiopathic pulmonary neuroendocrine cell hyperplasia	cancer_or_benign_tumor	cancer_or_benign_tumor	idiopathic_disease|cancer_or_benign_tumor	endocrinology|pulmonology|neurology	inflammatory_disease|cancer|autoimmune_diseases|cardiovascular_disorder	endocrine_disorder|lung_disorder	false	false	false	false	medium
MONDO:0022989	diomedi bernardi placidi syndrome	syndromic_disease	other	syndromic_disease	pediatric|cardiothoracic|genetics_and_genomics	cardiovascular_disorder|adrenal_gland_disease	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0022990	diphallus rachischisis imperforate anus	syndromic_disease	other	syndromic_disease	pediatric|urology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|congenital_anomaly	lower_gastrointestinal_disorder|spinal_disorder	false	false	false	false	high
MONDO:0022991	diploid-triploid mosaicism	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder|chromosomal_abnormality	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0022993	dipsogenic diabetes insipidus	urinary_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|urinary_system_disorder	renal_medicine|endocrinology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	endocrine_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0022998	distal arthrogryposis Moore weaver type	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0022999	distichiasis heart congenital anomalies	syndromic_disease	other	syndromic_disease	pediatric|cardiothoracic|congenital_anomalies|cardiology	congenital_anomalies|cardiovascular_disorder	heart_congenital_anomalies|heart_disorder	false	false	false	false	medium
MONDO:0023002	double discordia	syndromic_disease	other	syndromic_disease	psychiatry|neurology	adrenal_gland_disease|mental_health_disorder|neurodegenerative_disease	kidney_disorder|lower_gastrointestinal_disorder	false	false	false	false	none
MONDO:0023003	double fingernail of fifth finger	hereditary_disease	other	hereditary_disease	orthopaedic|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|joint_disorder	false	false	false	false	low
MONDO:0023005	double uterus-hemivagina-renal agenesis	syndromic_disease	other	syndromic_disease	urology|genetics_and_genomics|obstetrics_and_gynecology|renal_medicine	hemivagina|congenital_anomaly|double_uterus|renal_agenesis	kidney_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0023006	doxorubicin induced cardiomyopathy	musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder	oncology|cardiology	inflammatory_disease|cancer|cardiovascular_disorder	muscle_disorder|heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0023007	Drachtman Weinblatt Sitarz syndrome	musculoskeletal_system_disorder|syndromic_disease|hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder|syndromic_disease	rheumatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0023011	Wilson-Mikity syndrome	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|pulmonology	neurodegenerative_disease|metabolic_disorder	liver_disorder|lung_disorder	false	false	false	false	high
MONDO:0023013	Duker-Weiss-Siber syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder|kidney_disorder|eye_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0023015	duodenal atresia tetralogy of fallot	syndromic_disease	other	syndromic_disease	pediatric|cardiothoracic|gastroenterology	cardiovascular_disorder|congenital_abnormality	lower_gastrointestinal_disorder|heart_disorder	false	false	false	false	high
MONDO:0023016	duplication of leg mirror foot	syndromic_disease	other	syndromic_disease	orthopaedic|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	none
MONDO:0023017	duplication of the thumb unilateral biphalangeal	syndromic_disease	other	syndromic_disease	orthopaedic|pediatric	congenital_anomaly|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0023018	dupont sellier chochillon syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	blood_bone_marrow_disorder|liver_disorder|joint_disorder	false	false	false	true	very_high
MONDO:0023019	dwarfism bluish sclerae	syndromic_disease	other	syndromic_disease	genetics_and_genomics|endocrinology|pediatric	autoimmune_diseases|metabolic_disorder	endocrine_disorder|bone_disorder|joint_disorder|skin_disorder	false	false	false	false	low
MONDO:0023020	dwarfism deafness retinitis pigmentosa	syndromic_disease	other	syndromic_disease	ophthalmology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder|eye_disorder|bone_disorder	false	false	false	false	medium
MONDO:0023021	dwarfism lethal type advanced bone age	syndromic_disease	other	syndromic_disease	genetics_and_genomics|endocrinology|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0023022	dwarfism thin bones multiple fractures	syndromic_disease	other	syndromic_disease	orthopaedic|genetics_and_genomics|endocrinology|pediatrics	autoimmune_diseases|metabolic_disorder|bone_disease	bone_disorder	false	false	false	false	medium
MONDO:0023023	neonatal dacryocystitis	inflammatory_disease|disorder_of_visual_system	other	disorder_of_orbital_region|inflammatory_disease|disorder_of_visual_system	ophthalmology|pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	nose_disorder|eye_disorder	true	false	false	true	low
MONDO:0023030	dysmorphism cleft palate loose skin	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|dermatology	genetic_disease_is_incorrect_as_it_s_not_in_the_list|anemia|metabolic_disorder	loose_skin|skin_disorder|cleft_palate|teeth_disorder	false	false	false	true	high
MONDO:0023035	Eagle syndrome	syndromic_disease|nervous_system_disorder	other	nervous_system_disorder|syndromic_disease	neurology|otolaryngology	neurodegenerative_disease	throat_disorder|eye_disorder	false	false	false	false	medium
MONDO:0023039	eccrine mucinous carcinoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	adrenal_gland_disease|cancer	skin_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0023040	ectodermal dysplasia Bartalos type	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|dermatology	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0023042	ectodermal dysplasia margarita type	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|dermatology	neurodegenerative_disease|developmental_disorder|genetic_disorder	skin_disorder|eye_disorder|ear_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0023043	ectodermal dysplasia alopecia preaxial polydactyly	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|dermatology	developmental_disorder|autoimmune_diseases|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0023045	ectodermal dysplasia arthrogryposis diabetes mellitus	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|endocrinology|dermatology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|endocrine_disorder|eye_disorder|bone_disorder|joint_disorder	false	false	true	false	high
MONDO:0023046	ectodermal dysplasia blindness	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|teeth_disorder	false	false	false	false	high
MONDO:0023048	ectodermal dysplasia neurosensory deafness	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|psychiatry|neurology|otolaryngology	neurodegenerative_disease|autoimmune_diseases	skin_disorder|ear_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0023050	ectrodactyly cardiopathy dysmorphism	syndromic_disease	other	syndromic_disease	genetics_and_genomics|cardiology	cardiovascular_disorder	kidney_disorder|heart_disorder|joint_disorder	false	false	false	false	medium
MONDO:0023054	klumpke's paralysis	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0023059	Elliott ludman Teebi syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|ear_disorder|immune_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0023061	enamel hypoplasia cataract hydrocephaly	syndromic_disease	other	syndromic_disease	pediatric|neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder|teeth_disorder	false	false	false	false	high
MONDO:0023062	encephalocele anencephaly	syndromic_disease	other	syndromic_disease	pediatric|neurology	anencephaly_is_a_birth_defect_of_the_brain_and_skull_that_can_also_be_classified_as_neurodevelopmental_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0023066	enchondromatosis dwarfism deafness	syndromic_disease	other	syndromic_disease	genetics_and_genomics|orthopaedic|pediatric|otolaryngology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	ear_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0023067	endemic Kaposi sarcoma	infectious_disease|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|infectious_disease|cardiovascular_disorder	post_infectious_disorder|cancer_or_benign_tumor|infectious_disease|cardiovascular_disorder	hematology|dermatology|oncology	inflammatory_disease|anemia|autoimmune_diseases|cancer	skin_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0023068	Engelhard Yatziv syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases|metabolic_disorder	spine_disorder|bone_disorder|joint_disorder	false	false	false	as_of_my_last_knowledge_update_in_october_2023__there_are_no_known_efficacious_treatments_that_cure_engelhard_yatziv_syndrome__as_it_is_a_rare_genetic_disorder__therefore__the_answer_is_false	high
MONDO:0023069	enlarged vestibular aqueduct syndrome	musculoskeletal_system_disorder|otorhinolaryngologic_disease|auditory_system_disorder|syndromic_disease	other	auditory_system_disorder|otorhinolaryngologic_disease|syndromic_disease|musculoskeletal_system_disorder	neurology|otolaryngology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0023071	enterovirus antenatal infection	infectious_disease	infectious_disease	infectious_disease	pediatric|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder	true	false	false	false	high
MONDO:0023073	eosinophilic cryptitis	urinary_system_disorder|inflammatory_disease	other	urinary_system_disorder|inflammatory_disease	pediatric|gastroenterology|allergy_and_immunology|otolaryngology	inflammatory_disease|allergy|autoimmune_diseases	upper_gastrointestinal_disorder|immune_disorder	false	false	false	true	medium
MONDO:0023076	eosinophilic pustular folliculitis	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|inflammatory_disease	dermatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0023079	epidermal nevus vitamin D resistant rickets	syndromic_disease	other	syndromic_disease	dermatology|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0023083	epimetaphyseal dysplasia cataract	syndromic_disease	other	syndromic_disease	orthopaedic|ophthalmology|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disease_is_not_in_the_list_so__metabolic_disorder	bone_disorder|eye_disorder	false	false	false	false	low
MONDO:0023084	epiphyseal dysplasia dysmorphism camptodactyly	syndromic_disease	other	syndromic_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0023089	erythroplakia	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|dermatology	cancer|anemia	skin_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0023091	esophageal atresia coloboma talipes	syndromic_disease	other	syndromic_disease	gastroenterology|orthopaedic|pediatric	congenital_disorder|neurodegenerative_disease|birth_anomaly	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0023093	exertional headache	nervous_system_disorder	other	nervous_system_disorder	neurology	mental_health_disorder|cardiovascular_disorder|inflammatory_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0023094	exogenous ochronosis	connective_tissue_disorder|musculoskeletal_system_disorder|metabolic_disease	metabolic_disease	connective_tissue_disorder|musculoskeletal_system_disorder|metabolic_disease	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	skin_disorder|liver_disorder|joint_disorder	false	false	false	false	low
MONDO:0023098	extrasystoles short stature hyperpigmentation microcephaly	syndromic_disease	other	syndromic_disease	cardiology|pediatric|genetics_and_genomics|neurology	metabolic_disorder|cardiovascular_disorder|neurodegenerative_disease	brain_disorder|heart_disorder	true	false	false	false	medium
MONDO:0023099	FRAXD syndrome	chromosomal_disorder|hereditary_disease	other	chromosomal_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|bone_disorder|joint_disorder|eye_disorder	false	false	false	false	low
MONDO:0023100	facial clefting corpus callosum agenesis	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	facial_clefting|brain_disorder	false	false	false	false	high
MONDO:0023101	facio digito genital syndrome recessive form	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0023102	facio skeletal genital syndrome rippberger type	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|endocrinology	inflammatory_disease|autoimmune_diseases|metabolic_disorder|anemia	joint_disorder|reproductive_system_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0023106	Fairbank disease	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	rheumatology|orthopaedic	autoimmune_diseases|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0023111	familial capillaro-venous leptomeningeal angiomatosis	syndromic_disease	other	syndromic_disease	oncology|pediatric|genetics_and_genomics|neurology	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0023113	familial colorectal cancer	hereditary_disease|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|hereditary_disease	oncology|genetics_and_genomics|gastroenterology	familial_cancer|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0023119	familial myelofibrosis	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	anemia|cancer_or_benign_tumor	immune_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder	hematology|oncology|genetics_and_genomics	anemia|cancer	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0023121	familial partial paralysis	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	familial_partial_paralysis|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0023122	familial prostate carcinoma	cancer_or_benign_tumor|reproductive_system_disorder|hereditary_disease	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor|hereditary_disease	oncology|genetics_and_genomics|urology	genetic_disorder|cancer|familial_carcinoma	reproductive_system_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0023124	familial pulmonary arterial hypertension leucopenia and atrial septal defect	syndromic_disease	other	syndromic_disease	pulmonology|cardiology|pediatric|hematology	cardiovascular_disorder|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|heart_disorder|lung_disorder	false	false	false	false	high
MONDO:0023133	Faye-Petersen-Ward-Carey syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0023134	febrile ulceronecrotic Mucha-Habermann disease	immune_system_disorder|integumentary_system_disorder|inflammatory_disease|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|acute_disease|integumentary_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	immunology|pediatric|genetics_and_genomics|dermatology|gastroenterology	cancer|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder|skin_disorder	true	false	false	false	very_high
MONDO:0023137	feigenbaum Bergeron syndrome	syndromic_disease	other	syndromic_disease	rheumatology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	medium
MONDO:0023138	Feingold trainer syndrome	syndromic_disease	other	syndromic_disease	neurology|pediatric	mental_health_disorder|autoimmune_diseases|neurodegenerative_disease	immune_disorder|reproductive_system_disorder|eye_disorder|muscle_disorder|joint_disorder|throat_disorder|upper_gastrointestinal_disorder|bone_disorder|skin_disorder|liver_disorder|vascular_disorder|lymphatic_disorder|nose_disorder|ear_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0023142	fetal brain disruption sequence	syndromic_disease	other	syndromic_disease	obstetrics_and_gynecology|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0023143	fetal enterovirus syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|infectious_disease	infectious_disease	disorder_of_development_or_morphogenesis|syndromic_disease|infectious_disease	obstetrics_and_gynecology|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	false	high
MONDO:0023147	fetal parainfluenza virus type 3 syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|infectious_disease	infectious_disease	disorder_of_development_or_morphogenesis|syndromic_disease|infectious_disease	obstetrics_and_gynecology|pediatric	autoimmune_diseases|inflammatory_disease	respiratory_system_disorder_is_actually_not_in_the_list_but_a_more_accurate_answer_would_be_lung_disorder|lung_disorder	true	false	false	false	medium
MONDO:0023148	fetal phenothiazine syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease	pediatrics|psychiatry|obstetrics_and_gynecology|neonatology	mental_health_disorder|neurodegenerative_disease	lower_gastrointestinal_disorder|brain_disorder|upper_gastrointestinal_disorder|lung_disorder|liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0023149	infection due to clostridium perfringens	infectious_disease	infectious_disease	infectious_disease	pediatrics|gastroenterology	bacterial_infection|infectious_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0023152	fibrocartilaginous embolism	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|pulmonology|cardiology|rheumatology|orthopaedic|hematology	cardiovascular_disorder|inflammatory_disease	joint_disorder|bone_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0023153	tuberculous ascites	infectious_disease	infectious_disease	infectious_disease	pulmonology|hepatology|gastroenterology	cancer|autoimmune_diseases|inflammatory_disease	lung_disorder|liver_disorder|immune_disorder	true	false	false	true	high
MONDO:0023154	fibromatosis multiple non ossifying	syndromic_disease	other	syndromic_disease	rheumatology|orthopaedic|genetics_and_genomics	cancer|autoimmune_diseases|metabolic_disorder|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0023155	fibula aplasia complex brachydactyly	syndromic_disease	other	syndromic_disease	orthopaedic|genetics_and_genomics	birth_defect|genetic_diseases|metabolic_disorder	muscle_disorder|joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0023157	fibular hypoplasia scapulo pelvic dysplasia absent	syndromic_disease	other	syndromic_disease	orthopaedic|genetics_and_genomics	genetic_disorder|congenital_disorder|metabolic_disorder	muscle_disorder|joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0023158	Fitz-Hugh-Curtis syndrome	syndromic_disease|inflammatory_disease|reproductive_system_disorder	other	syndromic_disease|inflammatory_disease|reproductive_system_disorder	obstetrics_and_gynecology|pediatric	cancer|autoimmune_diseases|inflammatory_disease	liver_disorder|kidney_disorder	true	false	false	true	medium
MONDO:0023161	viral myocarditis	inflammatory_disease|musculoskeletal_system_disorder|cardiovascular_disorder|infectious_disease	cardiovascular_disorder|infectious_disease	cardiovascular_disorder|inflammatory_disease|infectious_disease|musculoskeletal_system_disorder	pulmonology|pediatrics|hepatology|cardiology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|heart_disorder|vascular_disorder	true	false	false	true	high
MONDO:0023164	viral pericarditis	inflammatory_disease|infectious_disease|cardiovascular_disorder	cardiovascular_disorder|infectious_disease	inflammatory_disease|infectious_disease|cardiovascular_disorder	cardiothoracic|cardiology|pediatric	cardiovascular_disorder|inflammatory_disease	heart_disorder|viral_disorder	true	false	false	true	medium
MONDO:0023165	florid cystic endosalpingiosis of the uterus	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics|endocrinology	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	reproductive_system_disorder|uterus_disorder	false	false	false	false	low
MONDO:0023167	focal alopecia congenital megalencephaly	syndromic_disease	other	syndromic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	congenital_disorder|brain_disorder	false	false	false	false	low
MONDO:0023170	focal or multifocal malformations in neuronal migration	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	mental_health_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0023171	foix chavany Marie syndrome	syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder	neurology|genetics_and_genomics	mental_health_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0023175	Fontaine farriaux blanckaert syndrome	syndromic_disease	other	syndromic_disease	neurology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	vascular_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0023176	formaldehyde poisoning	poisoning	other	poisoning	pulmonology|toxicology_is_not_in_the_list_but__allergy_and_immunology|hematology	metabolic_disorder|neurodegenerative_disease	respiratory_system_disorder|lung_disorder	false	false	false	true	high
MONDO:0023178	fragile X syndrome type 1	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0023179	fragile X syndrome type 2	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0023180	fragile X syndrome type 3	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0023182	Franceschini Vardeu Guala syndrome	cardiovascular_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|hereditary_disease	cancer_or_benign_tumor|cardiovascular_disorder	disorder_of_development_or_morphogenesis|syndromic_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	pediatrics|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder	false	false	false	as_of_my_last_update_in_october_2023__there_are_no_known_efficacious_treatments_that_cure__prevent__or_specifically_treat_franceschini_vardeu_guala_syndrome__therefore__the_answer_is_false	high
MONDO:0023186	Fraser Jequier Chen syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0023188	Freiberg disease	syndromic_disease|musculoskeletal_system_disorder	other	syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|rheumatology|orthopaedic	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0023193	Friedman Goodman syndrome	syndromic_disease	other	syndromic_disease	neurology|pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	endocrine_disorder|liver_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0023196	frontonasal malformation cloacal exstrophy	syndromic_disease	other	syndromic_disease	obstetrics_and_gynecology|pediatric|genetics_and_genomics	congenital_abnormality|metabolic_disorder	nose_disorder|brain_disorder	false	false	false	false	high
MONDO:0023197	frontonasal dysplasia Klippel feil syndrome	syndromic_disease	other	syndromic_disease	otolaryngology|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|ear_disorder|spinal_disorder|facial_disorder	false	false	false	false	medium
MONDO:0023199	frontonasal dysplasia phocomelic upper limbs	syndromic_disease	other	syndromic_disease	neurology|pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	nose_disorder|upper_gastrointestinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0023200	Fryns Fabry Remans syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	brain_disorder|skin_disorder	false	false	false	false	high
MONDO:0023201	Fryns Smeets Thiry syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder|brain_disorder|joint_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0023203	Fuchs atrophia gyrata chorioideae et retinae	syndromic_disease	other	syndromic_disease	neurology|ophthalmology	autoimmune_diseases|neurodegenerative_disease	eye_disorder|chorioidea_et_retinae_disorder	false	false	false	false	high
MONDO:0023204	Fukuda-Miyanomae-Nakata syndrome	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|syndromic_disease	other	hereditary_disease|nervous_system_disorder|syndromic_disease|musculoskeletal_system_disorder	allergy_and_immunology|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|lymphatic_disorder|immune_disorder|vascular_disorder	false	false	false	false	low
MONDO:0023206	functional pancreatic neuroendocrine tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|endocrinology|gastroenterology	neuroendocrine_tumor|cancer	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0023208	Fuqua Berkovitz syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|inflammatory_disease	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0023209	galactorrhoea-hyperprolactinaemia	disorder_of_development_or_morphogenesis|metabolic_disease|nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder|breast_disorder	metabolic_disease|endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|nervous_system_disorder|breast_disorder|metabolic_disease|reproductive_system_disorder	endocrinology|obstetrics_and_gynecology	endocrine_disorder_is_not_in_the_list_but_it_is_relevant_so_we_use_inflammatory_disease__as_an_alternative|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0023212	Garret-Tripp syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	ear_disorder|bone_disorder	false	false	false	false	high
MONDO:0023214	gas bloat syndrome	syndromic_disease	other	syndromic_disease	hepatology|cardiology|pulmonology|gastroenterology	metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0023221	Gaucher ichthyosis restrictive dermopathy	syndromic_disease	other	syndromic_disease	dermatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|skin_disorder|liver_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0023224	inherited reflex epilepsy	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	inherited_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0023226	gershinibaruch Leibo syndrome	syndromic_disease	other	syndromic_disease	neurology|pediatric	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0023227	gestational diabetes insipidus	urinary_system_disorder	other	urinary_system_disorder	obstetrics_and_gynecology|endocrinology	metabolic_disorder|gestational_diabetes	endocrine_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0023230	Ghose-Sachdev-Kumar syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0023232	giant cell myocarditis	inflammatory_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	inflammatory_disease|acute_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiothoracic|cardiology|pulmonology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	muscle_disorder|heart_disorder	true	false	false	true	very_high
MONDO:0023238	giant mammary hamartoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|gastroenterology	hamartoma|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0023240	gigantism advanced bone age hoarse cry	syndromic_disease	other	syndromic_disease	otolaryngology|pediatric|endocrinology	adrenal_gland_disease|metabolic_disorder	throat_disorder|bone_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0023243	glass-chapman-hockley syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|neurology|pediatrics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	low
MONDO:0023246	linear porokeratosis	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|cancer	skin_disorder|liver_disorder	false	false	false	false	low
MONDO:0023249	polyarticular juvenile rheumatoid arthritis	inflammatory_disease|immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	autoimmune_disease	inflammatory_disease|musculoskeletal_system_disorder|immune_system_disorder|connective_tissue_disorder	rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder|bone_disorder	false	false	false	true	high
MONDO:0023250	global disaccharide intolerance	hereditary_disease|digestive_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|digestive_system_disorder	gastroenterology|endocrinology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0023255	glossopalatine ankylosis micrognathia ear anomalies	syndromic_disease	other	syndromic_disease	otolaryngology|genetics_and_genomics|orthopaedic|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	teeth_disorder|ear_disorder|throat_disorder	false	false	false	false	high
MONDO:0023258	glycogen storage disease type 1 due to SLC37A4 mutation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|hepatology	glycogen_storage_disease|metabolic_disorder	liver_disorder|muscle_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0023263	glyceraldehyde-3-phosphate dehydrogenase deficiency	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|metabolic_disorders|pediatric	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|metabolic_disorder_is_not_available_in_list__so__endocrine_disorder	false	false	false	false	high
MONDO:0023267	goldstein hutt syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	immune_disorder|bone_disorder|liver_disorder|joint_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0023272	goniodysgenesis intellectual disability short stature	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|neurodegenerative_disease	brain_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0023273	pigmented dermatofibrosarcoma protuberans	connective_tissue_disorder|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	oncology|dermatology	tumor_disease|cancer|dermatological_cancer	skin_disorder|muscle_disorder	false	true	false	true	medium
MONDO:0023275	Graham-Boyle-Troxell syndrome	cancer_or_benign_tumor|respiratory_system_disorder|urinary_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|urinary_system_disorder|cancer_or_benign_tumor	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0023282	granulomatous hypophysitis	endocrine_system_disorder|nervous_system_disorder|inflammatory_disease|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|inflammatory_disease|nervous_system_disorder|endocrine_system_disorder	pulmonology|rheumatology|endocrinology|allergy_and_immunology|immunology	inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	immune_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0023283	ovarian granulosa cell tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0023286	graphite pneumoconiosis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|respiratory|occupationalmedicine	occupational_disease|inflammatory_disease|respiratory_disease	lower_gastrointestinal_disorder|lung_disorder	false	false	false	false	high
MONDO:0023288	green sandford davison syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0023290	grix Blankenship Peterson syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|spinal_disorder	false	false	false	false	high
MONDO:0023297	guttate psoriasis	hereditary_disease|inflammatory_disease|integumentary_system_disorder|immune_system_disorder	other	inflammatory_disease|immune_system_disorder|hereditary_disease|integumentary_system_disorder	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|skin_disorder	false	false	false	true	medium
MONDO:0023305	heavy metal poisoning	poisoning	other	poisoning	renal_medicine|neurology|pulmonology|hepatology|gastroenterology	toxic_exposure_disease|metabolic_disorder	liver_disorder|kidney_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0023368	Ho-Kaufman-McAlister syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0023369	disorder of facial skeleton	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|otolaryngology	metabolic_disorder|inflammatory_disease	facial_skeleton|bone_disorder	false	false	false	false	medium
MONDO:0023370	neoplastic disease or syndrome	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology	cancer|neoplastic_disease	lymphatic_disorder|reproductive_system_disorder|skin_disorder|vascular_disorder|urinary_tract_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0023388	pityriasis rotunda	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|skin_disorder	false	false	false	false	low
MONDO:0023415	congenital candidiasis	infectious_disease	infectious_disease	infectious_disease	genetics_and_genomics|dermatology|pediatric	metabolic_disorder|congenital_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0023419	hyperprolinemia	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|biochemistry____changed_to_correct_response_as_per_original_request____genetics_and_genomics|genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0023472	chondrodysplasia situs inversus imperforate anus polydactyly	syndromic_disease	other	syndromic_disease	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder	polydactyly_is_not_in_the_list__however_i_assume_you_meant_to_provide_another_condition_and_it_seems_like_a_limb_disorder_would_be_more_accurate_than_joint_or_bone_but_since_that_is_also_not_listed_we_have_the_following|bone_disorder|lower_gastrointestinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0023483	infectious myositis	inflammatory_disease|musculoskeletal_system_disorder|infectious_disease	infectious_disease	infectious_disease|inflammatory_disease|musculoskeletal_system_disorder	rheumatology|infectious_disease	autoimmune_diseases|inflammatory_disease	muscle_disorder|immune_disorder|joint_disorder	true	false	false	true	high
MONDO:0023510	Jaffer-Beighton syndrome	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0023513	Jeune syndrome situs inversus	musculoskeletal_system_disorder|respiratory_system_disorder|cardiovascular_disorder|integumentary_system_disorder|urinary_system_disorder|hereditary_disease|syndromic_disease	cardiovascular_disorder	cardiovascular_disorder|respiratory_system_disorder|integumentary_system_disorder|urinary_system_disorder|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	pediatric|orthopaedic|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|bone_disorder|heart_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0023521	Judge Misch wright syndrome	disorder_of_visual_system|integumentary_system_disorder|syndromic_disease	other	integumentary_system_disorder|syndromic_disease|disorder_of_orbital_region|disorder_of_visual_system	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	joint_disorder|vascular_disorder|brain_disorder	true	false	false	false	high
MONDO:0023528	KSHV inflammatory cytokine syndrome	syndromic_disease	other	syndromic_disease|post_infectious_disorder	allergy_and_immunology|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0023530	kallikrein hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|renal_medicine	cardiovascular_disorder|metabolic_disorder	kidney_disorder|vascular_disorder	false	false	false	false	high
MONDO:0023538	Kaplowitz-Bodurtha syndrome	disorder_of_visual_system|nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	pediatric|hepatology|gastroenterology|genetics_and_genomics	inflammatory_disease|anemia|metabolic_disorder|cancer|autoimmune_diseases	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0023540	Kashani-Strom-Utley syndrome	syndromic_disease	other	syndromic_disease	dermatology|genetics_and_genomics	neurodegenerative_disease|anemia|inflammatory_disease|autoimmune_diseases	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0023541	Kasznica-Carlson-Coppedge syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|allergy|autoimmune_diseases	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0023543	Katsantoni-Papadakou-Lagoyanni syndrome	integumentary_system_disorder|syndromic_disease	other	integumentary_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	liver_disorder|kidney_disorder	false	false	false	false	none
MONDO:0023551	C1q nephropathy	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|rheumatology	inflammatory_disease|autoimmune_diseases	kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0023554	acquired testicular failure	reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	renal_medicine|pediatric|urology|endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0023557	infective vaginitis	inflammatory_disease|reproductive_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|reproductive_system_disorder	pediatric|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0023558	Kocher-debre-Semelaigne syndrome	musculoskeletal_system_disorder|endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	musculoskeletal_system_disorder|syndromic_disease|endocrine_system_disorder	cardiology|pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder	false	false	false	false	high
MONDO:0023561	Koone-Rizzo-Elias syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatrics|neurology	autoimmune_diseases|neurodegenerative_disease	bone_disorder|kidney_disorder|skin_disorder|liver_disorder|vascular_disorder	false	false	false	false	high
MONDO:0023563	Kotzot-Richter syndrome	syndromic_disease|metabolic_disease|hereditary_disease|integumentary_system_disorder|hematologic_disorder	metabolic_disease	syndromic_disease|hematologic_disorder|integumentary_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatrics	cancer|neurodegenerative_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0023567	Kozlowski Brown Hardwick syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|dermatology|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0023569	Kozlowski Ouvrier syndrome	syndromic_disease|hereditary_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder|hereditary_disease	pulmonology|occupational_disease	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	liver_disorder	false	false	false	false	high
MONDO:0023571	Kozlowski Rafinski Klicharska syndrome	syndromic_disease|disorder_of_visual_system|hereditary_disease	other	syndromic_disease|disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	genetics_and_genomics|pediatrics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	liver_disorder	false	false	false	false	high
MONDO:0023573	Kozlowski Warren Fisher syndrome	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|endocrine_disorder|skin_disorder|upper_gastrointestinal_disorder|reproductive_system_disorder|eye_disorder|urinary_tract_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0023575	Krauss Herman Holmes syndrome	syndromic_disease|disorder_of_visual_system	other	syndromic_disease|disorder_of_orbital_region|disorder_of_visual_system	psychiatry|neurology	autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0023577	Krieble Bixler syndrome	syndromic_disease|disorder_of_visual_system	other	syndromic_disease|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0023579	Kuster Majewski Hammerstein syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0023581	Kuster syndrome	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	immune_disorder|genetic_disorder|developmental_disorder	false	false	false	false	high
MONDO:0023595	congenital myotonic dystrophy	syndromic_disease|hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0023597	laryngeal papillomatosis	cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder	oncology|pediatric|otolaryngology	cancer|inflammatory_disease	lymphatic_disorder|throat_disorder	true	false	false	false	high
MONDO:0023599	mesomelic dysplasia	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder	bone_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0023601	non-classic congenital adrenal hyperplasia	hereditary_disease|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	hereditary_disease|metabolic_disease|endocrine_system_disorder	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0023603	hereditary disorder of connective tissue	connective_tissue_disorder|hereditary_disease	other	connective_tissue_disorder|hereditary_disease	rheumatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|connective_tissue_is_related_to_joints_so_it_fits_here_as_well	false	false	false	false	high
MONDO:0023605	Laugier-Hunziker syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|dermatology	neurodegenerative_disease|cancer	bone_disorder|skin_disorder	false	false	false	false	low
MONDO:0023607	Laurence-Prosser-Rocker syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|dermatology	neurodegenerative_disease|metabolic_disorder	liver_disorder|genetic_disorder	false	false	false	false	high
MONDO:0023609	le Marec-Bracq-Picaud syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|anemia|metabolic_disorder	joint_disorder|blood_bone_marrow_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0023619	lentigo maligna melanoma	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|integumentary_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	skin_cancer|malignant_tumor|cancer	skin_disorder|eye_disorder	false	true	false	true	medium
MONDO:0023628	levator syndrome	syndromic_disease|digestive_system_disorder	other	digestive_system_disorder|syndromic_disease	obstetrics_and_gynecology|otolaryngology|neurology|ophthalmology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|mental_health_disorder	brain_disorder|eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0023642	Weber syndrome	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|eye_disorder|vascular_disorder	false	false	false	false	high
MONDO:0023644	lip and oral cavity carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology|otolaryngology	inflammatory_disease|cancer	teeth_disorder|oral_cavity_carcinoma	false	true	false	true	high
MONDO:0023646	lipodermatosclerosis	immune_system_disorder|connective_tissue_disorder|integumentary_system_disorder|inflammatory_disease	autoimmune_disease	inflammatory_disease|connective_tissue_disorder|immune_system_disorder|integumentary_system_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0023650	littoral cell angioma of the spleen	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	hepatology|oncology|hematology	adrenal_gland_disease|cancer	liver_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0023655	immunodeficiency 14b, autosomal recessive	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	allergy_and_immunology|pediatric|genetics_and_genomics|immunology	inflammatory_disease|immune_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0023657	intellectual developmental disorder, autosomal dominant 65	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	intellectual_developmental_disorder_autosomal_dominant_65|brain_disorder	false	false	false	false	high
MONDO:0023659	developmental and epileptic encephalopathy 96	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|developmental_disorder	encephalopathy|developmental_disorder|brain_disorder|epileptic_disorder	true	false	false	true	very_high
MONDO:0023660	angioedema, hereditary, 6	integumentary_system_disorder|hereditary_disease|inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|inflammatory_disease|cardiovascular_disorder|integumentary_system_disorder	allergy_and_immunology|pediatric|genetics_and_genomics	autoimmune_diseases|allergic_disease	immune_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0023662	lymphatic malformation 10	immune_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|immune_system_disorder	dermatology|pediatric|oncology|hematology	lymphatic|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0023664	spermatogenic failure 54	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|endocrinology	adrenal_gland_disease|metabolic_disorder|cancer	reproductive_system_disorder	false	false	false	false	low
MONDO:0023670	Bardet-Biedl syndrome 20	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0023671	oculopharyngodistal myopathy 3	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	throat_disorder|muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0023679	hematohidrosis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|hematology	adrenal_gland_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	low
MONDO:0023682	tympanic paraganglioma	endocrine_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|auditory_system_disorder|hereditary_disease|otorhinolaryngologic_disease	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|otorhinolaryngologic_disease|auditory_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|endocrine_system_disorder	oncology|neurology|otolaryngology	cancer|neurological_cancer	throat_disorder|ear_disorder	false	true	false	false	medium
MONDO:0023691	maple syrup urine disease type 1A	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|renal_medicine|pediatric	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0023692	maple syrup urine disease type 1B	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|renal_medicine|pediatric	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0023693	maple syrup urine disease type 2	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|genetics_and_genomics|renal_medicine	genetic_disorder|inherited_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0023696	Marinesco-Sjogren-like syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|rheumatology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0023699	Maroteaux Fonfria syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	vascular_disorder|ear_disorder|muscle_disorder|brain_disorder|eye_disorder|joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0023704	Martinez Monasterio Pinheiro syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|syndromic_disease|integumentary_system_disorder	genetics_and_genomics|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0023726	mediastinal yolk sac tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric	cancer	lung_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0023757	meralgia paresthetica	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	neurological_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0023809	Milner-Khallouf-Gibson syndrome	syndromic_disease	other	syndromic_disease	pediatric|hematatology|genetics_and_genomics|neurology|allergy_and_immunology	mental_health_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0023833	multifocal choroiditis	cardiovascular_disorder|disorder_of_visual_system|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease	immune_disorder|eye_disorder	true	false	false	true	high
MONDO:0023865	corneal infection	inflammatory_disease|infectious_disease|disorder_of_visual_system	infectious_disease	inflammatory_disease|disorder_of_orbital_region|disorder_of_visual_system|infectious_disease	ophthalmology|dermatology	allergy|autoimmune_diseases|inflammatory_disease	eye_disorder	true	false	false	true	high
MONDO:0023868	melanoma associated retinopathy	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder	ophthalmology|dermatology|oncology	autoimmune_diseases|cancer	skin_disorder|eye_disorder	true	false	false	true	high
MONDO:0023880	WHIM syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|immunology|pediatric	inflammatory_disease|anemia|autoimmune_diseases|metabolic_disorder	lymphatic_disorder|immune_disorder|bone_bone_marrow_disorder	false	false	false	true	high
MONDO:0023910	Martsolf syndrome	syndromic_disease|disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|disorder_of_visual_system|syndromic_disease|hereditary_disease	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	kidney_disorder|eye_disorder|joint_disorder|skin_disorder|liver_disorder	false	false	false	true	high
MONDO:0023961	visceral neuropathy, familial	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	familial_disorders___note__i_corrected_the_category_name_to_match_the_provided_list__familial_is_a_type_of_disorder__so_it_fits_under_neurodegenerative_disease|neurodegenerative_disease	muscle_disorder|nerve_disorder	false	false	false	false	medium
MONDO:0024171	radio-digito-facial dysplasia	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|facial_dysplasia	false	false	false	false	medium
MONDO:0024182	dry beriberi	nutritional_disorder	other	nutritional_disorder	cardiology|endocrinology|pediatric	metabolic_disorder|inflammatory_disease	endocrine_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0024183	wet beriberi	nervous_system_disorder|nutritional_disorder	other	nutritional_disorder|nervous_system_disorder	cardiology|rheumatology|endocrinology	cardiovascular_disorder|metabolic_disorder|inflammatory_disease	endocrine_disorder|vascular_disorder	false	false	false	true	high
MONDO:0024189	neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset	hereditary_disease	other	hereditary_disease	neurology|endocrinology|pediatric	infantile_onset|endocrine|multisystem|neurodegenerative_disease|pancreatic_disease	neurologic|endocrine	false	false	false	true	very_high
MONDO:0024193	portal hypertension, noncirrhotic	hereditary_disease	other	hereditary_disease	gastroenterology|cardiology|hepatology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0024227	miliaria pustulosa	integumentary_system_disorder|syndromic_disease	other	integumentary_system_disorder|syndromic_disease	dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	low
MONDO:0024228	miliaria profunda	integumentary_system_disorder|syndromic_disease	other	integumentary_system_disorder|syndromic_disease	dermatology|general_medicine____dermatology|general_medicine___corrected_to__dermatology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0024229	miliaria crystallina	integumentary_system_disorder|syndromic_disease	other	integumentary_system_disorder|syndromic_disease	dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder	false	false	false	true	low
MONDO:0024234	Seckel like syndrome majoor-krakauer type	syndromic_disease	other	syndromic_disease	neurology|pediatric|genetics_and_genomics	developmental_disorder|metabolic_disorder|genetic_disorder	endocrine_disorder|joint_disorder|spinal_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0024235	Brenner tumor	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	renal_medicine|oncology|hematology	cancer|adrenal_gland_disease	kidney_disorder|blood_bone_marrow_disorder	false	true	false	false	medium
MONDO:0024237	inherited neurodegenerative disorder	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|inherited_neurodegenerative_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0024238	cerebral degeneration	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|inflammatory_disease	brain_disorder|cerebral_disorder	false	false	false	false	very_high
MONDO:0024239	congenital anomaly of cardiovascular system	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic|pediatric	cardiovascular_disorder|congenital_anomaly_of_cardiovascular_system	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0024240	eccrine carcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	cancer|adrenal_gland_disease	skin_disorder|cutaneous_disorder	false	true	false	false	high
MONDO:0024245	ductal eccrine adenocarcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|liver_disorder|skin_disorder	false	true	false	false	high
MONDO:0024246	syringofibroadenoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	neurology|dermatology	cancer|adrenal_gland_disease	bone_disorder|spinal_disorder	false	false	false	false	low
MONDO:0024247	benign eccrine neoplasm	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	oncology|dermatology	neoplasm|cancer	skin_disorder	false	false	false	false	low
MONDO:0024249	pityriasis lichenoides	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|immune_system_disorder|inflammatory_disease|integumentary_system_disorder|cardiovascular_disorder	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0024250	acute lichenoid pityriasis	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|immune_system_disorder|acute_disease|inflammatory_disease|integumentary_system_disorder|cardiovascular_disorder	pediatric|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0024251	Minamata disease	nervous_system_disorder	other	nervous_system_disorder	neurology|toxicology_is_not_listed__but_closest_match_is_neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease	brain_disorder|nerve_disorder_is_not_in_the_list__so_i_ll_remove_it	false	false	false	true	very_high
MONDO:0024257	hereditary motor neuron disease	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|hereditary	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0024262	massive neonatal aspiration syndrome	syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|syndromic_disease	pulmonology|pediatric	respiratory_disease|inflammatory_disease	lower_gastrointestinal_disorder|throat_disorder|lung_disorder	false	false	false	false	high
MONDO:0024263	neonatal aspiration syndrome	syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|syndromic_disease	pulmonology|pediatric	respiratory_problem|neonatal_condition|inflammatory_disease	respiratory_disorder_is_not_in_the_list__so_i_ll_use_lung_disorder|lung_disorder	false	false	false	false	medium
MONDO:0024264	hypothyroidism, congenital, nongoitrous, 2	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	congenital_disorder|endocrine_disorder|thyroid_disorder	false	false	false	true	medium
MONDO:0024265	Duane syndrome type 1	nervous_system_disorder|syndromic_disease|disorder_of_visual_system|hereditary_disease	other	nervous_system_disorder|hereditary_disease|syndromic_disease|disorder_of_visual_system	neurology|genetics_and_genomics	neurodegenerative_disease|eye_disorder	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0024266	patent ductus arteriosus 3	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	pediatric|cardiology	cardiovascular_disorder|congenital_anomaly	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0024268	superficial mycosis	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	dermatology	allergy|autoimmune_diseases|inflammatory_disease	nose_disorder|skin_disorder	true	false	false	true	low
MONDO:0024270	parasitic intestinal disorder	infectious_disease|digestive_system_disorder	infectious_disease	digestive_system_disorder|infectious_disease	other____no__just_the_categories____gastroenterology_pediatric|pediatric|gastroenterology	parasitic_intestinal_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0024271	intestinal helminthiasis	infectious_disease|digestive_system_disorder	infectious_disease	digestive_system_disorder|infectious_disease	pediatric|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0024275	amebic dysentery	inflammatory_disease|infectious_disease|digestive_system_disorder	infectious_disease	acute_disease|digestive_system_disorder|inflammatory_disease|infectious_disease	gastroenterology|hepatology	gastrointestinal_infection|infectious_disease|inflammatory_disease	lower_gastrointestinal_disorder|liver_disorder	true	false	false	true	medium
MONDO:0024276	glandular cell neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|otolaryngology	cancer|glandular_cell_neoplasm	skin_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0024277	neonatal thrombocytopenia	hematologic_disorder	other	hematologic_disorder	hematology|pediatric	anemia|autoimmune_diseases|neonatal_thrombocytopenia	blood_bone_marrow_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0024278	proctocolitis	hereditary_disease|immune_system_disorder|inflammatory_disease|digestive_system_disorder	other	digestive_system_disorder|inflammatory_disease|immune_system_disorder|hereditary_disease	gastroenterology|hepatology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	medium
MONDO:0024279	chronic endometritis	inflammatory_disease|reproductive_system_disorder	other	reproductive_system_disorder|inflammatory_disease	gastroenterology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0024280	polyarticular arthritis	musculoskeletal_system_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|inflammatory_disease	pediatric|rheumatology	autoimmune_diseases|inflammatory_disease	joint_disorder|immune_disorder	false	false	false	true	high
MONDO:0024281	juvenile chronic polyarthritis	musculoskeletal_system_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|inflammatory_disease	pediatric|rheumatology	autoimmune_diseases|inflammatory_disease	joint_disorder|bone_disorder|immune_disorder	false	false	false	true	high
MONDO:0024282	mucinous ovarian cancer	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0024283	Demodex folliculitis	integumentary_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	integumentary_system_disorder|inflammatory_disease|infectious_disease	dermatology|pediatrics	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0024284	demodicidosis of sebaceous gland	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	dermatology|pediatric	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	low
MONDO:0024285	epsilon-heavy chain disease	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0024286	benign blood vessel neoplasm	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	oncology|hematology	benign_blood_vessel_neoplasm_is_actually_more_specifically_classified_as_a_type_of_cancer__which_means_it_fits_into_this_category__but_also_could_fit_into_the_cardiovascular_disorder_category_because_it_affects_blood_vessels|cancer	vascular_disorder	false	false	false	true	low
MONDO:0024287	congenital vascular malformation	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pediatric|genetics_and_genomics|vascular_surgery__removed_because_it_is_not_in_the_category_list|cardiology	congenital_vascular_malformation|cardiovascular_disorder	vascular_disorder	false	false	false	false	medium
MONDO:0024288	hyperbilirubinemia	metabolic_disease	metabolic_disease	metabolic_disease	hepatology|hematology|pediatric	metabolic_disorder|anemia|inflammatory_disease	biliary_disorder|liver_disorder	false	false	false	true	medium
MONDO:0024290	enuresis	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	urology|neurology|pediatric	metabolic_disorder|mental_health_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	true	low
MONDO:0024291	vascular malformation	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	orthopaedic|vascular_surgery_is_not_in_the_list_so|cardiology	vascular_malformation_can_also_be_categorized_as_an_inflammatory_disease|cardiovascular_disorder	blood_bone_marrow_disorder|joint_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0024292	gastrointestinal polyp	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	gastrointestinal_disease|tumor|cancer|benign_tumor|polyp_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0024294	skin disorder caused by infection	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	dermatology|infectious_diseases	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0024295	skin disease caused by bacterial infection	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	dermatology|pediatric	autoimmune_diseases|bacterial_infection_is_not_in_the_list_so__inflammatory_disease|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0024296	vascular neoplasm	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	vascular_neoplasm_is_primarily_classified_under_a_subset_of_oncology__but_the_closest_fitting_categories_from_the_given_list_would_be__oncology__cardiology_and_hematology|oncology|hematology|cardiology	cancer|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder	false	true	false	false	medium
MONDO:0024298	vitamin deficiency disorder	nutritional_disorder	other	nutritional_disorder	hepatology|endocrinology|gastroenterology	metabolic_disorder|anemia	endocrine_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0024299	vitamin D-dependent rickets	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	endocrinology|pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|inflammatory_disease	endocrine_disorder|bone_disorder	false	false	false	true	high
MONDO:0024300	hypophosphatemic rickets	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	pediatric|renal_medicine|endocrinology	hypophosphatemic_rickets|metabolic_disorder	bone_disorder__kidney_disorder	false	false	false	true	high
MONDO:0024301	acquired mineral metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|renal_medicine|endocrinology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|liver_disorder	false	false	false	false	high
MONDO:0024302	internal hirudiniasis	upper_digestive_tract_disorder|infectious_disease	infectious_disease	infectious_disease|upper_digestive_tract_disorder	urology|hematology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|gastrointestinal_disorder	false	false	false	false	medium
MONDO:0024303	external hirudiniasis	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology	external_parasitosis|parasitic_disease|wound_infection|infectious_disease|skin_infection	joint_disorder|skin_disorder|reproductive_system_disorder|muscle_disorder	true	false	false	true	low
MONDO:0024304	ichthyosis vulgaris	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0024305	acquired hyperprolactinemia	endocrine_system_disorder|reproductive_system_disorder|metabolic_disease|nervous_system_disorder	endocrine_system_disorder|metabolic_disease	nervous_system_disorder|endocrine_system_disorder|metabolic_disease|reproductive_system_disorder	psychiatry|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0024306	acquired lactic acidosis	metabolic_disease	metabolic_disease	metabolic_disease	cardiology|renal_medicine|pulmonology|endocrinology	metabolic_disorder|acquired_lactic_acidosis	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0024307	prothrombin deficiency	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|hematology	blood_disorder|cardiovascular_disorder|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0024308	pseudoxanthoma elasticum (inherited or acquired)	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0024309	neuropathy, hereditary sensory and autonomic, type 2A	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0024310	angiodysplasia of stomach	digestive_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|digestive_system_disorder	cardiology|hepatology|gastroenterology	cardiovascular_disorder|gastrointestinal_disease	vascular_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0024311	cancer affecting bone of limb skeleton	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	hematology|orthopaedic|oncology	cancer|autoimmune_diseases	bone_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0024312	cancer of short bone of upper limb	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	orthopaedic|oncology	cancer|adrenal_gland_disease	bone_disorder|subtype|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0024313	staphylococcal infection	infectious_disease	infectious_disease	infectious_disease	pediatric|dermatology|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0024314	parasitemia	infectious_disease|hematologic_disorder	infectious_disease	hematologic_disorder|infectious_disease	parasitology|hematology	cancer|anemia	immune_disorder|blood_bone_marrow_disorder	true	false	false	false	very_high
MONDO:0024315	parasitic endophthalmitis	infectious_disease|disorder_of_visual_system|inflammatory_disease	infectious_disease	infectious_disease|disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	ophthalmology	inflammatory_disease|autoimmune_diseases	parasitic_disorder|infection|eye_disorder	true	false	false	true	high
MONDO:0024316	physiological malfunction arising from mental factor	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	physiological_malfunction_arising_from_mental_factor|mental_health_disorder	mental_factor_is_often_related_to_brain_function_so_this_category_is_more_likely_correct_than_other_categories_in_the_list|brain_disorder	false	false	false	false	medium
MONDO:0024317	chronic pain syndrome	nervous_system_disorder	other	nervous_system_disorder	rheumatology|neurology	inflammatory_disease|mental_health_disorder|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0024318	viral infection of central nervous system	infectious_disease|nervous_system_disorder	infectious_disease	nervous_system_disorder|infectious_disease	pediatric|neurology	viral_infection_of_central_nervous_system____inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	central_nervous_system_disorder|brain_disorder	true	false	false	false	high
MONDO:0024320	inner ear neoplasm	otorhinolaryngologic_disease|cancer_or_benign_tumor|auditory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|auditory_system_disorder	otolaryngology|oncology|neurology	cancer	ear_disorder	false	true	false	false	medium
MONDO:0024321	disorder of GPI anchor biosynthesis	metabolic_disease	metabolic_disease	metabolic_disease	hematology|genetics_and_genomics|immunology	inflammatory_disease|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0024322	disorder of glycosylation	metabolic_disease	metabolic_disease	metabolic_disease	pediatric|metabolic_diseases|genetics_and_genomics|molecular_biology|biochemistry|endocrinology	metabolic_disorder|disorder_of_glycosylation	liver_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0024323	glomangiomyoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	gynecology|oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	kidney_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0024325	cutaneous glomangiomyoma	cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|general_surgery|plastic_surgery	cancer|neoplasm	muscle_disorder|skin_disorder	false	false	false	false	low
MONDO:0024326	pleural adenomatoid tumor	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	cardiothoracic|oncology|pulmonology	inflammatory_disease|cancer|other____note__i_have_included__inflammatory_disease__as_it_is_a_plausible_category_for_a_tumor__although_pleural_adenomatoid_tumor_is_specifically_a_type_of_cancer	lung_disorder|pleural_disorder|lower_gastrointestinal_disorder	false	true	false	false	low
MONDO:0024327	chronic renal failure syndrome	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	renal_failure_ssyndrome|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0024330	infectious otitis media	otorhinolaryngologic_disease|auditory_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|otorhinolaryngologic_disease|auditory_system_disorder|inflammatory_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	throat_disorder|ear_disorder	true	false	false	true	medium
MONDO:0024331	colorectal carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0024332	perennial allergic rhinitis	otorhinolaryngologic_disease|immune_system_disorder|inflammatory_disease|respiratory_system_disorder	other	immune_system_disorder|otorhinolaryngologic_disease|respiratory_system_disorder|inflammatory_disease	otolaryngology|pulmonology|allergy_and_immunology	inflammatory_disease|allergy	lung_disorder|nose_disorder|immune_disorder	false	false	false	true	low
MONDO:0024333	sciatica	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0024334	peripheral nerve lesion	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|nerve_disorder	false	false	false	false	high
MONDO:0024335	retrobulbar neuritis	inflammatory_disease|nervous_system_disorder|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|inflammatory_disease	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder|spinal_disorder	true	false	false	true	medium
MONDO:0024336	vulvar adenocarcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer|adenocarcinoma	skin_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0024337	urothelial neoplasm	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology	cancer|urothelial_neoplasm	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0024338	mucinous neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|gastroenterology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0024339	lymph node neoplasm	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	oncology|hematology	cancer|lymphoma|neoplasm	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0024340	retinal neuroblastoma	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|nervous_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_orbital_region|cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder|disorder_of_development_or_morphogenesis	ophthalmology|oncology|pediatric	cancer	eye_disorder|brain_disorder	false	true	false	true	high
MONDO:0024341	retinal cell neoplasm	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_visual_system	cancer_or_benign_tumor	disorder_of_orbital_region|cancer_or_benign_tumor|disorder_of_visual_system|nervous_system_disorder	ophthalmology|oncology|neurology	cancer|neurodegenerative_disease	eye_disorder	false	true	false	false	high
MONDO:0024343	pityriasis simplex	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	skin_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0024344	pityriasis folliculorum	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0024346	pityriasis amiantacea	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder	false	false	false	false	low
MONDO:0024349	pityriasis alba	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	skin_disorder|immunne_disorder	false	false	false	false	low
MONDO:0024350	pityriasis steatoides	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0024352	viral respiratory tract infection	infectious_disease|respiratory_system_disorder	infectious_disease	infectious_disease|respiratory_system_disorder	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	lung_disorder|respiratory_system_disorder|throat_disorder	true	false	false	false	medium
MONDO:0024354	cytomegalovirus pneumonia	infectious_disease|inflammatory_disease|respiratory_system_disorder	infectious_disease	infectious_disease|respiratory_system_disorder|inflammatory_disease	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0024355	respiratory tract infectious disorder	infectious_disease|respiratory_system_disorder	infectious_disease	infectious_disease|respiratory_system_disorder	otolaryngology|pulmonology|respiratory_tract_infectious_disorder	inflammatory_disease|infectious_disorder|autoimmune_diseases|respiratory_tract_infectious_disorder_is_not_in_the_list_so_we_ll_exclude_it	lung_disorder|respiratory_tract_infectious_disorder	true	false	false	true	high
MONDO:0024356	primary central sleep apnea syndrome	syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|sleep_disorder|syndromic_disease	pulmonology|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0024357	drug induced central sleep apnea	syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|sleep_disorder|syndromic_disease	pulmonology|neurology	cardiovascular_disorder|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0024358	complex sleep apnea	syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|sleep_disorder|syndromic_disease	pulmonology|neurology	cardiovascular_disorder|metabolic_disorder	lung_disorder|vascular_disorder	false	false	false	true	high
MONDO:0024359	central sleep apnea due to periodic breathing	syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|sleep_disorder|syndromic_disease	pulmonology|neurology	cardiovascular_disorder|metabolic_disorder	lung_disorder|brain_disorder	false	false	false	true	medium
MONDO:0024360	central sleep apnea caused by high altitude	syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|sleep_disorder|syndromic_disease	pulmonology|neurology	cardiovascular_disorder|metabolic_disorder|respiratory_disease	lung_disorder|brain_disorder	false	false	false	true	medium
MONDO:0024361	circadian rhythm sleep disorder	other	other	sleep_disorder	pulmonology|neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	endocrine_disorder|brain_disorder	false	false	false	true	medium
MONDO:0024363	rapid eye movement sleep disorder	other	other	sleep_disorder	neurology|psychiatry	autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	eye_disorder|brain_disorder	false	false	false	true	medium
MONDO:0024376	sleep disorder, initiating and maintaining sleep	other	other	sleep_disorder	neurology|psychiatry	sleep_disorder|initiating_and_maintaining_sleep|metabolic_disorder|neurodegenerative_disease|mental_health_disorder	sleep_disorder|brain_disorder	false	false	false	true	high
MONDO:0024377	circadian rhythm sleep disorder, delayed sleep phase type	other	other	sleep_disorder	genetics_and_genomics|neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	endocrine_disorder|brain_disorder	false	false	false	true	medium
MONDO:0024378	circadian rhythm sleep disorder, advanced sleep phase type	other	other	sleep_disorder	endocrinology|neurology	neurodegenerative_disease|mental_health_disorder	endocrine_disorder|brain_disorder	false	false	false	true	medium
MONDO:0024379	circadian rhythm sleep disorder, irregular sleep wake type	other	other	sleep_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	sleep_disorder|endocrine_disorder|brain_disorder	false	false	false	true	medium
MONDO:0024381	circadian rhythm sleep disorder, jet lag type	other	other	sleep_disorder	pulmonology|psychiatry|neurology	circadian_rhythm_sleep_disorder|mental_health_disorder	endocrine_disorder|brain_disorder	false	false	false	true	medium
MONDO:0024382	circadian rhythm sleep disorder, shift work type	other	other	sleep_disorder	sleep_disorder_type_is_removed_from_list_since_it_s_a_subtype_of_the_disease_category_which_is_neurology_so_best_categories_are_neurology|psychiatry|neurology	metabolic_disorder|mental_health_disorder	sleep_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0024386	large cell lung carcinoma, clear cell variant	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	oncology|pulmonology	autoimmune_diseases|inflammatory_disease|cancer|adrenal_gland_disease	lung_disorder	false	true	false	true	high
MONDO:0024387	benign ovarian sex cord-stromal tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0024388	Clostridium infectious disease	infectious_disease	infectious_disease	infectious_disease	obstetrics_and_gynecology|pediatric|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0024389	anaerobic bacteria infectious disease	infectious_disease	infectious_disease	infectious_disease	rheumatology|pulmonology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0024392	anaerobic balanitis	reproductive_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease|inflammatory_disease	pediatrics|dermatology|renal_medicine|urology|pulmonology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|lower_gastrointestinal_disorder	true	false	false	false	low
MONDO:0024410	infection caused by Bifidobacterium	infectious_disease	infectious_disease	infectious_disease	allergy_and_immunology|pediatrics|gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder	true	false	false	false	none
MONDO:0024412	Peptostreptococcus infectious disease	infectious_disease	infectious_disease	infectious_disease	gastroenterology|pulmonology	autoimmune_diseases|inflammatory_disease	throat_disorder|nose_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0024414	anaerobic cellulitis	integumentary_system_disorder|infectious_disease	infectious_disease	infectious_disease|integumentary_system_disorder	general_surgery|orthopaedic|dermatology|urology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	muscle_disorder|skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0024415	hemorrhagic duodenitis	digestive_system_disorder|inflammatory_disease	other	inflammatory_disease|digestive_system_disorder	hepatology|hematology|gastroenterology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	false	medium
MONDO:0024416	Neorickettsia infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|infectious_disease	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0024417	perceptual disorders	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	ear_disorder|eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0024418	muscular fibrosis multifocal obstructed vessels	syndromic_disease	other	syndromic_disease	genetics_and_genomics|cardiology|hematology|rheumatology|pulmonology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	muscle_disorder|vascular_disorder	false	false	false	false	high
MONDO:0024419	enthesitis	connective_tissue_disorder|musculoskeletal_system_disorder|inflammatory_disease	other	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|joint_disorder	false	false	false	true	high
MONDO:0024421	short stature contractures hypotonia	syndromic_disease	other	syndromic_disease	endocrinology|genetics_and_genomics|neurology	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0024422	auditory perceptual disorders	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	otolaryngology|neurology	mental_health_disorder|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0024429	Alice in Wonderland syndrome	nervous_system_disorder|syndromic_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	nervous_system_disorder|syndromic_disease|disorder_of_visual_system|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	lung_disorder|brain_disorder	false	false	false	false	medium
MONDO:0024430	allesthesia	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	low
MONDO:0024431	bilirubin metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|hepatology|hematology	metabolic_disorder|bilirubin_metabolism_disease_does_not_fit_any_category_from_the_list	liver_disorder|biliary_disorder	false	false	false	true	medium
MONDO:0024432	nerve plexus disorder	nervous_system_disorder	other	nervous_system_disorder	neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0024454	sacral nerve plexus disorder	nervous_system_disorder	other	nervous_system_disorder	obstetrics_and_gynecology|neurology|urology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0024455	autosomal dominant Robinow syndrome 1	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|neurology|pediatric	cardiovascular_disorder|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	skin_disorder|brain_disorder|eye_disorder|bone_disorder	false	false	false	false	medium
MONDO:0024456	anterior segment dysgenesis 3	disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system	other	disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|pediatric|ophthalmology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0024457	neurodegeneration with brain iron accumulation 2A	nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	metabolic_disease|neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|metabolic_disease|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0024458	disorder of visual system		other		neurology|ophthalmology	disorder_of_visual_system|neurodegenerative_disease	visual_system|eye_disorder	false	false	false	false	high
MONDO:0024459	Aeromonas hydrophila intestinal disease	digestive_system_disorder|infectious_disease	infectious_disease	infectious_disease|digestive_system_disorder	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0024461	angiomatosis	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	hematology|genetics_and_genomics|dermatology|neurology	cancer|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0024462	susceptibility to familial cutaneous melanoma	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	oncology|genetics_and_genomics|dermatology	cancer|familial_cancer_syndrome|genetic_disorder	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0024463	ovarian dysgenesis 1	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics	cancer|autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0024464	pituitary hormone deficiency, combined, 1	nervous_system_disorder|reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	nervous_system_disorder|hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrinology|neurology	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|pituitary_disorder	false	false	false	true	high
MONDO:0024465	surfactant metabolism dysfunction, pulmonary, 2	hereditary_disease|respiratory_system_disorder	other	hereditary_disease|respiratory_system_disorder	pulmonology|pediatric	pulmonary____if_it_were_one_category___inflammatory_disease|metabolic_disorder|inflammatory_disease	lung_disorder|pulmonary	false	false	false	false	high
MONDO:0024466	facial paresis, hereditary congenital, 1	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0024467	apocrine sweat gland disorder	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|genetic_disorder|endocrine_disorder	skin_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0024468	anterior pituitary gland disorder	nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder|reproductive_system_disorder	endocrinology|neurology	neurodegenerative_disease|endocrine_disorder	endocrine_disorder|brain_disorder	false	false	false	false	medium
MONDO:0024469	chondrogenic neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|orthopaedic	adrenal_gland_disease|cancer|neoplasm	joint_disorder|bone_disorder	false	true	false	false	medium
MONDO:0024470	benign chondrogenic neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|orthopaedic	cancer|benign_chondrogenic_neoplasm_falls_under_this_category_as_it_is_a_non_malignant_tumor_which_is_still_a_type_of_tumor	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	low
MONDO:0024472	boutonneuse fever	infectious_disease	infectious_disease	infectious_disease	rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	joint_disorder|skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0024473	Astrakhan spotted fever	infectious_disease	infectious_disease	infectious_disease	hepatology|hematology|pulmonology	autoimmune_diseases|inflammatory_disease	liver_disorder|skin_disorder	true	false	false	false	medium
MONDO:0024474	intraepithelial neoplasia	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pathology	intraepithelial_neoplasia_is_a_precancerous_lesion_that_has_the_potential_to_develop_into_cancer__so_it_fits_under_this_category|cancer	skin_disorder	false	true	false	true	medium
MONDO:0024475	squamous cell intraepithelial neoplasia	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pulmonology|dermatology	cancer|intraepithelial_neoplasia|squamous_cell_carcinoma	skin_disorder	false	true	false	true	medium
MONDO:0024476	epithelial neoplasm of rectum	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|epithelial_neoplasm	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0024477	liver and intrahepatic bile duct neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	hepatology|oncology|gastroenterology	cancer|liver_and_intrahepatic_bile_duct_neoplasm_is_already_a_cancer_so_this_category_is_redundant	biliary_disorder|liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0024478	mesenchymal hamartoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric|gastroenterology	cancer|adrenal_gland_disease	liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0024479	epithelial tumor of colon	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease|autoimmune_diseases|allergy|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0024480	dermatosis of eyelid	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	dermatology|ophthalmology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	medium
MONDO:0024481	skin appendage disorder	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	autoimmune_diseases|skin_appendage_disorder_is_often_a_symptom_of_autoimmune_conditions__such_as_psoriasis__a_type_of_autoimmune_disease_that_affects_the_skin__and_alopecia_areata__an_autoimmune_disorder_that_causes_hair_loss	skin_disorder|skin_appendage_disorder	false	false	false	false	low
MONDO:0024482	eccrine sweat gland hamartoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|dermatology	cancer|skin_disease	skin_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0024483	urothelial hyperplasia	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	renal_medicine|urology	cancer|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0024485	papillary urothelial hyperplasia	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	renal_medicine|urology	cancer|urotheial_carcinoma	urinary_tract_disorder|kidney_disorder	false	false	false	false	low
MONDO:0024487	nail infection	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0024498	glioma susceptibility 1	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	oncology|genetics_and_genomics|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0024499	vascular bone neoplasm	cardiovascular_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder|cardiovascular_disorder	orthopaedic|oncology	autoimmune_diseases|cancer|inflammatory_disease	vascular_disorder|bone_disorder	false	true	false	false	medium
MONDO:0024500	duodenal neuroendocrine neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|neuroendocrine_tumor	endocrine_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0024501	appendix neuroendocrine neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	neurology|endocrinology|oncology	cancer|endocrine_disorder|neuroendocrine_tumors	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0024502	gallbladder neuroendocrine neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	hepatology|oncology|gastroenterology	cancer|neuroendocrine_tumor_subcategory__note__this_is_a_subcategory_i_inferred_based_on_the_disease_name|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0024503	digestive system neuroendocrine neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	cancer|adrenal_gland_disease|neuroendocrine_neoplasm	liver_disorder|endocrine_disorder|lower_gastrointestinal_disorder	false	true	false	false	high
MONDO:0024504	enterochromaffin cell serotonin-producing pancreatic neuroendocrine tumor	cancer_or_benign_tumor|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|oncology|gastroenterology	cancer|pancreatic_neuroendocrine_tumor___wait__there_is_no__neuroendocrine_tumor__in_the_category_list___cancer|pancreatic_cancer|pancreatic_disease|neuroendocrine_tumor	endocrine_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0024506	Adams-Oliver syndrome 1	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|anemia|metabolic_disorder	muscle_disorder|vascular_disorder|skeletal_disorder	false	false	false	false	medium
MONDO:0024507	aniridia 1	disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	neurodegenerative_disease|eye_disorder|genetic_disorder	reproductive_system_disorder|eye_disorder	false	false	false	false	high
MONDO:0024508	epilepsy, hot water, 1	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0024516	familial acne inversa	hereditary_disease|inflammatory_disease|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease|hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0024517	SMARCB1-related schwannomatosis	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|integumentary_system_disorder|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	oncology|genetics_and_genomics	cancer|neurological_diseases	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0024518	reactive thrombocytosis	hematologic_disorder	other	hematologic_disorder	renal_medicine|hematology|cardiology	metabolic_disorder|inflammatory_disease	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0024519	renal hypodysplasia/aplasia 1	disorder_of_development_or_morphogenesis|hereditary_disease|urinary_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|urinary_system_disorder	urology|pediatric|renal_medicine	kidney_disease|renal_impairment____corrected_to____metabolic_disorder|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0024520	renal hypodysplasia/aplasia 3	disorder_of_development_or_morphogenesis|hereditary_disease|urinary_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|urinary_system_disorder	urology|pediatric|renal_medicine	kidney_disease|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0024521	aortic aneurysm, familial abdominal, 1	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	pulmonology|genetics_and_genomics|hematology|cardiology	familial_abdominal_aortic_anneurysm_does_not_exist_so_i_assume_you_meant_familial_abdominal|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0024522	amyloidosis, primary localized cutaneous, 1	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	renal_medicine|genetics_and_genomics|hematology|dermatology	autoimmune_diseases|metabolic_disorder	skin_disorder|lymphatic_disorder	false	false	false	true	medium
MONDO:0024523	aortic valve disease 1	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiothoracic|cardiology	aortic_valve_disease|autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0024524	dyschromatosis universalis hereditaria 1	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|dermatology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	genetic_disorder_is_not_in_the_list_but_it_can_be_inferred_that_blood_bone_marrow_disorder_could_be_included_too_since_dyschromatosis_universalis_hereditaria_affects_pigmentation_of_the_eyes_and_skin_and_is_a_genetic_disorder_affecting_the_bone_marrow|eye_disorder|skin_disorder	false	false	false	false	low
MONDO:0024525	Fanconi renotubular syndrome 1	hereditary_disease|syndromic_disease|urinary_system_disorder	other	syndromic_disease|hereditary_disease|urinary_system_disorder	pediatric|renal_medicine|genetics_and_genomics	kidney_disease|anemia|metabolic_disorder	blood_bone_marrow_disorder|kidney_disorder	false	false	false	true	high
MONDO:0024526	Zimmermann-Laband syndrome 1	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0024527	glomerulopathy with fibronectin deposits 1	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	nephrology|renal_medicine|rheumatology	autoimmune_diseases|inflammatory_disease	kidney_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0024528	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|nervous_system_disorder|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0024529	MVP1	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiothoracic|cardiology	autoimmune_diseases|cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	none
MONDO:0024530	Bethlem myopathy 1A	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|eye_disorder|immune_disorder	false	false	false	false	high
MONDO:0024531	myopathy, tubular aggregate, 1	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|myopathy	false	false	false	true	medium
MONDO:0024532	otofaciocervical syndrome 1	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|otolaryngology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	throat_disorder|ear_disorder	false	false	false	false	medium
MONDO:0024533	pulmonary hypertension, primary, 1	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	pulmonology|cardiology	primary____note__primary_pulmonary_hypertension_is_often_associated_with_cardiovascular_disease|cardiovascular_disorder	lung_disorder|vascular_disorder	false	false	false	true	high
MONDO:0024534	Dowling-Degos disease 1	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	dermatology|gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0024535	Singleton-Merten syndrome 1	disorder_of_development_or_morphogenesis|hereditary_disease|connective_tissue_disorder|syndromic_disease|musculoskeletal_system_disorder	other	connective_tissue_disorder|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	vascular_disorder|urinary_tract_disorder|liver_disorder|kidney_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0024536	glucocorticoid deficiency 1	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	endocrinology|pediatrics	adrenal_gland_disease|metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0024537	Brown-Vialetto-van Laere syndrome 1	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0024538	basal ganglia calcification, idiopathic, 1	hereditary_disease|nervous_system_disorder	other	idiopathic_disease|nervous_system_disorder|hereditary_disease	neurology|cardiothoracic|genetics_and_genomics|cardiology	neurodegenerative_disease|metabolic_disorder	brain_disorder|vascular_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0024539	choroidal dystrophy, central areolar, 1	hereditary_disease|disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder|psychiatric_disorder	disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder|cardiovascular_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0024540	Jervell and Lange-Nielsen syndrome 1	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|cardiovascular_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0024541	trichohepatoenteric syndrome 1	immune_system_disorder|hereditary_disease|connective_tissue_disorder|syndromic_disease|digestive_system_disorder	other	digestive_system_disorder|connective_tissue_disorder|syndromic_disease|hereditary_disease|immune_system_disorder	hepatology|genetics_and_genomics|gastroenterology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|liver_disorder	true	false	false	true	high
MONDO:0024542	cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1	hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	syndromic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|brain_disorder_is_repeated_so_it_should_be|spinal_disorder	false	false	false	false	very_high
MONDO:0024543	brittle cornea syndrome 1	disorder_of_development_or_morphogenesis|hereditary_disease|connective_tissue_disorder|disorder_of_visual_system|syndromic_disease	other	disorder_of_orbital_region|disorder_of_visual_system|connective_tissue_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	ophthalmology|genetics_and_genomics	metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|eye_disorder	false	false	false	false	high
MONDO:0024545	Miyoshi muscular dystrophy 1	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	true	high
MONDO:0024546	hypertrophic osteoarthropathy, primary, autosomal recessive, 1	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	rheumatology|pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0024547	pancreatic agenesis 1	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	endocrinology|pediatric|genetics_and_genomics|gastroenterology	congenital_disorder|developmental_disorder|metabolic_disorder	pancreatic_disorder|upper_gastrointestinal_disorder|liver_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0024548	peeling skin syndrome 1	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0024549	microphthalmia with coloboma 1	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0024550	frontometaphyseal dysplasia 1	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	genetic_disease|metabolic_disorder	muscle_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0024551	X-linked lymphoproliferative disease due to SH2D1A deficiency	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	oncology|pediatric|genetics_and_genomics	autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0024552	linear skin defects with multiple congenital anomalies 1	hereditary_disease|integumentary_system_disorder|disorder_of_visual_system|syndromic_disease	other	disorder_of_orbital_region|integumentary_system_disorder|disorder_of_visual_system|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder	false	false	false	false	high
MONDO:0024553	myopathy, lactic acidosis, and sideroblastic anemia 1	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|mitochondrial_disease|metabolic_disease|hematologic_disorder	anemia|metabolic_disease	metabolic_disease|mitochondrial_disease|hematologic_disorder|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|renal_medicine|hematology	anemia|metabolic_disorder	muscle_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0024554	D-2-hydroxyglutaric aciduria 1	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0024555	megalencephalic leukoencephalopathy with subcortical cysts 1	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0024556	epilepsy, familial focal, with variable foci 1	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0024557	ataxia-telangiectasia-like disorder 1	hereditary_disease|nervous_system_disorder|metabolic_disease	neurodegenerative_disease|metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	immune_disorder|joint_disorder|brain_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0024558	radioulnar synostosis with amegakaryocytic thrombocytopenia 1	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|hematologic_disorder	other	hematologic_disorder|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|hematology	anemia|genetic_disorder|metabolic_disorder	joint_disorder|blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0024559	aortic aneurysm, familial thoracic 1	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	pulmonology|genetics_and_genomics|cardiothoracic|cardiology	cardiovascular_disorder|metabolic_disorder|familial	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0024560	PDA1	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|cardiology	inflammatory_disease|neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	heart_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0024561	vitelliform macular dystrophy 3	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	neurology|ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0024562	sick sinus syndrome 1	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	pulmonology|cardiothoracic|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0024564	cerebroretinal microangiopathy with calcifications and cysts 1	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|premature_aging_syndrome	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease|nervous_system_disorder|premature_aging_syndrome	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	brain_disorder|vascular_disorder|eye_disorder	false	false	false	false	high
MONDO:0024565	ectodermal dysplasia-syndactyly syndrome 1	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	integumentary_system_disorder|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	skin_disorder|joint_disorder|eye_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0024566	febrile seizures, familial, 11	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0024567	hypotonia, infantile, with psychomotor retardation and characteristic facies 1	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|brain_disorder	true	false	false	true	very_high
MONDO:0024568	infantile liver failure syndrome 1	hereditary_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|hepatology	metabolic_disorder	lower_gastrointestinal_disorder|liver_disorder	false	false	false	true	very_high
MONDO:0024569	optic atrophy 8	mitochondrial_disease|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	neurodegenerative_disease	disorder_of_orbital_region|disorder_of_visual_system|mitochondrial_disease|hereditary_disease|nervous_system_disorder	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0024570	hyperparathyroidism 4	musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder|cancer_or_benign_tumor|endocrine_system_disorder|syndromic_disease	endocrine_system_disorder|cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|endocrine_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	endocrinology|renal_medicine	autoimmune_diseases|metabolic_disorder	endocrine_disorder|blood_bone_marrow_disorder|bone_disorder	false	false	false	true	medium
MONDO:0024571	AIDS-related disorder	immune_system_disorder	other	post_infectious_disorder|immune_system_disorder	psychiatry|pulmonology|allergy_and_immunology|immunology|pediatrics	inflammatory_disease|autoimmune_diseases|mental_health_disorder	lymphatic_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0024572	immunodeficiency-related disorder	immune_system_disorder	other	immune_system_disorder	allergy_and_immunology|immunology	immunodeficiency_related_disorder_also_belongs_to_inflammatory_disease_category|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0024573	familial hypertrophic cardiomyopathy	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	pediatric|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0024574	von Willebrand disease (hereditary or acquired)	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|hematology	blood_disorder|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0024575	pregnancy disorder	obstetric_disorder	other	obstetric_disorder	pediatrics|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	pregnancy_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0024582	male reproductive system neoplasm	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	adrenal_gland_disease|other___removed_cancer_as_it_is_too_broad____adrenal_gland_disease|cancer	reproductive_system_disorder|male_reproductive_system_neoplasm	false	true	false	false	high
MONDO:0024607	congenital muscular dystrophy with cataracts and intellectual disability	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	genetics_and_genomics|neurology|pediatric|ophthalmology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	muscle_disorder|eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0024608	dientamoebiasis	digestive_system_disorder|infectious_disease	infectious_disease	digestive_system_disorder|infectious_disease	hepatology|pediatric|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0024609	vulvar squamous cell carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|dermatology|oncology	cancer	reproductive_system_disorder|skin_disorder	false	true	false	false	high
MONDO:0024610	parasitic skin disorder	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|parasitic_skin_disorder	true	false	false	true	medium
MONDO:0024611	orbit neoplasm	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|disorder_of_orbital_region|musculoskeletal_system_disorder	oncology|ophthalmology	cancer|orbital_neoplasm_can_also_be_classified_under_a_specific_category_called_orbit_cancer_which_is_a_type_of_eye_cancer_that_starts_in_the_tissues_around_the_eye_socket__including_the_eyelids__lacrimal_gland__or_eye_muscles	brain_disorder|eye_disorder	false	true	false	false	high
MONDO:0024612	manic bipolar affective disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0024613	bipolar depression	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	bipolar_depression|mental_health_disorder	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0024614	neurotic depression	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	psychiatry|neurology	neurotic_depression|mental_health_disorder	mental_disorder|brain_disorder	false	false	false	true	high
MONDO:0024615	T-cell and NK-cell neoplasm	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|immune_disorder	false	true	false	false	very_high
MONDO:0024616	tympanitis	auditory_system_disorder|otorhinolaryngologic_disease|inflammatory_disease	other	inflammatory_disease|auditory_system_disorder|otorhinolaryngologic_disease	pediatrics|otolaryngology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|throat_disorder|ear_disorder	true	false	false	false	medium
MONDO:0024617	xanthogranuloma	immune_system_disorder	other	immune_system_disorder	dermatology|pulmonology	autoimmune_diseases|inflammatory_disease|cancer	skin_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0024618	poliovirus infection	infectious_disease	infectious_disease	infectious_disease	neurology|pediatric	inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	true	false	false	true	high
MONDO:0024619	central nervous system infectious disorder	nervous_system_disorder|infectious_disease	infectious_disease	nervous_system_disorder|infectious_disease	neurology|pediatric	neurodegenerative_disease|central_nervous_system_infectious_disorder	central_nervous_system_inflectious_disorder|brain_disorder	true	false	false	true	high
MONDO:0024620	meningitis caused by poliovirus	inflammatory_disease|nervous_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|nervous_system_disorder|infectious_disease	neurology|pediatric	inflammatory_disease|neurodegenerative_disease	upper_gastrointestinal_disorder|spinal_disorder|brain_disorder	true	false	false	false	high
MONDO:0024621	serous cystadenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	gynecology|oncology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|kidney_disorder	false	true	false	false	very_high
MONDO:0024622	thyroid gland adenocarcinoma	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	thyroid_gland_disease|autoimmune_diseases|cancer|adrenal_gland_disease	blood_bone_marrow_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0024623	otorhinolaryngologic disease		other		otorhinolaryngologic_disease|otolaryngology	autoimmune_diseases|otorhinolaryngologic_disease|inflammatory_disease	throat_disorder|ear_disorder	true	false	false	false	medium
MONDO:0024625	disorder of lacrimal gland	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|otolaryngology	autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	low
MONDO:0024626	defective phagocytic cell engulfment	immune_system_disorder	other	immune_system_disorder	hematology|allergy_and_immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	true	false	false	false	high
MONDO:0024627	phagocytic cell dysfunction	immune_system_disorder	other	immune_system_disorder	hematology|immunology|allergy_and_immunology	autoimmune_diseases|anemia|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0024630	defective phagocytic cell chemotaxis	immune_system_disorder	other	immune_system_disorder	hematology|rheumatology|allergy_and_immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0024632	defective phagocytic cell opsonization	immune_system_disorder	other	immune_system_disorder	hematology|allergy_and_immunology	autoimmune_diseases|anemia|inflammatory_disease	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0024633	hypertensive nephropathy	urinary_system_disorder	other	urinary_system_disorder	cardiology|renal_medicine	cardiovascular_disorder|metabolic_disorder	vascular_disorder|kidney_disorder	false	false	false	true	high
MONDO:0024634	large intestine disorder	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|hepatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0024635	small intestine disorder	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|hepatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0024636	inflammation of heart layer	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	cardiology|cardiothoracic	inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	true	false	false	true	high
MONDO:0024637	malignant soft tissue neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	orthopaedic|oncology	cancer|malignant_software_neoplasm	muscle_disorder|soft_tissue_neoplasm	false	true	false	false	high
MONDO:0024638	pancreatic gastrinoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	cancer|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0024639	gastric enterochromaffin cell serotonin-producing neuroendocrine tumor	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|endocrinology|oncology	neuroendocrine_tumor|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0024642	gastric neuroendocrine tumor G2	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	cancer|gastrointestinal_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0024643	myocardial disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0024644	myocardial ischemia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|pulmonology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0024645	retroperitoneal neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|general_surgery|oncology	adrenal_gland_disease|cancer	lymphatic_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|muscle_disorder|vascular_disorder|kidney_disorder	false	true	false	false	high
MONDO:0024647	urolithiasis	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	metabolic_disorder|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0024648	optic tract meningioma	psychiatric_disorder|disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder	psychiatric_disorder|cancer_or_benign_tumor	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|cancer_or_benign_tumor	neurology|ophthalmology|oncology	cancer|neurological_cancer	brain_disorder|eye_disorder	false	true	false	false	high
MONDO:0024649	optic tract astrocytoma	psychiatric_disorder|disorder_of_visual_system|cancer_or_benign_tumor|nervous_system_disorder	psychiatric_disorder|cancer_or_benign_tumor	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|cancer_or_benign_tumor	neurology|ophthalmology|oncology	neurodegenerative_disease|astrocytoma|cancer	brain_disorder|eye_disorder	false	true	false	false	high
MONDO:0024650	drug-induced osteoporosis	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	rheumatology|orthopaedic|endocrinology|renal_medicine|hematology	metabolic_disorder|inflammatory_disease	osteoporosis|bone_disorder	false	false	false	true	high
MONDO:0024651	corticosteroid-induced osteoporosis	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	rheumatology|endocrinology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	endocrine_disorder|bone_disorder	false	false	false	true	high
MONDO:0024652	embryonic cyst of fallopian tube	reproductive_system_disorder	other	reproductive_system_disorder	genetics_and_genomics|obstetrics_and_gynecology	cancer|reproductive_system_disorder|gynecological_disease	reproductive_system_disorder	false	false	false	false	low
MONDO:0024653	skull neoplasm	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0024654	skull disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	neurology|orthopaedic	neurodegenerative_disease|skull_disorder_can_also_be_related_to_inflammatory_disease	brain_disorder|skull_disorder_is_not_in_the_list__so_it_cannot_be_selected__however__skull_disorders_can_also_be_related_to_brain_disorders__therefore__bone_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0024655	rheumatic pericarditis	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	cardiology|rheumatology|cardiothoracic	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	immune_disorder|joint_disorder|heart_disorder	true	false	false	true	medium
MONDO:0024656	colorectal lymphoma	digestive_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|digestive_system_disorder	hematology|gastroenterology|oncology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|lower_gastrointestinal_disorder	true	true	false	true	high
MONDO:0024658	extrahepatic bile duct sarcoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology|hepatology	cancer|sarcoma	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0024659	colorectal Kaposi sarcoma	digestive_system_disorder|infectious_disease|cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder|infectious_disease	cardiovascular_disorder|post_infectious_disorder|infectious_disease|cancer_or_benign_tumor|digestive_system_disorder	dermatology|gastroenterology|oncology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|lower_gastrointestinal_disorder|skin_disorder	false	true	false	false	high
MONDO:0024660	tubular adenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|gastroenterology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0024661	tubulovillous adenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	gastroenterology|oncology|renal_medicine	adrenal_gland_disease|cancer	kidney_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0024662	colorectal tubulovillous adenoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0024663	primary skin meningioma	integumentary_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	meningioma_is_a_type_of_brain_tumor_which_can_be_treated_as_an_instance_of_cancer|cancer	brain_disorder|skin_disorder	false	false	false	false	low
MONDO:0024664	hypertension, pregnancy-induced	cardiovascular_disorder|obstetric_disorder	cardiovascular_disorder	cardiovascular_disorder|obstetric_disorder	cardiology|obstetrics_and_gynecology|renal_medicine	metabolic_disorder|cardiovascular_disorder	kidney_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0024665	indeterminate sex and/or pseudohermaphroditism	endocrine_system_disorder|reproductive_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	urology|genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0024666	benign epithelial skin neoplasm	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer|benign_epithelial_skin_neoplasm_is_actually_a_type_of_cancer	skin_disorder	false	false	false	true	low
MONDO:0024673	skin lymphangioma	cardiovascular_disorder|immune_system_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor|integumentary_system_disorder|immune_system_disorder	pediatric|dermatology	autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|skin_disorder	false	false	false	false	low
MONDO:0024674	Pancoast syndrome	cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease	neurology|pulmonology|otolaryngology	autoimmune_diseases|cancer|inflammatory_disease	lung_disorder|vascular_disorder|spinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0024675	adult kidney Wilms tumor	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology|pediatric	kidney_disease|cancer	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0024676	childhood kidney Wilms tumor	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology|pediatric	cancer|childhood_kidney_cancer	kidney_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0024677	pancreatic insulinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|oncology	cancer|metabolic_disorder	liver_disorder|endocrine_disorder|upper_gastrointestinal_disorder	false	true	true	true	high
MONDO:0024685	Philadelphia-positive myelogenous leukemia	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	hematology|oncology	leukemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	high
MONDO:0024686	tenosynovial giant cell tumor, diffuse type	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	rheumatology|orthopaedic	cancer|inflammatory_disease	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0024711	malignant mixed epithelial stromal tumor of the kidney	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	renal_medicine|urology|oncology	adrenal_gland_disease|kidney_cancer|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	very_high
MONDO:0024715	benign synovial neoplasm	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	rheumatology|oncology	benign_neoplasm|cancer	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0024744	childhood choroid plexus neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pediatric|neurology|oncology	cancer|neurodegenerative_disease	eye_disorder|brain_disorder	false	true	false	false	high
MONDO:0024746	immature teratoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0024757	cardiovascular neoplasm	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor	cardiology|oncology	cancer|cardiovascular_disorder	vascular_disorder|heart_disorder	false	true	false	false	high
MONDO:0024770	autoinflammatory syndrome, familial, X-linked, Behcet-like 2	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	hereditary_disease|connective_tissue_disorder|syndromic_disease	genetics_and_genomics|rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder|joint_disorder	false	false	false	false	high
MONDO:0024771	myopathy, distal, 7, adult-onset, X-linked	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	orthopaedic|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0024772	intellectual developmental disorder, X-linked, syndromic, Pilorge type	syndromic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|syndromic_disease	genetics_and_genomics|pediatric|psychiatry	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|intellectual_developmental_disorder	false	false	false	false	high
MONDO:0024773	spermatogenic failure, X-linked, 4	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	anemia|metabolic_disorder	reproductive_system_disorder|other____note__since_the_disease_is_x_linked__it_s_likely_to_be_a_genetic_disorder_affecting_males__however__none_of_the_provided_categories_directly_indicate_an_x_linked_condition__therefore___other__is_included_as_it_is_not_possible_to_determine_the_best_fitting_category_from_the_given_list	false	false	false	false	high
MONDO:0024777	immunodeficiency 98 with autoinflammation, X-linked	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|allergy_and_immunology|immunodeficiency	inflammatory_disease|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	true	false	false	true	very_high
MONDO:0024781	immunodeficiency 102	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|rheumatology|oncology|hematology|pediatric|allergy_and_immunology|immunology	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	true	false	false	true	very_high
MONDO:0024797	adult brain stem neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0024813	pulmonary sulcus neoplasm	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology	neurodegenerative_disease|cancer	lung_disorder|spinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0024857	immature extragonadal teratoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	true	high
MONDO:0024861	mixed teratoma and seminoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|urology	cancer|adrenal_gland_disease	reproductive_system_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0024863	small size posterior uveal melanoma	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|disorder_of_development_or_morphogenesis	oncology|ophthalmology	cancer|uveal_melanoma	eye_disorder|skin_disorder	true	true	false	true	medium
MONDO:0024864	medium/large size posterior uveal melanoma	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system|disorder_of_development_or_morphogenesis	oncology|ophthalmology	cancer	eye_disorder|skin_disorder	true	true	false	true	high
MONDO:0024868	metastatic carcinoma in the adrenal medulla	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	neurology|oncology|endocrinology	cancer|adrenal_gland_disease	endocrine_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0024873	clitoral carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder	false	true	false	true	high
MONDO:0024876	tendon sheath disorder	musculoskeletal_system_disorder|connective_tissue_disorder	other	musculoskeletal_system_disorder|connective_tissue_disorder	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0024877	clitoris neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology|urology	cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0024878	secondary carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology	cancer	lymphatic_disorder|upper_gastrointestinal_disorder|lung_disorder	false	true	false	false	high
MONDO:0024879	metastatic carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|cardiology|pulmonology|hematatology	cancer|metastatic_carcinoma	lymphatic_disorder|lung_disorder	false	true	false	true	very_high
MONDO:0024880	metastatic malignant neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|cardiology|hematology	cancer|metastatic_malignant_neoplasm	lymphatic_disorder|lung_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0024881	secondary malignant neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|hematology	secondary_malignant_neoplasm|cancer	lymphatic_disorder|secondary_malignant_neoplasm_does_not_exist_in_the_list_so__blood_bone_marrow_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0024882	secondary neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|neurology|hematology	cancer|secondary_neoplasm	lymphatic_disorder|vascular_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0024883	metastatic neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|neurology|hematology	metastatic_neoplasm|cancer	lymphatic_disorder|bone_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0024884	metastatic carcinoma in the bone	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	oncology|orthopaedic	cancer|inflammatory_disease|autoimmune_diseases	bone_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0024885	malignant ovarian serous tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease_is_incorrect____cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	true	false	false	very_high
MONDO:0024886	serous adenofibroma	reproductive_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|connective_tissue_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	reproductive_system_disorder	false	false	false	false	low
MONDO:0024888	mesonephric neoplasm	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|pediatric|urology	cancer|adrenal_gland_disease	kidney_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0024889	benign mesonephroma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	cancer|adrenal_gland_disease	kidney_disorder|lower_gastrointestinal_disorder	false	false	false	false	low
MONDO:0024890	pineal parenchymal cell neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0024891	non-infectious meningitis	inflammatory_disease|nervous_system_disorder	other	nervous_system_disorder|inflammatory_disease	pediatric|neurology	inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0024892	soft tissue amyloid neoplasm	cancer_or_benign_tumor|metabolic_disease	metabolic_disease|cancer_or_benign_tumor	metabolic_disease|cancer_or_benign_tumor	pathology|oncology|hematology|genetics_and_genomics	cancer|neoplastic_disease	muscle_disorder|soft_tissue_disorder	false	false	false	false	medium
MONDO:0024893	toxocara canis infection (canine roundworms)	infectious_disease	infectious_disease	infectious_disease	gastroenterology|hepatology|oncology|pulmonology|hematology|allergy_and_immunology|pediatric|obstetrics_and_gynecology	allergy|inflammatory_disease|autoimmune_diseases	immune_disorder_lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0024954	larva migrans, visceral	infectious_disease	infectious_disease	infectious_disease	pulmonology|allergy_and_immunology|pediatric|dermatology	inflammatory_disease|autoimmune_diseases|allergy	lymphatic_disorder|immune_disorder|joint_disorder|skin_disorder	true	false	false	true	medium
MONDO:0024988	sex cord-stromal benign neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease|sex_cord_stromal_tumors_fall_under_the_category_of_cancer__specifically_those_originating_in_the_adrenal_glands	endocrine_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0025193	oculopharyngodistal myopathy	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	ophthalmology|otolaryngology|genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	eye_disorder|throat_disorder|muscle_disorder	false	false	false	false	high
MONDO:0025294	tick-borne infectious disease	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|pediatrics|neurology|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0025303	anaplasmosis	infectious_disease	infectious_disease	infectious_disease	veterinary_science|hematology	autoimmune_diseases|anemia|inflammatory_disease	immune_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0025351	multiple congenital anomalies-neurodevelopmental syndrome, X-linked	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0025353	developmental and epileptic encephalopathy, 90	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	epileptic_disease|developmental_disorder|neurodegenerative_disease	brain_disorder|epileptic_disorder|developmental_disorder|spinal_disorder	false	false	false	true	high
MONDO:0025354	spermatogenic failure, X-linked, 3	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	anemia|metabolic_disorder	reproductive_system_disorder|bone_disorder	false	false	false	false	low
MONDO:0025356	azoospermia, obstructive, with nephrolithiasis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|renal_medicine|urology	obstructive|metabolic_disorder	kidney_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0025371	Parvoviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	hematology|allergy_and_immunology|pediatric	inflammatory_disease|autoimmune_diseases|anemia	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	medium
MONDO:0025445	Wieacker-Wolff syndrome (spectrum)	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|bone_disorder	false	false	false	false	medium
MONDO:0025512	type II hypersensitivity reaction disease	immune_system_disorder	autoimmune_disease	immune_system_disorder	immunology|allergy_and_immunology|rheumatology	allergy|autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0025513	autoimmune urticaria	immune_system_disorder|integumentary_system_disorder|inflammatory_disease	autoimmune_disease	immune_system_disorder|inflammatory_disease|integumentary_system_disorder	allergy_and_immunology|dermatology	allergy|autoimmune_diseases|inflammatory_disease	immune_disorder_skin_disorder	false	false	false	true	medium
MONDO:0025514	livedoid vasculopathy	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease|integumentary_system_disorder	hematology|rheumatology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	liver_disorder|vascular_disorder	false	false	false	false	high
MONDO:0025556	isocyanate induced asthma	respiratory_system_disorder|immune_system_disorder	other	immune_system_disorder|respiratory_system_disorder	pulmonology|allergy_and_immunology	allergy|inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	false	false	false	true	high
MONDO:0025598	pneumonia caused by chlamydia	respiratory_system_disorder|infectious_disease|reproductive_system_disorder|inflammatory_disease	infectious_disease	reproductive_system_disorder|inflammatory_disease|infectious_disease|respiratory_system_disorder	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	true	false	false	true	low
MONDO:0025622	Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0025667	limbal stem cell deficiency	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology	inflammatory_disease|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	true	high
MONDO:0025690	microcephaly, epilepsy, and diabetes syndrome 2	hereditary_disease	other	hereditary_disease	endocrinology|neurology|pediatric	epilepsy_is_not_in_the_category_list__metabolic_disorder|neurodegenerative_disease|metabolic_disorder	endocrine_disorder|brain_disorder	false	false	true	false	high
MONDO:0025691	dystonia 30	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0025699	Coffin-Siris syndrome 12	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|neurology|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	immune_disorder|bone_bone_marrow_disorder|skeletal_system_disorder	false	false	false	false	high
MONDO:0025701	leukodystrophy, hypomyelinating, 22	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|hypomyelinating|metabolic_disorder	brain_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0025708	megacystis-microcolon-intestinal hypoperistalsis syndrome 2	hereditary_disease|digestive_system_disorder|syndromic_disease	other	syndromic_disease|digestive_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0025712	angioedema, hereditary, 4	hereditary_disease|cardiovascular_disorder|integumentary_system_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|hereditary_disease|integumentary_system_disorder|cardiovascular_disorder	dermatology|allergy_and_immunology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|allergy	immune_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0025713	angioedema, hereditary, 7	hereditary_disease|cardiovascular_disorder|integumentary_system_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|hereditary_disease|integumentary_system_disorder|cardiovascular_disorder	hematology|dermatology|allergy_and_immunology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|allergy	immune_disorder|vascular_disorder	false	false	false	true	high
MONDO:0025956	ovarian remnant syndrome	reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder	pediatrics|obstetrics_and_gynecology|genetics_and_genomics	cancer|autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0025986	megacystis-microcolon-intestinal hypoperistalsis syndrome	syndromic_disease|digestive_system_disorder|hereditary_disease	other	digestive_system_disorder|syndromic_disease|hereditary_disease	gastroenterology|genetics_and_genomics|pediatric	neurodevelopmental_disorder|gastrointestinal_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0026045	prurigo nodularis	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	allergy|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	high
MONDO:0026404	X inactivation, familial skewed, 1	hereditary_disease	other	hereditary_disease	genetics_and_genomics|obstetrics_and_gynecology|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0026426	X inactivation, familial skewed, 2	hereditary_disease	other	hereditary_disease	pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|bone_disorder|sex_disorder	false	false	false	false	high
MONDO:0026720	mitochondrial complex I deficiency, nuclear type 12	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatrics|neurology|genetics_and_genomics|genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	false	very_high
MONDO:0026721	mitochondrial complex I deficiency, nuclear type 30	mitochondrial_disease|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|metabolic_disease	metabolic_disease	syndromic_disease|hereditary_disease|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatrics|neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	mitochondrial_disorders|muscle_disorder	false	false	false	false	very_high
MONDO:0026722	Mullegama-Klein-Martinez syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0026723	intellectual developmental disorder, X-linked 108	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatry|neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|intellectual_developmental_disorder_is_not_in_the_list_but_x_linked_suggests_it_may_be_linked_to_brain_disorder_so_x_linked_condition_that_also_points_towards_other_category_is_actually_more_likely_so___brain_disorder	false	false	false	true	high
MONDO:0026724	Paganini-Miozzo syndrome	nervous_system_disorder|psychiatric_disorder|syndromic_disease|hereditary_disease	psychiatric_disorder	nervous_system_disorder|syndromic_disease|hereditary_disease|psychiatric_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	skeletal_system_disorder|eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0026726	nephrotic syndrome, type 20	urinary_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|urinary_system_disorder	renal_medicine|pediatric|nephrology	autoimmune_diseases|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0026727	Shukla-Vernon syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	joint_disorder|kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0026729	congenital disorder of glycosylation, type ICC	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|congenital_disorder	liver_disorder	false	false	true	false	high
MONDO:0026730	Basilicata-Akhtar syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|allergy_and_immunology|dermatology	autoimmune_diseases|adrenal_gland_disease	liver_disorder	false	false	false	false	high
MONDO:0026731	hypothyroidism, congenital, nongoitrous, 8	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	endocrinology|pediatric|genetics_and_genomics	autoimmune_diseases|congenital|metabolic_disorder	congenital|endocrine_disorder	false	false	false	true	low
MONDO:0026732	hypothyroidism, congenital, nongoitrous, 9	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	endocrinology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	congenital____endocrine_disorder_is_used_since_the_subcategory_of__congenital__applies_to_a_specific_subtype_of_endocrine_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0026733	intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type	nervous_system_disorder|psychiatric_disorder|syndromic_disease|hereditary_disease	psychiatric_disorder	nervous_system_disorder|syndromic_disease|hereditary_disease|psychiatric_disorder	neurology|genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	other____corrected_list__brain_disorder|brain_disorder|intellectual_developmental_disorder	false	false	false	false	high
MONDO:0026762	Wieacker-Wolff syndrome, female-restricted	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	obstetrics_and_gynecology|pediatric|genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	liver_disorder|reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0026763	holoprosencephaly 13, X-linked	nervous_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease|syndromic_disease	endocrine_system_disorder	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease|syndromic_disease|endocrine_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0026765	congenital disorder of glycosylation, type IIr	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	congenital_disorder_of_glycosylation_is_a_metabolic_disorder_that_involves_the_abnormal_synthesis_of_n_glycans___corrected_answer___metabolic_disorder|metabolic_disorder	liver_disorder|glycosylation_is_related_to_carbohydrate_processing_in_the_liver	false	false	true	false	high
MONDO:0026767	immunodeficiency 74, COVID-19-related, X-linked	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|immunology|allergy_and_immunology	immunodeficiency|inflammatory_disease|autoimmune_diseases	immune_disorder	true	false	false	true	high
MONDO:0026771	developmental and epileptic encephalopathy, 85, with or without midline brain defects	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|developmental_disorder	developmental_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0026777	VEXAS syndrome	connective_tissue_disorder|hereditary_disease|syndromic_disease	other	connective_tissue_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|hematology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0027026	Buschke Lowenstein tumor	infectious_disease|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|infectious_disease	infectious_disease|cancer_or_benign_tumor|reproductive_system_disorder	dermatology|oncology	cancer|neurodegenerative_disease	skin_disorder|lower_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0027029	HHV-6 encephalitis	infectious_disease|nervous_system_disorder|inflammatory_disease	infectious_disease	inflammatory_disease|infectious_disease|acute_disease|nervous_system_disorder	pediatric|neurology	inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder|immune_disorder	true	false	false	true	high
MONDO:0027048	deafness, Y-linked 2	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	medium
MONDO:0027068	mitochondrial complex I deficiency, mitochondrial type 1	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	false	high
MONDO:0027069	mitochondrial complex 5 (ATP synthase) deficiency, mitochondrial type 1	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|cardiology|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder|mitochondrial_disorder_is_not_in_the_list_so__muscle_disorder	false	false	false	false	high
MONDO:0027091	xanthogranulomatous sialadenitis	inflammatory_disease|immune_system_disorder	other	immune_system_disorder|mouth_disorder|inflammatory_disease	otolaryngology|dermatology	autoimmune_diseases|cancer|inflammatory_disease	salivary_gland_disorder|skin_disorder	true	false	false	false	medium
MONDO:0027353	autosomal recessive dyskeratosis congenita 4	hereditary_disease|integumentary_system_disorder|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor|integumentary_system_disorder	pediatric|genetics_and_genomics|dermatology	neurodegenerative_disease|metabolic_disorder	bone_disorder|kidney_disorder|skin_disorder|liver_disorder|eye_disorder	false	false	false	false	high
MONDO:0027407	Kleefstra syndrome 1	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	vascular_disorder|liver_disorder	false	false	false	false	medium
MONDO:0027451	autosomal recessive cutis laxa type 2D	musculoskeletal_system_disorder|metabolic_disease|integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder|metabolic_disease	dermatology|genetics_and_genomics	autosomal_recessive_disease|metabolic_disorder	muscle_disorder|skin_disorder	false	false	false	false	high
MONDO:0027462	autosomal recessive cutis laxa type 2C	musculoskeletal_system_disorder|metabolic_disease|integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0027652	5-fluorouracil toxicity	poisoning	other	poisoning	oncology|gastroenterology|hepatology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0027653	abacavir toxicity	poisoning	other	poisoning	oncology|pulmonology|hematology|hepatology	toxicity_reactions|adverse_reaction	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0027655	allopurinol toxicity	poisoning	other	poisoning	renal_medicine|nephrotoxicity_is_often_associated_with_allopurinol_toxicity_so_this_category_would_be_a_good_fit_as_well_but_it_s_not_in_the_list_however__since_you_asked_for_categories_that_are_present_in_your_list_and_renal_medicine_is_related_to_nephrotoxicity_which_isn_t_an_option__renal_medicine_seems_like_a_reasonable_fit	metabolic_disorder|inflammatory_disease	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0027664	cisplatin toxicity	poisoning	other	poisoning	oncology|renal_medicine	cancer	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0027666	codeine toxicity	poisoning	other	poisoning	psychiatry|neurology|pediatrics	mental_health_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0027667	efavirenz toxicity	poisoning	other	poisoning	neurology|hepatology	mental_health_disorder|neurodegenerative_disease	liver_disorder	false	false	false	false	high
MONDO:0027668	flucloxacilline toxicity	poisoning	other	poisoning	gastroenterology|hepatology	metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	flucloxacillin_is_an_antibiotic_used_to_treat_bacterial_infections__but_like_many_medications__it_can_cause_side_effects_and_toxicity_in_some_individuals__the_potential_toxic_effects_of_flucloxacillin_include_liver_damage__hepatotoxicity___allergic_reactions__and_gastrointestinal_issues_such_as_nausea_and_diarrhea____to_manage_toxicity__it_s_essential_for_anyone_experiencing_adverse_effects_to_consult_a_healthcare_provider__in_cases_of_liver_toxicity__monitoring_liver_function_tests_and_discontinuing_the_drug_may_be_necessary____while_there_are_treatments_for_conditions_like_drug_induced_liver_injury__there_isn_t_a_specific__cure__for_flucloxacillin_toxicity_itself__rather__the_approach_focuses_on_supportive_care_and_avoidance_of_the_drug_in_the_future___in_summary__effective_management_strategies_exist_for_addressing_flucloxacillin_toxicity__but_a_defined__cure__is_not_applicable_as_it_is_a_condition_resulting_from_drug_use___thus__the_answer_is_false__while_treatments_to_manage_toxicity_exist__they_do_not__cure__flucloxacillin_toxicity_itself	high
MONDO:0027675	irinotecan toxicity	poisoning	other	poisoning	oncology|gastroenterology	toxicity|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0027676	congenital anomalies of kidney and urinary tract 2	hereditary_disease|urinary_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|urinary_system_disorder|disorder_of_development_or_morphogenesis	pediatric|urology	congenital_anomalies|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0027677	isoniazid toxicity	poisoning	other	poisoning	pulmonology|neurology	neurodegenerative_disease|metabolic_disorder	lung_disorder|liver_disorder	false	false	false	false	low
MONDO:0027687	raltegravir toxicity	poisoning	other	poisoning	gastroenterology|hematology|hepatology	metabolic_disorder|allergic_reaction	liver_disorder|vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0027694	amyotrophic lateral sclerosis type 23	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0027696	voriconazole toxicity	poisoning	other	poisoning	pulmonology|hepatology	inflammatory_disease|toxicity	liver_disorder|lung_disorder	false	false	false	voriconazole_is_an_antifungal_medication_used_to_treat_serious_fungal_infections__while_it_can_be_effective__it_also_has_potential_toxicities_and_side_effects__which_can_include___1____hepatotoxicity____voriconazole_can_cause_liver_enzyme_elevations_and_potentially_lead_to_liver_damage___2____visual_disturbances____some_patients_may_experience_visual_side_effects_such_as_blurred_vision__changes_in_color_perception__and_light_sensitivity___3____central_nervous_system_effects____there_can_be_neurotoxicity__manifesting_as_hallucinations_or_other_neurological_symptoms__particularly_with_higher_doses___4____skin_reactions____skin_rashes_can_occur__and_there_is_a_risk_of_more_severe_reactions_like_stevens_johnson_syndrome___5____qt_prolongation____voriconazole_may_cause_changes_in_heart_rhythm__leading_to_a_prolonged_qt_interval__which_can_increase_the_risk_of_arrhythmias___6____renal_toxicity____while_less_common__it_can_also_affect_kidney_function___while_voriconazole_is_efficacious_in_treating_certain_fungal_infections__it_is_important_for_healthcare_providers_to_monitor_for_these_toxicities_and_manage_them_appropriately__if_you_are_asking_about_whether_there_are_treatments_specifically_for_voriconazole_toxicity_itself_or_how_to_manage_it__the_answer_would_depend_on_the_specific_symptoms_and_the_severity_of_the_toxicity__treatment_may_include_dose_adjustment__temporary_discontinuation__or_symptomatic_management___in_summary__the_existence_of_efficacious_treatments_for_the_underlying_fungal_infections_that_voriconazole_targets_is_true__while_considerations_for_toxicity_management_are_also_essential__if_the_question_concerns_whether_voriconazole_toxicity_specifically_has_effective_treatments__that_is_more_nuanced_and_may_need_further_clarification	high
MONDO:0027749	serpinopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hepatology|rheumatology|hematology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0027766	generalized lipodystrophy	metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|metabolic_disease	endocrinology|dermatology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder_skin_disorder	false	false	true	false	very_high
MONDO:0027767	partial lipodystrophy	metabolic_disease|integumentary_system_disorder	metabolic_disease	integumentary_system_disorder|metabolic_disease	endocrinology|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|skin_disorder	false	false	true	false	medium
MONDO:0027772	lung colloid adenocarcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	pulmonology|oncology	cancer|lung_adenocarcinoma	lung_disorder	false	true	false	false	medium
MONDO:0028226	autosomal recessive severe congenital neutropenia	hematologic_disorder|immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder|hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0029000	poisoning		other		toxicology_is_not_in_the_list_but_gastroenterology_is_a_good_fit|gastroenterology	poisoning|acute_medical_condition|toxic_exposure	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0029130	polydactyly, postaxial, type A8	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0029131	peripheral neuropathy, autosomal recessive, with or without impaired intellectual development	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	autosomal_recessive_diseases__not_in_the_list_but_closest_match_is_metabolic_disorder|neurodegenerative_disease|metabolic_disorder	peripheral_neuropathy|muscle_disorder	false	false	false	false	high
MONDO:0029132	Liddle syndrome 3	syndromic_disease|urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|renal_medicine	metabolic_disorder|autoimmune_diseases|inflammatory_disease	endocrine_disorder|blood_bone_marrow_disorder|kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0029133	muscular dystrophy, limb-girdle, autosomal dominant 4	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|pediatrics|orthopaedic	neurodegenerative_disease|metabolic_disorder	spinal_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0029134	severe combined immunodeficiency due to CARMIL2 deficiency	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	pediatric|genetics_and_genomics|immunology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0029135	muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8	musculoskeletal_system_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder|metabolic_disease	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0029136	muscular dystrophy, limb-girdle, autosomal recessive 23	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0029137	hearing loss, autosomal dominant 74	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	otolaryngology|pediatric|genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	ear_disorder	false	false	false	false	medium
MONDO:0029138	developmental and epileptic encephalopathy, 67	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	developmental_disorder|neurodegenerative_disease|epileptic_encephalopathy|inflammatory_disease	developmental_and_epileptic_encephalopathy|brain_disorder	false	false	false	true	very_high
MONDO:0029140	glycosylphosphatidylinositol biosynthesis defect 18	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	inherited_metabolic_disorder|metabolic_disorder|lipid_storage_disease|lysosomal_storage_disease	false	false	false	false	high
MONDO:0029141	Usher syndrome, type 4	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	otolaryngology|pediatric|genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0029142	hearing loss, autosomal recessive 111	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	medium
MONDO:0029143	intellectual developmental disorder with hypertelorism and distinctive facies	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0029144	extraoral halitosis due to methanethiol oxidase deficiency	hereditary_disease	other	hereditary_disease	hepatology|otolaryngology|pediatric|genetics_and_genomics|gastroenterology|pulmonology	metabolic_disorder	liver_disorder|metabolic_disorder	false	false	false	false	low
MONDO:0029145	orofacial cleft 8	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	otolaryngology|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	teeth_disorder|facial_disorder|oral_disorder	false	false	false	false	high
MONDO:0029147	spermatogenic failure 33	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|pediatric|obstetrics_and_gynecology|endocrinology	adrenal_gland_disease|autoimmune_diseases|metabolic_disorder|anemia|cancer	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0029148	spermatogenic failure 34	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0029465	intellectual developmental disorder, autosomal dominant 69	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0030005	epilepsy, early-onset, with or without developmental delay	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	autoimmune_diseases|mental_health_disorder|neurodegenerative_disease|metabolic_disorder	developmental_delay|brain_disorder|early_onset	false	false	false	true	high
MONDO:0030006	combined oxidative phosphorylation deficiency 40	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|cardiology|neurology|pediatric|hepatology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0030007	combined oxidative phosphorylation deficiency 41	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	pediatrics|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0030008	combined oxidative phosphorylation deficiency 42	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0030009	alopecia-intellectual disability syndrome 4	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|intellectual_disability_syndrome_is_actually_listed_as_a_specific_disease_under_the_category_of__brain_disorder	false	false	false	false	medium
MONDO:0030010	hypogonadotropic hypogonadism 25 with anosmia	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrinology|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder|endocrine_disorder|nose_disorder	false	false	false	true	medium
MONDO:0030012	Diets-Jongmans syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|lower_gastrointestinal_disorder|joint_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0030013	immunodeficiency 66	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|infectious_diseases|pediatrics|allergy_and_immunology|immunology	immunodeficiency|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0030014	muscular dystrophy, limb-girdle, autosomal recessive 26	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0030015	bone marrow failure syndrome 6	hereditary_disease|immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	other	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics|oncology|pediatric|hematogenomics	anemia|cancer	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0030017	combined oxidative phosphorylation deficiency 43	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	genetics_and_genomics|renal_medicine|cardiology|neurology|pediatric|pulmonology|hepatology	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0030018	autoinflammation with episodic fever and lymphadenopathy	hereditary_disease	other	hereditary_disease	pediatrics|rheumatology|immunology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	immune_disorder|lymphatic_disorder|joint_disorder	true	false	false	true	medium
MONDO:0030019	anauxetic dysplasia 3	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0030020	combined oxidative phosphorylation deficiency 44	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	genetics_and_genomics|pediatric|neurology|metabolism_is_too_broad_for_this_format_so_i_have_excluded_it	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0030024	neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|neurological_disorder|structural_brain_abnormalities	false	false	false	true	high
MONDO:0030025	neurodevelopmental disorder with hypotonia, microcephaly, and seizures	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0030026	retinal dystrophy with leukodystrophy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0030027	tremor, hereditary essential, 6	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	hereditary_essential|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0030028	neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disorder_with_ataxia_tremor_optic_atrophy_and_cognitive_decline|neurodegenerative_disease|childhood_onset_neurodegenerative_disease	spinal_disorder|eye_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0030029	skeletal dysplasia, mild, with joint laxity and advanced bone age	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	skeletal_dysplasia___note__skeletal_dysplasias_are_a_group_of_disorders_that_affect_the_development_of_bones_and_cartilage__often_associated_with_metabolic_issues____corrected_response_to_match_format___metabolic_disorder|skeletal_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0030030	Nizon-Isidor syndrome	hereditary_disease	other	hereditary_disease	neurology|psychiatry	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0030031	lissencephaly 10	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0030033	seizures, early-onset, with neurodegeneration and brain calcifications	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	neurodegeneration_is_often_associated_with_brain_disorders_so_this_would_be_a_good_fit|brain_disorder	true	true	false	true	very_high
MONDO:0030034	epilepsy, progressive myoclonic, 11	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0030035	leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|developmental_delay|neurodegenerative_disease	developmental_delay|blood_bone_marrow_disorder|brain_disorder	true	false	false	false	high
MONDO:0030036	leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|motor_delay_syndrome	spinal_disorder|nervous_system_disorder|muscle_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0030037	neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|cerebellar_atrophy_indicates_brain_disorder_muscle_disorder_spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0030038	hereditary glaucoma, primary closed-angle	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0030042	proteinuria, chronic benign	hereditary_disease	other	hereditary_disease	nephrology|renal_medicine|urology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0030043	congenital disorder of glycosylation, type iit	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|congenital_disorder	liver_disorder	false	false	true	true	high
MONDO:0030044	pseudo-TORCH syndrome 3	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|eye_disorder|lymphatic_disorder|immune_disorder	true	false	false	false	high
MONDO:0030045	Liberfarb syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0030046	neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	spasticity|structural_brain_anomalies|neurodegenerative_disease|metabolic_disorder|seizures	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0030047	microcephaly, developmental delay, and brittle hair syndrome	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	developmental_delay_is_more_closely_associated_with_brain_disorder_than_the_other_categories_but_could_also_fit_in_other_categories__however_microcephaly_fits_most_accurately_here_so_this_is_a_primary_choice___developmental_delay_can_fit_into_multiple_categories__however_given_it_s_association_with_microcephaly_i_have_chosen_brain_disorder_as_the_first_category_and_then_removed_developmental_delay_from_further_consideration_because_of_its_ambiguity|brain_disorder	false	false	false	false	high
MONDO:0030048	harderoporphyria	metabolic_disease|integumentary_system_disorder|hereditary_disease	metabolic_disease	integumentary_system_disorder|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|dermatology	metabolic_disorder|anemia	skin_disorder|liver_disorder	false	false	false	false	high
MONDO:0030049	46,xx sex reversal 5	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0030051	intellectual developmental disorder with autistic features and language delay, with or without seizures	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|language_delay	false	false	false	false	high
MONDO:0030054	developmental and epileptic encephalopathy, 86	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	epileptic_disease|neurodegenerative_disease|developmental_disorder|encephalopathy	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0030055	neuronopathy, distal hereditary motor, autosomal recessive 8	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0030056	Fanconi renotubular syndrome 5	hereditary_disease|syndromic_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder|syndromic_disease	renal_medicine|genetics_and_genomics	metabolic_disorder|anemia|kidney_disease	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0030057	neurodevelopmental, jaw, eye, and digital syndrome	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodevelopmental|neurodegenerative_disease	joint_disorder|spinal_disorder|eye_disorder|brain_disorder|jaw_disorder	false	false	false	false	high
MONDO:0030058	hearing loss, autosomal dominant 77	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	pediatric|genetics_and_genomics|otolaryngology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0030059	developmental and epileptic encephalopathy, 87	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	epileptic_encephalopathy|inflammatory_disease|neurodegenerative_disease|developmental_disorder	epileptic_disorder|brain_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0030060	neurodevelopmental disorder with language impairment and behavioral abnormalities	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	high
MONDO:0030061	periventricular nodular heterotopia 9	hereditary_disease|syndromic_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease	pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0030062	arrhythmogenic right ventricular dysplasia, familial, 14	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|cardiovascular_disease_can_also_be_related_to_genetics_so_this_is_added_to_the_list_and_the_original_request_does_not_allow_for__other__but_since_there_is_no_other_category_that_fits_better__it_has_been_left_out|cardiology	familial|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0030063	neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics|neurodevelopmental_disorders	neurodegenerative_disease|metabolic_disorder	brain_disorder|neurodevelopmental_disorder	false	false	false	true	very_high
MONDO:0030064	episodic ataxia, type 9	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0030065	agenesis of corpus callosum, cardiac, ocular, and genital syndrome	hereditary_disease	other	hereditary_disease	pediatric|neurology|obstetrics_and_gynecology|genetics_and_genomics|urology|ophthalmology|cardiology	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	eye_disorder|brain_disorder|heart_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0030066	granulomatous disease, chronic, autosomal recessive, 5	immune_system_disorder|inflammatory_disease|hereditary_disease|hematologic_disorder	other	hereditary_disease|inflammatory_disease|hematologic_disorder|immune_system_disorder	pediatric|rheumatology|genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease	joint_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0030067	Treacher Collins syndrome 4	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	pediatric|genetics_and_genomics|otolaryngology	craniofacial_abnormality|neurodegenerative_disease|facial_deformity|congenital_disorder|developmental_disorder|genetic_condition	throat_disorder|teeth_disorder|ear_disorder	false	false	false	false	medium
MONDO:0030069	hyper-IgE recurrent infection syndrome 5, autosomal recessive	immune_system_disorder|hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder|immune_system_disorder	pediatric|genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0030070	heterotaxy, visceral, 9, autosomal, with male infertility	cardiovascular_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder	pediatric|genetics_and_genomics|urology	visceral|cardiovascular_disorder	kidney_disorder|reproductive_system_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0030071	retinitis pigmentosa 89	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0030072	developmental and epileptic encephalopathy, 88	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	developmental_and_epileptic_encephalopathy_is_a_rare_category_so_it_fits_best_in_other|metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	very_high
MONDO:0030073	Mitchell syndrome	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030074	spondylometaphyseal dysplasia with corneal dystrophy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0030077	vertebral, cardiac, renal, and limb defects syndrome 3	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|limb_defect|cardiovascular_disorder	spinal_disorder|vertebral	false	false	false	false	high
MONDO:0030087	diabetes mellitus, permanent neonatal 2	metabolic_disease|digestive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder|diabetes_mellitus|metabolic_disease	hereditary_disease|metabolic_disease|digestive_system_disorder|endocrine_system_disorder	pediatric|endocrinology	diabetes_mellitus|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0030088	diabetes mellitus, permanent neonatal 3	metabolic_disease|digestive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder|diabetes_mellitus|metabolic_disease	hereditary_disease|metabolic_disease|digestive_system_disorder|endocrine_system_disorder	pediatric|endocrinology	metabolic_disorder|autoimmune_diseases	kidney_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0030089	diabetes mellitus, permanent neonatal 4	metabolic_disease|digestive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder|diabetes_mellitus|metabolic_disease	hereditary_disease|metabolic_disease|digestive_system_disorder|endocrine_system_disorder	pediatric|endocrinology	metabolic_disorder|neonatal_condition_is_not_in_the_list_but_it_can_be_inferred_that_metabolic_disorder_would_still_apply_given_a_permanent_condition	kidney_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0030105	galactosemia 4	disorder_of_visual_system|hereditary_disease|metabolic_disease	metabolic_disease	disorder_of_orbital_region|disorder_of_visual_system|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0030116	silver-russell syndrome 2	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	muscle_disorder|teeth_disorder|endocrine_disorder|bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0030118	silver-russell syndrome 4	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|chromosomal_disorder	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0030134	oculopharyngodistal myopathy 2	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0030258	pontocerebellar hypoplasia, type 14	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0030259	pontocerebellar hypoplasia, type 15	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0030260	pontocerebellar hypoplasia, type 1E	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030261	pontocerebellar hypoplasia, type 1F	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030263	leukodystrophy, hypomyelinating, 21	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|hypomyelinating|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0030266	immunodeficiency 80 with or without congenital cardiomyopathy	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|immunodeficiency_80_is_likely_in_the_allergy_and_immunology_category__so_it_will_be_included__pediatric__cardiology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0030268	developmental and epileptic encephalopathy 6B	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|developmental_disorder	brain_disorder|epileptic_disorder|developmental_disorder	false	false	false	false	very_high
MONDO:0030270	lymphatic malformation 9	immune_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	immune_system_disorder|hereditary_disease|cardiovascular_disorder	oncology|pediatric|hematology	inflammatory_disease|cancer	lymphatic_disorder	false	false	false	false	medium
MONDO:0030281	arthrogryposis multiplex congenita 6	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0030293	angioedema, hereditary, 5	cardiovascular_disorder|hereditary_disease|integumentary_system_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder|integumentary_system_disorder|hereditary_disease	allergy_and_immunology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|allergy	immune_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0030294	megacystis-microcolon-intestinal hypoperistalsis syndrome 3	digestive_system_disorder|syndromic_disease|hereditary_disease	other	digestive_system_disorder|hereditary_disease|syndromic_disease	pediatric|gastroenterology|genetics_and_genomics	neurodevelopmental_disorder|metabolic_disorder|gastrointestinal_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0030296	megacystis-microcolon-intestinal hypoperistalsis syndrome 4	digestive_system_disorder|syndromic_disease|hereditary_disease	other	digestive_system_disorder|hereditary_disease|syndromic_disease	pediatric|gastroenterology|genetics_and_genomics	metabolic_disorder|gastrointestinal_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0030298	angioedema, hereditary, 8	cardiovascular_disorder|hereditary_disease|inflammatory_disease|integumentary_system_disorder	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder|hereditary_disease|integumentary_system_disorder	immunology|hematology|allergy_and_immunology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|allergy	immune_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0030300	cardiomyopathy, dilated, 2D	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder|autoimmune_diseases	heart_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0030302	immunodeficiency 81	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	allergy_and_immunology|immunology	inflammatory_disease|immunodeficiency____autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0030307	spermatogenic failure 55	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	urology|pediatric	metabolic_disorder|anemia|inflammatory_disease|autoimmune_diseases|cancer	spermatozoa|reproductive_system_disorder	false	false	false	false	medium
MONDO:0030308	immunodeficiency 82 with systemic inflammation	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	rheumatology|allergy_and_immunology|immunology	immunodeficiency|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0030309	Leber hereditary optic neuropathy, autosomal recessive	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	genetics_and_genomics|neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0030311	combined oxidative phosphorylation deficiency 52	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology|metabolism_related_categories_omitted	neurodegenerative_disease|metabolic_disorder	mitochondrial_disorder___however_i_assume_that__mitochondrial_disorder__was_not_in_the_original_list_so_i_will_provide_this_alternative____liver_disorder|muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0030312	spinocerebellar ataxia, autosomal recessive 29	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030314	inflammatory bowel disease (infantile ulcerative colitis) 31, autosomal recessive	hereditary_disease|immune_system_disorder|digestive_system_disorder	other	hereditary_disease|digestive_system_disorder|immune_system_disorder	genetics_and_genomics|pediatric|gastroenterology	autoimmune_diseases|inflammatory_disease	immune_disorder|inflammatory_bowel_disease|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0030316	lymphatic malformation 11	hereditary_disease|immune_system_disorder|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|immune_system_disorder|cardiovascular_disorder	oncology|genetics_and_genomics|pediatric	lymphatic_disorder|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0030317	cardiomyopathy, familial hypertrophic, 28	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|cardiology	cardiovascular_disorder|familial_hypertrophic_cardiomyopathy_is_not_in_the_list__so_using_cardiomyopathy_as_substitute__cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder|vascular_disorder	false	false	false	true	high
MONDO:0030318	spinocerebellar ataxia, autosomal recessive 30	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030323	spinocerebellar ataxia, autosomal recessive 31	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0030326	mitochondrial dna depletion syndrome 16B (neuroophthalmic type)	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	genetics_and_genomics|neurology|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0030329	megacystis-microcolon-intestinal hypoperistalsis syndrome 5	hereditary_disease|syndromic_disease|digestive_system_disorder	other	hereditary_disease|syndromic_disease|digestive_system_disorder	genetics_and_genomics|pediatric|gastroenterology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0030330	cardiomyopathy, familial restrictive, 6	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	genetics_and_genomics|cardiology|renal_medicine	cardiovascular_disorder|metabolic_disorder|familial_relatives_is_not_in_the_list_so_i_m_ignoring_it	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0030331	Ritscher-Schinzel syndrome 4	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder|joint_disorder|bone_disorder|brain_disorder|skin_disorder|vascular_disorder	false	false	false	false	high
MONDO:0030332	ciliary dyskinesia, primary, 46	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	hereditary_disease|syndromic_disease|respiratory_system_disorder	genetics_and_genomics|pulmonology|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	eye_disorder|lung_disorder	false	false	false	true	high
MONDO:0030333	immunodeficiency 84	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	allergy_and_immunology|immunology	immunodeficiency|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	true	false	false	false	high
MONDO:0030335	diarrhea 12, with microvillus atrophy	hereditary_disease|digestive_system_disorder	other	hereditary_disease|digestive_system_disorder	pediatric|gastroenterology	metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0030337	cutis laxa, autosomal recessive, type 2E	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	genetics_and_genomics|pediatric|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0030338	anencephaly 2	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0030339	microcephaly 28, primary, autosomal recessive	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|autosomal_recessive_diseases_category_is_not_in_the_list_but_microcephaly_28_primary_fits_into_neurodegenerative_disease_and_metabolic_disorder|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030341	myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive	syndromic_disease|nervous_system_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|genetic_disorder_is_not_in_the_list_but_autosomal_recessive_is_a_subtype_of_it__however_none_of_these_fit_so_we_have_neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	immune_disorder|muscle_disorder	false	false	false	false	high
MONDO:0030346	ciliary dyskinesia, primary, 47, and lissencephaly	syndromic_disease|respiratory_system_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|respiratory_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	brain_disorder|muscle_disorder|spinal_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0030353	Joubert syndrome 38	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	neurology|genetics_and_genomics|medical_genetics|pediatric	neurodegenerative_disease|anemia|metabolic_disorder	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0030354	facioscapulohumeral muscular dystrophy 3, digenic	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	bone_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0030355	facioscapulohumeral muscular dystrophy 4, digenic	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|muscular_dystrophy	muscle_disorder	false	false	false	false	high
MONDO:0030356	short-rib thoracic dysplasia 21 without polydactyly	syndromic_disease|respiratory_system_disorder|urinary_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|urinary_system_disorder|respiratory_system_disorder	genetics_and_genomics|pediatric	genetic_disorder|metabolic_disorder	bone_disorder|skeletal_disorder	false	false	false	false	high
MONDO:0030360	cholestasis, progressive familial intrahepatic, 6	hereditary_disease|syndromic_disease|metabolic_disease|digestive_system_disorder|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder	hereditary_disease|syndromic_disease|digestive_system_disorder|metabolic_disease|endocrine_system_disorder	gastroenterology|genetics_and_genomics|hepatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0030361	Aicardi-Goutieres syndrome 8	hereditary_disease|connective_tissue_disorder|immune_system_disorder|syndromic_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|syndromic_disease|nervous_system_disorder|immune_system_disorder|connective_tissue_disorder	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease	brain_disorder|kidney_disorder|immune_disorder|bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0030362	Aicardi-Goutieres syndrome 9	hereditary_disease|connective_tissue_disorder|immune_system_disorder|syndromic_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|syndromic_disease|nervous_system_disorder|immune_system_disorder|connective_tissue_disorder	neurology|genetics_and_genomics|ophthalmology|pediatric	autoimmune_diseases|neurodegenerative_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0030366	cardiomyopathy, dilated, 2E	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiovascular|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0030374	WHIM syndrome 2	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|immunology	metabolic_disorder|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0030375	neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2	hereditary_disease	other	hereditary_disease	neurology|multisystem|endocrine	metabolic_disorder|infantile_onset_disease_is_not_listed_so_it_can_be_ignored|neurodegenerative_disease	multisystem|infantile_onset|endocrine|neurologic	false	false	false	true	high
MONDO:0030376	Martsolf syndrome 2	syndromic_disease|disorder_of_visual_system|hereditary_disease	other	hereditary_disease|syndromic_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	liver_disorder|joint_disorder	false	false	false	false	high
MONDO:0030378	combined oxidative phosphorylation deficiency 53	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	pediatrics|neurology|genetics_and_genomics|hepatology	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0030397	portal hypertension, noncirrhotic, 2	hereditary_disease	other	hereditary_disease	gastroenterology|hepatology	inflammatory_disease|cardiovascular_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0030399	visceral neuropathy, familial, 2, autosomal recessive	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	lower_gastrointestinal_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030423	congenital disorder of glycosylation, type 2v	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric	congenital_disorder_of_glycosylation_type_2v_is_often_classified_under_this_category_because_it_is_a_disorder_of_glycosylation__which_affects_the_way_glycans_are_attached_to_proteins_or_lipids_in_cells__and_can_be_caused_by_mutations_in_genes_involved_in_n_glycosylation|metabolic_disorder	liver_disorder|developmental_disorder|genetic_disorder	false	false	true	false	high
MONDO:0030428	immunodeficiency 85 and autoimmunity	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	allergy_and_immunology|immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0030430	spermatogenic failure 56	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	endocrine_disease|metabolic_disorder	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0030433	Charcot-Marie-Tooth disease, axonal, type 2FF	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	axonal_disorder|neurodegenerative_disease|inherited_metabolic_disorder|peripheral_nervous_system_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0030436	anemia, sideroblastic, 5	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	oncology|hematology|pediatric|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|anemia	false	false	false	true	medium
MONDO:0030437	congenital disorder of glycosylation, type IIw	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	congenital_disorder|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	true	false	high
MONDO:0030438	pontocerebellar hypoplasia, type 16	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0030439	spermatogenic failure 57	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	cancer|anemia|metabolic_disorder	reproductive_system_disorder	false	false	false	false	medium
MONDO:0030440	cone-rod dystrophy 22	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	true	high
MONDO:0030448	immunodeficiency 86	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|genetics_and_genomics|pediatric|immunology	autoimmune_diseases|immunodeficiency|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0030449	hearing loss, autosomal recessive 118, with cochlear aplasia	hereditary_disease|nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|auditory_system_disorder|psychiatric_disorder	genetics_and_genomics|pediatric|otolaryngology	neurodegenerative_disease|metabolic_disorder	cochlear_aplasia|ear_disorder	false	false	false	false	very_high
MONDO:0030453	developmental and epileptic encephalopathy 97	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric	developmental_disorder|neurodegenerative_disease	brain_disorder|epileptic_disorder|developmental_disorder	false	false	false	true	high
MONDO:0030454	Joubert syndrome 39	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	neurology|pediatric|genetics_and_genomics	anemia|neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0030455	dystonia 31	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|muscledisorder	false	false	false	true	high
MONDO:0030456	muscular dystrophy, limb-girdle, autosomal recessive 27	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|orthopaedic|genetics_and_genomics	muscular_dystrophy_is_not_in_the_list_so_it_would_be__neurodegenerative_disease|neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0030457	immunodeficiency 87 and autoimmunity	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder	true	false	false	true	high
MONDO:0030458	Charcot-Marie-Tooth disease, axonal, Type 2HH	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|axonal_dysfunction	spinal_disorder|muscle_disorder|nerve_muscle_disorder_is_not_in_the_list_so__spinal_disorder	false	false	false	false	medium
MONDO:0030462	Joubert syndrome 40	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	neurology|pediatric|genetics_and_genomics	anemia|neurodegenerative_disease|metabolic_disorder	brain_disorder_kidney_disorder	false	false	false	false	high
MONDO:0030463	spermatogenic failure 58	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	anemia|autoimmune_diseases|cancer|metabolic_disorder	reproductive_system_disorder	false	false	false	false	medium
MONDO:0030465	cataract 49	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0030471	Galloway-Mowat syndrome 9	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|genetic_condition	liver_disorder|kidney_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0030472	developmental and epileptic encephalopathy 98	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	developmental_disorder|neurodegenerative_disease	developmental_disorder|brain_disorder|epileptic_disorder	false	false	false	true	very_high
MONDO:0030473	developmental and epileptic encephalopathy 99	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	epileptic_disease|developmental_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0030474	heterotaxy, visceral, 10, autosomal, with male infertility	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|pediatric|urology	metabolic_disorder|cardiovascular_disorder|autoimmune_diseases|adrenal_gland_disease|neurodegenerative_disease	kidney_disorder|visceral_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0030475	heterotaxy, visceral, 11, autosomal, with male infertility	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	genetics_and_genomics|urology	visceral|adrenal_gland_disease	kidney_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0030476	Galloway-Mowat syndrome 10	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|inflammatory_disease	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0030480	hearing loss, autosomal recessive 119	hereditary_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	pediatric|genetics_and_genomics|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	high
MONDO:0030482	spastic paraplegia 84, autosomal recessive	hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|syndromic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0030483	immunodeficiency 88	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	immunology|allergy_and_immunology	autoimmune_diseases|immunodeficiency	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0030484	immunodeficiency 89 and autoimmunity	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	rheumatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0030486	dystonia 32	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|psychiatry	autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0030487	spondylometaphyseal dysplasia, pagnamenta type	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|inflammatory_disease|adrenal_gland_disease|neurodegenerative_disease	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0030489	epidermolysis bullosa simplex 2A, generalized severe	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	pediatric|genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases	joint_disorder|skin_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0030490	oocyte maturation defect 11	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder	false	false	false	false	medium
MONDO:0030491	immunodeficiency 91 and hyperinflammation	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	rheumatology|pulmonology|immunology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder|hyperinflammation	false	false	false	true	very_high
MONDO:0030492	spermatogenic failure 59	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	metabolic_disorder|endocrine_disease	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0030493	spermatogenic failure 60	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	metabolic_disorder|endocrine_disorders	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0030498	immunodeficiency 92	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	immunology|allergy_and_immunology|pediatric	inflammatory_disease|autoimmune_diseases|immunodeficiency	lymphatic_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0030500	Loeys-Dietz syndrome 6	cardiovascular_disorder|hereditary_disease|syndromic_disease|connective_tissue_disorder	cardiovascular_disorder	syndromic_disease|hereditary_disease|connective_tissue_disorder|cardiovascular_disorder	genetics_and_genomics|pediatric	metabolic_disorder|cardiovascular_disorder	vascular_disorder|bone_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0030502	tetrasomy	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	genetic_disorder|genetic_disorder____corrected_response_based_on_tetrasomy_being_a_chromosomal_disorder____metabolic_disorder|metabolic_disorder	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030503	cholestasis, progressive familial intrahepatic, 7, with or without hearing loss	hereditary_disease|syndromic_disease|metabolic_disease|digestive_system_disorder|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder	digestive_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease|endocrine_system_disorder	hepatology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0030505	cholestasis, progressive familial intrahepatic, 8	hereditary_disease|syndromic_disease|metabolic_disease|digestive_system_disorder|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder	digestive_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease|endocrine_system_disorder	hepatology|genetics_and_genomics|pediatric|gastroenterology	metabolic_disorder|inflammatory_disease	liver_disorder|biliary_disorder	false	false	false	false	very_high
MONDO:0030506	ovarian dysgenesis 9	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	obstetrics_and_gynecology|genetics_and_genomics	cancer|metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0030507	spermatogenic failure 61	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	metabolic_disorder|anemia|autoimmune_diseases	reproductive_system_disorder	false	false	false	false	medium
MONDO:0030508	spermatogenic failure 62	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	metabolic_disorder|anemia	vascular_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0030512	spastic paraplegia 85, autosomal recessive	syndromic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0030513	dystonia 33	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0030514	leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|otolaryngology|genetics_and_genomics|cardiology|cardiothoracic|hepatology|neurology	metabolic_disorder|neurodegenerative_disease|cardiovascular_disorder|liver_dysfunction_is_not_in_this_list_however__metabolic_disorder__could_be_a_better_fit_than_the_other_options_given	blood_bone_marrow_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0030515	spermatogenic failure 63	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	metabolic_disorder|anemia|autoimmune_diseases	reproductive_system_disorder|spermatozoa_regeneration_failure	false	false	false	false	medium
MONDO:0030517	trichothiodystrophy 8, nonphotosensitive	syndromic_disease|hereditary_disease|integumentary_system_disorder|nervous_system_disorder	neurodegenerative_disease	syndromic_disease|hereditary_disease|integumentary_system_disorder|nervous_system_disorder	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	hair_disorder|skin_disorder	false	false	false	false	high
MONDO:0030518	trichothiodystrophy 9, nonphotosensitive	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	syndromic_disease|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	hair_disorder|skin_disorder	false	false	false	false	high
MONDO:0030519	agammaglobulinemia 9, autosomal recessive	hematologic_disorder|immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease|hematologic_disorder	pediatric|immunology|genetics_and_genomics|hematology	metabolic_disorder|anemia|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0030522	spermatogenic failure 64	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	metabolic_disorder|anemia	spinal_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0030523	oocyte maturation defect 12	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0030524	mucopolysaccharidosis, type 10	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|liver_disorder|vascular_disorder|upper_gastrointestinal_disorder|kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0030525	epidermolysis bullosa simplex 2B, generalized intermediate	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|muscle_disorder	false	false	false	true	high
MONDO:0030527	epidermolysis bullosa simplex 2C, localized	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	high
MONDO:0030528	immunodeficiency 93 and hypertrophic cardiomyopathy	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|cardiology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	immune_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0030529	agammaglobulinemia 10, autosomal dominant	hematologic_disorder|immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|autoimmune_diseases|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0030531	spermatogenic failure 65	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	metabolic_disorder|cancer|inflammatory_disease|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0030533	intellectual developmental disorder, autosomal recessive 73	psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	metabolic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	intellectual_developmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0030534	hypogonadotropic hypogonadism 26 with or without anosmia	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrinology|genetics_and_genomics|pediatrics|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0030535	epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0030537	central hypoventilation syndrome, congenital, 2, and autonomic dysfunction	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	autonomic_dysfunction|neurodegenerative_disease	spinal_disorder|autonomic_dysfunction_is_not_in_the_list_so_removed_it|brain_disorder	false	false	false	false	high
MONDO:0030538	dystonia 34, myoclonic	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0030539	central hypoventilation syndrome, congenital, 3	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0030543	combined oxidative phosphorylation deficiency 54	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0030549	hearing loss, autosomal dominant 81	psychiatric_disorder|hereditary_disease|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	genetics_and_genomics|otolaryngology|pediatric	autosomal_dominant_disorder_is_a_category_that_isn_t_in_the_list__but_based_on_the_description_it_would_fit_best_in_neurodegenerative_disease|neurodegenerative_disease	ear_disorder	false	false	false	false	medium
MONDO:0030553	acromesomelic dysplasia 4	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0030602	Klebsiella pneumonia	infectious_disease|inflammatory_disease|respiratory_system_disorder	infectious_disease	inflammatory_disease|infectious_disease|respiratory_system_disorder	pulmonology	autoimmune_diseases|inflammatory_disease	immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0030603	Klebsiella infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder|urinary_tract_disorder|lung_disorder	true	false	false	true	high
MONDO:0030604	cystic partially differentiated nephroblastoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	oncology|urology|pediatric|renal_medicine	cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0030606	Bryant-Li-Bhoj neurodevelopmental syndrome 1	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	neurodevelopmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0030607	Bryant-Li-Bhoj neurodevelopmental syndrome 2	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	neurodevelopmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0030608	interstitial lung disease 1	hereditary_disease	other	hereditary_disease	hematology|rheumatology|allergy_and_immunology|cardiothoracic|pulmonology	autoimmune_diseases|inflammatory_disease	immune_disorder|vascular_disorder|lung_disorder	false	false	false	false	high
MONDO:0030619	retinitis pigmentosa 92	metabolic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	metabolic_disease|psychiatric_disorder	disorder_of_orbital_region|metabolic_disease|disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	vascular_disorder|eye_disorder	false	false	false	false	high
MONDO:0030625	dyskinesia with orofacial involvement, autosomal recessive	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric|psychiatry	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0030634	leukoencephalopathy, hereditary diffuse, with spheroids 2	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0030639	Teebi hypertelorism syndrome	hereditary_disease	other	hereditary_disease	otolaryngology|genetics_and_genomics|pediatric	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	eye_disorder|bone_disorder|upper_gastrointestinal_disorder|throat_disorder	false	false	false	false	medium
MONDO:0030669	gastrointestinal defects and immunodeficiency syndrome 2	digestive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|digestive_system_disorder|hereditary_disease	gastroenterology|genetics_and_genomics|pediatrics|allergy_and_immunology	immunodeficiency|gastrointestinal_defects|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|immune_disorder|liver_disorder|gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0030673	spastic paraplegia 86, autosomal recessive	syndromic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0030674	Teebi hypertelorism syndrome 2	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	cardiovascular_disorder|metabolic_disorder	upper_gastrointestinal_disorder|heart_disorder|eye_disorder	false	false	false	false	medium
MONDO:0030676	parkinsonism-dystonia 3, childhood-onset	syndromic_disease|hereditary_disease|nervous_system_disorder	other	syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0030677	Charcot-Marie-Tooth disease, demyelinating, IIA 1I	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|demyelinating	spinal_disorder|muscle_disorder|demyelinating	false	false	false	false	medium
MONDO:0030679	Noonan syndrome 14	cardiovascular_disorder|syndromic_disease|hereditary_disease|immune_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|immune_system_disorder|cardiovascular_disorder	cardiothoracic|genetics_and_genomics|endocrinology|otolaryngology|cardiology|pediatric	cardiovascular_disorder|metabolic_disorder|autoimmune_diseases|mental_health_disorder	vascular_disorder|joint_disorder|heart_disorder	false	false	false	false	high
MONDO:0030680	cardiomyopathy, dilated, 2F	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiothoracic|cardiology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	muscle_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0030681	immunodeficiency 94 with autoinflammation and dysmorphic facies	immune_system_disorder|hereditary_disease|hematologic_disorder	other	hereditary_disease|immune_system_disorder|hematologic_disorder	immunology|genetics_and_genomics|pediatric|allergy_and_immunology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	genetic_disorder|lymphatic_disorder|immune_disorder|autoimmune_disorder	true	false	false	true	high
MONDO:0030684	hypogonadotropic hypogonadism 27 without anosmia	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	genetics_and_genomics|endocrinology	endocrine_system_disorder|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0030689	Charcot-Marie-Tooth disease, demyelinating, IIA 1H	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0030690	pulmonary fibrosis and/or bone marrow failure, telomere-related, 6	hereditary_disease|premature_aging_syndrome|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease|premature_aging_syndrome	genetics_and_genomics|pulmonology|hematogenetics|hematology	autoimmune_diseases|inflammatory_disease|anemia|cancer	lung_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0030692	immunodeficiency 95	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	immunology|genetics_and_genomics|pediatric|allergy_and_immunology	immunodeficiency_is_not_in_the_list_so_i_will_use_its_closest_match__immune_disorder_is_also_not_in_the_list__however__an_option_can_be_made__autoimmune_diseases|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0030693	immunodeficiency 96	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	immunology|genetics_and_genomics|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|immunodeficiency_can_be_related_to_immune_system_issues_so_these_categories_seem_most_relevant	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0030695	developmental and epileptic encephalopathy 100	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	epileptic_disorder|neurodegenerative_disease|developmental_disorder	brain_disorder|encephalopathy|epileptic_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0030696	mitochondrial DNA depletion syndrome 20 (mngie type)	hereditary_disease|syndromic_disease|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|musculoskeletal_system_disorder	metabolic_disease	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatrics	metabolic_disorder|neurodegenerative_disease|anemia	muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0030697	myopia 28, autosomal recessive	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	autosomal_recessive|eye_disorder	false	false	false	false	medium
MONDO:0030700	autoimmune glomerulonephritis	urinary_system_disorder|immune_system_disorder|inflammatory_disease	autoimmune_disease	immune_system_disorder|inflammatory_disease|urinary_system_disorder	rheumatology|renal_medicine	autoimmune_diseases|inflammatory_disease	immune_disorder|kidney_disorder	false	false	false	true	high
MONDO:0030701	autoimmune cardiomyopathy	cardiovascular_disorder|musculoskeletal_system_disorder|immune_system_disorder	autoimmune_disease|cardiovascular_disorder	immune_system_disorder|cardiovascular_disorder|musculoskeletal_system_disorder	genetics_and_genomics|rheumatology|allergy_and_immunology|cardiology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	heart_disorder|immune_disorder|muscledisorder	false	false	false	false	high
MONDO:0030702	autoimmune atherosclerosis	cardiovascular_disorder|immune_system_disorder	autoimmune_disease|cardiovascular_disorder	immune_system_disorder|cardiovascular_disorder	rheumatology|cardiology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	immune_disorder|vascular_disorder	false	false	false	true	high
MONDO:0030703	autoimmune vasculitis	cardiovascular_disorder|immune_system_disorder|inflammatory_disease	autoimmune_disease|cardiovascular_disorder	immune_system_disorder|inflammatory_disease|cardiovascular_disorder	hematology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|vascular_disorder	false	false	false	true	high
MONDO:0030705	Trichomonas prostatitis	reproductive_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|reproductive_system_disorder|inflammatory_disease	urology	urological_disease|inflammatory_disease|sexually_transmitted_infection|prostate_gland_disease|genitourinary_disorder	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	low
MONDO:0030706	Trichomonas cystitis	reproductive_system_disorder|urinary_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|reproductive_system_disorder|inflammatory_disease|urinary_system_disorder	urology	urinary_infection|genitourinary_disorder	urinary_tract_disorder|kidney_disorder	true	false	false	true	medium
MONDO:0030707	Trichomonas balanoposthitis	reproductive_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|reproductive_system_disorder|inflammatory_disease	urology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|reproductive_system_disorder	true	false	false	true	low
MONDO:0030708	Trichomonas cervicitis	reproductive_system_disorder|infectious_disease	infectious_disease	infectious_disease|reproductive_system_disorder	pediatric|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0030711	Anemia, congenital dyserythropoietic, type IIIb, autosomal recessive	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	bone_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0030712	oculopharyngodistal myopathy 4	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	throat_disorder|muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0030714	osteogenesis imperfecta, IIA 22	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030716	spermatogenic failure 66	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	metabolic_disorder|anemia	reproductive_system_disorder	false	false	false	false	medium
MONDO:0030717	immunodeficiency 97 with autoinflammation	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	immunology|allergy_and_immunology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	true	false	false	true	very_high
MONDO:0030718	spermatogenic failure 67	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	metabolic_disorder|endocrine_disease__note__actual_category_provided_was_adrenal_gland_disease_which_is_a_subset_of_endocrine	reproductive_system_disorder	false	false	false	false	medium
MONDO:0030719	hearing loss, autosomal dominant 82	psychiatric_disorder|auditory_system_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder|hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	autosomal_dominant_disorder_is_typically_associated_with_a_genetic_basis_but_this_category_is_not_present_in_the_list_therefore_we_have_to_choose_from_available_categories__however_it_can_also_be_associated_with__metabolic_disorder|neurodegenerative_disease	ear_disorder|autosomal_dominant	false	false	false	false	high
MONDO:0030720	trichomonal vulvovaginitis	infectious_disease|inflammatory_disease|reproductive_system_disorder|urinary_system_disorder	infectious_disease	infectious_disease|inflammatory_disease|reproductive_system_disorder|urinary_system_disorder	dermatology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	vaginal_infection_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0030721	spermatogenic failure 68	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	endocrinology|urology|genetics_and_genomics	metabolic_disorder|endocrine_disorder	reproductive_system_disorder	false	false	false	false	medium
MONDO:0030723	hearing loss, autosomal dominant 83	psychiatric_disorder|auditory_system_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|otolaryngology	autosomal_dominant_disorder|neurodegenerative_disease	autosomal_dominant_disorder|ear_disorder	false	false	false	true	high
MONDO:0030724	hearing loss, autosomal dominant 84	psychiatric_disorder|auditory_system_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|pediatric|otolaryngology	note__there_seems_to_be_a_missing_category_for_genetic_disorders_like__autosomal_dominant_disorder___however__based_on_the_provided_options|autosomal_dominant_disorder_is_more_specific_but_the_closest_match_in_this_list|neurodegenerative_disease	ear_disorder|autosomal_dominant_is_a_genetic_disorder_so_it_could_also_fit_into_the_category_of_other_but_since_you_asked_for_no__other__i_left_that_out	false	false	false	true	high
MONDO:0030726	neutropenia, severe congenital, 9, autosomal dominant	hematologic_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology|pediatric	metabolic_disorder|autoimmune_diseases|anemia|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0030727	developmental and epileptic encephalopathy 101	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology	neurodegenerative_disease|developmental_disorder	brain_disorder	false	false	false	false	very_high
MONDO:0030729	Tessadori-van Haaften neurodevelopmental syndrome 1	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|neurodevelopmental_disorder	false	false	false	false	high
MONDO:0030730	Tessadori-van Haaften neurodevelopmental syndrome 2	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	neurodevelopmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0030731	aortic aneurysm, familial thoracic 12	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	hematology|cardiothoracic|cardiology|genetics_and_genomics	familial_condition|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0030732	spermatogenic failure 69	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|anemia	reproductive_system_disorder	false	false	false	false	high
MONDO:0030733	spermatogenic failure 70	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0030736	ovarian dysgenesis 10	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|cancer	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0030746	epidermolysis bullosa, junctional 2A, intermediate	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0030747	epidermolysis bullosa, junctional 2B, severe	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|joint_disorder|skin_disorder	false	false	false	true	very_high
MONDO:0030748	epidermolysis bullosa, junctional 3A, intermediate	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0030749	epidermolysis bullosa, junctional 3B, severe	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0030750	epidermolysis bullosa, junctional 4, intermediate	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0030756	Stuve-Wiedemann syndrome 2	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	immune_disorder|joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0030768	epidermolysis bullosa, junctional 5A, intermediate	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	dermatology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|immunedisorder	false	false	false	false	high
MONDO:0030770	congenital disorder of deglycosylation 2	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	other___note__since_the_categories_provided_don_t_directly_relate_to__congenital_disorder_of_deglycosylation___i_ve_made_an_educated_guess_based_on_the_fact_that_such_disorders_often_have_a_systemic_impact_and_can_be_related_to_various_organs__including_the_liver__however__this_might_not_be_the_exact_or_best_fitting_category_for_every_case_of_congenital_disorder_of_deglycosylation___in_2021__it_was_reported_that_defects_in_the_mgat2_gene_cause_congenital_disorder_of_deglycosylation_type_ii__cddgii___it_s_worth_noting_that_some_forms_of_congenital_disorders_of_glycosylation_are_associated_with_neurological_symptoms|liver_disorder	false	false	false	false	high
MONDO:0030781	restrictive dermopathy 2	hereditary_disease	other	hereditary_disease	pulmonology|dermatology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0030785	intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly	psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	pediatric|psychiatry|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	neurodevelopmental_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0030787	spermatogenic failure 71	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|anemia	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0030796	leukoencephalopathy, hereditary diffuse, with spheroids	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|hereditary_disorder	blood_bone_marrow_disorder|brain_disorder	false	false	false	false	high
MONDO:0030797	retinitis pigmentosa 93	psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder|disorder_of_visual_system	metabolic_disease|psychiatric_disorder	disorder_of_orbital_region|metabolic_disease|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0030798	immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	hematology|allergy_and_immunology	inflammatory_disease|anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0030800	cholestasis, progressive familial intrahepatic, 9	syndromic_disease|metabolic_disease|endocrine_system_disorder|hereditary_disease|digestive_system_disorder	metabolic_disease|endocrine_system_disorder	digestive_system_disorder|hereditary_disease|syndromic_disease|metabolic_disease|endocrine_system_disorder	gastroenterology|genetics_and_genomics|hepatology	metabolic_disorder|inflammatory_disease|cardiovascular_disorder	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0030801	monosomy 7 myelodysplasia and leukemia syndrome 2	syndromic_disease|cancer_or_benign_tumor|hematologic_disorder|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|oncology|hematology	anemia|cancer	blood_bone_marrow_disorder|leukemia	false	true	false	false	very_high
MONDO:0030805	spinocerebellar ataxia 49	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030809	spermatogenic failure 72	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder	false	false	false	false	medium
MONDO:0030810	cholestasis, progressive familial intrahepatic, 10	syndromic_disease|metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder	metabolic_disease|endocrine_system_disorder	digestive_system_disorder|hereditary_disease|syndromic_disease|metabolic_disease|endocrine_system_disorder	gastroenterology|hepatology	metabolic_disorder|inflammatory_disease	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0030813	immunodeficiency 101 (varicella zoster virus-specific)	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	allergy_and_immunology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder	true	false	false	true	high
MONDO:0030815	cholestasis, progressive familial intrahepatic, 11	syndromic_disease|metabolic_disease|hereditary_disease|endocrine_system_disorder|digestive_system_disorder	metabolic_disease|endocrine_system_disorder	digestive_system_disorder|hereditary_disease|syndromic_disease|metabolic_disease|endocrine_system_disorder	genetics_and_genomics|hepatology|gastroenterology	metabolic_disorder|inflammatory_disease	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0030818	spermatogenic failure 73	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	metabolic_disorder|anemia	reproductive_system_disorder	false	false	false	false	medium
MONDO:0030819	meckel syndrome 14	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder	lower_gastrointestinal_disorder|liver_disorder|kidney_disorder|joint_disorder	false	false	false	false	medium
MONDO:0030822	renal hypodysplasia/aplasia 4	disorder_of_development_or_morphogenesis|hereditary_disease|urinary_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|urinary_system_disorder	renal_medicine|urology|pediatric	metabolic_disorder|renal_hydropathy|anemia	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0030827	macrothrombocytopenia, isolated, 2, autosomal dominant	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|autoimmune_diseases|anemia	blood_bone_marrow_disorder|immune_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0030831	gastrointestinal defect and immunodeficiency syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|digestive_system_disorder	other	hereditary_disease|disorder_of_development_or_morphogenesis|digestive_system_disorder	immunology|gastroenterology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	immune_disorder|gastrointestinal_disorder	true	false	false	false	high
MONDO:0030835	developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy	hereditary_disease	other	hereditary_disease	endocrinology|neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	neurodegenerative_disorder|nervous_system_disorder|growth_disorder|spinal_disorder|developmental_delay|neuromuscular_disorder|brain_disorder	false	false	false	false	high
MONDO:0030837	neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	neurological_disorder|brain_disorder	false	false	false	the_description_you_provided_suggests_a_complex_neurodevelopmental_disorder_that_may_include_conditions_such_as_microcephaly_and_various_associated_symptoms__while_specific_treatments_for_neurodevelopmental_disorders_can_vary_greatly__there_is_ongoing_research_in_the_field__and_some_specific_disorders_may_have_targeted_therapies__however__many_neurodevelopmental_disorders_currently_do_not_have_a_definitive_cure___in_general__while_there_may_be_interventions_that_can_improve_specific_symptoms__such_as_medications_to_manage_epilepsy_or_therapies_for_language_development___a_comprehensive_cure_that_addresses_the_underlying_disorder_may_not_exist___given_that_information__i_would_return_false_for_the_existence_of_efficacious_treatments_that_cure__prevent__or_treat_this_specific_disease_comprehensively__unless_you_specify_a_particular_diagnosed_condition_within_that_broader_category	very_high
MONDO:0030839	thyroid hormone metabolism, abnormal, 2	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	thyroid_hormone_metabolism|endocrine_disorder	false	false	false	false	medium
MONDO:0030840	mismatch repair cancer syndrome 2	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|oncology	mismatch_repair_cancer_syndrome_2_does_not_fit_well_in_any_other_category|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0030841	mismatch repair cancer syndrome 3	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|oncology	genetic_disorder|cancer	immune_disorder|lymphatic_disorder|kidney_disorder	false	false	false	true	high
MONDO:0030843	mismatch repair cancer syndrome 4	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|oncology	genetic_disorder_is_not_listed_but_given_the_context_of_mismatch_repair_it_implies_cancer|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0030844	spermatogenic failure 47	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	metabolic_disorder|anemia|cancer	reproductive_system_disorder	false	false	false	false	medium
MONDO:0030846	spermatogenic failure 48	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|anemia	reproductive_system_disorder|spermatic_failing_is_also_a_type_of_reproductive_system_disorder	false	false	false	false	medium
MONDO:0030847	arthrogryposis, distal, type 1C	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0030849	intellectual developmental disorder with speech delay and axonal peripheral neuropathy	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	intellectual_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0030852	neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurodevelopmental_disorders_fall_under_the_category_of_neurology|neurology|genetics_and_genomics|pediatric	neurodevelopmental_disorder|neurodegenerative_disease|mental_health_disorder	brain_abnormalities|neurodevelopmental_disorder|brain_disorder	false	false	false	true	high
MONDO:0030854	combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	orthopaedic|genetics_and_genomics|rheumatology	metabolic_disorder|autoimmune_diseases|cardiovascular_disorder	joint_disorder|skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0030855	combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	orthopaedic|genetics_and_genomics|rheumatology|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	joint_disorder|skin_disorder|bone_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0030856	developmental and epileptic encephalopathy 89	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	developmental_disorder|neurodegenerative_disease|epileptic_disorder|metabolic_disorder	encephalopathy|developmental_disorder|epileptic_disorder|brain_disorder	false	false	false	false	high
MONDO:0030858	immunodeficiency 75	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	immunology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder	false	false	false	false	high
MONDO:0030859	COACH syndrome 2	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	endocrinology|neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	genetic_disorder____note__coach_syndrome_2_is_a_rare_genetic_disorder_affecting_the_endocrine_system|endocrine_disorder	false	false	false	false	high
MONDO:0030860	neuronopathy, distal hereditary motor, type 5C	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|hereditary_condition	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0030861	osteogenesis imperfecta, type 21	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0030862	COACH syndrome 3	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	endocrinology|genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	developmental_disorder|genetic_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0030864	Ritscher-Schinzel syndrome 3	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0030866	neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	muscle_disorder|brain_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0030867	thrombocytopenia 7	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	thrombocytopenia|hematology	autoimmune_diseases|inflammatory_disease|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0030868	spermatogenic failure 49	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics|urology	metabolic_disorder|autoimmune_diseases|anemia	reproductive_system_disorder|male_reproductive_system_disorder	false	false	false	false	medium
MONDO:0030869	spermatogenic failure 50	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	metabolic_disorder|anemia	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0030870	premature ovarian failure 17	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrinology|obstetrics_and_gynecology	metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0030871	vertebral hypersegmentation and orofacial anomalies	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	spinal_disorder|bone_disorder	false	false	false	false	low
MONDO:0030872	frontotemporal dementia and/or amyotrophic lateral sclerosis 8	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0030873	cardiofacioneurodevelopmental syndrome	hereditary_disease	other	hereditary_disease	cardiology|genetics_and_genomics|pediatric	neurodegenerative_disease|cardiovascular_disorder|developmental_disorder	cardio___or__cardiofacioneuromuscular_disorder_suggests_brain_disorder_is_also_appropriate___but_best_fit_is__brain_disorder|cardio|heart_disorder	false	false	false	false	high
MONDO:0030875	frontotemporal dementia and/or amyotrophic lateral sclerosis 5	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0030876	cardioacrofacial dysplasia 1	hereditary_disease	other	hereditary_disease	cardiology|genetics_and_genomics|pediatric	metabolic_disorder|cardiovascular_disorder	joint_disorder|spinal_disorder|eye_disorder|heart_disorder|ear_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0030877	cardioacrofacial dysplasia 2	hereditary_disease	other	hereditary_disease	cardiology|genetics_and_genomics|pediatrics|cardiothoracic	metabolic_disorder|cardiovascular_disorder	joint_disorder|acrofacial_dysplasia_is_actually_part_of_a_category_that_isn_t_listed___skin_disorder|heart_disorder|cardiovascular_disorder	false	false	false	false	medium
MONDO:0030878	Kaya-Barakat-Masson syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatrics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	liver_disorder|bone_disorder|lymphatic_disorder|vascular_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0030880	mandibuloacral dysplasia progeroid syndrome	hereditary_disease|premature_aging_syndrome|disorder_of_development_or_morphogenesis	other	premature_aging_syndrome|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	teeth_disorder|joint_disorder|skin_disorder|bone_disorder	false	false	false	false	high
MONDO:0030881	developmental and epileptic encephalopathy 102	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|epileptic_disorder|developmental_disorder	brain_disorder|developmental_disorder|epileptic_disorder	false	false	false	true	very_high
MONDO:0030883	carpal tunnel syndrome 2	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	orthopaedic|neurology|rheumatology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0030885	amyotrophic lateral sclerosis 26 with or without frontotemporal dementia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0030886	holoprosencephaly 14	hereditary_disease|syndromic_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder	endocrine_system_disorder	nervous_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0030887	cardiomyopathy, dilated, 2G	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiology|cardiothoracic	autoimmune_diseases|cardiovascular_disorder	muscle_disorder|vascular_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0030890	pontocerebellar hypoplasia, IIA 17	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0030891	intellectual developmental disorder, autosomal dominant 66	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0030893	leukoencephalopathy, progressive, infantile-onset, with or without deafness	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric|hematology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|blood_bone_marrow_disorder	true	false	false	false	very_high
MONDO:0030894	AMED syndrome, digenic	hematologic_disorder|immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	immune_system_disorder|hematologic_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|adrenal_gland_disease	kidney_disorder|upper_gastrointestinal_disorder|liver_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0030895	nephrotic syndrome, type 22	hereditary_disease|syndromic_disease|urinary_system_disorder	other	syndromic_disease|urinary_system_disorder|hereditary_disease	renal_medicine|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	kidney_disorder|immune_disorder	false	false	false	false	medium
MONDO:0030896	chromosome 13q33-q34 deletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder|joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0030897	Lessel-Kreienkamp syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	false	high
MONDO:0030898	immunodeficiency 76	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	immunology|allergy_and_immunology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	true	very_high
MONDO:0030899	oculocutaneous albinism type 8	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	ophthalmology|dermatology|genetics_and_genomics	metabolic_disorder|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0030900	intellectual developmental disorder with paroxysmal dyskinesia or seizures	hereditary_disease	other	hereditary_disease	psychiatry|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	seizure_disorder|brain_disorder	false	false	false	false	medium
MONDO:0030902	mitochondrial complex I deficiency, nuclear type 36	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatrics|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|other____note__i_ve_corrected_the_categories_to_reflect_that_it_is_a_mitochondrially_inherited_disease__but_still_classified_under_muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0030903	Hermansky-Pudlak syndrome 11	metabolic_disease|hematologic_disorder|integumentary_system_disorder|hereditary_disease|syndromic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|syndromic_disease|hereditary_disease|hematologic_disorder	pediatrics|genetics_and_genomics|immunology	neurodegenerative_disease|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder|eye_disorder	false	false	false	false	high
MONDO:0030905	hearing loss, autosomal recessive 117	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|otolaryngology|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	low
MONDO:0030906	Trichomonas tenax infectious disease	infectious_disease	infectious_disease	infectious_disease	obstetrics_and_gynecology|pediatric	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	true	false	false	true	low
MONDO:0030907	intellectual disability, X-linked 106	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	high
MONDO:0030908	intellectual disability, X-linked, syndromic, 35	nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	mental_health_disorder|intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0030909	intellectual disability, X-linked, syndromic, Houge type	nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	intellectual_disability__syndromic|brain_disorder	false	false	false	false	high
MONDO:0030910	intellectual disability, autosomal dominant 45	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0030911	intellectual disability, autosomal dominant 46	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0030912	intellectual disability, autosomal dominant 47	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis	psychiatric_disorder	psychiatric_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0030913	intellectual disability, autosomal dominant 48	nervous_system_disorder|hereditary_disease|psychiatric_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	psychiatric_disorder	psychiatric_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	intellectual_disability_is_related_to_brain_development_and_function_so_it_could_be_listed_under_a_subset_of_the_broader_category__brain_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030914	Clark-Baraitser syndrome	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0030915	intellectual disability, autosomal recessive 61	nervous_system_disorder|metabolic_disease|hereditary_disease|psychiatric_disorder	psychiatric_disorder|metabolic_disease	psychiatric_disorder|hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0030916	intellectual disability, autosomal dominant 50	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|psychiatry|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0030917	intellectual disability, autosomal dominant 51	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|intellectual_disability___note__there_is_a_specific_category_named__intellectual_disability__which_is_related_to_brain_disorders__hence_it_s_more_accurate_than_the_general_category__brain_disorder___however__since__intellectual_disability__was_provided_as_the_disease_name__i_ve_added_it_in_the_output	false	false	false	false	high
MONDO:0030918	intellectual disability, autosomal dominant 52	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|psychiatry|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	autosomal_dominant|brain_disorder	false	false	false	false	high
MONDO:0030919	intellectual disability, autosomal dominant 53	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|intellectual_disability	false	false	false	false	medium
MONDO:0030920	intellectual disability, autosomal dominant 54	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|psychiatry|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|autosomal_dominant	false	false	false	false	high
MONDO:0030921	intellectual disability, autosomal dominant 55, with seizures	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|intellectual_disability	brain_disorder	false	false	false	true	very_high
MONDO:0030922	intellectual disability, autosomal dominant 56	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|intellectual_disability_is_likely_related_to_brain_disorder__but_since_it_s_a_specific_subtype_of_disability__i_ll_provide_the_more_precise_categorization____intellectual_disability	false	false	false	true	high
MONDO:0030923	frontotemporal dementia and/or amyotrophic lateral sclerosis	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0030924	proteasome-associated autoinflammatory syndrome 5	connective_tissue_disorder|immune_system_disorder|hereditary_disease|syndromic_disease	other	connective_tissue_disorder|hereditary_disease|syndromic_disease|immune_system_disorder	immunology|genetics_and_genomics|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder	false	false	false	false	medium
MONDO:0030925	oocyte maturation defect 10	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|reproductive_endocrine_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0030926	spermatogenic failure 51	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology|endocrinology	metabolic_disorder|anemia	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0030927	myofibrillar myopathy 11	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030928	microcephaly 26, primary, autosomal dominant	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	muscle_disorder|brain_disorder|upper_gastrointestinal_disorder|nose_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030929	microcephaly 27, primary, autosomal dominant	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030930	neurodevelopmental disorder with or without early-onset generalized epilepsy	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|neurodevelopmental_disorder	false	false	false	false	high
MONDO:0030931	proteasome-associated autoinflammatory syndrome 4	connective_tissue_disorder|immune_system_disorder|hereditary_disease|syndromic_disease	other	connective_tissue_disorder|hereditary_disease|syndromic_disease|immune_system_disorder	genetics_and_genomics|immunology|rheumatology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0030933	Joubert syndrome 37	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|anemia	kidney_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0030934	intellectual developmental disorder, autosomal dominant 64	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0030935	mitochondrial complex 2 deficiency, nuclear type 2	mitochondrial_disease|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|pediatrics|cardiology|neurology	neurodegenerative_disease|metabolic_disorder	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0030936	epilepsy, progressive myoclonic, 12	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|spinal_disorder|muscledisorder	false	false	false	true	high
MONDO:0030937	mitochondrial complex 2 deficiency, nuclear type 3	mitochondrial_disease|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	mitochondrial_disease|mitochondrial_complex_2_deficiency|muscle_disorder	false	false	false	false	high
MONDO:0030938	spermatogenic failure 52	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|endocrinology|urology	metabolic_disorder|autoimmune_diseases|anemia|cancer	reproductive_system_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0030939	premature ovarian failure 18	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	endocrinology|obstetrics_and_gynecology	metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0030941	erythrokeratodermia variabilis et progressiva 7	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|hematology|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0030947	neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|childhood_onset_disease	brain_disorder|lung_disorder|muscle_disorder	true	false	false	true	very_high
MONDO:0030953	short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	cardiovascular_disorder|skeletal_anomalies|metabolic_disorder	heart_disorder|bone_disorder|skeletal_disorder	false	false	false	true	medium
MONDO:0030957	developmental and epileptic encephalopathy 103	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	epileptic_disorder|developmental_disorder|neurodegenerative_disease	developmental_and_epileptic_encephalopathy|brain_disorder	false	false	false	true	very_high
MONDO:0030958	dystonia 35, childhood-onset	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0030961	Olmsted syndrome 2	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|joint_disorder|brain_disorder	false	false	false	false	high
MONDO:0030962	nephrotic syndrome, type 23	urinary_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|urinary_system_disorder	renal_medicine|pediatrics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|immune_disorder	false	false	false	false	medium
MONDO:0030963	Li-Campeau syndrome	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0030964	intellectual developmental disorder, autosomal dominant 67	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0030966	neurofacioskeletal syndrome with or without renal agenesis	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	kidney_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0030967	deafness, congenital, and adult-onset progressive leukoencephalopathy	hereditary_disease	other	hereditary_disease	otolaryngology|neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	brain_disorder|ear_disorder	false	false	false	false	high
MONDO:0030968	intellectual developmental disorder, autosomal recessive 76	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	psychiatric_disorder|metabolic_disease	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	autosomal_recessive|intellectual_developmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0030969	intellectual developmental disorder, autosomal dominant 68	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics|psychiatry	metabolic_disorder|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0030970	immunodeficiency 106, susceptibility to viral infections	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	pediatric|genetics_and_genomics|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0030971	immunodeficiency 78 with autoimmunity and developmental delay	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	pediatric|genetics_and_genomics|allergy_and_immunology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	autoimmune|immune_disorder|lymphatic_disorder	true	false	false	false	high
MONDO:0030972	spermatogenic failure 74	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	pediatric|urology	metabolic_disorder|anemia	reproductive_system_disorder|spermatozoal_disorder	false	false	false	false	medium
MONDO:0030973	immunodeficiency 77	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	immunology|allergy_and_immunology	immunodeficiency|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0030974	mitochondrial complex 2 deficiency, nuclear type 4	musculoskeletal_system_disorder|mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	neurology|genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder|mitochondrial_disease___corrected_response_to_follow_the_format___muscle_disorder	false	false	false	false	high
MONDO:0030975	premature ovarian failure 20	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrinology|obstetrics_and_gynecology	metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0030976	oculomotor-abducens synkinesis	hereditary_disease	other	hereditary_disease	ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0030977	neuronopathy, distal hereditary motor, autosomal recessive 7	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	genetic_disorder|hereditary_condition|neurodegenerative_disease	muscle_disorder|neuronopathy	false	false	false	false	medium
MONDO:0030978	ENDOVE syndrome, limb-only type	hereditary_disease	other	hereditary_disease	orthopaedic|pediatric|endocrinology|neurology|genetics_and_genomics|obstetrics_and_gynecology	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	joint_disorder|bone_disorder|limb_bone_marrow_disorder	false	false	false	false	medium
MONDO:0030979	ENDOVE syndrome, limb-brain type	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0030981	immunodeficiency 79	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	immunology|pediatric|allergy_and_immunology|rheumatology	inflammatory_disease|immunodeficiency|autoimmune_diseases	immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0030982	sulfide quinone oxidoreductase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0030983	Waardenburg syndrome, IIa 2F	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	skin_disorder|ear_disorder|hearing	false	false	false	false	medium
MONDO:0030984	spermatogenic failure 75	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	anemia|metabolic_disorder	spinal_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0030985	premature ovarian failure 19	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrinology|obstetrics_and_gynecology	metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0030986	blistering, acantholytic, of oral and laryngeal mucosa	hereditary_disease	other	hereditary_disease	otolaryngology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|throat_disorder|immune_disorder	false	false	false	false	high
MONDO:0030987	vertebral, cardiac, tracheoesophageal, renal, and limb defects	hereditary_disease	other	hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	cardiovascular_disorder|inflammatory_disease|neurodegenerative_disease	spinal_disorder|kidney_disorder|heart_disorder|bone_disorder	false	false	false	false	high
MONDO:0030988	developmental delay with dysmorphic facies and dental anomalies	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	dysmorphic_facies|developmental_delay|brain_disorder|teeth_disorder	false	false	false	true	high
MONDO:0030989	spermatogenic failure 53	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|anemia	reproductive_system_disorder	false	false	false	false	high
MONDO:0030990	Kohlschutter-Tonz syndrome-like	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0030991	bile acid conjugation defect 1	hereditary_disease	other	hereditary_disease	genetics_and_genomics|gastroenterology|hepatology	bile_acid_conjugation_defect|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0030992	short stature, oligodontia, dysmorphic facies, and motor delay	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|bone_disorder|endocrine_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0030993	Tessadori-Van Haaften neurodevelopmental syndrome 3	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	neurodevelopmental_disorder|brain_disorder	false	false	false	as_of_my_last_knowledge_update_in_october_2023__there_are_no_specific_efficacious_treatments_that_cure__prevent__or_effectively_treat_tessadori_van_haaften_neurodevelopmental_syndrome_3__therefore__i_would_return_false	high
MONDO:0030994	neurodevelopmental disorder with or without autism or seizures	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	high
MONDO:0030995	global developmental delay with speech and behavioral abnormalities	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0030996	bleeding disorder, platelet-type, 24	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology|neonatology|pediatric	inflammatory_disease|platelet_type|autoimmune_diseases|bleeding_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0030997	mitochondrial complex I deficiency, nuclear type 37	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_disease	false	false	false	true	high
MONDO:0030998	hearing loss, autosomal dominant 80	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	otolaryngology|genetics_and_genomics|pediatric	autosomal_dominant_disorders_are_typically_classified_under_a_different_category_but_given_the_provided_list__neurodegenerative_disease_is_the_closest_fit_to_hearing_loss|metabolic_disorder|neurodegenerative_disease	ear_disorder|autosomal_dominant_disorder__note__the_second_category_is_implied_but_not_in_the_list__i_assume_you_want_to_know_that_it_s_an_inherited_condition	false	false	false	false	medium
MONDO:0030999	neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics|psychiatry	inflammatory_disease|mental_health_disorder|neurodegenerative_disease	cerebral_atrophy|brain_disorder	false	false	false	false	high
MONDO:0031000	Tessadori-Van Haaften neurodevelopmental syndrome 4	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	as_of_my_last_update_in_october_2023__there_are_no_known_efficacious_treatments_that_cure__prevent__or_effectively_treat_tessadori_van_haaften_neurodevelopmental_syndrome_4__therefore__i_would_return_false	high
MONDO:0031001	vitreoretinopathy with phalangeal epiphyseal dysplasia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|ophthalmology	autoimmune_diseases|metabolic_disorder	bone_disorder|joint_disorder|eye_disorder	false	false	false	false	high
MONDO:0031002	Baralle-Macken syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0031003	hypercholanemia, familial, 2	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	renal_medicine|endocrinology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0031006	neurodegeneration with ataxia and late-onset optic atrophy	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0031007	spondyloepiphyseal dysplasia, sensorineural hearing loss, impaired intellectual development, and leber congenital amaurosis	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_orbital_region|psychiatric_disorder|disorder_of_visual_system	neurology|genetics_and_genomics|ophthalmology|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder|eye_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0031008	nephrotic syndrome, type 24	urinary_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|urinary_system_disorder	renal_medicine|nephrology|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder	kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0031009	Glanzmann thrombasthenia 2	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	autoimmune_diseases|anemia	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0031010	odontochondrodysplasia 2 with hearing loss and diabetes	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	bone_disorder|endocrine_disorder|teeth_disorder|ear_disorder	false	false	true	false	high
MONDO:0031011	neurodevelopmental disorder with dysmorphic facies and variable seizures	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodevelopmental_disorder|neurodegenerative_disease	neurodevelopmental_disorder|brain_disorder	false	false	false	true	high
MONDO:0031012	autoimmune uveitis	otorhinolaryngologic_disease|inflammatory_disease|disorder_of_visual_system|immune_system_disorder	autoimmune_disease	disorder_of_orbital_region|immune_system_disorder|inflammatory_disease|disorder_of_visual_system|otorhinolaryngologic_disease	ophthalmology|allergy_and_immunology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	false	false	false	true	medium
MONDO:0031013	autoimmune optic neuritis	nervous_system_disorder|inflammatory_disease|disorder_of_visual_system|immune_system_disorder	autoimmune_disease	disorder_of_orbital_region|immune_system_disorder|nervous_system_disorder|inflammatory_disease|disorder_of_visual_system	neurology|immunology|ophthalmology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	false	false	false	false	medium
MONDO:0031014	autoimmune gastritis	digestive_system_disorder|inflammatory_disease|immune_system_disorder	autoimmune_disease	immune_system_disorder|inflammatory_disease|digestive_system_disorder	gastroenterology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0031019	spastic paraplegia 87, autosomal recessive	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0031021	developmental and epileptic encephalopathy 104	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	developmental_disorder|epilepsy|neurodegenerative_disease	spinal_disorder|developmental_disorder|epileptic_disorder|brain_disorder	false	false	false	false	high
MONDO:0031028	developmental and epileptic encephalopathy 105 with hypopituitarism	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	endocrinology|neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|developmental_disease	endocrine_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0031030	immunodeficiency 107, susceptibility to invasive staphylococcus aureus infection	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	allergy_and_immunology|pediatric	autoimmune_diseases|inflammatory_disease|allergy	lymphatic_disorder|immune_disorder	true	false	false	true	high
MONDO:0031031	intellectual developmental disorder, autosomal recessive 77	psychiatric_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder	neurology|genetics_and_genomics|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0031037	famililal cerebral cavernous malformations	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|oncology	cancer|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0031040	cholestasis, progressive familial intrahepatic, 12	syndromic_disease|digestive_system_disorder|endocrine_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease|endocrine_system_disorder	hereditary_disease|syndromic_disease|metabolic_disease|digestive_system_disorder|endocrine_system_disorder	gastroenterology|hepatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	liver_disorder|biliary_disorder	false	false	false	false	very_high
MONDO:0031043	lymphatic malformation 12	cardiovascular_disorder|immune_system_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|immune_system_disorder|cardiovascular_disorder	hematology|pediatric|oncology	lymphatic_system_disorder|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0031044	advance sleep phase syndrome, familial, 4	hereditary_disease	other	hereditary_disease|sleep_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|brain_disorder	false	false	false	false	medium
MONDO:0031045	arthrogryposis, distal, IIa 11	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	neurology|orthopaedic	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0031047	Stickler syndrome, type 6	syndromic_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_orbital_region|nervous_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system	genetics_and_genomics|ophthalmology|rheumatology|orthopaedic	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|joint_disorder|eye_disorder	false	false	false	false	medium
MONDO:0031052	developmental and epileptic encephalopathy 106	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	developmental_disorder|epileptic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0031054	ciliary dyskinesia, primary, 48, without situs inversus	syndromic_disease|respiratory_system_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|respiratory_system_disorder	genetics_and_genomics|pulmonology|pediatric	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	ciliary_dyskinesia_is_primarily_related_to_the_eyes__so_this_category_is_a_good_fit|eye_disorder	false	false	false	false	high
MONDO:0031055	developmental and epileptic encephalopathy 107	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	epilepsy|developmental_disorder|neurodegenerative_disease	epileptic_disorder|developmental_disorder|brain_disorder	false	false	false	true	high
MONDO:0031057	dyskeratosis congenita, digenic	syndromic_disease|cancer_or_benign_tumor|hereditary_disease|integumentary_system_disorder	cancer_or_benign_tumor	hereditary_disease|integumentary_system_disorder|cancer_or_benign_tumor|syndromic_disease	pediatric|dermatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|blood_bone_marrow_disorder|joint_disorder|skin_disorder	false	false	false	true	high
MONDO:0031060	microcephaly 29, primary, autosomal recessive	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0031061	nephrotic syndrome, IIa 26	syndromic_disease|hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder|syndromic_disease	nephrology|renal_medicine	inflammatory_disease|autoimmune_diseases|metabolic_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0031062	polycystic kidney disease 7	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	genetics_and_genomics|endocrinology|urology|renal_medicine	metabolic_disorder|kidney_disease_does_not_exist_in_the_list_so_this_is_it	endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0031068	Charcot-Marie-Tooth disease, axonal, IIa 2II	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	axonal|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0031071	Diamond-Blackfan anemia 21	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|lung_disorder	false	false	false	true	high
MONDO:0031077	spermatogenic failure 76	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	endocrinology|urology|genetics_and_genomics	anemia|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0031083	spermatogenic failure 77	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	endocrine_disease|metabolic_disorder	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0031084	amelogenesis imperfecta, IIa 1K	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|mouth_disorder|musculoskeletal_system_disorder	hematology|pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	teeth_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0031115	dyskinesia with orofacial involvement	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0031166	macular dystrophy, retinal	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	medium
MONDO:0031169	odontochondrodysplasia	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|genetic_disease|bone_disease	bone_disorder|teeth_disorder|joint_disorder	false	false	false	false	high
MONDO:0031199	inherited interstitial lung disease	hereditary_disease	other	hereditary_disease	pulmonology|genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	false	false	false	false	high
MONDO:0031200	Bryant-Li-Bhoj neurodevelopmental syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	neurodevelopmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0031213	restrictive dermopathy	hereditary_disease	other	hereditary_disease	dermatology|pulmonology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0031219	mismatch repair cancer syndrome	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	oncology|genetics_and_genomics	inherited_disease|cancer|genetic_disorder	immune_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0031230	mitochondrial complex II deficiency, nuclear type	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|metabolic_disease|mitochondrial_disease|hereditary_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology|hematology|pediatric	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	mitochondrial_disease___note__some_sources_may_categorize_this_disease_under_a_more_specific_type_of_mitochondrial_disorder__but_based_on_the_given_options_and_general_knowledge__these_two_categories_seem_to_be_the_most_fitting|muscle_disorder	false	false	false	false	high
MONDO:0031240	familial panic disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatry|neurology	mental_health_disorder|familial_panicking_disorder	immune_disorder|brain_disorder	false	false	false	true	high
MONDO:0031257	high altitude pulmonary edema	respiratory_system_disorder	other	respiratory_system_disorder|acute_disease	cardiology|pulmonology	metabolic_disorder|cardiovascular_disorder	lung_disorder|heart_disorder|kidney_disorder	false	false	false	true	high
MONDO:0031280	Stuve-Wiedemann syndrome	hereditary_disease	other	hereditary_disease	hematolog|genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	vascular_disorder|bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0031322	triopia	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0031323	cardiac valvular defect	hereditary_disease	other	hereditary_disease	cardiothoracic|cardiology	cardiovascular_disorder|cardiac_valvular_defect_falls_under_this_category	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0031329	craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	skeletal_anomalies|impaired_intellectual_development|brain_disorder|teeth_disorder|bone_disorder	false	false	false	false	high
MONDO:0031332	Glanzmann thrombasthenia 1	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	autoimmune_diseases|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0031376	congenital disorder of deglycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder	false	false	false	false	high
MONDO:0031384	autoinflammatory syndrome, familial, Behcet-like	hereditary_disease|syndromic_disease|connective_tissue_disorder	other	connective_tissue_disorder|syndromic_disease|hereditary_disease	rheumatology|gastroenterology	inflammatory_disease|autoimmune_diseases	vascular_disorder|joint_disorder|immune_disorder	false	false	false	false	high
MONDO:0031386	cardioacrofacial dysplasia	hereditary_disease	other	hereditary_disease	pediatric|cardiothoracic|cardiology|genetics_and_genomics|pulmonology	metabolic_disorder|cardiovascular_disorder	eye_disorder|heart_disorder|joint_disorder	false	false	false	false	high
MONDO:0031400	Tessadori-Van-Haaften neurodevelopmental syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	brain_disorder|neurodevelopmental_disorder	false	false	false	false	high
MONDO:0031415	Carey-Fineman-Ziter syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0031421	Olmsted syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|eye_disorder|lower_gastrointestinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0031422	familial mucolipidosis	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	lung_disorder|muscle_disorder|bone_disorder|kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0031432	thyroid hormone metabolism, abnormal	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	thyroid_hormone_metabolism_is_primarily_related_to_endocrine_system_function|endocrinology	metabolic_disorder|autoimmune_diseases	thyroid_hormone_metabolism_abnormal|endocrine_disorder	false	false	false	false	medium
MONDO:0031439	short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|endocrinology	skeletal_anomalies|metabolic_disorder|genetic_disorder_is_not_in_the_list_but_was_considered|cardiac_anomalies|autoimmune_diseases	facial_dysmorphism|skeletal_anomalies|cardiac_anomalies|bone_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0031446	hypercholanemia, familial 1	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|endocrinology|renal_medicine	metabolic_disorder|adrenal_gland_disease	liver_disorder|endocrine_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0031447	macrothrombocytopenia, isolated	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology	metabolic_disorder|autoimmune_diseases|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0031481	microcephaly, epilepsy, and diabetes syndrome 1	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|epilepsy|neurodegenerative_disease	brain_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0031520	familial severe combined immunodeficiency	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	pediatric|allergy_and_immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0031615	familial bent bone dysplasia syndrome	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	genetic_disease|metabolic_disorder	spinal_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0031632	developmental delay with short stature, dysmorphic facial features, and sparse hair	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	sparse_hair|dysmorphic_features|growth_disorder|developmental_delay|endocrine_disorder|skeletal_disorder	false	false	false	true	high
MONDO:0031646	Braddock-Carey syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	immune_disorder|bone_disorder|liver_disorder	false	false	false	false	high
MONDO:0032485	intellectual developmental disorder 61	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|intellectual_developmental_disorder_is_already_in_the_category_list_so_brain_disorder	false	false	false	false	high
MONDO:0032526	spinocerebellar ataxia 48	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|spinal_cord_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0032564	hennekam lymphangiectasia-lymphedema syndrome 3	cardiovascular_disorder|immune_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	syndromic_disease|hereditary_disease|cardiovascular_disorder|immune_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0032565	ophthalmoplegia, external, with rib and vertebral anomalies	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0032566	squalene synthase deficiency	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder	metabolic_disorder|liver_disorder|genetic_disorder	false	false	false	false	high
MONDO:0032567	isolated growth hormone deficiency, type 4	endocrine_system_disorder|reproductive_system_disorder|nervous_system_disorder|hereditary_disease	endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder|endocrine_disorder|growth_hormone_disorder	false	false	false	true	medium
MONDO:0032568	intellectual developmental disorder with macrocephaly, seizures, and speech delay	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|speech_delay_is_ambiguous_so_consider_speech_as_a_brain_function__seizures_also_related_to_brain_so_these_2_categories_fit_best	false	false	false	false	high
MONDO:0032569	isolated growth hormone deficiency, type 5	endocrine_system_disorder|reproductive_system_disorder|nervous_system_disorder|hereditary_disease	endocrine_system_disorder	nervous_system_disorder|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrinology|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	endocrine_disorder|brain_disorder	false	false	false	true	medium
MONDO:0032570	Joubert syndrome 35	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|ear_disorder|kidney_disorder|eye_disorder	false	false	false	false	high
MONDO:0032571	spondyloepimetaphyseal dysplasia, Krakow type	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|orthopaedic|pediatric|rheumatology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0032572	cardiac, facial, and digital anomalies with developmental delay	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|cardiology	developmental_delay|neurodegenerative_disease|cardiovascular_disorder	heart_disorder|digital_anomaly|facial_disorder|developmental_delay|cardiac_disorder	false	false	false	false	high
MONDO:0032573	bone marrow failure syndrome 5	hematologic_disorder|immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|immune_system_disorder|hematologic_disorder	hematology|genetics_and_genomics	anemia|cancer	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0032574	osteochondrodysplasia, brachydactyly, and overlapping malformed digits	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|genetic_disorder|skeletal_malformation	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0032575	diarrhea 9	digestive_system_disorder|hereditary_disease	other	hereditary_disease|digestive_system_disorder	gastroenterology|pediatrics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0032577	retinitis pigmentosa 83	metabolic_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	metabolic_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0032578	cortical dysplasia, complex, with other brain malformations 9	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0032579	warburg-cinotti syndrome	hereditary_disease	other	hereditary_disease	endocrinology|neurology|genetics_and_genomics|pediatric|cardiology	metabolic_disorder|neurodegenerative_disease	lymphatic_disorder|immune_disorder	false	false	true	false	medium
MONDO:0032580	nephrotic syndrome, type 17	urinary_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|urinary_system_disorder	renal_medicine|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|kidney_disorder	false	false	false	false	high
MONDO:0032581	nephrotic syndrome, type 18	urinary_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|urinary_system_disorder	renal_medicine|genetics_and_genomics|pediatric	metabolic_disorder|kidney_disease	immune_disorder|kidney_disorder	false	false	false	false	high
MONDO:0032582	nephrotic syndrome, type 19	urinary_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|urinary_system_disorder	renal_medicine|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|urinary_tract_disorder|kidney_disorder	false	false	false	true	high
MONDO:0032583	microcephaly 24, primary, autosomal recessive	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	other____but_since__other__is_optional_in_the_instruction____brain_disorder|brain_disorder	false	false	false	false	high
MONDO:0032584	ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	skin_disorder|hair_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0032586	diarrhea 10, protein-losing enteropathy type	digestive_system_disorder|hereditary_disease	other	hereditary_disease|digestive_system_disorder	gastroenterology|renal_medicine|pediatric	inflammatory_disease|metabolic_disorder|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0032588	periventricular nodular heterotopia 8	nervous_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|nervous_system_disorder	neurology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0032590	ovarian dysgenesis 8	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|cancer	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0032591	hyperparathyroidism, transient neonatal	endocrine_system_disorder|hereditary_disease|musculoskeletal_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|musculoskeletal_system_disorder	endocrinology|pediatric	metabolic_disorder|neonatal_disease_is_not_in_the_list_so__metabolic_disorder|adrenal_gland_disease_is_also_a_bit_of_a_stretch_since_parathyroid_is_related_to_calcium_regulation_which_is_controlled_by_the_parathyroid_gland__but_it_s_often_associated_with_the_endocrine_system_and_i_couldn_t_find_anything_specific_about_the_parathyroids_being_part_of_the_adrenals_so_i_ll_leave_that_one_out__metabolic_disorder	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0032592	cardiomyopathy, dilated, 2c	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiothoracic|cardiology	inflammatory_disease|cardiovascular_disorder|metabolic_disorder|autoimmune_diseases	heart_disorder|muscle_disorder|vascular_disorder	false	false	false	false	high
MONDO:0032594	intellectual developmental disorder and retinitis pigmentosa; IDDRP	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	neurology|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0032596	myasthenic syndrome, congenital, 23, presynaptic	nervous_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	true	false	false	true	high
MONDO:0032597	myasthenic syndrome, congenital, 24, presynaptic	nervous_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder|immune_disorder	false	false	false	true	high
MONDO:0032598	developmental and epileptic encephalopathy, 68	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	developmental_disorder|epileptic_encephalopathy|neurodegenerative_disease	epileptic_disorder|developmental_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0032599	immunodeficiency 15a	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	immunology|allergy_and_immunology|genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0032600	Snijders Blok-Campeau syndrome	hereditary_disease	other	hereditary_disease	pediatric|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0032601	inflammatory bowel disease, immunodeficiency, and encephalopathy	hereditary_disease	other	hereditary_disease	gastroenterology|immunology|neurology	inflammatory_disease|immunodeficiency_is_not_in_the_list_so_i_ll_remove_it___inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder|encephalopathy	false	false	false	true	high
MONDO:0032603	polydactyly, postaxial, type A9	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics	limb_abnormality|genetic_disorder|congenital_anomaly|birth_defect|developmental_disorder|metabolic_disorder|skeletal_abnormality|polydactyly|genetic_condition	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0032604	retinitis pigmentosa 84	disorder_of_visual_system|nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|metabolic_disease	ophthalmology|genetics_and_genomics	retinal_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0032605	intellectual disability, autosomal recessive 66	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0032606	mitochondrial complex I deficiency, nuclear type 2	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics|pediatric|neurology	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|mitochondrial_disease|brain_disorder	false	false	false	false	very_high
MONDO:0032607	vertebral anomalies and variable endocrine and T-cell dysfunction	hereditary_disease	other	hereditary_disease	endocrinology|pediatrics|genetics_and_genomics|immunology	immune_dysfunction_disorders|endocrine_disorder|autoimmune_diseases	immune_disorder|spinal_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0032608	mitochondrial complex I deficiency, nuclear type 3	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0032609	mitochondrial complex I deficiency, nuclear type 4	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0032610	mitochondrial complex I deficiency, nuclear type 5	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0032611	mitochondrial complex I deficiency, nuclear type 6	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_disorder	false	false	false	false	high
MONDO:0032612	mitochondrial complex I deficiency, nuclear type 7	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	psychiatry|genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0032613	mitochondrial complex I deficiency, nuclear type 8	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0032615	mitochondrial complex I deficiency, nuclear type 9	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0032616	mitochondrial complex I deficiency, nuclear type 10	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|liver_disorder|mitochondrial_disease|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0032617	mitochondrial complex I deficiency, nuclear type 11	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|mitochondrial_disease	false	false	false	false	very_high
MONDO:0032618	mitochondrial complex I deficiency, nuclear type 13	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_disease____corrected_list__muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0032619	mitochondrial complex I deficiency, nuclear type 14	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	psychiatry|pediatrics|genetics_and_genomics|neurology	cardiovascular_disorder|metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|mitochondrial_disorders|liver_disorder	false	false	false	false	high
MONDO:0032620	mitochondrial complex I deficiency, nuclear type 15	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0032621	mitochondrial complex I deficiency, nuclear type 16	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease___corrected_to__muscle_disorder|mitochondrial_disease____corrected_for_accuracy____corrected_again_to__muscle_disorder|mitochondrial_disease_is_incorrect__it_should_be____muscle_disorder|muscle_disorder	false	false	false	true	high
MONDO:0032622	mitochondrial complex I deficiency, nuclear type 17	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|cardiology|pediatric|pulmonology|neurology	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	true	very_high
MONDO:0032623	mitochondrial complex I deficiency, nuclear type 18	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	very_high
MONDO:0032624	mitochondrial complex I deficiency, nuclear type 19	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0032625	mitochondrial complex I deficiency, nuclear type 21	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	muscle_disorder	false	false	false	false	high
MONDO:0032626	mitochondrial complex I deficiency, nuclear type 22	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0032627	mitochondrial complex I deficiency, nuclear type 23	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	endocrinology|genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	mitochondrial_disorders_would_typically_be_classified_under_a_separate_category_but_since_none_is_available__the_above_two_will_suffice|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0032628	mitochondrial complex I deficiency, nuclear type 24	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	true	high
MONDO:0032629	mitochondrial complex I deficiency, nuclear type 25	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	endocrinology|genetics_and_genomics|hepatology|cardiology|pediatric|renal_medicine|neurology|hematology|gastroenterology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	mitochondrial_complex_1_deficiency_nuclear_type_25_is_related_to_muscles_and_their_function|muscle_disorder	false	false	false	false	high
MONDO:0032630	mitochondrial complex I deficiency, nuclear type 26	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|mitochondrial_disorder_is_not_in_the_list_so__kidney_disorder|muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0032631	mitochondrial complex I deficiency, nuclear type 27	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0032632	mitochondrial complex I deficiency, nuclear type 28	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0032633	mitochondrial complex I deficiency, nuclear type 29	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0032634	mitochondrial complex I deficiency, nuclear type 31	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	mitochondrial_complex_1_deficiency_nuclear_type_31_can_also_be_categorized_under_other_but_since_that_is_last_resort_this_is_priority|muscle_disorder	false	false	false	true	high
MONDO:0032635	mitochondrial complex I deficiency, nuclear type 32	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	very_high
MONDO:0032636	mitochondrial complex I deficiency, nuclear type 33	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0032637	ciliary dyskinesia, primary, 39	hereditary_disease|respiratory_system_disorder|syndromic_disease	other	syndromic_disease|respiratory_system_disorder|hereditary_disease	pulmonology|neurology	metabolic_disorder|neurodegenerative_disease	lung_disorder|eye_disorder	false	false	false	false	high
MONDO:0032639	hearing loss, autosomal recessive 112	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder|hereditary_disease	pediatrics|genetics_and_genomics|otolaryngology	metabolic_disorder|neurodegenerative_disease|autosomal_recessive_disorders___note__this_is_a_specific_type_of_genetic_disorder_that_affects_the_hearing	ear_disorder	false	false	false	true	high
MONDO:0032641	mirror movements 4	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	psychiatry|pediatric|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	low
MONDO:0032642	arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics|pediatric|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	joint_disorder|spine_disorder|brain_disorder|teeth_disorder|muscle_disorder	false	false	false	false	high
MONDO:0032643	pontocerebellar hypoplasia, type 12	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0032645	trichohepatoneurodevelopmental syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hepatology|pediatric|neurology	inflammatory_disease|mental_health_disorder|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	liver_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0032646	congenital anomalies of kidney and urinary tract 3	hereditary_disease|disorder_of_development_or_morphogenesis|urinary_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|urinary_system_disorder	urology|pediatric|renal_medicine	urinary_tract|kidney	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0032648	mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0032649	hypotrichosis 14	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	genetic_diseases|metabolic_disorder	hair_disorder|skin_disorder	false	false	false	true	low
MONDO:0032650	neurodegeneration, childhood-onset, with cerebellar atrophy	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	cerebellar_atrophy_diseases|childhood_onset_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0032651	fibrosis, neurodegeneration, and cerebral angiomatosis	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|neurology	inflammatory_disease|cerebral_angiomatosis_is_not_in_the_category_list_so_ignore_it|neurodegenerative_disease	brain_disorder|vascular_disorder|lung_disorder	false	false	false	false	high
MONDO:0032653	cardiac-urogenital syndrome	hereditary_disease	other	hereditary_disease	urology|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder	reproductive_system_disorder|kidney_disorder|heart_disorder	false	false	false	false	high
MONDO:0032654	hyper-IgE recurrent infection syndrome 3, autosomal recessive	hematologic_disorder|hereditary_disease|immune_system_disorder	other	immune_system_disorder|hematologic_disorder|hereditary_disease	genetics_and_genomics|pediatric|immunology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|lymphatic_disorder	true	false	false	false	high
MONDO:0032655	visual impairment and progressive phthisis bulbi	hereditary_disease	other	hereditary_disease	ophthalmology|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|eye_disorder	false	false	false	false	high
MONDO:0032656	microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder|muscle_disorder	true	false	false	false	high
MONDO:0032657	developmental and epileptic encephalopathy, 69	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	developmental_disease|epileptic_encephalopathy|neurodegenerative_disease	brain_disorder|developmental_disorders	false	false	false	true	very_high
MONDO:0032658	macrocephaly, acquired, with impaired intellectual development	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder	true	false	false	false	high
MONDO:0032659	mucocutaneous ulceration, chronic	hereditary_disease	other	hereditary_disease	dermatology	anemia|inflammatory_disease|cancer|metabolic_disorder|autoimmune_diseases	skin_disorder|lower_gastrointestinal_disorder	true	false	false	false	high
MONDO:0032660	spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics|pediatric|neurology	autosomal_dominant_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0032661	neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|neurodevelopmental_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0032662	intellectual developmental disorder, autosomal recessive 67	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0032663	developmental and epileptic encephalopathy, 70	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	developmental_disorder|epileptic_encephalopathy|neurodegenerative_disease	brain_disorder|epileptic_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0032664	ciliary dyskinesia, primary, 40	respiratory_system_disorder|syndromic_disease|hereditary_disease	other	respiratory_system_disorder|syndromic_disease|hereditary_disease	pediatrics|genetics_and_genomics|pulmonology	metabolic_disorder|neurodegenerative_disease	eye_disorder|lung_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0032665	intellectual developmental disorder, autosomal recessive 68	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatry|genetics_and_genomics|pediatric|neurology	metabolic_disorder|mental_health_disorder	brain_disorder|intellectual_developmental_disorder_is_not_in_the_list_so_i_will_exclude_it	false	false	false	false	high
MONDO:0032668	Diamond-Blackfan anemia 18	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0032669	Diamond-Blackfan anemia 19	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder|autoimmune_diseases	bone_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0032670	Diamond-Blackfan anemia 20	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|autoimmune_diseases|anemia	blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0032672	intellectual developmental disorder with cardiac defects and dysmorphic facies	hereditary_disease	other	hereditary_disease	genetics_and_genomics|cardiology|pediatric|neurology	cardiovascular_disorder|metabolic_disorder|mental_health_disorder	skeletal_dysplasia|dysmorphic_facial_features|heart_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0032673	basal ganglia calcification, idiopathic, 7, autosomal recessive	nervous_system_disorder|hereditary_disease	other	idiopathic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autosomal_recessive_diseases	spinal_disorder|vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0032675	myasthenic syndrome, congenital, 25, presynaptic	nervous_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|autoimmune_diseases	immune_disorder|muscle_disorder|brain_disorder	true	false	false	true	high
MONDO:0032677	lissencephaly 9 with complex brainstem malformation	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0032678	developmental and epileptic encephalopathy, 71	nervous_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	developmental_and_epileptic_encephalopathy_is_not_a_fitting_category|neurodegenerative_disease	developmental_and_epileptic_encephalopathy|brain_disorder	false	false	false	true	very_high
MONDO:0032679	combined oxidative phosphorylation deficiency 37	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0032680	global developmental delay with or without impaired intellectual development	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0032681	encephalopathy, progressive, early-onset, with episodic rhabdomyolysis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0032684	intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	obstetrics_and_gynecology|endocrinology|genetics_and_genomics|pediatric|allergy_and_immunology	metabolic_disorder|adrenal_gland_disease	immune_disorder|bone_disorder|endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0032685	infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development	hereditary_disease	other	hereditary_disease	ophthalmology|genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	eye_disorder|endocrine_disorder|brain_disorder	true	false	false	false	high
MONDO:0032686	spermatogenic failure 35	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	endocrine_system_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0032687	intellectual developmental disorder with abnormal behavior, microcephaly, and short stature	hereditary_disease	other	hereditary_disease	endocrinology|genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	microcephaly_is_often_associated_with_other_conditions_but_primarily_falls_under_the_category_of_brain_disorder_however_microcephaly_can_be_a_symptom_of_an_endocrine_disorder_so_that_should_also_be_included__however_since_we_have_to_provide_only_best_fitting_categories_in_case_of_microcephaly__it_would_be_more_accurate_to_choose_one_between_them|endocrine_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0032688	polymicrogyria with or without vascular-type Ehlers-Danlos syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0032689	retinitis pigmentosa 85	disorder_of_visual_system|nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|metabolic_disease	ophthalmology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0032690	microcephaly, growth deficiency, seizures, and brain malformations	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|inflammatory_diseases|autoimmune_diseases|neurodegenerative_disease	brain_disorder|growth_deficiency|brain_malformations	true	false	false	false	very_high
MONDO:0032691	Galloway-Mowat syndrome 6	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease	kidney_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0032692	Galloway-Mowat syndrome 7	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0032693	Galloway-Mowat syndrome 8	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|inflammatory_disease	gastrointestinal_disorder|kidney_disorder|immune_disorder|liver_disorder	false	false	false	false	high
MONDO:0032694	microcephaly 25, primary, autosomal recessive	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	skin_disorder|brain_disorder|ear_disorder	false	false	false	false	high
MONDO:0032696	oocyte maturation defect 6	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder	reproductive_system_disorder	false	false	false	false	medium
MONDO:0032697	Houge-Janssens syndrome 3	nervous_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	immune_disorder|endocrine_disorder|skin_disorder|joint_disorder	false	false	false	false	high
MONDO:0032698	neurodevelopmental disorder with central and peripheral motor dysfunction	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0032702	Coffin-Siris syndrome 8	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	genetics_and_genomics|pediatric|neurology	inflammatory_disease|cancer|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	skeletal_system_disorder|bone_bone_marrow_disorder	false	false	false	false	high
MONDO:0032703	short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|skeletal_dysplasia_with_scoliosis_is_not_in_the_list_so_i_removed_it	bone_disorder|skeletal_dysplasia_is_not_in_the_list_so_it_will_be_excluded|spinal_disorder	false	false	false	false	medium
MONDO:0032705	neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination	hereditary_disease|metabolic_disease|nervous_system_disorder	neurodegenerative_disease|metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|neurodevelopmental_disorder	false	false	false	false	very_high
MONDO:0032706	spinocerebellar ataxia, autosomal recessive 27	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0032707	turnpenny-fry syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|cardiology|obstetrics_and_gynecology|pediatrics|neurology	metabolic_disorder|neurodegenerative_disease	vascular_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0032710	developmental and epileptic encephalopathy, 72	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	epileptic_disorder|developmental_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0032712	combined oxidative phosphorylation deficiency 38	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	metabolic_disease	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	genetics_and_genomics|pediatrics|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0032714	facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|dermatology|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|teeth_disorder|skin_disorder	false	false	false	false	high
MONDO:0032715	intellectual developmental disorder, autosomal recessive 69	hereditary_disease|psychiatric_disorder|metabolic_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	genetics_and_genomics|pediatric|neurology	mental_health_disorder|metabolic_disorder	brain_disorder|intellectual_developmental_disorder	false	false	false	false	high
MONDO:0032716	leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate	hereditary_disease	other	hereditary_disease|acute_disease	renal_medicine|hematology|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|urinary_tract_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0032717	amelogenesis imperfecta, type 3C	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|mouth_disorder|musculoskeletal_system_disorder	genetics_and_genomics|dermatology|pediatrics	metabolic_disorder|anemia	teeth_disorder|bone_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0032721	spondyloepiphyseal dysplasia, kondo-fu type	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0032723	immunodeficiency 60	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	allergy_and_immunology|immunodeficiency_is_also_somewhat_related_to_genetics_and_genomics_and_pediatric_but_the_first_one_fits_best	inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0032724	spondyloepimetaphyseal dysplasia with joint laxity, type 3	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|rheumatology	inflammatory_disease|metabolic_disorder	joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0032725	developmental and epileptic encephalopathy, 74	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	epilepsy|developmental_disorder|neurodegenerative_disease	neurological_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0032726	combined oxidative phosphorylation deficiency 39	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0032728	Charcot-Marie-Tooth disease, axonal, type 2EE	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	axonal_dysfunction|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0032729	intellectual developmental disorder, autosomal recessive 70	hereditary_disease|psychiatric_disorder|metabolic_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	genetics_and_genomics|pediatric|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0032730	leukodystrophy, hypomyelinating, 18	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	hypomyelinating|metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|brain_disorder	false	false	false	false	high
MONDO:0032732	hearing loss, autosomal recessive 113	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|otolaryngology|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder	false	false	false	false	medium
MONDO:0032733	global developmental delay, progressive ataxia, and elevated glutamine	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	true	false	false	based_on_the_information_provided__it_appears_that_you_are_referring_to_a_medical_condition_that_involves_global_developmental_delay__progressive_ataxia__and_elevated_glutamine_levels__these_symptoms_could_be_associated_with_a_variety_of_neurological_or_metabolic_disorders___while_some_conditions_causing_these_symptoms_may_have_specific_treatments_or_management_strategies__the_effectiveness_and_availability_of_those_treatments_can_vary_widely_depending_on_the_underlying_cause_of_the_symptoms___for_example__if_the_elevated_glutamine_is_due_to_a_metabolic_disorder_such_as_urea_cycle_disorders__specific_dietary_interventions_or_medications_may_be_effective__however__other_conditions_may_not_have_a_definitive_cure_and_can_only_be_managed_symptomatically___therefore__without_more_specific_information_about_the_underlying_cause_of_these_symptoms__it_is_difficult_to_definitively_state_whether_efficacious_treatments_exist___as_such__the_return_value_would_be___false	high
MONDO:0032735	cataract 48	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	general_medicine|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0032736	metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression	hereditary_disease	other	hereditary_disease	neurology|pediatric	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|muscle_disorder|metabolic_crisis	false	false	false	false	very_high
MONDO:0032737	spastic paraplegia 80, autosomal dominant	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0032738	gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy	hereditary_disease	other	hereditary_disease	urology|endocrinology|genetics_and_genomics|neurology|obstetrics_and_gynecology|ophthalmology	myopathy_is_a_subset_of_this_category_so_removing_that_one_leaves__neurodegenerative_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0032739	spermatogenic failure 36	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	anemia|metabolic_disorder	reproductive_system_disorder	false	false	false	false	high
MONDO:0032740	hearing loss, autosomal recessive 100	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|otolaryngology|pediatric	neurodegenerative_disease|metabolic_disorder	autosomal_recessive|ear_disorder	false	false	false	false	medium
MONDO:0032741	neurodevelopmental disorder with impaired speech and hyperkinetic movements	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	psychiatry|neurology|pediatric	autoimmune_diseases|neurodevelopmental_disease|mental_health_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0032744	spermatogenic failure 37	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	anemia|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0032745	developmental delay with variable intellectual impairment and behavioral abnormalities	hereditary_disease	other	hereditary_disease	psychiatry|neurology|pediatric	mental_health_disorder|neurodegenerative_disease|developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities_is_not_in_the_list__so_it_can_be_ignored	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0032746	hydatidiform mole, recurrent, 3	reproductive_system_disorder|hereditary_disease|obstetric_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|reproductive_system_disorder|cancer_or_benign_tumor|obstetric_disorder	oncology|genetics_and_genomics|obstetrics_and_gynecology	gynecological_disease___corrected_to_original_request___cancer|cancer|reproductive_system_disease	reproductive_system_disorder	false	false	false	true	medium
MONDO:0032747	hydatidiform mole, recurrent, 4	reproductive_system_disorder|hereditary_disease|obstetric_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|reproductive_system_disorder|cancer_or_benign_tumor|obstetric_disorder	hematology|oncology|genetics_and_genomics|obstetrics_and_gynecology	gestational_tumor|pregnancy_complication|malignant_placenta|malignant_disease|cancer|placental_abnormality	reproductive_system_disorder	false	false	false	true	medium
MONDO:0032748	spermatogenic failure 38	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	autoimmune_diseases|anemia|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0032749	hearing loss, autosomal recessive 94	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|otolaryngology|pediatric	neurodegenerative_disease|metabolic_disorder|autosomal_recessive	ear_disorder|autosomal_recessive_disorder_is_not_in_the_list_so_i_ll_exclude_it	false	false	false	true	medium
MONDO:0032750	arthrogryposis, distal, type 2B2	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|neurology|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	muscle_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0032751	arthrogryposis, distal, type 2B3	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0032752	developmental and epileptic encephalopathy, 75	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|developmental_disorder	encephalopathy_disorder|developmental_disorder|brain_disorder|epileptic_disorder	false	false	false	false	very_high
MONDO:0032753	spastic ataxia 9, autosomal recessive	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0032755	neurodevelopmental disorder with or without variable brain abnormalities; NEDBA	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	neurodevelopmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0032756	long QT syndrome 8	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|cardiology|pediatric	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0032757	ciliary dyskinesia, primary, 41	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	hereditary_disease|syndromic_disease|respiratory_system_disorder	genetics_and_genomics|pediatric|pulmonology	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0032758	neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|hematolog|neurology	anemia|neurodegenerative_disease|metabolic_disorder	muscle_disorder|blood_bone_marrow_disorder|brain_disorder	false	false	false	false	high
MONDO:0032759	intellectual developmental disorder with short stature and variable skeletal anomalies	hereditary_disease	other	hereditary_disease	orthopaedic|endocrinology|genetics_and_genomics|pediatric	genetic_disorder|skeletal_anomaly|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	true	medium
MONDO:0032760	developmental delay with or without dysmorphic facies and autism	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease|developmental_disorder	developmental_delay_category|brain_disorder	false	false	false	false	high
MONDO:0032761	hearing loss, autosomal recessive 114	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	genetics_and_genomics|otolaryngology|pediatric	neurodegenerative_disease|autosomal_recessive_diseases_is_not_in_the_list__however__autosomal_recessive_category_is_similar_to_hearing_loss__autosomal_recessive_and_could_be_used_as_a_synonym_______no___i_will_use_the_closest_match__neurodegenerative_disease|metabolic_disorder	hearing_loss|ear_disorder	false	false	false	false	medium
MONDO:0032762	hearing loss, autosomal recessive 115	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	genetics_and_genomics|otolaryngology|pediatric	autosomal_recessive_is_not_in_the_list_so_ignore_it|neurodegenerative_disease|metabolic_disorder	autosomal_recessive|ear_disorder	false	false	false	false	medium
MONDO:0032763	immunodeficiency 62	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	immunology|pediatric|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|immunodeficiency	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0032764	Khan-Khan-Katsanis syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|lower_gastrointestinal_disorder|kidney_disorder	false	false	false	false	high
MONDO:0032765	bleeding disorder, platelet-type, 22	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology|platelet_type_diseases_often_fall_under_this_category	platelet_type____removed__anemia|bleeding_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0032766	hypoalphalipoproteinemia, primary, 2	hereditary_disease	other	hereditary_disease	endocrinology|genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	true	low
MONDO:0032767	pheochromocytoma/paraganglioma syndrome 6	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|nervous_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	oncology|otolaryngology|neurology	cancer|neurodegenerative_disease	endocrine_disorder|brain_disorder	false	true	false	false	high
MONDO:0032768	developmental and epileptic encephalopathy, 76	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|developmental_disorder	developmental_disorder|brain_disorder|epileptic_disorder	false	false	false	false	very_high
MONDO:0032770	intellectual developmental disorder with severe speech and ambulation defects	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0032771	pheochromocytoma/paraganglioma syndrome 7	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|nervous_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|endocrine_system_disorder|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	oncology|neurology	neurocancer|cancer	endocrine_disorder|brain_disorder	false	true	false	true	high
MONDO:0032772	brain abnormalities, neurodegeneration, and dysosteosclerosis	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|orthopaedic	neurodegenerative_disease|dysosteosclerosis|brain_abnormalities	neurodegeneration|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0032773	uridine-cytidineuria	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	metabolism__implied_by_genetics__was_incorrect_so_i_removed_it|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	metabolic_disorder|urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0032774	cerebellar, ocular, craniofacial, and genital syndrome	hereditary_disease	other	hereditary_disease	psychiatry|genetics_and_genomics|neurology|pediatric	craniofacial|ocular|neurodegenerative_disease	eye_disorder|reproductive_system_disorder|brain_disorder|craniofacial	false	false	false	false	high
MONDO:0032775	neurodevelopmental disorder with seizures and speech and walking impairment	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	neurodevelopmental_disorder|brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0032776	hearing loss, autosomal recessive 99	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	genetics_and_genomics|otolaryngology|pediatric	autosomal_recessive_is_associated_with_genetic_conditions_which_can_be_a_subtype_of_metabolic_disorders___however_since_the_instruction_was_to_use_categories_from_given_list_i_m_assuming_you_want_the_category_that_best_describes_it____neurodegenerative_disease|metabolic_disorder	autosomal_recessive|ear_disorder	false	false	false	false	high
MONDO:0032777	generalized epilepsy with febrile seizures plus, type 10	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	generalized_epilepsy|brain_disorder	false	false	false	false	high
MONDO:0032778	arthrogryposis multiplex congenita 3, myogenic type	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|rheumatology|neurology|pediatric|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0032779	neurodevelopmental disorder with microcephaly and structural brain anomalies	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease|neurodevelopmental_disorder	structural_braian_anomalies____corrected_to__brain_disorder|neurodevelopmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0032780	hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	autoimmune_diseases|mental_health_disorder|neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder|brain_disorder	true	false	false	false	high
MONDO:0032781	congenital hypotonia, epilepsy, developmental delay, and digital anomalies	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	developmental_delay|neurodegenerative_disease	muscle_disorder|developmental_delay|brain_disorder	false	false	false	false	high
MONDO:0032782	immunodeficiency 63 with lymphoproliferation and autoimmunity	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|immunology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder_lymphatic_disorder	true	false	false	true	high
MONDO:0032783	aortic valve disease 3	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiothoracic|cardiology	autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0032784	neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0032785	polydactyly, postaxial, type a10	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics	congenital_abnormality|skeletal_dysplasia|developmental_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0032786	Noonan syndrome 11	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease|immune_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	immune_system_disorder|cardiovascular_disorder|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	cardiovascular_disorder|mental_health_disorder|metabolic_disorder	joint_disorder|heart_disorder	false	false	false	false	medium
MONDO:0032787	holoprosencephaly 12 with or without pancreatic agenesis	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|nervous_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0032788	cerebellar atrophy with seizures and variable developmental delay	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	developmental_delays_are_generally_associated_with_brain_disorders__but_since_the_question_asks_for_categories_related_to_the_given_disease__we_ll_only_consider_the_presence_of_seizures_which_is_more_specifically_related_to_brain_disorder_than_spinal|brain_disorder|spinal_disorder	true	false	false	false	high
MONDO:0032789	intellectual developmental disorder, autosomal recessive 71	hereditary_disease|psychiatric_disorder|nervous_system_disorder|metabolic_disease	psychiatric_disorder|metabolic_disease	psychiatric_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	mental_disorder_is_not_in_the_list_so_it_will_be_removed|brain_disorder	false	false	false	false	high
MONDO:0032790	neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	neurodevelopmental_disorder|skeletal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0032791	Coffin-Siris syndrome 10	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	vascular_disorder|bone_disorder|joint_disorder|blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	high
MONDO:0032792	neuropathy, hereditary motor and sensory, type VIc, with optic atrophy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|ophthalmology	hereditary_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0032793	O'Donnell-Luria-Rodan syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|ear_disorder|urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0032794	Leber congenital amaurosis 19	hereditary_disease|disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0032795	intellectual developmental disorder 59	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatry|neurology|pediatric	intellectual_developmental_disorders_are_not_in_the_list_so_i_will_use__mental_health_disorder|neurodegenerative_disease|mental_health_disorder	intellectual_developmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0032796	hyper-IgE recurrent infection syndrome 4, autosomal recessive	hereditary_disease|hematologic_disorder|immune_system_disorder	other	hematologic_disorder|immune_system_disorder|hereditary_disease	genetics_and_genomics|immunology|pediatric	autoimmune_diseases|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	true	false	false	false	high
MONDO:0032797	myopathy, congenital, with tremor	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology	congenital_disease|neurodegenerative_disease	muscle_disorder|congenital_disease	false	false	false	false	high
MONDO:0032798	ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|skin_disorder	false	false	false	false	high
MONDO:0032799	mitochondrial DNA depletion syndrome 16 (hepatic type)	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	metabolic_disease	mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|hepatology	inflammatory_disease|hepatic_type_suggests_a_liver_involvement_so_also__adrenal_gland_disease_is_less_likely_and_i_will_leave_it_out__metabolic_disorder|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0032800	robinow syndrome, autosomal recessive 2	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0032801	erythrokeratodermia variabilis et progressiva 6	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0032802	hearing loss, autosomal dominant 37	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|neurology|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant_disorders	ear_disorder	false	false	false	false	high
MONDO:0032803	immunodeficiency 64	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	allergy_and_immunology|genetics_and_genomics|immunology|pediatric	immunodeficiency|inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	true	very_high
MONDO:0032804	ectodermal dysplasia 15, hypohidrotic/hair type	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	syndromic_disease|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	ear_disorder|teeth_disorder|skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0032805	hypopigmentation, organomegaly, and delayed myelination and development	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	skin_disorder|brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0032806	trichothiodystrophy 7, nonphotosensitive	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	syndromic_disease|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	skin_disorder|hair_disorder____note__i_assume__hair_disorder__is_implied_as_it_is_a_relevant_category_for_trichothiodystrophy__which_affects_the_structure_of_hair	false	false	false	false	medium
MONDO:0032807	neurodevelopmental disorder with visual defects and brain anomalies	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|brain_anomalies	brain_disorder|eye_disorder	true	false	false	false	high
MONDO:0032808	developmental and epileptic encephalopathy, 77	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	inflammatory_disease|epileptic_disease|neurodegenerative_disease|developmental_disease	spinal_disorder|developmental_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0032810	oocyte maturation defect 7	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics	genetic_disorder|metabolic_disorder	reproductive_system_disorder|ovarian_disorder	false	false	false	false	high
MONDO:0032811	night blindness, congenital stationary, type1i	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|genetics_and_genomics|ophthalmology	neurodegenerative_disease|congenital_stationary_night_blindness_is_a_rare_genetic_disorder_affecting_the_retina__also_known_as_cone_monochromacy_or_congenital_stationary_night_blindness_type_1	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0032812	developmental and epileptic encephalopathy, 78	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	developmental_disorder|neurodegenerative_disease	developmental_and_epileptic_encephalopathy_is_more_specifically_classified_under_a_broader_category__brain_disorder|spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0032813	developmental and epileptic encephalopathy, 79	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	epileptic_disease|neurodegenerative_disease|developmental_disease|encephalopathy	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0032814	microangiopathy and leukoencephalopathy, pontine, autosomal dominant	nervous_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|hereditary_disease|cardiovascular_disorder	neurology|hematology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0032815	mitochondrial DNA depletion syndrome 17	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|mitochondrial_disease	false	false	false	false	very_high
MONDO:0032816	neurodevelopmental disorder with ataxia, hypotonia, and microcephaly	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|neurodevelopmental_disorder|metabolic_disorder	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0032817	neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|endocrine_disorder|eye_disorder	false	false	false	false	high
MONDO:0032818	neurodevelopmental disorder with cerebellar hypoplasia and spasticity	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0032819	hypothyroidism, congenital, nongoitrous, 7	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	congenital_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0032820	neurodevelopmental disorder with structural brain anomalies and dysmorphic facies	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	neurodevelopmental_disorder|structural_brain_anomalies|brain_disorder	false	false	false	false	high
MONDO:0032821	myopathy, congenital, progressive, with scoliosis	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics|pediatric|orthopaedic	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0032822	developmental and epileptic encephalopathy, 80	nervous_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|epileptic_encephalopathy|developmental_disorder	epileptic_disorder|developmental_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0032823	intellectual developmental disorder 60 with seizures	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	seizures_is_closely_related_to_another_category__brain_disorder|brain_disorder	false	false	false	false	high
MONDO:0032824	glycosylphosphatidylinositol biosynthesis defect 21	hereditary_disease	other	hereditary_disease	genetic_and_genomics|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0032826	nephrotic syndrome, type 21	urinary_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease|urinary_system_disorder	renal_medicine|pediatric|nephrology	renal_disease|genetic_disorder|metabolic_disorder	kidney_disorder|immune_disorder	false	false	false	true	high
MONDO:0032828	spastic tetraplegia and axial hypotonia, progressive	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0032829	neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease|mental_health_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0032830	snijders blok-fisher syndrome	hereditary_disease	other	hereditary_disease	rheumatology|otolaryngology|dermatology	autoimmune_diseases|inflammatory_disease	liver_disorder|joint_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0032831	pontocerebellar hypoplasia, type 13	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0032832	intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	nose_disorder|brain_disorder|skeletal_disorder	false	false	false	false	high
MONDO:0032833	lower urinary tract obstruction, congenital	hereditary_disease	other	hereditary_disease	urology|pediatric	congenital_anomalies|urological_disorders	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0032834	retinitis pigmentosa 86	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system|metabolic_disease	psychiatric_disorder|metabolic_disease	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|psychiatric_disorder|disorder_of_orbital_region|metabolic_disease	genetics_and_genomics|ophthalmology	retinitis_pigmentosa_is_sometimes_associated_with_other_diseases_that_have_a_genetic_basis_such_as_neurodegenerative_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0032835	spondyloepiphyseal dysplasia, nishimura type	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic	genetic_disease|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0032836	Weiss-Kruszka syndrome	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0032837	abdominal obesity-metabolic syndrome 4	nutritional_disorder|hereditary_disease|syndromic_disease|metabolic_disease	metabolic_disease	hereditary_disease|syndromic_disease|metabolic_disease|nutritional_disorder	gastroenterology|endocrinology	cardiovascular_disorder|metabolic_disorder	metabolic_disorder|upper_gastrointestinal_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0032838	neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	structural_anomalies_disorder|joint_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0032839	noonan syndrome 12	cardiovascular_disorder|immune_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|cardiovascular_disorder|musculoskeletal_system_disorder|immune_system_disorder	neurology|obstetrics_and_gynecology|genetics_and_genomics|pediatric|cardiology	cardiovascular_disorder|metabolic_disorder	lymphatic_disorder|vascular_disorder|joint_disorder|heart_disorder	false	false	false	false	medium
MONDO:0032841	Usher syndrome, type 1M	hereditary_disease	other	hereditary_disease	otolaryngology|genetics_and_genomics|ophthalmology|pediatric	neurodegenerative_disease|metabolic_disorder	ear_disorder|eye_disorder|genetic_disorder	false	false	false	false	high
MONDO:0032842	Siddiqi syndrome	hereditary_disease	other	hereditary_disease	neurology|pediatric	autoimmune_diseases|inflammatory_disease|mental_health_disorder|neurodegenerative_disease	immune_disorder|kidney_disorder|liver_disorder|blood_bone_marrow_disorder|lower_gastrointestinal_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0032843	oculopharyngeal myopathy with leukoencephalopathy 1	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	muscle_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0032844	infantile liver failure syndrome 3	endocrine_system_disorder|digestive_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|digestive_system_disorder	gastroenterology|hepatology|genetics_and_genomics|pediatric	infants_disease|metabolic_disorder	liver_disorder|lower_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0032845	spermatogenic failure 39	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|anemia|cancer|metabolic_disorder	muscle_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0032846	osteogenesis imperfecta, type 20	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	rheumatology|genetics_and_genomics|pediatric|orthopaedic	genetic_disorder|metabolic_disorder	spinal_disorder|bone_disorder|teeth_disorder|joint_disorder	false	false	false	false	high
MONDO:0032848	immunodeficiency 65, susceptibility to viral infections	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	allergy_and_immunology|genetics_and_genomics|immunology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0032849	neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|neurodevelopmental_disorder|optic_atrophy_seizures|structural_brain_anomalies	muscle_disorder|spinal_disorder|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0032850	neurooculocardiogenitourinary syndrome	hereditary_disease	other	hereditary_disease	neurology|urology|cardiology	autoimmune_diseases|neurodegenerative_disease|cardiovascular_disorder|neurooculocardiogenitourinary_syndrome_suggests_a_disorder_affecting_the_nerves__eyes__heart__and_urinary_system__so_it_fits_with_categories_related_to_the_nervous_system|metabolic_disorder	heart_disorder|kidney_disorder|urinary_tract_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0032851	intellectual developmental disorder with impaired language and dysmorphic facies	hereditary_disease	other	hereditary_disease	neurology|psychiatry|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	brain_disorder|intellectual_developmental_disorder	false	false	false	false	medium
MONDO:0032852	myopathy, congenital, with structured cores and z-line abnormalities	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	neurology|genetics_and_genomics|pediatric	congenital_myopathies|neurodegenerative_disease	muscle_disorder|congenital_disorder	false	false	false	true	high
MONDO:0032853	myopathy, distal, 6, adult-onset, autosomal dominant	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant_disorder_is_not_in_the_list_so_it_can_be_ignored	muscle_disorder|lower_skeletal_muscle_disorder|skeletal_muscle_disorder	false	false	false	false	medium
MONDO:0032854	Zimmermann-Laband syndrome 3	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0032855	neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|psychiatry|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder|brain_disorder	false	false	false	true	high
MONDO:0032857	diarrhea 11, malabsorptive, congenital	digestive_system_disorder|hereditary_disease	other	hereditary_disease|digestive_system_disorder	gastroenterology|malabsorptive_conditions_often_cause_diarrhea|pediatric	inflammatory_disease|malabsorptive|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0032858	developmental and epileptic encephalopathy, 81	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	developmental_disorder|inflammatory_disease|neurodegenerative_disease|epileptic_disorder	epileptic_disorder|developmental_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0032859	spermatogenic failure 40	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|pediatric	anemia|metabolic_disorder	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0032860	intellectual developmental disorder, autosomal recessive 72	metabolic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder|metabolic_disease	nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	psychiatry|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	brain_disorder|intellectual_developmental_disorder	false	false	false	false	high
MONDO:0032862	hydrocephalus, congenital communicating, 1	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	congenital_condition|inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0032863	spermatogenic failure 41	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	hormonal_disorder|metabolic_disorder|reproductive_system_disease	male_reproductive_disorder|reproductive_system_disorder|infertility_disorder|spermatic_cord_disorder	false	false	false	false	high
MONDO:0032864	intellectual developmental disorder with speech delay, autism, and dysmorphic facies	hereditary_disease	other	hereditary_disease	neurology|psychiatry|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	brain_disorder|intellectual_developmental_disorder	false	false	false	false	high
MONDO:0032865	pulmonary fibrosis and/or bone marrow failure, telomere-related, 5	premature_aging_syndrome|respiratory_system_disorder|hereditary_disease	other	premature_aging_syndrome|hereditary_disease|respiratory_system_disorder	pulmonology|hematology|genetics_and_genomics	telomere_related_diseases_category_is_not_present_in_the_list_but_closest_match_is_metabolic_disorder|bone_marrow_failure|anemia	lung_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0032866	cortical dysplasia, complex, with other brain malformations 10	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|other_brain_malformations	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0032867	pancreatic cancer, susceptibility to, 5	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	gastroenterology|oncology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0032868	lessel-kubisch syndrome	hereditary_disease	other	hereditary_disease	pediatric|endocrinology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	liver_disorder	false	false	false	false	medium
MONDO:0032869	mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6	metabolic_disease|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	neurology|pediatrics|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|mitochondrial_complex_5__atp_synthase__deficiency__nuclear_type_6_can_be_associated_with_other_disorders	false	false	false	false	high
MONDO:0032870	intellectual developmental disorder with short stature and behavioral abnormalities	hereditary_disease	other	hereditary_disease	pediatric|neurology|endocrinology|genetics_and_genomics	metabolic_disorder|mental_health_disorder	brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0032871	leukodystrophy, hypomyelinating, 19, transient infantile	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|brain_disorder	false	false	false	false	high
MONDO:0032872	ciliary dyskinesia, primary, 42	respiratory_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|respiratory_system_disorder	neurology|pulmonology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	lung_disorder|eye_disorder	false	false	false	false	high
MONDO:0032873	retinitis pigmentosa 87 with choroidal involvement	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	metabolic_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease	vascular_disorder|eye_disorder	false	false	false	false	high
MONDO:0032874	ciliary dyskinesia, primary, 43	respiratory_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|respiratory_system_disorder	pediatric|pulmonology	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|respiratory_disorder_is_not_an_option_so_i_will_leave_out_lung_disorder|eye_disorder	false	false	false	false	high
MONDO:0032875	short stature and microcephaly with genital anomalies	hereditary_disease	other	hereditary_disease	pediatric|endocrinology|genetics_and_genomics	metabolic_disorder|genetic_disorders	reproductive_system_disorder|bone_disorder|brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0032876	neurodevelopmental disorder with absent language and variable seizures	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|neurodevelopmental_disorder	false	false	false	true	very_high
MONDO:0032877	neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0032878	neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0032879	megabladder, congenital	hereditary_disease	other	hereditary_disease	pediatric|urology|genetics_and_genomics	adrenal_gland_disease|congenital_anomaly	kidney_disorder|urinary_tract_disorder	false	false	false	false	none
MONDO:0032880	developmental and epileptic encephalopathy, 82	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|developmental_disorder	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0032881	premature ovarian failure 16	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrinology|obstetrics_and_gynecology	metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0032882	Heyn-Sproul-Jackson syndrome	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0032883	intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	craniofacial_dysmorphism|brain_disorder|seizure_disorder	false	false	false	false	high
MONDO:0032884	ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|mental_health_disorder	skin_disorder|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0032885	spondyloepimetaphyseal dysplasia, Isidor-Toutain type	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0032886	Liang-Wang syndrome	hereditary_disease	other	hereditary_disease	pediatric|neurology	neurodegenerative_disease|mental_health_disorder	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0032887	neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0032888	neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0032889	Poirier-Bienvenu neurodevelopmental syndrome	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0032890	neuromuscular disease and ocular or auditory anomalies with or without seizures	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|ocular_and_auditory_anomalies_seizures|autoimmune_diseases	ear_disorder|muscle_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0032891	aneurysm, intracranial berry, 12	cardiovascular_disorder|hereditary_disease|nervous_system_disorder	cardiovascular_disorder	nervous_system_disorder|hereditary_disease|cardiovascular_disorder	neurology|cardiovascular	neurodegenerative_disease|cardiovascular_disorder	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0032892	structural brain anomalies with impaired intellectual development and craniosynostosis	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|structural_abnormality	brain_disorder|structural_braın_anomalies	false	false	false	false	high
MONDO:0032893	pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|dysmorphic_facies|pachygyria|developmental_delay|seizures|microcephaly	microcephaly|seizures|pachygyria|brain_disorder|dysmorphic_facies|developmental_delay	false	false	false	false	very_high
MONDO:0032894	neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0032895	developmental and epileptic encephalopathy, 83	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	epileptic_encephalopathy|neurodegenerative_disease|developmental_disorder	developmental_disorder|brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0032896	spermatogenic failure 42	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	metabolic_disorder|anemia	reproductive_system_disorder|endoctrine_disorder	false	false	false	false	high
MONDO:0032897	intellectual developmental disorder with hypotonia and behavioral abnormalities	hereditary_disease	other	hereditary_disease	neurology|psychiatry|pediatric	metabolic_disorder|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0032898	spermatogenic failure 43	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|cancer	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0032899	neutropenia, severe congenital, 8, autosomal dominant	immune_system_disorder|hematologic_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder|hematologic_disorder	hematology|immunology|oncology|genetics_and_genomics|pediatric	metabolic_disorder|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0032900	neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|psychiatry|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|neurodevelopmental_disorder|muscle_disorder	false	false	false	true	high
MONDO:0032901	Catifa syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	bone_disorder|joint_disorder|immune_disorder|spinal_disorder|muscle_disorder	false	false	false	false	none
MONDO:0032902	Joubert syndrome 36	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	anemia|neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder|eye_disorder	false	false	false	false	high
MONDO:0032903	arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|joint_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0032904	corneal dystrophy, Meesmann, 2	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	medium
MONDO:0032905	spastic paraplegia 81, autosomal recessive	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0032906	spastic paraplegia 82, autosomal recessive	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0032907	lymphatic malformation 8	cardiovascular_disorder|immune_system_disorder|hereditary_disease	cardiovascular_disorder	immune_system_disorder|cardiovascular_disorder|hereditary_disease	hematology|oncology|pediatric	lymphatic_disorder|vascular_anomaly|genetic_disorder|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0032908	CEBALID syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0032909	mitochondrial complex III deficiency, nuclear type 10	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatrics	neurodegenerative_disease|metabolic_disorder	heart_disorder|mitochondrial_disease|muscle_disorder	false	false	false	true	high
MONDO:0032910	mitochondrial complex I deficiency, nuclear type 34	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	pediatric|neurology|genetics_and_genomics|other____i_ve_corrected_it_to_remove__other	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0032911	hearing loss, autosomal dominant 75	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	ear_disorder	false	false	false	false	high
MONDO:0032912	Coffin-Siris syndrome 11	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|oncology	metabolic_disorder|neurodegenerative_disease	bone_disorder|muscle_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0032913	congenital heart defects, multiple types, 7	hereditary_disease	other	hereditary_disease	pediatric|cardiology	metabolic_disorder|cardiovascular_disorder	blood_bone_marrow_disorder|heart_disorder	false	false	false	true	high
MONDO:0032914	ciliary dyskinesia, primary, 44	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	syndromic_disease|hereditary_disease|respiratory_system_disorder	neurology|genetics_and_genomics|pulmonology	metabolic_disorder|neurodegenerative_disease	lung_disorder|eye_disorder	false	false	false	false	high
MONDO:0032915	long QT syndrome 16	hereditary_disease|cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	syndromic_disease|hereditary_disease|cardiovascular_disorder	pediatric|cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0032916	Imagawa-Matsumoto syndrome	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|adrenal_gland_disease|inflammatory_disease	liver_disorder|immune_disorder	false	false	false	false	high
MONDO:0032917	hearing loss, autosomal dominant 76	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|auditory_system_disorder|hereditary_disease|nervous_system_disorder	otolaryngology|genetics_and_genomics	neurodegenerative_disease|autosomal_dominant_disorders_is_not_in_the_list_so_removing_that_part__neurodegenerative_disease	bone_disorder|neurological_disorder|genetic_disorder|ear_disorder	false	false	false	false	medium
MONDO:0032918	developmental and epileptic encephalopathy, 84	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	developmental_disorder|epilepsy|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0032919	intellectual developmental disorder 62	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	intellectual_disorder_is_not_in_the_list_so_i_will_use_brain_disorder|brain_disorder	false	false	false	false	high
MONDO:0032920	juvenile arthritis due to defect in LACC1	hereditary_disease	other	hereditary_disease	rheumatology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease	bone_disorder|immune_disorder|joint_disorder	false	false	false	true	high
MONDO:0032921	neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0032922	Beck-Fahrner syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|endocrinology|pediatrics	metabolic_disorder|autoimmune_diseases|anemia	liver_disorder|kidney_disorder|bone_disorder|eye_disorder	false	false	false	false	medium
MONDO:0032923	spinocerebellar ataxia, autosomal recessive 28	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0032924	ciliary dyskinesia, primary, 45	syndromic_disease|respiratory_system_disorder|hereditary_disease	other	syndromic_disease|hereditary_disease|respiratory_system_disorder	pediatric|neurology|pulmonology	metabolic_disorder|neurodegenerative_disease	lung_disorder|eye_disorder	false	false	false	false	high
MONDO:0032925	respiratory papillomatosis, juvenile recurrent, congenital	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|pulmonology	autoimmune_diseases|cancer|inflammatory_disease	throat_disorder|lung_disorder	true	false	false	true	high
MONDO:0032926	sandestig-stefanova syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|kidney_disorder|immune_disorder	false	false	false	false	medium
MONDO:0032927	triokinase and FMN cyclase deficiency syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0032928	T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant	hereditary_disease	other	hereditary_disease	pediatric|allergy_and_immunology|genetics_and_genomics|hematology	autoimmune_diseases|anemia	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0032930	intellectual developmental disorder with poor growth and with or without seizures or ataxia	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|endocrine_disorder|intellectual_developmental_disorder_is_not_in_the_list_so_none	false	false	false	false	high
MONDO:0032931	pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal	hereditary_disease	other	hereditary_disease	neurology|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|lung_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0032932	mitochondrial DNA depletion syndrome 18	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0032933	chromosome 1p36.33 duplication syndrome, atad3 gene cluster, autosomal dominant	hereditary_disease|chromosomal_disorder	other	chromosomal_disorder|hereditary_disease	neurology|genetics_and_genomics|psychiatry|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	immune_disorder|lymphatic_disorder|kidney_disorder|muscle_disorder|brain_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|eye_disorder|joint_disorder|heart_disorder	false	false	false	false	high
MONDO:0032934	genitourinary and/or brain malformation syndrome	hereditary_disease	other	hereditary_disease	urology|neurology|genetics_and_genomics	brain_malformation_syndrome__closest_match_is_not_explicitly_listed____corrected__neurodegenerative_disease|genitourinary_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0032935	rhizomelic limb shortening with dysmorphic features	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0032936	myopathy, congenital, with respiratory insufficiency and bone fractures	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|orthopaedic|pulmonology|pediatric	metabolic_disorder|neurodegenerative_disease|congenital_myopathies_can_be_caused_by_mutations_in_genes_involved_in_energy_production__which_links_to_both_neurodegenerative_disease_and_metabolic_disorder	bone_disorder|muscle_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0032937	myopathy, congenital proximal, with minicore lesions	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	congenital_disorder|muscle_disorder|myopathy_disorder	false	false	false	false	high
MONDO:0032938	basal ganglia calcification, idiopathic, 8, autosomal recessive	hereditary_disease|nervous_system_disorder	other	idiopathic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autosomal_recessive_diseases	vascular_disorder|brain_disorder	false	false	false	false	medium
MONDO:0032939	intellectual developmental disorder, autosomal dominant 63, with macrocephaly	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	intellectual_developmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0032940	retinitis pigmentosa 88	hereditary_disease|psychiatric_disorder|metabolic_disease|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder|metabolic_disease	metabolic_disease|disorder_of_visual_system|psychiatric_disorder|hereditary_disease|disorder_of_orbital_region|nervous_system_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0032941	myopia 27	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	neurology|ophthalmology|pediatric	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	true	medium
MONDO:0032942	neurodevelopmental disorder with microcephaly and dysmorphic facies	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	microcephaly|brain_disorder	false	false	false	true	very_high
MONDO:0032943	neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|endocrinology|pediatric	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease|endocrine_anomalies	brain_disorder|endocrine_disorder|heart_disorder	false	false	false	false	high
MONDO:0033004	polycystic kidney disease 4	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	genetics_and_genomics|renal_medicine|endocrinology	kidney_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0033005	Galloway-Mowat syndrome 1	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	liver_disorder|kidney_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0033006	Galloway-Mowat syndrome 2, X-linked	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0033007	Galloway-Mowat syndrome 3	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0033008	Galloway-Mowat syndrome 4	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0033009	Galloway-Mowat syndrome 5	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0033010	erythrokeratodermia variabilis et progressiva 1	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	hematology|genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0033012	erythrokeratodermia variabilis et progressiva 2	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	hematology|genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0033013	erythrokeratodermia variabilis et progressiva 3	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	hematatology|rheumatology|genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0033014	erythrokeratodermia variabilis et progressiva 4	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	hematology|genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0033015	erythrokeratodermia variabilis et progressiva 5	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology	inflammatory_disease|anemia|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0033043	spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0033044	Meckel syndrome 13	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	genetic_disorder_is_not_in_the_list_so___metabolic_disorder|metabolic_disorder|cardiovascular_disorder	lower_gastrointestinal_disorder|liver_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0033045	orofaciodigital syndrome 16	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	oral_disorder|bone_disorder|digit_disorder|teeth_disorder|face_disorder	false	false	false	false	high
MONDO:0033046	Meier-Gorlin syndrome 8	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics	genetic_disorders|metabolic_disorder	skeletal_disorder|bone_disorder	false	false	false	false	high
MONDO:0033047	Perrault syndrome 6	endocrine_system_disorder|metabolic_disease|hereditary_disease|mitochondrial_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease|endocrine_system_disorder	reproductive_system_disorder|mitochondrial_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0033091	ichthyosis, congenital, autosomal recessive 14	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	skin_disorder|congenital_disorder	false	false	false	false	medium
MONDO:0033092	ichthyosis, congenital, autosomal recessive 13	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases	skin_disorder|congenital	false	false	false	false	medium
MONDO:0033115	spinocerebellar ataxia, autosomal recessive 25	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0033116	spinocerebellar ataxia, autosomal recessive 26	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0033123	exudative vitreoretinopathy 7	disorder_of_visual_system|hereditary_disease|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	ophthalmology	inflammatory_disease|cancer|autoimmune_diseases	eye_disorder|vitreoretinopathy_is_a_type_of_eye_disorder	false	false	false	false	high
MONDO:0033135	Charcot-Marie-Tooth disease, demyelinating, type 1G	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	hereditary|neurology|genetics_and_genomics|genetic	demyelinating|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder|nerve_disorder	false	false	false	false	medium
MONDO:0033169	curariform drugs toxicity	poisoning	other	poisoning	pulmonology|neurology	inflammatory_disease|neurodegenerative_disease	muscle_disorder|neuromuscular_disorder	false	false	false	false	high
MONDO:0033170	statin toxicity	poisoning	other	poisoning	hepatology|gastroenterology|cardiology	metabolic_disorder|cardiovascular_disorder	liver_disorder|muscle_disorder	false	false	false	false	low
MONDO:0033181	phenytoin or carbamazepine toxicity	poisoning	other	poisoning	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	liver_disorder|brain_disorder	false	false	false	false	high
MONDO:0033198	hearing loss, autosomal recessive 106	psychiatric_disorder|nervous_system_disorder|hereditary_disease|auditory_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	autosomal_recessive|ear_disorder	false	false	false	false	low
MONDO:0033199	hearing loss, autosomal recessive 107	psychiatric_disorder|nervous_system_disorder|hereditary_disease|auditory_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder|auditory_system_disorder	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|neurodegenerative_disease	hearing_loss|ear_disorder	false	false	false	false	medium
MONDO:0033200	hearing loss, autosomal recessive 108	nervous_system_disorder|auditory_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder|autosomal_recessive	false	false	false	true	high
MONDO:0033201	hearing loss, autosomal recessive 57	nervous_system_disorder|auditory_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder|bone_disorder|hearing_loss	false	false	false	true	medium
MONDO:0033202	hearing loss, autosomal recessive 109	nervous_system_disorder|auditory_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	false	medium
MONDO:0033203	nephrotic syndrome 14	syndromic_disease|hereditary_disease|urinary_system_disorder|metabolic_disease	metabolic_disease	metabolic_disease|urinary_system_disorder|syndromic_disease|hereditary_disease	nephrology|renal_medicine	metabolic_disorder|autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	true	high
MONDO:0033204	ciliary dyskinesia, primary, 37	syndromic_disease|hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pulmonology	metabolic_disorder|ciliary_dyskinesia_is_not_directly_listed_so_it_would_be_best_fitting_in_a_metabolic_disorder_but_it_can_also_be_related_to_neurodegenerative_disease__since_primary_ciliary_dyskinesia_has_been_linked_with_some_neurological_features|neurodegenerative_disease	lung_disorder|eye_disorder|respiratory_disorder___corrected_list_to_match_the_requested_format___eye_disorder	false	false	false	false	medium
MONDO:0033258	hearing loss, autosomal dominant 71	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	genetics_and_genomics|pediatric|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder|bone_disorder	false	false	false	false	medium
MONDO:0033259	hearing loss, autosomal dominant 72	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	genetics_and_genomics|neurology|pediatric|otolaryngology	autosomal_dominant_disorder|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0033260	hearing loss, autosomal dominant 73	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	genetics_and_genomics|pediatric|otolaryngology	autosomal_dominant_is_a_genetic_disorder_category_but_none_of_the_provided_categories_explicitly_mention__genetic__so_the_best_fit_remains_neurodegenerative_disease|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0033261	hearing loss, autosomal dominant 34, with or without inflammation	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder|auditory_system_disorder	neurology|genetics_and_genomics|otolaryngology	autosomal_dominant_genetic_disorder|neurodegenerative_disease|inflammatory_disease	ear_disorder|bone_disorder	false	false	false	false	medium
MONDO:0033262	nephrotic syndrome 15	syndromic_disease|hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease|syndromic_disease	nephrology__not_listed__so_ignore|renal_medicine|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0033280	nephrotic syndrome 16	syndromic_disease|urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|syndromic_disease|hereditary_disease	pediatric|renal_medicine	autoimmune_diseases|metabolic_disorder|inflammatory_disease	kidney_disorder|urinary_tract_disorder|immune_disorder	false	false	false	false	medium
MONDO:0033281	polycystic kidney disease 5	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	urology|renal_medicine|genetics_and_genomics	kidney_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0033282	multiple mitochondrial dysfunctions syndrome 5	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|cardiovascular_disorder	mitochondrial_disease____note__mitochondrial_disease_is_a_broader_category_that_encompasses_multiple_mitochondrial_dysfunction_syndromes|muscle_disorder	false	false	false	false	high
MONDO:0033304	nonsyndromic deafness, Y-linked	hereditary_disease|nervous_system_disorder|psychiatric_disorder|auditory_system_disorder	psychiatric_disorder	hereditary_disease|auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	otolaryngology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0033308	Joubert syndrome 30	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0033309	Joubert syndrome 32	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	false	medium
MONDO:0033310	Joubert syndrome 31	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics|psychiatry	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	kidney_disorder|spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0033311	Joubert syndrome 33	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0033312	schizophrenia 19	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0033352	neuropathy, congenital hypomelinating	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0033361	developmental and epileptic encephalopathy, 52	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	epileptic_disorder|brain_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0033362	developmental and epileptic encephalopathy, 53	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|epileptic_disorder|developmental_disorder	epileptic_disorder|brain_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0033363	developmental and epileptic encephalopathy, 54	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	epilepsy|neurodegenerative_disease|developmental_disorder	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0033364	developmental and epileptic encephalopathy, 55	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|developmental_and_epileptic_encephalopathy_is_a_condition_of_the_brain_therefore_it_can_be_classified_as_neurodegenerative_disease	epileptic_disorder|brain_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0033365	developmental and epileptic encephalopathy, 56	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|developmental_disorder	epileptic_disorder|brain_disorder|developmental_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0033366	developmental and epileptic encephalopathy, 57	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|developmental_disorder	epileptic_disorder|brain_disorder|developmental_disorder|encephalopathy	false	false	false	true	very_high
MONDO:0033367	developmental and epileptic encephalopathy, 58	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|developmental_disorder	epileptic_disorder|brain_disorder|developmental_disorder|neurological_disorder	false	false	false	true	very_high
MONDO:0033368	developmental and epileptic encephalopathy, 59	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|developmental_disorder	epileptic_disorder|brain_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0033369	developmental and epileptic encephalopathy, 60	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|developmental_disorder	epileptic_disorder|brain_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0033370	developmental and epileptic encephalopathy, 61	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|developmental_and_epileptic_encephalopathy	developmental_and_epileptic_encephalopathy|brain_disorder	false	false	false	true	very_high
MONDO:0033371	developmental and epileptic encephalopathy, 62	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	developmental_disorder|neurodegenerative_disease|epileptic_disorder	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0033372	developmental and epileptic encephalopathy, 63	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	developmental_disorder|neurodegenerative_disease|epileptic_disorder	epileptic_disorder|brain_disorder|developmental_disorder	false	false	false	true	very_high
MONDO:0033373	developmental and epileptic encephalopathy, 64	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	developmental_disorder|neurodegenerative_disease|epileptic_disease	epileptic_disorder|brain_disorder|developmental_disorder|neurological_disorder	false	false	false	true	very_high
MONDO:0033374	developmental and epileptic encephalopathy, 65	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	developmental_disorder|epilepsy|neurodegenerative_disease	epileptic_disorder|brain_disorder|developmental_disorder|neurological_disorder	false	false	false	true	very_high
MONDO:0033375	orofaciodigital syndrome 17	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder|ear_disorder|teeth_disorder	false	false	false	false	high
MONDO:0033479	spinocerebellar ataxia 44	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0033480	spinocerebellar ataxia 45	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0033481	spinocerebellar ataxia 46	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|inflammatory_disease|cardiovascular_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0033482	spinocerebellar ataxia 47	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0033483	erythrocytosis, familial, 5	hereditary_disease|immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	other	hereditary_disease|hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|blood_disorder|hereditary_disorder|hematological_disorder	false	false	false	false	medium
MONDO:0033485	short-rib thoracic dysplasia 19 with or without polydactyly	respiratory_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|urinary_system_disorder	other	hereditary_disease|syndromic_disease|respiratory_system_disorder|urinary_system_disorder|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0033486	leukodystrophy, hypomyelinating, 14	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0033492	Coffin-Siris syndrome 6	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0033493	fibromatosis, gingival, 5	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|mouth_disorder	orthopaedic|rheumatology|genetics_and_genomics|dermatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|cancer	bone_disorder|joint_disorder	false	false	false	false	low
MONDO:0033532	Suleiman-El-Hattab syndrome	hereditary_disease	other	hereditary_disease	pediatrics|neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0033533	combined oxidative phosphorylation deficiency 45	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	kidney_disorder|liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0033534	combined oxidative phosphorylation deficiency 46	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatrics|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0033537	combined oxidative phosphorylation deficiency 47	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	pediatrics|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0033541	immunodeficiency 69	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|pediatric|immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0033542	immunodeficiency 70	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|immunodeficiency|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0033543	cone-rod synaptic disorder syndrome, congenital nonprogressive	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	true	high
MONDO:0033544	Tolchin-Le Caignec syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	liver_disorder	false	false	false	false	medium
MONDO:0033545	mitochondrial DNA depletion syndrome 19	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	mitochondrial_disease|muscle_disorder	false	false	false	false	very_high
MONDO:0033546	neurodegeneration, infantile-onset, biotin-responsive	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0033547	Li-Ghorbani-Weisz-Hubshman syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	as_of_october_2023__there_are_no_known_specific_treatments_that_cure__prevent__or_effectively_treat_li_ghorbani_weisz_hubshman_syndrome__this_condition_is_a_rare_genetic_disorder__and_management_typically_focuses_on_symptomatic_treatment_and_supportive_care_rather_than_a_definitive_cure__therefore__the_answer_is_false	low
MONDO:0033548	myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	inflammatory_disease|respiratory_disease|genetic_disorder|congenital_disorder|neurodegenerative_disease|metabolic_disorder	congenital_disorder|respiratory_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0033549	optic atrophy 12	hereditary_disease|disorder_of_visual_system|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease|disorder_of_visual_system	neurology|ophthalmology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0033551	immunodeficiency 72 with autoinflammation	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|genetics_and_genomics|rheumatology|immunology	autoimmune_diseases|inflammatory_disease|immunodeficiency_72_with_autoinflammation	immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0033554	immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|hematology|immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0033555	immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|genetics_and_genomics|hematology|rheumatology|pediatric|immunology	autoimmune_diseases|inflammatory_disease|immunodeficiency	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0033556	muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0033557	hemophagocytic lymphohistiocytosis, familial, 6	immune_system_disorder|syndromic_disease|hereditary_disease	other	immune_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|hematology	metabolic_disorder|autoimmune_diseases|inflammatory_disease|anemia	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	very_high
MONDO:0033558	autoinflammation, immune dysregulation, and eosinophilia	hereditary_disease	other	hereditary_disease	allergy_and_immunology|rheumatology|immunology_is_not_in_the_list_but_it_can_be_replaced_by_allergy_and_immunology|pediatric	autoimmune_diseases|inflammatory_disease|allergy	immune_disorder|lung_disorder|joint_disorder	true	false	false	true	high
MONDO:0033559	intellectual developmental disorder with seizures and language delay	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	language_disorder_is_not_in_the_list_so_brain_disorder|brain_disorder	false	false	false	true	high
MONDO:0033560	mitochondrial complex 1 deficiency, nuclear type 35	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0033561	deeah syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	vascular_disorder|ear_disorder|bone_disorder|spinal_disorder|muscle_disorder|joint_disorder|lymphatic_disorder|brain_disorder|immune_disorder	false	false	false	false	high
MONDO:0033562	neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotonia	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurodevelopmental_disorders|neurology|genetics_and_genomics|pediatric	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	muscle_disorder|neurodevelopmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0033563	retinitis pigmentosa 90	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|metabolic_disease	psychiatric_disorder|metabolic_disease	hereditary_disease|disorder_of_visual_system|psychiatric_disorder|disorder_of_orbital_region|metabolic_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0033564	oocyte maturation defect 8	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|anemia	reproductive_system_disorder	false	false	false	false	medium
MONDO:0033565	oocyte maturation defect 9	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder	reproductive_system_disorder	false	false	false	false	medium
MONDO:0033566	combined oxidative phosphorylation deficiency 48	mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0033569	combined oxidative phosphorylation deficiency 49	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0033570	combined oxidative phosphorylation deficiency 50	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0033572	intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|psychiatry|pediatric	adrenal_gland_disease|mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	true	false	false	false	high
MONDO:0033613	neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0033614	spastic paraplegia 83, autosomal recessive	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0033615	coenzyme q10 deficiency, primary, 9	mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	metabolic_disease	mitochondrial_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics|cardiology	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	muscle_disorder|liver_disorder	false	false	false	true	high
MONDO:0033618	Vissers-Bodmer syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	skeletal_rare_disease_disorder|bone_disorder	false	false	false	false	high
MONDO:0033619	myopathy, epilepsy, and progressive cerebral atrophy	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0033620	myofibrillar myopathy 10	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder	false	false	false	false	high
MONDO:0033621	spinal muscular atrophy, infantile, James type	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0033622	spermatogenic failure 44	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	anemia|metabolic_disorder|reproductive_disorder	reproductive_system_disorder|spermatozoa_disorder	false	false	false	false	medium
MONDO:0033630	neurodevelopmental disorder with speech impairment and dysmorphic facies	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	speech_disorder|facial_abnormality|brain_disorder|developmental_disorder	false	false	false	true	medium
MONDO:0033631	combined oxidative phosphorylation deficiency 51	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	mitochondrial_disorder|liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0033635	mitochondrial complex IV deficiency, nuclear type 3	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|mitochondrialdisease_is_not_an_actual_category__however_it_can_be_categorized_under_the_following___muscle_disorder|muscle_disorder|other___corrected_response___muscle_disorder	false	false	false	false	high
MONDO:0033636	mitochondrial complex IV deficiency, nuclear type 4	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatrics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	true	high
MONDO:0033637	mitochondrial complex IV deficiency, nuclear type 7	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0033638	mitochondrial complex IV deficiency, nuclear type 8	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	high
MONDO:0033639	mitochondrial complex IV deficiency, nuclear type 10	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0033640	vitamin D-dependent rickets, type 3	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|endocrinology|orthopaedic|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0033641	cleft palate, proliferative retinopathy, and developmental delay	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|autoimmune_diseases|cleft_palate|proliferative_retinopathy|developmental_delay|neurodegenerative_disease	bone_disorder|teeth_disorder|developmental_delay__joint_disorder|eye_disorder	false	false	false	true	high
MONDO:0033642	neurodevelopmental disorder with alopecia and brain abnormalities	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|neurodevelopmental_disorders_are_not_listed_so_cannot_be_included|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_abnormalities|brain_disorder|neurodevelopmental_disorder	false	false	false	false	high
MONDO:0033643	inflammatory bowel disease 30	immune_system_disorder|digestive_system_disorder|hereditary_disease	other	immune_system_disorder|digestive_system_disorder|hereditary_disease	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	immune_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0033644	microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|ophthalmology	metabolic_disorder|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	to_provide_accurate_categorizations_for_the_qalys_lost_due_to_microcornea__rod_cone_dystrophy__cataract__and_posterior_staphyloma_1__i_would_categorize_them_as_follows_____microcornea__low____rod_cone_dystrophy__high____cataract__medium____posterior_staphyloma_1__high
MONDO:0033645	mitochondrial complex IV deficiency, nuclear type 11	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0033646	mitochondrial complex IV deficiency, nuclear type 12	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	neurology|genetics_and_genomics|pediatric	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0033649	mitochondrial complex IV deficiency, nuclear type 14	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0033650	mitochondrial complex IV deficiency, nuclear type 15	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0033651	mitochondrial complex IV deficiency, nuclear type 16	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0033652	mitochondrial complex IV deficiency, nuclear type 17	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	pediatrics|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	heart_disorder|brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0033653	mitochondrial complex IV deficiency, nuclear type 18	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	pediatrics|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0033654	mitochondrial complex IV deficiency, nuclear type 19	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	pediatric|neurology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	high
MONDO:0033655	mitochondrial complex IV deficiency, nuclear type 20	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0033656	mitochondrial complex IV deficiency, nuclear type 21	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|mitochondrial_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	pediatrics|neurology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|neurodegenerative_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0033657	leukodystrophy, hypomyelinating, 20	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0033658	neurodevelopmental disorder with seizures and brain atrophy	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	seizure_disorder|neurodegenerative_disease	neurodevelopmental_disorder|brain_disorder	false	false	false	true	high
MONDO:0033662	neurodevelopmental disorder with microcephaly, seizures, and brain atrophy	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	seizures|brain_disorder|neurodevelopmental_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0033664	Kilquist syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|neurology	metabolic_disorder|neurodegenerative_disease	vascular_disorder|immune_disorder|bone_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0033665	hearing loss, autosomal dominant 78	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|otolaryngology	autosomal_dominant_is_a_pattern_typically_associated_with_genetic_disorders__which_often_fall_under_the_category_of_neurodegenerative_disease|neurodegenerative_disease	ear_disorder|autosomal_dominant	false	false	false	false	medium
MONDO:0033667	Delpire-McNeill syndrome	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	liver_disorder|kidney_disorder|joint_disorder|eye_disorder	false	false	false	false	high
MONDO:0033668	hearing loss, autosomal dominant 79	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|otolaryngology	autosomal_dominant_disorder_is_not_in_the_list_but_a_more_general_category_would_be_metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	false	high
MONDO:0033669	Noonan syndrome 13	syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|immune_system_disorder|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|cardiology|cardiothoracic|pediatric	metabolic_disorder|cardiovascular_disorder	endocrine_disorder|joint_disorder|heart_disorder	false	false	false	false	medium
MONDO:0033670	hearing loss, autosomal recessive 116	psychiatric_disorder|auditory_system_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	otolaryngology|pediatric|genetics_and_genomics	autosomal_recessive____note__i_corrected_the_disease_name_to__autosomal_recessive_hearing_loss|metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	medium
MONDO:0033671	spermatogenic failure 45	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0033672	Duane anomaly-myopathy-scoliosis syndrome	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0033673	spermatogenic failure 46	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|endocrinology|genetics_and_genomics	anemia|metabolic_disorder|autoimmune_diseases	reproductive_system_disorder	false	false	false	false	medium
MONDO:0033682	skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome	disorder_of_development_or_morphogenesis|immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder	dermatology|immunology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|developmental_delay	immune_disorder|developmental_delay|skeletal_dysplasia|bone_disorder	false	false	false	false	high
MONDO:0033683	congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome	hematologic_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|connective_tissue_disorder|immune_system_disorder|hereditary_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|immune_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|hematologic_disorder|connective_tissue_disorder	hematology|pediatric|genetics_and_genomics	anemia|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|bone_disorder	false	false	false	false	high
MONDO:0033717	congenital cerebellar ataxia due to RNU12 mutation	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0033809	isolated blepharochalasis	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	low
MONDO:0033810	isolated iridoschisis	disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system	other	disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|eye_disorder	false	false	false	false	none
MONDO:0033816	thygeson superficial punctate keratopathy	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	medium
MONDO:0033818	Terrien marginal degeneration	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0033821	fungal keratitis	infectious_disease|inflammatory_disease|disorder_of_visual_system	infectious_disease	infectious_disease|disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	ophthalmology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|eye_disorder	true	false	false	true	high
MONDO:0033838	radiation-induced plexopathy	nervous_system_disorder	other	nervous_system_disorder|radiation_induced_disorder	oncology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0033839	osteoradionecrosis of the mandible	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|mouth_disorder|radiation_induced_disorder	orthopaedic|oncology	cancer|inflammatory_disease	bone_disorder|teeth_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0033850	autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	liver_disorder|nervous_system_disorder|muscle_disorder|vascular_disorder	false	false	false	false	high
MONDO:0033853	congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	hepatology|genetics_and_genomics|ophthalmology|pediatric	neurodegenerative_disease|global_developmental_delay_syndrome|metabolic_disorder	global_developmental_delay|liver_disorder|eye_disorder	false	false	false	true	very_high
MONDO:0033856	LAMA5-related multisystemic syndrome	connective_tissue_disorder|hereditary_disease	other	connective_tissue_disorder|hereditary_disease	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	kidney_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0033862	primary autoimmune enteropathy	digestive_system_disorder|immune_system_disorder	autoimmune_disease	immune_system_disorder|digestive_system_disorder	gastroenterology|allergy_and_immunology|pediatric|immunology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0033864	infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome	nervous_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|nervous_system_disorder|syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0033885	mitochondrial complex IV deficiency, nuclear-type	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	mitochondrial_disease|muscle_disorder	false	false	false	false	high
MONDO:0033925	pediatric-onset Graves disease	immune_system_disorder|inflammatory_disease|endocrine_system_disorder	endocrine_system_disorder|autoimmune_disease	endocrine_system_disorder|inflammatory_disease|immune_system_disorder	endocrinology|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	endocrine_disorder|pediatric_onset_graves_disease	false	false	false	true	high
MONDO:0033926	prepubertal anorexia nervosa	psychiatric_disorder|nutritional_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nutritional_disorder|nervous_system_disorder	endocrinology|psychiatry|pediatric	neurodegenerative_disease|mental_health_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	very_high
MONDO:0033938	acute radiation syndrome	syndromic_disease	other	acute_disease|syndromic_disease	radiology|hematoloty|oncology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0033946	hereditary angioedema with C1Inh deficiency	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease|hereditary_disease	cardiovascular_disorder	inflammatory_disease|hereditary_disease|cardiovascular_disorder|integumentary_system_disorder	genetics_and_genomics|hematology|immunology_is_not_in_the_list_so_it_s_removed_to__allergy_and_immunology|allergy_and_immunology	allergy|metabolic_disorder|autoimmune_diseases	vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0033948	acquired angioedema with C1Inh deficiency	integumentary_system_disorder|cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder|integumentary_system_disorder	genetics_and_genomics|hematology|allergy_and_immunology|immunology	allergy|metabolic_disorder|autoimmune_diseases	vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0033954	monoclonal mast cell activation syndrome	hematologic_disorder|syndromic_disease|immune_system_disorder	other	immune_system_disorder|syndromic_disease|hematologic_disorder	hematology|allergy_and_immunology|immunology|oncology	autoimmune_diseases|cancer|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0033968	immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	hematology|gastroenterology|rheumatology|immunology	autoimmune_diseases|inflammatory_disease|lymphopenia_is_often_associated_with_other_immune_system_disorders_so_also__anemia	lymphatic_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0033969	inflammatory bowel disease-recurrent sinopulmonary infections syndrome	immune_system_disorder	other	immune_system_disorder	gastroenterology|rheumatology|pulmonology|immunology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0033980	RELA fusion-positive ependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0034021	spondylodysplastic Ehlers-Danlos syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|connective_tissue_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|rheumatology	inflammatory_disease|metabolic_disorder	spinal_disorder|bone_disorder|joint_disorder|vascular_disorder	false	false	false	false	high
MONDO:0034022	Bethlem myopathy 2	nervous_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	false	high
MONDO:0034041	congenital axonal neuropathy with encephalopathy	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|congenital_axonal_neuropathy_with_encephalopathy_falls_under_this_category_as_it_primarily_affects_the_nervous_system__specifically_the_axons_of_neurons	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0034054	severe combined immunodeficiency due to CD70 deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|allergy_and_immunology|pediatric	inflammatory_disease|autoimmune_diseases|anemia	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0034092	optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome	mitochondrial_disease|hereditary_disease|nervous_system_disorder	other	mitochondrial_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	inflammatory_disease|neurodegenerative_disease|global_developmental_delay_syndrome	eye_disorder|spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0034103	infection-related hemolytic uremic syndrome	hematologic_disorder	other	post_infectious_disorder|hematologic_disorder	hematology|renal_medicine|pediatric	autoimmune_diseases|inflammatory_disease|anemia	urinary_tract_disorder|immune_disorder|kidney_disorder	true	false	false	true	high
MONDO:0034106	developmental and epileptic encephalopathy, 73	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|developmental_disorder	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0034109	congenital myopathy with reduced type 2 muscle fibers	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|muscular_diseases	muscle_disorder	false	false	false	false	high
MONDO:0034110	atypical Fanconi syndrome-neonatal hyperinsulinism syndrome	urinary_system_disorder	other	urinary_system_disorder	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	kidney_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0034121	NAD(P)HX dehydratase deficiency	nervous_system_disorder|metabolic_disease|hereditary_disease	neurodegenerative_disease|metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	high
MONDO:0034127	IgA pemphigus	immune_system_disorder|integumentary_system_disorder|inflammatory_disease	autoimmune_disease	integumentary_system_disorder|inflammatory_disease|immune_system_disorder	allergy_and_immunology|immunology|dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	high
MONDO:0034142	pancreatic agenesis-holoprosencephaly syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|gastroenterology|neurology	neurodegenerative_disease|developmental_disorder|congenital_disorder	brain_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0034143	early-onset calcifying leukoencephalopathy-skeletal dysplasia	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|skeletal_dysplasias_can_sometimes_be_associated_with_other_disorders|metabolic_disorder	brain_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0034145	oculocerebrodental syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	teeth_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0034146	spastic ataxia-dysarthria due to glutaminase deficiency	nervous_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	nervous_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0034150	idiopathic gastroparesis	digestive_system_disorder	other	idiopathic_disease|digestive_system_disorder	gastroenterology|neurology	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0034186	autosomal recessive extra-oral halitosis	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatrics|otolaryngology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	oral_disorder_is_not_included_in_the_list_so_i_will_use_throat_disorder_as_a_reasonable_substitute_since_it_s_related_to_halitosis|teeth_disorder	false	false	false	based_on_current_knowledge_up_to_october_2023__there_are_no_known_efficacious_treatments_that_specifically_cure__prevent__or_treat_autosomal_recessive_extra_oral_halitosis__halitosis_can_result_from_various_underlying_conditions__and_treatment_usually_focuses_on_the_specific_cause_rather_than_a_direct_treatment_for_halitosis_itself__therefore__the_answer_is_false	none
MONDO:0034189	primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome	inflammatory_disease|endocrine_system_disorder|immune_system_disorder|digestive_system_disorder	endocrine_system_disorder|autoimmune_disease	digestive_system_disorder|inflammatory_disease|endocrine_system_disorder|immune_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0034204	syndromic congenital sodium diarrhea	digestive_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease|digestive_system_disorder	pediatric|genetics_and_genomics|gastroenterology	metabolic_disorder|adrenal_gland_disease	lower_gastrointestinal_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0034212	methotrexate toxicity	poisoning	other	poisoning	oncology|hematology|rheumatology	autoimmune_diseases|inflammatory_disease|anemia|cancer	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0034216	resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha	hereditary_disease|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	hereditary_disease|endocrine_system_disorder|metabolic_disease	endocrinology|genetics_and_genomics	metabolic_disorder|endocrine_system_disease	endocrine_disorder|thyroid_disorder|genetic_disorder	false	false	false	true	high
MONDO:0034556	vibratory angioedema	integumentary_system_disorder|inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|integumentary_system_disorder|inflammatory_disease	renal_medicine|dermatology|allergy_and_immunology|hematology	autoimmune_diseases|allergy|inflammatory_disease	vascular_disorder|immune_disorder	false	false	false	false	medium
MONDO:0034676	overgrowth syndrome with 2q37 translocation	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|oncology	neurodegenerative_disease|cancer|metabolic_disorder|autoimmune_diseases	spinal_disorder|immune_disorder|bone_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0034820	cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome	syndromic_disease	other	syndromic_disease	otolaryngology|pulmonology|cardiothoracic|pediatric|cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder|hearing_loss|congenital_heart_defect	ear_disorder|heart_disorder|teeth_disorder|joint_disorder	false	false	false	false	high
MONDO:0034846	primary desmosis coli	digestive_system_disorder	other	digestive_system_disorder	genetics_and_genomics|rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0034895	congenital brachyesophagus-intrathoracic stomach-vertebral anomalies syndrome	syndromic_disease	other	syndromic_disease	pediatric|otolaryngology|genetics_and_genomics	vertebral_anomalies|neurodegenerative_disease	spinal_disorder|bone_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0034971	isolated congenital entropion	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|dermatology	inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0034976	iatrogenic Creutzfeldt-Jakob disease	nervous_system_disorder|iatrogenic_disease|infectious_disease	infectious_disease	nervous_system_disorder|iatrogenic_disease|infectious_disease	genetics_and_genomics|neurology	iatrogenic|neurodegenerative_disease	brain_disorder|spinal_disorder	true	false	false	false	very_high
MONDO:0034978	isolated foveal hypoplasia	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0034987	intraductal tubulopapillary neoplasm of pancreas	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer|intraductal_tubulopapillary_neoplasm_of_pancreas_is_also_classified_as_a_type_of_pancreatic_cancer_which_falls_under_the_larger_category_of_cancer_so_it_can_be_categorized_in_both_but_i_will_leave_off_the_second_instance_and_just_list_cancer	pancreas_is_closely_related_to_the_biliary_system_so___biliary_disorder|liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0034989	intellectual disability-cardiac anomalies-short stature-joint laxity syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	joint_disorder|heart_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0034991	intrauterine growth restriction-congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome	syndromic_disease	other	syndromic_disease	obstetrics_and_gynecology|pediatrics|genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases	skin_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0035004	serine biosynthesis pathway deficiency, infantile/juvenile form	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	metabolic_disorder|liver_disorder|other____blood_bone_marrow_disorder_was_incorrectly_excluded	false	false	false	true	very_high
MONDO:0035008	isolated splenic vein thrombosis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	gastroenterology|cardiology|hepatology|hematology	inflammatory_disease|cardiovascular_disorder	vascular_disorder|liver_disorder	false	false	false	false	medium
MONDO:0035009	isolated mesenteric vein thrombosis	cardiovascular_disorder|digestive_system_disorder	cardiovascular_disorder	cardiovascular_disorder|digestive_system_disorder	gastroenterology|cardiology|hematology	inflammatory_disease|adrenal_gland_disease|cardiovascular_disorder	lower_gastrointestinal_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0035018	frontonasal dysplasia-bifid nose-upper limb anomalies syndrome	syndromic_disease	other	syndromic_disease	orthopaedic|pediatric|genetics_and_genomics	other___however__a_more_specific_match_would_be__developmental_disorder|neurodegenerative_disease|metabolic_disorder|skeletal_dysplasia__not_present_in_the_original_list	nose_disorder|upper_limb_anomalies_syndrome_suggests_additional_categories_like_bone_disorder_or_joint_disorder_but_none_of_them_have_a_direct_relation_so_i_removed_them_to_give_you_this_list__nose_disorder|upper_limbs_disorder	false	false	false	false	very_high
MONDO:0035027	microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|congenital_disorder	bone_disorder|eye_disorder|muscle_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0035105	diaphragmatic hernia-short bowel-asplenia syndrome	syndromic_disease	other	syndromic_disease	general_surgery|pediatric|gastroenterology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0035112	acute myeloid leukemia with BCR-ABL1	musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|immune_system_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	oncology|hematology	leukemia|cancer	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0035121	myeloid/lymphoid neoplasm associated with JAK2 rearrangement	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	anemia|cancer|myeloid_lymphoid_neoplasm_associated_with_jak2_rearrangement_is_primarily_classified_as_a_type_of_blood_cancer_and_can_be_more_specifically_categorized_under_leukemia_which_falls_under_the_broader_category_of__anemia__since_it_affects_the_production_or_function_of_red_blood_cells__but_in_a_medical_context__it_s_generally_considered_a_cancer	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0035122	GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder	nervous_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	developmental_disorder|mental_health_disorder|neurodegenerative_disease	autism_spectrum_disorder|intellectual_disability|developmental_delay|brain_disorder	false	false	false	false	high
MONDO:0035124	linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|skin_disorder|brain_disorder	false	false	false	false	high
MONDO:0035133	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics|pediatric|endocrinology|psychiatry	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	endocrine_disorder|intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0035136	isolated melanotic schwannoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	skin_disorder|brain_disorder	false	false	false	false	medium
MONDO:0035149	secondary erythromelalgia	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	rheumatology|neurology|dermatology	metabolic_disorder|inflammatory_disease	endocrine_disorder|liver_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0035151	17q24.2 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|joint_disorder|vascular_disorder|immune_disorder|spinal_disorder|muscle_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0035153	male infertility due to acephalic spermatozoa	reproductive_system_disorder	other	reproductive_system_disorder	genetics_and_genomics|urology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder|male_infertility|muscle_disorder	false	false	false	false	high
MONDO:0035159	dermoid or epidermoid cyst of the central nervous system	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0035161	progressive dementia with neuroserpin inclusion bodies	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	true	false	false	false	high
MONDO:0035173	9q21.13 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0035220	PLG-related hereditary angioedema with normal C1inh	hereditary_disease|inflammatory_disease|integumentary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|inflammatory_disease|integumentary_system_disorder	immunology|hematology|genetics_and_genomics	allergy|inflammatory_disease|cardiovascular_disorder	vascular_disorder|immune_disorder	false	false	false	true	medium
MONDO:0035235	classic pyoderma gangrenosum	connective_tissue_disorder|integumentary_system_disorder|syndromic_disease	other	connective_tissue_disorder|syndromic_disease|integumentary_system_disorder	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0035236	pustular pyoderma gangrenosum	connective_tissue_disorder|integumentary_system_disorder|syndromic_disease	other	connective_tissue_disorder|syndromic_disease|integumentary_system_disorder	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0035237	bullous pyoderma gangrenosum	connective_tissue_disorder|integumentary_system_disorder|syndromic_disease	other	connective_tissue_disorder|syndromic_disease|integumentary_system_disorder	allergy_and_immunology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0035238	vegetative pyoderma gangrenosum	connective_tissue_disorder|integumentary_system_disorder|syndromic_disease	other	connective_tissue_disorder|syndromic_disease|integumentary_system_disorder	allergy_and_immunology|hematology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder_skin_disorder	false	false	false	false	low
MONDO:0035290	atypical hemolytic uremic syndrome with complement gene abnormality	hematologic_disorder|syndromic_disease|immune_system_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder|immune_system_disorder|syndromic_disease	genetics_and_genomics|renal_medicine|pediatric|hematology	autoimmune_diseases|anemia	kidney_disorder|immune_disorder	false	false	false	true	high
MONDO:0035293	streptococcus pneumoniae-associated hemolytic uremic syndrome	hematologic_disorder	other	post_infectious_disorder|hematologic_disorder	renal_medicine|pediatric|hematology	inflammatory_disease|autoimmune_diseases|anemia	kidney_disorder|vascular_disorder|immune_disorder	true	false	false	true	high
MONDO:0035295	congenital primary megaureter, refluxing and obstructed form	urinary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|urinary_system_disorder	urology|pediatric	congenital_condition|urogenital_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0035312	fibrohistiocytic inflammatory pseudotumor of the liver	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	oncology|immunology|hepatology	inflammatory_disease|autoimmune_diseases|cancer	immune_disorder|liver_disorder	false	false	false	false	medium
MONDO:0035313	lymphoplasmacytic inflammatory pseudotumor of the liver	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	hematology|oncology|immunology|hepatology	inflammatory_disease|autoimmune_diseases|cancer	immune_disorder|lymphatic_disorder|liver_disorder	false	false	false	false	low
MONDO:0035320	early-onset familial hypoaldosteronism	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics|pediatric|renal_medicine	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0035321	late-onset familial hypoaldosteronism	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|genetics_and_genomics|renal_medicine	adrenal_gland_disease|familial_disorders|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	false	low
MONDO:0035337	Duane retraction syndrome with congenital deafness	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|syndromic_disease	other	syndromic_disease|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	ophthalmology|genetics_and_genomics|pediatric|neurology	autoimmune_diseases|congenital_deafness|neurodegenerative_disease	eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0035344	acute bilirubin encephalopathy	nervous_system_disorder	other	acute_disease|nervous_system_disorder	hepatology|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0035345	chronic bilirubin encephalopathy	nervous_system_disorder	other	nervous_system_disorder	hepatology|pediatric|neurology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	liver_disorder|brain_disorder	false	false	false	false	high
MONDO:0035349	localized dystrophic epidermolysis bullosa	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0035350	letrozole toxicity	poisoning	other	poisoning	endocrinology|obstetrics_and_gynecology	endocrine_system_disorder|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	letrozole_is_a_medication_used_primarily_to_treat_hormone_receptor_positive_breast_cancer_in_postmenopausal_women__while_it_can_be_effective__it_may_also_cause_toxicity_and_have_side_effects__some_common_side_effects_of_letrozole_include___1__hot_flashes__2__joint_pain_or_stiffness__3__fatigue__4__nausea__5__bone_density_loss__which_could_lead_to_an_increased_risk_of_fractures__6__mood_changes__7__increased_sweating__severe_adverse_effects__although_less_common__can_include_____heart_problems____liver_function_abnormalities____increased_risk_of_blood_clots__it_s_important_for_patients_to_be_monitored_during_treatment__and_any_unusual_symptoms_should_be_reported_to_a_healthcare_provider__adjustments_to_treatment_or_supportive_care_may_be_necessary_to_manage_toxicity___for_specific_and_comprehensive_guidance__individuals_should_consult_their_healthcare_providers_regarding_risks_and_benefits_of_using_letrozole_in_their_particular_situation	high
MONDO:0035357	portosinusoidal vascular disease	digestive_system_disorder|endocrine_system_disorder|cardiovascular_disorder	endocrine_system_disorder|cardiovascular_disorder	digestive_system_disorder|endocrine_system_disorder|cardiovascular_disorder	cardiology|hepatology	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	vascular_disorder|liver_disorder	false	false	false	false	high
MONDO:0035362	TRIM22-related inflammatory bowel disease	hereditary_disease|digestive_system_disorder|immune_system_disorder	other	hereditary_disease|immune_system_disorder|digestive_system_disorder	gastroenterology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0035370	ALPI-related inflammatory bowel disease	hereditary_disease|digestive_system_disorder|immune_system_disorder	other	hereditary_disease|immune_system_disorder|digestive_system_disorder	gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|liver_disorder|immune_disorder	false	false	false	false	high
MONDO:0035375	multisystem inflammatory syndrome in children and adults	other	other	post_infectious_disorder	gastroenterology|hepatology|rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder	true	false	false	true	high
MONDO:0035400	seronegative autoimmune hepatitis	endocrine_system_disorder|immune_system_disorder|inflammatory_disease|digestive_system_disorder	autoimmune_disease|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|immune_system_disorder|inflammatory_disease	rheumatology|allergy_and_immunology|hepatology	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder	false	false	false	true	high
MONDO:0035401	isolated anencephaly	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology	neurodegenerative_disease|anencephaly_is_a_condition_present_at_birth_where_a_major_portion_of_the_brain_is_absent	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0035402	isolated exencephaly	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0035403	serous cystadenoma of childhood	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|pediatric	adrenal_gland_disease|cancer	kidney_disorder|upper_gastrointestinal_disorder|reproductive_system_disorder|liver_disorder	false	false	false	false	low
MONDO:0035404	mucinous cystadenoma of childhood	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|pediatric	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0035405	seromucinous cystadenoma of childhood	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	oncology|pediatric	cancer	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	low
MONDO:0035406	furuncular myiasis due to Dermatobia hominis	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	pediatric|dermatology	infectious_disease|skin_disease|inflammatory_disease	skin_disorder|muscle_disorder	true	false	false	true	medium
MONDO:0035407	furuncular myiasis due to Cordylobia anthropophaga	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	pediatric|dermatology	skin_disease|inflammatory_disease	skin_disorder	true	false	false	true	medium
MONDO:0035408	furuncular myiasis due to Cordylobia rodhaini	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|infectious_disease	pediatrics|dermatology	inflammatory_disease	skin_disorder|upper_gastrointestinal_disorder|immune_disorder	true	false	false	true	medium
MONDO:0035410	isolated congenital aglossia	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis|mouth_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	musculoskeletal_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0035411	isolated congenital hypoglossia	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis|mouth_disorder|hereditary_disease|musculoskeletal_system_disorder	otolaryngology|pediatric	congenital__disorder|neurodegenerative_disease	throat_disorder|congenital_disorder	false	false	false	false	medium
MONDO:0035423	triglyceride deposit cardiomyovasculopathy	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|cardiology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	muscle_disorder|heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0035432	POMGNT2-related limb-girdle muscular dystrophy R24	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology|pediatric	muscular_dystrophy|neurodegenerative_disease|metabolic_disorder	muscle_disorder|lower_gastrointestinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0035437	CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome	connective_tissue_disorder|syndromic_disease	other	syndromic_disease|connective_tissue_disorder	genetics_and_genomics|immunology|pediatric	inflammatory_disease|neutrophil_dysfunction_syndrome_is_related_to_an_immune_system_disorder__so_it_fits_into_autoimmune_diseases_category_as_well|autoimmune_diseases	immune_disorder|immunodeficiency|neutrophil_dysfunction|autoinflammation	false	false	false	true	high
MONDO:0035441	congenital autosomal recessive small-platelet thrombocytopenia	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics|obstetrics_and_gynecology|pediatric	metabolic_disorder|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0035444	acute mast cell leukemia	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|hereditary_disease	cancer_or_benign_tumor	hematologic_disorder|acute_disease|cancer_or_benign_tumor|hereditary_disease|immune_system_disorder	hematology|oncology	leukemia|cancer	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0035445	chronic mast cell leukemia	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|hereditary_disease	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|hereditary_disease|immune_system_disorder	hematology|immunology|oncology	inflammatory_disease|autoimmune_diseases|cancer|allergy	immune_disorder|blood_bone_marrow_disorder	false	true	false	false	medium
MONDO:0035447	liver adenomatosis	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	gastroenterology|hepatology|others|oncology	metabolic_disorder|inflammatory_disease|cancer	liver_disorder	false	false	false	false	medium
MONDO:0035449	atelencephaly	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0035450	aprosencephaly	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0035452	mueller-weiss syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics	metabolic_disorder|anemia	bone_disorder|vascular_disorder|joint_disorder	false	false	false	false	high
MONDO:0035459	idiopathic multidrug-resistant nephrotic syndrome	hereditary_disease|syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|syndromic_disease|hereditary_disease|idiopathic_disease	pediatric|renal_medicine	inflammatory_disease|autoimmune_diseases|metabolic_disorder	immune_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0035460	idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunosuppressive therapy	syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|syndromic_disease|idiopathic_disease	allergy_and_immunology|hematology|pediatric|renal_medicine	inflammatory_disease|autoimmune_diseases	immune_disorder|kidney_disorder	false	false	false	true	high
MONDO:0035472	GJC2-related late-onset primary lymphedema	immune_system_disorder	other	immune_system_disorder	genetics_and_genomics|cardiology|neurology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	lymphatic_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0035473	warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome	immune_system_disorder|syndromic_disease	other	syndromic_disease|immune_system_disorder	immunology|dermatology|obstetrics_and_gynecology|oncology	inflammatory_disease|genital_dysplasia|lymphedema|autoimmune_diseases|cancer	skin_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0035475	EPHB4-related lymphatic-related hydrops fetalis	immune_system_disorder	other	immune_system_disorder	genetics_and_genomics|obstetrics_and_gynecology|pediatric	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases|metabolic_disorder	lymphatic_disorder|vascular_disorder	false	false	false	false	high
MONDO:0035499	CELSR1-related late-onset primary lymphedema	immune_system_disorder	other	immune_system_disorder	immunology|hematology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0035500	congenital primary lymphedema of Gordon	immune_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|immune_system_disorder|cardiovascular_disorder	pediatric|hematology|genetics_and_genomics	cardiovascular_disorder|congenital_disease___note__this_answer_is_corrected_from_the_original_response_which_incorrectly_included__congenital__as_a_category	congenital_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0035511	ricin poisoning	poisoning	other	poisoning	hematology|pulmonology|allergy_and_immunology	autoimmune_diseases	upper_gastrointestinal_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0035521	blepharophimosis-ptosis-epicanthus inversus syndrome plus	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|ophthalmology	adrenal_gland_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|eye_disorder|skin_disorder|joint_disorder	false	false	false	false	medium
MONDO:0035524	blepharophimosis-ptosis-epicanthus inversus syndrome type 1	endocrine_system_disorder|hereditary_disease|disorder_of_visual_system|reproductive_system_disorder	endocrine_system_disorder	disorder_of_orbital_region|endocrine_system_disorder|disorder_of_visual_system|reproductive_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|ophthalmology	metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0035525	blepharophimosis-ptosis-epicanthus inversus syndrome type 2	endocrine_system_disorder|hereditary_disease|disorder_of_visual_system|reproductive_system_disorder	endocrine_system_disorder	disorder_of_orbital_region|endocrine_system_disorder|disorder_of_visual_system|reproductive_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|ophthalmology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0035529	infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|pulmonology|genetics_and_genomics|allergy_and_immunology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder_lung_disorder	false	false	false	false	very_high
MONDO:0035534	DONSON-related microcephaly-short stature-limb abnormalities spectrum	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|short_stature|limb_abnormalities	false	false	false	false	very_high
MONDO:0035540	pheochromocytoma-paraganglioma	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology|renal_medicine|cardiology	endocrine_disorder|cancer|metabolic_disorder|adrenal_gland_disease	vascular_disorder|endocrine_disorder	false	true	false	true	medium
MONDO:0035551	cathepsin a-related arteriopathy-strokes-leukoencephalopathy	hereditary_disease|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|hereditary_disease|cardiovascular_disorder	genetics_and_genomics|neurology|cardiology	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	vascular_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0035562	acquired human prion disease	nervous_system_disorder|infectious_disease	neurodegenerative_disease|infectious_disease	nervous_system_disorder|infectious_disease	neurology|genetics_and_genomics	neurodegenerative_disease|acquired_prion_diseases	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0035584	punctate inner choroidopathy	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0035586	Cramp-fasciculation syndrome	syndromic_disease	other	syndromic_disease	neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0035592	congenital infiltrating lipomatosis of the face	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	oncology|pediatric|dermatology|genetics_and_genomics	inflammatory_disease|cancer|cardiovascular_disorder	muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0035605	B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	leukemia|lymphoma|cancer	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0035614	sporadic fatal insomnia	nervous_system_disorder|infectious_disease	infectious_disease|neurodegenerative_disease	infectious_disease|nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|cancer|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0035639	mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)	hematologic_disorder|connective_tissue_disorder|immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|hereditary_disease|hematologic_disorder|immune_system_disorder|acute_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder	oncology|hematology	cancer|acute_leukemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0035642	mixed phenotype acute leukemia with t(v;11q23.3)	hematologic_disorder|connective_tissue_disorder|immune_system_disorder|hereditary_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|hereditary_disease|hematologic_disorder|acute_disease|immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	genetics_and_genomics|hematology|oncology	cancer	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	true	true	false	false	very_high
MONDO:0035646	congenital-onset Steinert myotonic dystrophy	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|hereditary_disease|syndromic_disease|cardiovascular_disorder|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	joint_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0035647	childhood-onset Steinert myotonic dystrophy	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0035648	juvenile-onset Steinert myotonic dystrophy	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	joint_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0035649	adult-onset Steinert myotonic dystrophy	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0035650	late-onset Steinert myotonic dystrophy	syndromic_disease|hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	nervous_system_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0035651	choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|endocrinology	developmental_dysfunction|metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder|growth_disorder	false	false	false	false	high
MONDO:0035660	GNAO1-related developmental delay-seizures-movement disorder spectrum	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	developmental_delay_seizures_movement_disorder_spectrum_is_more_closely_related_to_neurodevelopmental_disorders_than_the_provided_category_list__but_since_that_option_is_not_available__the_best_fit_would_be___neurodegenerative_disease|neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0035661	TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|cardiology	developmental_disorder|congenital_disorder|cardiovascular_disorder	congenital_disorder|developmental_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0035663	neuromyelitis optica spectrum disorder with anti-AQP4 antibodies	disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	allergy_and_immunology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder|eye_disorder|immune_disorder	false	false	false	true	high
MONDO:0035664	neuromyelitis optica spectrum disorder with anti-MOG antibodies	disorder_of_visual_system|nervous_system_disorder|inflammatory_disease|disorder_of_development_or_morphogenesis	neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|immunology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0035665	neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies	disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0035666	acute transverse myelitis with anti-MOG antibodies	nervous_system_disorder|inflammatory_disease|disorder_of_development_or_morphogenesis	neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|inflammatory_disease|acute_disease	genetics_and_genomics|neurology	autoimmune_diseases|inflammatory_disease	spinal_disorder|immune_disorder	true	false	false	true	high
MONDO:0035667	isolated optic neuritis without anti-MOG antibodies	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease	brain_disorder|eye_disorder|immune_disorder	true	false	false	false	medium
MONDO:0035668	isolated optic neuritis with anti-MOG antibodies	disorder_of_visual_system|nervous_system_disorder|inflammatory_disease|disorder_of_development_or_morphogenesis	neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|inflammatory_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	autoimmune_diseases|inflammatory_disease	brain_disorder|eye_disorder|immune_disorder	true	false	false	true	medium
MONDO:0035669	acute disseminated encephalomyelitis with anti-MOG antibodies	nervous_system_disorder|inflammatory_disease|infectious_disease|disorder_of_development_or_morphogenesis	neurodegenerative_disease|infectious_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|inflammatory_disease|post_infectious_disorder|acute_disease|infectious_disease	pediatrics|rheumatology|neurology	autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder|immune_disorder	true	false	false	true	high
MONDO:0035670	acute disseminated encephalomyelitis without anti-MOG antibodies	inflammatory_disease|infectious_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	infectious_disease|neurodegenerative_disease	inflammatory_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|post_infectious_disorder|acute_disease|infectious_disease	allergy_and_immunology|neurology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|spinal_disorder|brain_disorder	true	false	false	false	high
MONDO:0035678	Timothy syndrome type 1	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder	immune_disorder|kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0035679	Timothy syndrome type 2	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	cardiology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder	immune_disorder|liver_disorder	false	false	false	false	high
MONDO:0035694	combined immunodeficiency due to RELA haploinsufficiency	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	immunology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0035696	incomplete septal cirrhosis	endocrine_system_disorder|digestive_system_disorder|cardiovascular_disorder	cardiovascular_disorder|endocrine_system_disorder	cardiovascular_disorder|digestive_system_disorder|endocrine_system_disorder	cardiology|gastroenterology|pulmonology|cardiothoracic|hepatology	liver_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	false	medium
MONDO:0035706	SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome	nervous_system_disorder|hereditary_disease|syndromic_disease|psychiatric_disorder	psychiatric_disorder	syndromic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|intellectual_disability|multiple_congenital_anomalies_syndrome	false	false	false	false	very_high
MONDO:0035707	blepharophimosis-intellectual disability syndrome/genitopatellar overlap syndrome	syndromic_disease	other	syndromic_disease	pediatric|neurology|ophthalmology|orthopaedic|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|joint_disorder|reproductive_system_disorder|eye_disorder	false	false	false	false	high
MONDO:0035734	hereditary angioedema with normal C1inh not related to F12 or PLG variant	hereditary_disease|integumentary_system_disorder|inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	integumentary_system_disorder|hereditary_disease|cardiovascular_disorder|inflammatory_disease	allergy_and_immunology|pediatrics|cardiology|dermatology|renal_medicine|rheumatology|hematology|pulmonology|gastroenterology|genetics_and_genomics	allergy|inflammatory_disease|metabolic_disorder	immune_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0035735	acquired hemophilia A	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics	inflammatory_disease|adrenal_gland_disease|anemia|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0035736	acquired hemophilia B	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics	inflammatory_disease|anemia|metabolic_disorder|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0035737	acquired factor V deficiency	hematologic_disorder	other	hematologic_disorder	pediatric|hematology|genetics_and_genomics	blood_disorder|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0035738	acquired factor VII deficiency	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0035740	acquired factor XI deficiency	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0035742	factor V short isoforms-related bleeding disorder	hematologic_disorder	other	hematologic_disorder	obstetrics_and_gynecology|pediatric|hematology|genetics_and_genomics	bleeding_disorder|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0035743	factor V amsterdam bleeding disorder	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0035759	factor V atlanta bleeding disorder	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics	bleeding_disorder|metabolic_disorder|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0035763	idiopathic non-lupus full-house nephropathy	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|nephrology	inflammatory_disease|metabolic_disorder	kidney_disorder|immune_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0035764	idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance	syndromic_disease|urinary_system_disorder	other	syndromic_disease|urinary_system_disorder|idiopathic_disease	pediatric|renal_medicine	inflammatory_disease|metabolic_disorder|autoimmune_diseases	kidney_disorder|immune_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0035774	NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|neurodevelopmental_disorder	brain_disorder|lower_gastrointestinal_disorder|sleep_wake_cycle_disturbance_could_be_classified_as_a_neurological_disorder__brain_disorder__and_sleep_disturbance_is_related_to_brain_function__however_the_specific_symptom_of_chronic_constipation_would_classify_as_a_gastrointestinal_issue__lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0035775	CCNK-related neurodevelopmental disorder-severe intellectual disability-facial dysmorphism syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	brain_disorder|neurodevelopmental_disorder	false	false	false	false	very_high
MONDO:0035776	combined deficiency of factor VII and factor X	hematologic_disorder	other	hematologic_disorder	pediatric|hematology|genetics_and_genomics	inherited_diseases|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0035777	parenteral nutrition-associated cholestasis	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0035782	non-syndromic anorectal malformation with rectourethral fistula, bulbar type	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	urology|pediatric	neurodegenerative_disease|surgical_condition|anorectal_fistula	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0035783	non-syndromic anorectal malformation with rectourethral fistula, prostatic type	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	urology|gastroenterology	inflammatory_disease|cancer|autoimmune_diseases	lower_gastrointestinal_disorder|urinary_tract_disorder	false	false	false	true	high
MONDO:0035819	cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	hematology|neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|anemia|growth_retardation	muscle_disorder|brain_disorder|bone_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0035821	isolated female hypospadias	reproductive_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|reproductive_system_disorder	urology|obstetrics_and_gynecology	metabolic_disorder|autoimmune_diseases|adrenal_gland_disease	reproductive_system_disorder|lower_gastrointestinal_disorder|urinary_tract_disorder	false	false	false	false	low
MONDO:0035823	KLHL7-related Bohring-Opitz-like syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	endocrinology|neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	bone_disorder|skeletal_rare_disease_disorder	false	false	false	false	high
MONDO:0035824	KLHL7-related cold-induced sweating-like syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	skin_disorder	false	false	false	false	medium
MONDO:0035826	symptomatic form of X-linked centronuclear myopathy in female carriers	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0035838	idiopathic multicentric Castleman disease	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	hematology|rheumatology|oncology	inflammatory_disease|cancer|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0035875	ivermectin toxicity	poisoning	other	poisoning	neurology|toxicity	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	kidney_disorder|liver_disorder	false	false	false	false	none
MONDO:0035876	belinostat toxicity or dose selection	poisoning	other	poisoning	pulmonology|neurology|dermatology|genetics_and_genomics|oncology|renal_medicine|hematology	metabolic_disorder|inflammatory_disease|anemia|cancer	kidney_disorder|lower_gastrointestinal_disorder|immune_disorder|liver_disorder|bone_disorder|vascular_disorder|lymphatic_disorder	false	false	false	belinostat_is_a_medication_used_primarily_for_the_treatment_of_patients_with_relapsed_or_refractory_peripheral_t_cell_lymphoma__as_with_many_cancer_treatments__belinostat_can_have_toxicities_associated_with_its_use__the_main_toxicities_include__but_are_not_limited_to__thrombocytopenia__low_platelet_counts___anemia__fatigue__nausea__vomiting__and_potential_liver_enzyme_elevation____dose_selection_for_belinostat_is_critical_to_minimize_these_toxicities_while_maintaining_efficacy__the_recommended_dosage_must_be_carefully_determined_based_on_the_patient_s_overall_health__renal_function__and_liver_function__as_well_as_any_concomitant_medications_they_may_be_taking_that_could_interact_with_belinostat___if_you_have_specific_questions_about_the_toxicity_profile_or_dosage_regimen_for_belinostat__i_recommend_discussing_them_with_a_healthcare_professional_who_specializes_in_oncology	none
MONDO:0035879	granuloma faciale	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0035882	chronic intervillositis of unknown etiology	obstetric_disorder	other	obstetric_disorder	immunology|hematology	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0035892	Mills syndrome	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	musculoskeletal_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0035930	neu-laxova syndrome due to 3-phosphoserine phosphatase deficiency	metabolic_disease|hereditary_disease|integumentary_system_disorder|syndromic_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease	integumentary_system_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|metabolic_disease	genetics_and_genomics|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	liver_disorder|brain_disorder|muscle_disorder|upper_gastrointestinal_disorder|kidney_disorder	false	false	false	true	high
MONDO:0035940	B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	genetics_and_genomics|hematology|oncology	leukemia|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0035941	B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	pediatric|hematology|oncology	leukemia|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0035942	B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1)	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	leukemia|cancer|lymphoma	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0035943	B-lymphoblastic leukemia/lymphoma with hyperdiploidy	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	genetics_and_genomics|hematology|oncology	cancer|lymphoma	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0035944	B-lymphoblastic leukemia/lymphoma with hypodiploidy	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	genetics_and_genomics|hematology|oncology	cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0035945	B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3)	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	leukemia|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0036025	toxicity to dolutegravir	poisoning	other	poisoning	hepatology|dermatology|hematology	adverse_reaction|toxicity|drug_side_effect|pharmacological_disease	liver_disorder|kidney_disorder	false	false	false	false	none
MONDO:0036042	KAT6B-related multiple congenital anomalies syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	joint_disorder|muscle_disorder|skin_disorder	false	false	false	false	high
MONDO:0036045	euthyroid dysprealbuminemic hyperthyroxinemia	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	hepatology|endocrinology|hematology	anemia|metabolic_disorder|autoimmune_diseases	liver_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0036189	oculogastrointestinal-neurodevelopmental syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|neurology|pediatric|gastroenterology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0036193	parkinsonism with polyneuropathy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0036212	spastic paraparesis-cataracts-speech delay syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0036217	lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to a point mutation	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0036218	lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene cluster	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0036482	retinitis pigmentosa 81	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	psychiatric_disorder|metabolic_disease	psychiatric_disorder|nervous_system_disorder|metabolic_disease|disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0036483	short-rib thoracic dysplasia 18 with polydactyly	respiratory_system_disorder|urinary_system_disorder|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	other	respiratory_system_disorder|syndromic_disease|urinary_system_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	genetic_disorder|metabolic_disorder	skeletal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0036484	Charcot-Marie-Tooth disease, dominant intermediate G	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|orthopaedic	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0036501	refractory malignant neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology	refractory_disorder|cancer|refractory_malignant_neoplasm_is_best_fit_into|malignant_neoplasm	blood_bone_marrow_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0036511	childhood malignant kidney neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|pediatric|oncology	childhood_malignant_kidney_neoplasm_can_also_be_classified_as_a_specific_type_of_cancer_known_as_renal_cell_carcinoma_in_children_but_the_provided_list_does_not_have_this_category_so_we_will_stick_to_the_general_category_of_cancer_which_is_appropriate_for_this_disease|cancer	kidney_disorder|lymphatic_disorder|urinary_tract_disorder	false	true	false	true	high
MONDO:0036591	adrenal cortex neoplasm	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	oncology|endocrinology	adrenal_gland_disease|cancer	adrenal_cortex_neoplasm_is_actually_a_subset_of_this_category__so_endocrine_disorder_is_the_best_fit|endocrine_disorder	false	true	false	false	high
MONDO:0036595	ovarian Sertoli-Leydig cell tumor	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	endocrinology|obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer|endocrine_disorder	reproductive_system_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0036688	rhabdomyoma	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric|oncology	cancer|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	low
MONDO:0036696	spleen neoplasm	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	spleen_neoplasm_falls_under_this_category_since_it_refers_to_a_tumor_or_cancer_of_the_spleen|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0036779	axillary neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|dermatology	adrenal_gland_disease|cancer	skin_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0036781	benign axillary neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|dermatology	cancer	lymphatic_disorder|skin_disorder	false	false	false	false	low
MONDO:0036870	lymphatic vessel neoplasm	cancer_or_benign_tumor|cardiovascular_disorder|immune_system_disorder	cancer_or_benign_tumor|cardiovascular_disorder	immune_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder	hematology|oncology	lymphatic_vessel_neoplasm|cancer	vascular_disorder|lymphatic_disorder	false	true	false	false	medium
MONDO:0036915	benign ovarian mucinous tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer|ovarian_tumor	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	true	low
MONDO:0036918	punctate acrokeratoderma freckle-like pigmentation	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	low
MONDO:0036976	benign epithelial neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pathology|oncology	neoplasm|cancer	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0036990	benign Leydig cell tumor	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|endocrinology|genetics_and_genomics	adrenal_gland_disease|cancer	endocrine_disorder|reproductive_system_disorder	false	false	false	true	low
MONDO:0037002	benign phyllodes tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	surgical_oncology_is_not_an_option_so_use__oncology|oncology	cancer	skin_disorder|breast_disorder	false	false	false	false	low
MONDO:0037003	malignant phyllodes tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cardiothoracic|oncology	malignant_tumor|cancer	lymphatic_disorder|vascular_disorder|breast_lung_disorder	false	true	false	false	high
MONDO:0037105	lung germ cell tumor	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology	cancer|autoimmune_diseases	reproductive_system_disorder|lung_disorder	false	true	false	true	high
MONDO:0037149	HSD10 disease, atypical type	metabolic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|mitochondrial_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|nervous_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0037250	childhood testicular neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	urology|oncology|pediatric	pediatric_cancer|childhood_neoplasm|cancer	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0037251	congestive splenomegaly	hematologic_disorder|immune_system_disorder	other	hematologic_disorder|immune_system_disorder	hematology|hepatology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	lymphatic_disorder|liver_disorder|vascular_disorder	false	false	false	false	high
MONDO:0037252	thecoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|dermatology	adrenal_gland_disease|cancer	reproductive_system_disorder|skin_disorder	false	true	false	false	medium
MONDO:0037253	ovarian thecoma	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0037254	transitional cell neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	urology|oncology|renal_medicine	cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0037255	ovarian serous tumor	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0037256	serous neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|urinary_tract_disorder|kidney_disorder	false	true	false	false	very_high
MONDO:0037398	pneumonia caused by pseudomonas aeruginosa infection	respiratory_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	respiratory_system_disorder|infectious_disease|inflammatory_disease	pediatric|pulmonology	cancer|autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0037735	sebaceous gland cancer	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	oncology|dermatology	autoimmune_diseases|cancer	skin_disorder|reproductive_system_disorder	false	true	false	false	medium
MONDO:0037736	infratentorial neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neoplasm	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0037737	peritoneal solitary fibrous tumor	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	oncology|genetics_and_genomics|hematology	autoimmune_diseases|cancer	muscle_disorder|soft_tissue_disorder	false	false	false	false	medium
MONDO:0037738	cauda equina cancer	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0037739	benign neoplasm of cauda equina	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer|neoplasm|benign_cancer	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0037740	malignant central nervous system mesenchymal, non-meningothelial neoplasm	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	malignant_central_nervous_system_mesenchymal__non_meningothelial_neoplasm_fits_within_this_category_as_it_refers_to_a_type_of_cancer_that_affects_the_central_nervous_system|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0037742	endometrioid stromal and related neoplasms	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0037743	mediastinal soft tissue cancer	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pulmonology|oncology|cardiothoracic	cancer	lymphatic_disorder|lung_disorder	false	true	false	false	very_high
MONDO:0037744	neoplasm of retromolar area	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	neurology|oncology|ophthalmology	cancer|neoplasm	eye_disorder	false	true	false	false	high
MONDO:0037745	fibromyxoid tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|rheumatology|orthopaedic	cancer|inflammatory_disease	muscle_disorder|joint_disorder|vascular_disorder|bone_disorder	false	true	false	false	medium
MONDO:0037746	malignant vaginal mixed epithelial and mesenchymal neoplasm	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer|malignant_vaginal_mixed_epithelial_and_mesenchymal_neoplasm	reproductive_system_disorder	false	true	false	false	very_high
MONDO:0037748	hyperlipoproteinemia	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|endocrinology|hepatology|cardiology	metabolic_disorder|cardiovascular_disorder	liver_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0037792	carbohydrate metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	renal_medicine|endocrinology|genetics_and_genomics|hepatology	carbohydrate_metabolism_disease|metabolic_disorder	liver_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0037807	glycerol metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	hepatology|metabolic_disorders_typically_involve_genetics_or_endocrine_systems_but_can_also_impact_liver_and_kidneys|renal_medicine|endocrinology|genetics_and_genomics	metabolic_disorder|glycerol_metabolism_disease	liver_disorder|glycogen_storage_disease	false	false	false	true	medium
MONDO:0037821	porphyrin metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	hematology|neurology|genetics_and_genomics|hepatology	neurodegenerative_disease|anemia|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	high
MONDO:0037829	purine metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|endocrinology|pediatrics|hepatology	purine_metabolism_disease|metabolic_disorder	upper_gastrointestinal_disorder|kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0037847	vertebral joint disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	neurology|rheumatology|orthopaedic	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0037858	inherited fatty acid metabolism disorder	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatrics	inherited_fatty_acid_metabolism_disorder|metabolic_disorder	liver_disorder	false	false	false	true	high
MONDO:0037870	valine metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	metabolism_disease|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0037871	amino acid metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	metabolism_disease|genetics_and_genomics	metabolic_disorder|amino_acid_metabolism_disease	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0037872	bordetellosis	infectious_disease	infectious_disease	infectious_disease	pulmonology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|immune_disorder|vascular_disorder	true	false	false	true	low
MONDO:0037937	pyrimidine metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|hepatology|metabolic_diseases|pediatrics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0037938	inborn disorder of aspartate family metabolism	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatrics	metabolic_disorder|inborn_disorder	liver_disorder	false	false	false	true	high
MONDO:0037939	porphyria	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|dermatology|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|skin_disorder|liver_disorder	false	false	false	false	medium
MONDO:0037940	inherited auditory system disease	hereditary_disease|auditory_system_disorder	other	hereditary_disease|auditory_system_disorder	otolaryngology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inherited_auditory_system_disease_does_not_fit_any_category_in_the_provided_list_so_it_is_excluded	ear_disorder	false	false	false	true	medium
MONDO:0040500	glycosylphosphatidylinositol biosynthesis defect 16	psychiatric_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	psychiatric_disorder|metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0040501	Ehlers-Danlos syndrome, arthrochalasia type, 2	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	orthopaedic|rheumatology	cardiovascular_disorder|metabolic_disorder|inflammatory_disease|autoimmune_diseases	joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0040502	glucocorticoid deficiency 5	endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology|pediatric	adrenal_gland_disease|metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0040503	blepharocheilodontic syndrome 2	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|disorder_of_visual_system|syndromic_disease	other	disorder_of_visual_system|disorder_of_development_or_morphogenesis|disorder_of_orbital_region|syndromic_disease|hereditary_disease|integumentary_system_disorder	genetics_and_genomics|ophthalmology|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0040566	inherited glutathione metabolism disease	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	inherited|genetics_and_genomics	inherited_disease_is_not_listed_but_one_possible_fitting_category_is__metabolic_disorder|metabolic_disorder	metabolic_disorder|liver_disorder	false	false	false	false	high
MONDO:0040653	autosomal recessive ocular albinism	hereditary_disease|disorder_of_visual_system|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|pediatric|ophthalmology	genetic_disease|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0040654	autosomal dominant oculocutaneous albinism	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	dermatology|genetics_and_genomics|ophthalmology	anemia|metabolic_disorder|autoimmune_diseases	skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0040671	class V glucose-6-phosphate dehydrogenase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|hematology|endocrinology	metabolic_disorder|anemia	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0040673	malignant peritoneal germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	reproductive_system_disorder	false	true	false	false	high
MONDO:0040674	orgasm disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry|urology	neurodegenerative_disease|mental_health_disorder	muscle_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0040675	myofibroblastoma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	genetics_and_genomics|oncology|pathology	cancer	muscle_disorder|lymphatic_disorder	false	true	false	false	low
MONDO:0040676	great vessel cancer	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiothoracic|oncology	cardiovascular_disorder|cancer	vascular_disorder|heart_disorder	false	true	false	false	high
MONDO:0040677	invasive carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|hepatology|hematology|urology	invasive_carcinoma|cancer	liver_disorder|lung_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0040678	infiltrating urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	true	very_high
MONDO:0040679	urothelial carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	cancer|urothelial_carcinoma	urinary_tract_disorder|kidney_disorder	false	true	false	true	high
MONDO:0040698	subacute bursitis	inflammatory_disease|musculoskeletal_system_disorder	other	acute_disease|inflammatory_disease|musculoskeletal_system_disorder	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	muscle_disorder|joint_disorder	false	false	false	true	medium
MONDO:0040699	necrotizing scleritis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	false	false	false	false	high
MONDO:0040700	orbital dermoid cyst	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease|disorder_of_orbital_region	ophthalmology|dermatology|pediatric|oncology	cancer|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	true	low
MONDO:0040728	Campylobacter fetus infectious disease	inflammatory_disease|digestive_system_disorder|infectious_disease	infectious_disease	digestive_system_disorder|infectious_disease|inflammatory_disease	pediatric|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0040732	Pseudomonas aeruginosa infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0040753	latent tuberculosis infection	infectious_disease	infectious_disease	infectious_disease	pulmonology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|lung_disorder|immune_disorder	true	false	false	true	medium
MONDO:0040870	primary polydipsia	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	endocrinology|renal_medicine	adrenal_gland_disease|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0040871	psychogenic polydipsia	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0040872	non-psychogenic polydipsia	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	endocrinology|renal_medicine	autoimmune_diseases|metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0040922	latent early syphilis	infectious_disease|reproductive_system_disorder	infectious_disease	reproductive_system_disorder|infectious_disease	dermatology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|ear_disorder|vascular_disorder|reproductive_system_disorder|skin_disorder	true	false	false	true	low
MONDO:0040923	late latent syphilis	infectious_disease|reproductive_system_disorder	infectious_disease	reproductive_system_disorder|infectious_disease	neurology|dermatology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	vascular_disorder|immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0040925	latent yaws	infectious_disease|reproductive_system_disorder	infectious_disease	reproductive_system_disorder|infectious_disease	pediatric|rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder|skin_disorder	true	false	false	true	medium
MONDO:0040998	Pasteurella multocida infectious disease	infectious_disease	infectious_disease	infectious_disease	otolaryngology|pediatric	inflammatory_disease|autoimmune_diseases	nose_disorder|ear_disorder|throat_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0041052	postherpetic neuralgia	nervous_system_disorder	other	post_infectious_disorder|nervous_system_disorder	dermatology|neurology	inflammatory_disease|autoimmune_diseases	nerve_disorder|skin_disorder	false	false	false	false	high
MONDO:0041086	mixed anxiety and depressive disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	mental_health_disorder|mixed_anxiety_and_depressive_disorder	brain_disorder|mental_health_disorder	false	false	false	true	high
MONDO:0041093	central retinal vein occlusion with macular edema	cardiovascular_disorder|nervous_system_disorder|disorder_of_visual_system	cardiovascular_disorder	disorder_of_orbital_region|cardiovascular_disorder|nervous_system_disorder|disorder_of_visual_system	neurology|ophthalmology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	vascular_disorder|eye_disorder	false	false	false	true	high
MONDO:0041095	malignant otitis externa caused by Pseudomonas aeruginosa	otorhinolaryngologic_disease|inflammatory_disease|auditory_system_disorder|infectious_disease	infectious_disease	post_infectious_disorder|auditory_system_disorder|otorhinolaryngologic_disease|inflammatory_disease|infectious_disease	pulmonology|infectious_diseases|otolaryngology	inflammatory_disease|cancer	ear_disorder|throat_disorder	true	false	false	true	high
MONDO:0041114	peripheral ischemia	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|cardiology|vascular_disease_is_not_listed_so_closest_would_be_cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder	false	false	false	true	high
MONDO:0041154	disorder of neck of urinary bladder	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	urinary_system_issue|urological_disorder|genitourinary_disorder	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0041167	carcinoid crisis	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	cardiology|oncology	adrenal_gland_disease|cancer|cardiovascular_disorder	lung_disorder|endocrine_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0041182	polymorphic light eruption	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|radiation_induced_disorder|inflammatory_disease	dermatology|genetics_and_genomics	inflammatory_disease|allergy|autoimmune_diseases	liver_disorder|skin_disorder	false	false	false	true	low
MONDO:0041186	Rowell syndrome	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	immune_system_disorder|connective_tissue_disorder	allergy_and_immunology|dermatology|immunology|pediatric	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder|vascular_disorder|skin_disorder|joint_disorder	false	false	false	false	high
MONDO:0041259	diphtheritic myocarditis	inflammatory_disease|cardiovascular_disorder|musculoskeletal_system_disorder|infectious_disease	cardiovascular_disorder|infectious_disease	cardiovascular_disorder|inflammatory_disease|musculoskeletal_system_disorder|infectious_disease	cardiology|pediatric	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	heart_disorder|vascular_disorder	true	false	false	true	high
MONDO:0041261	disorder of acid-base balance	metabolic_disease	metabolic_disease	metabolic_disease	nephrology|renal_medicine	metabolic_disorder|acid_base_balance_is_closely_related_to_metabolic_functions	kidney_disorder|liver_disorder	false	false	false	true	medium
MONDO:0041284	primary motor cortex epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0041295	acute papillary necrosis	urinary_system_disorder	other	acute_disease|urinary_system_disorder	hematology|hepatology	metabolic_disorder|cancer|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	true	false	false	false	high
MONDO:0041366	acute epiglottitis	inflammatory_disease|otorhinolaryngologic_disease|respiratory_system_disorder	other	respiratory_system_disorder|otorhinolaryngologic_disease|acute_disease|inflammatory_disease	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	throttle_disorder|throat_disorder|nose_disorder	true	false	false	true	high
MONDO:0041403	toxic amblyopia	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	true	high
MONDO:0041447	metastatic malignant neoplasm in the colon	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology|gastroenterology	metastatic_malignant_neoplasm_in_the_colon|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0041448	metastasis from malignant tumor of colon	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	malignancy|cancer|metastatic_cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0041526	pregnancy disorder with abortive outcome	obstetric_disorder	other	obstetric_disorder	obstetrics_and_gynecology	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	pregnancy_disorder|reproductive_system_disorder	true	false	false	false	very_high
MONDO:0041535	mesenteric lymphadenitis due to Yersinia infection	infectious_disease|inflammatory_disease|immune_system_disorder	infectious_disease	immune_system_disorder|inflammatory_disease|infectious_disease	pediatric|gastroenterology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	medium
MONDO:0041536	Far-East scarlet-like fever	infectious_disease	infectious_disease	infectious_disease	tropical_medicine|infectious_diseases|pediatric	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder	true	false	false	false	medium
MONDO:0041656	ST-elevation myocardial infarction	cardiovascular_disorder	cardiovascular_disorder	acute_disease|cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	very_high
MONDO:0041751	multibacillary leprosy	infectious_disease	infectious_disease	infectious_disease	dermatology|infectious_diseases	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0041752	paucibacillary leprosy	infectious_disease	infectious_disease	infectious_disease	pulmonology|dermatology|hematology|renal_medicine|immunology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0041755	twin reversal arterial perfusion syndrome	hematologic_disorder|immune_system_disorder	anemia	hematologic_disorder|immune_system_disorder	cardiology|obstetrics_and_gynecology|pediatrics	prenatal_condition|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0041775	intraoperative floppy iris syndrome	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|anemia	eye_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0041806	drug-resistant tuberculosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|infectious_diseases	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder|lung_disorder	true	false	false	true	very_high
MONDO:0041825	bacterial meningitis caused by gram-negative bacteria	infectious_disease|nervous_system_disorder|inflammatory_disease	infectious_disease	inflammatory_disease|nervous_system_disorder|infectious_disease	pediatric|neurology	bacterial_meningitis|inflammatory_disease	spinal_disorder|lymphatic_disorder|immune_disorder|brain_disorder	true	false	false	true	high
MONDO:0041850	pneumonia caused by gram negative bacteria	infectious_disease|respiratory_system_disorder|inflammatory_disease	infectious_disease	inflammatory_disease|infectious_disease|respiratory_system_disorder	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0041879	staphylococcus aureus pneumonia	infectious_disease|respiratory_system_disorder|inflammatory_disease	infectious_disease	infectious_disease|respiratory_system_disorder|inflammatory_disease	respiratory|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|throat_disorder|immune_disorder	true	false	false	true	high
MONDO:0041903	gonococcal infection of joint	inflammatory_disease|infectious_disease|reproductive_system_disorder|musculoskeletal_system_disorder	infectious_disease	reproductive_system_disorder|inflammatory_disease|musculoskeletal_system_disorder|infectious_disease	urology|rheumatology	autoimmune_diseases|inflammatory_disease	joint_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0041959	fibrosis of bile duct	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0041996	thallium poisoning	poisoning	other	poisoning	hematology|neurology	metabolic_disorder|neurodegenerative_disease|cardiovascular_disorder	liver_disorder|kidney_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0042233	disseminated candidiasis	infectious_disease	infectious_disease	infectious_disease	pediatrics|dermatology|immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	true	very_high
MONDO:0042370	Yersinia enterocolitica infectious disease	infectious_disease	infectious_disease	infectious_disease	gastroenterology|renal_medicine|pediatrics	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0042433	mycotic endocarditis	cardiovascular_disorder|infectious_disease|inflammatory_disease	cardiovascular_disorder|infectious_disease	cardiovascular_disorder|inflammatory_disease|infectious_disease	cardiovascular|cardiology	cancer|inflammatory_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	true	false	false	true	high
MONDO:0042451	endomyometritis	reproductive_system_disorder|inflammatory_disease	other	inflammatory_disease|reproductive_system_disorder	endocrinology|gynecology_is_not_in_the_list_so_use_obstetrics_and_gynecology_instead|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0042452	tertiary lesion of yaws	reproductive_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease	pediatric|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|joint_disorder|bone_disorder	true	false	false	true	medium
MONDO:0042458	Trichinella spiralis infectious disease	infectious_disease|inflammatory_disease|musculoskeletal_system_disorder	infectious_disease	inflammatory_disease|musculoskeletal_system_disorder|infectious_disease	gastroenterology|parasitology_is_not_in_the_list_so_gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|muscle_disorder	true	false	false	true	low
MONDO:0042484	disseminated sporotrichosis	infectious_disease	infectious_disease	infectious_disease	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0042485	infective arthritis	musculoskeletal_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	inflammatory_disease|infectious_disease|musculoskeletal_system_disorder	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder	true	false	false	true	medium
MONDO:0042486	polyposis syndrome, hereditary mixed, 1	hereditary_disease|digestive_system_disorder|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|hereditary_disease|syndromic_disease	gastroenterology|oncology|genetics_and_genomics|pediatric	metabolic_disorder|inflammatory_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0042487	uterine cervix carcinoma in situ	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	oncology|obstetrics_and_gynecology	cancer	reproductive_system_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	low
MONDO:0042488	Cestode infectious disease	infectious_disease	infectious_disease	infectious_disease	parasitology_is_not_in_the_list_but_gastroenterology|hepatology|pediatric	parasitic_disease|worm_infection|infectious_disease	gastrointestinal_disorder|infectious_disease|liver_disorder	true	false	false	true	low
MONDO:0042490	neutropenia, severe congenital, 1, autosomal dominant	hematologic_disorder|immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0042491	cervical squamous intraepithelial neoplasia	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	cancer	reproductive_system_disorder|throat_disorder	false	false	false	true	medium
MONDO:0042493	gastric non-hodgkin lymphoma	hematologic_disorder|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder|hematologic_disorder	gastroenterology|oncology|hematology	inflammatory_disease|cancer|autoimmune_diseases	lymphatic_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0042494	childhood malignant melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	oncology|dermatology|pediatric	childhood_malignant_melanoma_can_also_fit_in_the_category__childhood_cancer__which_is_a_subset_of_cancer_but_since__cancer__is_more_general__it_will_be_considered_as_the_best_fitting_category_here|cancer	skin_disorder	false	true	false	false	high
MONDO:0042495	arteriosclerotic retinopathy	nervous_system_disorder|disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_visual_system|disorder_of_orbital_region|nervous_system_disorder	cardiology|ophthalmology	cardiovascular_disorder|metabolic_disorder	eye_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0042496	ergotism	poisoning|infectious_disease	infectious_disease	infectious_disease|poisoning	psychiatry|neurology|pulmonology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	vascular_disorder|upper_gastrointestinal_disorder|muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0042497	mycotoxicosis	poisoning|infectious_disease	infectious_disease	infectious_disease|poisoning	gastroenterology|pulmonology|hepatology	cancer	lower_gastrointestinal_disorder|liver_disorder	true	false	false	false	high
MONDO:0042498	Ruzicka-Goerz-Anton syndrome	syndromic_disease	other	syndromic_disease	dermatology|neurology	neurodegenerative_disease|autoimmune_diseases	skin_disorder|liver_disorder	false	false	false	false	high
MONDO:0042499	benign familial neonatal-infantile seizures 1	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	neonatal_infantile_seizures|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0042600	Sammartino-Decreccio syndrome	syndromic_disease	other	syndromic_disease	endocrinology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0042601	Samson-Gardner syndrome	syndromic_disease	other	syndromic_disease	endocrinology|dermatology|genetics_and_genomics|pediatrics	adrenal_gland_disease|metabolic_disorder	skin_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0042602	Samson-Viljoen syndrome	syndromic_disease	other	syndromic_disease	dermatology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	skin_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0042603	Sanderson-Fraser syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0042604	Sandhaus-Ben-Ami syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics|cardiology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0042605	Y chromosome infertility due to DAZ1 deletion	hereditary_disease|chromosomal_disorder|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease|chromosomal_disorder	urology|genetics_and_genomics	genetic_disorder|infertility_condition|reproductive_disease	chromosomal_disorder|genetic_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0042705	prostatic malacoplakia associated with prostatic abscess	syndromic_disease	other	syndromic_disease	urology|renal_medicine	inflammatory_disease|cancer|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	false	medium
MONDO:0042717	Saul-Wilkes-Stevenson syndrome	syndromic_disease	other	syndromic_disease	rheumatology|otolaryngology|dermatology	inflammatory_disease|autoimmune_diseases	joint_disorder|spinal_disorder|vascular_disorder|liver_disorder|eye_disorder|skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0042726	macrogyria, pseudobulbar palsy and intellectual disability	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|intellectual_disability|neurodegenerative_disease	spinal_disorder|intellectual_disability|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0042727	sacrococcygeal teratoma	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	oncology|pediatric	cancer	spinal_disorder|sacroiliac_region_disorder_is_implied_but_no_specific_category_exists_so_omitted|reproductive_system_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0042911	Schwartz-Cohen-addad-Lambert syndrome	syndromic_disease	other	syndromic_disease	neurology|ophthalmology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|immune_disorder|eye_disorder	false	false	false	false	medium
MONDO:0042912	Schlegelberger-Grote syndrome	syndromic_disease	other	syndromic_disease	immunology|genetics_and_genomics|pediatrics	autoimmune_diseases|metabolic_disorder	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0042913	Schrander-stumpel-Theunissen-Hulsmans syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	lymphatic_disorder|bone_disorder	false	false	false	false	none
MONDO:0042956	Saal-Bulas syndrome	syndromic_disease	other	syndromic_disease	neurology|psychiatry	neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0042960	Sackey-Sakati-Aur syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder|lower_gastrointestinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0042961	sacral hemangiomas multiple congenital abnormalities	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|oncology|hematology|genetics_and_genomics|pediatric	metabolic_disorder|congenital_abnormalities	skin_disorder|vascular_disorder	false	false	false	false	high
MONDO:0042962	Slti-Salem syndrome	syndromic_disease|integumentary_system_disorder|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|syndromic_disease|endocrine_system_disorder|integumentary_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	blood_bone_marrow_disorder|kidney_disorder|liver_disorder|immune_disorder	false	false	false	false	high
MONDO:0042963	wandering spleen	hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder	hepatology|hematology|gastroenterology	metabolic_disorder|inflammatory_disease	lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0042964	Machado-Joseph disease type 4	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0042966	inherited mitral valve disease	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|genetics_and_genomics	inherited_disease|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0042967	rheumatic disease of mitral valve	cardiovascular_disorder|connective_tissue_disorder	cardiovascular_disorder	connective_tissue_disorder|cardiovascular_disorder	cardiology|rheumatology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	heart_disorder|joint_disorder	true	false	false	true	medium
MONDO:0042968	partial duplication of chromosome 12	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	kidney_disorder	false	false	false	false	low
MONDO:0042969	partial duplication of the long arm of chromosome 12	chromosomal_disorder	other	chromosomal_disorder	oncology|genetics_and_genomics|pediatric	genetic_disorder|neurodegenerative_disease|chromosomal_abnormality|developmental_disorder	skeletal_system_disorder|bone_disorder	false	false	false	false	high
MONDO:0042970	disorder of glutamate decarboxylase	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0042971	congenital herpes virus infection	infectious_disease|disorder_of_development_or_morphogenesis	infectious_disease	infectious_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|obstetrics_and_gynecology|pediatric	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	false	medium
MONDO:0042972	meningococcemia	infectious_disease	infectious_disease	infectious_disease	allergy_and_immunology|hematology|pediatric|neurology	inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder|vascular_disorder	true	false	false	true	high
MONDO:0042973	familial osteosclerosis	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics	genetic_disorder|metabolic_disorder	vascular_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0042974	parainfluenza virus type 3 infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|throat_disorder|lung_disorder	true	false	false	false	medium
MONDO:0042976	vitamin B deficiency	nutritional_disorder	other	nutritional_disorder	hematatology|endocrinology|gastroenterology	metabolic_disorder|anemia	endocrine_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0042977	trichoepithelioma, multiple familial, 1	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	oncology|genetics_and_genomics	cancer|autoimmune_diseases	skin_disorder	false	false	false	false	low
MONDO:0042979	hypokalemic periodic paralysis, type 1	nutritional_disorder|metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|nutritional_disorder|metabolic_disease	renal_medicine|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0042980	Westphal disease	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|neurology	neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0042981	aortic valve stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0042982	GATA2 deficiency with susceptibility to MDS/AML	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	hematology|genetics_and_genomics	cancer|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0042983	neurocutaneous syndrome	nervous_system_disorder	other	nervous_system_disorder	dermatology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0043003	familial acanthosis nigricans	integumentary_system_disorder|hereditary_disease|inflammatory_disease	other	hereditary_disease|integumentary_system_disorder|inflammatory_disease	genetics_and_genomics|dermatology	metabolic_disorder|adrenal_gland_disease	skin_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0043004	Weil's disease	infectious_disease	infectious_disease	infectious_disease	hepatology|rheumatology|hematology	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder	true	false	false	true	high
MONDO:0043009	hereditary lethal multiple congenital anomalies/dysmorphic syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	congenital_anomalies|metabolic_disorder	kidney_disorder|joint_disorder|lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0043069	Zerres Rietschel Majewski syndrome	endocrine_system_disorder|syndromic_disease	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0043071	Zazam Sheriff Phillips syndrome	disorder_of_development_or_morphogenesis|disorder_of_visual_system|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis|disorder_of_orbital_region|disorder_of_visual_system	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0043073	Zadik-Barak-Levin syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	skeletal_dysplasia|joint_disorder	false	false	false	false	high
MONDO:0043075	neuroaxonal dystrophy renal tubular acidosis	metabolic_disease|nervous_system_disorder|urinary_system_disorder	metabolic_disease|neurodegenerative_disease	urinary_system_disorder|nervous_system_disorder|metabolic_disease	neurology|renal_medicine|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|kidney_disorder|muscle_disorder	false	false	false	false	high
MONDO:0043077	weinstein kliman scully syndrome	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|metabolic_disease|syndromic_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|reproductive_system_disorder|syndromic_disease|metabolic_disease|hereditary_disease	genetics_and_genomics|endocrinology|pediatrics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	endocrine_disorder|eye_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0043083	coronal synostosis, syndactyly and jejunal atresia	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	gastroenterology|genetics_and_genomics|pediatric	genetic_disorder__note__this_is_a_specific_category_in_the_list_that_would_be_more_fitting_for_the_given_disease|metabolic_disorder	upper_gastrointestinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0043085	chromosome 1, uniparental disomy 1q12 q21	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatrics	genetic_disorder|mental_health_disorder|neurodegenerative_disease	other____corrected__spinal_disorder|spinal_disorder|chromosome_abnormality	false	false	false	false	high
MONDO:0043087	thickened earlobes with conductive deafness from incus-stapes abnormalities	syndromic_disease	other	syndromic_disease	otolaryngology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	ear_disorder|bone_disorder	false	false	false	false	low
MONDO:0043089	acute posterior multifocal placoid pigment epitheliopathy	cardiovascular_disorder|disorder_of_visual_system|inflammatory_disease	cardiovascular_disorder	acute_disease|inflammatory_disease|cardiovascular_disorder|disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0043094	ichthyosis, follicular	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0043096	holoacardius amorphus	disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiology|cardiothoracic|hematology	anemia|cardiovascular_disorder	heart_disorder|blood_bone_marrow_disorder	true	false	false	false	none
MONDO:0043099	Hordnes Engebretsen Knudtson syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|otolaryngology	metabolic_disorder|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	ear_disorder|bone_disorder	false	false	false	false	high
MONDO:0043101	hypothalamic dysfunction	nervous_system_disorder	other	nervous_system_disorder	endocrinology|neurology	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	endocrine_disorder|brain_disorder	false	false	false	false	high
MONDO:0043103	hypothyroidism due to iodide transport defect	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	endocrine_disorder	false	false	false	true	high
MONDO:0043106	ichthyosis linearis circumflexa	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	pediatric|dermatology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0043108	infantile striato thalamic degeneration	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|neurology	infantile_striatothalamic_degeneration_is_not_clearly_related_to_another_category|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0043110	jones hersh yusk syndrome	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|neurology|pediatrics	metabolic_disorder|inflammatory_disease|autoimmune_diseases|anemia	joint_disorder|liver_disorder|bone_disorder|kidney_disorder	true	false	false	false	medium
MONDO:0043112	lachiewicz sibley syndrome	urinary_system_disorder	other	urinary_system_disorder	rheumatology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	upper_gastrointestinal_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0043114	Landy-Donnai syndrome	syndromic_disease	other	syndromic_disease	dermatology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	skin_disorder|eye_disorder|ear_disorder|bone_disorder	false	false	false	false	high
MONDO:0043116	Iida Kannari syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|joint_disorder|liver_disorder|immune_disorder|ear_disorder|bone_disorder|kidney_disorder	false	false	false	false	high
MONDO:0043120	male pseudohermaphroditism due to defective lh molecule	reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	urology|endocrinology|genetics_and_genomics	endocrine_disorder|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0043123	massa casaer ceulemans syndrome	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	other____actually_massa_casaer_ceulemans_syndrome_is_a_condition_affecting_the_muscles_of_the_face|muscle_disorder	false	false	false	false	high
MONDO:0043125	mcpherson robertson cammarano syndrome	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0043127	mehta lewis patton syndrome	hereditary_disease|musculoskeletal_system_disorder|disorder_of_visual_system|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	mouth_disorder|hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0043129	merlob grunebaum reisner syndrome	syndromic_disease	other	syndromic_disease	urology|genetics_and_genomics|pediatric	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	kidney_disorder|reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0043131	Michels Caskey syndrome	reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	joint_disorder|eye_disorder|skin_disorder|brain_disorder|muscle_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0043133	microcephaly micropenis convulsions	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	genetics_and_genomics|neurology|pediatric	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder|brain_disorder|muscle_disorder	true	false	false	false	high
MONDO:0043135	microcephaly microphthalmos blindness	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	true	false	false	false	high
MONDO:0043137	isolated microcephaly	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0043139	microcephaly sparse hair intellectual disability seizures	psychiatric_disorder|integumentary_system_disorder|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	integumentary_system_disorder|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	neurology|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	seizures|brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0043141	microdontia hypodontia short stature	hereditary_disease|musculoskeletal_system_disorder|endocrine_system_disorder	endocrine_system_disorder	mouth_disorder|hereditary_disease|musculoskeletal_system_disorder|endocrine_system_disorder	endocrinology|genetics_and_genomics|pediatric	anemia|autoimmune_diseases|metabolic_disorder	teeth_disorder|bone_disorder	false	false	false	false	medium
MONDO:0043143	microphthalmia microtia fetal akinesia	hereditary_disease|syndromic_disease|disorder_of_visual_system|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease|disorder_of_orbital_region|disorder_of_visual_system	genetics_and_genomics|ophthalmology|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	ear_disorder|eye_disorder	false	false	false	false	high
MONDO:0043152	negative rheumatoid factor polyarthritis	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder	false	false	false	true	high
MONDO:0043154	neonatal ovarian cyst	reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|pediatric	metabolic_disorder|inflammatory_disease	reproductive_system_disorder	false	false	false	true	medium
MONDO:0043156	nephrotic syndrome ocular anomalies	syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|syndromic_disease	urology|pediatric|nephrology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	kidney_disorder|eye_disorder	false	false	false	true	medium
MONDO:0043162	pagon stephan syndrome	endocrine_system_disorder|syndromic_disease|reproductive_system_disorder|nervous_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|nervous_system_disorder|syndromic_disease|endocrine_system_disorder|reproductive_system_disorder	rheumatology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	liver_disorder|kidney_disorder|joint_disorder|eye_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0043164	palmer pagon syndrome	nervous_system_disorder	other	nervous_system_disorder	pediatric|dermatology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|bone_disorder	false	false	false	false	high
MONDO:0043166	pancreatic lipomatosis duodenal stenosis	musculoskeletal_system_disorder|digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor|endocrine_system_disorder	musculoskeletal_system_disorder|connective_tissue_disorder|digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	pediatric|gastroenterology|hepatology	metabolic_disorder|cancer|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0043168	panostotic fibrous dysplasia	musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|connective_tissue_disorder	anemia|cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	orthopaedic|endocrinology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|anemia|inflammatory_disease	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0043170	Pavone Fiumara Rizzo syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	joint_disorder|bone_disorder|liver_disorder	false	false	false	false	high
MONDO:0043172	pfeiffer rockelein syndrome	syndromic_disease	other	syndromic_disease	pulmonology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0043174	Pfeiffer Tietze Welte syndrome	syndromic_disease	other	syndromic_disease	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|kidney_disorder|immune_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	high
MONDO:0043176	phosphoribosylpyrophosphate synthetase deficiency	syndromic_disease|metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease|syndromic_disease	pediatrics|genetics_and_genomics	metabolic_disorder|genetic_disorder	enzyme_deficiency|liver_disorder	false	false	false	false	high
MONDO:0043179	piepkorn karp hickok syndrome	syndromic_disease	other	syndromic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	kidney_disorder|lower_gastrointestinal_disorder	false	false	false	false	none
MONDO:0043183	podder-tolmie syndrome	syndromic_disease	other	syndromic_disease	pediatric|neurology|endocrinology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	immune_disorder|bone_disorder	false	false	false	false	high
MONDO:0043185	pointer syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	immune_disorder|brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0043191	radial defect robin sequence	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	muscle_disorder|joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0043193	richieri-costa guion-almeida cohen syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0043195	Rubinstein Taybi like syndrome	syndromic_disease	other	syndromic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|eye_disorder|brain_disorder|bone_disorder	false	false	false	false	high
MONDO:0043197	ruvalcaba churesigaew myhre syndrome	syndromic_disease	other	syndromic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|joint_disorder|bone_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0043199	short limb dwarf lethal colavita kozlowski type	syndromic_disease	other	syndromic_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disease	joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0043206	trichostasis spinulosa	disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder	neurology|dermatology	inflammatory_disease|neurodegenerative_disease	skin_disorder|bone_disorder	false	false	false	false	low
MONDO:0043207	urethral obstruction sequence	disorder_of_development_or_morphogenesis|urinary_system_disorder	other	disorder_of_development_or_morphogenesis|urinary_system_disorder	urology|pediatric	urinary_system_disorder|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0043209	albinism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	dermatology|genetics_and_genomics|pediatric|ophthalmology	anemia|autoimmune_diseases|metabolic_disorder	bone_bone_marrow_disorder|eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0043218	neurovascular disorder	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	cardiology|neurology	inflammatory_disease|cardiovascular_disorder|neurodegenerative_disease|autoimmune_diseases	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0043219	migraine with brainstem aura	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	psychiatry|neurology	inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0043224	multi-infarct dementia	cardiovascular_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|cardiovascular_disorder	nervous_system_disorder|psychiatric_disorder|cardiovascular_disorder	neurology|cardiology	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	true	high
MONDO:0043226	postpartum amenorrhea-galactorrhea syndrome	endocrine_system_disorder|nervous_system_disorder|reproductive_system_disorder|metabolic_disease|obstetric_disorder|breast_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder|metabolic_disease	nervous_system_disorder|metabolic_disease|obstetric_disorder|reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis|breast_disorder	obstetrics_and_gynecology|endocrinology	endocrine_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0043230	ciguatera fish poisoning	poisoning	other	poisoning	toxicology|gastroenterology	metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0043233	exfoliative dermatitis	inflammatory_disease|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease	dermatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	liver_disorder|skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0043237	glossodynia	nervous_system_disorder	other	nervous_system_disorder|mouth_disorder	neurology|otolaryngology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	teeth_disorder|throat_disorder	false	false	false	false	medium
MONDO:0043240	hemophilic arthropathy	musculoskeletal_system_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|inflammatory_disease	hematology|rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0043243	leukoplakia	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	dermatology|hematology	inflammatory_disease|cancer	skin_disorder|oral_disorder	false	false	false	false	medium
MONDO:0043247	Mallory-Weiss syndrome	syndromic_disease	other	syndromic_disease	gastroenterology|hepatology	inflammatory_disease|gastrointestinal_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0043251	odontoma	cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor	pediatric|orthopaedic|oncology	cancer|bone_disease___note__i_corrected_the_output_to_use_the_correct_terminology_for_the_category_of_a_dental_condition_like_odontoma	teeth_disorder|bone_disorder	false	false	false	true	low
MONDO:0043254	papular urticaria	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder	dermatology|allergy_and_immunology	allergy|inflammatory_disease|autoimmune_diseases	skin_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	low
MONDO:0043257	pemphigus and fogo selvagem	immune_system_disorder|integumentary_system_disorder|inflammatory_disease	autoimmune_disease	inflammatory_disease|immune_system_disorder|integumentary_system_disorder	dermatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder_skin_disorder	false	false	false	true	high
MONDO:0043264	post-traumatic epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0043267	rheumatoid vasculitis	cardiovascular_disorder|musculoskeletal_system_disorder|immune_system_disorder|connective_tissue_disorder|inflammatory_disease	autoimmune_disease|cardiovascular_disorder	connective_tissue_disorder|inflammatory_disease|musculoskeletal_system_disorder|cardiovascular_disorder|immune_system_disorder	rheumatology|hematology	inflammatory_disease|autoimmune_diseases	joint_disorder|vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0043275	TORCH syndrome	syndromic_disease	other	post_infectious_disorder|syndromic_disease	pediatric|dermatology|neurology	inflammatory_disease|autoimmune_diseases	eye_disorder|skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0043277	mosaic trisomy 6	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|cancer	spinal_disorder|brain_disorder	false	false	false	false	low
MONDO:0043280	Wallerian degeneration	nervous_system_disorder	other	nervous_system_disorder	neurology	inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0043283	silicosiderosis	respiratory_system_disorder	other	respiratory_system_disorder	occupational_diseases__implied_by_silicosis__is_closely_related_to_other_category_in_list__however___other__is_typically_not_recommended|pulmonology	inflammatory_disease|metabolic_disorder	liver_disorder|lung_disorder	false	false	false	false	high
MONDO:0043287	superior vena cava syndrome	syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease	cardiothoracic|pulmonology|oncology	inflammatory_disease|cancer	upper_gastrointestinal_disorder|lung_disorder|lymphatic_disorder|vascular_disorder	false	false	false	false	high
MONDO:0043291	Rokitansky-Aschoff sinuses of the gallbladder	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|cancer|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0043294	linear scleroderma	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	connective_tissue_disorder|immune_system_disorder	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|muscle_disorder|joint_disorder	false	false	false	true	medium
MONDO:0043297	vibrio vulnificus infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|gastroenterology	infectious_disease|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|liver_disorder	true	false	false	true	high
MONDO:0043300	actinic cheilitis	inflammatory_disease	other	mouth_disorder|inflammatory_disease	dermatology|oncology	inflammatory_disease|cancer	upper_gastrointestinal_disorder|skin_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0043303	hyperacusis	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder|otorhinolaryngologic_disease	psychiatric_disorder	psychiatric_disorder|otorhinolaryngologic_disease|auditory_system_disorder|nervous_system_disorder	neurology|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0043310	amaurosis fugax	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	vascular_disorder|eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0043314	aquarium granuloma	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease	dermatology|pediatric	inflammatory_disease|autoimmune_diseases|cancer	immune_disorder|liver_disorder|skin_disorder	true	false	false	true	medium
MONDO:0043317	amyopathic dermatomyositis	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease|idiopathic_disease|musculoskeletal_system_disorder|connective_tissue_disorder	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|muscle_disorder|skin_disorder	false	false	false	false	high
MONDO:0043320	piriformis syndrome	nervous_system_disorder|syndromic_disease	other	syndromic_disease|nervous_system_disorder	orthopaedic|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	true	low
MONDO:0043327	cerebrospinal fluid leak	nervous_system_disorder	other	nervous_system_disorder	neurology|neurosurgery	neurological_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0043330	Mirizzi syndrome	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	gastroenterology|urology|general_surgery	inflammatory_disease|abdominal_disease	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0043339	lathyrism	poisoning	other	poisoning	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0043343	Chilaiditi syndrome	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0043346	progressive transformation of germinal centers	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	immunology|hematology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0043349	intravascular papillary endothelial hyperplasia	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cardiothoracic|pulmonology|cardiology|renal_medicine	cardiovascular_disorder|vascular_disease|inflammatory_disease___note__i_corrected_the_original_list_to_match_the_provided_category_name_exactly__which_is_intravascular_papillary_endothelial_hyperplasia	kidney_disorder|vascular_disorder	false	false	false	false	low
MONDO:0043352	fournier gangrene	reproductive_system_disorder|infectious_disease	infectious_disease	infectious_disease|reproductive_system_disorder	orthopaedic|vascular_surgery|emergency_medicine|general_surgery|pediatric	inflammatory_disease|autoimmune_diseases	vascular_disorder|lower_gastrointestinal_disorder|skin_disorder	true	false	false	true	very_high
MONDO:0043355	collagenous gastritis	inflammatory_disease|digestive_system_disorder	other	inflammatory_disease|digestive_system_disorder	gastroenterology|rheumatology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0043358	engraftment syndrome	syndromic_disease	other	disease_related_to_transplantation|syndromic_disease	oncology|hematology	inflammatory_disease|cancer|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0043361	May-Thurner syndrome	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|vascular____i_corrected_the_final_answer_to_reflect_that_may_thurner_syndrome_is_a_condition_related_to_blood_flow_and_pressure_in_the_legs__which_would_be_more_accurately_categorized_under__vascular___even_though_it_wasn_t_listed_directly	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|joint_disorder	false	false	false	false	medium
MONDO:0043364	eosinophil peroxidase deficiency	hematologic_disorder|hereditary_disease|immune_system_disorder	other	hereditary_disease|hematologic_disorder|immune_system_disorder	genetics_and_genomics|allergy_and_immunology|hematology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	low
MONDO:0043370	secondary adrenal insufficiency	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	endocrinology|neurology|pediatric	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	endocrine_disorder|secondary_adrenal_insufficiency_is_not_in_the_list_but_its_a_subset_of_endocrine_disorder_so_the_answer_remains_endocrine_disorder	false	false	false	true	high
MONDO:0043373	sudden sensorineural hearing loss	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|acute_disease|nervous_system_disorder	neurology|otolaryngology	neurodegenerative_disease|autoimmune_diseases	ear_disorder|vascular_disorder|brain_disorder	false	false	false	true	high
MONDO:0043377	juvenile spondyloarthropathy	connective_tissue_disorder|musculoskeletal_system_disorder|inflammatory_disease|immune_system_disorder	autoimmune_disease	musculoskeletal_system_disorder|connective_tissue_disorder|inflammatory_disease|immune_system_disorder	orthopaedic|rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	joint_disorder|spinal_disorder	false	false	false	true	high
MONDO:0043424	digestive system infectious disorder	digestive_system_disorder|infectious_disease	infectious_disease	digestive_system_disorder|infectious_disease	hepatology|gastroenterology	digestive_system_infectious_disorder|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0043452	chromosome 8, trisomy	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|chromosomal_disorder	heart_disorder|upper_gastrointestinal_disorder|bone_disorder|kidney_disorder|immune_disorder	false	false	false	false	medium
MONDO:0043455	humoral hypercalcemia of malignancy	cancer_or_benign_tumor|metabolic_disease|hematologic_disorder|syndromic_disease	cancer_or_benign_tumor|metabolic_disease	syndromic_disease|hematologic_disorder|metabolic_disease|cancer_or_benign_tumor	renal_medicine|endocrinology|oncology	cancer|metabolic_disorder|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0043459	radiation-induced disorder	other	other		radiology|oncology	cancer|radiation_induced_disorder	lung_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0043465	achlorhydria	digestive_system_disorder	other	digestive_system_disorder	hepatology|gastroenterology|endocrinology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0043468	acne keloid	inflammatory_disease|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease	dermatology	autoimmune_diseases|inflammatory_disease	nose_disorder|skin_disorder|blood_bone_marrow_disorder|lymphatic_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0043472	ectopic ACTH secretion syndrome	endocrine_system_disorder|cancer_or_benign_tumor|syndromic_disease	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|syndromic_disease	endocrinology|neurology	autoimmune_diseases|adrenal_gland_disease	endocrine_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0043475	Adams-Stokes syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	neurology|cardiology	neurodegenerative_disease|cardiovascular_disorder	heart_disorder|brain_disorder	false	false	false	true	high
MONDO:0043479	adenoviridae infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric	autoimmune_diseases|inflammatory_disease|cancer	eye_disorder|respiratory_disorder__note__i_assume_you_meant_to_write__respiratory_disorder__instead_of__lung_disorder|immune_disorder	true	false	false	true	medium
MONDO:0043494	arteritis	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	rheumatology|cardiothoracic	autoimmune_diseases|inflammatory_disease	vascular_disorder|immune_disorder|joint_disorder	true	false	false	true	high
MONDO:0043510	brain injury	nervous_system_disorder|injury	other	nervous_system_disorder	neurology|psychiatry	neurodegenerative_disease|inflammatory_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0043512	traumatic encephalopathy	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|inflammatory_disease|traumatic_brain_injury	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0043523	cadmium poisoning	poisoning	other	poisoning	renal_medicine|cardiology|hematology	cardiovascular_disorder	vascular_disorder|kidney_disorder	false	false	false	true	high
MONDO:0043529	carcinoid heart disease	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	oncology|cardiology	cancer|cardiovascular_disorder	heart_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0043537	cluster headache syndrome	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	neurology|otolaryngology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder|brain_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0043541	viral conjunctivitis	inflammatory_disease|disorder_of_visual_system|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|pediatric	viral_conjunctivitis_is_not_in_the_original_list_so_it_will_not_be_included|inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	true	false	false	true	low
MONDO:0043543	iatrogenic disease		other		genetics_and_genomics	iatrogenic_disease_can_sometimes_be_related_to_improper_treatment_of_cardiovascular_disorders|inflammatory_disease|certain_treatments_can_trigger_autoimmune_reactions|improper_treatment_can_lead_to_inflammation|improper_treatment_or_medication_can_affect_mental_health|cardiovascular_disorder|mental_health_disorder|autoimmune_diseases	liver_disorder	false	false	false	false	high
MONDO:0043544	nosocomial infection	infectious_disease|iatrogenic_disease	infectious_disease	iatrogenic_disease|infectious_disease	allergy_and_immunology|general|pulmonology|pediatric	infectious_disease|inflammatory_disease	nosocomial_infection_is_often_caused_by_bacterial_infections_in_hospitals__which_can_also_be_linked_to_a_compromised_immune_system|immunedisorder	true	false	false	true	high
MONDO:0043549	crush syndrome	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|other__no__just_renal|nephrology	inflammatory_disease|cardiovascular_disorder|metabolic_disorder	muscle_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0043555	infantile diarrhea	inflammatory_disease|digestive_system_disorder|infectious_disease	infectious_disease	digestive_system_disorder|inflammatory_disease|acute_disease|infectious_disease	gastroenterology|pediatric	inflammatory_disease|gastrointestinal_disorder|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0043576	endarteritis	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	rheumatology|cardiothoracic|hematology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	vascular_disorder|immune_disorder	true	false	false	false	high
MONDO:0043579	enteritis	inflammatory_disease|digestive_system_disorder	other	inflammatory_disease|digestive_system_disorder	pediatric|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0043653	herpes labialis	infectious_disease	infectious_disease	mouth_disorder|infectious_disease	dermatology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	true	false	false	true	low
MONDO:0043678	chromosome inversion disorder	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	genetic_disorder|neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|chromosomal_abnormality	false	false	false	false	medium
MONDO:0043683	Leriche syndrome	syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder	renal_medicine|pulmonology|oncology|cardiothoracic|hematology	autoimmune_diseases|inflammatory_disease|cardiovascular_disorder	vascular_disorder|liver_disorder	false	false	false	true	medium
MONDO:0043693	alcoholic liver diseases	psychiatric_disorder|endocrine_system_disorder|digestive_system_disorder	psychiatric_disorder|endocrine_system_disorder	endocrine_system_disorder|psychiatric_disorder|digestive_system_disorder	gastroenterology|hepatology	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0043726	multiple organ dysfunction syndrome	syndromic_disease	other	syndromic_disease	neurology|renal_medicine|pulmonology	inflammatory_disease|cardiovascular_disorder	kidney_disorder|liver_disorder|lung_disorder	false	false	false	false	high
MONDO:0043731	lytic metastatic bone lesion	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|hematology|oncology	lytic_metastatic_bone_lesion_is_often_associated_with_a_spread_of_cancer_to_the_bones|cancer	bone_disorder|blood_bone_marrow_disorder|spinal_disorder	false	true	false	false	high
MONDO:0043735	osteoradionecrosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|radiation_induced_disorder	orthopaedic|oncology|rheumatology	inflammatory_disease|osteoporosis_is_close_but_incorrect_for_the_following_reason__it_can_also_be_categorized_under_cancer__given_that_it_s_caused_by_radiation|cancer	bone_disorder|spinal_disorder	false	false	false	true	high
MONDO:0043759	abdominal ectopic pregnancy	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology	gynecological_condition|obstetric_complication|miscarriage_risk	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0043762	tubal pregnancy	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology	inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	reproductive_system_disorder	false	false	false	false	medium
MONDO:0043765	presbycusis	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	neurology|otolaryngology	mental_health_disorder|neurodegenerative_disease	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0043768	thrombocytopenic purpura	immune_system_disorder|hematologic_disorder	other	hematologic_disorder|immune_system_disorder	hematology	inflammatory_disease|anemia|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0043771	radiodermatitis	integumentary_system_disorder|inflammatory_disease	other	integumentary_system_disorder|radiation_induced_disorder|inflammatory_disease	dermatology|radiation_oncology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0043775	respiratory paralysis	respiratory_system_disorder|nervous_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|respiratory_system_disorder|nervous_system_disorder	neurology|pulmonology	respiratory_paralysis_is_a_condition_that_can_be_caused_by_diseases_affecting_the_nervous_system_so_it_could_also_fit_in_neurodegenerative_disease_category__however__the_most_fitting_categorization_of_this_disease_would_be_neurological_disorder|neurodegenerative_disease	muscle_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0043777	rhinophyma	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|otolaryngology	inflammatory_disease|autoimmune_diseases	skin_disorder|nose_disorder	false	false	false	true	low
MONDO:0043783	sclerema neonatorum	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	skin_disorder|muscle_disorder	true	false	false	false	high
MONDO:0043786	serositis	inflammatory_disease	other	inflammatory_disease	nephrology|hematology|rheumatology	autoimmune_diseases|inflammatory_disease	liver_disorder|immune_disorder	true	false	false	false	medium
MONDO:0043789	serum sickness	immune_system_disorder	autoimmune_disease	immune_system_disorder	allergy_and_immunology|rheumatology	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	medium
MONDO:0043797	spinal cord injury	injury|nervous_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder	neurology|orthopaedic	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	joint_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0043836	tuberculosis, spinal	musculoskeletal_system_disorder|infectious_disease	infectious_disease	infectious_disease|musculoskeletal_system_disorder	pulmonology|neurology	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|spinal_disorder|lung_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0043839	ulcer disease	other	other		gastroenterology|hepatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0043862	voice disorders	respiratory_system_disorder	other	respiratory_system_disorder	pulmonary|otolaryngology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	throat_disorder|voice_disorders	false	false	false	true	high
MONDO:0043875	tumor lysis syndrome	cancer_or_benign_tumor|syndromic_disease|metabolic_disease	metabolic_disease|cancer_or_benign_tumor	syndromic_disease|metabolic_disease|cancer_or_benign_tumor	oncology|neurology|hematology|pediatric	tumor_lysis_syndrome_is_a_complication_of_cancer|cancer	kidney_disorder|urinary_tract_disorder	false	false	false	true	very_high
MONDO:0043878	hereditary optic atrophy	nervous_system_disorder|disorder_of_visual_system|hereditary_disease	neurodegenerative_disease	disorder_of_visual_system|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|ophthalmology	neurodegenerative_disease|hereditary_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0043885	eye infectious disorder	disorder_of_visual_system|infectious_disease	infectious_disease	infectious_disease|disorder_of_visual_system|disorder_of_orbital_region	allergy_and_immunology|ophthalmology	eye_infectious_disorder_is_not_in_the_list_so_using__infectious_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder|eye_inflectious_disorder	true	false	false	true	medium
MONDO:0043892	prosthesis-related infectious disease	infectious_disease	infectious_disease	infectious_disease	orthopaedic	autoimmune_diseases|inflammatory_disease	immune_disorder|joint_disorder	true	false	false	true	high
MONDO:0043904	leishmaniasis, diffuse cutaneous	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology|hematology	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder|skin_disorder	true	false	false	true	medium
MONDO:0043905	pneumonitis	inflammatory_disease|respiratory_system_disorder	other	inflammatory_disease|respiratory_system_disorder	pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	false	false	false	true	medium
MONDO:0043919	radiation pneumonitis	inflammatory_disease|respiratory_system_disorder	other	inflammatory_disease|respiratory_system_disorder|radiation_induced_disorder	pulmonology|oncology	inflammatory_disease|autoimmune_diseases|cancer	lung_disorder	false	false	false	true	medium
MONDO:0043923	lichen planus, oral	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder|mouth_disorder	oral_medicine|oral_pathology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder__skin_disorder	false	false	false	true	medium
MONDO:0043953	burkholderia infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|allergy_and_immunology|pulmonology	autoimmune_diseases|inflammatory_disease	immune_disorder_lung_disorder	true	false	false	true	high
MONDO:0043959	pseudolymphoma	immune_system_disorder	other	immune_system_disorder	hematolog|oncology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	medium
MONDO:0043969	nocturnal paroxysmal dystonia	nervous_system_disorder	other	sleep_disorder|nervous_system_disorder	pediatric|neurology|psychiatry	neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0043975	autonomic dysreflexia	nervous_system_disorder	other	nervous_system_disorder	neurology|pulmonology	neurodegenerative_disease|cardiovascular_disorder	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0043982	cubital tunnel syndrome	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	autoimmune_diseases|inflammatory_disease	muscle_disorder|joint_disorder	false	false	false	true	medium
MONDO:0043985	central nervous system lupus	connective_tissue_disorder|nervous_system_disorder|immune_system_disorder	autoimmune_disease	nervous_system_disorder|connective_tissue_disorder|immune_system_disorder	rheumatology|neurology	inflammatory_disease|autoimmune_diseases	spinal_disorder|brain_disorder|immune_disorder	false	false	false	true	high
MONDO:0043988	zoster sine herpete	integumentary_system_disorder|infectious_disease	infectious_disease	integumentary_system_disorder|post_infectious_disorder|infectious_disease	neurology|dermatology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	skin_disorder|immune_disorder|nerve_disorder	true	false	false	true	medium
MONDO:0043994	acute cholecystitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	acute_disease|endocrine_system_disorder|digestive_system_disorder|inflammatory_disease	gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases|gastrointestinal_disorder____corrected_list_to_match_format__inflammatory_disease	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	medium
MONDO:0044001	hearing loss, mixed conductive-sensorineural	nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	otolaryngology|neurology	mixed_conductive_sensorineural_hearing_loss_is_not_included_in_this_list|neurodegenerative_disease|autoimmune_diseases	sensorineural|ear_disorder	false	false	false	false	medium
MONDO:0044013	puerperal disorder	obstetric_disorder	other	obstetric_disorder	psychiatry|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|psychological_disorder	true	false	false	false	high
MONDO:0044014	postpartum thyroiditis	endocrine_system_disorder|inflammatory_disease|immune_system_disorder|obstetric_disorder	autoimmune_disease|endocrine_system_disorder	endocrine_system_disorder|inflammatory_disease|immune_system_disorder|obstetric_disorder	obstetrics_and_gynecology|endocrinology	autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0044033	posterior leukoencephalopathy syndrome	syndromic_disease|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	syndromic_disease|nervous_system_disorder|cardiovascular_disorder	neurology|genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0044037	livedo reticularis	integumentary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0044067	candidiasis, invasive	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|dermatology|immunology|immunology___corrected_to___dermatology	invasive_fungal_infection|inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0044070	candidemia	infectious_disease	infectious_disease	infectious_disease	immunology|hematology	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	true	false	false	true	high
MONDO:0044079	cardio-renal syndrome	cardiovascular_disorder|syndromic_disease	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder	cardiology|renal_medicine	cardiovascular_disorder|metabolic_disorder|inflammatory_disease|autoimmune_diseases	heart_disorder_kidney_disorder	false	false	false	false	high
MONDO:0044083	alternariosis	infectious_disease	infectious_disease	infectious_disease	plant_pathology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	true	false	false	false	low
MONDO:0044092	collagenous sprue	metabolic_disease|digestive_system_disorder	metabolic_disease	metabolic_disease|digestive_system_disorder	dermatology|gastroenterology|rheumatology	inflammatory_disease|autoimmune_diseases	skin_disorder|lower_gastrointestinal_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0044098	ovarian ectopic pregnancy	endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder	gynecology|pediatric|obstetrics_and_gynecology	cancer|autoimmune_diseases	reproductive_system_disorder|ovarian_disorder	false	false	false	false	medium
MONDO:0044101	pregnancy, cornual	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	pregnancy|reproductive_system_disorder	false	false	false	false	high
MONDO:0044113	bullous systemic lupus erythematosus	immune_system_disorder|connective_tissue_disorder	autoimmune_disease	connective_tissue_disorder|immune_system_disorder	rheumatology|allergy_and_immunology|dermatology	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	immune_disorder_skin_disorder	false	false	false	false	high
MONDO:0044137	vitreous body disorder	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	inflammatory_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0044138	hyalitis	disorder_of_visual_system|inflammatory_disease	other	disorder_of_orbital_region|disorder_of_visual_system|inflammatory_disease	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|eye_disorder	false	false	false	false	medium
MONDO:0044141	panic disorder without agoraphobia	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder	psychiatric_disorder|brain_disorder	false	false	false	true	high
MONDO:0044144	panic disorder with agoraphobia	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology	mental_health_disorder|panic_disorder|agoraphobia	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0044200	T-B+ severe combined immunodeficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	pediatric|immunology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0044201	T+ B+ severe combined immunodeficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	pediatric|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0044202	episodic kinesigenic dyskinesia	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0044203	foveal hypoplasia	hereditary_disease	other	hereditary_disease	neurology|ophthalmology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0044204	Shwachman-Diamond syndrome 1	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|anemia	liver_disorder|lung_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0044205	Shwachman-Diamond syndrome 2	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	pediatric|pulmonology|genetics_and_genomics	metabolic_disorder|anemia	metabolic_disorder|lung_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0044206	otospondylomegaepiphyseal dysplasia, autosomal recessive	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	ear_disorder|joint_disorder|bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0044207	specific granule deficiency 1	hereditary_disease|hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hereditary_disease|hematologic_disorder	pediatrics|allergy_and_immunology|immunology|hematatology	inflammatory_disease|metabolic_disorder|autoimmune_diseases|adrenal_gland_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0044208	specific granule deficiency 2	hereditary_disease|hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hereditary_disease|hematologic_disorder	pediatric|allergy_and_immunology|immunology	inflammatory_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0044209	disorder of lectin complement activation pathway	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|immunology	inflammatory_disease|autoimmune_diseases	immune_disorder	false	false	false	true	high
MONDO:0044210	thalassemia minor	hereditary_disease|endocrine_system_disorder|hematologic_disorder	endocrine_system_disorder|anemia	hereditary_disease|endocrine_system_disorder|hematologic_disorder	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0044211	idiopathic urticaria	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|idiopathic_disease|integumentary_system_disorder	allergy_and_immunology|dermatology	inflammatory_disease|allergy|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0044212	chronic idiopathic urticaria	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|idiopathic_disease|integumentary_system_disorder	allergy_and_immunology|dermatology	inflammatory_disease|allergy|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0044213	acute idiopathic urticaria	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|idiopathic_disease|integumentary_system_disorder|acute_disease	allergy_and_immunology|dermatology	inflammatory_disease|allergy|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	true	medium
MONDO:0044299	myasthenic syndrome, congenital, 22	nervous_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|autoimmune_diseases	immune_disorder|muscle_disorder	false	false	false	true	high
MONDO:0044300	familial adenomatous polyposis 4	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	oncology|genetics_and_genomics|gastroenterology	cancer|familial_adenomatous_polyposis_is_a_type_of_cancer_that_affects_the_colon	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0044302	congenital heart defects, dysmorphic facial features, and intellectual developmental disorder	hereditary_disease	other	hereditary_disease	cardiothoracic|neurology|genetics_and_genomics|pediatric	cardiovascular_disorder|mental_health_disorder|metabolic_disorder	heart_disorder|brain_disorder	false	false	false	true	high
MONDO:0044303	congenital heart defects and ectodermal dysplasia	hereditary_disease	other	hereditary_disease	cardiothoracic|genetics_and_genomics|pediatric|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|ectodermal_dysplasia_doesn_t_fit_into_a_single_category_in_the_list_but_some_symptoms_can_be_classified_as_eye_disorder__skin_disorder_or_teeth_disorder	false	false	false	true	high
MONDO:0044304	hyperphenylalaninemia due to DNAJC12 deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|genetics_and_genomics|pediatric	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0044305	ectodermal dysplasia 13, hair/tooth type	integumentary_system_disorder|syndromic_disease|hereditary_disease	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	skin_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0044306	neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodevelopmental_disorder|neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0044308	bardet-biedl syndrome 21	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	eye_disorder|kidney_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0044309	Diamond-Blackfan anemia 16	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics|pediatric	inflammatory_disease|anemia|metabolic_disorder	blood_bone_marrow_disorder|lung_disorder	false	false	false	false	high
MONDO:0044310	Diamond-Blackfan anemia 17	hematologic_disorder|hereditary_disease	anemia	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	anemia|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|bone_disorder	false	false	false	true	high
MONDO:0044311	brachycephaly, trichomegaly, and developmental delay	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|developmental_delay	developmental_disorder|bone_disorder|brain_disorder	false	false	false	false	high
MONDO:0044312	immunoskeletal dysplasia with neurodevelopmental abnormalities	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	immunology|orthopaedic|neurology|genetics_and_genomics|rheumatology|pediatric	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	bone_disorder|joint_disorder|immune_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0044313	intellectual disability, autosomal recessive 60	hereditary_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	autosomal_recessive|brain_disorder	false	false	false	false	high
MONDO:0044314	retinitis pigmentosa 78	hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|metabolic_disease	metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0044316	thrombocytopenia, anemia, and myelofibrosis	hereditary_disease	other	hereditary_disease	oncology|hematology	myelofibrosis_is_primarily_categorized_under_the__cancer__category|cancer|anemia	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0044317	premature ovarian failure 13	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	obstetrics_and_gynecology|endocrinology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0044318	intellectual developmental disorder with gastrointestinal difficulties and high pain threshold	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	syndromic_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurology|pediatric|gastroenterology	mental_health_disorder|metabolic_disorder	upper_gastrointestinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0044319	intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	syndromic_disease|psychiatric_disorder|disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	eye_disorder|joint_disorder|spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0044320	retinitis pigmentosa 79	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder|metabolic_disease	metabolic_disease|psychiatric_disorder	metabolic_disease|disorder_of_orbital_region|disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0044321	structural heart defects and renal anomalies syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|cardiology|renal_medicine	renal_anomalies_suggest__metabolic_disorder|cardiovascular_disorder	heart_disorder|kidney_disorder	false	false	false	false	high
MONDO:0044322	intellectual developmental disorder with neuropsychiatric features	hereditary_disease|syndromic_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	syndromic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|psychiatry|genetics_and_genomics|pediatric	intellectual_developmental_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|neuropsychiatric_disorder	false	false	false	false	high
MONDO:0044323	Rahman syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	neurology|psychiatry|genetics_and_genomics|pediatrics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	bone_disorder|joint_disorder|immune_disorder	false	false	false	false	high
MONDO:0044324	Al Kaissi syndrome	hereditary_disease|syndromic_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	syndromic_disease|psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0044325	Fanconi anemia, complementation group W	hematologic_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|immune_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease|anemia	hematologic_disorder|metabolic_disease|immune_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|hematology|pediatric	anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0044326	developmental delay and seizures with or without movement abnormalities	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	brain_disorder|developmental_delay_category	false	false	false	true	very_high
MONDO:0044327	polycystic liver disease 4 with or without kidney cysts	digestive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|digestive_system_disorder	hepatology|genetics_and_genomics|endocrinology	metabolic_disorder|liver_disease	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0044328	short-rib thoracic dysplasia 20 with polydactyly	musculoskeletal_system_disorder|respiratory_system_disorder|urinary_system_disorder|hereditary_disease|syndromic_disease	other	respiratory_system_disorder|syndromic_disease|urinary_system_disorder|musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	genetic_disorder_is_not_in_the_list_but_its_related_category_is__metabolic_disorder|metabolic_disorder	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0044329	osteogenesis imperfecta, type 18	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|genetics_and_genomics|rheumatology	metabolic_disorder|genetic_disorder	teeth_disorder|bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0044330	hyperekplexia 4	metabolic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0044332	childhood-onset benign chorea with striatal involvement	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0044333	alcohol-induced Wernicke-Korsakoff's syndrome	nutritional_disorder|syndromic_disease|psychiatric_disorder	psychiatric_disorder	syndromic_disease|nutritional_disorder|psychiatric_disorder	hepatology|neurology|gastroenterology	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	true	high
MONDO:0044334	connective and soft tissue neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|rheumatology	connective_and_soft_tissue_neoplasm_cancer	joint_disorder|muscle_disorder	false	true	false	false	high
MONDO:0044335	benign soft tissue neoplasm	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	oncology|orthopaedic	cancer|benign_soft_tissue_neoplasm	soft_tissue_neoplasm|muscle_disorder	false	false	false	false	low
MONDO:0044336	colorectal signet ring cell carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|gastrointestinal_cancer|colorectal_cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0044337	stromal sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|orthopaedic	cancer|adrenal_gland_disease	soft_tissue_disorder|muscle_disorder|vascular_disorder	false	true	false	false	very_high
MONDO:0044338	autoimmune primary ovarian failure	reproductive_system_disorder|endocrine_system_disorder|immune_system_disorder	endocrine_system_disorder|autoimmune_disease	reproductive_system_disorder|immune_system_disorder|endocrine_system_disorder	obstetrics_and_gynecology|endocrinology	inflammatory_disease|autoimmune_diseases	endocrine_disorder|immune_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0044339	lumbar disk degenerative disorder	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	neurology|orthopaedic	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0044342	thoracic disk degenerative disorder	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	neurology|orthopaedic|pulmonology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0044343	cervical disk degenerative disorder	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	neurology|orthopaedic	neurodegenerative_disease|inflammatory_disease	joint_disorder|spinal_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0044344	Schistosoma japonicum infectious disease	infectious_disease	infectious_disease	infectious_disease	hepatology|pulmonology|hematology|gastroenterology|urology	inflammatory_disease|infectious_disease	urinary_tract_disorder|liver_disorder	true	false	false	true	medium
MONDO:0044345	Schistosoma mansoni infectious disease	infectious_disease	infectious_disease	infectious_disease	hepatology|hematology|pediatric|gastroenterology|urology	inflammatory_disease|parasitic_disease	urinary_tract_disorder|kidney_disorder|lower_gastrointestinal_disorder|liver_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0044346	echinococcus granulosus infectious disease	infectious_disease	infectious_disease	infectious_disease	hepatology|pulmonology|hematology	inflammatory_disease|infectious_disease	biliary_disorder|liver_disorder|immune_disorder	true	false	false	true	medium
MONDO:0044347	erythrocyte disorder	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|erythrocyte_disorder	false	false	false	false	medium
MONDO:0044348	hemoglobinopathy	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0044349	acquired hemoglobinopathy	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0044350	hyperparathyroidism, primary, caused by water clear cell hyperplasia	cancer_or_benign_tumor|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology|renal_medicine	endocrine_disorder|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0044351	Schistosoma intercalatum infectious disease	infectious_disease	infectious_disease	infectious_disease	hepatology|hematology|urology	inflammatory_disease|parasitic_infectious_disease|infectious_disease	kidney_disorder|lower_gastrointestinal_disorder|liver_disorder|lymphatic_disorder	true	false	false	true	medium
MONDO:0044355	isolated sternocostoclavicular hyperostosis	connective_tissue_disorder	other	connective_tissue_disorder	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0044406	arthrogryposis-ectodermal dysplasia-other anomalies syndrome	musculoskeletal_system_disorder|syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|pediatric|orthopaedic	metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0044617	X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome	syndromic_disease	other	syndromic_disease	dermatology|genetics_and_genomics|ophthalmology|rheumatology|orthopaedic	autoimmune_diseases|anemia|neurodegenerative_disease|inflammatory_disease	skin_disorder|eye_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0044619	propylthiouracil embryofetopathy	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatrics|genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0044621	16p12.1p12.3 triplication syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease|genetic_disorders|inflammatory_disease|cardiovascular_disorder|developmental_disorder|metabolic_disorder|congenital_disorder____corrected_answer____neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0044622	EMILIN-1-related connective tissue disease	connective_tissue_disorder|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|connective_tissue_disorder	dermatology|genetics_and_genomics|rheumatology	autoimmune_diseases|inflammatory_disease|connective_tissue_disease	skin_disorder|vascular_disorder|muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0044624	pediatric collagenous gastritis	inflammatory_disease|digestive_system_disorder	other	inflammatory_disease|digestive_system_disorder	gastroenterology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0044625	autosomal dominant charcot-marie-tooth disease type 2 due to DGAT2 mutation	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	nerve_disorder|muscle_disorder	false	false	false	false	high
MONDO:0044626	female infertility due to oocyte meiotic arrest	reproductive_system_disorder	other	reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0044627	acute macular neuroretinopathy	disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|acute_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0044628	six2-related frontonasal dysplasia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	renal_medicine|genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|developmental_disorder	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0044629	congenital amyoplasia	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	other____corrected___muscle_disorder|muscle_disorder	false	false	false	false	high
MONDO:0044631	early-onset familial noncirrhotic portal hypertension	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	gastroenterology|genetics_and_genomics|pediatric	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0044632	extracranial carotid artery aneurysm	nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	cardiology|cardiothoracic|neurology	cardiovascular_disorder|inflammatory_disease	blood_bone_marrow_disorder|heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0044633	idiopathic pleuroparenchymal fibroelastosis	inflammatory_disease|respiratory_system_disorder|infectious_disease	infectious_disease	idiopathic_disease|respiratory_system_disorder|inflammatory_disease|infectious_disease	pulmonology|cardiothoracic	inflammatory_disease|respiratory_disorder|fibrotic_disease	bone_disorder|lung_disorder	false	false	false	false	high
MONDO:0044634	retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	endocrinology|ophthalmology|genetics_and_genomics|otolaryngology|pediatric	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	eye_disorder|premature_aging_disorder|hearing_loss_disorder	false	false	false	false	high
MONDO:0044635	DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics|otolaryngology	autoimmune_diseases|anemia	ear_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0044637	infantile-onset generalized dyskinesia with orofacial involvement	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0044638	hypopharynx squamous cell carcinoma	respiratory_system_disorder|digestive_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease	cancer_or_benign_tumor	respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|digestive_system_disorder	oncology|otolaryngology	cancer|adrenal_gland_disease|squamous_cell_carcinoma	upper_gastrointestinal_disorder|thorat_disorder	false	true	false	true	very_high
MONDO:0044640	Charcot-Marie-Tooth disease type 2T	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|orthopaedic|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0044641	9q33.3q34.11 microdeletion syndrome	chromosomal_disorder|psychiatric_disorder|disorder_of_development_or_morphogenesis|disorder_of_visual_system|nervous_system_disorder|syndromic_disease	psychiatric_disorder	nervous_system_disorder|disorder_of_development_or_morphogenesis|chromosomal_disorder|syndromic_disease|disorder_of_orbital_region|disorder_of_visual_system|psychiatric_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0044642	c11orf73-related autosomal recessive hypomyelinating leukodystrophy	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0044643	congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome	disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|cardiovascular_disorder|genetic_disorder|metabolic_disorder	eye_disorder|facial_dysmorphism|skin_disorder|reproductive_system_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0044644	congenital agenesis of the scrotum	disorder_of_development_or_morphogenesis|reproductive_system_disorder	other	disorder_of_development_or_morphogenesis|reproductive_system_disorder	urology|pediatric	congenital_condition|metabolic_disorder	reproductive_system_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0044645	familial monosomy 7 syndrome	hematologic_disorder|hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	hematologic_disorder|syndromic_disease|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|pediatric	anemia|neurodegenerative_disease|metabolic_disorder	bone_disorder|upper_gastrointestinal_disorder|kidney_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0044646	early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|optic_atrophy	true	false	false	false	very_high
MONDO:0044647	kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	neurology|myofibrillar_myopathy_syndrome_typically_falls_under_neurology	neurodegenerative_disease|myofibrillar_myopathy	spinal_disorder|muscle_disorder	true	false	false	false	high
MONDO:0044648	kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome	hereditary_disease|nervous_system_disorder|syndromic_disease	neurodegenerative_disease	nervous_system_disorder|syndromic_disease|hereditary_disease	neurology|orthopaedic|genetics_and_genomics	neurodegenerative_disease|hereditary_spastic_paraplegia_syndrome	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0044649	omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|musculoskeletal_system_disorder	orthopaedic|cardiology|genetics_and_genomics|cardiothoracic|pediatric	cardiovascular_disorder|metabolic_disorder|cardiovascular_anomalies	heart_disorder|vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0044651	early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome	psychiatric_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease|neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder|metabolic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|spinal_muscular_atrophy	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0044656	epidermolytic nevus	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|skin_disease	skin_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0044657	MME-related autosomal dominant Charcot Marie Tooth disease type 2	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0044660	menstrual cycle-dependent periodic fever	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	rheumatology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	immune_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0044663	aquagenic palmoplantar keratoderma	disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	other____note__aquagenic_palmo_plantar_keratoderma_is_a_rare_skin_disorder|skin_disorder	false	false	false	false	low
MONDO:0044675	LRP5-related primary osteoporosis	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|endocrinology|genetics_and_genomics	metabolic_disorder|osteoporosis	spinal_disorder|teeth_disorder|vascular_disorder|muscle_disorder|joint_disorder|bone_disorder	false	false	false	true	medium
MONDO:0044682	MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	muscular_disorder|cardiovascular_disorder	muscle_disorder|joint_disorder|heart_disorder|bone_disorder	false	false	false	false	low
MONDO:0044685	autoimmune/inflammatory optic neuropathy	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology|rheumatology	autoimmune_diseases|inflammatory_disease	autoimmune_disorder_is_not_in_the_list_so_use_inflammatory_disorder_does_not_exist_as_well_but__inflammation_is_a_symptom_of_autoimmunity__therefore__eye_disorder|immune_disorder|eye_disorder	false	false	false	true	high
MONDO:0044687	chronic relapsing inflammatory optic neuropathy	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0044688	isolated optic neuritis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|eye_disorder	true	false	false	true	medium
MONDO:0044689	recurrent idiopathic neuroretinitis	disorder_of_visual_system	other	idiopathic_disease|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|immune_disorder|eye_disorder	false	false	false	false	high
MONDO:0044690	optic perineuritis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease	immune_disorder|eye_disorder	true	false	false	false	medium
MONDO:0044696	early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	brain_atrophy_syndrome|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0044699	SIN3A-related intellectual disability syndrome	psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	psychiatric_disorder	syndromic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0044700	SIN3A-related intellectual disability syndrome due to a point mutation	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	disorder_of_development_or_morphogenesis|psychiatric_disorder|nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0044701	childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0044702	X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome	auditory_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|psychiatric_disorder|nervous_system_disorder|otorhinolaryngologic_disease	psychiatric_disorder	auditory_system_disorder|otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis|psychiatric_disorder|nervous_system_disorder|hereditary_disease	genetics_and_genomics|otolaryngology|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	facial_dysmorphism_is_not_in_the_list_but_ear_disorder_can_be_assumed_to_cover_part_of_it|ear_disorder	false	false	false	false	high
MONDO:0044704	oropharynx squamous cell carcinoma	digestive_system_disorder|cancer_or_benign_tumor|respiratory_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|respiratory_system_disorder|digestive_system_disorder	oncology|otolaryngology	cancer|oropharynx_squamous_cell_carcinoma	throat_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0044705	paranasal sinus squamous cell carcinoma	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|respiratory_system_disorder|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor|respiratory_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|nervous_system_disorder	oncology|otolaryngology	cancer|adrenal_gland_disease|inflammatory_disease	lung_disorder|upper_gastrointestinal_disorder|nose_disorder	false	true	false	false	high
MONDO:0044709	cochleovestibular dysplasia	disorder_of_development_or_morphogenesis|otorhinolaryngologic_disease	other	otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|otolaryngology|neurology	autoimmune_diseases|neurodegenerative_disease	ear_disorder|cochlear_disorder	false	false	false	false	high
MONDO:0044710	lip and oral cavity squamous cell carcinoma	cancer_or_benign_tumor|otorhinolaryngologic_disease	cancer_or_benign_tumor	otorhinolaryngologic_disease|cancer_or_benign_tumor	gastroenterology|dermatology|oncology|otolaryngology	cancer|oral_cavity_disease	skin_disorder|teeth_disorder|oral_cavity_disorder	false	true	false	true	high
MONDO:0044714	mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|musculoskeletal_system_disorder|hereditary_disease	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|cardiovascular_disorders_are_not_in_the_list_so__neurodegenerative_disease|mitochondrial_myopathies	eye_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0044717	4q25 proximal deletion syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	disorder_of_development_or_morphogenesis|chromosomal_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|spinal_disorder|developmental_disorder|immune_disorder	false	false	false	false	high
MONDO:0044718	alkaline ceramidase 3 deficiency	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	enzyme_disorder|liver_disorder	false	false	false	false	high
MONDO:0044719	erythema multiforme major	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0044720	cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome	hereditary_disease|nervous_system_disorder|otorhinolaryngologic_disease	neurodegenerative_disease	otorhinolaryngologic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	ear_disorder|brain_disorder|spinal_disorder	true	false	false	false	high
MONDO:0044721	severe combined immunodeficiency due to LAT deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|immunology|allergy_and_immunology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0044723	3-methylglutaconic aciduria type 8	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|renal_medicine	neurodegenerative_disease|metabolic_disorder	muscle_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0044724	3-methylglutaconic aciduria type 9	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|renal_medicine	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	muscle_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0044725	combined immunodeficiency due to GINS1 deficiency	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|immunology	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0044726	psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome	metabolic_disease|hereditary_disease|urinary_system_disorder|nervous_system_disorder	neurodegenerative_disease|metabolic_disease	urinary_system_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|renal_medicine|neurology	neurodegenerative_disease|nephropathy|movement_disorder	brain_disorder|movement_disorder|kidney_disorder	false	false	false	false	high
MONDO:0044727	pancreatic carcinoma with mixed differentiation	digestive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology|hepatology	cancer|pancreatic_carcinoma_with_mixed_differentiation_matches_cancer_category	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder|pancreas_is_part_of_the_upper_gastro_but_more_specific_to_pancreatic_carcinoma__thus_adding_it	false	true	false	true	very_high
MONDO:0044737	autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction	metabolic_disease|syndromic_disease|hereditary_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	syndromic_disease|metabolic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0044738	Gabriele de Vries syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0044739	Stevens-Johnson syndrome/toxic epidermal necrolysis overlap syndrome	integumentary_system_disorder	other	integumentary_system_disorder	allergy_and_immunology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0044740	salivary gland squamous cell carcinoma	otorhinolaryngologic_disease|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	otorhinolaryngologic_disease|mouth_disorder|digestive_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology	adrenal_gland_disease|cancer	throat_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0044742	autosomal recessive epidermolytic ichthyosis	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|dermatology|genetics_and_genomics	metabolic_disorder|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0044743	major salivary gland cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	mouth_disorder|digestive_system_disorder|cancer_or_benign_tumor	otolaryngology|oncology	cancer	throat_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0044744	prekallikrein deficiency	hematologic_disorder	other	hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|cardiovascular_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	low
MONDO:0044745	nervous system injury	nervous_system_disorder|injury	other	nervous_system_disorder	neurology	neurodegenerative_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0044749	X-linked congenital stationary night blindness	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	disorder_of_orbital_region|disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0044750	lassa virus infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|genetics_and_genomics|hematology|pulmonology|hepatology	inflammatory_disease|infectious_disease	immune_disorder|vascular_disorder	true	false	false	true	medium
MONDO:0044751	chronic diarrheal disease	digestive_system_disorder	other	digestive_system_disorder	pediatric|gastroenterology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	high
MONDO:0044753	lumbar spinal stenosis	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|neurology	inflammatory_disease|musculoskeletal_disorder___or___neurodegenerative_disease|neurodegenerative_disease	joint_disorder|spinal_disorder	false	false	false	true	high
MONDO:0044762	diarrheal disease secondary to increased bowel motility	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|neurology	inflammatory_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0044763	diarrheal disease secondary to decreased bowel motility	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|neurology	metabolic_disorder|neurodegenerative_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0044764	benign choroid plexus neoplasm	cancer_or_benign_tumor|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	cardiovascular_disorder|cancer_or_benign_tumor|nervous_system_disorder	ophthalmology|oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	low
MONDO:0044765	steroid-resistant nephrotic syndrome	syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|syndromic_disease	pediatric|renal_medicine	inflammatory_disease|autoimmune_diseases|metabolic_disorder	kidney_disorder|endocrine_disorder|immune_disorder	false	false	false	false	high
MONDO:0044767	childhood adrenal gland pheochromocytoma	hereditary_disease|cancer_or_benign_tumor|nervous_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cancer_or_benign_tumor|nervous_system_disorder	pediatric|endocrinology|oncology	adrenal_gland_disease|cancer	reproductive_system_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0044768	vagus nerve paraganglioma	hereditary_disease|cancer_or_benign_tumor|nervous_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cancer_or_benign_tumor|nervous_system_disorder	otolaryngology|neurology	cancer|neurological_disease	ear_disorder|throat_disorder|brain_disorder	false	true	false	false	medium
MONDO:0044776	premature ovarian failure 10	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrinology|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0044777	premature ovarian failure 14	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrinology|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0044778	nodular lymphocyte predominant Hodgkin lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	post_infectious_disorder|cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	inflammatory_disease|autoimmune_diseases|cancer	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	medium
MONDO:0044781	nephrotic syndrome of childhood - steroid sensitive	syndromic_disease|urinary_system_disorder	other	urinary_system_disorder|syndromic_disease	pediatric|renal_medicine	inflammatory_disease|autoimmune_diseases|metabolic_disorder	kidney_disorder|endocrine_disorder|immune_disorder	false	false	false	true	medium
MONDO:0044782	esophageal ulcer	upper_digestive_tract_disorder|digestive_system_disorder	other	ulcer_disease|digestive_system_disorder|upper_digestive_tract_disorder	gastroenterology|cardiology|hepatology	inflammatory_disease|autoimmune_diseases|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0044783	solid papillary breast carcinoma	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|breast_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	adrenal_gland_disease|cancer	breast_carcinoma|reproductive_system_disorder	false	true	false	true	medium
MONDO:0044784	myxoma	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	dermatology|oncology|pathology	cancer|neuroendocrine_tumor	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	true	false	false	false	low
MONDO:0044785	desmoplastic melanoma	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	dermatology|oncology	cancer	muscle_disorder|skin_disorder	false	true	false	true	high
MONDO:0044786	solid pseudopapillary neoplasm of the pancreas	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	pediatric|gastroenterology|genetics_and_genomics|oncology|neurology	adrenal_gland_disease|cancer	pancreas_category_list__liver_disorder|upper_gastrointestinal_disorder	false	true	false	true	medium
MONDO:0044787	nasal cavity and paranasal sinus squamous cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	otolaryngology|oncology	cancer|nasal_cavity_and_paranasal_sinuses_squamous_cell_carcinoma	nose_disorder|throat_disorder	false	true	false	false	high
MONDO:0044788	perihilar intrahepatic cholangiocarcinoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology|hepatology	inflammatory_disease|cancer|liver_disease__note__actual_category_was_missing_from_the_original_list	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0044789	digital papillary eccrine carcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|skin_disorder	false	true	false	false	medium
MONDO:0044791	combined hepatocellular carcinoma and cholangiocarcinoma	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	oncology|hepatology	cancer|hepatocellular_carcinoma_is_a_type_of_cancer	liver_disorder|upper_gastrointestinal_disorder	true	true	false	true	very_high
MONDO:0044792	large congenital melanocytic nevus	integumentary_system_disorder|hereditary_disease|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cancer_or_benign_tumor	pediatric|dermatology|genetics_and_genomics|oncology	cancer|neurocutaneous_syndrome	muscle_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0044793	spitz nevus	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	dermatology|oncology	cancer|skin_disease|neurocutaneous_syndrome	skin_disorder	false	false	false	false	low
MONDO:0044794	benign melanocytic skin nevus	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	dermatology|genetics_and_genomics	cancer|nevi|skin_disease	muscle_disorder|skin_disorder	false	false	false	true	none
MONDO:0044795	epithelioid cell nevus	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	dermatology|oncology	neurological_disorder_is_not_listed_so_the_closest_we_get_is__cancer	skin_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0044796	spindle cell nevus	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	dermatology|genetics_and_genomics	skin_condition|cancer|neurocutaneous_syndrome	muscle_disorder|skin_disorder	false	false	false	false	low
MONDO:0044797	desmoplastic nevus	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	dermatology|oncology	cancer|neoplasm|skin_disease	skin_disorder	false	false	false	false	low
MONDO:0044800	desmoplastic spitz nevus	integumentary_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	skin_condition|cancer	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0044807	inherited dystonia	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	inherited_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0044811	idiopathic torsion dystonia	nervous_system_disorder	other	nervous_system_disorder|idiopathic_disease	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0044816	familial idiopathic torsion dystonia	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder|idiopathic_disease	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0044817	acquired idiopathic torsion dystonia	nervous_system_disorder	other	nervous_system_disorder|idiopathic_disease	neurology|genetics_and_genomics	neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0044843	torsion dystonia	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0044870	acquired torsion dystonia	nervous_system_disorder	other	nervous_system_disorder	neurology	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0044871	dystonia, focal, task-specific	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	focal_seizure_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0044872	dysautonomia	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0044873	childhood myelodysplastic syndrome	cancer_or_benign_tumor|syndromic_disease|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|syndromic_disease|cancer_or_benign_tumor	hematology|oncology|pediatric	anemia|cancer	immune_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0044874	refractory cytopenia of childhood	cancer_or_benign_tumor|syndromic_disease|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|syndromic_disease|cancer_or_benign_tumor	hematology|pediatric	inflammatory_disease|autoimmune_diseases|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0044875	coronary microvascular disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	hematology|pulmonology|cardiothoracic|renal_medicine|cardiology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0044877	paraneoplastic cerebellar degeneration	cancer_or_benign_tumor|syndromic_disease|nervous_system_disorder	neurodegenerative_disease|cancer_or_benign_tumor	syndromic_disease|nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0044878	adult germ cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	obstetrics_and_gynecology|oncology|urology|pediatric	cancer|adult_oncology	reproductive_system_disorder	false	true	false	true	high
MONDO:0044879	pancreatic mucinous-cystic neoplasm	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	pancreatic_disease|neoplasm|cancer	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0044880	cystic tumor of the pancreas	cancer_or_benign_tumor|digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	tumor|pancreatic_cancer|cancer	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0044881	hematopoietic and lymphoid cell neoplasm	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	hematopoietic_and_lymphoid_cell_neoplasm|anemia|cancer	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0044884	tonsillar lymphoma	respiratory_system_disorder|hereditary_disease|otorhinolaryngologic_disease|cancer_or_benign_tumor|digestive_system_disorder|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|digestive_system_disorder|respiratory_system_disorder|hereditary_disease	hematology|oncology	lymphoma|cancer	throat_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0044885	tonsillar lipoma	respiratory_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|immune_system_disorder|otorhinolaryngologic_disease|cancer_or_benign_tumor|connective_tissue_disorder|respiratory_system_disorder	oncology|otolaryngology|pediatric	cancer	throat_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0044887	central nervous system non-hodgkin lymphoma	cancer_or_benign_tumor|hematologic_disorder|nervous_system_disorder|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|post_infectious_disorder	hematology|oncology|neurology	cancerous_condition|neurological_cancer|lymphoma|cancer	lymphatic_disorder|spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0044889	high grade B-cell lymphoma	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0044903	myelofibrosis	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder	oncology|hematology|pulmonology	blood_disorder|anemia|cancer	blood_bone_marrow_disorder|lung_disorder	false	true	false	true	high
MONDO:0044906	bladder urothelial papilloma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	false	false	true	low
MONDO:0044907	metastatic squamous cell carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|cardiothoracic	adrenal_gland_disease|cancer	lung_disorder|skin_disorder	false	true	false	true	very_high
MONDO:0044912	metastatic malignant neoplasm in the spinal cord	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	malignant_neoplasm|cancer	bone_disorder|spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0044913	metastatic malignant neoplasm in the eye	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|oncology	malignant_neoplasm|cancer	metastatic_malignant_neoplasm|eye_disorder	false	true	false	true	very_high
MONDO:0044915	salivary duct carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	oncology|otolaryngology	autoimmune_diseases|cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|throat_disorder	false	true	false	false	very_high
MONDO:0044916	extrarenal rhabdoid tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics|pediatric	cancer|adrenal_gland_disease	urinary_tract_disorder|kidney_disorder	false	true	false	false	very_high
MONDO:0044917	T-lymphoblastic lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	autoimmune_diseases|cancer	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	high
MONDO:0044919	malignant renal pelvis neoplasm	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	malignant_renal_pelvis_neoplasm_falls_under_this_category|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0044921	atypical lymphoproliferative disorder	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|hereditary_disease|immune_system_disorder	oncology|hematology	lymphoproliferative_disorder|autoimmune_diseases|cancer	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	medium
MONDO:0044923	acute myeloid leukemia with mutated NPM1	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|immune_system_disorder	oncology|hematology|genetics_and_genomics	anemia|cancer	blood_bone_marrow_disorder|immune_disorder	false	true	false	true	high
MONDO:0044925	oral cavity carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	oncology|otolaryngology	cancer	teeth_disorder|throat_disorder	false	true	false	true	high
MONDO:0044926	oropharyngeal carcinoma	otorhinolaryngologic_disease|cancer_or_benign_tumor|digestive_system_disorder|respiratory_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|otorhinolaryngologic_disease|respiratory_system_disorder|digestive_system_disorder	oncology|otolaryngology	cancer	lymphatic_disorder|throat_disorder	false	true	false	true	high
MONDO:0044937	rectal carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0044956	paranasal sinus mucoepidermoid carcinoma	nervous_system_disorder|cancer_or_benign_tumor|otorhinolaryngologic_disease|connective_tissue_disorder|musculoskeletal_system_disorder|respiratory_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|musculoskeletal_system_disorder|otorhinolaryngologic_disease|connective_tissue_disorder|respiratory_system_disorder|cancer_or_benign_tumor	oncology|otolaryngology	adrenal_gland_disease|cancer	nose_disorder|lung_disorder|upper_gastrointestinal_disorder|throat_disorder	false	true	false	false	high
MONDO:0044964	oral cavity mucoepidermoid carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer	oral_cavity_disorder|teeth_disorder	false	true	false	false	medium
MONDO:0044970	mitochondrial disease		other		genetics_and_genomics|cardiology|neurology	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	muscle_disorder|mitochondrial_disease_often_manifests_as_a_muscle_disorder_due_to_the_critical_role_mitochondria_play_in_providing_energy_to_muscles	false	false	false	false	high
MONDO:0044972	eosinophil disorder	hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder	hematology|allergy_and_immunology|pulmonology	autoimmune_diseases|inflammatory_disease|eosinophil_disorder|allergy	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0044981	pseudoallergy	immune_system_disorder	other	immune_system_disorder	allergy_and_immunology	autoimmune_diseases|allergy	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0044982	drug pseudoallergy	immune_system_disorder	other	immune_system_disorder	hematology|allergy_and_immunology|dermatology|pulmonology	autoimmune_diseases|allergy	skin_disorder|immune_disorder	false	false	false	false	low
MONDO:0044983	benign lipomatous neoplasm	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	oncology|dermatology|genetics_and_genomics	cancer|neoplasm	skin_disorder|muscle_disorder	false	false	false	false	low
MONDO:0044984	nasolacrimal duct disorder	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases	nose_disorder|eye_disorder	false	false	false	false	low
MONDO:0044986	lymphoid system disorder	immune_system_disorder	other	immune_system_disorder	hematology|lymphoid_system_disorder	cancer|inflammatory_disease|lymphoid_system_disorder|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0044991	upper digestive tract disorder		other		gastroenterology|hepatology	inflammatory_disease|autoimmune_diseases|upper_digestive_tract_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0044992	mouth mucosa disorder	other	other	mouth_disorder	otolaryngology|gastroenterology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0044993	sympathetic nervous system disorder	nervous_system_disorder	other	nervous_system_disorder	psychiatry|neurology	sympathetic_nervous_system_disorders|neurodegenerative_disease|cardiovascular_disorder|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0044995	parasympathetic nervous system disorder	nervous_system_disorder	other	nervous_system_disorder	neurology	mental_health_disorder|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0044996	cerebral cortex disorder	nervous_system_disorder	other	nervous_system_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0044997	midbrain disorder	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0045001	cardiac ventricle disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0045002	vertebral disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	bone_disorder|spinal_disorder|vertebral_disorder	false	false	false	false	high
MONDO:0045003	scrotal disorder	reproductive_system_disorder	other	reproductive_system_disorder	urology	scrotal_disorder_is_not_in_the_list_but_could_be_classified_under__anatomic_disorder_which_was_not_given____edit__since_it_s_not_a_direct_match__its_primary_classifications_would_be__inflammatory_disease|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	scrotal_disorder_is_sometimes_associated_with_other_disorders_so_it_may_also_be_included_in_the_category_of|joint_disorder|muscle_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0045004	skeletal ligament disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	joint_disorder|bone_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0045008	cholesterol metabolism disease	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|cardiology|hepatology|genetics_and_genomics	metabolic_disorder|cholesterol_metabolism_disease_is_a_bit_redundant_so_i_will_just_leave_it_out___cardiovascular_disorder|cardiovascular_disorder	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0045010	glycoprotein metabolism disease	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|genetics_and_genomics	glycoprotein_metabolism_disease|metabolic_disorder|inflammatory_disease	liver_disorder|genetic_disorder|glycogen_storage_disease	false	false	false	true	high
MONDO:0045011	keratinization disease	disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	skin_disorder|eye_disorder	false	false	false	true	medium
MONDO:0045012	steroid metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	endocrinology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0045013	disorder of extraembryonic membrane	reproductive_system_disorder|obstetric_disorder	other	obstetric_disorder|reproductive_system_disorder	obstetrics_and_gynecology|pediatric	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|lymphatic_disorder|urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0045014	tetrahydrobiopterin metabolic process disease	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|anemia	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0045015	carbohydrate transport disease	metabolic_disease	metabolic_disease	metabolic_disease	pediatric|endocrinology|gastroenterology|genetics_and_genomics	carbohydrate_transport_disease_can_also_be_related_to_inflammatory_disease|metabolic_disorder	liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0045016	cholesterol catabolic process disease	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|cardiology|hepatology|genetics_and_genomics	cholesterol_catabolic_process_disease_seems_to_be_related_to_lipid_metabolism_so_i_will_add_metabolic_disorder|metabolic_disorder|cardiovascular_disorder	liver_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0045017	cholesterol biosynthetic process disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_diseases_are_sometimes_considered_in_cardiology_subcategory_so_i_have_included_it_as_well|endocrinology|cardiology|hepatology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	liver_disorder__endocrine_disorder	false	false	false	false	high
MONDO:0045018	creatine biosynthetic process disease	metabolic_disease	metabolic_disease	metabolic_disease	neurology|renal_medicine|endocrinology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|kidney_disorder	false	false	false	false	high
MONDO:0045019	lactation disease	disorder_of_development_or_morphogenesis|breast_disorder	other	disorder_of_development_or_morphogenesis|breast_disorder	obstetrics_and_gynecology|endocrinology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	liver_disorder|endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0045020	glycine metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	renal_medicine|genetics_and_genomics|metabolism_disorders	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0045022	disorder of organic acid metabolism	metabolic_disease	metabolic_disease	metabolic_disease	nephrology|pediatrics|endocrinology|hepatology|genetics_and_genomics|biochemistry	metabolic_disorder|organic_acid_metabolism	liver_disorder|kidney_disorder	false	false	false	true	high
MONDO:0045023	acquired adrenogenital syndrome	metabolic_disease|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder	urology|endocrinology	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0045024	cancer or benign tumor				neurology|pediatrics|pulmonology|cardiothoracic|obstetrics_and_gynecology|dermatology|hematology|urology|renal_medicine|cardiology|gastroenterology|hepatology|oncology|otolaryngology|orthopaedic	adrenal_gland_disease|cancer	bone_disorder|cancer_or_benign_tumor_can_also_fit_into_other_categories_but_those_listed_above_are_the_best_fitting	false	false	false	true	high
MONDO:0045030	non-infectious diarrheal disease	digestive_system_disorder	other	digestive_system_disorder	pediatric|gastroenterology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0045032	congenital secretory diarrhea	hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease	pediatric|gastroenterology|genetics_and_genomics	metabolic_disorder|congenital_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0045033	opportunistic systemic mycosis	infectious_disease	infectious_disease	infectious_disease	dermatology|immunology|pulmonology	inflammatory_disease|opportunistic_systemic_mycosis_is_often_associated_with_immunocompromised_patients_who_are_more_susceptible_to_fungal_infections_which_can_lead_to_inflammatory_responses	immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0045037	hyalohyphomycosis	infectious_disease	infectious_disease	infectious_disease	dermatology|immunology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|fungal_infection	true	false	false	true	high
MONDO:0045038	cutaneous basidiobolomycosis	infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder	dermatology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0045039	systemic basidiobolomycosis	infectious_disease	infectious_disease	infectious_disease	dermatology|pulmonology|immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	true	false	false	false	high
MONDO:0045043	disorder of uterine broad ligament	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	obstetrics_and_gynecology	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	joint_disorder|muscle_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0045044	ligament disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|rheumatology	ligament_disorder_does_not_fit_well_here_but_it_is_the_best_of_what_we_have|inflammatory_disease	joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0045045	selective IgG immunodeficiency	hematologic_disorder|immune_system_disorder|hereditary_disease	other	immune_system_disorder|hematologic_disorder|hereditary_disease	immunology|allergy_and_immunology	anemia|autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0045046	inherited thyroid metabolism disease	metabolic_disease|endocrine_system_disorder|hereditary_disease	metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease|hereditary_disease	pediatric|endocrinology|genetics_and_genomics	metabolic_disorder|inherited_thyroid_metabolism_disease	inherited_disease|endocrine_disorder	false	false	false	true	high
MONDO:0045047	neurosarcoidosis	syndromic_disease|nervous_system_disorder|connective_tissue_disorder	other	nervous_system_disorder|syndromic_disease|connective_tissue_disorder	neurology|immunology|oncology	neurodegenerative_disease|cancer|autoimmune_diseases|inflammatory_disease	brain_disorder|immune_disorder|spinal_disorder	false	false	false	true	high
MONDO:0045048	toxemia of pregnancy	cardiovascular_disorder|obstetric_disorder	cardiovascular_disorder	obstetric_disorder|cardiovascular_disorder	obstetrics_and_gynecology|renal_medicine	metabolic_disorder|autoimmune_diseases|inflammatory_disease	reproductive_system_disorder|endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0045049	hypermature cataract	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	medium
MONDO:0045050	nuclear cataract	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	ophthalmology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	true	high
MONDO:0045051	cortical cataract	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	neurology|ophthalmology	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	true	medium
MONDO:0045052	benign osteogenic neoplasm	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	orthopaedic|oncology	cancer	bone_disorder	false	false	false	false	low
MONDO:0045053	osteogenic neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	orthopaedic|oncology	osteogenic_neoplasm|cancer	blood_bone_marrow_disorder|bone_disorder|osteogenic_neoplasm_suggests_bone_marrow_disorder_as_well_so__blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0045054	cancer-related condition	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology	cancer_related_condition|cancer	cancer_related_conditions_often_affect_the_lymphatic_system|lymphatic_disorder	false	false	false	true	very_high
MONDO:0045055	glycogen-rich carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hepatology|endocrinology|oncology	metabolic_disorder|adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	high
MONDO:0045056	grade II meningioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0045057	delirium	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	upper_gastrointestinal_disorder|brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0045058	ACTH-producing pituitary gland neoplasm	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder|nervous_system_disorder|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|endocrine_system_disorder	endocrinology|oncology	adrenal_gland_disease|cancer	brain_disorder|pituitary_gland_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0045059	cribriform carcinoma of breast	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|otolaryngology	adrenal_gland_disease|cancer	brain_disorder|throat_disorder|ear_disorder	false	true	false	false	high
MONDO:0045060	intraductal cribriform breast adenocarcinoma	breast_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|breast_disorder	breast_cancer|assuming__breast_cancer__is_the_best_fitting_category_for_intraductal_cribriform_breast_adenocarcinoma___corrected_answer__oncology|oncology	intraductal_breast_adenocarcinoma|cancer	cancer_disorder|breast_disorder|reproductive_system_disorder|adenocarcinoma_disorder	false	true	false	false	medium
MONDO:0045063	major salivary gland adenoid cystic carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|mouth_disorder	otolaryngology|oncology	inflammatory_disease|adrenal_gland_disease|cancer|autoimmune_diseases	teeth_disorder|oral_disorder	false	true	false	false	high
MONDO:0045068	minor salivary gland adenoid cystic carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|mouth_disorder	oncology|otolaryngology	gland_disease|cancer	teeth_disorder|mouth_disorder|throat_disorder	false	true	false	true	high
MONDO:0045069	minor salivary gland carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|mouth_disorder	oncology|otolaryngology	inflammatory_disease|adrenal_gland_disease|cancer	upper_gastrointestinal_disorder|throat_disorder	false	true	false	false	medium
MONDO:0045070	digestive system melanoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|digestive_system_disorder|cancer_or_benign_tumor	gastroenterology|oncology	inflammatory_disease|digestive_system|adrenal_gland_disease|cancer|autoimmune_diseases	lower_gastrointestinal_disorder|skin_disorder	false	true	false	false	high
MONDO:0045071	mycosis fungoides variant	hematologic_disorder|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	hematologic_disorder|integumentary_system_disorder|cancer_or_benign_tumor	dermatology|oncology	cancer|autoimmune_diseases	immune_disorder|skin_disorder|lymphatic_disorder	true	true	false	true	high
MONDO:0045072	ectopic hormone secretion syndrome associated with neoplasia	syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor	endocrinology|oncology	neoplasia|adrenal_gland_disease|cancer	reproductive_system_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0049221	myopia 26, X-linked, female-limited	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0049222	intellectual disability, X-linked 107	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatrics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	intellectual_disability|brain_disorder	false	false	false	false	high
MONDO:0049223	osteogenesis imperfecta, type 19	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics	genetic_disease|metabolic_disorder	bone_disorder|teeth_disorder|joint_disorder	false	false	false	false	high
MONDO:0054549	peroxisome biogenesis disorder 10B	hereditary_disease|syndromic_disease|nervous_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease|neurodegenerative_disease	syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|metabolic_disease|hereditary_disease	pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisome_biogenesis_disorder	false	false	false	false	very_high
MONDO:0054550	avascular necrosis of femoral head, primary, 1	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|connective_tissue_disorder	other	connective_tissue_disorder|syndromic_disease|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|hematology	cardiovascular_disorder|metabolic_disorder	bone_disorder|vascular_disorder	false	false	false	false	high
MONDO:0054551	avascular necrosis of femoral head, primary, 2	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|hematology	cardiovascular_disorder|metabolic_disorder	bone_disorder|vascular_disorder	false	false	false	false	high
MONDO:0054559	congenital disorder of glycosylation, type IIq	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	congenital_disorder|metabolic_disorder	liver_disorder	false	false	true	false	high
MONDO:0054560	anauxetic dysplasia 1	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	developmental_biology|pediatric|medical_genetics|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	immune_disorder|blood_bone_marrow_disorder|muscle_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0054561	anauxetic dysplasia 2	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	immune_disorder|musculoskeletal_disorder_is_not_in_the_list_but_it_s_implied_as_anauxetic_dysplasia_2_primarily_affects_bones_and_joints|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0054565	short-rib thoracic dysplasia 17 with or without polydactyly	hereditary_disease|urinary_system_disorder|syndromic_disease|musculoskeletal_system_disorder|respiratory_system_disorder	other	urinary_system_disorder|respiratory_system_disorder|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|genetic_disorder	skeletal_system_disorder|bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0054573	Lopes-Maciel-Rodan syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	dermatology|otolaryngology|cardiology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	bone_disorder|eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0054577	bleeding disorder, platelet-type, 21	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	platelet_type|hematology	bleeding_disorder|platelet_type	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0054581	Townes-Brocks syndrome 1	hereditary_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	heart_disorder|lung_disorder|respiratory_bone_disorder	false	false	false	false	medium
MONDO:0054582	Townes-Brocks syndrome 2	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	cardiothoracic|pediatric|genetics_and_genomics	genetic_disorder_is_not_in_the_list_but_this_is_similar_to_it|metabolic_disorder	kidney_disorder|heart_disorder|immune_disorder|bone_disorder|eye_disorder|lung_disorder|joint_disorder	false	false	false	false	medium
MONDO:0054588	Noonan syndrome-like disorder with loose anagen hair 2	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|integumentary_system_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|integumentary_system_disorder	dermatology|pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	skin_disorder|heart_disorder|hair_disorder_is_not_in_the_list_but__skin_disorder_is_likely_the_closest_match_so_remove_it__heart_disorder|joint_disorder	false	false	false	false	medium
MONDO:0054591	Stankiewicz-Isidor syndrome	hereditary_disease|syndromic_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|syndromic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	liver_disorder|kidney_disorder|bone_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0054593	microcephaly 18, primary, autosomal dominant	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|blood_bone_marrow_disorder|muscle_disorder	false	false	false	false	high
MONDO:0054601	pituitary adenoma 5, multiple types	endocrine_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor|reproductive_system_disorder|hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	connective_tissue_disorder|hereditary_disease|nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|reproductive_system_disorder|endocrine_system_disorder	neurology|endocrinology	cancer__neurodegenerative_disease	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0054602	gaze palsy, familial horizontal, with progressive scoliosis, 2	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|orthopaedic	neurodegenerative_disease|familial_disorder|genetic_disorder	spinal_disorder|muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0054615	spermatogenic failure 18	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	autoimmune_diseases|cancer|metabolic_disorder|anemia	reproductive_system_disorder	false	false	false	true	high
MONDO:0054636	Skraban-Deardorff syndrome	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|dermatology|pediatrics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	bone_disorder|skin_disorder|joint_disorder	false	false	false	false	high
MONDO:0054637	Noonan syndrome-like disorder with loose anagen hair 1	hereditary_disease|musculoskeletal_system_disorder|integumentary_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder|musculoskeletal_system_disorder|integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric	cardiovascular_disorder|metabolic_disorder	hair_disorder|bone_disorder|skin_disorder	false	false	false	false	medium
MONDO:0054654	combined oxidative phosphorylation deficiency 32	mitochondrial_disease|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0054665	pituitary adenoma 3, multiple types	cancer_or_benign_tumor|reproductive_system_disorder|hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|endocrine_system_disorder|connective_tissue_disorder	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder|musculoskeletal_system_disorder|endocrine_system_disorder|connective_tissue_disorder|hereditary_disease	endocrinology|neurology	neurodegenerative_disease|cancer	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0054666	ovarian dysgenesis 5	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|cancer	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0054669	pontocerebellar hypoplasia, type 11	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0054677	combined oxidative phosphorylation deficiency 33	mitochondrial_disease|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	neurology|genetics_and_genomics|metabolic_disorders_category_was_excluded_but_can_be_inferred_from_the_answer|pediatric	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0054680	epiphyseal dysplasia, multiple, 7	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|orthopaedic|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0054691	immunodeficiency, common variable, 14	cancer_or_benign_tumor|syndromic_disease|hereditary_disease|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|syndromic_disease|hereditary_disease	pediatric|rheumatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|immunodeficiency	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0054695	myopathy, centronuclear, 6, with fiber-type disproportion	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|myopathy|metabolic_disorder	muscle_disorder|centronuclear_myopathies_often_affect_the_muscle_type_fibers_disproportionately	false	false	false	false	high
MONDO:0054696	immunodeficiency 53	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	pediatric|allergy_and_immunology|immunology	autoimmune_diseases|inflammatory_disease|immunodeficiency_does_not_match_any_category__but_closest_is_autoimmue_diseases_and_inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0054697	immunodeficiency 11b with atopic dermatitis	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	dermatology|pediatric|allergy_and_immunology|immunology	autoimmune_diseases|inflammatory_disease|allergy	immune_disorder_skin_disorder	true	false	false	true	high
MONDO:0054698	proteasome-associated autoinflammatory syndrome 1	connective_tissue_disorder|syndromic_disease|hereditary_disease|immune_system_disorder	other	connective_tissue_disorder|immune_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|rheumatology|immunology	autoimmune_diseases|inflammatory_disease	immune_disorder	false	false	false	false	very_high
MONDO:0054699	proteasome-associated autoinflammatory syndrome 3	connective_tissue_disorder|syndromic_disease|hereditary_disease|immune_system_disorder	other	connective_tissue_disorder|immune_system_disorder|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder	false	false	false	true	high
MONDO:0054700	proteasome-associated autoinflammatory syndrome 2	hereditary_disease|immune_system_disorder|syndromic_disease|connective_tissue_disorder	other	hereditary_disease|immune_system_disorder|syndromic_disease|connective_tissue_disorder	rheumatology|genetics_and_genomics|allergy_and_immunology|pediatric|immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|liver_disorder|joint_disorder	false	false	false	false	high
MONDO:0054701	Kleefstra syndrome 2	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatrics|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0054708	retinitis pigmentosa 80	hereditary_disease|nervous_system_disorder|metabolic_disease|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder|metabolic_disease	metabolic_disease|nervous_system_disorder|disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0054716	microcephaly 19, primary, autosomal recessive	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0054722	geleophysic dysplasia 3	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic	genetic_disorder|neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0054723	spermatogenic failure 19	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	anemia|metabolic_disorder	reproductive_system_disorder	false	false	false	false	high
MONDO:0054724	spermatogenic failure 20	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|endocrinology	anemia|metabolic_disorder|autoimmune_diseases	spermatozoa_is_part_of_the_male_reproductive_system__so_this_category_fits|reproductive_system_disorder	false	false	false	false	high
MONDO:0054725	spermatogenic failure 21	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	anemia|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0054726	spermatogenic failure 22	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	anemia|metabolic_disorder|autoimmune_diseases	reproductive_system_disorder	false	false	false	false	medium
MONDO:0054727	spermatogenic failure 23	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	anemia|metabolic_disorder	reproductive_system_disorder	false	false	false	false	low
MONDO:0054728	spermatogenic failure 24	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	anemia|metabolic_disorder	reproductive_system_disorder	false	false	false	false	medium
MONDO:0054729	spermatogenic failure 25	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics|endocrinology	anemia|metabolic_disorder|cancer|autoimmune_diseases	reproductive_system_disorder	false	false	false	false	medium
MONDO:0054730	spermatogenic failure 26	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	adrenal_gland_disease|metabolic_disorder	reproductive_system_disorder	false	false	false	false	high
MONDO:0054731	spermatogenic failure 27	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	endocrinology|urology	anemia|autoimmune_diseases|cancer|metabolic_disorder	reproductive_system_disorder	false	false	false	false	high
MONDO:0054732	spermatogenic failure 28	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	endocrinology|genetics_and_genomics|urology	autoimmune_diseases|adrenal_gland_disease|inflammatory_disease|cancer|metabolic_disorder	spermatozoa_related_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0054733	spermatogenic failure 29	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	anemia|autoimmune_diseases|cancer|metabolic_disorder	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0054736	mosaic variegated aneuploidy syndrome 3	cancer_or_benign_tumor|chromosomal_disorder|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|chromosomal_disorder|cancer_or_benign_tumor	neurology|genetics_and_genomics|pediatric|oncology	neurodegenerative_disease|cancer	lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0054737	Fraser syndrome 1	disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|pediatric	metabolic_disorder|genetic_condition|congenital_disorder	eye_disorder__ear_disorder__upper_gastrointestinal_disorder__reproductive_system_disorder	false	false	false	false	high
MONDO:0054738	Fraser syndrome 2	disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	kidney_disorder|throat_disorder|lymphatic_disorder|nose_disorder|ear_disorder|bone_disorder|immune_disorder|eye_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|teeth_disorder	false	false	false	false	high
MONDO:0054739	Fraser syndrome 3	disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|pediatric|otolaryngology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	face_disorder|joint_disorder|ear_disorder|eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0054740	blepharocheilodontic syndrome 1	integumentary_system_disorder|disorder_of_visual_system|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system|integumentary_system_disorder|disorder_of_orbital_region	genetics_and_genomics|pediatric|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0054741	combined oxidative phosphorylation deficiency 34	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	metabolic_disease	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	neurology|genetics_and_genomics|pediatric|metabolic	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0054742	combined oxidative phosphorylation deficiency 35	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	metabolic_disease	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	neurology|pediatrics|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0054743	polycystic liver disease 3 with or without kidney cysts	endocrine_system_disorder|digestive_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|digestive_system_disorder|endocrine_system_disorder	genetics_and_genomics|renal_medicine|hepatology	inflammatory_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0054748	Fanconi anemia, complementation group S	metabolic_disease|hematologic_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|immune_system_disorder	metabolic_disease|anemia	immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder|hematologic_disorder|disorder_of_development_or_morphogenesis|metabolic_disease	genetics_and_genomics|hematology	anemia|autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0054752	multiple synostoses syndrome 4	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|orthopaedic	congenital_dysmorphic_syndrome|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0054761	microcephaly 20, primary, autosomal recessive	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder|primary	false	false	false	false	high
MONDO:0054763	neurodegeneration with brain iron accumulation 7	metabolic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	metabolic_disease|psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0054764	neurodegeneration with brain iron accumulation 8	metabolic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	metabolic_disease|psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	neurology|genetics_and_genomics|neurodegeneration	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0054765	amyloidosis, primary localized cutaneous, 3	metabolic_disease|hereditary_disease|integumentary_system_disorder	metabolic_disease	hereditary_disease|metabolic_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	liver_disorder|skin_disorder	false	false	false	true	medium
MONDO:0054770	orofaciodigital syndrome 18	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	genetic_disease|metabolic_disorder	joint_disorder|bone_disorder|oral_disorder|facial_disorder|teeth_disorder	false	false	false	false	high
MONDO:0054771	keratoconus 9	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	pediatric|ophthalmology	eye_disease|autoimmune_diseases|genetic_disorder|inflammatory_disease	eye_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0054776	epilepsy, familial focal, with variable foci 4	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0054780	elliptocytosis 3	hematologic_disorder	anemia	hematologic_disorder	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|red_cell_disorder	false	false	false	true	high
MONDO:0054781	combined oxidative phosphorylation deficiency 36	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	metabolic_disease	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	genetics_and_genomics|pediatrics|neurology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0054782	leukodystrophy, hypomyelinating, 15	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|blood_bone_marrow_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0054785	multiple mitochondrial dysfunctions syndrome 6	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	metabolic_disease	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	mitochondrial_dysfunction|muscle_disorder	false	false	false	false	high
MONDO:0054791	leukodystrophy, hypomyelinating, 16	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|blood_bone_marrow_disorder|brain_disorder	false	false	false	false	high
MONDO:0054794	hydrocephalus, congenital, 3, with brain anomalies	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0054801	erythrocytosis, familial, 6	musculoskeletal_system_disorder|immune_system_disorder|hereditary_disease|hematologic_disorder	other	hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|erythrocytosis_familial_6	false	false	false	true	medium
MONDO:0054802	erythrocytosis, familial, 7	musculoskeletal_system_disorder|immune_system_disorder|hereditary_disease|hematologic_disorder	other	hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|hereditary_disease	hematology|genetics_and_genomics	anemia|autoimmune_diseases|metabolic_disorder|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0054804	microcephaly 21, primary, autosomal recessive	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	bone_disorder|brain_disorder|ear_disorder	false	false	false	false	high
MONDO:0054805	microcephaly 22, primary, autosomal recessive	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|autosomal_recessive_diseases_typically_fall_under_one_of_these_categories__but_the_provided_list_does_not_contain_a_specific_category_for_this_condition	brain_disorder|congenital_disorder	false	false	false	false	high
MONDO:0054806	microcephaly 23, primary, autosomal recessive	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|head_disorder|developmental_disorder	false	false	false	false	high
MONDO:0054813	Ehlers-Danlos syndrome, classic-like, 2	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	dermatology|genetics_and_genomics|rheumatology	autoimmune_diseases|metabolic_disorder|cardiovascular_disorder	joint_disorder|skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0054817	leukodystrophy, hypomyelinating, 17	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0054831	Coffin-Siris syndrome 7	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	syndromic_disease|hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	joint_disorder|blood_bone_marrow_disorder|spinal_disorder|vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0054832	corneal dystrophy, posterior polymorphous, 4	disorder_of_visual_system|hereditary_disease	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	genetics_and_genomics|ophthalmology	neurodegenerative_disease|autoimmune_diseases	eye_disorder|immune_disorder	false	false	false	false	medium
MONDO:0054833	Charcot-Marie-tooth disease, axonal, type 2DD	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|orthopaedic|neurology	neurodegenerative_disease|axonal	spinal_disorder|muscle_disorder|nerve_disorder	false	false	false	false	high
MONDO:0054835	classic dopamine transporter deficiency syndrome	syndromic_disease|nervous_system_disorder|hereditary_disease	other	syndromic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	true	high
MONDO:0054837	intellectual disability, autosomal dominant 57	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0054838	cardiomyopathy, familial hypertrophic 27	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|cardiology	metabolic_disorder|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0054842	polycystic kidney disease 6 with or without polycystic liver disease	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	genetics_and_genomics|nephrology|endocrinology	kidney_disease|metabolic_disorder	endocrine_disorder|kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0054843	ciliary dyskinesia, primary, 38	syndromic_disease|hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease|syndromic_disease	pulmonology|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	eye_disorder|lung_disorder	false	false	false	false	high
MONDO:0054844	pontocerebellar hypoplasia, type 1D	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0054845	developmental and epileptic encephalopathy, 66	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|inflammatory_disease|epileptic_encephalopathy|developmental_disorder|metabolic_disorder	developmental_disorder|epileptic_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0054846	epilepsy, familial adult myoclonic, 6	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|epilepsy	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0054847	epilepsy, familial adult myoclonic, 7	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0054849	inflammatory bowel disease 29	hereditary_disease|immune_system_disorder|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease|immune_system_disorder	gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0054850	ovarian dysgenesis 6	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|cancer	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0054852	peeling skin syndrome 6	integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder	dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	true	false	false	false	high
MONDO:0054860	hearing loss, autosomal recessive 110	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|neurodegenerative_disease	hearing_loss|ear_disorder	false	false	false	false	medium
MONDO:0054861	intellectual disability, autosomal recessive 63	nervous_system_disorder|metabolic_disease|hereditary_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder	hereditary_disease|metabolic_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0054862	premature ovarian failure 15	endocrine_system_disorder|reproductive_system_disorder|immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder|hematologic_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|musculoskeletal_system_disorder|reproductive_system_disorder|hematologic_disorder|immune_system_disorder	endocrinology|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0054865	encephalopathy due to mitochondrial and peroxisomal fission defect	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease	metabolic_disease	mitochondrial_disease|metabolic_disease|hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0054866	sudden arrhythmia death syndrome	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiovascularthoracic|cardiology	adrenal_gland_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0054867	paraomphalocele	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neonatology|pediatric|genetics_and_genomics|obstetrics_and_gynecology	adrenal_gland_disease|neurodegenerative_disease	bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0054868	meconium ileus	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|pediatric|obstetrics_and_gynecology	metabolic_disorder|gastrointestinal_disease|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0054869	nondystrophic myotonia	musculoskeletal_system_disorder|syndromic_disease	other	musculoskeletal_system_disorder|syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	medium
MONDO:0056795	X-linked spermatogenic failure 1	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	autoimmune_diseases|anemia|metabolic_disorder	reproductive_system_disorder	false	false	false	false	high
MONDO:0056796	obstructive nephropathy	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology	metabolic_disorder|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	true	high
MONDO:0056797	neurodevelopmental disorder with midbrain and hindbrain malformations	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0056798	disorder of appendix	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|general_surgery	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0056799	synovium disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology	autoimmune_diseases|inflammatory_disease	joint_disorder|immune_disorder	false	false	false	false	medium
MONDO:0056802	synovial bursa disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0056803	sulfur metabolism disease	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|metabolism__note__this_is_a_custom_category	adrenal_gland_disease|metabolic_disorder	metabolic_disorder|liver_disorder	false	false	false	false	high
MONDO:0056804	benign neoplasm of peripheral nervous system	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	cancer|neoplasm	muscle_disorder|nerve_disorder	false	false	false	false	low
MONDO:0056805	benign peripheral nerve granular cell tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	nerve_disorder|muscle_disorder	false	false	false	false	low
MONDO:0056806	non-small cell squamous lung carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|pulmonology	carcinoma|cancer|lung_cancer	lung_disorder	false	true	false	true	very_high
MONDO:0056813	hormone-resistant breast carcinoma	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	obstetrics_and_gynecology|oncology	cancer|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	true	false	false	very_high
MONDO:0056814	hormone-resistant prostate carcinoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|reproductive_system_disorder	urology|oncology	cancer	reproductive_system_disorder|endocrine_disorder	false	true	false	true	very_high
MONDO:0056815	liver adenosquamous carcinoma	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	hepatology|gastroenterology|oncology	adenocarcinoma|cancer|liver_disease	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0056816	vulvar neuroendocrine carcinoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	cancer|neuroendocrine_carcinoma	reproductive_system_disorder|endocrine_disorder	false	true	false	false	very_high
MONDO:0056817	rectal adenosquamous carcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	gastroenterology|oncology	inflammatory_disease|cancer|adrenal_gland_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0056818	skin adenosquamous carcinoma	integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|integumentary_system_disorder	dermatology|oncology	skin_disease|cancer|adenosquamous_carcinoma	lymphatic_disorder|immune_disorder|skin_disorder	false	true	false	true	high
MONDO:0056819	nasal cavity and paranasal sinus carcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	otolaryngology|oncology	cancer|nasal_cavity_and_paranasal_sinus_carcinoma	nose_disorder|throat_disorder	false	true	false	false	high
MONDO:0056820	nasal cavity and paranasal sinus neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	otolaryngology|oncology	cancer	nose_disorder|throat_disorder	false	true	false	false	high
MONDO:0056822	amyotonia congenita	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0060455	X-linked congenital hemolytic anemia	hematologic_disorder|hereditary_disease	anemia	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0060456	cerebral sclerosis, diffuse, scholz type	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0060457	autoinflammation with arthritis and dyskeratosis	hereditary_disease	other	hereditary_disease	rheumatology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|immune_disorder	false	false	false	true	high
MONDO:0060486	arthrogryposis multiplex congenita 1, neurogenic, with myelin defect	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|orthopaedic|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:0060489	46,XX sex reversal 4	endocrine_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease|sex_reversal	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0060490	neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	muscle_disorder|brain_disorder|neurodevelopmental_disorder	false	false	false	false	very_high
MONDO:0060491	neurodevelopmental disorder with involuntary movements	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0060496	neurodevelopmental disorder with hypotonia, neuropathy, and deafness	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|otolaryngology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	ear_disorder|muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0060502	neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0060507	retinal dystrophy with or without macular staphyloma	hereditary_disease	other	hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0060510	Cohen-Gibson syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	musculoskeletal_disorder_is_incorrect____joint_disorder|joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0060527	maleylacetoacetate isomerase deficiency	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	genetic_disorder|metabolic_disorder|neurodegenerative_disease	muscle_disorder|liver_disorder	false	false	false	true	high
MONDO:0060532	congenital heart defects and skeletal malformations syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|cardiology	cardiovascular_disorder|skeletal_malformations_syndrome	heart_disorder|skeletal_disorder	false	false	false	true	high
MONDO:0060533	microcephaly, short stature, and limb abnormalities	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|endocrinology	adrenal_gland_disease|short_stature|limb_abnormalities|metabolic_disorder|microcephaly|neurodegenerative_disease	brain_disorder|bone_disorder	false	false	false	false	high
MONDO:0060549	congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay	hereditary_disease	other	hereditary_disease	pediatric|urology|genetics_and_genomics	congenital_anomalies|metabolic_disorder	ear_disorder|kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0060550	polydactyly, postaxial, type a7	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0060551	cerebellar atrophy, developmental delay, and seizures	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	seizure_disorder|developmental_disorder|neurodegenerative_disease	developmental_delay|spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0060554	vertebral, cardiac, renal, and limb defects syndrome 1	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|orthopaedic|renal_medicine|genetics_and_genomics|cardiology	developmental_disorder|cardiovascular_disorder|metabolic_disorder	kidney_disorder|spinal_disorder|joint_disorder|vascular_disorder|muscle_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0060555	vertebral, cardiac, renal, and limb defects syndrome 2	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|orthopaedic|neurology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder|limb_defect	kidney_disorder|spinal_disorder|vascular_disorder|limb_defect	false	false	false	false	high
MONDO:0060556	joint laxity, short stature, and myopia	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|orthopaedic|endocrinology|ophthalmology	growth_hormone_deficiency|metabolic_disorder	endocrine_disorder|joint_disorder|eye_disorder	false	false	false	false	medium
MONDO:0060562	encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|neurology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0060564	HELIX syndrome	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0060568	Pilarowski-Bjornsson syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	bone_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0060577	neurodevelopmental disorder with microcephaly, ataxia, and seizures	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	neurodevelopmental_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0060578	neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|mitochondrial_diseases_are_not_listed_so_nothing|neurodegenerative_disease	brain_disorder|muscle_disorder	true	false	false	true	very_high
MONDO:0060582	auditory neuropathy-optic atrophy syndrome	hereditary_disease|mitochondrial_disease	other	hereditary_disease|mitochondrial_disease	genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	ear_disorder|eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0060583	platelet abnormalities with eosinophilia and immune-mediated inflammatory disease	hereditary_disease	other	hereditary_disease	rheumatology|hematology|immunology	anemia|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	true	false	false	false	high
MONDO:0060585	neuronopathy, distal hereditary motor, type 9	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	motor_neuron_disorder|hereditary_disease|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0060589	facial palsy, congenital, with ptosis and velopharyngeal dysfunction	hereditary_disease	other	hereditary_disease	otolaryngology|neurology|pediatric	congenital_condition|autoimmune_diseases|neurodegenerative_disease|cranial_nerve_disorder____however__since_the_original_list_didn_t_have_those_specific_categories__i_will_choose_from_it___neurological_disorder|neurological_disorder	ear_disorder|muscle_disorder|throat_disorder	true	false	false	false	high
MONDO:0060591	immunodeficiency, developmental delay, and hypohomocysteinemia	hereditary_disease	other	hereditary_disease	immunology|allergy_and_immunology|pediatric|genetics_and_genomics	metabolic_disorder|developmental_delay|autoimmune_diseases	developmental_delay|immune_disorder	true	false	false	true	medium
MONDO:0060592	Sweeney-Cox syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0060596	neurodevelopmental disorder with dysmorphic facies and distal limb anomalies	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodevelopmental_disorder|neurodegenerative_disease	musculoskeletal_disorder__note__original_list_didn_t_have_this_category_but_based_on_description_it_fits_best|brain_disorder	false	false	false	true	high
MONDO:0060611	combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatrics|hematology	anemia|metabolic_disorder	upper_gastrointestinal_disorder|immune_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0060621	neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics|neurodevelopmental_disorder_is_often_classified_under_developmental_pediatrics_so_likely_the_best_fit_is_just_pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	cortical_atrophy|spinal_disorder|brain_disorder	false	false	false	the_description_provided_suggests_a_neurodevelopmental_disorder__potentially_related_to_conditions_such_as_congenital_zika_syndrome_or_other_genetic_metabolic_disorders__however__as_of_my_last_knowledge_update_in_october_2023__there_are_generally_no_specific_cures_for_neurodevelopmental_disorders__including_those_characterized_by_microcephaly__seizures__and_cortical_atrophy__treatments_may_focus_on_managing_symptoms_and_improving_quality_of_life__but_they_do_not_cure_the_underlying_disorder___based_on_this_understanding__the_response_would_be__false	very_high
MONDO:0060622	neurodevelopmental disorder with severe motor impairment and absent language	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0060624	neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0060627	glycosylphosphatidylinositol biosynthesis defect 15	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0060629	neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0060631	Alkuraya-Kucinskas syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|cancer|neurodegenerative_disease	bone_disorder|liver_disorder|joint_disorder	false	false	false	false	high
MONDO:0060640	neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	neurodevelopmental_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0060641	neurodevelopmental disorder with or without seizures and gait abnormalities	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0060642	neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|psychiatry	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0060650	Leber congenital amaurosis with early-onset deafness	disorder_of_visual_system|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease	otolaryngology|pediatric|genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0060659	neurodevelopmental disorder with poor language and loss of hand skills	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	neurodevelopmental_disorder|brain_disorder	false	false	false	true	high
MONDO:0060662	Diamond-Blackfan anemia-like	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0060663	congenital heart defects, multiple types, 5	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiology|pediatric	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0060664	neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics|renal_medicine	renal_abnormalities_is_not_in_the_list_so_i_will_remove_it__neurodegenerative_disease|neurodegenerative_disease|metabolic_disorder	kidney_disorder|eye_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0060666	hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	teeth_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0060677	chromosome 1p35 deletion syndrome	chromosomal_disorder|hereditary_disease	other	hereditary_disease|chromosomal_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	developmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0060688	hyperthyroxinemia, euthyroid, caused by generalized 5-prime-deiodinase deficiency	hereditary_disease	other	hereditary_disease	genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder	thyroid_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0060690	phenytoin toxicity	poisoning	other	poisoning	neurology|psychiatry	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	liver_disorder|brain_disorder	false	false	false	false	medium
MONDO:0060702	spondyloepimetaphyseal dysplasia, di rocco type	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0060704	neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodevelopmental_disorder|seizure|neurodegenerative_disease|brain_abnormalities	spinal_disorder|muscle_disorder|brain_abnormalities|brain_disorder	false	false	false	true	very_high
MONDO:0060707	Ververi-Brady syndrome	nervous_system_disorder|hereditary_disease|syndromic_disease|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|syndromic_disease|hereditary_disease	neurology|pediatrics	mental_health_disorder|neurodegenerative_disease	vascular_disorder|joint_disorder	false	false	false	false	high
MONDO:0060711	Jaberi-Elahi syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|pediatrics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0060713	deafness, congenital heart defects, and posterior embryotoxon	hereditary_disease	other	hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	cardiovascular_disorder|congenital_heart_defects	ear_disorder|heart_disorder	true	false	false	false	high
MONDO:0060714	tumoral calcinosis, hyperphosphatemic, familial, 2	hereditary_disease|integumentary_system_disorder|endocrine_system_disorder|metabolic_disease|cancer_or_benign_tumor	endocrine_system_disorder|metabolic_disease|cancer_or_benign_tumor	metabolic_disease|integumentary_system_disorder|endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor	rheumatology|renal_medicine|genetics_and_genomics|oncology	cancer|metabolic_disorder	bone_disorder|kidney_disorder	false	false	false	true	high
MONDO:0060715	tumoral calcinosis, hyperphosphatemic, familial, 3	hereditary_disease|integumentary_system_disorder|endocrine_system_disorder|metabolic_disease|cancer_or_benign_tumor	endocrine_system_disorder|metabolic_disease|cancer_or_benign_tumor	metabolic_disease|integumentary_system_disorder|endocrine_system_disorder|hereditary_disease|cancer_or_benign_tumor	pediatric|endocrinology|renal_medicine|genetics_and_genomics|oncology	familial|cancer|metabolic_disorder	bone_disorder|endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0060720	congenital disorder of glycosylation with defective fucosylation	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|all_other_options_do_not_fit_the_description_of_a_congenital_disorder|genetics_and_genomics	congenital_disorder|metabolic_disorder	liver_disorder|other____liver_disorder_is_the_primary_location_of_a_defect_in_fucosylation__but_since_it_is_a_congenital_disorder_of_glycosylation__it_also_falls_under_the_broader_category_of__other	false	false	true	false	high
MONDO:0060724	glycosylphosphatidylinositol biosynthesis defect 17	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatrics|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease|inflammatory_disease|metabolic_disorder	liver_disorder|metabolic_disorder	false	false	false	false	high
MONDO:0060729	protoporphyria, erythropoietic, 2	hereditary_disease|integumentary_system_disorder|digestive_system_disorder|endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease	metabolic_disease|integumentary_system_disorder|endocrine_system_disorder|digestive_system_disorder|hereditary_disease	dermatology|hematology|genetics_and_genomics	anemia|metabolic_disorder	liver_disorder|skin_disorder	false	false	false	true	high
MONDO:0060732	tetraamelia syndrome 2	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|medical_genetics	neurodegenerative_disease|metabolic_disorder	limb_abnormality|bone_disorder|vascular_disorder	false	false	false	false	high
MONDO:0060733	humerofemoral hypoplasia with radiotibial ray deficiency	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic	autoimmune_diseases|inflammatory_disease|metabolic_disorder	bone_disorder|vascular_disorder|joint_disorder	false	false	false	false	high
MONDO:0060745	intellectual developmental disorder with or without epilepsy or cerebellar ataxia	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	cerebellar_ataxia|brain_disorder	false	false	false	false	high
MONDO:0060752	neurodevelopmental disorder with spasticity and poor growth	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	brain_disorder|poor_growth_is_associated_with_endocrine_disorder_or_other_but_those_aren_t_the_best_fit_so_it_s__brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0060758	spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0060759	neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures	nervous_system_disorder|syndromic_disease|hereditary_disease	other	nervous_system_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|spinal_disorder|muscle_disorder	true	false	false	true	very_high
MONDO:0060760	intellectual developmental disorder with dysmorphic facies and behavioral abnormalities	nervous_system_disorder|psychiatric_disorder|syndromic_disease|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|syndromic_disease|hereditary_disease	psychiatry|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|intellectual_disdevelopmental_disorder	false	false	false	false	high
MONDO:0060761	neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|neurodevelopmental_disorder	neurodevelopmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0060763	intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities	nervous_system_disorder|psychiatric_disorder|hereditary_disease|syndromic_disease	psychiatric_disorder	nervous_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease	immunology|genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases	immune_disorder|brain_disorder	true	false	false	false	high
MONDO:0060764	tetraamelia syndrome 1	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|lower_gastrointestinal_disorder|immune_disorder|lymphatic_disorder|upper_gastrointestinal_disorder|spinal_disorder	false	false	false	false	high
MONDO:0060765	fibroepithelial polyp	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	gastroenterology|oncology|otolaryngology	tumor|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	low
MONDO:0060766	anal polyp	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|urology	gastrointestinal_disease|neoplastic_disease|colorectal_cancer|cancer	lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0060768	gingival fibroepithelial polyp	cancer_or_benign_tumor|musculoskeletal_system_disorder	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	oral_pathology|pediatric|otolaryngology	inflammatory_disease|cancer	skin_disorder|teeth_disorder|oral_disorder	false	false	false	false	low
MONDO:0060774	vaginal fibroepithelial polyp	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	gynecological_disorder|benign_tumor|genital_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0060777	cervical fibroepithelial polyp	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	inflammatory_disease|cancer	lower_gastrointestinal_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0060778	adult Fanconi syndrome	urinary_system_disorder|syndromic_disease	other	urinary_system_disorder|syndromic_disease	genetics_and_genomics|pulmonology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	bone_bone_marrow_disorder|kidney_disorder	true	false	false	true	high
MONDO:0060779	acquired Fanconi syndrome	urinary_system_disorder|syndromic_disease	other	urinary_system_disorder|syndromic_disease	genetics_and_genomics|pulmonology|endocrinology|renal_medicine	metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|kidney_disorder	true	false	false	false	high
MONDO:0060781	Preeyasombat-Varavithya syndrome	urinary_system_disorder|syndromic_disease	other	urinary_system_disorder|syndromic_disease	pediatric|obstetrics_and_gynecology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	liver_disorder	false	false	false	false	high
MONDO:0060782	premalignant hematological system disease	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	hematology|oncology|genetics_and_genomics	anemia|premalignant_hematological_system_disease____cancer	premalignant_hematological_system_disease|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0060783	classic congenital adrenal hyperplasia	metabolic_disease|endocrine_system_disorder|hereditary_disease	metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0100000	MED12-related intellectual disability syndrome	psychiatric_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|syndromic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100001	alpha-gal syndrome	immune_system_disorder	other	immune_system_disorder	dermatology|allergy_and_immunology|gastroenterology	allergy|autoimmune_diseases	immune_disorder|food_allergy_disorder|skin_disorder	false	false	false	false	medium
MONDO:0100002	food protein-induced allergic proctocolitis	inflammatory_disease|digestive_system_disorder|hereditary_disease|immune_system_disorder	other	inflammatory_disease|digestive_system_disorder|hereditary_disease|immune_system_disorder	pediatrics|gastroenterology	inflammatory_disease|allergy|autoimmune_diseases	lower_gastrointestinal_disorder|immune_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0100004	mast cell activation syndrome	hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder	allergy_and_immunology|hematology	inflammatory_disease|allergy|autoimmune_diseases	immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0100006	secondary mast cell activation syndrome	hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hematologic_disorder	immunology|allergy_and_immunology|hematology	inflammatory_disease|allergy|autoimmune_diseases	immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0100008	food protein-induced enterocolitis syndrome	hereditary_disease	other	hereditary_disease	pediatric|gastroenterology	inflammatory_disease|allergy	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0100009	structural congenital heart disease, multiple types - GATA4	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|cardiology|genetics_and_genomics	cardiovascular_disorder|structural_congenital_heart_disease	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0100010	disease of the tendon	musculoskeletal_system_disorder|connective_tissue_disorder	other	connective_tissue_disorder|musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0100011	tendinosis	musculoskeletal_system_disorder|connective_tissue_disorder	other	connective_tissue_disorder|musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease	joint_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0100012	paratenonitis	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	other	inflammatory_disease|connective_tissue_disorder|musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|muscle_disorder	false	false	false	false	low
MONDO:0100013	paratenonitis with tendinosis	inflammatory_disease|musculoskeletal_system_disorder|connective_tissue_disorder	other	inflammatory_disease|connective_tissue_disorder|musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0100014	autoimmune retinopathy	otorhinolaryngologic_disease|nervous_system_disorder|immune_system_disorder|disorder_of_visual_system	autoimmune_disease	nervous_system_disorder|disorder_of_visual_system|immune_system_disorder|disorder_of_orbital_region|otorhinolaryngologic_disease	rheumatology|ophthalmology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	false	false	false	false	high
MONDO:0100015	adult-onset segmental dystonia	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0100016	early-onset generalized dystonia	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|adrenal_gland_disease|autoimmune_diseases	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100017	pityriasis rubra pilaris	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0100018	adult onset pityriasis rubra pilaris	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder|muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0100019	ECHS1-related paroxysmal dyskinesia	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0100020	atypical childhood epilepsy with centrotemporal spikes	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|inflammatory_disease|mental_health_disorder|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0100021	photosensitive occipital lobe epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|epilepsy	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0100022	neonatal/infantile epilepsy syndrome	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0100023	self-limited familial neonatal epilepsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0100024	self-limited familial infantile epilepsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	true	low
MONDO:0100025	epilepsy of infancy with migrating focal seizures	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0100026	myoclonic encephalopathy in non-progressive disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0100028	immune epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|immunology_is_not_in_the_list_but_closest_match_is_allergy_and_immunology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder	false	false	false	true	high
MONDO:0100029	antibody mediated epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|immunology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder	false	false	false	false	high
MONDO:0100033	metabolic epilepsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0100034	cerebral folate deficiency	hereditary_disease|nutritional_disorder|metabolic_disease	metabolic_disease	nutritional_disorder|hereditary_disease|metabolic_disease	pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0100035	structural epilepsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|structural___note__structural_epilepsy_is_a_type_of_epilepsy_that_involves_abnormal_electrical_activity_in_the_brain_due_to_physical_changes_in_the_brain_s_structure	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100037	juvenile onset pityriasis rubra pilaris	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder|joint_disorder	false	false	false	true	medium
MONDO:0100038	complex neurodevelopmental disorder	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100039	CDKL5 disorder	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder|reproductive_system_disorder	false	false	false	false	very_high
MONDO:0100040	FOXG1 disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100041	secondary trimethylaminuria	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatrics|hepatology|genetics_and_genomics|renal_medicine	metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	true	low
MONDO:0100042	cardiac conduction defect	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder|autoimmune_diseases	heart_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0100044	acrofrontofacionasal dysostosis 1	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	skeletal_dysplasia|metabolic_disorder|genetic_disorder	spinal_disorder|bone_disorder|teeth_disorder|joint_disorder	false	false	false	false	medium
MONDO:0100050	Usher syndrome, type 1D/F	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	pediatric|neurology|ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0100051	idiopathic mast cell activation syndrome	immune_system_disorder|hematologic_disorder	other	hematologic_disorder|immune_system_disorder|idiopathic_disease	hematolog|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0100053	anaphylaxis	immune_system_disorder	other	immune_system_disorder	pediatric|allergy_and_immunology	allergy|autoimmune_diseases	allergic_reaction|immune_disorder	false	false	false	true	high
MONDO:0100054	idiopathic anaphylaxis	immune_system_disorder	other	immune_system_disorder|idiopathic_disease	pulmonology|dermatology|allergy_and_immunology	allergy|inflammatory_disease|autoimmune_diseases	immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0100055	intraosseous spindle cell rhabdomyosarcoma with TFCP2/NCOA2 rearrangements	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology|genetics_and_genomics	cancer	muscle_disorder|bone_disorder	false	true	false	false	very_high
MONDO:0100056	exercise-induced anaphylaxis	immune_system_disorder	other	immune_system_disorder	pediatrics|allergy_and_immunology	allergy|inflammatory_disease|autoimmune_diseases	allergic_reaction|immune_disorder|anaphylaxis	false	false	false	true	medium
MONDO:0100057	food-dependent exercise-induced anaphylaxis	immune_system_disorder	other	immune_system_disorder	pediatric|allergy_and_immunology	allergy|autoimmune_diseases	upper_gastrointestinal_disorder|immune_disorder	false	false	false	true	medium
MONDO:0100058	hypervalinemia and hyperleucine-isoleucinemia	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0100059	hypereosinophilia of undetermined significance	musculoskeletal_system_disorder|cardiovascular_disorder|immune_system_disorder|syndromic_disease|hematologic_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|hematologic_disorder|syndromic_disease|cardiovascular_disorder|immune_system_disorder	immunology|hematology|allergy_and_immunology	allergy|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	low
MONDO:0100060	congenital/infantile spindle cell rhabdomyosarcoma with VGLL2/NCOA2/CITED2 rearrangements	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology|genetics_and_genomics	congenital_infantile_spindle_cell_rhabdomyosarcoma|cancer	muscle_disorder|childhood_disorder	false	true	false	false	very_high
MONDO:0100061	PRPS1 deficiency disorder	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|blood_bone_marrow_disorder|joint_disorder	false	false	false	false	high
MONDO:0100062	genetic developmental and epileptic encephalopathy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|developmental_disorder|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0100063	Pericytoma with t(7;12)	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics	cancer|adrenal_gland_disease	brain_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0100064	tyrosine hydroxylase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0100065	TH-deficient infantile parkinsonism and motor delay	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0100066	TH-deficient progressive infantile encephalopathy	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0100067	childhood spindle cell rhabdomyosarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology	cancer	muscle_disorder	false	true	false	true	very_high
MONDO:0100068	SLC10A7-congenital disorder of glycosylation	musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	congenital_disorder_of_glycosylation|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0100069	hearing impairment and infertile male syndrome	syndromic_disease	other	syndromic_disease	otolaryngology|urology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder|ear_disorder	false	false	false	true	medium
MONDO:0100070	neuroendocrine disorder	endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder	endocrine_system_disorder|nervous_system_disorder	neurology|endocrinology	metabolic_disorder|autoimmune_diseases|neuroendocrine_disorder____neurodegenerative_disease	neurodisorder|endocrine_disorder|brain_disorder	false	false	false	false	high
MONDO:0100071	cardiocutaneous syndrome	syndromic_disease	other	syndromic_disease	dermatology|cardiology|cardiothoracic	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	vascular_disorder|skin_disorder|heart_disorder	false	false	false	false	high
MONDO:0100072	neonatal diabetes, congenital sensorineural hearing loss and congenital cataracts	syndromic_disease	other	syndromic_disease	ophthalmology|genetics_and_genomics|pediatric|endocrinology	metabolic_disorder|autoimmune_diseases|congenital_condition	eye_disorder|ear_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0100073	methicillin-resistant staphylococcus aureus infectious disease	infectious_disease	infectious_disease	infectious_disease	dermatology|infectious_disease|renal_medicine|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0100074	norovirus infectious disease	infectious_disease	infectious_disease	infectious_disease	gastroenterology|infectious_disease	viral_infection|gastrointestinal_disorder|infectious_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0100076	juvenile idiopathic scoliosis	musculoskeletal_system_disorder	other	idiopathic_disease|musculoskeletal_system_disorder	orthopaedic|pediatric	inflammatory_disease|neurodegenerative_disease	bone_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0100077	congenital alveolar dysplasia	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|pulmonology	metabolic_disorder|congenital_disease	bone_disorder|lung_disorder	false	false	false	false	high
MONDO:0100078	resistant hypertension	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	renal_medicine|cardiology	metabolic_disorder|cardiovascular_disorder	vascular_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0100079	developmental and epileptic encephalopathy, 6A	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	developmental_disorder|neurodegenerative_disease|epileptic_disorder	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0100080	cardioectodermal syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|pediatric|cardiology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	eye_disorder|ear_disorder|heart_disorder	false	false	false	false	high
MONDO:0100081	sleep disorder	other	other		neurology|psychiatry|pulmonology	metabolic_disorder|mental_health_disorder	sleep_disorder_is_not_in_the_list_so_this_answer_will_be_a_subset_of_brain_disorder___however__sleep_disorder_can_also_relate_to_nervous_system_disorders_which_isn_t_listed_here_but_it_can_also_overlap_with_upper_gastrointestinal_disorder_due_to_relationship_between_digestive_and_sleep|brain_disorder	false	false	false	true	medium
MONDO:0100082	LEOPARD syndrome 1	disorder_of_development_or_morphogenesis|syndromic_disease|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	dermatology|genetics_and_genomics|pediatric	metabolic_disorder|cardiovascular_disorder	bone_disorder|eye_disorder|vascular_disorder|skin_disorder|heart_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100083	hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	syndromic_disease|cancer_or_benign_tumor|hematologic_disorder|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|hematologic_disorder|cancer_or_benign_tumor	genetics_and_genomics|hematology|oncology	anemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0100084	alpha-actinopathy	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	neurology|genetics_and_genomics|cardiology|pulmonology	muscular_dystrophy|neurodegenerative_disease	lower_gastrointestinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100085	cancer of long bone of upper limb	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	orthopaedic|oncology	inflammatory_disease|autoimmune_diseases|cancer	bone_disorder|blood_bone_marrow_disorder|subtype	false	true	false	false	high
MONDO:0100086	perinatal disease		other		obstetrics_and_gynecology|pediatric	metabolic_disorder|perinatal_disease|autoimmune_diseases	perinatal_disease|reproductive_system_disorder	true	false	false	false	high
MONDO:0100087	familial Alzheimer disease	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	bone_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0100089	GATA1-Related X-Linked Cytopenia	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	anemia|autoimmune_diseases|genetic_disorder|i_removed__other__because_it_was_not_one_of_the_best_fitting_categories	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0100090	congenital alveolar dysplasia due to FGF10	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|pulmonology	cardiovascular_disorder|metabolic_disorder	lung_disorder|teeth_disorder	false	false	false	false	high
MONDO:0100091	inherited pseudoxanthoma elasticum	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	metabolic_disorder|genetic_disease|inherited_diseases|skin_condition	skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0100092	myoclonus, familial, 2	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	familial____note__i_corrected_the_category__familial__to_be_a_subcategory_of_neurodegenerative_disease__as_myoclonus_is_often_associated_with_certain_genetic_disorders|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100093	myoclonus, familial, 1	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	familial|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100094	cannabinoid hyperemesis syndrome	syndromic_disease	other	syndromic_disease	hepatology|neurology|gastroenterology|psychiatry	metabolic_disorder|mental_health_disorder	upper_gastrointestinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0100095	neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	variable_ataxia_and_seizures|childhood_onset|neurodegenerative_disease|stress_induced	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0100096	COVID-19	infectious_disease	infectious_disease	infectious_disease	infectious_disease|pulmonology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|lung_disorder|immune_disorder	true	false	false	true	very_high
MONDO:0100097	congenital alveolar dysplasia due to TBX4	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|pulmonology	metabolic_disorder|congenital_disease|developmental_disorder	lung_disorder|respiratory_system_disorder_is_not_listed_so_we_will_assume_it_s_a_lung_disorder	false	false	false	false	high
MONDO:0100098	dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|autosomal_recessive_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0100099	retrograde cricopharyngeus dysfunction	syndromic_disease	other	syndromic_disease	neurology|otolaryngology	autoimmune_diseases|neurodegenerative_disease	throat_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0100100	SELENON-related myopathy	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	true	very_high
MONDO:0100101	fetal akinesia deformation sequence 1	respiratory_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	disorder_of_development_or_morphogenesis|respiratory_system_disorder|hereditary_disease|syndromic_disease	obstetrics_and_gynecology|genetics_and_genomics|pediatric	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100102	fetal akinesia deformation sequence 2	respiratory_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	disorder_of_development_or_morphogenesis|respiratory_system_disorder|hereditary_disease|syndromic_disease	obstetrics_and_gynecology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100103	fetal akinesia deformation sequence 3	respiratory_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	disorder_of_development_or_morphogenesis|respiratory_system_disorder|hereditary_disease|syndromic_disease	pediatric|obstetrics_and_gynecology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100104	fetal akinesia deformation sequence 4	respiratory_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	disorder_of_development_or_morphogenesis|respiratory_system_disorder|hereditary_disease|syndromic_disease	pediatric|obstetrics_and_gynecology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100105	brain small vessel disease 3	cardiovascular_disorder|hereditary_disease|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|nervous_system_disorder	neurology|cardiovascular_disease_is_a_subset_of_cardiology_which_is_in_the_category_list_but_brain_small_vessel_disease_specifically_falls_under_neurology_as_it_deals_directly_with_issues_affecting_blood_vessels_within_the_brain	neurodegenerative_disease|cardiovascular_disorder	brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0100107	non-neonatal early infantile epileptic encephalopathy	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0100108	TPM3-related myopathy	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease	muscle_disorder|bone_disorder	false	false	false	true	high
MONDO:0100109	Zinner syndrome	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	lower_gastrointestinal_disorder|liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0100110	adenovirus renal infection	urinary_system_disorder|infectious_disease	infectious_disease	urinary_system_disorder|infectious_disease	renal_medicine|pediatric	autoimmune_diseases|inflammatory_disease|renal_infection	urinary_tract_disorder|kidney_disorder	true	false	false	true	high
MONDO:0100111	focal segmental glomerulosclerosis and neurodevelopmental syndrome	hereditary_disease	other	hereditary_disease	renal_medicine|neurology|pediatric|psychiatry|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|mental_health_disorder	neurodevelopmental_syndrome_is_more_complex_and_can_be_categorized_under_brain_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0100112	acyl-CoA binding domain containing protein 5 deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100113	hearing loss with skin disease	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	dermatology|otolaryngology	autoimmune_diseases|inflammatory_disease	skin_disorder|ear_disorder	true	false	false	true	medium
MONDO:0100114	dry age related macular degeneration	psychiatric_disorder|hereditary_disease|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease	neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0100115	acute flaccid myelitis	nervous_system_disorder|inflammatory_disease	other	nervous_system_disorder|inflammatory_disease|acute_disease	neurology|pediatric	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder_spinal_disorder_muscle_disorder	true	false	false	false	high
MONDO:0100116	Middle East respiratory syndrome	respiratory_system_disorder|infectious_disease	infectious_disease	respiratory_system_disorder|infectious_disease	pulmonology|infectious_diseases	autoimmune_diseases|inflammatory_disease|respiratory_syndrome	lower_gastrointestinal_disorder|immune_disorder|lung_disorder	true	false	false	false	high
MONDO:0100118	hereditary skin disorder	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0100119	Knobloch syndrome 2	hereditary_disease|nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	medical_genetics|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0100120	vector-borne disease	infectious_disease	infectious_disease	infectious_disease	infectious_disease_is_not_in_the_list__but_vector_borne_implies_a_connection_to_infectious_diseases_which_could_be_categorized_under_pediatric__children_are_often_affected|pediatric	autoimmune_diseases|vector_borne_diseases_often_involve_a_vector_such_as_an_insect_transmitting_the_disease_so_another_category_could_be__infectious_disease|inflammatory_disease	immune_disorder|vascular_disorder	true	false	false	true	high
MONDO:0100121	SCN4A-related myopathy, autosomal recessive	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0100122	GNPTAB-mucolipidosis	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	lymphatic_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0100123	toxic bronchiolitis	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease	lung_disorder|lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0100124	NAA10-related syndrome	psychiatric_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|syndromic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|developmental_disorder|developmental_disorder___corrected_to__brain_disorder	false	false	false	false	high
MONDO:0100125	hallucinogen-persisting perception disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	mental_health_disorder|hallucinations	brain_disorder	false	false	false	false	medium
MONDO:0100126	P5CS deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|nephrology	nevrodegenerative_disease|metabolic_disorder	amino_acid_metabolism_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100127	toxic bronchiolitis obliterans	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0100128	coinfection	infectious_disease	infectious_disease	infectious_disease	microbiology|immunology|pulmonology|infectious_diseases|allergy_and_immunology|infection	autoimmune_diseases|inflammatory_disease	immune_disorder|upper_gastrointestinal_disorder	true	false	false	false	high
MONDO:0100129	intracranial arachoid cyst	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|pediatric	cancer|inflammatory_disease|neurological_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0100130	adult acute respiratory distress syndrome	respiratory_system_disorder|syndromic_disease	other	respiratory_system_disorder|syndromic_disease|acute_disease	pulmonology|cardiology|cardiothoracic	respiratory_disease___corrected_list_to_match_request___inflammatory_disease|inflammatory_disease|cardiovascular_disorder	lung_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0100131	pediatric acute respiratory distress syndrome	respiratory_system_disorder|syndromic_disease	other	respiratory_system_disorder|syndromic_disease|acute_disease	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease|respiratory_disease_is_not_in_the_list_but_could_be_a_better_fit_than_some_of_these_options__the_best_fitting_categories_from_this_list_would_be_inflammatory_disease	lung_disorder|respiratory_distress_syndrome	false	false	false	false	high
MONDO:0100132	intrahepatic bile duct adenosquamous carcinoma	digestive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	hepatology|oncology	autoimmune_diseases|cancer|inflammatory_disease|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder|biliary_disorder	false	true	false	false	very_high
MONDO:0100133	mitochondrial complex I deficiency	mitochondrial_disease|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0100134	mitochondrial complex I deficiency, mitochondrial type	mitochondrial_disease|metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder	false	false	false	false	high
MONDO:0100135	Dravet syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	neurological_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0100137	telomere syndrome	premature_aging_syndrome	other	premature_aging_syndrome	pediatrics|genetics_and_genomics	metabolic_disorder|cancer|neurodegenerative_disease	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	high
MONDO:0100138	X-linked recessive mitochondrial myopathy	mitochondrial_disease|metabolic_disease|hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease	nervous_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease|musculoskeletal_system_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	mitochodrial_myopathy|muscle_disorder	false	false	false	false	very_high
MONDO:0100144	Uner Tan Syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics|allergy_and_immunology	autoimmune_diseases|neurodegenerative_disease	immune_disorder|skin_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0100146	ATP6AP2-related disorder	psychiatric_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|syndromic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|kidney_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0100147	SATB2 associated disorder	psychiatric_disorder|syndromic_disease|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|syndromic_disease|hereditary_disease	pediatric|psychiatry|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	spinal_disorder|bone_disorder	false	false	false	true	very_high
MONDO:0100148	X-linked complex neurodevelopmental disorder	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0100149	PNPLA6-related spastic paraplegia with or without ataxia	syndromic_disease|metabolic_disease|hereditary_disease|nervous_system_disorder	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|metabolic_disease|syndromic_disease|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100150	RYR1-related myopathy	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|orthopaedic|genetics_and_genomics	muscle_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0100151	nephropathic cystinosis	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	urology|genetics_and_genomics|renal_medicine	metabolic_disorder|neurodegenerative_disease	urinary_tract_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0100152	DKC1-related disorder	syndromic_disease|integumentary_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|anemia|neurodegenerative_disease	blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0100153	tubulinopathy	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	tubulinvopathy|neurodegenerative_disease	muscle_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100154	TUBB3-related tubulinopathy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0100155	retinal dystrophy-ataxia-pituitary hormone abnormality-hypogonadism syndrome	syndromic_disease	other	syndromic_disease	neurology|ophthalmology|genetics_and_genomics|endocrinology	hypogonadism_syndrome|hormonal_disorder|adrenal_gland_disease|pituitary_disease|genetic_disorder|neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	endocrine_disorder|brain_disorder|spinal_disorder|reproductive_system_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0100156	Imerslund-Grasbeck syndrome type 1	hematologic_disorder|hereditary_disease|nutritional_disorder|syndromic_disease|metabolic_disease	metabolic_disease|anemia	nutritional_disorder|metabolic_disease|hereditary_disease|syndromic_disease|hematologic_disorder	pediatrics|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0100157	Imerslund-Grasbeck syndrome type 2	hematologic_disorder|hereditary_disease|nutritional_disorder|syndromic_disease|metabolic_disease	metabolic_disease|anemia	nutritional_disorder|metabolic_disease|hereditary_disease|syndromic_disease|hematologic_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0100158	CHRNG-associated hypo-akinesia disorder of prenatal onset	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0100159	pulmonary hypertension, neonatal	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	pediatric|pulmonology|cardiology	cardiovascular_disorder|pulmonary_hypertension_neonatal_is_not_a_recognized_medical_term_for_the_given_disease_so_it_should_be_removed_from_consideration__cardiovascular_disorder	lung_disorder|vascular_disorder	false	false	false	true	high
MONDO:0100160	alcoholic ketoacidosis	metabolic_disease	metabolic_disease	metabolic_disease	gastroenterology|neurology|renal_medicine|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|liver_disorder	false	false	false	true	medium
MONDO:0100161	hyperkalemic renal tubular acidosis	urinary_system_disorder|metabolic_disease	metabolic_disease	urinary_system_disorder|metabolic_disease	renal_medicine|pediatric|genetics_and_genomics	renal_tubular_acidosis|metabolic_disorder	muscle_disorder|kidney_disorder	false	false	false	true	high
MONDO:0100162	IKBKG-related immunodeficiency with or without ectodermal dysplasia	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	immunology|pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	ectodermal_dysplasia|immune_disorder	true	false	false	true	high
MONDO:0100163	COVID-19–associated multisystem inflammatory syndrome in children	infectious_disease	infectious_disease	post_infectious_disorder|infectious_disease	pediatric|pulmonology|rheumatology	inflammatory_disease|autoimmune_diseases	lung_disorder|liver_disorder|immune_disorder|kidney_disorder	true	false	false	true	very_high
MONDO:0100164	permanent neonatal diabetes mellitus	digestive_system_disorder|hereditary_disease|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|diabetes_mellitus|metabolic_disease	endocrine_system_disorder|digestive_system_disorder|metabolic_disease|hereditary_disease	pediatric|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|immune_disorder	false	false	true	true	high
MONDO:0100165	permanent neonatal diabetes mellitus 1	digestive_system_disorder|hereditary_disease|metabolic_disease|endocrine_system_disorder	endocrine_system_disorder|diabetes_mellitus|metabolic_disease	endocrine_system_disorder|digestive_system_disorder|metabolic_disease|hereditary_disease	pediatric|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder	false	false	true	true	high
MONDO:0100166	PPP2R1A-related intellectual disability	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100168	desmoid tumor caused by somatic mutation	cancer_or_benign_tumor|hereditary_disease|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|hereditary_disease	dermatology|oncology|genetics_and_genomics	cancer|adrenal_gland_disease	reproductive_system_disorder|muscle_disorder|skin_disorder	false	false	false	true	high
MONDO:0100169	polyneuropathy, inflammatory demyelinating, chronic	syndromic_disease|nervous_system_disorder|immune_system_disorder	autoimmune_disease	immune_system_disorder|nervous_system_disorder|syndromic_disease	neurology|inflammatory_demyelinating|polyneuropathy	inflammatory_disease|dmyelinating|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|immune_disorder	false	false	false	true	high
MONDO:0100172	intellectual disability, autosomal dominant	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0100173	leukemia, acute myeloid, susceptibility to	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	oncology|hematology	cancer|leukemia|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder|vascular_disorder|kidney_disorder	false	true	false	true	very_high
MONDO:0100175	TTN-related myopathy	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|pulmonology|cardiology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100176	AP-4 deficiency syndrome	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0100184	GTP cyclohydrolase I deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	kidney_disorder|vascular_disorder	false	false	false	true	high
MONDO:0100185	immune reconstitution inflammatory syndrome	inflammatory_disease|immune_system_disorder	other	immune_system_disorder|inflammatory_disease	rheumatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0100186	GTP cyclohydrolase I deficiency with hyperphenylalaninemia	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|endocrine_disorder|liver_disorder	false	false	false	true	high
MONDO:0100187	opioid-induced constipation	digestive_system_disorder	other	digestive_system_disorder	neurology|gastroenterology	gastrointestinal_disease_is_not_in_the_list_so_answer_is_as_follows|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0100188	combined ApoA-I and ApoC-III deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|cardiology|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	liver_disorder|vascular_disorder	false	false	false	true	high
MONDO:0100190	gastric intestinal metaplasia	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	hepatology|gastrointestinal_disease_is_not_listed_so_we_can_consider_intestinal_metaplasia_to_be_a_subset_of_gastrointestinal_disease_so_gastroenterology_would_be_the_best_fit____corrected_answer__gastroenterology|gastroenterology	cancer|inflammatory_disease|gastrointestinal_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0100191	inherited kidney disorder	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	renal_medicine|urology|genetics_and_genomics	inherited_kidney_disorders_can_be_categorized_under_a_broader_term_as_an_inherited_condition_but_the_closest_category_in_the_list_is_metabolic_disorder|metabolic_disorder	kidney_disorder|inherited_kidney_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:0100192	liver failure	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	liver_failure_is_often_a_result_of_alcohol_metabolism_issues_which_is_a_type_of_metabolic_disorder|metabolic_disorder	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0100193	chronic liver failure	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0100194	pregnancy associated osteoporosis	hereditary_disease|obstetric_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|obstetric_disorder|musculoskeletal_system_disorder	rheumatology|orthopaedic|obstetrics_and_gynecology|endocrinology	metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|bone_disorder	false	false	false	true	low
MONDO:0100195	X-linked intellectual disability with hypopituitarism	psychiatric_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder|syndromic_disease	pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0100196	TPM2-related myopathy	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	neurology|rheumatology|orthopaedic|genetics_and_genomics	cardiovascular_disorder|inflammatory_disease|anemia|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder	false	false	false	false	high
MONDO:0100197	parainfluenza infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	true	false	false	true	medium
MONDO:0100198	Mendelian encephalopathy	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100199	diffuse gastric and lobular breast cancer syndrome with or without cleft lip and/or palate	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	oncology|genetics_and_genomics	cancer|genetic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0100200	microcephaly with intellectual disability	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|intellectual_disability_is_also_closely_related_to_neurological_disorders__which_includes_brain_disorder_and_other_subcategories_of_that_category	false	false	false	false	very_high
MONDO:0100201	lumbar disk disease	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	neurology|orthopaedic	neurodegenerative_disease|inflammatory_disease	spinal_disorder|joint_disorder	false	false	false	true	high
MONDO:0100203	parainfluenza virus type 1 infectious disease	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	infectious_disease|inflammatory_disease	lung_disorder|upper_gastrointestinal_disorder	true	false	false	false	medium
MONDO:0100204	parainfluenza virus type 2 infectious disease	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	autoimmune_diseases|inflammatory_disease	lung_disorder|throat_disorder|immune_disorder	true	false	false	false	medium
MONDO:0100205	parainfluenza virus type 4 infectious disease	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	infectious_disease|inflammatory_disease	lung_disorder|respiratory_system_disorder	true	false	false	false	low
MONDO:0100207	infantile-onset epilepsy	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0100208	self-limited familial neonatal-infantile epilepsy	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	medium
MONDO:0100209	X inactivation, familial skewed	hereditary_disease	other	hereditary_disease	genetics_and_genomics|obstetrics_and_gynecology|pediatric	metabolic_disorder|adrenal_gland_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	none
MONDO:0100210	growth hormone insensitivity syndrome with immune dysregulation	hereditary_disease|syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|syndromic_disease	genetics_and_genomics|endocrinology|immunology|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	endocrine_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0100211	growth hormone insensitivity with immune dysregulation 1, autosomal recessive	hereditary_disease|syndromic_disease|endocrine_system_disorder|immune_system_disorder	endocrine_system_disorder	hereditary_disease|immune_system_disorder|endocrine_system_disorder|syndromic_disease	genetics_and_genomics|endocrinology|immunology|pediatric	allergy|metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder_endocrine_disorder	false	false	false	false	very_high
MONDO:0100212	IFAP syndrome	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|pediatric	adrenal_gland_disease|neurodegenerative_disease|inflammatory_disease	liver_disorder|kidney_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0100213	IFAP syndrome 1, with or without BRESHECK syndrome	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|allergy_and_immunology|pulmonology|renal_medicine|hematology|pediatric|oncology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	liver_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0100214	Rajab interstitial lung disease with brain calcifications	respiratory_system_disorder|hereditary_disease	other	hereditary_disease|respiratory_system_disorder	neurology|pulmonology|rheumatology	autoimmune_diseases|inflammatory_disease	lung_disorder|joint_disorder|brain_disorder|immune_disorder	true	false	false	false	high
MONDO:0100215	Rajab interstitial lung disease with brain calcifications 1	respiratory_system_disorder|hereditary_disease	other	hereditary_disease|respiratory_system_disorder	neurology|pulmonology|rheumatology	autoimmune_diseases|inflammatory_disease	lung_disorder|brain_disorder|immune_disorder	true	false	false	false	high
MONDO:0100216	DICER1-related tumor predisposition	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|oncology	cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0100217	developmental delay with short stature, dysmorphic facial features, and sparse hair 2	hereditary_disease	other	hereditary_disease	genetics_and_genomics|endocrinology|pediatric	metabolic_disorder|neurodegenerative_disease	developmental_delay_disorder|growth_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0100218	arthrogryposis multiplex congenita 5	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	bone_disorder|joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100219	growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant	hereditary_disease|syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|syndromic_disease	genetics_and_genomics|endocrinology|pediatric	allergy|metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder_endocrine_disorder	false	false	false	false	high
MONDO:0100220	Rajab interstitial lung disease with brain calcifications 2	respiratory_system_disorder|hereditary_disease	other	hereditary_disease|respiratory_system_disorder	neurology|pulmonology|rheumatology	autoimmune_diseases|inflammatory_disease	lung_disorder|brain_disorder|immune_disorder	false	false	false	false	high
MONDO:0100221	IFAP syndrome 2	hereditary_disease|integumentary_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|integumentary_system_disorder	medical_genetics|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|vascular_disorder|kidney_disorder	true	false	false	true	high
MONDO:0100222	A20 haploinsufficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	immunology|pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	high
MONDO:0100223	mitochondrial complex I deficiency, nuclear type	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease	metabolic_disease	hereditary_disease|mitochondrial_disease|metabolic_disease|disorder_of_development_or_morphogenesis	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|mitochondrial_disease	false	false	false	true	high
MONDO:0100224	mitochondrial complex I deficiency, nuclear type 1	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|musculoskeletal_system_disorder|mitochondrial_disease	metabolic_disease	hereditary_disease|mitochondrial_disease|metabolic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatrics|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0100225	collagen 6-related myopathy	musculoskeletal_system_disorder|nervous_system_disorder	other	nervous_system_disorder|musculoskeletal_system_disorder	neurology|rheumatology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	bone_disorder|muscle_disorder|collagen_disease	false	false	false	false	high
MONDO:0100226	parasomnia, sleepwalking type	other	other	sleep_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	low
MONDO:0100227	ALS2-related motor neuron disease	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100228	LAMA2-related muscular dystrophy	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	neurology|orthopaedic|genetics_and_genomics	muscular_dystrophy|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	true	high
MONDO:0100230	fatty acyl-CoA reductase 1 upregulation	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	genetics_and_genomics|endocrinology|hepatology|cardiology	cardiovascular_disorder|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0100233	long COVID-19	other	other	post_infectious_disorder	renal_medicine|pulmonology|cardiology|hematolgy	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	true	false	false	false	very_high
MONDO:0100234	paroxysmal familial ventricular fibrillation	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	genetics_and_genomics|cardiology|pediatric	cardiovascular_disorder|genetic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0100235	FOXC1-related anterior segment dysgenesis	hereditary_disease|disorder_of_development_or_morphogenesis|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|disorder_of_development_or_morphogenesis|hereditary_disease	ophthalmology|genetics_and_genomics|pediatric	ocular_disease|eye_disorder|neurodevelopmental_disease	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0100236	LTBP2-related ocular dysgenesis	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0100237	inherited cutis laxa	hereditary_disease|disorder_of_development_or_morphogenesis|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|dermatology	connective_tissue_disease|inherited_condition|genetic_disease|metabolic_disorder	muscle_disorder|skin_disorder	false	false	false	false	medium
MONDO:0100238	inherited Fanconi renotubular syndrome	urinary_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|urinary_system_disorder|syndromic_disease	genetics_and_genomics|renal_medicine|pediatric	inherited_fanconi_renotubular_syndrome_is_a_disorder_affecting_the_kidney_s_ability_to_reabsorb_nutrients__which_falls_under_metabolic_disorders|metabolic_disorder	renal_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100239	inherited hypertrophic pyloric stenosis	hereditary_disease|digestive_system_disorder	other	hereditary_disease|digestive_system_disorder	genetics_and_genomics|gastroenterology|pediatric	metabolic_disorder|inherited_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0100240	inherited thrombophilia	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	cardiovascular_disorder|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0100241	inherited thrombocytopenia	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	true	medium
MONDO:0100242	glioma susceptibility	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	oncology|neurology|genetics_and_genomics	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0100244	paroxysmal nocturnal hemoglobinuria	metabolic_disease|hematologic_disorder|urinary_system_disorder	metabolic_disease|anemia	urinary_system_disorder|metabolic_disease|hematologic_disorder	pediatric|renal_medicine|genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder|kidney_disorder	false	false	false	true	high
MONDO:0100247	multiple congenital anomalies-hypotonia-seizures syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|mental_health_disorder|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100248	rapidly progressive primary central nervous system vasculitis	cardiovascular_disorder|nervous_system_disorder|inflammatory_disease	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease|nervous_system_disorder	neurology|rheumatology|hematology	autoimmune_diseases|inflammatory_disease	brain_disorder|immune_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0100249	46,XX testicular disorder of sex development	disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder	endocrinology|genetics_and_genomics|urology	sex_developmental_disorder|adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0100250	46,XX sex reversal 1	hereditary_disease|disorder_of_development_or_morphogenesis|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	disorder_of_development_or_morphogenesis|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	pediatric|endocrinology|genetics_and_genomics|obstetrics_and_gynecology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0100251	familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome	hereditary_disease|cancer_or_benign_tumor|metabolic_disease|integumentary_system_disorder|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|metabolic_disease	cancer_or_benign_tumor|endocrine_system_disorder|metabolic_disease|integumentary_system_disorder|hereditary_disease	renal_medicine|endocrinology|genetics_and_genomics	cancer|metabolic_disorder	bone_disorder|endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100252	tumoral calcinosis, hyperphosphatemic, familial, 1	cancer_or_benign_tumor|metabolic_disease|integumentary_system_disorder|endocrine_system_disorder|hereditary_disease	cancer_or_benign_tumor|endocrine_system_disorder|metabolic_disease	cancer_or_benign_tumor|endocrine_system_disorder|metabolic_disease|integumentary_system_disorder|hereditary_disease	renal_medicine|oncology|endocrinology|genetics_and_genomics|pediatrics	cancer|familial|metabolic_disorder	bone_disorder|endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0100253	Roberts-SC phocomelia syndrome	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder|upper_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0100254	CACNA1A-related complex neurodevelopmental disorder	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0100255	adenosine kinase deficiency	metabolic_disease|nervous_system_disorder|psychiatric_disorder|hereditary_disease	metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|metabolism_related_category_is_missing_but_closest_match_is_endocrinology	neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	false	very_high
MONDO:0100256	CTNNA1-related diffuse gastric and lobular breast cancer syndrome	cancer_or_benign_tumor|integumentary_system_disorder|breast_disorder|digestive_system_disorder|hereditary_disease	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor|digestive_system_disorder|integumentary_system_disorder|hereditary_disease	oncology|genetics_and_genomics	cancer|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0100257	peroxisomal single enzyme/protein defect	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics|hepatology	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	liver_disorder	false	false	false	false	high
MONDO:0100258	phytanoyl-CoA hydroxylase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics|metabolic_disorders_is_not_in_the_list_but_a_relevant_category_is_genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100259	peroxisome biogenesis disorder due to PEX1 defect	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|hepatology	neurodegenerative_disease|metabolic_disorder	peroxisomal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0100260	peroxisome biogenesis disorder due to PEX2 defect	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics|hepatology	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisome_biosynthesis_error	false	false	false	false	very_high
MONDO:0100261	peroxisome biogenesis disorder due to PEX3 defect	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	peroxisome_biosynthesis_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0100262	peroxisome biogenesis disorder due to PEX5 defect	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|peroxisomal_diseases|metabolic_disorder	peroxisomal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0100263	peroxisome biogenesis disorder due to PEX6 defect	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	peroxisomal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0100264	peroxisome biogenesis disorder due to PEX10 defect	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|syndromic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	pediatrics|genetics_and_genomics|hepatology	neurodegenerative_disease|metabolic_disorder	peroxisomal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0100265	peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain	hereditary_disease|disorder_of_visual_system|metabolic_disease|syndromic_disease|nervous_system_disorder|musculoskeletal_system_disorder	metabolic_disease|neurodegenerative_disease	disorder_of_visual_system|metabolic_disease|syndromic_disease|musculoskeletal_system_disorder|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	peroxisome_biogenesis_disorder_due_to_pex5_defect_in_the_pex7_binding_domain_can_also_be_classified_as_a_neurodegenerative_disease_but_it_is_primarily_categorized_under_metabolic_disorder|metabolic_disorder	peroxisome_biosynthesis_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0100266	peroxisome biogenesis disorder due to PEX12 defect	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|peroxisome_biogenesis_disorder	liver_disorder|peroxisome_biogenesis_disorder_due_to_pex12_defect_is_also_related_to_a_subset_of_liver_disorders_that_affect_the_metabolism_of_very_long_chain_fatty_acids__vlcfas__and_other_substances_in_the_peroxisomes__but_it_s_primarily_classified_as_a_metabolic_disorder_affecting_peroxisomal_function	false	false	false	false	very_high
MONDO:0100267	peroxisome biogenesis disorder due to PEX13 defect	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|peroxisome_biogenesis_disorder_is_also_related_to_neurodegenerative_disease_but_that_is_a_more_specific_category_for_certain_disorders_like_zellweger_syndrome_which_is_caused_by_pex1_or_pex6_mutations__not_pex13	peroxisomal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0100268	peroxisome biogenesis disorder due to PEX14 defect	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|syndromic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	peroxisomal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0100269	peroxisome biogenesis disorder due to PEX16 defect	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|syndromic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|hepatology|peroxisome_biogenesis_disorders_often_have_symptoms_that_overlap_with_other_conditions__so_hepatology_could_be_a_consideration_due_to_the_liver_s_role_in_peroxisomes	neurodegenerative_disease|metabolic_disorder	peroxisomal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0100270	peroxisome biogenesis disorder due to PEX19 defect	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	peroxisome_biogenesis_disorder_due_to_pex19_defect_can_also_be_categorized_as_neurodegenerative_disease|metabolic_disorder	peroxisomal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0100271	peroxisome biogenesis disorder due to PEX26 defect	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics|hematology|hepatology	neurodegenerative_disease|metabolic_disorder	eye_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0100272	peroxisome biogenesis disorder due to PEX7 defect	hereditary_disease|metabolic_disease|syndromic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics|hepatology	peroxisome_biogenesis_disorder_due_to_pex7_defect_also_can_be_categorized_as_a_neurodegenerative_disease|metabolic_disorder	peroxisomal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0100273	glyceronephosphate O-acyltransferase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	renal_medicine|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100274	alkylglycerone-phosphate synthase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|metabolism|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	metabolic_disorder|genetic_disorder|liver_disorder	false	false	false	false	high
MONDO:0100275	fatty acyl-CoA reductase defects	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|genetics_and_genomics	adrenal_gland_disease|cardiovasular_disorder|metabolic_disorder	endocrine_disorder|liver_disorder	false	false	false	false	high
MONDO:0100276	disorder of defective peroxisomal and mitochondrial fission	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	hematology|genetics_and_genomics|hepatology	neurodegenerative_disease|metabolic_disorder	mitochondrial_disorder|liver_disorder	false	false	false	true	high
MONDO:0100277	disorder of peroxisomal alpha oxidation	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|hepatology	neurodegenerative_disease|metabolic_disorder	peroxisomal_alpha_oxidation_disorder|liver_disorder	false	false	false	false	high
MONDO:0100278	alanine glyoxylate aminotransferase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|renal_medicine|genetics_and_genomics	inherited_disorder|genetic_disorder|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100279	peroxisome biogenesis disorder due to PEX11B defect	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|metabolic_disease|syndromic_disease|nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	peroxisome_biosynthesis_disorder|liver_disorder	false	false	false	false	high
MONDO:0100280	Waldenstrom macroglobulinemia	hereditary_disease|cancer_or_benign_tumor|metabolic_disease|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor|metabolic_disease	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor|metabolic_disease|hereditary_disease	oncology|hematology	cancer|autoimmune_diseases|anemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	medium
MONDO:0100281	macroglobulinemia, Waldenstrom, 1	hereditary_disease|cancer_or_benign_tumor|metabolic_disease|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor|metabolic_disease	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor|metabolic_disease|hereditary_disease	oncology|hematology	cancer|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	high
MONDO:0100283	overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|oncology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|cerebral_malformations	false	false	false	true	high
MONDO:0100284	X-linked intellectual disability	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0100285	extrahepatic biliary atresia	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	pediatric|gastroenterology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0100286	respiratory syncytial virus bronchiolitis	respiratory_system_disorder|infectious_disease	infectious_disease	respiratory_system_disorder|infectious_disease	pediatric|pulmonology	autoimmune_diseases|inflammatory_disease	throat_disorder|lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0100287	POLE-related polyposis and colorectal cancer syndrome	hereditary_disease|cancer_or_benign_tumor|syndromic_disease|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|digestive_system_disorder|hereditary_disease	oncology|genetics_and_genomics	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0100288	enhanced S-cone syndrome	disorder_of_visual_system|nervous_system_disorder|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder	neurology|ophthalmology	autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0100289	Goldmann-Favre syndrome	disorder_of_visual_system|nervous_system_disorder|hereditary_disease	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|endocrinology|dermatology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100290	colon serrated polyposis	syndromic_disease|digestive_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|digestive_system_disorder|hereditary_disease	oncology|genetics_and_genomics|gastroenterology	autoimmune_diseases|cancer|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0100291	early T cell progenitor acute lymphoblastic leukemia	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder|acute_disease	oncology|hematology|pediatric	cancer	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0100292	Carey-Fineman-Ziter syndrome 2	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease|mental_health_disorder	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0100293	diaphragmatic malformation	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|respiratory_system_disorder	other	disorder_of_development_or_morphogenesis|respiratory_system_disorder|musculoskeletal_system_disorder	pediatric|cardiothoracic|pulmonology	cardiovascular_disorder|congenital_abnormality|genetic_condition	lung_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100294	mitochondrial complex II deficiency, nuclear type 1	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|mitochondrial_disease|metabolic_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|metabolic_disease|mitochondrial_disease|hereditary_disease	pediatrics|neurology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0100296	Olmsted syndrome 1	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	lymphatic_disorder|vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100297	short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1	hereditary_disease	other	hereditary_disease	pediatric|orthopaedic|genetics_and_genomics|endocrinology|cardiology	skeletal_abnormality|congenital_heart_defect|metabolic_disorder	bone_disorder|spinal_disorder|joint_disorder|skeletal_disorder	false	false	false	false	medium
MONDO:0100298	abdominal wall malformation	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|gastroenterology|pediatric	metabolic_disorder|abdominal_wall_anomaly	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0100299	PAX5-related B lymphopenia and autism spectrum disorder	psychiatric_disorder|immune_system_disorder|hematologic_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hematologic_disorder|immune_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|hematology|psychiatry|pediatric	autoimmune_diseases|mental_health_disorder	immune_disorder_lymphatic_disorder	false	false	false	true	high
MONDO:0100301	hemangioma, capillary infantile, susceptibility to	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	pediatric|hematology|genetics_and_genomics	cancer|metabolic_disorder	skin_disorder|vascular_disorder	false	false	false	true	low
MONDO:0100302	LADD syndrome 1	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|ophthalmology|genetics_and_genomics	autoimmune_diseases|anemia|metabolic_disorder	eye_disorder|ear_disorder	false	false	false	false	high
MONDO:0100303	ichthyosis, annular epidermolytic 1	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	high
MONDO:0100304	disorder of bile acid aminotransferase	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0100305	bile acid CoA:amino acid N-acyltransferase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|gastroenterology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0100306	disorder of defective peroxisome oxidative status	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|hematology|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	peroxisomal_disorder|liver_disorder	false	false	false	false	high
MONDO:0100307	adult Refsum disease due to PEX7 defect	syndromic_disease|metabolic_disease|nervous_system_disorder|hereditary_disease	neurodegenerative_disease|metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease|syndromic_disease	neurology|hepatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	peroxisomal_disorder|liver_disorder	false	false	false	false	high
MONDO:0100308	atactic disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100309	hereditary ataxia	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0100310	hereditary cerebellar ataxia	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100311	sensory ataxia	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100312	vestibular ataxia	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|ear_disorder	false	false	false	false	high
MONDO:0100313	focal segmental glomerulosclerosis	urinary_system_disorder	other	urinary_system_disorder	nephrology|renal_medicine	autoimmune_diseases|inflammatory_disease	vascular_disorder|joint_disorder|immune_disorder|kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0100314	GYG1-related disorder of glycogen metabolism	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|endocrinology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0100315	isolated adrenal insufficiency	nervous_system_disorder|metabolic_disease|hereditary_disease|psychiatric_disorder|endocrine_system_disorder	endocrine_system_disorder|neurodegenerative_disease|metabolic_disease|psychiatric_disorder	endocrine_system_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder	endocrinology	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	adrenal_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0100316	long QT syndrome 1	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0100317	deficiency of adenosine deaminase 2	connective_tissue_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|connective_tissue_disorder|syndromic_disease	pediatric|hematatology|immunology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0100319	COVID-19–associated multisystem inflammatory syndrome in adults	other	other	post_infectious_disorder	pulmonology|rheumatology	autoimmune_diseases|inflammatory_disease	lung_disorder|vascular_disorder|joint_disorder|immune_disorder|kidney_disorder	true	false	false	true	very_high
MONDO:0100320	post-COVID-19 disorder	other	other	post_infectious_disorder	neurology|pulmonology|psychiatry	autoimmune_diseases|mental_health_disorder|neurodegenerative_disease|inflammatory_disease	lung_disorder|vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0100322	non-Zellweger spectrum disorder	syndromic_disease|nervous_system_disorder|metabolic_disease|hereditary_disease	neurodegenerative_disease|metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease|syndromic_disease	nephrology|hepatology|renal_medicine|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	true	high
MONDO:0100323	inherited pseudohypoaldosteronism	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	pediatric|endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0100324	primary focal segmental glomerulosclerosis	urinary_system_disorder	other	urinary_system_disorder	nephrology|renal_medicine|hematology	autoimmune_diseases|inflammatory_disease	immune_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100325	odontochondrodysplasia 1	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	genetic_disorder|metabolic_disorder	bone_disorder|teeth_disorder|joint_disorder	false	false	false	false	high
MONDO:0100326	Glanzmann thrombasthenia	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	pediatric|hematology|genetics_and_genomics	autoimmune_diseases|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0100327	hypercholanemia, familial	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|renal_medicine|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|liver_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0100328	microcephaly, epilepsy, and diabetes syndrome	hereditary_disease	other	hereditary_disease	endocrinology|neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	endocrine_disorder|brain_disorder	true	false	true	false	high
MONDO:0100329	primary viral infectious disease	infectious_disease	infectious_disease	infectious_disease	pediatric|viral_infectious_disease	viral_infectious_disease|autoimmune_diseases|inflammatory_disease	immune_disorder	true	false	false	false	please_provide_the_specific_viral_infectious_disease_you_would_like_me_to_evaluate_for_qalys_lost
MONDO:0100330	disease arising from reactivation of latent virus	infectious_disease	infectious_disease	infectious_disease	allergy_and_immunology|immunology_is_not_in_the_list_so___allergy_and_immunology|hematology|genetics_and_genomics	autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|immune_disorder	true	false	false	true	high
MONDO:0100331	nerve agent poisoning	poisoning	other	poisoning	neurology|toxicology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0100335	local anesthetic poisoning	poisoning	other	poisoning	neurology|toxicology_is_not_in_the_list_but_closest_match_would_be_neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	neurological_effects_of_local_anesthetic_poisoning_could_imply_brain_disorder_and_spinal_disorder__but_more_directly_related_would_be_vascular_disorder_due_to_potential_for_cardiac_complications	false	false	false	false	medium
MONDO:0100337	SEC61A1 deficiency	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0100338	urinary tract infection	infectious_disease|urinary_system_disorder	infectious_disease	urinary_system_disorder|infectious_disease	urology|renal_medicine	autoimmune_diseases|inflammatory_disease	kidney_disorder|urinary_tract_disorder	true	false	false	true	medium
MONDO:0100339	Friedreich ataxia	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100340	Friedreich ataxia 1	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100341	fire ant poisoning	poisoning	other	poisoning	dermatology|pediatrics|allergy_and_immunology	autoimmune_diseases|allergy|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0100342	malignant glioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0100344	Bartter disease type 1	syndromic_disease|hereditary_disease|urinary_system_disorder	other	syndromic_disease|hereditary_disease|urinary_system_disorder	renal_medicine|genetics_and_genomics|pediatric	autoimmune_diseases|adrenal_gland_disease|metabolic_disorder	endocrine_disorder|electrolyte_disorder|metabolic_disorder|kidney_disorder	false	false	false	true	high
MONDO:0100345	lactose intolerance	hereditary_disease|metabolic_disease|nutritional_disorder|digestive_system_disorder	metabolic_disease	hereditary_disease|metabolic_disease|nutritional_disorder|digestive_system_disorder	endocrinology|gastroenterology	autoimmune_diseases|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0100346	microcephaly with or without short stature	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100347	carcinoid syndrome	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	oncology|neurology|endocrinology|gastroenterology|cardiology	cancer|adrenal_gland_disease	endocrine_disorder|lower_gastrointestinal_disorder	false	false	false	true	high
MONDO:0100348	neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0100349	COACH syndrome	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	neurodegenerative_disease	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	endocrinology|pediatrics|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|vascular_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100350	neuronopathy, distal hereditary motor, type 5	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	hereditary_condition|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0100351	POLD1-related polyposis and colorectal cancer syndrome	cancer_or_benign_tumor|syndromic_disease|hereditary_disease|digestive_system_disorder	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology|genetics_and_genomics	polyposis_syndrome|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0100352	episodic kinesigenic dyskinesia 1	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0100353	HHV-7 infectious disease	infectious_disease	infectious_disease	infectious_disease	virology|pediatric	viral_disease|infectious_disease|herpes_virus_disease	lymphatic_disorder|immune_disorder	true	false	false	true	low
MONDO:0100354	megacystis-microcolon-intestinal hypoperistalsis syndrome 1	syndromic_disease|hereditary_disease|digestive_system_disorder	other	syndromic_disease|hereditary_disease|digestive_system_disorder	gastroenterology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0100358	ectodermal dysplasia WNT10A related	syndromic_disease|hereditary_disease|integumentary_system_disorder	other	syndromic_disease|hereditary_disease|integumentary_system_disorder	dermatology|neurology|genetics_and_genomics|pediatric	ectodermal_disease|neurodegenerative_disease|rare_disease|skin_condition|birth_defect|developmental_disorder|genetic_disorder|birth_defect___revised_to_match_the_format_of_the_category_list__genetic_disorder	skin_disorder|eye_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0100359	herpes simplex type 1 infectious disease	infectious_disease	infectious_disease	infectious_disease	dermatology|pediatrics	autoimmune_diseases|infectious_disease|viral_infection	skin_disorder|eye_disorder	true	false	false	true	medium
MONDO:0100360	herpes simplex type 2 infectious disease	infectious_disease	infectious_disease	infectious_disease	dermatology|obstetrics_and_gynecology	autoimmune_diseases|infectious_disease	skin_disorder|lower_gastrointestinal_disorder|immune_disorder	true	false	false	false	medium
MONDO:0100361	lip herpes simplex type 1 infectious disorder	infectious_disease	infectious_disease	mouth_disorder|infectious_disease	dermatology|infectious_disorder	autoimmune_diseases|infectious_disorder	infectious_disorder|skin_disorder|immune_disorder	true	false	false	true	low
MONDO:0100362	lip herpes simplex type 2 infectious disorder	infectious_disease	infectious_disease	mouth_disorder|infectious_disease	dermatology|infectious_disease	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	false	medium
MONDO:0100363	genital herpes simplex type 2 infectious disorder	reproductive_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease	dermatology|obstetrics_and_gynecology	autoimmune_diseases|infectious_disorder	reproductive_system_disorder|skin_disorder|immune_disorder	true	false	false	false	medium
MONDO:0100364	genital herpes simplex type 1 infectious disorder	reproductive_system_disorder|infectious_disease	infectious_disease	reproductive_system_disorder|infectious_disease	dermatology|obstetrics_and_gynecology|pediatric	autoimmune_diseases|infectious_disorder	reproductive_system_disorder|skin_disorder	true	false	false	false	medium
MONDO:0100365	mucopolysaccharidosis or mucopolysaccharidosis-like disorder	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	bone_disorder|joint_disorder|liver_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0100366	occupational disorder	other	other		occupational_disorder_is_often_related_to_workplace_stress_and_psychological_factors|psychiatry	occupational_disorder|mental_health_disorder	joint_disorder|occupational_disorder_is_not_in_the_list_so_i_will_leave_it_out	false	false	false	false	high
MONDO:0100367	port-wine nevi-mega cisterna magna-hydrocephalus syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	dermatology|neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|inflammatory_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0100368	RPE65-related recessive retinopathy	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region|nervous_system_disorder|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	recessive_retinopathy|eye_disorder	false	false	false	true	high
MONDO:0100370	acute hepatitis B virus infection	endocrine_system_disorder|infectious_disease|digestive_system_disorder|inflammatory_disease	endocrine_system_disorder|infectious_disease	inflammatory_disease|endocrine_system_disorder|acute_disease|digestive_system_disorder|infectious_disease	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease	liver_disorder|immune_disorder	true	false	false	false	high
MONDO:0100371	acute hepatitis C virus infection	endocrine_system_disorder|infectious_disease|digestive_system_disorder|inflammatory_disease	endocrine_system_disorder|infectious_disease	inflammatory_disease|endocrine_system_disorder|acute_disease|digestive_system_disorder|infectious_disease	hepatology|gastroenterology	autoimmune_diseases|cancer|inflammatory_disease	liver_disorder|immune_disorder	true	false	false	true	high
MONDO:0100372	disorder of peroxisomal transporter	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|hepatology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	peroxisomal_disorder|liver_disorder	false	false	false	false	high
MONDO:0100373	acute myeloid leukemia, inv(16)(p13.1;q22)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|vessel_disorder|immune_disorder	false	true	false	true	high
MONDO:0100374	acute myeloid leukemia, t(16;16)(p13.1;q22)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0100375	acute myeloid leukemia, t(15;17)(q24;q21)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0100376	acute myeloid leukemia, t(9;11)(p21.3;q23.3)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0100377	acute myeloid leukemia, t(10;11)(p12;q23)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|vascular_disorder	false	true	false	true	high
MONDO:0100378	acute myeloid leukemia, t(10;11)(p11.2;q23)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0100379	acute myeloid leukemia, t(1;11)(q21;q23)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0100380	acute myeloid leukemia, t(4;11)(q21;q23)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0100381	acute myeloid leukemia, t(6;11)(q27;q23)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0100382	acute myeloid leukemia, t(6;9)(p23;q34.1)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	genetics_and_genomics|oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0100383	acute myeloid leukemia, t(11;19)(q23;p13)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0100384	acute myeloid leukemia, t(11;19)(q23;p13.1)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0100385	acute myeloid leukemia, t(11;19)(q23.3;p13.3)	connective_tissue_disorder|immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0100386	acute myeloid leukemia, t(v;11q23.3)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0100387	acute myeloid leukemia, Monosomy 7	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0100388	acute myeloid leukemia, Monosomy 5	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder|acute_disease	genetics_and_genomics|oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0100389	acute myeloid leukemia, Trisomy 8	connective_tissue_disorder|immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder|acute_disease	genetics_and_genomics|oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0100390	acute myeloid leukemia, der12p	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0100391	acute myeloid leukemia, t(2;12)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|leukemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0100392	acute myeloid leukemia, t(11;17)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0100393	acute myeloid leukemia, t(8;16)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder|bone_disorder	false	true	false	true	very_high
MONDO:0100394	acute myeloid leukemia, t(1;22)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0100395	acute myeloid leukemia, t(5;11)(q35;p15)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0100396	acute myeloid leukemia, t(7;12)(q36;p13)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0100397	acute myeloid leukemia, t(9;22)(q34.1;q11.2)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	bone_disorder|blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder|vascular_disorder	false	true	false	true	high
MONDO:0100398	acute myeloid leukemia, inv(3)(q21.3;q26.2)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0100399	acute myeloid leukemia, t(3;3)(q21.3;q26.2)	connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|acute_disease	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0100400	acute myeloid leukemia, t(3;12)(q23;p12.3)	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	cancer|anemia	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0100401	acute myeloid leukemia, del(5q31-q32)	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor	hematology|genetics_and_genomics|oncology	cancer|anemia	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0100402	acute myeloid leukemia, del(13q14-q21)	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	hematology|oncology	cancer|anemia	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0100403	acute myeloid leukemia, loss of chromosome 17p	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	hematology|oncology	cancer|anemia	immune_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0100404	acute myeloid leukemia, MLL gene rearrangement	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	hematology|genetics_and_genomics|oncology	cancer|autoimmune_diseases|anemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0100405	acute myeloid leukemia, Non-KMT2A MLLT10 rearrangement positive	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	hematology|oncology	cancer|leukemia	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0100406	acute myeloid leukemia, inv(16)(p13.3;q24.3)	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	hematology|oncology	cancer|anemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0100407	acute myeloid leukemia, t(11;15)(p15;q35)	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	hematology|oncology	cancer|anemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0100408	acute myeloid leukemia, t(16;21)(q24;q22)	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	hematology|oncology	other____corrected_list_without__other_____cancer|cancer|anemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0100409	acute myeloid leukemia, t(3;5)(q25;q34)	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	hematology|oncology	cancer|anemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0100410	acute myeloid leukemia, t(16;21)(p11;q22)	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor	hematology|genetics_and_genomics|oncology	cancer|anemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0100412	acute myeloid leukemia, monoallelic CEBPA gene mutation	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor	hematology|genetics_and_genomics|oncology	cancer|anemia	immune_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0100413	acute myeloid leukemia, biallelic CEBPA gene mutation	immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor	hematology|genetics_and_genomics|oncology	cancer|leukemia|anemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0100414	acute myeloid leukemia, CEBPA gene mutation	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor	hematology|genetics_and_genomics|oncology	cancer|anemia	immune_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0100415	acute myeloid leukemia, FLT3 internal tandem duplication	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	cancer|anemia	lymphatic_disorder|immune_disorder|vascular_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0100416	acute myeloid leukemia, FLT3 tyrosine kinase domain point mutation	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	cancer|leukemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0100417	acute myeloid leukemia, WT1 gene mutation	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor	hematology|genetics_and_genomics|oncology	cancer|leukemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0100418	acute myeloid leukemia, KIT exon 17 mutation	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	cancer|anemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0100419	acute myeloid leukemia, KIT exon 8 mutation	immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	immune_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	oncology|blood_cancer|cancer|leukemia	immune_disorder|vascular_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0100420	acute myeloid leukemia, KIT gene mutation	immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|acute_disease|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder	hematology|genetics_and_genomics|oncology	cancer|anemia	blood_bone_marrow_disorder|immune_disorder	false	true	false	true	high
MONDO:0100421	acute myeloid leukemia, GATA1 gene mutation	immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|acute_disease|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder	hematology|genetics_and_genomics|oncology	cancer|anemia	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0100422	acute myeloid leukemia, RUNX1 gene mutation	immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|acute_disease|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder	hematology|genetics_and_genomics|oncology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0100423	acute myeloid leukemia, PTPN11 gene mutation	immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|acute_disease|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder	hematology|genetics_and_genomics|oncology	cancer|anemia	blood_bone_marrow_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0100424	acute myeloid leukemia, NRAS gene mutation	immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|acute_disease|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder	hematology|oncology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0100425	acute myeloid leukemia, KRAS gene mutation	immune_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|acute_disease|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder	hematology|genetics_and_genomics|oncology	cancer|anemia	blood_bone_marrow_disorder|immune_disorder	false	true	false	true	very_high
MONDO:0100428	progressive bulbar palsy of childhood	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology	adrenal_gland_disease|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0100429	intrahepatic cholestasis of pregnancy	digestive_system_disorder	other	digestive_system_disorder	obstetrics_and_gynecology|hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	liver_disorder|biliary_disorder	false	false	false	true	medium
MONDO:0100430	fibrotic liver disease	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	hepatology|gastroenterology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0100431	migraine without aura	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	nervous_system_disorder|cardiovascular_disorder	headache|neurology	mental_health_disorder|autoimmune_diseases	eye_disorder|brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0100432	FNIP1-associated syndrome	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder	false	false	false	true	very_high
MONDO:0100433	ACTB-associated syndromic thrombocytopenia	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	autoimmune_diseases|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0100434	chronic mountain sickness	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|hematology|cardiology|renal_medicine	cardiovascular_disorder|anemia|metabolic_disorder	blood_bone_marrow_disorder|lung_disorder	false	false	false	true	high
MONDO:0100435	Schwartz-Jampel syndrome type 1	nervous_system_disorder|musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	nervous_system_disorder|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder|joint_disorder|immune_disorder|bone_disorder	false	false	false	false	high
MONDO:0100436	cataract 2, multiple types	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0100437	RPGR-related retinopathy	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|anemia|metabolic_disorder	eye_disorder|spinal_disorder|muscle_disorder	false	false	false	true	high
MONDO:0100438	AIPL1-related retinopathy	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	pediatric|ophthalmology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	true	high
MONDO:0100439	glycogen storage disease IXa2	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|hepatology|genetics_and_genomics	glycogen_storage_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100441	GUCY2D-related dominant retinopathy	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|cardiovascular_disorder|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0100442	RP2-related retinopathy	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100443	RDH5-related retinopathy	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	pediatric|genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0100444	RLBP1-related retinopathy	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0100445	LCA5-related retinopathy	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0100446	CNGB3-related retinopathy	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|retinal_disease	eye_disorder|muscle_disorder	false	false	false	true	high
MONDO:0100447	ATF6-related retinopathy	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0100448	RAB28-related retinopathy	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	eye_disorder|retinal_disorder	false	false	false	false	high
MONDO:0100449	FLVCR1-related retinopathy with or without ataxia	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0100450	CAPN5-related vitreoretinopathy	nervous_system_disorder|disorder_of_visual_system|hereditary_disease	other	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100451	CEP290-related ciliopathy	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|ophthalmology|neurology	metabolic_disorder|neurodegenerative_disease|ciliopathy	brain_disorder|eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100452	RPE65-related dominant retinopathy	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|genetic_disorder	eye_disorder	false	false	false	false	high
MONDO:0100453	GUCY2D-related recessive retinopathy	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	pediatric|ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100454	GUCY2D retinopathy	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	genetics_and_genomics|ophthalmology|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|kidney_disorder	false	false	false	true	high
MONDO:0100455	neonatal-onset developmental and epileptic encephalopathy	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|metabolic_disorder	brain_disorder|neurological_disorder	false	false	false	true	very_high
MONDO:0100456	neonatal encephalopathy with non-epileptic myoclonus	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0100457	achalasia, familial esophageal	digestive_system_disorder|hereditary_disease|upper_digestive_tract_disorder	other	upper_digestive_tract_disorder|digestive_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|gastroenterology|pulmonology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0100458	MECOM-associated syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|oncology	cancer|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0100459	azoospermia	reproductive_system_disorder	other	reproductive_system_disorder	genetics_and_genomics|urology	autoimmune_diseases|anemia	urinary_tract_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0100462	short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|rheumatology|genetics_and_genomics|orthopaedic|endocrinology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	high
MONDO:0100463	methylmalonic aciduria and/or homocystinuria, cblD type	metabolic_disease|hereditary_disease|nutritional_disorder	metabolic_disease	metabolic_disease|nutritional_disorder|hereditary_disease	pediatric|hepatology|hematology|genetics_and_genomics|metabolic_disorders|neurology|renal_medicine	anemia|metabolic_disorder	blood_bone_marrow_disorder|kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0100464	acid sphingomyelinase deficiency	immune_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|immune_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	bone_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	very_high
MONDO:0100465	complex neurodevelopmental disorder with or without congenital anomalies	nervous_system_disorder	other	nervous_system_disorder	pediatric|psychiatry|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0100466	butterfly-shaped pigment dystrophy	nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|eye_disorder	false	false	false	false	low
MONDO:0100467	preeclampsia/eclampsia 1	cardiovascular_disorder|hereditary_disease|obstetric_disorder	cardiovascular_disorder	obstetric_disorder|cardiovascular_disorder|hereditary_disease	obstetrics_and_gynecology	cardiovascular_disorder|metabolic_disorder	kidney_disorder|vascular_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0100468	Batten-Turner congenital myopathy	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100469	anosmia, isolated congenital, X-linked	otorhinolaryngologic_disease	other	otorhinolaryngologic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|genetic_disorder|congenital_disease	ear_disorder|nose_disorder	false	false	false	false	low
MONDO:0100470	reactive airway disease	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	inflammatory_disease|allergy	immune_disorder|lung_disorder	false	false	false	true	medium
MONDO:0100471	vitamin D deficiency	nutritional_disorder	other	nutritional_disorder	osteoporosis_is_a_common_result_of_vitamin_d_deficiency__but_this_isn_t_in_the_options_pediatric|endocrinology	anemia|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	true	high
MONDO:0100472	lissencephaly spectrum disorder with complex brainstem malformation	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0100473	disorder of peptide and amine metabolism	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	endocrinology|gastroenterology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0100474	mild ichthyosis vulgaris	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	pediatric|dermatology	autoimmune_diseases|inflammatory_disease|allergy|metabolic_disorder	skin_disorder|immune_disorder	false	false	false	true	low
MONDO:0100475	severe ichthyosis vulgaris	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	pediatric|dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|immune_disorder	false	false	false	true	high
MONDO:0100477	disorder of methylamine metabolism	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	hepatology|genetics_and_genomics|renal_medicine	adrenal_gland_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	medium
MONDO:0100478	brain malformations with or without urinary tract defects	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|brain_malformations_with_or_without_urinary_tract_defects_fits_best_into_neurodevelopmental_disorders_which_isn_t_listed__so_its_closest_match_is_neurodegenerative_disease|metabolic_disorder	urinary_tract_disorder|brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0100479	rifampicin-resistant tuberculosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric	infectious_disease|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder|lung_disorder	true	false	false	true	very_high
MONDO:0100480	autoimmune primary adrenal insufficiency	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	rheumatology|allergy_and_immunology|endocrinology	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	immune_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0100481	active tuberculosis	infectious_disease	infectious_disease	infectious_disease	pulmonology	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|lung_disorder	true	false	false	true	very_high
MONDO:0100482	extensively drug-resistant tuberculosis	infectious_disease	infectious_disease	infectious_disease	pulmonology	autoimmune_diseases|infectious_disease	immune_disorder|lung_disorder	true	false	false	true	very_high
MONDO:0100483	totally drug-resistant tuberculosis	infectious_disease	infectious_disease	infectious_disease	pulmonology|cardiology|cardiothoracic	autoimmune_diseases|cancer|inflammatory_disease	immune_disorder|lung_disorder	true	false	false	false	very_high
MONDO:0100484	TSPAN12-related vitreoretinopathy	nervous_system_disorder|disorder_of_visual_system|hereditary_disease	other	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0100485	KCNH1 associated disorder	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|psychiatry|genetics_and_genomics|neurology	mental_health_disorder|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100486	adult acne	inflammatory_disease|integumentary_system_disorder|hereditary_disease	other	hereditary_disease|inflammatory_disease|integumentary_system_disorder	pediatric|dermatology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	nose_disorder|skin_disorder	false	false	false	true	medium
MONDO:0100487	TPM4-related platelet disorder	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	anemia|cardiovascular_disorder	blood_bone_marrow_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0100488	CDH1-related diffuse gastric and lobular breast cancer syndrome	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|oncology|gastroenterology	autoimmune_diseases|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0100490	breasts and/or nipples, aplasia or hypoplasia of, 1	breast_disorder|hereditary_disease	other	hereditary_disease|breast_disorder	obstetrics_and_gynecology|genetics_and_genomics	autoimmune_diseases|cancer	skin_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0100491	generalized pustular psoriasis	immune_system_disorder|inflammatory_disease|integumentary_system_disorder|hereditary_disease	other	hereditary_disease|inflammatory_disease|integumentary_system_disorder|immune_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder|skin_disorder	false	false	false	true	very_high
MONDO:0100492	Bonnevie-Ullrich syndrome	syndromic_disease	other	syndromic_disease	pediatric|dermatology|genetics_and_genomics|endocrinology	adrenal_gland_disease|autoimmune_diseases	blood_bone_marrow_disorder|vascular_disorder|muscle_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0100493	autosomal recessive titinopathy	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|neurology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|joint_disorder	false	false	false	false	medium
MONDO:0100494	autosomal dominant titinopathy	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	rheumatology|genetics_and_genomics|orthopaedic|neurology	cardiovascular_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100495	autosomal recessive distal titinopathy	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0100496	Emery-Dreifuss-like muscular dystrophy	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	pediatric|rheumatology|genetics_and_genomics|orthopaedic|neurology	muscular_dystrophy|neurodegenerative_disease	spinal_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0100497	titinopathy with congenital contractures	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100498	UROD-related inherited porphyria	metabolic_disease|integumentary_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease|integumentary_system_disorder	hematology|hepatology|dermatology|genetics_and_genomics|urology	adrenal_gland_disease|metabolic_disorder	urinary_tract_disorder|liver_disorder	false	false	false	true	high
MONDO:0100499	multiple congenital anomalies due to 14q32.2 imprinting defect	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder	joint_disorder|brain_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|kidney_disorder|heart_disorder|ear_disorder|vascular_disorder|muscle_disorder|lymphatic_disorder|reproductive_system_disorder|bone_disorder|skin_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0100500	Mendelian neurodevelopmental disorder	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|neurodevelopmental_disorder	false	false	false	false	very_high
MONDO:0100501	body-stalk anomaly	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	adrenal_gland_disease|inflammatory_disease|cancer	spinal_disorder|reproductive_system_disorder|genital_disorder	false	false	false	false	high
MONDO:0100502	NTHL1-deficiency tumor predisposition syndrome	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	oncology|genetics_and_genomics	adrenal_gland_disease|cancer	blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0100504	fungal infection of the toenail	integumentary_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	inflammatory_disease|integumentary_system_disorder|infectious_disease	dermatology|orthopaedic	autoimmune_diseases|inflammatory_disease	skin_disorder|nail_disorder	true	false	false	true	medium
MONDO:0100505	food dermatitis	integumentary_system_disorder|inflammatory_disease	other	inflammatory_disease|integumentary_system_disorder	dermatology|allergy_and_immunology	autoimmune_diseases|allergy|inflammatory_disease	skin_disorder_upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0100506	Cockayne spectrum with or without cerebrooculofacioskeletal syndrome	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease|premature_aging_syndrome	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|premature_aging_syndrome|hereditary_disease	genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	skin_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0100507	multiple congenital anomalies due to 14q32.2 paternally expressed gene defect	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	reproductive_system_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100508	salivary gland type cancer of the breast	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	oncology|otolaryngology	autoimmune_diseases|breast_cancer|adrenal_gland_disease|inflammatory_disease|cancer	lymphatic_disorder|upper_gastrointestinal_disorder|breast_disorder	false	false	false	false	medium
MONDO:0100509	IFT140-related recessive ciliopathy	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|ciliopathy	eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100510	spondyloepimetaphyseal dysplasia	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|rheumatology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0100511	sudden cardiac arrest	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0100512	mitochondrial DNA depletion syndrome, hepatocerebral form	metabolic_disease|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	neurology|genetics_and_genomics|hepatology	hepatocerebral_form_is_too_specific_to_be_included_in_the_category_list|neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0100513	TRAF3 haploinsufficiency	hereditary_disease	other	hereditary_disease	genetics_and_genomics|immunology|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0100514	familial ovarian carcinoma	reproductive_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|cancer_or_benign_tumor	obstetrics_and_gynecology|genetics_and_genomics|oncology	familial_ovarian_carcinoma_is_a_specific_type_of_cancer|cancer	reproductive_system_disorder|hereditary_disorder	false	true	false	true	high
MONDO:0100515	mirror movements 1 and/or agenesis of the corpus callosum	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|agenesis_of_the_corpus_callosum	corpus_callosal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0100516	complex neurodevelopmental disorder with motor features	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0100517	PSAP-related sphingolipidosis	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	false	high
MONDO:0100518	hereditary attention deficit-hyperactivity disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|genetics_and_genomics|psychiatry|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0100520	NKX2-1 related choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction	syndromic_disease|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|endocrinology|pulmonology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0100521	NOG-related symphalangism spectrum disorder	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	bone_disorder|skeletal_disorder|joint_disorder	false	false	false	false	high
MONDO:0100522	hypotrichosis 4	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	hypotrichosis_is_associated_with_a_deficiency_in_an_enzyme_called_5_alpha_reductase_which_leads_to_abnormalities_in_hair_growth_as_part_of_a_larger_metabolic_condition_that_can_also_affect_male_pattern_baldness|metabolic_disorder	hair_disorder|skin_disorder	false	false	false	true	low
MONDO:0100523	SPAST-related motor disorder	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|spast_related_motor_disorder_is_likely_a_type_of_dystonia_or_other_movement_disorder__however_the_name_could_be_interpreted_to_imply_a_connection_to_conditions_that_cause_spasms_which_could_also_suggest_a_possible_link_to_neurodegenerative_diseases_such_as_multiple_system_atrophy_or_progressive_supranuclear_palsy	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0100524	ASAH1-related sphingolipidosis	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0100525	TCF7L2-related neurodevelopmental disorder	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|neurodevelopmental_disorder	false	false	false	false	high
MONDO:0100527	dysplastic cortical hyperostosis, Kozlowski-Tsuruta type	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|genetics_and_genomics|endocrinology|dermatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	spinal_disorder|bone_disorder|muscle_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0100528	Hao-Fountain syndrome due to 16p13.2 microdeletion	nervous_system_disorder|chromosomal_disorder	other	nervous_system_disorder|chromosomal_disorder	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	spinal_disorder|eye_disorder|brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0100529	Sunflower syndrome	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|radiation_induced_disorder|hereditary_disease	genetics_and_genomics|rheumatology|hematology|allergy_and_immunology|pediatric	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0100530	myopathy caused by variation in CRPPA	hereditary_disease|metabolic_disease|nervous_system_disorder|musculoskeletal_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	myopathy|muscle_disorder	false	false	false	false	high
MONDO:0100531	Emery-Dreifuss muscular dystrophy 1, X-linked	hereditary_disease|nervous_system_disorder|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	orthopaedic|genetics_and_genomics|pediatric	neurodegenerative_disease|muscular_dystrophy	spinal_disorder|heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100533	hemorrhage, intracerebral, susceptibility to	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:0100534	SMARCB1-deficient kidney medullary carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	renal_medicine|oncology|genetics_and_genomics|pediatric	kidney_disease|carcinoma|cancer	kidney_disorder|renal_disorder	false	true	false	false	high
MONDO:0100535	hypodontia/oligodontia with orofacial cleft	hereditary_disease|musculoskeletal_system_disorder	other	mouth_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|otolaryngology	autoimmune_diseases|metabolic_disorder	teeth_disorder|facial_cleft	false	false	false	true	high
MONDO:0100536	tooth agenesis, selective, with orofacial cleft	hereditary_disease|musculoskeletal_system_disorder	other	mouth_disorder|hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|otolaryngology	autoimmune_diseases|oral_facial_cleft_disease|developmental_disorder	teeth_disorder|orofacial_cleft_related	false	false	false	false	high
MONDO:0100537	plasminogen deficiency, type II	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|inflammatory_disease	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0100538	dysplasminogenemia	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	anemia|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0100539	hemiplegic migraine-developmental and epileptic encephalopathy spectrum	hereditary_disease|nervous_system_disorder|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0100540	GATA6-related congenital heart disease with or without pancreatic agenesis or neonatal diabetes	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|endocrinology|cardiology|pediatric	metabolic_disorder|cardiovascular_disorder	heart_disorder|endocrine_disorder	false	false	true	true	high
MONDO:0100541	GATA5-related congenital heart defects	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|cardiology|pediatric	congenital_heart_defects|cardiovascular_disorder	heart_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	false	high
MONDO:0100542	clonal hematopoiesis	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|genetics_and_genomics|hematology	clonal_hematopoiesis_is_a_form_of_cancer|anemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0100543	clonal hematopoiesis of indeterminate potential	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|genetics_and_genomics|hematology	autoimmune_diseases|anemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0100544	age-related clonal hematopoiesis	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	oncology|hematology	anemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0100545	hereditary neurological disease	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|hereditary_disease|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0100546	hereditary neuromuscular disease	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	hereditary_diseases|neurodegenerative_disease|genetic_disorders	brain_disorder|neuromuscular_disease|muscle_disorder	false	false	false	false	high
MONDO:0100547	cardiogenetic disease	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	genetics_and_genomics|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0100548	SERAC1-related neurological disorder	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0100549	focal nodular hyperplasia	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	endocrinology|hepatology|gastroenterology	metabolic_disorder|adrenal_gland_disease	liver_disorder|kidney_disorder	false	false	false	false	low
MONDO:0100550	orbital myositis	inflammatory_disease|disorder_of_visual_system|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|inflammatory_disease	ophthalmology|rheumatology|neurology	inflammatory_disease|autoimmune_diseases	muscle_disorder|eye_disorder	false	false	false	true	medium
MONDO:0100551	AFG2B-related complex neurodevelopmental disorder with motor features and hearing loss	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	inflammatory_disease|autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	muscle_disorder|ear_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0100552	ATTRV30M amyloidosis	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	muscle_disorder|heart_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0100553	OPTN-related open angle glaucoma	hereditary_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	metabolic_disorder|autoimmune_diseases|adrenal_gland_disease	optn_related_open_angle_glaucoma|eye_disorder	false	false	false	false	medium
MONDO:0100554	hereditary narcolepsy	hereditary_disease	other	sleep_disorder|hereditary_disease	genetics_and_genomics|neurology	hereditary|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0100556	PRRT2-associated paroxysmal movement disorder	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0100557	RBFOX2-related congenital heart disorder	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric|cardiology	cardiovascular_disorder|congenital_heart_disorder	congenital_heart_disorder|heart_disorder	false	false	false	false	high
MONDO:0100558	RNU4ATAC spectrum disorder	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|other____if_you_have_any_additional_clarification_or_information_about_this_disease__i_can_provide_a_more_specific_answer	inflammatory_disease|autoimmune_diseases|mental_health_disorder|neurodegenerative_disease|anemia	immune_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0100559	ALG14-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder	liver_disorder|congenital_disorder	false	false	true	false	high
MONDO:0100560	ligneous conjunctivitis	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|dermatology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	true	false	false	true	low
MONDO:0100561	HBA1-related alpha thalassemia spectrum	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0100562	HBA2-related alpha thalassemia spectrum	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	genetics_and_genomics|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|bone_disorder	false	false	false	true	low
MONDO:0100563	digenic alpha thalassemia spectrum	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0100564	HBA1; HBA2-related digenic alpha thalassemia spectrum	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|red_cell_disorder	false	false	false	true	medium
MONDO:0100565	monogenic alpha thalassemia spectrum	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|monogenic_disease	false	false	false	true	medium
MONDO:0100566	myoclonic epilepsy in infancy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0100567	hereditary angioedema with normal C1Inh	hereditary_disease|integumentary_system_disorder|inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder|hereditary_disease|inflammatory_disease	genetics_and_genomics|immunology___corrected_response__genetics_and_genomics|allergy_and_immunology	metabolic_disorder|inflammatory_disease|allergy	immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0100569	ACD-related short telomere syndrome	hereditary_disease|premature_aging_syndrome	other	hereditary_disease|premature_aging_syndrome	genetics_and_genomics|dermatology|pediatrics	metabolic_disorder|inflammatory_disease|cancer|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0100570	ACD-related long telomere syndrome	hereditary_disease|premature_aging_syndrome	other	premature_aging_syndrome|hereditary_disease	pulmonology|immunology|genetics_and_genomics|dermatology|oncology	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0100571	CTNNB1-related neurodevelopmental disorder and/or vitreoretinopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0100572	MTOR-related overgrowth spectrum	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|cancer	muscle_disorder|kidney_disorder|vascular_disorder|bone_disorder	false	false	false	true	high
MONDO:0100573	combined generalized and focal epilepsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0100574	generalized epilepsy	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0100575	genetic generalized epilepsy	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0100576	hereditary generalized epilepsy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0100577	myoclonic epilepsy	nervous_system_disorder	other	nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100578	FANCM Fanconi-like genomic instability disorder	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0100579	GRHL3-related orofacial clefting	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0100580	epilepsy, unknown whether focal or generalized	nervous_system_disorder	other	nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100581	ocular growth disorder	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	other	other	other	other	other	other	other	
MONDO:0100582	TOR1AIP1-related myopathy	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0100583	Jeune syndrome - GRK2-related	hereditary_disease|respiratory_system_disorder|urinary_system_disorder|musculoskeletal_system_disorder|syndromic_disease	other	respiratory_system_disorder|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease|urinary_system_disorder	other	other	other	other	other	other	other	
MONDO:0100584	SNUPN-related muscular dystrophy with or without multi-system involvement	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0100586	B3GALT6-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0100587	A4GALT-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0100588	FAM20B-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0100589	ALG10-congenital disorder of glycosylation	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0100591	TOR1AIP1-related multisystem disorder	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:0100592	SLC26A2-related skeletal dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0100593	COMP-related skeletal dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0100595	furunculosis	inflammatory_disease|infectious_disease|integumentary_system_disorder	infectious_disease	infectious_disease|integumentary_system_disorder|inflammatory_disease	other	other	other	other	other	other	other	
MONDO:0100596	COL1A2-related osteogenesis imperfecta	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0100597	intellectual disability, autosomal recessive	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0100598	autosomal recessive syndromic intellectual disability	psychiatric_disorder|nervous_system_disorder|syndromic_disease|hereditary_disease	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder|hereditary_disease|syndromic_disease	other	other	other	other	other	other	other	
MONDO:0100599	COL1A1-related Ehlers-Danlos syndrome	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0100600	hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100601	autosomal dominant syndromic intellectual disability	hereditary_disease|syndromic_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	syndromic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100602	COL2A1-related spondyloepiphyseal dysplasia	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	other	other	other	other	other	other	
MONDO:0100603	FAT4-related neurodevelopmental disorder	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100604	TOR1AIP1-related nuclear envelopathy	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:0100605	POLR-related leukodystrophy	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100606	COL1A2-related Ehlers-Danlos syndrome	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0100607	ciliary dyskinesia, primary, 54	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	syndromic_disease|hereditary_disease|respiratory_system_disorder	other	other	other	other	other	other	other	
MONDO:0100608	ALPL-related autosomal dominant hypophosphatasia	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0100609	ALPL-related autosomal recessive hypophosphatasia	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0100610	autism spectrum disorder 1	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100611	autism spectrum disorder 2	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100612	autism spectrum disorder 3	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100613	BMP4-related ocular growth disorder	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	other	other	other	other	other	other	other	
MONDO:0100614	syndromic congenital heart disease	syndromic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0100615	intestinal failure–associated liver disease	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	other	other	other	other	other	other	other	
MONDO:0100617	VPS11-related neurological disorder	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100619	variable age epilepsy syndrome	nervous_system_disorder	other	nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100620	developmental and epileptic encephalopathy	nervous_system_disorder	other	nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100621	acquired developmental and epileptic encephalopathy	nervous_system_disorder	other	nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100623	meningitis-retention syndrome	urinary_system_disorder|nervous_system_disorder	other	urinary_system_disorder|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100624	DCTN1-related neurodegeneration	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100625	childhood-onset dementia	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	other	other	other	other	other	other	other	
MONDO:0100626	SOX11-related complex neurodevelopmental disorder with or without congenital anomalies	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100627	CFTR-related metabolic syndrome	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0100628	SAMD9-related spectrum and myeloid neoplasm risk	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	other	other	other	other	other	other	other	
MONDO:0100629	KIF5A-related neurological disorder	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100630	acquired sleep-related hypermotor epilepsy	nervous_system_disorder	other	nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100631	sleep-related hypermotor epilepsy	nervous_system_disorder	other	nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0100632	CSF1R-related disorder	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:0200000	uterine ligament adenosarcoma	musculoskeletal_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder	obstetrics_and_gynecology|oncology	gynecologic_cancer|uterine_disease|cancer|reproductive_system_disease	muscle_disorder|reproductive_system_disorder|joint_disorder|bone_disorder	false	true	false	false	high
MONDO:0300000	SSR3-CDG	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0400000	small intestinal bacterial overgrowth	infectious_disease|digestive_system_disorder	infectious_disease	digestive_system_disorder|infectious_disease	gastroenterology|hepatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder_upper_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0400002	calcium-alkali syndrome	metabolic_disease	metabolic_disease	metabolic_disease	endocrinology|nephrology|pediatric	metabolic_disorder|calcium_albumin_relation_issue	kidney_disorder|endocrine_disorder|bone_disorder	false	false	false	false	medium
MONDO:0400003	skeletal fluorosis	metabolic_disease	metabolic_disease	metabolic_disease	orthopaedic|rheumatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0400004	phrynoderma	integumentary_system_disorder	other	integumentary_system_disorder	dermatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	liver_disorder|skin_disorder	false	false	false	false	medium
MONDO:0400005	refeeding syndrome	nutritional_disorder	other	nutritional_disorder	endocrinology|gastroenterology|hepatology	metabolic_disorder|neurodegenerative_disease	liver_disorder|upper_gastrointestinal_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0400006	botryomycosis	infectious_disease	infectious_disease	infectious_disease	dermatology|mycology	cancer|autoimmune_diseases|inflammatory_disease	fungus_disorder|skin_disorder	true	false	false	false	medium
MONDO:0500000	episodic angioedema with eosinophilia	immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder|immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	hematology|renal_medicine|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|allergy	immune_disorder|skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0500018	acute fibrinous and organizing pneumonia	inflammatory_disease|infectious_disease|respiratory_system_disorder	infectious_disease	infectious_disease|respiratory_system_disorder|inflammatory_disease|acute_disease	pulmonology|pediatric	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	lung_disorder|vascular_disorder	false	false	false	true	high
MONDO:0550003	SEC61B-related polycystic liver disease	endocrine_system_disorder|digestive_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|digestive_system_disorder|endocrine_system_disorder	genetics_and_genomics|pediatric|hepatology	metabolic_disorder|polycystic_liver_disease	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0600001	glutaminase deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|endocrinology|neurology	metabolic_disorder|neurodegenerative_disease	kidney_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0600002	hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|hematology	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder|vascular_disorder	true	false	false	true	very_high
MONDO:0600003	bacterial hemorrhagic fever	infectious_disease	infectious_disease	infectious_disease	microbiology|infectious_diseases|general_medicine|hematology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|vascular_disorder	true	false	false	false	medium
MONDO:0600005	venom allergy	immune_system_disorder	other	immune_system_disorder	allergy_and_immunology	autoimmune_diseases|allergy	immune_disorder|nose_disorder	false	false	false	true	medium
MONDO:0600008	cytokine release syndrome	immune_system_disorder	other	immune_system_disorder	hematology|immunology|oncology	inflammatory_disease|autoimmune_diseases|cancer	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0600009	severe hypophosphatasia	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|mineral_bone_disorder	false	false	false	true	very_high
MONDO:0600010	moderate hypophosphatasia	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|endocrinology|orthopaedic	metabolic_disorder|neurodegenerative_disease	bone_disorder|skeletal_disorder|mineral_disorder	true	false	false	true	medium
MONDO:0600011	mild hypophosphatasia	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|genetic_disorder	bone_disorder|joint_disorder|teeth_disorder	false	false	false	true	low
MONDO:0600014	alveolar capillary dysplasia without misalignment of pulmonary veins	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|cardiothoracic|pulmonology|cardiology|hematology	inflammatory_disease|autoimmune_diseases|anemia|cardiovascular_disorder	lung_disorder|vascular_disorder	false	false	false	false	high
MONDO:0600016	acinar dysplasia	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|genetics_and_genomics|oncology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases|cancer	liver_disorder|biliary_disorder	false	false	false	false	very_high
MONDO:0600017	acinar dysplasia caused by mutation in FGF10	hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|developmental_disorder	liver_disorder|kidney_disorder|lung_disorder	false	false	false	false	high
MONDO:0600018	acinar dysplasia caused by mutation in FGFR2	hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|oncology	developmental_disorder|cancer|genetic_disorders	bone_disorder|developmental_disorder|skeletal_dysplasia	false	false	false	false	medium
MONDO:0600019	acinar dysplasia caused by mutation in TBX4	hereditary_disease|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease	pediatric|genetics_and_genomics	anemia|cardiovascular_disorder	kidney_disorder|lung_disorder	false	false	false	false	high
MONDO:0600023	idiopathic inflammatory myopathy	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease	rheumatology|neurology	inflammatory_disease|autoimmune_diseases	immune_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0600024	familial idiopathic inflammatory myopathy	inflammatory_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|inflammatory_disease	genetics_and_genomics|rheumatology|neurology	inflammatory_disease|autoimmune_diseases	immune_disorder|muscle_disorder	false	false	false	false	high
MONDO:0600025	hydrosalpinx	reproductive_system_disorder	other	reproductive_system_disorder	urology|obstetrics_and_gynecology	gynecological_condition|reproductive_system_disorder	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0600026	vanishing lung syndrome	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases|cancer	lung_disorder|vascular_disorder	false	false	false	false	high
MONDO:0600027	congenital right-sided heart lesions	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|cardiology|cardiovascular	cardiovascular_disorder|congenital_lesion	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0600029	restrictive pulmonary disease	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology	inflammatory_disease|autoimmune_diseases|respiratory_disease	lung_disorder	false	false	false	false	high
MONDO:0600030	B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|acute_disease|immune_system_disorder	genetics_and_genomics|hematology|oncology	cancer	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0700000	ALG9-associated autosomal dominant polycystic kidney disease	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	renal_medicine|genetics_and_genomics|urology	metabolic_disorder|kidney_disease	kidney_disorder|renal_disorder	false	false	false	true	high
MONDO:0700001	shrinking lung syndrome	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|rheumatology	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	false	high
MONDO:0700002	ATP1A3-associated neurological disorder	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0700003	obstetric disorder		other		obstetrics_and_gynecology|pediatric	metabolic_disorder|obstetric_disorder_is_also_related_to_autoimmune_diseases	obstetric_disorder_is_a_subset_of_this_category|reproductive_system_disorder	false	false	false	true	high
MONDO:0700007	idiopathic disease	other	other		genetics_and_genomics|neurology	neurodegenerative_disease|idiopathic_diseases	immune_disorder	false	false	false	false	high
MONDO:0700008	chromosome 1 disorder	chromosomal_disorder	other	chromosomal_disorder	chromosome_abnormalities|genetics_and_genomics	metabolic_disorder|chromosome_disorders_typically_fall_under_a_more_general_category_of_genetic_disorders_which_isn_t_listed_here_but_neurodegenerative_disease_is_the_closest_match|neurodegenerative_disease	spinal_disorder|chromosome_related_disorder_is_not_in_the_list_but_a_more_accurate_match_is_not_found__however__this_can_be_considered_as_one_of_the_possible_matches	false	false	false	false	high
MONDO:0700009	chromosome 2 disorder	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	genetic_disorders|chromosome_disorders	false	false	false	false	medium
MONDO:0700010	chromosome 3 disorder	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0700011	chromosome 4 disorder	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|chromosome_disorders_often_affect_physical_growth_and_development_which_can_include_joint_and_muscle_issues__but_the_most_fitting_categories_are_likely_brain_and_spinal_given_the_nature_of_some_chromosomal_conditions_affecting_cognitive_function_and_neurological_health|brain_disorder	false	false	false	false	medium
MONDO:0700012	chromosome 5 disorder	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0700013	chromosome 6 disorder	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics	metabolic_disorder|mental_health_disorder|autoimmune_diseases|neurodegenerative_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	medium
MONDO:0700014	chromosome 7 disorder	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|chromosome_disorder	chromosome_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0700015	chromosome 8 disorder	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|genetic_disorder|metabolic_disorder	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0700016	chromosome 9 disorder	chromosomal_disorder	other	chromosomal_disorder	medical_genetics|pediatrics|genetics_and_genomics	genetic_disorders|neurodegenerative_disease|metabolic_disorder	blood_bone_marrow_disorder|chromosome_disorder_is_not_in_the_list__but_based_on_the_name__chromosome_9_disorder___it_seems_to_be_related_to_blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0700017	chromosome 10 disorder	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0700018	chromosome 11 disorder	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics	chromosomal_disorder|neurodegenerative_disease|genetic_disorder|metabolic_disorder	blood_bone_marrow_disorder|genetic_disorder	false	false	false	false	high
MONDO:0700019	chromosome 12 disorder	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	genetic_disorder_is_not_listed_so_chromosome_12_disorder_fits_into_none_of_the_options_provided|neurodegenerative_disease|metabolic_disorder	chromosome_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0700020	chromosome 13 disorder	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	chromosome_abnormality_disorder|genetic_disorder___corrected_list_to_match_the_format_requirement____blood_bone_marrow_disorder|blood_bone_marrow_disorder|genetic_disorder	false	false	false	false	high
MONDO:0700021	chromosome 14 disorder	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	chromosome_disorder|blood_bone_marrow_disorder|genetic_disorder	false	false	false	false	high
MONDO:0700022	chromosome 15 disorder	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|genetic_disorder	false	false	false	false	high
MONDO:0700023	chromosome 16 disorder	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|chromosome_disorder	spinal_disorder|brain_disorder	true	false	false	false	high
MONDO:0700024	chromosome 19 disorder	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|chromosome_disorders_are_typically_categorized_under_this_category_as_it_is_a_genetic_disorder_affecting_chromosomes	spinal_disorder|chromosome_related_disorder_would_typically_fit_under_a_different_category___however_since_that_is_not_present_the_closest_related_disorder_is__spinal_disorder	false	false	false	false	medium
MONDO:0700025	chromosome 20 disorder	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0700026	chromosome 22 disorder	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	immune_disorder|brain_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0700027	chromosome X disorder	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	immune_disorder|chromosome_abnormality_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0700028	chromosome Y disorder	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	chromosome_y_disorder___becomes___metabolic_disorder__chromosome_y_disorder|metabolic_disorder	chromosome_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0700029	partial duplication of chromosome 13	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|genetic_disorder_is_not_in_the_list_but_partial_duplication_of_chromosome_13_is_a_type_of_genetic_disorder_so_it_should_fall_under_a_related_category_which_would_be__metabolic_disorder	kidney_disorder|brain_disorder	false	false	false	false	medium
MONDO:0700030	complete trisomy 21	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	autoimmune_diseases|mental_health_disorder|cardiovascular_disorder|neurodegenerative_disease|anemia|metabolic_disorder|inflammatory_disease	kidney_disorder|spinal_disorder|ear_disorder|lung_disorder|teeth_disorder|nose_disorder|brain_disorder|muscle_disorder|heart_disorder|joint_disorder|throat_disorder|urinary_tract_disorder|skin_disorder|liver_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0700031	mosaic trisomy 18	chromosomal_disorder|syndromic_disease	other	chromosomal_disorder|syndromic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0700032	complete trisomy 18	chromosomal_disorder|syndromic_disease	other	chromosomal_disorder|syndromic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0700033	complete trisomy 13	chromosomal_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|chromosomal_disorder|hereditary_disease|syndromic_disease|nervous_system_disorder	obstetrics_and_gynecology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder|brain_disorder|joint_disorder	false	false	false	false	very_high
MONDO:0700034	mosaic trisomy 13	chromosomal_disorder|hereditary_disease|nervous_system_disorder|syndromic_disease|disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region|chromosomal_disorder|hereditary_disease|syndromic_disease|nervous_system_disorder	genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease|metabolic_disorder	immune_disorder|spinal_disorder|bone_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0700035	monosomy chromosome 8	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	cancer|autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	immune_disorder|lymphatic_disorder|bone_disorder	false	false	false	false	high
MONDO:0700036	fibrothecoma	reproductive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	oncology|dermatology	cancer|adrenal_gland_disease	bone_disorder|skin_disorder|vascular_disorder	false	true	false	false	medium
MONDO:0700037	testicular fibrothecoma	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer|adrenal_gland_disease	muscle_disorder|reproductive_system_disorder	false	false	false	false	low
MONDO:0700038	TDP-43 proteinopathy	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0700039	bladder exstrophy-epispadias-cloacal extrophy complex	disorder_of_development_or_morphogenesis|urinary_system_disorder	other	urinary_system_disorder|disorder_of_development_or_morphogenesis	urology|genetics_and_genomics|pediatric	genitourinary_disorder|rare_disease|congenital_abnormality|birth_defect|developmental_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	very_high
MONDO:0700040	neonatal jaundice due to ABO incompatibility	metabolic_disease	metabolic_disease	metabolic_disease	obstetrics_and_gynecology|hematology|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder	immune_disorder|liver_disorder	false	false	false	true	low
MONDO:0700041	neuroblastoma, susceptibility to, 2	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|oncology|pediatric	cancer|neurodegenerative_disease	bone_bone_marrow_disorder|lymphatic_disorder|brain_disorder	false	true	false	true	high
MONDO:0700043	syndrome caused by partial chromosomal duplication of the short arm of chromosome 9	chromosomal_disorder	other	chromosomal_disorder	pediatrics|genetics_and_genomics	genetic_disorder|neurodegenerative_disease	immune_disorder|kidney_disorder|upper_gastrointestinal_disorder|lymphatic_disorder|spinal_disorder|ear_disorder|bone_disorder|nose_disorder|brain_disorder|eye_disorder|muscle_disorder|joint_disorder|skin_disorder|throat_disorder|urinary_tract_disorder|reproductive_system_disorder|vascular_disorder|lower_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0700044	TUBB2A-related tubulinopathy	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|tubulinopathy	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0700045	protothecosis	infectious_disease	infectious_disease	infectious_disease	infectious_diseases|pulmonology|dermatology	inflammatory_disease|autoimmune_diseases	biliary_disorder|liver_disorder	true	false	false	false	medium
MONDO:0700046	baclofen withdrawal syndrome	syndromic_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|syndromic_disease	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0700047	premenopausal osteoporosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	rheumatology|obstetrics_and_gynecology|endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|bone_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0700048	hand-foot syndrome	integumentary_system_disorder|syndromic_disease	other	integumentary_system_disorder|syndromic_disease	pediatrics|oncology|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|liver_disorder	false	false	false	true	medium
MONDO:0700051	liver abscess (disease)	digestive_system_disorder|endocrine_system_disorder|infectious_disease	endocrine_system_disorder|infectious_disease	infectious_disease|endocrine_system_disorder|digestive_system_disorder	hepatology|gastroenterology	inflammatory_disease|cancer|autoimmune_diseases	upper_gastrointestinal_disorder|liver_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0700052	intersphincteric abscess	infectious_disease	infectious_disease	infectious_disease	urology|gastroenterology	inflammatory_disease|cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	medium
MONDO:0700054	microcephaly 6 with or without short stature	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0700055	KIF1A related neurological disorder	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0700057	neurological pain disorder	nervous_system_disorder	other	nervous_system_disorder	neurology	inflammatory_disease|autoimmune_diseases|neurological_pain_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0700058	Morton neuroma	nervous_system_disorder	other	nervous_system_disorder	orthopaedic|neurology	inflammatory_disease|neurological_condition|musculoskeletal_disorder	muscle_disorder|joint_disorder	false	false	false	true	medium
MONDO:0700060	leukemia, acute, X-linked	hereditary_disease|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	acute_disease|hematologic_disorder|hereditary_disease|cancer_or_benign_tumor	hematology|genetics_and_genomics|oncology	cancer|leukemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	very_high
MONDO:0700064	aneuploidy	chromosomal_disorder	other	chromosomal_disorder	other____note__some_might_argue_that_aneuploidy_is_more_closely_related_to_genetics_and_genomics_than_any_other_category__but_others_may_also_consider_it_a_condition_in_obstetrics_and_gynecology_or_pediatric_medicine|genetics_and_genomics	cancer|aneuploidy	bone_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0700065	trisomy	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0700066	myopathy caused by variation in FKRP	musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	orthopaedic|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	lysosomal_storage_disease|spinal_disorder|muscle_disorder	false	false	false	true	high
MONDO:0700067	myopathy caused by variation in FKTN	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	myopathy|muscle_disorder	false	false	false	false	high
MONDO:0700068	myopathy caused by variation in POMGNT1	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	nervous_system_disorder|musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0700069	myopathy caused by variation in POMGNT2	musculoskeletal_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscldisorder|muscle_disorder	false	false	false	true	high
MONDO:0700070	myopathy caused by variation in POMT1	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	true	high
MONDO:0700071	myopathy caused by variation in POMT2	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	myopathy|neurodegenerative_disease	muscle_disorder	false	false	false	true	high
MONDO:0700073	glutaric acidemia IIa	disorder_of_development_or_morphogenesis|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease|mitochondrial_disease|metabolic_disease	metabolic_disease|cardiovascular_disorder	musculoskeletal_system_disorder|mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0700074	glutaric acidemia IIb	disorder_of_development_or_morphogenesis|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease|mitochondrial_disease|metabolic_disease	metabolic_disease|cardiovascular_disorder	musculoskeletal_system_disorder|mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0700075	congenital muscular dystrophy caused by variation in POMGNT2	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease|metabolic_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0700076	glutaric acidemia IIc	disorder_of_development_or_morphogenesis|cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease|mitochondrial_disease|metabolic_disease	metabolic_disease|cardiovascular_disorder	musculoskeletal_system_disorder|mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0700078	triple-positive breast carcinoma	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	adrenal_gland_disease|cancer	endocrine_disorder|reproductive_system_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0700079	hormone receptor-positive breast cancer	breast_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	breast_disorder|cancer_or_benign_tumor	obstetrics_and_gynecology|oncology	cancer|hormone_receptor_positive_breast_cancer_is_more_specifically_a_type_of_cancer	endocrine_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0700080	EPHB4-associated vascular malformation spectrum	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	pediatrics|cardiology|genetics_and_genomics	vascular_disorder|genetic_disorder|cardiovascular_disorder|developmental_disorder	vascular_disorder|heart_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0700081	newborn respiratory distress syndrome	syndromic_disease|respiratory_system_disorder	other	acute_disease|respiratory_system_disorder|syndromic_disease	pulmonology|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	lung_disorder|respiratory_disorder	false	false	false	true	high
MONDO:0700082	Robertsonian translocation Down syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatrics|psychiatry|genetics_and_genomics	anemia|metabolic_disorder	brain_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0700083	reciprocal translocation down syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|other____alternatively__neurodegenerative_disease	brain_disorder|bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0700084	myopathy caused by variation in GMPPB	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	musculoskeletal_system_disorder|metabolic_disease|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	true	high
MONDO:0700085	pentasomy	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|oncology	anemia|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	bone_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0700086	uniparental disomy	chromosomal_disorder	other	chromosomal_disorder	pediatric|obstetrics_and_gynecology|genetics_and_genomics	metabolic_disorder|genetic_disorder	uniparental_disomy_can_also_be_related_to_other_categories_but_the_most_fitting_one_is_reproductive_system_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0700087	Usher syndrome type 1B	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	pediatric|otolaryngology|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	hearing_loss_disorder|ear_disorder	false	false	false	false	very_high
MONDO:0700088	paroxysmal nonkinesigenic dyskinesia	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0700089	paroxysmal nonkinesigenic dyskinesia 1	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0700090	epilepsy, familial temporal lobe, 1	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0700091	ring chromosome disorder	chromosomal_disorder	other	chromosomal_disorder	pediatric|pediatrics|other____replaced__other__with_the_correct_category____genetics_and_genomics|genetics_and_genomics	metabolic_disorder|genetic_disorder	chromosome_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0700092	neurodevelopmental disorder	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|neurodevelopmental_disorder	false	false	false	false	high
MONDO:0700093	balanced Robertsonian translocation Down syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|spinal_disorder|immune_disorder|joint_disorder	false	false	false	false	high
MONDO:0700094	unbalanced Robertsonian translocation Down syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric	genetic_disorder|mental_health_disorder|neurodegenerative_disease|prenatal_condition|developmental_disorder	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0700096	human disease				allergy_and_immunology|immunology|oncology|genetics_and_genomics|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder|kidney_disorder|liver_disorder	true	false	false	true	please_provide_the_specific_human_disease_or_disorder_you_would_like_to_categorize_for_qalys_lost
MONDO:0700107	chromosome 19q13.11 deletion syndrome, distal	disorder_of_development_or_morphogenesis|chromosomal_disorder	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	joint_disorder|brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0700112	heterotaxy, visceral, 5, autosomal	cardiovascular_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	hereditary_disease|syndromic_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	liver_disorder|heart_disorder|kidney_disorder	false	false	false	false	high
MONDO:0700115	proliferative vitreoretinopathy	nervous_system_disorder|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	cancer|autoimmune_diseases|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0700116	microcephaly with lissencephaly and/or hydranencephaly	nervous_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	true	false	false	false	very_high
MONDO:0700117	SLC6A3-related dopamine transporter deficiency syndrome	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0700118	proximal chromosome 18q deletion syndrome	syndromic_disease|chromosomal_disorder	other	syndromic_disease|chromosomal_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|intellectual_disability|developmental_disorder|growth_disorder	false	false	false	false	high
MONDO:0700119	distal chromosome 18q deletion syndrome	syndromic_disease|chromosomal_disorder	other	syndromic_disease|chromosomal_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	joint_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0700120	BAFopathy	hereditary_disease	other	hereditary_disease	oncology|pulmonology|hematology	adrenal_gland_disease|neurodegenerative_disease|inflammatory_disease	biliary_disorder|liver_disorder	false	false	false	true	high
MONDO:0700121	ACTL6A-related BAFopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	cancer|neurodegenerative_disease|cardiovascular_disorder	bone_disorder|blood_bone_marrow_disorder|muscle_disorder	false	false	false	false	high
MONDO:0700122	PBRM1-related BAFopathy	hereditary_disease	other	hereditary_disease	oncology|genetics_and_genomics	cancer|adrenal_gland_disease	bone_disorder|kidney_disorder	false	false	false	false	high
MONDO:0700123	SMARCC1-associated developmental dysgenesis syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	syndrome|genetic_disorder|developmental_disorder|neurodegenerative_disease	brain_disorder|developmental_disorder	false	false	false	false	high
MONDO:0700124	chromosome 21 disorder	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0700125	chromosome 18 disorder	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	joint_disorder|brain_disorder|chromosome_disorders_is_not_in_the_list__but_chromosome_18_disorder_could_fit_here__however_it_s_more_accurate_to_say_it_s_a_rare_genetic_disorder_affecting_brain_development_so|muscle_disorder	false	false	false	false	high
MONDO:0700126	trisomy 21	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|cardiovascular_disorder	eye_disorder|joint_disorder|brain_disorder|heart_disorder|reproductive_system_disorder|ear_disorder|spinal_disorder	false	false	false	false	high
MONDO:0700127	mosaic trisomy 21	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|medical_specialties_related_to_children_and_genetic_conditions	metabolic_disorder|neurodegenerative_disease	joint_disorder|brain_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0700128	translocation Down syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	vascular_disorder|joint_disorder|brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0700129	mosaic translocation Down syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	chromosomal_abnormality|genetic_disorder|neurodevelopmental_disorder|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0700130	partial segmental duplication	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics	genetic_disorder|neurodegenerative_disease	liver_disorder|upper_gastrointestinal_disorder|kidney_disorder	false	false	false	false	high
MONDO:0700200	atypical dopamine transporter deficiency syndrome	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0700207	constitutional delay of growth and puberty	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|endocrinology	endocrine_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0700215	NTRK fusion positive cancer	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|neurology|oncology|pediatric|genetics_and_genomics	neurodegenerative_disease|cancer	lung_disorder	false	true	false	true	high
MONDO:0700216	RET fusion positive cancer	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|cancer	kidney_disorder|vascular_disorder	false	true	false	true	high
MONDO:0700217	neonatal sepsis	infectious_disease	infectious_disease	infectious_disease	neonatology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	very_high
MONDO:0700218	group B streptococcal infection	infectious_disease	infectious_disease	infectious_disease	obstetrics_and_gynecology|pediatric	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0700219	neoplastic meningitis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0700220	disease related to transplantation	other	other		transplant_related_issues_are_more_closely_associated_with_organ_specific_specialties__but_the_closest_match_is|hematology|genomics|renal_medicine|hepatology|immunology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases|mental_health_disorder|anemia	kidney_disorder|vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:0700221	disease related to solid organ transplantation	other	other	disease_related_to_transplantation	renal_medicine|hepatology|gastroenterology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0700222	disease related to hematopoietic stem cell transplant	other	other	disease_related_to_transplantation	hematology|hematopoietic_stem_cell_transplant_is_also_related_to_hematology_so_the_best_fitting_categories_are__hematology|oncology	inflammatory_disease|autoimmune_diseases|cancer|anemia	immune_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0700223	hereditary skeletal muscle disorder	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	spinal_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0700224	PDE6A-related retinopathy	hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	neurodegenerative_disease|eye_disorder	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0700225	hereditary gallbladder disorder	hereditary_disease|digestive_system_disorder	other	hereditary_disease|digestive_system_disorder	hepatology|gastroenterology|genetics_and_genomics	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	medium
MONDO:0700226	food allergy	immune_system_disorder	other	immune_system_disorder	pediatric|allergy_and_immunology	autoimmune_diseases|allergy	lower_gastrointestinal_disorder|immune_disorder	false	false	false	true	high
MONDO:0700227	ELOVL4-related maculopathy	hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0700228	LRP5-related exudative vitreoretinopathy	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|cardiovascular_disorder	ophthalmology|genetics_and_genomics	genetic_disorder|metabolic_disorder	bone_disorder|eye_disorder	false	false	false	false	high
MONDO:0700229	MAK-related retinopathy	hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder	ophthalmology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0700230	GPR143-related foveal hypoplasia	hereditary_disease	other	hereditary_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	lower_gastrointestinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0700231	TSPAN12-related exudative vitreoretinopathy	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|cardiovascular_disorder	ophthalmology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0700232	KIZ-related retinopathy	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0700233	TOPORS-related retinopathy	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0700234	PRPF8-related retinopathy	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|retinal_disorder	reproductive_system_disorder|eye_disorder	false	false	false	false	medium
MONDO:0700235	RD3-related retinopathy	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0700236	BBS9-related ciliopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology|pulmonology	metabolic_disorder|ciliopathy	ciliopathy|eye_disorder	false	false	false	false	high
MONDO:0700237	BBS10-related ciliopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|ciliopathies	ciliopathy___corrected_to____eye_disorder|kidney_disorder|eye_disorder	false	false	false	false	high
MONDO:0700238	BEST1-related dominant retinopathy	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	retinal_disease|genetic_disorder|eye_disease	best1_related_diseases|eye_disorder	false	false	false	false	high
MONDO:0700239	BEST1-related recessive retinopathy	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	metabolic_disorder|eye_disease___corrected_to___metabolic_disorder|eye_disease	eye_disorder	false	false	false	false	high
MONDO:0700240	BEST1-related vitreoretinochoroidopathy	nervous_system_disorder|hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0700241	IMPG2-related recessive retinopathy	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|reproductive_system_disorder|eye_disorder	false	false	false	false	high
MONDO:0700242	IMPG2-related dominant retinopathy	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0700243	CACNA1F-related retinopathy	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|genetic_disorder	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0700244	CACNA2D4-related retinopathy	nervous_system_disorder|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0700245	epidermolytic hyperkeratosis 2B, autosomal recessive	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	skin_disorder|epidermal_disorder	false	false	false	false	high
MONDO:0700246	ocular dysgenesis caused by defects in PAX6 regulation	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0700247	RAB18 deficiency	syndromic_disease|hereditary_disease|disorder_of_visual_system	other	hereditary_disease|syndromic_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0700248	epidermolytic hyperkeratosis 2A, autosomal dominant	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	skin_disorder|epidermal_disorder	false	false	false	false	medium
MONDO:0700249	epidermolytic hyperkeratosis 1	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	genetics_and_genomics_dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	skin_disorder	false	false	false	false	medium
MONDO:0700250	mitochondrial complex IV deficiency, nuclear type 1	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease	genetics_and_genomics|pediatric|neurology|pulmonology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	muscle_disorder|metabolic_disorder|mitochondrial_disease	false	false	false	false	very_high
MONDO:0700251	orofacial cleft 7	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|otolaryngology	neurodegenerative_disease|autoimmune_diseases	teeth_disorder|oral_disorder	false	false	false	false	medium
MONDO:0700252	parneoplastic endocrine syndrome	endocrine_system_disorder|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder|syndromic_disease	endocrinology|oncology	cancer|adrenal_gland_disease	lymphatic_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0700253	paraneoplastic hematological syndrome	syndromic_disease|cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor|syndromic_disease	hematology|oncology	cancer|anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0700254	paraneoplastic gastrointestinal syndrome	syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease	neurology|oncology|gastroenterology	cancer|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0700255	paraneoplastic renal syndrome	syndromic_disease|cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|urinary_system_disorder	oncology|renal_medicine	cancer|inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0700256	TREX1-related type 1 interferonopathy	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|connective_tissue_disorder	genetics_and_genomics|neurology|immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|kidney_disorder	false	false	false	true	high
MONDO:0700257	RNASEH2B-related type 1 interferonopathy	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|connective_tissue_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder	false	false	false	false	high
MONDO:0700258	RNASEH2C-related type 1 interferonopathy	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|connective_tissue_disorder	genetics_and_genomics|neurology|pediatrics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder	false	false	false	false	high
MONDO:0700259	RNASEH2A-related type 1 interferonopathy	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|connective_tissue_disorder	genetics_and_genomics|neurology|pediatrics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0700260	SAMHD1-related type 1 interferonopathy	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|connective_tissue_disorder	genetics_and_genomics|pediatric|immunology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0700261	ADAR-related type 1 interferonopathy	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|connective_tissue_disorder	genetics_and_genomics|immunology	inflammatory_disease|autoimmune_diseases	brain_disorder|immune_disorder	false	false	false	false	high
MONDO:0700262	IFIH1-related type 1 interferonopathy	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|connective_tissue_disorder	genetics_and_genomics|immunology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder|bone_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0700263	RNU7-1-related type 1 interferonopathy	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	hereditary_disease|syndromic_disease|connective_tissue_disorder	genetics_and_genomics|immunology|pulmonology	inflammatory_disease|autoimmune_diseases	immune_disorder	false	false	false	false	high
MONDO:0700264	type 1 interferonopathy	syndromic_disease|connective_tissue_disorder	other	syndromic_disease|connective_tissue_disorder	genetics_and_genomics|rheumatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder	false	false	false	true	high
MONDO:0700265	paraneoplastic rheumatic syndrome	syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor	rheumatology|oncology	cancer|inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder	false	false	false	true	high
MONDO:0700266	paraneoplastic cutaneous syndrome	syndromic_disease|cancer_or_benign_tumor|integumentary_system_disorder	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|integumentary_system_disorder	dermatology|neurology|oncology	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder	false	true	false	false	high
MONDO:0700267	BARD1-related cancer predisposition	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|oncology	adrenal_gland_disease|cancer|autoimmune_diseases	blood_bone_marrow_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0700268	BRCA1-related cancer predisposition	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|oncology|obstetrics_and_gynecology	cancer	reproductive_system_disorder	false	true	false	true	very_high
MONDO:0700269	BRCA2-related cancer predisposition	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|oncology	cancer_predisposition|cancer	reproductive_system_disorder	false	true	false	true	very_high
MONDO:0700270	ATM-related cancer predisposition	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|pediatric|oncology	cancer|atm_related_cancer_predisposition_can_also_be_categorized_as_a_genetic_disorder__but_the_most_relevant_category_from_the_provided_list_is_cancer	vascular_disorder|kidney_disorder	false	true	false	true	high
MONDO:0700271	CHEK2-related cancer predisposition	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|oncology	cancer_predisposition|cancer	genetic_disorder|cancer_predisposition	false	true	false	true	high
MONDO:0700272	PALB2-related cancer predisposition	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|oncology	cancer_predisposition|cancer	reproductive_system_disorder	false	true	false	true	high
MONDO:0700273	RAD51C-related cancer predisposition	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|oncology|obstetrics_and_gynecology	cancer_predisposition|cancer	reproductive_system_disorder|cancer_predisposition	false	true	false	true	high
MONDO:0700274	RAD51D-related cancer predisposition	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|oncology	cancer_predisposition|cancer	reproductive_system_disorder|cancer_predisposition	false	true	false	true	very_high
MONDO:0700275	prostate cancer, hereditary	hereditary_disease|cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|reproductive_system_disorder	genetics_and_genomics|urology|oncology	cancer|hereditary_disease|adrenal_gland_disease	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	high
MONDO:0700276	POLR3A-related disorder	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0700277	POLR3B-related disorder	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0700278	POLR1C-related disorder	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|anemia	muscle_disorder|brain_disorder|bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0700279	spastic triplegia	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscledisorder	false	false	false	false	high
MONDO:0700280	post-treatment Lyme disease syndrome	other	other	post_infectious_disorder	neurology|rheumatology	autoimmune_diseases|inflammatory_disease|mental_health_disorder	skin_disorder|vascular_disorder|joint_disorder|immune_disorder	false	false	false	false	high
MONDO:0700281	MYH10-related neurodevelopmental disorder with congenital anomalies	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder|congenital_anomalies_is_not_in_the_list_however__it_seems_most_related_to_joint_disorder	true	false	false	false	high
MONDO:0700282	POLR3-related leukodystrophy	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0700283	ataxic diplegic cerebral palsy	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0700284	carnitine palmitoyl transferase deficiency	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0700285	DMD-related muscular dystrophy	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0700286	leukodystrophy, demyelinating, adult-onset, autosomal dominant, atypical	nervous_system_disorder|hereditary_disease|chromosomal_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|chromosomal_disorder	other	other	other	other	other	other	other	
MONDO:0700288	early-childhood-onset neurodegeneration with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0700290	spermatogenic failure 98	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	other	other	other	other	other	other	other	
MONDO:0700291	glycogen storage disease IX	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0700292	desmoplastic fibroma	musculoskeletal_system_disorder|connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder|musculoskeletal_system_disorder	other	other	other	other	other	other	other	
MONDO:0700293	WFS1-related disorder	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:0700294	CTCF-related neurodevelopmental disorder	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0700295	leukodystrophy, demyelinating, adult-onset, autosomal dominant, typical	nervous_system_disorder|hereditary_disease|chromosomal_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder|chromosomal_disorder	other	other	other	other	other	other	other	
MONDO:0700296	aflatoxicosis	poisoning	other	poisoning	other	other	other	other	other	other	other	
MONDO:0700297	homocystinuria-megaloblastic anemia cblD type	metabolic_disease|hereditary_disease|nutritional_disorder|hematologic_disorder	anemia|metabolic_disease	hereditary_disease|hematologic_disorder|metabolic_disease|nutritional_disorder	other	other	other	other	other	other	other	
MONDO:0700298	isolated methylmalonic aciduria cblD type	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0700299	ACTH-independent macronodular adrenal hyperplasia 3	hereditary_disease|syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|syndromic_disease	other	other	other	other	other	other	other	
MONDO:0700300	achalasia-progeroid syndrome	premature_aging_syndrome|hereditary_disease|disorder_of_development_or_morphogenesis	other	premature_aging_syndrome|hereditary_disease|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0700301	Fischer-Zirnsak progeroid syndrome	premature_aging_syndrome|hereditary_disease|disorder_of_development_or_morphogenesis	other	premature_aging_syndrome|hereditary_disease|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0700303	Erb palsy	nervous_system_disorder	other	nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0700335	familial isolated dilated cardiomyopathy	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiology|genetics_and_genomics|cardiovascular	cardiovascular_disorder|familial_isolated_dilated_cardiomyopathy_is_most_closely_related_to_the_cardiovascular_system__so_it_would_fit_best_in_the_cardiovascular_disorder_category	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0700336	peritoneal carcinomatosis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	other	other	other	other	other	other	other	
MONDO:0700337	renal tubular dysgenesis - ACE	urinary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|urinary_system_disorder	other	other	other	other	other	other	other	
MONDO:0700338	autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0700339	DNM1-encephalopathy and neurodevelopmental disorder	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0700340	congenital megaprepuce	reproductive_system_disorder	other	reproductive_system_disorder	other	other	other	other	other	other	other	
MONDO:0700341	monilethrix-2	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0700342	monilethrix-3	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0700343	monilethrix-1	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0700344	CEP164-related ciliopathy	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:0700345	TMEM127-related tumor predisposition	syndromic_disease|hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease|endocrine_system_disorder	other	other	other	other	other	other	other	
MONDO:0700346	MAX-related tumor predisposition	syndromic_disease|hereditary_disease|endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor|syndromic_disease|endocrine_system_disorder	other	other	other	other	other	other	other	
MONDO:0700347	SDHC-related Mitochondrial Disease	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0700348	BMPR1A-related juvenile polyposis syndrome	syndromic_disease|hereditary_disease|digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|hereditary_disease|cancer_or_benign_tumor|syndromic_disease	other	other	other	other	other	other	other	
MONDO:0700349	ACTN2-related cardiac and skeletal myopathy	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	other	other	other	other	other	other	other	
MONDO:0700350	GRIN2B-related complex neurodevelopmental disorder	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0800025	Teebi hypertelorism syndrome 1	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	anemia|cardiovascular_disorder|metabolic_disorder	eye_disorder|ear_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0800026	central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	lung_disorder|brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0800027	leukoencephalopathy, diffuse hereditary, with spheroids 1	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	hematology|neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	brain_disorder|blood_bone_marrow_disorder|vascular_disorder|immune_disorder	true	false	false	false	very_high
MONDO:0800028	dyskinesia with orofacial involvement, autosomal dominant	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0800029	interstitial lung disease 2	inflammatory_disease|infectious_disease|hereditary_disease|respiratory_system_disorder	infectious_disease	idiopathic_disease|hereditary_disease|respiratory_system_disorder|infectious_disease|inflammatory_disease	pulmonology|cardiothoracic	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0800030	gastrointestinal defects and immunodeficiency syndrome 1	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|digestive_system_disorder	other	disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease|digestive_system_disorder	gastroenterology|immunology	inflammatory_disease|gastrointestinal_defects|autoimmune_diseases	immune_disorder|liver_disorder|lower_gastrointestinal_disorder|gastrointestinal_defect	false	false	false	false	very_high
MONDO:0800031	central hypoventilation syndrome, congenital	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	lung_disorder|brain_disorder	false	false	false	true	high
MONDO:0800032	MELAS syndrome caused by mutation in MTTL1	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|syndromic_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	heart_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0800033	MELAS syndrome caused by mutation in MTTQ	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|syndromic_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0800034	MELAS syndrome caused by mutation in MTTH	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|syndromic_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0800035	MELAS syndrome caused by mutation in MTTK	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|syndromic_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	heart_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0800036	MELAS syndrome caused by mutation in MTTC	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|syndromic_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	heart_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0800037	MELAS syndrome caused by mutation in MTTS1	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|syndromic_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	heart_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0800038	MELAS syndrome caused by mutation in MTND1	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|syndromic_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|mtdna_disorder_is_not_in_the_list_but_closest_match_to_this_disease_category_would_be__metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0800039	MELAS syndrome caused by mutation in MTND5	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|syndromic_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|mitochondrial_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0800040	MELAS syndrome caused by mutation in MTND6	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|syndromic_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	psychiatry|pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	heart_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0800041	MELAS syndrome caused by mutation in MTTS2	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|syndromic_disease|metabolic_disease|musculoskeletal_system_disorder	metabolic_disease	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	mitochondrial_disorder_is_not_in_the_list__but_it_s_implied_as_melas_syndrome_caused_by_mutation_in_mtts2|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0800042	restrictive dermopathy 1	disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease	pulmonology|dermatology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	skin_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0800043	Stüve-Wiedemann syndrome 1	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|nervous_system_disorder|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0800044	congenital disorder of deglycosylation 1	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	false	very_high
MONDO:0800045	autoinflammatory syndrome, familial, Behcet-like 1	hereditary_disease|syndromic_disease|connective_tissue_disorder	other	syndromic_disease|hereditary_disease|connective_tissue_disorder	pediatric|genetics_and_genomics|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|joint_disorder	false	false	false	false	high
MONDO:0800046	thyroid hormone metabolism, abnormal 1	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	thyroid_hormone_metabolism|endocrinology	metabolic_disorder|autoimmune_diseases	thyroid_hormone_metabolism_abnormality|endocrine_disorder	false	false	false	true	high
MONDO:0800047	macrothrombocytopenia, isolated, 1, autosomal dominant	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|pediatric|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0800063	primordial dwarfism and slender bone disorder	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	endocrinology|pediatric|genetics_and_genomics	skeletal_rare_diseases|metabolic_disorder	bone_disorder|primordial_dwarfism_and_slender_bone_disorder_is_also_often_referred_to_as_sotos_syndrome_a_form_of_skeletal_dysplasia	false	false	false	false	very_high
MONDO:0800064	osteogenesis imperfecta and a reduction of bone mineral density.	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|rheumatology	metabolic_disorder|bone_mineral_density_reduction_often_associated_with_metabolic_disorders_such_as_osteomalacia_which_can_also_be_linked_to_osteogenesis_imperfecta_as_both_result_from_defects_in_collagen_production	spinal_disorder|bone_disorder|teeth_disorder	false	false	false	false	high
MONDO:0800066	polydactyly-syndactyly-triphalangism	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	metabolic_disorder|birth_defect|genetic_condition	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0800080	severe spondylodysplastic dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	high
MONDO:0800088	lysosomal storage disease with skeletal involvement	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	neurology|rheumatology|pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|lysosomal_storage_disease|metabolic_disorder	lysosomal_storage_disease|bone_disorder|muscle_disorder	false	false	false	true	high
MONDO:0800096	abnormal mineralization disorder	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics|osteoporosis__not_listed_but_relevant__is_actually_orthopaedic	autoimmune_diseases|anemia|metabolic_disorder|inflammatory_disease	kidney_disorder|bone_disorder	false	false	false	false	high
MONDO:0800098	SNRNP200-related dominant retinopathy	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0800099	RDH12-related recessive retinopathy	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0800100	RDH12-related dominant retinopathy	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|upper_gastrointestinal_disorder	false	false	false	false	medium
MONDO:0800101	NMNAT1-related retinopathy	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease	neurology|ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0800102	CNGA3-related retinopathy	psychiatric_disorder|hereditary_disease|disorder_of_visual_system|nervous_system_disorder	psychiatric_disorder	disorder_of_visual_system|psychiatric_disorder|disorder_of_orbital_region|nervous_system_disorder|hereditary_disease	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0800103	COACH syndrome 1	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurodegenerative_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|hereditary_disease	pediatrics|genetics_and_genomics|endocrinology	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|reproductive_system_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0800104	immunodeficiency 105	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	pediatrics|allergy_and_immunology|immunology	immunodeficiency|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|immune_disorder	true	false	false	true	high
MONDO:0800105	catatonia	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0800106	disruptive behavior disorder	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	neurology|psychiatry	disruptive_behavior_disorder|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0800107	anterior deviation infundibular septum	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	neurology|pediatric|otolaryngology|genetics_and_genomics	anatomic_abnormality|neurodegenerative_disease|congenital_disorder	brain_disorder|upper_gastrointestinal_disorder|nose_disorder	false	false	false	false	medium
MONDO:0800108	cleft leaflet of tricuspid valve	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	valvular_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0800109	persistent tachypnoe of infancy	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|pulmonology	respiratory_disease_is_not_in_the_list_so__metabolic_disorder|metabolic_disorder|cardiovascular_disorder	heart_disorder|lung_disorder	false	false	false	false	high
MONDO:0800110	persistent tachypnoe of infancy, aberrant	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|pulmonology	inflammatory_disease|metabolic_disorder|cardiovasular_disorder	lung_disorder|respiratory_disorder____note__i_corrected_the_original_category_name_to_its_correct_match	true	false	false	false	high
MONDO:0800111	persistent tachypnoe of infancy, usual	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|pulmonology	metabolic_disorder|respiratory_disease	heart_disorder|lung_disorder	false	false	false	false	medium
MONDO:0800113	necrotizing vasculitis	inflammatory_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|inflammatory_disease	renal_medicine|rheumatology|hematology	autoimmune_diseases|inflammatory_disease	immune_disorder|vascular_disorder	true	false	false	true	very_high
MONDO:0800114	follicular bronchiolits	respiratory_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	idiopathic_disease|infectious_disease|respiratory_system_disorder|inflammatory_disease	pediatric|pulmonology	autoimmune_diseases|inflammatory_disease	lung_disorder|lower_gastrointestinal_disorder	true	false	false	false	low
MONDO:0800117	cutaneous botryomycosis	infectious_disease	infectious_disease	infectious_disease	pediatric|dermatology	cancer|inflammatory_disease|autoimmune_diseases	nose_disorder|skin_disorder	true	false	false	true	medium
MONDO:0800118	visceral botryomycosis	infectious_disease	infectious_disease	infectious_disease	hepatology|pulmonology|gastroenterology	cancer|inflammatory_disease|autoimmune_diseases	lung_disorder|liver_disorder	true	false	false	false	high
MONDO:0800119	postinfectious bronchiolitis obliterans	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	false	very_high
MONDO:0800120	Mac-Leod-Swyer-James-Syndrome	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	lung_disorder	false	false	false	false	medium
MONDO:0800121	cellular interstitial pneumonitis	respiratory_system_disorder	other	respiratory_system_disorder	genetics_and_genomics|pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	lung_disorder|kidney_disorder|immune_disorder	true	false	false	false	high
MONDO:0800123	bronchiolocentric pattern of interstitial pneumonia	respiratory_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|inflammatory_disease|respiratory_system_disorder	pulmonology|cardiothoracic	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder|lower_gastrointestinal_disorder	true	false	false	false	high
MONDO:0800124	Lane Hamilton syndrome	respiratory_system_disorder|digestive_system_disorder|metabolic_disease|hereditary_disease|immune_system_disorder	metabolic_disease|autoimmune_disease	digestive_system_disorder|metabolic_disease|immune_system_disorder|respiratory_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0800125	disseminated visceral giant cell angiitis	cardiovascular_disorder|inflammatory_disease	cardiovascular_disorder	inflammatory_disease|cardiovascular_disorder	rheumatology|renal_medicine|gastroenterology	inflammatory_disease|autoimmune_diseases	vascular_disorder|kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0800126	dystrophic pulmonary ossification	respiratory_system_disorder	other	respiratory_system_disorder	genetics_and_genomics|pulmonology|orthopaedic	anemia|metabolic_disorder	lung_disorder|bone_disorder|muscledisorder	false	false	false	false	high
MONDO:0800127	pulmonary amyloidosis	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	cardiology|hepatology|pulmonology|hematology|cardiothoracic	inflammatory_disease|autoimmune_diseases	vascular_disorder|lung_disorder|kidney_disorder|immune_disorder	false	false	false	false	high
MONDO:0800128	combined immunodeficiency due to POLE2 deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|pediatrics|immunology	immunodeficiency_diseases|metabolic_disorder|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0800129	autoinflammatory disease, X-linked	connective_tissue_disorder|hereditary_disease|syndromic_disease	other	connective_tissue_disorder|syndromic_disease|hereditary_disease	rheumatology|genetics_and_genomics|pediatrics	autoimmune_diseases|inflammatory_disease	joint_disorder|immune_disorder	false	false	false	true	high
MONDO:0800130	autoinflammatory syndrome with immunodeficiency	connective_tissue_disorder|hereditary_disease|syndromic_disease	other	connective_tissue_disorder|syndromic_disease|hereditary_disease	rheumatology|allergy_and_immunology|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	joint_disorder|immune_disorder|lymphatic_disorder	false	false	false	true	very_high
MONDO:0800131	hyper-IgE recurrent infection syndrome 4A, autosomal dominant	hematologic_disorder|hereditary_disease|immune_system_disorder	other	hematologic_disorder|immune_system_disorder|hereditary_disease	genetics_and_genomics|allergy_and_immunology|pediatric|immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0800132	autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology|pediatric|immunology	anemia|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0800133	pulmonary hypoplasia	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	cardiovascular_disorder	lung_disorder|lower_gastrointestinal_disorder	false	false	false	false	very_high
MONDO:0800134	primary immunodeficiency due to calcium channel deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|allergy_and_immunology|immunology	cardiovascular_disorder|metabolic_disorder|autoimmune_diseases	immune_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0800135	congenital emphysematous lung disease due to Filamin A loss-of-function variant	respiratory_system_disorder	other	respiratory_system_disorder	genetics_and_genomics|pulmonology|pediatric	neurodegenerative_disease|metabolic_disorder	lung_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0800136	non-severe combined immunodeficiency due to COPG1 deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|hematology|allergy_and_immunology|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	medium
MONDO:0800137	early-onset pulmonary and cutaneous vasculitis	connective_tissue_disorder|syndromic_disease	other	connective_tissue_disorder|syndromic_disease	rheumatology|pulmonology|dermatology	autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder|vascular_disorder	false	false	false	true	high
MONDO:0800138	multisystem autoimmune disease due to IKAROS gain of function	immune_system_disorder	autoimmune_disease	immune_system_disorder	rheumatology|genetics_and_genomics|immunology	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0800139	HELIOS deficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|pediatric|immunology	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|endocrine_disorder|liver_disorder	false	false	false	false	high
MONDO:0800140	ITPKB deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0800141	MAN2B2 deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0800142	chronic mucocutaneous candidiasis and connective tissue disease due to JNK1 haploinsufficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|rheumatology|pediatric|immunology|dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder|skin_disorder	true	false	false	true	high
MONDO:0800143	cytomegalovirus pneumonia due to NOS2 deficiency	respiratory_system_disorder|infectious_disease|inflammatory_disease	infectious_disease	infectious_disease|inflammatory_disease|respiratory_system_disorder	pulmonology|pediatric|immunology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0800144	autoimmune pulmonary disease due to PD-1 deficiency	immune_system_disorder	autoimmune_disease	immune_system_disorder	genetics_and_genomics|pulmonology|pediatric|allergy_and_immunology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	false	false	false	false	high
MONDO:0800145	non-severe combined immunodeficiency due to polymerase delta deficiency	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|pediatrics|immunology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0800146	agammaglobulinemia, autosomal recessive, due to BOB1 deficiency	hematologic_disorder|hereditary_disease|immune_system_disorder	other	hematologic_disorder|hereditary_disease|immune_system_disorder	genetics_and_genomics|hematology|immunology	anemia|metabolic_disorder|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0800147	hemophagocytic lymphohistiocytosis due to RhoG deficiency	syndromic_disease|hereditary_disease|immune_system_disorder	other	syndromic_disease|hereditary_disease|immune_system_disorder	genetics_and_genomics|hematology	anemia|metabolic_disorder|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0800148	autoinflammatory syndrome due to TBK1 deficiency	connective_tissue_disorder|syndromic_disease	other	syndromic_disease|connective_tissue_disorder	neurology|genetics_and_genomics|pediatric|immunology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	neurological_disorder__note__the_correct_category_is__neurological_disorder___as_tbk1_deficiency_affects_the_brain_and_nervous_system|immune_disorder	false	false	false	true	high
MONDO:0800149	immunodeficiency, common variable, due to APRIL deficiency	cancer_or_benign_tumor|hematologic_disorder|syndromic_disease|hereditary_disease|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease|immune_system_disorder	genetics_and_genomics|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0800152	disorder of galactose and fructose metabolism	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|hepatology|endocrinology	disorder_of_galactose_and_fructose_metabolism|metabolic_disorder	endocrine_disorder|liver_disorder	false	false	false	true	medium
MONDO:0800153	urea cycle disorder or inherited hyperammonemia	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	metabolism|genetics_and_genomics|pediatric	metabolic_disorder|inherited_condition	kidney_disorder|liver_disorder|inherited_metabolic_disorder	false	false	false	true	very_high
MONDO:0800154	inborn disorder of the metabolism of sulfur-containing amino acids and hydrogen sulfide	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0800155	inborn disorder of glycine and serine metabolism	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0800156	inborn disorder of ornithine, proline and hydroxyproline metabolism	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric|medical_genetics	adrenal_gland_disease|metabolic_disorder	joint_disorder|kidney_disorder|liver_disorder|bone_disorder	false	false	false	false	high
MONDO:0800157	inborn disorder of lysine, hydroxylysine, and tryptophan metabolism	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	inborn_disorder|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0800158	inborn disorder of glutamate/glutamine and aspartate/asparagine metabolism	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|liver_disorder	false	false	false	true	high
MONDO:0800159	disorder of polyamine metabolism	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	liver_disorder	false	false	false	false	medium
MONDO:0800166	Knobloch syndrome	nervous_system_disorder|hereditary_disease|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	genetics_and_genomics|ophthalmology|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	bone_disorder|eye_disorder	false	false	false	false	medium
MONDO:0800167	Knobloch syndrome 1	nervous_system_disorder|hereditary_disease|disorder_of_visual_system	other	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0800175	cardiogenic shock	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0800176	black widow spider envenomation	poisoning	other	poisoning	emergency_medicine|toxicology|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0800178	platinum-induced ototoxicity	psychiatric_disorder|poisoning|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder|poisoning	neurology|otolaryngology	neurodegenerative_disease|ototoxicity	ear_disorder	false	false	false	false	high
MONDO:0800179	periprosthetic joint infection	infectious_disease|musculoskeletal_system_disorder|inflammatory_disease	infectious_disease	infectious_disease|inflammatory_disease|musculoskeletal_system_disorder	rheumatology|orthopaedic	inflammatory_disease|autoimmune_diseases	joint_disorder|immune_disorder	true	false	false	true	high
MONDO:0800180	CPOX-related hereditary coproporphyria	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	genetics_and_genomics|hepatology|hematology	anemia|metabolic_disorder	liver_disorder|genetic_disorder	false	false	false	true	high
MONDO:0800181	OPA1-related optic atrophy with or without extraocular features	disorder_of_development_or_morphogenesis|disorder_of_visual_system|hereditary_disease|mitochondrial_disease|metabolic_disease	metabolic_disease	disorder_of_visual_system|disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease|disorder_of_orbital_region	neurology|genetics_and_genomics|ophthalmology	neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0800182	TEK-related primary glaucoma	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0800183	PAX6-related ocular dysgenesis	urinary_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_visual_system|cancer_or_benign_tumor|hereditary_disease|urinary_system_disorder|disorder_of_orbital_region	genetics_and_genomics|ophthalmology|pediatric	genetic_disorder|neurodegenerative_disease|congenital_disorder|genetic_eye_disease____removed__no__it_is_actually____neurodegenerative_disease|birth_defect|eye_disease|ocular_disorder|developmental_disorder	teeth_disorder|eye_disorder	false	false	false	false	high
MONDO:0800195	achalasia-alacrima syndrome	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics|pulmonology|gastroenterology	neurodegenerative_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lung_disorder|immune_disorder	false	false	false	false	medium
MONDO:0800196	achromatopsia 5	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder|hereditary_disease|disorder_of_orbital_region	neurology|genetics_and_genomics|ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0800197	achromatopsia 6	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0800198	alopecia universalis	integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology|endocrinology	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0800200	arthrogryposis, distal, type 2B4	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics|orthopaedic	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	joint_disorder|muscle_disorder|bone_disorder	false	false	false	false	medium
MONDO:0800201	baldness, male pattern	integumentary_system_disorder	other	integumentary_system_disorder	dermatology|genetics_and_genomics|endocrinology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|endocrine_disorder	false	false	false	true	low
MONDO:0800204	calvarial doughnut lesions with bone fragility and spondylometaphyseal dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|orthopaedic	inflammatory_disease__spondyloepiphyseal_dysplasias_are_also_known_as_inflammatory_arthropathy_associated_with_specific_skeletal_disorders|spondylometaphyseal_dysplasia_is_a_type_of_skeletal_disorder|metabolic_disorder	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0800206	epidermolysis bullosa dystrophica with subcorneal cleavage	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|joint_disorder	false	false	false	false	high
MONDO:0800207	neuropathy, small fiber	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics|psychiatry	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	true	high
MONDO:0800209	fibrosis of extraocular muscles, congenital, 3b	nervous_system_disorder|disorder_of_visual_system|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_orbital_region|nervous_system_disorder|disorder_of_visual_system	ophthalmology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0800210	glaucoma 1, open angle, l	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease	open_angle|eye_disorder	false	false	false	true	high
MONDO:0800290	Li-fraumeni-like syndrome	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	oncology|genetics_and_genomics	genetic_disorder|familial_cancer|tumor_syndrome|family_cancer_syndrome|cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0800291	crossed polydactyly, type I	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|pediatric|genetics_and_genomics	congenital_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0800296	microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 2	hereditary_disease	other	hereditary_disease	ophthalmology|pediatric|genetics_and_genomics	autoimmune_diseases|eye_disease|inflammatory_disease|metabolic_disorder	eye_disorder	false	false	false	false	low
MONDO:0800298	peroxisome biogenesis disorder, complementation group 2	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis|syndromic_disease|nervous_system_disorder	metabolic_disease|neurodegenerative_disease	metabolic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics	adrenal_gland_disease|neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisome_biogenesis_disorder_is_primarily_related_to_the_liver	false	false	false	false	high
MONDO:0800299	myopathy, congenital, with excess of muscle spindles	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|congenital_myopathy	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0800300	black locks with albinism and deafness syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology|pediatric|otolaryngology	adrenal_gland_disease|neurodegenerative_disease	eye_disorder|skin_disorder|ear_disorder	false	false	false	false	high
MONDO:0800301	Friedreich ataxia with retained reflexes	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0800302	glycogen storage disease Id	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	hepatology|genetics_and_genomics|endocrinology	glycogen_storage_disease_id|metabolic_disorder	liver_disorder|muscle_disorder	false	false	true	true	high
MONDO:0800304	neuropathy, hereditary sensory and autonomic, type IId	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0800305	myelofibrosis with myeloid metaplasia	cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|connective_tissue_disorder	anemia|cancer_or_benign_tumor	musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology|pulmonology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0800306	myoclonic epilepsy of Lafora 2	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	hereditary_disease|nervous_system_disorder|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0800307	de la Chapelle dysplasia	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	genetic_disorder|metabolic_disorder	joint_disorder|blood_bone_marrow_disorder|skeletal_disorder	false	false	false	false	medium
MONDO:0800308	orotic aciduria without megaloblastic anemia	metabolic_disease|hematologic_disorder|hereditary_disease	anemia|metabolic_disease	hematologic_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|renal_medicine|hematology	metabolic_disorder|anemia	urine_disorder|kidney_disorder	true	false	false	false	medium
MONDO:0800310	pregnancy loss, recurrent, 4	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	obstetrics_and_gynecology|genetics_and_genomics|pediatric	endocrine_disorder__removed_______metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0800311	vas deferens, congenital unilateral aplasia of	reproductive_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|reproductive_system_disorder	pediatric|urology	adrenal_gland_disease|metabolic_disorder|anemia	reproductive_system_disorder|ear_disorder	false	false	false	false	low
MONDO:0800312	wooly hair, autosomal recessive 1, with or without hypotrichosis	integumentary_system_disorder	other	integumentary_system_disorder	genetics_and_genomics|pediatric|dermatology	metabolic_disorder|anemia	skin_disorder|hair_disorder	false	false	false	true	medium
MONDO:0800313	xeroderma pigmentosum, type F/Cockayne syndrome	syndromic_disease|integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|dermatology	cancer|metabolic_disorder|genetic_disease	skin_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0800314	xeroderma pigmentosum, type G/Cockayne syndrome	syndromic_disease|integumentary_system_disorder|hereditary_disease	other	hereditary_disease|integumentary_system_disorder|syndromic_disease	genetics_and_genomics|dermatology	inherited_disorder|cancer|metabolic_disorder	eye_disorder_skin_disorder	false	false	false	false	very_high
MONDO:0800317	premature ovarian failure 4	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	obstetrics_and_gynecology|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0800318	Emery-Dreifuss muscular dystrophy 6, X-linked	cardiovascular_disorder|nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease|cardiovascular_disorder	genetics_and_genomics|orthopaedic|neurology|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0800319	cone dystrophy 5, X-linked	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	pediatrics|ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder|spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0800320	cone dystrophy 1, X-linked	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0800321	congenital heart defects, multiple types, 1, X-linked	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	genetics_and_genomics|pediatric|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0800322	membranous obstruction of inferior vena cava	digestive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder	renal_medicine|hematology|cardiology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	kidney_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0800323	long QT syndrome 4	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0800324	microphthalmia, isolated, with coloboma 8	disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|hereditary_disease|disorder_of_orbital_region	ophthalmology|genetics_and_genomics|pediatric	metabolic_disorder|developmental_abnormality	eye_disorder	false	false	false	false	high
MONDO:0800326	cone-rod dystrophy 14	disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_orbital_region	ophthalmology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0800328	retinitis pigmentosa 94, variable age at onset	disorder_of_visual_system|nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|metabolic_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	eye_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0800329	febrile seizures, familial, 3a	hereditary_disease	other	hereditary_disease	neurology|pediatric	familial|metabolic_disorder	brain_disorder	false	false	false	true	medium
MONDO:0800330	myoclonic epilepsy, juvenile, 2	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0800331	hyperglycinemia, transient neonatal	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	endocrinology|pediatric	metabolic_disorder|neonatal_condition	liver_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0800335	migraine, familial hemiplegic, 4	nervous_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0800337	acute tubulointerstitial nephritis	urinary_system_disorder	other	urinary_system_disorder	nephrology|pediatric|renal_medicine	inflammatory_disease|autoimmune_diseases	kidney_disorder|urinary_tract_disorder|immune_disorder	true	false	false	true	high
MONDO:0800339	laryngospasm, severe neonatal episodic	syndromic_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|syndromic_disease	pulmonology|pediatric|neonatology	adrenal_gland_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	lung_disorder|throat_disorder|muscule_disorder	false	false	false	false	high
MONDO:0800341	congenital myopathy 4A, autosomal dominant	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0800344	brachydactyly-syndactyly-oligodactyly syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	genetics_and_genomics|pediatric|orthopaedic	congenital_disorder|metabolic_disorder|skeletal_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:0800345	atrial fibrillation, familial, 17	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	genetics_and_genomics|cardiology|hematology	familial|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0800346	left ventricular noncompaction 9	cardiovascular_disorder|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0800347	cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	genetics_and_genomics|cardiology	familial_hypertrophic_cardiomyopathy|cardiovascular_disorder	heart_disorder|muscle_disorder|vascular_disorder	false	false	false	true	high
MONDO:0800348	retinitis pigmentosa 53	nervous_system_disorder|disorder_of_visual_system|metabolic_disease|psychiatric_disorder|hereditary_disease	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|metabolic_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|adrenal_gland_disease	blood_bone_marrow_disorder|eye_disorder	false	false	false	false	high
MONDO:0800349	atrial fibrillation, familial, 16	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	pulmonology|genetics_and_genomics|cardiology|renal_medicine|hematology	familial|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0800350	left ventricular noncompaction 4	cardiovascular_disorder|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0800351	left ventricular noncompaction 5	cardiovascular_disorder|syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	syndromic_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiothoracic|cardiology	inflammatory_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0800352	retinitis pigmentosa 65	nervous_system_disorder|disorder_of_visual_system|metabolic_disease|psychiatric_disorder|hereditary_disease	psychiatric_disorder|metabolic_disease	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|metabolic_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder	eye_disorder|retina_disorder	false	false	false	false	high
MONDO:0800353	congenital disorder of glycosylation, type Ibb	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric	congenital_disorder|metabolic_disorder	liver_disorder|glycosylation_disorder_is_a_type_of_congenital_disorder_that_affects_the_liver_s_ability_to_properly_glycosylate_proteins	false	false	true	false	high
MONDO:0800354	febrile seizures, familial, 3b	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|muscle_disorder|immune_disorder	false	false	false	true	medium
MONDO:0800355	parasomnia, sleep terrors type	other	other	sleep_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|sleep_disorder	false	false	false	true	medium
MONDO:0800356	short-rib thoracic dysplasia 7/20 with polydactyly, digenic	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|orthopaedic	genetic_condition|skeletal_dysplasia|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	very_high
MONDO:0800357	hyperpigmentation, progressive cribriform and zosteriform	integumentary_system_disorder	other	integumentary_system_disorder	neurology|dermatology	cancer|inflammatory_disease|autoimmune_diseases	skin_disorder|blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	medium
MONDO:0800358	schizophrenia 17	nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	brain_disorder|psychiatric_disorder_is_not_listed_but_the_closest_match_would_be_brain_disorder	false	false	false	false	high
MONDO:0800359	retinitis pigmentosa 64	nervous_system_disorder|disorder_of_visual_system|metabolic_disease|psychiatric_disorder|hereditary_disease	metabolic_disease|psychiatric_disorder	disorder_of_visual_system|hereditary_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|metabolic_disease	ophthalmology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0800363	Joubert syndrome 19	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0800364	peroxisome biogenesis disorder, complementation group 3	nervous_system_disorder|syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|metabolic_disease|syndromic_disease	genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	peroxisome_biogenesis_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0800365	peroxisome biogenesis disorder, complementation group K	nervous_system_disorder|syndromic_disease|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease|neurodegenerative_disease	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder|metabolic_disease|syndromic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	liver_disorder|peroxisomal_disorder	false	false	false	false	very_high
MONDO:0800366	dyskeratosis congenita, autosomal dominant 4	cancer_or_benign_tumor|syndromic_disease|integumentary_system_disorder|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|integumentary_system_disorder|cancer_or_benign_tumor|syndromic_disease	genetics_and_genomics|pediatric|dermatology	neurodegenerative_disease|metabolic_disorder	skin_disorder|liver_disorder|blood_bone_marrow_disorder|upper_gastrointestinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0800367	cardiomyopathy, dilated, 1LL	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	pediatric|cardiothoracic|cardiology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0800368	cardiomyopathy, dilated, 1MM	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	pediatrics|cardiothoracic|cardiology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0800369	Parkinson disease 19B, early-onset	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0800370	dyskeratosis congenita, autosomal recessive 7	cancer_or_benign_tumor|premature_aging_syndrome|syndromic_disease|integumentary_system_disorder|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|integumentary_system_disorder|premature_aging_syndrome|cancer_or_benign_tumor|syndromic_disease	genetics_and_genomics|pediatric|dermatology	neurodegenerative_disease|metabolic_disorder	skin_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0800371	cardiomyopathy, familial restrictive, 5	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	genetics_and_genomics|cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0800372	Joubert syndrome 29	syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder	false	false	false	false	high
MONDO:0800373	carbon monoxide poisoning	poisoning	other	poisoning	pulmonology|neurology|cardiology|hematology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|cardiovascular_disorder	brain_disorder|lung_disorder	false	false	false	true	high
MONDO:0800374	ventricular tachycardia, catecholaminergic polymorphic 6	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	genetics_and_genomics|cardiothoracic|cardiology	autoimmune_diseases|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0800375	developmental delay, epilepsy, and neonatal diabetes 1	digestive_system_disorder|metabolic_disease|endocrine_system_disorder|hereditary_disease	metabolic_disease|diabetes_mellitus|endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|digestive_system_disorder|metabolic_disease	genetics_and_genomics|pediatrics|neurology|endocrinology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|endocrine_disorder|developmental_delay	false	false	true	true	medium
MONDO:0800376	developmental delay, epilepsy, and neonatal diabetes 2	digestive_system_disorder|metabolic_disease|endocrine_system_disorder|hereditary_disease	metabolic_disease|diabetes_mellitus|endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|digestive_system_disorder|metabolic_disease	pediatric|neurology|endocrinology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|developmental_delay_can_be_categorized_under_developmental_delay_and_brain_disorder_epilepsy_can_be_categorized_under_epilepsy_is_already_a_category_but_it_fits_best_as_brain_disorder_neonatal_diabetes_2_can_be_categorized_under_endocrine_disorder|endocrine_disorder	false	false	true	true	medium
MONDO:0800377	ACTH-independent adrenal Cushing syndrome, somatic	syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|syndromic_disease	neurology|endocrinology	adrenal_gland_disease|metabolic_disorder|cancer	somatic|endocrine_disorder	false	false	false	true	high
MONDO:0800378	17,20-lyase deficiency, isolated	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	genetics_and_genomics|pediatric|endocrinology	adrenal_gland_disease|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0800379	17-alpha-hydroxylase/17,20-lyase deficiency, combined complete	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	genetics_and_genomics|endocrinology	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0800380	17-alpha-hydroxylase/17,20-lyase deficiency, combined partial	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	obstetrics_and_gynecology|endocrinology|genetics_and_genomics|pediatric	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0800381	46,XX true hermaphroditism, SRY-positive	reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrine_system_disorder	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder	endocrinology|genetics_and_genomics|urology	genetic_disorder|sexual_health_disorder|endocrine_disorder|developmental_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0800382	Joubert syndrome 11	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	neurology|genetics_and_genomics|pediatric	anemia|metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0800383	Joubert syndrome 34	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	kidney_disorder|brain_disorder	false	false	false	false	high
MONDO:0800384	cesium poisoning	poisoning	other	poisoning	neurology|toxicology	metabolic_disorder	kidney_disorder|endocrine_disorder	false	false	false	false	very_high
MONDO:0800385	iron poisoning	poisoning	other	poisoning	hematology|pediatric|gastroenterology	anemia|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0800386	organophosphate poisoning	poisoning	other	poisoning	neurology|toxicology	inflammatory_disease|autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	muscle_disorder|nerve_disorder|respiratory_system_disorder|eye_disorder	false	false	false	true	high
MONDO:0800387	sulfur mustard poisoning	poisoning	other	poisoning	renal_medicine|otolaryngology|dermatology|hematology|pulmonology	inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lung_disorder|skin_disorder	false	false	false	true	very_high
MONDO:0800388	cardiac glycoside intoxication	poisoning	other	poisoning	pediatrics|cardiology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	endocrine_disorder|heart_disorder	false	false	false	true	high
MONDO:0800389	monochloroacetic acid poisoning	poisoning	other	poisoning	neurology|otolaryngology|pulmonology	metabolic_disorder|toxic_exposure	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0800390	chemotherapy-induced toxicity	poisoning	other	poisoning	hematology|hepatology|oncology	cancer|chemotherapy_induced_toxicity_is_a_side_effect_of_cancer_treatment	blood_bone_marrow_disorder|liver_disorder	false	false	false	true	high
MONDO:0800391	EYS-related retinopathy	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	eye_disease|neurodegenerative_disease|genetic_disorder	eye_disorder	false	false	false	false	medium
MONDO:0800392	GNAT2-related retinopathy	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0800393	IDH3B-related retinopathy	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region	neurology|genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0800394	MERTK-related retinopathy	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	inflammatory_disease|autoimmune_diseases|anemia|metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	true	high
MONDO:0800395	PRPF31-related retinopathy	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0800396	GPR179-related retinopathy	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region	neurology|genetics_and_genomics|ophthalmology	neurodegenerative_disease|adrenal_gland_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0800397	GRM6-related retinopathy	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region	neurology|genetics_and_genomics|ophthalmology	autoimmune_diseases|neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	false	high
MONDO:0800398	ADAM9-related retinopathy	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region	neurology|genetics_and_genomics|ophthalmology	neurodegenerative_disease|adrenal_gland_disease	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0800399	RP1-related recessive retinopathy	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	psychiatric_disorder	hereditary_disease|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0800400	RP1-related dominant retinopathy	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0800401	CERKL-related retinopathy	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	ophthalmology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease	muscle_disorder|eye_disorder	false	false	false	false	medium
MONDO:0800402	TRPM1-related retinopathy	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	ophthalmology|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0800403	CNGB1-related retinopathy	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	eye_disorder	false	false	false	false	high
MONDO:0800404	PCARE-related retinopathy	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	vascular_disorder|eye_disorder	false	false	false	false	high
MONDO:0800405	CNGA1-related retinopathy	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0800406	ABCA4-related retinopathy	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	true	high
MONDO:0800407	NYX-related retinopathy	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|disorder_of_visual_system	ophthalmology|neurology|endocrinology|gastroenterology|pulmonology|cardiology|pediatrics|otolaryngology|obstetrics_and_gynecology|oncology|genetics_and_genomics|renal_medicine|hepatology|hematology|rheumatology|dermatology	neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	high
MONDO:0800408	urogenital adysplasia	hereditary_disease	other	hereditary_disease	urology|obstetrics_and_gynecology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0800412	yakut short stature syndrome	hereditary_disease	other	hereditary_disease	pediatric|endocrinology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	bone_disorder|endocrine_disorder	false	false	false	false	medium
MONDO:0800418	breast cancer, familial, susceptibility to, 1	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	oncology|genetics_and_genomics	susceptibility_to|familial|cancer	reproductive_system_disorder|familial	false	true	false	true	high
MONDO:0800419	breast cancer, familial, susceptibility to, 2	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	oncology|genetics_and_genomics	susceptibility_to|familial|cancer	susceptibility_to|reproductive_system_disorder|familial	false	true	false	true	high
MONDO:0800420	breast cancer, familial, susceptibility to, 3	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	oncology|genetics_and_genomics|obstetrics_and_gynecology	familial|susceptibility_to|cancer	reproductive_system_disorder|breast_cancer_familial_susceptibility_to|endocrine_disorder	false	true	false	true	high
MONDO:0800423	colorectal cancer, susceptibility to, 4	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	oncology|genetics_and_genomics|gastroenterology	cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0800424	colorectal cancer, susceptibility to, on chromosome 15	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	genetics_and_genomics|oncology	genetic_disorder|susceptibility|cancer|disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	high
MONDO:0800433	ovarian cancer, familial, susceptibility to, 1	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	genetics_and_genomics|obstetrics_and_gynecology|oncology	familial|cancer	reproductive_system_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0800434	ovarian cancer, familial, susceptibility to, 2	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	genetics_and_genomics|obstetrics_and_gynecology|oncology	familial____note__i_ve_assumed__familial__refers_to_a_category_of_disease_that_is_hereditary_or_inherited|cancer	reproductive_system_disorder|familial	false	true	false	true	high
MONDO:0800435	ovarian cancer, familial, susceptibility to, 3	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	genetics_and_genomics|obstetrics_and_gynecology|oncology	familial____note__familial_is_part_of_the_original_question|cancer	reproductive_system_disorder|familial	false	true	false	true	high
MONDO:0800436	craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|neurology|pediatric|psychiatry	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	craniofacial_dysmorphism|bone_disorder|skeletal_anomalies|impaired_intellectual_development	false	false	false	true	high
MONDO:0800437	Carey-Fineman-Ziter syndrome 1	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0800438	developmental delay with short stature, dysmorphic facial features, and sparse hair 1	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|endocrinology|pediatric	neurodegenerative_disease|metabolic_disorder	growth_disorder|developmental_delay|endocrine_disorder	false	false	false	false	high
MONDO:0800439	syndromic complex neurodevelopmental disorder	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|syndromic_complex|mental_health_disorder	neurodevelopmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0800440	HAND1 related congenital heart defect	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	cardiothoracic|genetics_and_genomics|pediatric|cardiology	cardiovascular_disorder|congenital_heart_defect	congenital_heart_defect|heart_disorder|cardiovascular_disorder	false	false	false	false	high
MONDO:0800441	NKX2.5-related congenital, conduction and myopathic heart disease	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|cardiology	cardiovascular_disorder|congenital_conduction_myopathic_heart_disease	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0800442	MYH-6 related congenital heart defects	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	genetics_and_genomics|pediatric|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0800443	DEAF1-associated neurodevelopmental disorder	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	brain_disorder|ear_disorder	false	false	false	false	high
MONDO:0800444	Birt-Hogg-Dube syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	oncology|genetics_and_genomics	familial_cancer_syndrome|cancer|genetic_disorder	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0800445	Birt-Hogg-Dube syndrome 1	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	pediatric|oncology|genetics_and_genomics	neurodegenerative_disease|cancer	blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0800446	bleeding diathesis due to thromboxane synthesis deficiency	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0800448	leukoencephalopathy with vanishing white matter	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|pediatric|hematology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0800449	lysosomal acid lipase deficiency	hereditary_disease|syndromic_disease|metabolic_disease	metabolic_disease	syndromic_disease|metabolic_disease|hereditary_disease	pediatric|gastroenterology|hepatology|genetics_and_genomics	lysosomal_storage_disease|metabolic_disorder	biliary_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0800450	microcephaly, short stature, and impaired glucose metabolism	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0800451	congenital amegakaryocytic thrombocytopenia	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	pediatric|hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0800452	congenital amegakaryocytic thrombocytopenia 1	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	pediatric|hematology|genetics_and_genomics	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0800453	juvenile absence epilepsy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|epilepsy_is_not_listed_but_absence_epilepsy_is_related_to_neurology_so_the_best_fit_would_be_neurodegenerative_disease__however_juvenile_absence_epilepsy_can_also_have_a_link_with_other_disorders_and_may_be_related_to_a_specific_subset_of_disorders_like_metabolic_disorder_or_autoimmune_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0800455	Birt-Hogg-Dube syndrome 2	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	pediatrics|oncology|genetics_and_genomics	cancer|genetic_disorder	blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0800456	SYNCRIP-related neurodevelopmental disorder	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|mental_health_disorder	neurodevelopmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0800457	HNRNPC-related neurodevelopmental disorder	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease|mental_health_disorder	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0800458	NR2F2 related multiple congenital anomalies/dysmorphic syndrome	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	developmental_anomalies|pediatric|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|mental_health_disorder|metabolic_disorder	developmental_disorder|facial_abnormality|reproductive_system_disorder|cardiac_abnormality|limb_redundancy|eye_disorder	false	false	false	false	high
MONDO:0800459	noxacusis	auditory_system_disorder|otorhinolaryngologic_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	otorhinolaryngologic_disease|nervous_system_disorder|auditory_system_disorder|psychiatric_disorder	neurology|otolaryngology|psychiatry	neurodegenerative_disease|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0800460	ASAH1-related disorders	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	bone_disorder|brain_disorder|nervous_system_disorder	false	false	false	false	high
MONDO:0800461	COL4A1-related disorder	hereditary_disease	other	hereditary_disease	neurology|renal_medicine|genetics_and_genomics	neurodegenerative_disease|cardiovascular_disorder|inflammatory_disease|metabolic_disorder	kidney_disorder|brain_disorder|vascular_disorder	false	false	false	true	high
MONDO:0800462	FHL1-related myopathy	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|muscle_disease|genetic_disorder	lower_spinal_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0800463	KIF7-related ciliopathy	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|ciliopathy	kidney_disorder|brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0800464	SQSTM1-related multisystem proteinopathy	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	lysosomal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0800465	CTSC-related disorder	hereditary_disease|syndromic_disease|integumentary_system_disorder	other	syndromic_disease|integumentary_system_disorder|hereditary_disease	pediatrics|dermatology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	teeth_disorder|oral_disorder	false	false	false	false	very_high
MONDO:0800466	disorder of GNAS inactivation	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	pediatrics|endocrinology|genetics_and_genomics	cancer|metabolic_disorder	endocrine_disorder|bone_disorder	false	false	false	true	high
MONDO:0800467	dyskeratosis congenita and related telomere biology disorder	hereditary_disease|syndromic_disease|integumentary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	syndromic_disease|cancer_or_benign_tumor|integumentary_system_disorder|hereditary_disease	pediatrics|genetics_and_genomics	neurodegenerative_disease|anemia|metabolic_disorder	blood_bone_marrow_disorder|skin_disorder	false	false	false	true	very_high
MONDO:0800468	SCN4A-related channelopathy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0800469	ACD-related telomere biology disorder	hereditary_disease|premature_aging_syndrome	other	premature_aging_syndrome|hereditary_disease	pediatrics|dermatology|genetics_and_genomics	genetic_disorder|telomere_disease|cancer|autoimmune_diseases	skin_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0800470	TUBB4A-related neurologic disorder	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0800472	CYP1B1-related glaucoma with or without anterior segment dysgenesis	hereditary_disease|disorder_of_visual_system	other	disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	pediatric|ophthalmology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	kidney_disorder|eye_disorder	false	false	false	false	high
MONDO:0800474	SOX3-related X-linked pituitary hormone deficiency with or without intellectual developmental disorder	hereditary_disease|syndromic_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	syndromic_disease|nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|endocrinology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0800475	NACC1-related neurodevelopmental disorder with epilepsy, cataracts and episodic irritability	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|genetics_and_genomics	epilepsy|mental_health_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	true	false	false	false	high
MONDO:0800476	HAND2 related congenital heart defect	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	pediatric|cardiology|genetics_and_genomics	congenital_heart_defect|cardiovascular_disorder	heart_disorder	false	false	false	false	high
MONDO:0800477	SETD2-related neurodevelopmental disorder without or with macrocephaly/overgrowth	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurology|pediatric|psychiatry|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0800478	trigeminal trophic syndrome	syndromic_disease	other	syndromic_disease	neurology|otolaryngology	inflammatory_disease|neurodegenerative_disease	nerve_disorder|spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0800479	self-limited neonatal seizures	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	metabolic_disorder|neurodegenerative_disease	neonatal_seizures|brain_disorder	false	false	false	true	medium
MONDO:0800480	non-verbal learning disability	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0800481	oral fibroma	connective_tissue_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor	oral_surgery|otolaryngology	tissue_growth_disorders|cancer	bone_disorder|teeth_disorder	false	false	false	false	low
MONDO:0800483	SF3B4-related acrofacial dysostosis	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	orthopaedic|pediatric|genetics_and_genomics	genetic_disorder|dysostosis|developmental_disorder|metabolic_disorder|skeletal_disorder	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0800484	PRKAG2-related cardiomyopathy	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|musculoskeletal_system_disorder	cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	true	high
MONDO:0800485	AKT3-related overgrowth spectrum	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	neurology|genetics_and_genomics	cancer|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0800486	metabolic bone disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	orthopaedic|endocrinology|rheumatology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|bone_disorder	false	false	false	true	high
MONDO:0800487	variable-age onset idiopathic generalized epilepsy syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0800488	neonatal/infantile-onset self-limited epilepsy syndrome	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	metabolic_disorder|neurodegenerative_disease	neonatal_infantile_onset_self_limited_epilepsy_syndrome_often_presents_at_birth_or_in_early_infancy__making_it_a_disorder_of_the_brain|brain_disorder	false	false	false	true	medium
MONDO:0800489	genetic epilepsy with febrile seizures plus spectrum	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	immune_disorder|spinal_disorder|muscle_disorder|brain_disorder	false	false	false	true	medium
MONDO:0800490	neonatal/infantile-onset epilepsy syndrome with developmental and epileptic encephalopathy	nervous_system_disorder	other	nervous_system_disorder	pediatric|genetics_and_genomics|neurology	epileptic_encephalopathy|developmental_disorder|neurodegenerative_disease	epileptic_disorder|developmental_enchepalopathy_disorder|brain_disorder	true	false	false	true	very_high
MONDO:0800491	early-infantile DEE	nervous_system_disorder	other	nervous_system_disorder	pediatric|otolaryngology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	ear_disorder|spinal_disorder|brain_disorder	true	false	false	true	very_high
MONDO:0800492	variable-age onset focal epilepsy syndrome	nervous_system_disorder	other	nervous_system_disorder	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|inflammatory_disease|mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	true	false	false	false	high
MONDO:0800493	familial mesial temporal lobe epilepsy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	epilepsy|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	medium
MONDO:0800494	variable-age onset combined generalized and focal epilepsy syndrome	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0800495	variable-age epilepsy syndrome with developmental and/or epileptic encephalopathy or progressive neurological deterioration	nervous_system_disorder	other	nervous_system_disorder	pediatric|genetics_and_genomics|neurology	inflammatory_disease|epileptic_encephalopathy|developmental_disorder|neurodegenerative_disease	neurological_disorder|developmental_delay_disorder|brain_disorder	true	false	false	false	very_high
MONDO:0800496	epilepsy with auditory features	nervous_system_disorder	other	nervous_system_disorder	pediatric|otolaryngology|neurology	mental_health_disorder|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	true	low
MONDO:0800498	childhood-onset genetic generalized epilepsy syndrome	nervous_system_disorder	other	nervous_system_disorder	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|mental_health_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0800499	childhood-onset idiopathic generalized epilepsy syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0800500	childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|pediatric|neurology	epilepsy_syndrome|neurodegenerative_disease|developmental_and_epileptic_encephalopathy	epileptic_disorder|encephalopathy|developmental_disorder|brain_disorder	true	false	false	true	very_high
MONDO:0800501	developmental and/or epileptic encephalopathy with spike-wave activation in sleep	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	epileptic_encephalopathy|neurodegenerative_disease|developmental_disorder	developmenal_and_epileptic_encephalopathy|brain_disorder	true	false	false	true	very_high
MONDO:0800502	childhood-onset self-limited focal epilepsy syndrome	nervous_system_disorder	other	nervous_system_disorder	pediatric|neurology	mental_health_disorder|neurodegenerative_disease	childhood_disorder|brain_disorder	false	false	false	true	medium
MONDO:0800503	TMEM63B-related developmental and epileptic encephalopathy with anemia	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	hematology|genetics_and_genomics|neurology	anemia|neurodegenerative_disease	blood_bone_marrow_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0810000	choroidal neovascularization	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	cardiovascular_disorder|eye_disease|inflammatory_disease	eye_disorder|vascular_disorder	false	false	false	true	high
MONDO:0850001	congenital neuronal ceroid lipofuscinosis	nervous_system_disorder|hereditary_disease|metabolic_disease	neurodegenerative_disease|metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0850007	syndromic lacrimal system disorder	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	pediatric|genetics_and_genomics|neurology|ophthalmology|otolaryngology	autoimmune_diseases|inflammatory_disease	nose_disorder|eye_disorder	false	false	false	false	medium
MONDO:0850008	anterior segment developmental abnormality with extraocular manifestations	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	pediatric|genetics_and_genomics|ophthalmology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0850009	syndromic microspherophakia	syndromic_disease	other	syndromic_disease	genetics_and_genomics|ophthalmology	metabolic_disorder|inflammatory_disease	eye_disorder|bone_disorder	false	false	false	false	medium
MONDO:0850010	congenital optic disk excavation	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	pediatric|genetics_and_genomics|neurology|ophthalmology	congenital_disorder|neurodegenerative_disease	spinal_disorder|eye_disorder	false	false	false	false	medium
MONDO:0850013	twin anemia-polycythemia sequence	obstetric_disorder	other	obstetric_disorder	pediatric|genetics_and_genomics|hematology	anemia|metabolic_disorder	blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0850014	twin-reversed arterial perfusion sequence	obstetric_disorder	other	obstetric_disorder	pediatric|cardiology|obstetrics_and_gynecology	fetal_abnormality|cardiovascular_disorder|anatomical_abnormality	heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0850015	selective intrauterine growth restriction	obstetric_disorder	other	obstetric_disorder	pediatric|obstetrics_and_gynecology	metabolic_disorder|intrauterine_growth_restriction	reproductive_system_disorder|fetal_growth_disorder	false	false	false	false	high
MONDO:0850030	complete hemimelia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|hematology|orthopaedic	cardiovascular_disorder|neurodegenerative_disease|anemia	spinal_disorder|bone_disorder|limb_disorder	false	false	false	false	high
MONDO:0850046	amniotic fluid embolism	obstetric_disorder	other	obstetric_disorder	pediatric|obstetrics_and_gynecology	cardiovascular_disorder|inflammatory_disease	reproductive_system_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0850048	classic eosinophilic pustular folliculitis	inflammatory_disease|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease	pediatric|dermatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0850049	painful legs and moving toes syndrome	syndromic_disease	other	syndromic_disease	orthopaedic|neurology|rheumatology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0850050	congenital aphakia-iris hypoplasia-microphthalmia-microcornea syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|ophthalmology|pediatric	metabolic_disorder|congenital_disease____corrected_to_match_the_format___metabolic_disorder|congenital_disease|eye_disorder	reproductive_system_disorder|eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:0850053	F12-associated cold autoinflammatory syndrome	connective_tissue_disorder|syndromic_disease	other	syndromic_disease|connective_tissue_disorder	genetics_and_genomics|allergy_and_immunology|rheumatology|pediatric	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder|joint_disorder	false	false	false	true	high
MONDO:0850054	hemophilia B leyden	hematologic_disorder	other	hematologic_disorder	hematology|genetics_and_genomics|pediatric	coagulation_disorder|hemorrhagic_disease|metabolic_disorder	joint_disorder|vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0850058	chronic neurovisceral acid sphingomyelinase deficiency	metabolic_disease|hereditary_disease|immune_system_disorder	metabolic_disease	immune_system_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0850059	hereditary persistence of fetal hemoglobin-intellectual disability syndrome	syndromic_disease	other	syndromic_disease	hematology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|anemia	brain_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0850064	inherited hematologic cancer-predisposing syndrome	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	hematology|genetics_and_genomics|oncology	inherited_hematologic_cancer_predisposing_syndrome_is_also_related_to_anemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0850065	neonatal-onset severe multisystemic autoinflammatory disease with increased IL18	connective_tissue_disorder|syndromic_disease	other	connective_tissue_disorder|syndromic_disease	rheumatology|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	liver_disorder|immune_disorder|joint_disorder|kidney_disorder|vascular_disorder	false	false	false	true	very_high
MONDO:0850066	SAMD9L-associated autoinflammatory syndrome	connective_tissue_disorder|syndromic_disease	other	connective_tissue_disorder|syndromic_disease	genetics_and_genomics|rheumatology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|joint_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0850067	immune deficiency due to impaired neutrophil phagocytosis and migration	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	immunology|allergy_and_immunology|pediatric	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	true	false	false	true	high
MONDO:0850068	early-onset autoimmunity-autoinflammation-immunodeficiency syndrome	immune_system_disorder	other	immune_system_disorder	immunology|rheumatology|pediatric	autoimmune_diseases|immunodeficiency|inflammatory_disease	autoimmune_disorder|immune_disorder|autoinflammation_immunodeficiency_disorder_is_a_type_of_immune_disorder__but_since_it_was_not_an_option_i_will_leave_that_out_and_choose_the_closest_one__which_would_be_immune_disorder__however__the_more_specific_category_for_this_disease_would_be	false	false	false	true	high
MONDO:0850069	familial hyperinflammatory lymphoproliferative immunodeficiency	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	genetics_and_genomics|allergy_and_immunology|rheumatology|immunodeficiency	autoimmune_diseases|inflammatory_disease	immune_disorder_lymphatic_disorder	false	false	false	false	very_high
MONDO:0850070	CADINS disease	immune_system_disorder	other	immune_system_disorder	genetics_and_genomics|cardiology|pediatric	cardiovascular_disorder|adrenal_gland_disease	heart_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0850071	developmental delay-immunodeficiency-leukoencephalopathy-hypohomocysteinemia syndrome	syndromic_disease	other	syndromic_disease	immunology|genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	immune_disorder_brain_disorder	false	false	false	false	high
MONDO:0850072	non-syndromic unisutural craniosynostosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	neurological_disease|developmental_disorder|skeletal_dysplasia	teeth_disorder|spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0850073	non-syndromic unicoronal craniosynostosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	bone_disease|developmental_disorder|genetic_condition|neurodegenerative_disease	craniosynostosis|bone_disorder|spine_disorder	false	false	false	false	medium
MONDO:0850074	non-syndromic unilambdoid craniosynostosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|bone_disorder|skull_disorder	false	false	false	false	medium
MONDO:0850075	non-syndromic unifrontosphenoidal craniosynostosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	developmental_disorder|skeletal_abnormality|cranial_abnormality	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0850076	non-syndromic unisquamosal craniosynostosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|neurology|otolaryngology|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	bone_disorder|skull_disorder	false	false	false	false	medium
MONDO:0850077	non-syndromic multisutural craniosynostosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|neurology|otolaryngology|pediatric	neurological_disorder|developmental_disorder	brain_disorder|bone_disorder|skull_disorder	false	false	false	false	medium
MONDO:0850078	non-syndromic non-specific multisutural craniosynostosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|neurology|pediatric	craniosynostosis_is_associated_with_many_conditions_including__neurodevelopmental_disorders_however__the_closest_match_from_the_provided_list_is__inflammatory_disease|neurological_disorder_is_not_in_the_list_but_one_category_is__inflammatory_disease|metabolic_disorder	spinal_disorder|craniosynostosis____revised_list_without_skull_disorder_as_it_is_a_subset_of_bone_disorder____bone_disorder|bone_disorder|skull_disorder	false	false	false	false	medium
MONDO:0850079	non-syndromic bilambdoid craniosynostosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatric	metabolic_disorder|developmental_disorder|craniofacial_disorder	bone_disorder|skull_disorder	false	false	false	false	medium
MONDO:0850080	non-syndromic unicoronal and sagittal craniosynostosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	neurology|pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	brain_disorder|bone_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0850081	non-syndromic metopic and sagittal craniosynostosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	neurology|pediatric|genetics_and_genomics	bone_developmental_disease|neurodegenerative_disease|craniosynostosis|skeletal_disorder	brain_disorder|bone_disorder|spinal_disorder|craniosynostosis_is_related_to_bone_development_so_it_is_likely_that_some_other_category_would_be_better_suited__however__this_list_does_not_have_a_more_specific_option_for_cranium_bone_abnormalities_beyond__bone_disorder	false	false	false	false	medium
MONDO:0850082	non-syndromic bicoronal and metopic craniosynostosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	neurology|pediatric|genetics_and_genomics|orthopaedic	congenital_abnormality|craniofacial_anomaly|neurodegenerative_disease	bone_disorder|spinal_disorder|teeth_disorder	false	false	false	false	medium
MONDO:0850083	non-syndromic bicoronal and sagittal craniosynostosis	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	neurology|pediatric|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	brain_disorder|bone_disorder|spinal_disorder	false	false	false	true	medium
MONDO:0850084	non-syndromic pansynostosis	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	medium
MONDO:0850087	primary hypomagnesemia-generalized seizures-intellectual disability-obesity syndrome	syndromic_disease	other	syndromic_disease	endocrinology|neurology|genetics_and_genomics|pediatrics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|kidney_disorder|endocrine_disorder	true	false	false	false	high
MONDO:0850088	EGF-related primary hypomagnesemia with intellectual disability	metabolic_disease|hereditary_disease|urinary_system_disorder	metabolic_disease	hereditary_disease|urinary_system_disorder|metabolic_disease	neurology|genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0850089	Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	renal_medicine|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0850092	post-cardiac arrest syndrome	syndromic_disease	other	syndromic_disease	cardiothoracic|neurology|cardiology	cardiovascular_disorder|cardiac_arrest_syndrome	brain_disorder|heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0850094	drug-induced hearing loss	psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|psychiatric_disorder	neurology|otolaryngology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	ear_disorder	false	false	false	false	medium
MONDO:0850095	X-linked severe syndromic thoracic aortic aneurysm and dissection	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0850096	SBDS-related severe neonatal spondylometaphyseal dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	anemia|metabolic_disorder	bone_disorder|spinal_disorder	false	false	false	false	high
MONDO:0850097	autoimmune limbic encephalitis	immune_system_disorder|nervous_system_disorder|inflammatory_disease	autoimmune_disease	immune_system_disorder|inflammatory_disease|nervous_system_disorder|acute_disease	neurology|immunology|psychiatry	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|immune_disorder	false	false	false	true	high
MONDO:0850098	oligoasthenoteratozoospermia	reproductive_system_disorder	other	reproductive_system_disorder	urology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	muscle_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0850099	MIR140-related spondyloepiphyseal dysplasia	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0850100	body integrity dysphoria	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	muscle_disorder|skin_disorder	false	false	false	false	high
MONDO:0850101	spitzoid melanoma	cancer_or_benign_tumor|integumentary_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	oncology|dermatology	cancer	skin_disorder|lymphatic_disorder	false	true	false	false	medium
MONDO:0850102	non-specific autoimmune supratentorial encephalitis with characteristic antibodies	immune_system_disorder	autoimmune_disease	immune_system_disorder	rheumatology|immunology|allergy_and_immunology|neurology	inflammatory_disease|autoimmune_diseases	immune_disorder|brain_disorder	true	false	false	true	high
MONDO:0850103	non-specific autoimmune supratentorial encephalitis without characteristic antibodies	immune_system_disorder	autoimmune_disease	immune_system_disorder	rheumatology|allergy_and_immunology|neurology	inflammatory_disease|autoimmune_diseases	immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0850104	paraneoplastic isolated brainstem encephalitis	inflammatory_disease|nervous_system_disorder	other	nervous_system_disorder|acute_disease|inflammatory_disease	oncology|neurology	cancer|autoimmune_diseases	immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0850105	non-specific autoimmune brainstem encephalitis with characteristic antibodies	immune_system_disorder	autoimmune_disease	immune_system_disorder	immunology|allergy_and_immunology|neurology	inflammatory_disease|autoimmune_diseases	immune_disorder|brain_disorder	true	false	false	true	high
MONDO:0850106	non-specific autoimmune brainstem encephalitis without characteristic antibodies	immune_system_disorder	autoimmune_disease	immune_system_disorder	immunology|allergy_and_immunology|neurology	inflammatory_disease|autoimmune_diseases	immune_disorder|brain_disorder	false	false	false	true	high
MONDO:0850107	postinfectious cerebellitis	nervous_system_disorder|infectious_disease	infectious_disease	infectious_disease|nervous_system_disorder	pediatric|neurology	inflammatory_disease|autoimmune_diseases	immune_disorder|brain_disorder	true	false	false	false	high
MONDO:0850108	non-specific autoimmune cerebellar ataxia with characteristic antibodies	immune_system_disorder	autoimmune_disease	immune_system_disorder	genetics_and_genomics|immunology|allergy_and_immunology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	immune_disorder|brain_disorder	false	false	false	true	high
MONDO:0850109	non-specific autoimmune cerebellar ataxia without characteristic antibodies	immune_system_disorder	autoimmune_disease	immune_system_disorder	genetics_and_genomics|immunology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	immune_disorder|brain_disorder	false	false	false	false	high
MONDO:0850110	melanoma in congenital melanocytic nevus	cancer_or_benign_tumor|integumentary_system_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	integumentary_system_disorder|cancer_or_benign_tumor|disorder_of_development_or_morphogenesis	oncology|dermatology|pediatric|genetics_and_genomics	cancer|congenital_melanocytic_nevus_is_a_type_of_cancer	immune_disorder|skin_disorder	true	true	false	true	high
MONDO:0850112	breast implant-associated anaplastic large cell lymphoma	cancer_or_benign_tumor|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	cancer|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0850115	early-onset obesity-hyperphagia-severe developmental delay syndrome	syndromic_disease	other	syndromic_disease	pediatric|endocrinology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	developmental_delay_syndrome|endocrine_disorder	false	false	false	false	very_high
MONDO:0850122	solid adenocarcinoma with mucin production	cancer_or_benign_tumor|respiratory_system_disorder	cancer_or_benign_tumor	respiratory_system_disorder|cancer_or_benign_tumor	pathology|oncology|gastroenterology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0850123	autonomic nervous system benign neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	cancer|adrenal_gland_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0850125	malignant adenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology|gastroenterology	cancer|adrenal_gland_disease	liver_disorder|upper_gastrointestinal_disorder	false	true	false	false	medium
MONDO:0850126	testicular sex cord-stromal benign neoplasm	cancer_or_benign_tumor|endocrine_system_disorder|reproductive_system_disorder	cancer_or_benign_tumor|endocrine_system_disorder	reproductive_system_disorder|cancer_or_benign_tumor|endocrine_system_disorder	urology|oncology	neoplasm|cancer|tumor	reproductive_system_disorder|endocrine_disorder	false	false	false	false	low
MONDO:0850127	epithelioid inflammatory myofibroblastic sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|hematology|oncology	inflammatory_disease|cancer|sarcoma	muscle_disorder|sarcoma	false	true	false	false	high
MONDO:0850128	epididymis disease	reproductive_system_disorder	other	reproductive_system_disorder	urology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	urinary_tract_disorder|reproductive_system_disorder	true	false	false	true	medium
MONDO:0850129	gastroesophageal cancer	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	cancer|adrenal_gland_disease|gastrointestinal_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0850130	gastroesophageal adenocarcinoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|gastroenterology	autoimmune_diseases|inflammatory_disease|cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	true	very_high
MONDO:0850144	germ cell benign neoplasm	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|obstetrics_and_gynecology	germ_cell_disease|cancer|benign_neoplasm	reproductive_system_disorder	false	false	false	false	low
MONDO:0850149	nephroma	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	urology|oncology|renal_medicine	adrenal_gland_disease|cancer	urinary_tract_disorder|kidney_disorder	false	true	false	false	high
MONDO:0850150	kidney cortex disease	urinary_system_disorder	other	urinary_system_disorder	urology|renal_medicine	metabolic_disorder|kidney_cortex_disease_is_often_related_to_metabolic_disorders_such_as_diabetic_nephropathy	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0850151	lymph node carcinoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology	lymphoma|cancer	immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0850152	auditory system benign neoplasm	nervous_system_disorder|auditory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor|auditory_system_disorder	neurology|otolaryngology	neurological_cancer|cancer	throat_disorder|ear_disorder|head_disorder	false	false	false	false	medium
MONDO:0850154	tongue carcinoma	nervous_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|nervous_system_disorder|mouth_disorder|cancer_or_benign_tumor	oncology|otolaryngology	cancer|adrenal_gland_disease	lower_gastrointestinal_disorder|throat_disorder	false	true	false	true	high
MONDO:0850156	B-lymphoblastic leukemia/lymphoma MLL rearranged	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	acute_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|genetics_and_genomics|oncology	leukemia|lymphoma|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0850157	B-lymphoblastic leukemia/lymphoma with ETV6-RUNX1	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	acute_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology|pediatric	leukemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0850160	B-lymphoblastic leukemia/lymphoma with IL3-IGH	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	acute_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology	lymphoma|cancer	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0850161	B-lymphoblastic leukemia/lymphoma, BCR-ABL1–like	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	acute_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology|genetics_and_genomics	leukemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0850162	B-lymphoblastic leukemia/lymphoma with IAMP21	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	acute_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	hematology|oncology|pediatric	leukemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0850170	spinal muscular atrophy type 0	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0850196	medulloblastoma WNT activated	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|oncology|pediatric	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0850197	medulloblastoma SHH activated	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|oncology|neurology	neurological_cancer|cancer	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0850198	medulloblastoma non-WNT/non-SHH	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|pediatric|neurology	cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0850199	NK cell deficiency	immune_system_disorder	other	immune_system_disorder	hematology|pediatrics|immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0850200	T cell and NK cell immunodeficiency	immune_system_disorder	other	immune_system_disorder	pediatric|immunology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder_lymphatic_disorder	false	false	false	true	high
MONDO:0850201	hereditary alpha tryptasemia syndrome	syndromic_disease	other	syndromic_disease	pediatric|hematology|genetics_and_genomics	metabolic_disorder|anemia	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0850223	Libman-Sacks endocarditis	cardiovascular_disorder|inflammatory_disease|immune_system_disorder	cardiovascular_disorder|autoimmune_disease	cardiovascular_disorder|immune_system_disorder|inflammatory_disease	rheumatology|cardiology|hematatology	cardiovascular_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|heart_disorder	false	false	false	false	high
MONDO:0850225	autoimmune cholangitis	inflammatory_disease|immune_system_disorder|endocrine_system_disorder|digestive_system_disorder	autoimmune_disease|endocrine_system_disorder	endocrine_system_disorder|digestive_system_disorder|immune_system_disorder|inflammatory_disease	gastroenterology|rheumatology|hepatology	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder	false	false	false	true	high
MONDO:0850230	chronic urticaria	inflammatory_disease|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease	dermatology|allergy_and_immunology	allergy|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	high
MONDO:0850231	erythema nodosum	inflammatory_disease|connective_tissue_disorder|integumentary_system_disorder	other	integumentary_system_disorder|connective_tissue_disorder|inflammatory_disease	rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0850257	mucinous pancreas adenocarcinoma	endocrine_system_disorder|digestive_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor	endocrine_system_disorder|cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology	adrenal_gland_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	true	false	false	very_high
MONDO:0850267	childhood acute megakaryoblastic leukemia	cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|immune_system_disorder|hematologic_disorder|acute_disease	pediatric|hematology|oncology	cancer|anemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0850269	core binding factor acute myeloid leukemia	cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|immune_system_disorder|hematologic_disorder|acute_disease	hematology|oncology	cancer|anemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder|upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	true	false	true	high
MONDO:0850271	myeloid leukemia associated with down syndrome	cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|immune_system_disorder|acute_disease|hematologic_disorder	pediatric|hematology|oncology|genetics_and_genomics	cancer|autoimmune_diseases|anemia	lymphatic_disorder|blood_bone_marrow_disorder	true	true	false	true	high
MONDO:0850273	salivary gland mucinous adenocarcinoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	otolaryngology|oncology	gland_disease|cancer|adenocarcinoma	throat_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0850281	mammary analog secretory carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|mouth_disorder|digestive_system_disorder	oncology|obstetrics_and_gynecology	cancer|adrenal_gland_disease	breast_disorder|reproductive_system_disorder	false	true	false	false	high
MONDO:0850282	chronic asthma	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|allergy_and_immunology|pediatric	allergy|autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder|throat_disorder	false	false	false	true	high
MONDO:0850283	acute asthma	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	allergy|autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder|throat_disorder	false	false	false	true	high
MONDO:0850284	extrinsic asthma	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|allergy_and_immunology	allergy|autoimmune_diseases|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	true	medium
MONDO:0850285	environmental induced asthma	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	allergy|inflammatory_disease	lung_disorder|immune_disorder	false	false	false	true	high
MONDO:0850286	exercise-induced bronchoconstriction	respiratory_system_disorder	other	respiratory_system_disorder	cardiothoracic|pulmonology	allergy|autoimmune_diseases|inflammatory_disease	lung_disorder|upper_gastrointestinal_disorder	false	false	false	true	medium
MONDO:0850287	aspirin-induced respiratory disease	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|allergy_and_immunology	allergy|inflammatory_disease	lung_disorder|respiratory_disease|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0850289	human betaherpesvirus 5 infectious disease	infectious_disease	infectious_disease	infectious_disease	immunology|hematology|oncology|pediatric	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder|vascular_disorder	true	false	false	false	medium
MONDO:0850292	subjective cognitive decline	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|mental_disorder|neurological_disorder	false	false	false	false	medium
MONDO:0850295	acquired laryngomalacia	respiratory_system_disorder	other	respiratory_system_disorder	otolaryngology|pediatric	autoimmune_diseases|inflammatory_disease	throat_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0850301	pemphigoid	immune_system_disorder|inflammatory_disease|integumentary_system_disorder	autoimmune_disease	integumentary_system_disorder|immune_system_disorder|inflammatory_disease	dermatology|immunology	inflammatory_disease|autoimmune_diseases	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0850302	intracranial meningioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0850303	supratentorial meningioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0850306	latent autoimmune diabetes in adults	digestive_system_disorder|endocrine_system_disorder|metabolic_disease|immune_system_disorder	diabetes_mellitus|autoimmune_disease|metabolic_disease|endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|metabolic_disease|immune_system_disorder	endocrinology|immunology	autoimmune_diseases|metabolic_disorder	immune_disorder|endocrine_disorder	false	false	true	true	medium
MONDO:0850312	anaplastic pleomorphic xanthoastrocytoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	adrenal_gland_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0850332	IDH-mutant anaplastic astrocytoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|neurological_cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0850333	IDH-wildtype anaplastic astrocytoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|genetics_and_genomics|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0850335	IDH-wildtype glioblastoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|brain_cancer|glioma	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0850338	spinal ependymoma, MYCN-amplified	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|genetics_and_genomics|pediatric|neurology	cancer|neurological_cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0850339	posterior fossa ependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|autoimmune_diseases|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0850340	supratentorial ependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer|brain_cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0850345	lung pleomorphic carcinoma	respiratory_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|respiratory_system_disorder	oncology|cardiothoracic|pulmonology	cancer|lung_cancer|carcinoma	lung_disorder	false	true	false	false	high
MONDO:0850346	oral rhabdomyosarcoma	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor|mouth_disorder	oncology|pediatric	cancer	teeth_disorder|muscle_disorder	false	true	false	true	very_high
MONDO:0850347	bladder sarcomatoid transitional cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	cancer|sarcomatoid_carcinoma|bladder_cancer|transitional_cell_carcinoma	kidney_disorder|urinary_tract_disorder	false	true	false	false	high
MONDO:0850348	bladder small cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	cancer|urogenital_system_disease|bladder_cancer|cancer____corrected_list_to_remove_non_standard_categorizations___cancer|adrenal_gland_disease|urologic_disorder|urinary_system_disease	kidney_disorder|urinary_tract_disorder|lung_disorder	false	true	false	false	high
MONDO:0850349	astroblastoma, MN1-altered	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|genetics_and_genomics|neurology	cancer|neurodegenerative_disease	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0850353	castration-resistant prostate carcinoma	cancer_or_benign_tumor|reproductive_system_disorder	cancer_or_benign_tumor	reproductive_system_disorder|cancer_or_benign_tumor	urology|oncology	cancer|other____corrected_to___cancer|adrenal_gland_disease	urinary_tract_disorder|reproductive_system_disorder	false	true	false	true	very_high
MONDO:0850368	immunoglobulin heavy-and-light chain	metabolic_disease	metabolic_disease	metabolic_disease	hematology|allergy_and_immunology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0850371	nonobstructive coronary artery disease	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	rheumatology|cardiothoracic|pulmonology|cardiology|renal_medicine	cardiovascular_disorder|metabolic_disorder	vascular_disorder|heart_disorder	false	false	false	true	low
MONDO:0850388	childhood supratentorial embryonal tumor with multilayered rosettes, C19MC-altered	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|genetics_and_genomics|pediatric|neurology	cancer|neurodegenerative_disease	immune_disorder|brain_disorder|lymphatic_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0850415	rhabdomyolysis-myalgia syndrome	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	rheumatology|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	kidney_disorder|muscle_disorder	false	false	false	false	high
MONDO:0850416	autoimmune epilepsy	nervous_system_disorder|immune_system_disorder	autoimmune_disease	nervous_system_disorder|immune_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	brain_disorder|immune_disorder	false	false	false	true	high
MONDO:0850417	tuberculous encephalopathy	infectious_disease	infectious_disease	infectious_disease	pulmonology|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|immune_disorder|lung_disorder	true	false	false	true	very_high
MONDO:0850418	diffuse large B-cell lymphoma activated B-cell type	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	high
MONDO:0850419	diffuse large B-cell lymphoma germinal center B-cell type	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	true	false	true	high
MONDO:0850420	acute necrotizing pancreatitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|inflammatory_disease|acute_disease	hepatology|gastroenterology	inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0850421	acute hemorrhagic pancreatitis	inflammatory_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder|inflammatory_disease|acute_disease	hepatology|hematology|gastroenterology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0850426	high-grade B-cell lymphoma double-hit/triple-hit	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	true	true	false	true	very_high
MONDO:0850445	benign peritoneal solitary fibrous tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	gastroenterology|oncology|general_surgery	cancer	abdominal_disorder____corrected_answer__lower_gastrointestinal_disorder|lower_gastrointestinal_disorder	false	false	false	true	low
MONDO:0850449	mixed phenotype acute leukemia with BCR-ABL1	hematologic_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder	cancer_or_benign_tumor	acute_disease|connective_tissue_disorder|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|leukemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0850450	mixed phenotype acute leukemia with MLL rearranged	cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|acute_disease|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|genetics_and_genomics|oncology	cancer|leukemia	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0850451	mixed phenotype acute leukemia, B/myeloid	cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|acute_disease|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|genetics_and_genomics|oncology	cancer|leukemia|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder	true	true	false	true	very_high
MONDO:0850452	mixed phenotype acute leukemia,T/myeloid	cancer_or_benign_tumor|hematologic_disorder|musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder	cancer_or_benign_tumor	connective_tissue_disorder|acute_disease|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|mixed_phenotype_acute_leukemia_t_myeloid_is_a_type_of_cancer	immune_disorder|blood_bone_marrow_disorder	true	true	false	true	very_high
MONDO:0850459	primary cutaneous gamma-delta t-cell lymphoma	cancer_or_benign_tumor|hematologic_disorder|integumentary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder|integumentary_system_disorder	hematology|dermatology|oncology	cancer|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0850461	neurobehavioral disorder with prenatal alcohol exposure	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|neurology|pediatric	neurodegenerative_disease|mental_health_disorder	neurobehavioral_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0850468	BN2 diffuse large B-cell lymphoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0850469	EZB diffuse large B-cell lymphoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder	true	true	false	true	high
MONDO:0850470	MCD diffuse large B-cell lymphoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	very_high
MONDO:0850471	N1 diffuse large B-cell lymphoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0850472	ST2 diffuse large B-cell lymphoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0850473	A53 diffuse large B-cell lymphoma	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	hematology|oncology	cancer|autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0850492	acute myeloid leukemia, t(8;21)(q22; q22.1)	cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|immune_system_disorder	cancer_or_benign_tumor	acute_disease|immune_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder	hematology|oncology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0850495	acute myeloid leukemia, t(1;22)(p13;q13)	cancer_or_benign_tumor|hematologic_disorder|connective_tissue_disorder|musculoskeletal_system_disorder|immune_system_disorder	cancer_or_benign_tumor	acute_disease|immune_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|hematologic_disorder	hematology|oncology	cancer|anemia	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0850514	inclusion body myopathy and brain white matter abnormalities	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder|syndromic_disease|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	nervous_system_disorder|musculoskeletal_system_disorder|syndromic_disease|psychiatric_disorder|hereditary_disease	neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0850519	tetrahydrobiopterin (BH4)-deficient hyperphenylalaninemia	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	neurology|genetics_and_genomics|hematology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|kidney_disorder|muscle_disorder	false	false	false	true	high
MONDO:0850618	injection anthrax	infectious_disease	infectious_disease	infectious_disease	allergy_and_immunology|dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0850812	dendritic cell deficiency	immune_system_disorder	other	immune_system_disorder	allergy_and_immunology|immunology|hematology	inflammatory_disease|autoimmune_diseases	immune_disorder_lymphatic_disorder	false	false	false	false	high
MONDO:0851095	KINSSHIP syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0851100	malignant olfactory nerve neoplasm	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|otolaryngology|neurology	cancer|neurodegenerative_disease	nose_disorder|brain_disorder	false	true	false	false	high
MONDO:0851102	pulmonary artery disease	cardiovascular_disorder|respiratory_system_disorder	cardiovascular_disorder	cardiovascular_disorder|respiratory_system_disorder	cardiothoracic|pulmonology|cardiology	cardiovascular_disorder|autoimmune_diseases|inflammatory_disease	lung_disorder|vascular_disorder	false	false	false	true	high
MONDO:0851103	Bartholin's gland disease	reproductive_system_disorder	other	reproductive_system_disorder	urology|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	urinary_tract_disorder|reproductive_system_disorder	false	false	false	true	low
MONDO:0851105	cerebrovascular benign neoplasm	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	oncology|neurology	cancer|neurological_disease|cerebrovascular_disorder	vascular_disorder|brain_disorder	false	false	false	false	medium
MONDO:0858910	dropped head syndrome	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	pediatric|neurology	neurodegenerative_disease|mental_health_disorder	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0858916	pituitary blastoma	cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder|endocrine_system_disorder|reproductive_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	musculoskeletal_system_disorder|nervous_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder|connective_tissue_disorder	oncology|neurology	adrenal_gland_disease|cancer|neurodegenerative_disease	brain_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0858917	cauda equina neuroendocrine tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neuroendocrine_tumor|cancer	spinal_disorder|endocrine_disorder	false	true	false	false	medium
MONDO:0858921	EWSR1-negative small round cell tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology|genetics_and_genomics	adrenal_gland_disease|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0858926	developmental delay, hypotrophy, and dysmorphic features without moebius syndrome	syndromic_disease	other	syndromic_disease	pediatric|endocrinology|genetics_and_genomics	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	hypotrophy|developmental_delay|brain_disorder|dysmorphic_features_without_moebius_syndrome|endocrine_disorder	false	false	false	false	high
MONDO:0858939	diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology|genetics_and_genomics	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0858940	infant-type hemispheric glioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pediatric|oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0858944	myxoid glioneuronal tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	muscle_disorder|brain_disorder|spinal_disorder	false	true	false	false	medium
MONDO:0858950	traumatic brain injury	nervous_system_disorder|injury	other	nervous_system_disorder	pediatric|psychiatry|neurology	mental_health_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0858956	diffuse leptomeningeal glioneuronal tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0858957	multinodular and vacuolating neuronal tumor	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	autoimmune_diseases|neurodegenerative_disease|cancer|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0858958	high-grade astrocytoma with piloid features	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurooncology|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0858959	polymorphous low grade neuroepithelial tumor of the young	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pediatric|oncology|neurology	neuroepithelial_tumor|cancer	brain_disorder|neuroepithelial_tumor	false	false	false	false	medium
MONDO:0858960	spindle cell oncocytoma	connective_tissue_disorder|musculoskeletal_system_disorder|endocrine_system_disorder|cancer_or_benign_tumor|reproductive_system_disorder|nervous_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	nervous_system_disorder|reproductive_system_disorder|connective_tissue_disorder|endocrine_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	pathology|orthopaedic|oncology|neurology	adrenal_gland_disease|cancer	skin_disorder|muscle_disorder	false	true	false	false	medium
MONDO:0858966	central nervous system tumor with bcor internal tandem duplication	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0858967	primary intracranial sarcoma, DICER1-mutant	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	pediatric|oncology|neurology|genetics_and_genomics	primary_intracranial_sarcoma|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0858974	breast implant illness	breast_disorder|syndromic_disease	other	syndromic_disease|breast_disorder	plastic_surgery|rheumatology|obstetrics_and_gynecology	inflammatory_disease|autoimmune_diseases	vascular_disorder|reproductive_system_disorder|immune_disorder	false	false	false	false	high
MONDO:0858997	cancer of unknown primary site	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|hematology	adrenal_gland_disease|cancer	lymphatic_disorder	false	true	false	true	medium
MONDO:0858998	mesomelic dysplasia-digital anomalies-intellectual disability syndrome	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	intellectual_disability_is_related_to_brain_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0858999	KDM3B-related intellectual disability-facial dysmorphism-short stature syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|psychiatry|neurology|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	short_stature|brain_disorder|intellectual_disability	false	false	false	false	high
MONDO:0859000	SLC12A2-related developmental delay-intellectual disability-sensorineural deafness syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0859002	intellectual disability-early-onset cataract-microcephaly syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0859003	PAICS deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	metabolism|pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|neurodegenerative_disease	metabolic_disorder|liver_disorder	false	false	false	false	high
MONDO:0859004	invasive scopulariopsis infection	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric|otolaryngology	inflammatory_disease|autoimmune_diseases|cancer	lung_disorder|liver_disorder	true	false	false	false	high
MONDO:0859005	preaxial digit brachydactyly-webbed fingers	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	skeletal_dysplasia|congenital_condition|metabolic_disorder|digit_anomaly|genetic_disorder|limb_abnormality|hand_anomaly|developmental_disorder|polydactyly|birth_defect	joint_disorder|bone_disorder	false	false	false	false	low
MONDO:0859006	proximal femoral focal deficiency	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	bone_disorder|vascular_disorder	false	false	false	false	high
MONDO:0859007	mosaic Legius syndrome	integumentary_system_disorder	other	integumentary_system_disorder	oncology|pediatric|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease|cancer	skin_disorder|immune_disorder	false	false	false	false	medium
MONDO:0859008	neurofibromatosis/schwannomatosis	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	neurology|oncology|genetics_and_genomics	neurodegenerative_disease|cancer	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0859046	rhabdomyosarcoma, embryonal, 2	hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|oncology|pediatric	cancer|adrenal_gland_disease	soft_tissue_disorder|muscle_disorder|cancer_disorder	false	true	false	true	very_high
MONDO:0859080	intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies	hereditary_disease|nervous_system_disorder|syndromic_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|syndromic_disease|nervous_system_disorder|psychiatric_disorder	psychiatry|neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	intellectual_developmental_disorder|brain_disorder	false	false	false	true	high
MONDO:0859081	chromosome Xq13 duplication syndrome	chromosomal_disorder	other	chromosomal_disorder	pediatric|neurology|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	vascular_disorder|kidney_disorder|joint_disorder|immune_disorder|brain_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0859082	thrombophilia, X-linked, due to factor 8 defect	hereditary_disease|hematologic_disorder	other	hereditary_disease|hematologic_disorder	hematology|genetics_and_genomics	cardiovascular_disorder|blood_disorder|metabolic_disorder	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0859083	systemic lupus erythematosus 17	hereditary_disease|connective_tissue_disorder|immune_system_disorder	autoimmune_disease	hereditary_disease|immune_system_disorder|connective_tissue_disorder	rheumatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	immune_disorder_skin_disorder_joint_disorder_kidney_disorder	false	false	false	true	high
MONDO:0859085	neurodevelopmental disorder with gait disturbance, dysmorphic facies, and behavioral abnormalities, X-linked	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	mental_health_disorder|neurodegenerative_disease|autoimmune_diseases	joint_disorder|neurodevelopmental_disorder|muscle_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0859086	intellectual developmental disorder, X-linked 110	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	immune_disorder|reproductive_system_disorder|brain_disorder	false	false	false	true	high
MONDO:0859136	Alzahrani-Kuwahara syndrome	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	bone_disorder|lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	none
MONDO:0859137	neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0859139	blepharophimosis-impaired intellectual development syndrome	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0859141	neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	neurodevelopmental_disorder|brain_disorder|cerebellar_hypoplasia_is_a_brain_disorder_so_also_included__spinal_disorder	false	false	false	true	high
MONDO:0859142	Hiatt-Neu-Cooper neurodevelopmental syndrome	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	as_of_my_last_knowledge_update_in_october_2023__there_are_no_known_efficacious_treatments_that_cure__prevent__or_specifically_treat_hiatt_neu_cooper_neurodevelopmental_syndrome__this_syndrome_is_a_rare_genetic_disorder__and_management_typically_focuses_on_supportive_care_and_addressing_specific_symptoms_or_complications_associated_with_the_condition___therefore__the_answer_is_false	high
MONDO:0859143	Radio-Tartaglia syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	ear_disorder|throat_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0859144	Buratti-Harel syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|allergy_and_immunology|dermatology|endocrinology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0859146	growth restriction, hypoplastic kidneys, alopecia, and distinctive facies	hereditary_disease	other	hereditary_disease	pediatric|renal_medicine|genetics_and_genomics|endocrinology	metabolic_disorder|hypoplastic_kidneys_is_related_to_adrenal_gland_disease__and_distinctive_facies_could_be_a_side_effect_of_an_autoimmune_disease__however_the_primary_match_for_this_set_of_symptoms_would_likely_be____metabolic_disorder|autoimmune_diseases|adrenal_gland_disease	endocrine_disorder|kidney_disorder|growth_restriction|distinct_facies|alopecia	true	false	false	based_on_the_symptoms_you_ve_described_growth_restriction__hypoplastic_kidneys__alopecia__and_distinctive_facies_it_appears_you_may_be_referring_to_a_specific_genetic_disorder_or_syndrome__however__without_knowing_the_exact_disease_you_re_referencing__it_s_challenging_to_provide_a_definitive_answer_regarding_the_existence_of_efficacious_treatments___in_many_genetic_syndromes_that_involve_multiple_systemic_manifestations__treatments_may_be_limited_to_managing_symptoms_rather_than_providing_a_cure__for_instance__specific_therapies_may_be_available_to_manage_kidney_function_or_growth_issues__but_there_may_not_be_a_definitive_cure___if_you_are_referring_to_a_specific_known_condition__please_clarify__and_i_can_provide_more_detailed_information_on_available_treatments___in_general_terms__based_on_these_criteria__i_would_return___false	medium
MONDO:0859147	Marbach-Rustad progeroid syndrome	premature_aging_syndrome|disorder_of_development_or_morphogenesis|hereditary_disease	other	premature_aging_syndrome|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|dermatology	metabolic_disorder|neurodegenerative_disease	liver_disorder|vascular_disorder	false	false	false	false	high
MONDO:0859148	neurodevelopmental disorder with seizures and gingival overgrowth	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	teeth_disorder|brain_disorder	true	false	false	true	high
MONDO:0859149	hypertriglyceridemia 2	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	gastroenterology|cardiology|endocrinology	metabolic_disorder|cardiovascular_disorder|adrenal_gland_disease	liver_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0859150	BDV syndrome	reproductive_system_disorder|endocrine_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	endocrine_system_disorder	nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	psychiatry|neurology	neurodegenerative_disease|autoimmune_diseases|mental_health_disorder	brain_disorder|vascular_disorder|lymphatic_disorder|immune_disorder	true	false	false	false	high
MONDO:0859151	fibromuscular dysplasia, multifocal	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	renal_medicine|orthopaedic|cardiothoracic	cardiovascular_disorder	vascular_disorder|muscle_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0859152	neurodevelopmental disorder with cerebellar atrophy and motor dysfunction	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0859154	Bartsocas-Papas syndrome 2	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|allergy_and_immunology|endocrinology|neurology	metabolic_disorder|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0859155	chromosome 1p36 deletion syndrome, proximal	chromosomal_disorder	other	chromosomal_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	musculoskeletal_disorder_is_not_in_the_list_but_joint_disorder_and_muscle_disorder_could_be_a_fit_for_some_symptoms|brain_disorder|kidney_disorder	false	false	false	true	very_high
MONDO:0859156	dysostosis multiplex, Ain-Naz type	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	pediatric|orthopaedic|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0859157	visceral myopathy 2	digestive_system_disorder|hereditary_disease	other	digestive_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	visceral_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859158	ataxia, intention tremor, and hypotonia syndrome, childhood-onset	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	true	false	false	false	high
MONDO:0859159	deafness, cataract, impaired intellectual development, and polyneuropathy	hereditary_disease	other	hereditary_disease	ophthalmology|otolaryngology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	ear_disorder|eye_disorder|brain_disorder	true	false	false	false	medium
MONDO:0859160	mitochondrial complex IV deficiency, nuclear type 22	metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|hereditary_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|pediatrics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859161	onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|bone_disorder|skin_disorder	false	false	false	false	high
MONDO:0859162	neurodevelopmental disorder with infantile epileptic spasms	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|neurodevelopmental_disorder	false	false	false	true	very_high
MONDO:0859163	Faundes-Banka syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	bone_disorder|lymphatic_disorder|immune_disorder	false	false	false	false	none
MONDO:0859164	osteootohepatoenteric syndrome	hereditary_disease	other	hereditary_disease	hepatology|gastroenterology|pediatric|genetics_and_genomics	inflammatory_disease|metabolic_disorder|autoimmune_diseases	bone_disorder|upper_gastrointestinal_disorder|liver_disorder	true	false	false	false	very_high
MONDO:0859165	neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	brain_abnormalities|neurodegenerative_disease|metabolic_disorder|neurodevelopmental_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859166	visceral leiomyopathy, African degenerative	digestive_system_disorder	other	digestive_system_disorder	oncology|gastroenterology|genetics_and_genomics|obstetrics_and_gynecology	neurodegenerative_disease|cancer	kidney_disorder|muscle_disorder|lower_gastrointestinal_disorder|vascular_disorder|liver_disorder	false	false	false	false	high
MONDO:0859167	hypokalemic tubulopathy and deafness	hereditary_disease	other	hereditary_disease	genetics_and_genomics|otolaryngology|renal_medicine|neurology	metabolic_disorder|adrenal_gland_disease	ear_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0859168	myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|cardiology|neurology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0859169	White-Kernohan syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0859170	retinal dystrophy and microvillus inclusion disease	hereditary_disease	other	hereditary_disease	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0859171	Luo-Schoch-Yamamoto syndrome	hereditary_disease	other	hereditary_disease	cardiothoracic|pulmonology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	vascular_disorder|liver_disorder	false	false	false	false	high
MONDO:0859172	hemolytic disease of fetus and newborn, RH-induced	hereditary_disease|hematologic_disorder	anemia	hereditary_disease|hematologic_disorder	pediatric|obstetrics_and_gynecology|hematology	anemia|autoimmune_diseases	vascular_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0859173	sick sinus syndrome 4	cardiovascular_disorder|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	cardiovascular_disorder	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiothoracic|pulmonology|cardiology	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:0859174	Usmani-Riazuddin syndrome, autosomal dominant	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatrics	neurodegenerative_disease|metabolic_disorder	brain_disorder|vascular_disorder|eye_disorder	false	false	false	false	high
MONDO:0859175	nephronophthisis-like nephropathy 2	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	genetics_and_genomics|renal_medicine	inflammatory_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0859176	neurodevelopmental disorder with motor and speech delay and behavioral abnormalities	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859177	VISS syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0859178	developmental delay, impaired speech, and behavioral abnormalities	hereditary_disease	other	hereditary_disease	pediatric|psychiatry|neurology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder|autoimmune_diseases	brain_disorder|behavioral_abnormalities|impaired_speech__brain_disorder|developmental_delay__brain_disorder	false	false	false	false	medium
MONDO:0859179	neurodevelopmental disorder with dysmorphic facies and thin corpus callosum	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|genetic_disease_is_replaced_with__neurodevelopmental_disorder__so_the_answer_is__neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|neurodevelopmental_disorder	false	false	false	true	high
MONDO:0859180	bile acid malabsorption, primary, 2	hereditary_disease	other	hereditary_disease	hepatology|gastroenterology	inflammatory_disease|metabolic_disorder	lower_gastrointestinal_disorder|liver_disorder	false	false	false	true	high
MONDO:0859181	DEGCAGS syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|autoimmune_diseases	lymphatic_disorder|immune_disorder|joint_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0859182	Short stature, Dauber-Argente type	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	endocrinology|pediatric|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease|autoimmune_diseases	endocrine_disorder|bone_disorder	false	false	false	true	medium
MONDO:0859184	ventriculomegaly and arthrogryposis	hereditary_disease	other	hereditary_disease	pediatric|neurology|orthopaedic	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|arthrogryposis_is_often_associated_with_congenital_muscular_dystrophy_which_is_a_form_of_neurodegenerative_disease__however_the_given_disease_description_includes_ventriculomegaly_which_may_be_more_specifically_related_to_metabolic_disorders_such_as_non_ketotic_hyperglycinemia_or_other_metabolic_disorders|autoimmune_diseases	brain_disorder|muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0859185	neurodevelopmental disorder with hypotonia and dysmorphic facies	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|neurodevelopmental_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0859186	Chopra-Amiel-Gordon syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	immune_disorder|skin_disorder|joint_disorder	false	false	true	false	high
MONDO:0859187	neurodevelopmental disorder with hypotonia and brain abnormalities	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	true	high
MONDO:0859188	neurodevelopmental disorder with seizures and brain abnormalities	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|neurodevelopmental_disorder	brain_disorder|neurodevelopmental_disorder|brain_abnormalities	true	false	false	false	high
MONDO:0859189	muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|genetics_and_genomics|orthopaedic	neurodegenerative_disease|metabolic_disorder	muscle_disorder|reproductive_system_disorder|ear_disorder	false	false	false	false	high
MONDO:0859190	neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|renal_medicine|neurology	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	brain_disorder|kidney_disorder|heart_disorder	false	false	false	false	high
MONDO:0859191	biliary, renal, neurologic, and skeletal syndrome	hereditary_disease	other	hereditary_disease	hepatology|gastroenterology|rheumatology|renal_medicine|neurology	neurologic__skeletal|biliary__renal__metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0859192	cerebral cavernous malformation 4	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	oncology|genetics_and_genomics|neurology	neurological_disease|cancer	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0859193	neuroocular syndrome	disorder_of_visual_system|nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|disorder_of_visual_system|disorder_of_orbital_region|hereditary_disease	neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	eye_disorder|brain_disorder	true	false	false	false	high
MONDO:0859194	Boudin-Mortier syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|nervous_system_disorder	false	false	false	false	high
MONDO:0859196	Usmani-Riazuddin syndrome, autosomal recessive	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0859197	intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|psychiatry|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder|mental_health_disorder|autoimmune_diseases	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859198	short stature, impaired intellectual development, microcephaly, hypotonia, and ocular anomalies	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0859199	developmental delay with or without intellectual impairment or behavioral abnormalities	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|developmental_delays|mental_health_disorder	brain_disorder|developmental_disorder	false	false	false	false	medium
MONDO:0859200	cerebellar ataxia, brain abnormalities, and cardiac conduction defects	hereditary_disease	other	hereditary_disease	cardiology|genetics_and_genomics|neurology	brain_abnormalities|neurodegenerative_disease|cardiovascular_disorder	brain_abnormalities|brain_disorder|heart_disorder	false	false	false	false	high
MONDO:0859201	neurodevelopmental disorder with impaired language and ataxia and with or without seizures	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	spinal_disorder|brain_disorder	false	false	false	true	high
MONDO:0859202	developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|developmental_delay__hypotonia__musculoskeletal_defects__behavioral_abnormalities	muscle_disorder|brain_disorder|musculoskeletal_defects	false	false	false	true	medium
MONDO:0859203	rhizomelic dysplasia, Ain-Naz type	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859204	fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|mental_health_disorder|genetic_disorders|neurodegenerative_disease|polygenic_disease	lung_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0859205	delayed puberty, self-limited	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	pediatric|endocrinology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0859206	neurodevelopmental disorder with hearing loss and spasticity	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder|ear_disorder	false	false	false	true	high
MONDO:0859207	neurodevelopmental disorder with hypotonia and gross motor and speech delay	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0859208	Hengel-Maroofian-Schols syndrome	hereditary_disease	other	hereditary_disease	pulmonology|dermatology|cardiology|genetics_and_genomics|pediatric	metabolic_disorder|anemia|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	immune_disorder|joint_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0859209	Zaki syndrome	hereditary_disease	other	hereditary_disease	pulmonology|cardiology|genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0859210	chromosome 16q12 duplication syndrome	chromosomal_disorder	other	chromosomal_disorder	genetics_and_genomics|pediatric|neurology	chromosomal_disorder|neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder|skin_disorder|reproductive_system_disorder|joint_disorder|upper_gastrointestinal_disorder|immune_disorder	false	false	false	false	low
MONDO:0859211	neurodevelopmental disorder with hyperkinetic movements and dyskinesia	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|psychiatry|neurology	neurodegenerative_disease|mental_health_disorder|neurodevelopmental_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0859212	neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology	neurodegenerative_disease|mental_health_disorder|inflammatory_disease|autoimmune_diseases|allergy	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0859213	congenital heart defects, multiple types, 8, with or without heterotaxy	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0859214	Marbach-Schaaf neurodevelopmental syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0859215	dystonia, early-onset, and/or spastic paraplegia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|psychiatry|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	muscle_disorder|brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0859216	neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurodevelopmental_disorder_can_sometimes_be_associated_with_other_categories_but_it_is_most_specifically_related_to_the_above_listed_areas_of_medicine|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|seizures_suggest_that_brain_disorder_is_the_primary_category|liver_disorder	false	false	false	false	high
MONDO:0859217	Brunet-Wagner neurodevelopmental syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	as_of_my_last_knowledge_update_in_october_2021__there_are_no_specific_treatments_that_cure_brunet_wagner_neurodevelopmental_syndrome__management_typically_focuses_on_addressing_the_individual_symptoms_and_developmental_challenges_that_patients_may_experience__given_that_knowledge_in_medical_research_is_continually_evolving__i_recommend_checking_the_latest_literature_or_resources_for_any_updates_on_potential_treatments__the_answer_based_on_the_available_information_up_to_that_time_would_be_false	high
MONDO:0859218	developmental delay with variable neurologic and brain abnormalities	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|developmental_disorder|neurologic_disorder	false	false	false	false	high
MONDO:0859219	Rauch-Steindl syndrome	hereditary_disease	other	hereditary_disease	rheumatology|genetics_and_genomics|pediatrics|neurology|ophthalmology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	joint_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0859220	Ferguson-Bonni neurodevelopmental syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	neurodevelopmental_disorder_is_not_in_the_list_so_use_none_of_the_other_categories|brain_disorder	false	false	false	false	high
MONDO:0859221	Yoon-Bellen neurodevelopmental syndrome	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0859222	heterotaxy, visceral, 12, autosomal	hereditary_disease|cardiovascular_disorder|syndromic_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	metabolic_disorder|visceral_disease	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0859223	congenital disorder of glycosylation, type Iw, autosomal dominant	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder	skin_disorder|liver_disorder	false	false	true	false	high
MONDO:0859224	intellectual disability and myopathy syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0859225	neurodevelopmental disorder with or without variable movement or behavioral abnormalities	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology	neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0859226	craniotubular dysplasia, Ikegawa type	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|skull_bone_disorder	false	false	false	false	low
MONDO:0859228	combined oxidative phosphorylation deficiency 55	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease	metabolic_disease|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|metabolic_disorders|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0859229	cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|impaired_intellectual_development_is_most_closely_associated_with_mental_health_disorder|hypogonadotrophic_hypogonadism_is_also_associated_with_metabolic_disorder	brain_disorder|endocrine_disorder|spinal_disorder	false	false	false	false	high
MONDO:0859230	Kury-Isidor syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	joint_disorder|upper_gastrointestinal_disorder|blood_bone_marrow_disorder|liver_disorder	false	false	false	false	medium
MONDO:0859231	macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|anemia|autoimmune_diseases	brain_disorder|immune_disorder|lymphatic_disorder	true	false	false	false	medium
MONDO:0859232	neurodevelopmental disorder with central hypotonia and dysmorphic facies	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|psychiatry|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0859233	epidermolysis bullosa, junctional 6, with pyloric atresia	hereditary_disease|integumentary_system_disorder	other	integumentary_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|dermatology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|skin_disorder	false	false	false	false	very_high
MONDO:0859234	agammaglobulinemia 8b, autosomal recessive	hereditary_disease|hematologic_disorder|immune_system_disorder	other	immune_system_disorder|hereditary_disease|hematologic_disorder	genetics_and_genomics|hematology|pediatric|immunology	metabolic_disorder|anemia|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0859235	auditory neuropathy, autosomal dominant 3	hereditary_disease|psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|otolaryngology|neurology	neurodegenerative_disease|autosomal_dominant_disorders	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0859236	neurodevelopmental disorder with neuromuscular and skeletal abnormalities	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|bone_disorder|joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0859237	3-methylglutaconic aciduria, type VIIA	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	muscle_disorder|kidney_disorder	false	false	false	false	high
MONDO:0859238	hypoalphalipoproteinemia, primary, 2, intermediate	hereditary_disease	other	hereditary_disease	endocrinology|genetics_and_genomics|pediatrics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|biliary_disorder|liver_disorder	false	false	false	false	high
MONDO:0859239	Chilton-Okur-Chung neurodevelopmental syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0859240	intellectual developmental disorder with or without peripheral neuropathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0859241	neurodegeneration, childhood-onset, with progressive microcephaly	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|childhood_onset	brain_disorder|spinal_disorder|neurodegeneration	false	false	false	false	very_high
MONDO:0859242	leukodystrophy, hypomyelinating, 24	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|leukodystrophy_is_a_type_of_hypomyelinating_disease	brain_disorder|spinal_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0859243	neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|psychiatry|neurology	neurodegenerative_disease|mental_health_disorder|neurodevelopmental_disorder	brain_disorder|neurodevelopmental_disorder	false	false	false	false	high
MONDO:0859244	phosphoribosylaminoimidazole carboxylase deficiency	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|metabolic_disorders	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0859245	spinocerebellar ataxia, autosomal recessive 32	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|cardiovascular_disorder	brain_disorder_spinal_disorder	false	false	false	false	high
MONDO:0859246	leukodystrophy, childhood-onset, remitting	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|spinal_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0859247	neurocardiofaciodigital syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|cardiology|neurology	neurodegenerative_disease|metabolic_disorder|cardiovascular_disorder	brain_disorder|heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859248	corneal dystrophy, punctiform and polychromatic pre-descemet	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|ophthalmology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	eye_disorder	false	false	false	false	medium
MONDO:0859249	parenti-mignot neurodevelopmental syndrome	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|neurodevelopmental_disorder	false	false	false	false	high
MONDO:0859250	neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|psychiatry|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|seizure_disorder_is_not_in_the_list_so__brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0859251	Dentici-Novelli neurodevelopmental syndrome	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	teeth_disorder|brain_disorder	false	false	false	false	high
MONDO:0859252	neurodevelopmental disorder with poor growth and skeletal anomalies	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	bone_disorder|brain_disorder|growth_disorder_is_not_in_the_list__so_use__brain_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0859253	osteoporosis, childhood- or juvenile-onset, with developmental delay	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|neurology|orthopaedic	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	bone_disorder|spinal_disorder|joint_disorder	false	false	false	true	very_high
MONDO:0859254	hepatorenocardiac degenerative fibrosis	hereditary_disease	other	hereditary_disease	hepatology|cardiology|cardiothoracic	hepatorenocardiác_degenerative_fibrosis_seems_to_be_related_to_liver__so_also__hepatorenocardiác_degenerative_fibrosis_appears_to_be_connected_to_the_liver_and_heart__thus_also__cardiovascular_disorder|metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0859255	peripheral motor neuropathy, childhood-onset, biotin-responsive	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	true	high
MONDO:0859256	neurodevelopmental disorder with language delay and seizures	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	neurodevelopmental_disorder|brain_disorder	false	false	false	true	high
MONDO:0859257	intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859258	neurodevelopmental disorder with dystonia and seizures	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|neurodevelopmental_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859260	Dworschak-Punetha neurodevelopmental syndrome	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	as_of_my_last_knowledge_update_in_october_2023__there_are_no_known_specific_efficacious_treatments_that_cure__prevent__or_effectively_treat_dworschak_punetha_neurodevelopmental_syndrome__therefore__the_answer_is_false	high
MONDO:0859261	attention deficit-hyperactivity disorder 8	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|nervous_system_disorder	pediatric|psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	medium
MONDO:0859262	ACCES syndrome	hereditary_disease	other	hereditary_disease	endocrinology|pediatric|cardiology|neurology	metabolic_disorder|adrenal_gland_disease	vascular_disorder|liver_disorder	false	false	false	true	high
MONDO:0859263	developmental delay, impaired speech, and behavioral abnormalities, with or without seizures	hereditary_disease	other	hereditary_disease	pediatric|psychiatry|neurology	neurodegenerative_disease|inflammatory_disease|mental_health_disorder|autoimmune_diseases	behavioral_abnormalities|brain_disorder|developmental_delay|speech_impairment	false	false	false	true	medium
MONDO:0859264	congenital myopathy 11	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859265	neurodevelopmental disorder with epilepsy and brain atrophy	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	very_high
MONDO:0859266	neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|cerebral_hypomyelination|brain_atrophy	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0859267	tumor predisposition syndrome 2	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	syndromic_disease|hereditary_disease|cancer_or_benign_tumor	genetics_and_genomics|oncology	tumor_predisposition_syndrome_2|cancer	immune_disorder	false	false	false	false	high
MONDO:0859271	glycosylphosphatidylinositol biosynthesis defect 25	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|lysosomal_storage_disease|liver_disorder	false	false	false	false	high
MONDO:0859272	neurodevelopmental disorder with speech delay and variable ocular anomalies	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|neurodevelopmental_disorder	brain_disorder|speech_delay|eye_disorder	false	false	false	true	medium
MONDO:0859273	liver disease, severe congenital	hereditary_disease|endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|digestive_system_disorder	genetics_and_genomics|hepatology|pediatric	metabolic_disorder|liver_disease	liver_disease|liver_disorder	false	false	false	false	high
MONDO:0859274	neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|spinal_disorder|muscle_disorder|eye_disorder	false	false	false	true	high
MONDO:0859275	neurodevelopmental disorder with spasticity, seizures, and brain abnormalities	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0859276	primordial dwarfism-immunodeficiency-lipodystrophy syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|immunology	metabolic_disorder|inflammatory_disease|immunodeficency_disease|autoimmune_diseases	bone_disorder|skin_disorder|immune_disorder	false	false	false	false	high
MONDO:0859277	intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	bone_disorder|brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859278	keratoderma-ichthyosis-deafness syndrome, autosomal recessive	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	neurodegenerative_disease|metabolic_disorder	ear_disorder|skin_disorder	false	false	false	false	high
MONDO:0859279	spinal muscular atrophy, distal, autosomal recessive, 6	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	spinal_disorder|muscle_disorder	false	false	false	true	high
MONDO:0859280	developmental delay, hypotonia, and impaired language	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|mental_health_disorder	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859281	intellectual developmental disorder with autism and dysmorphic facies	hereditary_disease	other	hereditary_disease	genetics_and_genomics|psychiatry|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder|intellectual_developmental_disorder	false	false	false	false	high
MONDO:0859282	neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0859283	neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0859285	neurodevelopmental disorder with microcephaly, short stature, and speech delay	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|endocrine_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859286	neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|skeletal_disorder|muscle_disorder	false	false	false	true	high
MONDO:0859287	neurodevelopmental disorder with microcephaly, hypotonia, and absent language	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0859288	bone marrow failure and diabetes mellitus syndrome	hereditary_disease	other	hereditary_disease	endocrinology|hematology	metabolic_disorder|anemia|autoimmune_diseases	blood_bone_marrow_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0859289	intestinal dysmotility syndrome	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|neurology	neurodegenerative_disease|intestinal_disorder|metabolic_disorder|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0859290	familial apolipoprotein gene cluster deletion syndrome	metabolic_disease	metabolic_disease	metabolic_disease	genetics_and_genomics|cardiology	neurodegenerative_disease|metabolic_disorder	liver_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0859292	developmental delay, behavioral abnormalities, and neuropsychiatric disorders	hereditary_disease	other	hereditary_disease	pediatrics|neurology	neuropsychiatric_disorders|behavioral_abnormalities|developmental_delay	neuropsychiatric_disorders|brain_disorder	false	false	false	false	high
MONDO:0859293	neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	cerebral_atrophy|eye_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0859295	neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	upper_gastrointestinal_disorder|endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0859296	neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|otolaryngology|pediatric|neurology	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	ear_disorder|muscle_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0859297	neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases|metabolic_disorder	skeletal_disorder|brain_disorder|neurodevelopmental_disorder	false	false	false	true	very_high
MONDO:0859298	neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-pelger-huet anomaly	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology|psychiatry	neurodegenerative_disease|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder|brain_disorder	false	false	false	based_on_the_description_you_ve_provided__it_seems_like_you_are_referring_to_a_complex_neurodevelopmental_disorder_that_includes_specific_physical_and_developmental_features__however__as_of_my_last_update_in_october_2023__neurodevelopmental_disorders_typically_do_not_have_definitive_cures__treatments_generally_focus_on_managing_symptoms__providing_supportive_care__and_improving_quality_of_life___since_there_are_no_efficacious_treatments_that_cure__prevent__or_specifically_treat_the_underlying_causes_of_neurodevelopmental_disorders_featuring_those_characteristics__the_answer_is___false	very_high
MONDO:0859300	neuronopathy, distal hereditary motor, autosomal dominant 10	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autosomal_dominant|hereditary_condition	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0859301	neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology|psychiatry	neurodegenerative_disease|metabolic_disorder|skeletal_defects_is_not_in_the_list_so_i_ll_remove_it__leaving___neurodegenerative_disease	spinal_disorder|skeletal_defects|brain_disorder|joint_disorder	false	false	false	true	high
MONDO:0859302	hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2	hereditary_disease	other	hereditary_disease	metabolism_related_categories_likely_belong_in_endocrinology__genetics_and_genomics_because_of_genetic_factors__pediatric_because_it_can_affect_children|pediatric|genetics_and_genomics|endocrinology	neurodegenerative_disease|metabolic_disorder|hypermetabolism|cardiovascular_disorder	endocrine_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859303	intellectual developmental disorder with ocular anomalies and distinctive facial features	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology|ophthalmology	mental_health_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0859304	neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|childhood_onset_diseases_often_fall_under_neurodegenerative_categories	false	false	false	false	very_high
MONDO:0859305	neurodevelopmental disorder with eye movement abnormalities and ataxia	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0859306	developmental delay with variable intellectual disability and dysmorphic facies	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|genetic_disorder|metabolic_disorder|autoimmune_diseases|intellectual_disability|developmental_delay	dysmorphic_facies_disorder|skeletal_dysplasia_disorder|brain_disorder|developmental_delays_disorder|intellectual_disability_disorder	false	false	false	false	high
MONDO:0859307	cleidocranial dysplasia 2	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics|orthopaedic	bone_dysplasia|genetic_disorder|metabolic_disorder|skeletal_disease	skeletal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0859308	retinitis pigmentosa 95	nervous_system_disorder|metabolic_disease|disorder_of_visual_system|hereditary_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder	metabolic_disease|disorder_of_visual_system|disorder_of_orbital_region|psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	eye_disorder	false	false	false	false	medium
MONDO:0859309	spastic paraplegia 88, autosomal dominant	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859310	orofaciodigital syndrome 19	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	bone_disorder|ear_disorder|teeth_disorder|spinal_disorder	false	false	false	false	high
MONDO:0859311	Charcot-Marie-Tooth disease, demyelinating, type 1J	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|other_is_incorrect_since_it_s_a_disease_related_to_nerves__so_neurology_is_the_best_fit_neurology	neurodegenerative_disease|demyelinating|autoimmune_diseases	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0859312	neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	neurodevelopmental_disorder|brain_disorder|corpus_callosum_abnormality|growth_retardation	false	false	false	false	high
MONDO:0859313	neurodevelopmental disorder with speech impairment and with or without seizures	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|mental_health_disorder	speech_disorder|brain_disorder	false	false	false	true	high
MONDO:0859314	developmental and epileptic encephalopathy 108	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|developmental_disorder|epileptic_encephalopathy	developmental_disorder|brain_disorder|epileptic_disorder	false	false	false	true	very_high
MONDO:0859317	pseudohypoaldosteronism, type IB2, autosomal recessive	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	pediatric|genetics_and_genomics|endocrinology|renal_medicine	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0859318	pseudohypoaldosteronism, type IB3, autosomal recessive	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	pediatric|genetics_and_genomics|endocrinology|renal_medicine	metabolic_disorder|adrenal_gland_disease|autosomal_recessive_diseases_are_implied_but_this_is_a_categorical_list_so_i_will_just_use_the_first_two_categories	endocrine_disorder|kidney_disorder	false	false	false	true	high
MONDO:0859319	dyskeratosis congenita, autosomal recessive 8	cancer_or_benign_tumor|syndromic_disease|integumentary_system_disorder|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor|integumentary_system_disorder	pediatric|genetics_and_genomics|dermatology	neurodegenerative_disease|metabolic_disorder	skin_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0859320	mitochondrial complex I deficiency, nuclear type 39	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	mitochondrial_disease__becomes__muscle_disorder|muscle_disorder|mitochondrial_disease|mitochondrial_disease___corrected_to_match_the_exact_request___muscle_disorder	false	false	false	false	very_high
MONDO:0859321	mitochondrial complex III deficiency, nuclear type 11	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease|cardiovascular_disorder	muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0859322	myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis	hereditary_disease	other	hereditary_disease	neurology|rheumatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	kidney_disorder|muscle_disorder	false	false	false	true	high
MONDO:0859323	combined oxidative phosphorylation deficiency 56	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0859324	developmental delay, language impairment, and ocular abnormalities	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder|ocular_abnormalities|developmental_delay|language_impairment	brain_disorder|language_impairment_can_be_classified_under_brain_disorder____therefore__brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0859325	developmental and epileptic encephalopathy 109	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|developmental_disorder|epilepsy	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0859327	developmental and epileptic encephalopathy 110	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|developmental_disorder|epileptic_encephalopathy	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0859328	hypomagnesemia 7, renal, with or without dilated cardiomyopathy	urinary_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|urinary_system_disorder|metabolic_disease	renal_medicine|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|kidney_disorder	false	false	false	true	high
MONDO:0859329	mosaic variegated aneuploidy syndrome 4	cancer_or_benign_tumor|syndromic_disease|chromosomal_disorder|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor|chromosomal_disorder	pediatric|oncology|genetics_and_genomics	neurodegenerative_disease|cancer	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0859330	oocyte maturation defect 13	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|genetic_disorder_is_not_in_the_list_so__metabolic_disorder	reproductive_system_disorder	false	false	false	false	medium
MONDO:0859331	Rabin-Pappas syndrome	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease	bone_disorder|brain_disorder|skeletal_system_disorder_is_not_in_the_list_so__brain_disorder|eye_disorder|joint_disorder	false	false	false	false	high
MONDO:0859332	cortical dysplasia, complex, with other brain malformations 11	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:0859333	intellectual developmental disorder, autosomal dominant 70	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0859334	spinocerebellar ataxia 50	nervous_system_disorder|hereditary_disease|psychiatric_disorder	neurodegenerative_disease|psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	adrenal_gland_disease|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0859335	congenital myopathy 15	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859336	muscular dystrophy, congenital, with or without seizures	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0859337	combined oxidative phosphorylation deficiency 57	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859338	spermatogenic failure 78	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology|obstetrics_and_gynecology	metabolic_disorder|anemia	reproductive_system_disorder|spermatic_cord_disorder	false	false	false	false	medium
MONDO:0859339	tooth agenesis, selective, 10	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|mouth_disorder	pediatric|genetics_and_genomics|oral_and_dental_surgery__removed__this_is_not_in_the_original_list	genetic_disorder|metabolic_disorder|developmental_disorder	oral_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0859340	spinocerebellar ataxia 27B, late-onset	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	hereditary_disease|psychiatric_disorder|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	medium
MONDO:0859341	hypotrichosis 15	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	skin_disorder	false	false	false	true	low
MONDO:0859342	microcephaly 30, primary, autosomal recessive	nervous_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	high
MONDO:0859346	mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition	cancer_or_benign_tumor|hereditary_disease|syndromic_disease|chromosomal_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|chromosomal_disorder|syndromic_disease	oncology|pediatric|genetics_and_genomics	cancer|inflammatory_disease	liver_disorder|immune_disorder|lymphatic_disorder|upper_gastrointestinal_disorder	false	true	false	false	high
MONDO:0859347	neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	skin_disorder|muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0859350	neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	growth_disorder_is_not_in_the_list_but_it_can_be_inferred_as_urinary_tract_disorder_is_present_so_a_disorder_related_to_the_system_that_controls_growth_would_also_relate_to_a_disorder_of_another_system_such_as_brain_or_endocrine|endocrine_disorder|ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0859351	obesity and hypopigmentation	hereditary_disease	other	hereditary_disease	dermatology|endocrinology|pediatric	autoimmune_diseases|inflammatory_disease|metabolic_disorder	skin_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0859352	spermatogenic failure 79	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	anemia|metabolic_disorder	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0859353	ciliary dyskinesia, primary, 49, without situs inversus	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	hereditary_disease|respiratory_system_disorder|syndromic_disease	pulmonology|pediatric|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder|neurodegenerative_disease	muscle_disorder|lung_disorder|eye_disorder	false	false	false	false	high
MONDO:0859354	thyroid hormone metabolism, abnormal, 3	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder	endocrinology|thyroid_hormone_metabolism_falls_under_endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|thyroid_hormone_metabolism_is_a_subset_of_endocrine_disorder	false	false	false	false	high
MONDO:0859355	inflammatory poikiloderma with hair abnormalities and acral keratoses	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|inflammatory_poikiloderma	skin_disorder|immune_disorder	true	false	false	false	low
MONDO:0859356	congenital disorder of glycosylation, type IIy	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|genetic_disorder	liver_disorder	false	false	true	false	high
MONDO:0859357	congenital disorder of glycosylation, type IIz	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	pediatric|genetics_and_genomics	metabolic_disorder|congenital_disorder	liver_disorder	false	false	false	false	high
MONDO:0859358	cardiomyopathy, dilated, 2H	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiothoracic|cardiology	autoimmune_diseases|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	true	high
MONDO:0859360	spinocerebellar ataxia, autosomal recessive 33	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0859361	neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	bone_disorder|developmental_disorder|brain_disorder	false	false	false	true	high
MONDO:0859362	hyperinsulinemic hypoglycemia, familial, 8	metabolic_disease|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder|metabolic_disease	hereditary_disease|metabolic_disease|endocrine_system_disorder	endocrinology|pediatrics|genetics_and_genomics	autoimmune_diseases|metabolic_disorder	endocrine_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	true	true	high
MONDO:0859363	spastic paraplegia 79A, autosomal dominant, with ataxia	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0859364	spermatogenic failure 80	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	pediatric|urology	autoimmune_diseases|anemia|metabolic_disorder	reproductive_system_disorder|spermatic_failure_is_actually_more_specific_to_the_male_reproductive_system_specifically_so_the_best_fit_would_be_reproductive_system_disorder	false	false	false	false	high
MONDO:0859365	neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	bone_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0859366	hearing loss, autosomal dominant 85	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	otolaryngology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	autosomal_dominant_disorder_is_not_in_the_category_list_but_the_closest_match_would_be_brain_disorder_and_ear_disorder|ear_disorder	false	false	false	false	high
MONDO:0859367	retinitis pigmentosa 96	nervous_system_disorder|psychiatric_disorder|metabolic_disease|disorder_of_visual_system|hereditary_disease	psychiatric_disorder|metabolic_disease	hereditary_disease|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease|nervous_system_disorder	neurology|ophthalmology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:0859368	short QT syndrome 7	cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder	cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:0859369	joint contractures, osteochondromas, and B-cell lymphoma	hereditary_disease	other	hereditary_disease	orthopaedic|rheumatology|oncology|hematology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|bone_disorder|joint_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0859370	respiratory infections, recurrent, and failure to thrive with or without diarrhea	hereditary_disease	other	hereditary_disease	pulmonology|pediatric	inflammatory_disease|respiratory_infections|failure_to_thrive_with_or_without_diarrhea|recurrent	lung_disorder|lower_gastrointestinal_disorder	true	false	false	true	very_high
MONDO:0859372	cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiothoracic|cardiology|genetics_and_genomics	familial_hypertrophic_cardiomyopathy_is_a_subtype_of_the_first_one|metabolic_disorder|cardiovascular_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0859373	intellectual developmental disorder, autosomal recessive 78	nervous_system_disorder|psychiatric_disorder|metabolic_disease|hereditary_disease	psychiatric_disorder|metabolic_disease	hereditary_disease|psychiatric_disorder|metabolic_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	intellectual_developmental_disorder|brain_disorder	false	false	false	false	medium
MONDO:0859374	hearing loss, autosomal recessive 120	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder|auditory_system_disorder|nervous_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder|hearing_disorder	false	false	false	false	medium
MONDO:0859375	developmental delay with hypotonia, myopathy, and brain abnormalities	hereditary_disease	other	hereditary_disease	neurology|pediatric|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0859377	neurodevelopmental disorder with poor growth and behavioral abnormalities	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	endocrine_disorder|brain_disorder	false	false	false	true	high
MONDO:0859378	leukodystrophy, hypomyelinating, 25	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	leukodystrophy_is_not_explicitly_listed_but_hypomyelinating_suggests_a_neurodegenerative_disorder_of_the_central_nervous_system_which_would_be_related_to_metabolic_disorders_as_they_can_be_caused_by_defects_in_metabolism_leading_to_a_lack_or_excess_of_certain_chemicals|metabolic_disorder|neurodegenerative_disease	brain_disorder_spinal_disorder	false	false	false	false	very_high
MONDO:0859379	lymphatic malformation 13	immune_system_disorder|cardiovascular_disorder|hereditary_disease	cardiovascular_disorder	immune_system_disorder|hereditary_disease|cardiovascular_disorder	oncology|pediatric|hematology	cancer|lymphatic_condition	blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	false	medium
MONDO:0859380	episodic kinesigenic dyskinesia 3	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	psychiatry|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859381	cardiomyopathy, dilated, 100	cardiovascular_disorder|hereditary_disease|musculoskeletal_system_disorder	cardiovascular_disorder	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiology|cardiothoracic	inflammatory_disease|metabolic_disorder|cardiovascular_disorder|autoimmune_diseases	muscle_disorder|heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0859382	cataract 50 with or without glaucoma	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology|pediatric	metabolic_disorder|neurodegenerative_disease	glaucoma_is_a_separate_condition_but_sometimes_categorized_under_eye_disorder_as_well|eye_disorder	false	false	false	true	high
MONDO:0859383	ichthyosis hystrix	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases	skin_disorder	false	false	false	false	high
MONDO:0859390	epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	mental_health_disorder|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0859393	Atelis syndrome	hereditary_disease	other	hereditary_disease	psychiatry|neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|vascular_disorder|bone_disorder	false	false	false	false	high
MONDO:0859477	spermatogenic failure, X-linked, 5	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	metabolic_disorder	reproductive_system_disorder	false	false	false	true	high
MONDO:0859478	spermatogenic failure, X-linked, 6	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology|pediatric	autoimmune_diseases|anemia|metabolic_disorder	reproductive_system_disorder	false	false	false	false	high
MONDO:0859514	congenital myopathy 18	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	false	medium
MONDO:0859515	congenital myopathy 10b, mild variant	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder	false	false	false	false	medium
MONDO:0859516	neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0859517	congenital myopathy 2b, severe infantile, autosomal recessive	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	very_high
MONDO:0859518	leukodystrophy, hypomyelinating, 26, with chondrodysplasia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0859519	neurodevelopmental disorder with absent speech and movement and behavioral abnormalities	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0859520	mitochondrial complex IV deficiency, nuclear type 23	metabolic_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|hereditary_disease	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|metabolic_disease|mitochondrial_disease	pediatric|metabolic_disorders|neurology|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0859521	oocyte maturation defect 14	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|reproductive_system_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0859522	spermatogenic failure 81	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	metabolic_disorder|anemia	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0859523	congenital myopathy 2c, severe infantile, autosomal dominant	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0859524	hearing loss, autosomal dominant 86	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|autosomal_dominant_disorders_are_typically_classified_under_a_different_category_but_the_closest_would_be_metabolic_disorder_due_to_its_impact_on_auditory_function_through_inner_ear_metabolism	autosomal_dominant|ear_disorder	false	false	false	false	high
MONDO:0859525	hearing loss, autosomal dominant 87	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease	otolaryngology|genetics_and_genomics|pediatrics	autoimmune_diseases|hearing_loss|neurodegenerative_disease	bone_disorder|ear_disorder	false	false	false	false	high
MONDO:0859526	immunodeficiency 109 with lymphoproliferation	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|immunodeficiency_109_with_lymphoproliferation_fits_best_into_these_categories|hematology|oncology	autoimmune_diseases|inflammatory_disease|cancer	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0859527	hearing loss, autosomal dominant 88	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease	pediatric|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	true	high
MONDO:0859528	hearing loss, autosomal dominant 89	auditory_system_disorder|psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	pediatric|genetic_and_genomic|otolaryngology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	ear_disorder|bone_disorder	false	false	false	false	high
MONDO:0859529	amyotrophic lateral sclerosis 27, juvenile	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0859530	myopathy, sarcoplasmic body	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	muscle_disorder	false	false	false	false	medium
MONDO:0859531	neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|psychiatry|genetics_and_genomics	autoimmune_diseases|mental_health_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|neurodevelopmental_disorder	false	false	false	true	high
MONDO:0859532	congenital heart defects, multiple types, 9	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|hereditary_disease|cardiovascular_disorder	pediatric|cardiology	metabolic_disorder|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0859564	epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	reproductive_system_disorder|brain_disorder	false	false	false	false	high
MONDO:0859565	atrioventricular septal defect	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder|hereditary_disease	cardiothoracic|cardiology|pediatric	congenital_abnormality|inflammatory_disease|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	true	high
MONDO:0859567	craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2	syndromic_disease|hereditary_disease	other	syndromic_disease|hereditary_disease	neurology|psychiatry|genetics_and_genomics|pediatric	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	skeletal_anomalies|brain_disorder|bone_disorder	false	false	false	false	high
MONDO:0859568	macular dystrophy, retinal, 4	disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|retina_was_not_specified_however_one_of_the_main_categories_is_likely_ophthalmology|genetics_and_genomics	neurodegenerative_disease|retinal___corrected_list_without_duplication___retinal	eye_disorder|retinal	false	false	false	false	high
MONDO:0859569	Braddock-Carey syndrome 1	hereditary_disease	other	hereditary_disease	pediatric|genetic_disorders|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|kidney_disorder	false	false	false	false	high
MONDO:0859570	braddock-carey syndrome 2	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatrics	metabolic_disorder|neurodegenerative_disease	vascular_disorder|kidney_disorder|blood_bone_marrow_disorder|bone_disorder|immune_disorder	false	false	false	false	high
MONDO:0859571	diaphragmatic hernia 4, with cardiovascular defects	hereditary_disease|respiratory_system_disorder|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|respiratory_system_disorder	cardiothoracic|cardiology|pediatric	cardiovascular_defects|cardiovascular_disorder	heart_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0859572	cardiac valvular dysplasia 2	hereditary_disease	other	hereditary_disease	cardiothoracic|cardiology	cardiovascular_disorder	heart_disorder|cardiovascular_disorder	false	false	false	false	high
MONDO:0859573	bent bone dysplasia syndrome 2	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	genetic_disorder|metabolic_disorder	blood_bone_marrow_disorder|bone_disorder	false	false	false	false	high
MONDO:0859574	ichthyosis, annular epidermolytic, 2	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	allergy|metabolic_disorder|anemia|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|skin_disorder	false	false	false	false	high
MONDO:0859575	Atelis syndrome 1	hereditary_disease|syndromic_disease|cancer_or_benign_tumor|chromosomal_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|chromosomal_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:0859576	Atelis syndrome 2	hereditary_disease|syndromic_disease|cancer_or_benign_tumor|chromosomal_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|chromosomal_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0859577	lacrimoauriculodentodigital syndrome 2	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder|eye_disorder|joint_disorder|skin_disorder|teeth_disorder	false	false	false	false	high
MONDO:0859578	lacrimoauriculodentodigital syndrome 3	disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	ophthalmology|otolaryngology|genetics_and_genomics|pediatric	metabolic_disorder|genetic_disorder_is_implied_but_it_is_not_in_the_list_so_i_removed_it	eye_disorder|joint_disorder|teeth_disorder	false	false	false	false	high
MONDO:0859588	keratosis pilaris atrophicans faciei	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	dermatology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	low
MONDO:0859591	childhood low-grade glioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology|pediatric	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0859592	IDH-mutant and 1p/19q-codeleted oligodendroglioma	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|genetics_and_genomics|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0859597	cns neuroblastoma with FOXR2 activation	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor	neurology|genetics_and_genomics|oncology|pediatric	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0859598	erythroleukemia	connective_tissue_disorder|immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|acute_disease|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder|connective_tissue_disorder	hematology|oncology	anemia|cancer	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0859614	diffuse low-grade glioma, MAPK pathway–altered	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	genetics_and_genomics|neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	medium
MONDO:0859615	diffuse astrocytoma, MYB- or MYBL1-altered	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	genetics_and_genomics|neurology|oncology	central_nervous_system_cancer|brain_cancer|cancer	brain_disorder	false	true	false	true	medium
MONDO:0859689	hepatobiliary benign neoplasm	cancer_or_benign_tumor|digestive_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|digestive_system_disorder	oncology|gastroenterology|hepatology	hepatobiliary_benign_neoplasm|cancer	biliary_disorder|upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	medium
MONDO:0859690	malignant cystadenoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|urology	malignant_cystadenoma|cancer|adrenal_gland_disease	upper_gastrointestinal_disorder|liver_disorder	false	true	false	false	medium
MONDO:0859692	immune-mediated cerebellar ataxia	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics|immunology	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	immune_disorder|brain_disorder	false	false	false	true	high
MONDO:0859747	grade I lymphomatoid granulomatosis	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|hematologic_disorder	oncology|hematology|immunology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	true	true	false	false	medium
MONDO:0859748	grade II lymphomatoid granulomatosis	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|hematologic_disorder	oncology|hematology|pulmonology	cancer|autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	true	true	false	false	high
MONDO:0859749	grade III lymphomatoid granulomatosis	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|post_infectious_disorder|cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	cancer|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	true	false	false	high
MONDO:0859763	mosaic neurofibromatosis type 1	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	pediatric|oncology|genetics_and_genomics|neurology	cancer|neurofibromatosis_type_1|genetic_disorder____i_corrected_the_answer_to_match_the_category__neurofibromatosis_type_1__which_is_actually_a_type_of_cancer	spinal_disorder|brain_disorder|skin_disorder	false	false	false	false	medium
MONDO:0859764	mosaic NF2-related schwannomatosis	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|neurology	cancer|neurological_disorder	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0859765	mosaic schwannomatosis	hereditary_disease|cancer_or_benign_tumor|syndromic_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	genetics_and_genomics|neurology	cancer|neurodegenerative_disease	spinal_disorder|eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0956962	benign teratoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pediatric	adrenal_gland_disease|cancer	reproductive_system_disorder	false	false	false	true	low
MONDO:0956964	medulloblastoma SHH activated and TP53 mutant	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|genetics_and_genomics|pediatric	neurological_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0956965	medulloblastoma SHH activated and TP53 wild-type	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|genetics_and_genomics|pediatric	cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0956966	medulloblastoma non-WNT/non-SHH group 3	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|genetics_and_genomics|pediatric	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	very_high
MONDO:0956967	medulloblastoma non-WNT/non-SHH group 4	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|genetics_and_genomics|pediatric	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	true	high
MONDO:0956969	chronic inducible urticaria	inflammatory_disease|integumentary_system_disorder	other	integumentary_system_disorder|inflammatory_disease	dermatology|allergy_and_immunology	autoimmune_diseases|allergy|inflammatory_disease	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:0956971	intermittent asthma	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases|allergy	immune_disorder|lung_disorder	false	false	false	true	low
MONDO:0956975	T2-high asthma	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases|allergy	immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0956976	T2-low asthma	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|pediatric	inflammatory_disease|autoimmune_diseases|allergy|metabolic_disorder	immune_disorder|lung_disorder	false	false	false	true	high
MONDO:0956977	near-fatal asthma	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|allergy	respiratory_disorder|lung_disorder	false	false	false	true	high
MONDO:0956979	nocturnal asthma	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases|allergy	lung_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0956980	vascular parkinsonism	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology|cardiology	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:0956981	astrocytoma, IDH-mutant, grade 4	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology	cancer	brain_disorder	false	true	false	true	very_high
MONDO:0956983	pleomorphic xanthoastrocytoma BRAF mutant	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology|genetics_and_genomics	neurodegenerative_disease|adrenal_gland_disease|cancer	other____corrected___brain_disorder|brain_disorder	false	true	false	true	high
MONDO:0956984	YAP1-MAMLD1 fusion-positive supratentorial ependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|genetics_and_genomics	supratentorial_ependymoma|cancer	spinal_disorder|neurological_disorder|brain_disorder	false	true	false	false	high
MONDO:0956985	lipofibromatosis-like neural tumor	cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	neurology|oncology	neural_tumor|cancer	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0956986	solitary fibrous tumor/hemangiopericytoma	cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|connective_tissue_disorder	hematology|neurology|pulmonology|oncology|cardiothoracic	cancer	vascular_disorder|bone_disorder	false	true	false	true	medium
MONDO:0956987	EZB-MYC+ diffuse large B-cell lymphoma	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|cancer|inflammatory_disease	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	true	true	false	true	very_high
MONDO:0956988	EZB-MYC- diffuse large B-cell lymphoma	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	immune_system_disorder|hematologic_disorder|cancer_or_benign_tumor	hematology|oncology	autoimmune_diseases|lymphoma|cancer|inflammation_disease	lymphatic_disorder|immune_disorder	false	true	false	true	high
MONDO:0956989	CIC-rearranged sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|oncology|genetics_and_genomics	adrenal_gland_disease|cancer	lymphatic_disorder|muscle_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0956990	supratentorial ependymoma, ZFTA fusion–positive	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0956991	supratentorial ependymoma, YAP1 fusion–positive	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology|genetics_and_genomics	adrenal_gland_disease|cancer	spinal_disorder|brain_disorder	false	true	false	return_true	high
MONDO:0956992	posterior fossa group A ependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0956993	posterior fossa group B ependymoma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	high
MONDO:0956994	astrocytoma, IDH-mutant, grade 2	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology|genetics_and_genomics	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0956995	astrocytoma, IDH-mutant, grade 3	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0956996	oligodendroglioma, IDH-mutant and 1p/19q-codeleted grade 2	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	medium
MONDO:0956997	oligodendroglioma, IDH-mutant and 1p/19q-codeleted, grade 3	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	high
MONDO:0957003	hereditary neuro-ophthalmological disease	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|hereditary	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0957008	hereditary cerebral malformation	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0957018	autoinflammatory syndrome of childhood	connective_tissue_disorder|syndromic_disease	other	connective_tissue_disorder|syndromic_disease	pediatric|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|liver_disorder|joint_disorder	false	false	false	true	high
MONDO:0957048	isolated macular dystrophy	disorder_of_visual_system|nervous_system_disorder	other	disorder_of_orbital_region|nervous_system_disorder|disorder_of_visual_system	genetics_and_genomics|ophthalmology	neurodegenerative_disease|metabolic_disorder|inflammatory_disease	eye_disorder	false	false	false	true	medium
MONDO:0957097	hereditary hemolytic uremic syndrome	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	pediatric|renal_medicine|hematology	autoimmune_diseases|inflammatory_disease|metabolic_disorder|anemia	kidney_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0957111	neurological muscular channelopathy due to a genetic sodium channel defect	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics	neurological_muscular_channelopathy_due_to_a_genetic_sodium_channel_defect|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0957112	neurological muscular channelopathy due to a genetic chloride channel defect	nervous_system_disorder	other	nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder|neurological	false	false	false	true	high
MONDO:0957113	neurological muscular channelopathy due to a genetic calcium channel defect	nervous_system_disorder	other	nervous_system_disorder	cardiology|neurology|genetics_and_genomics	muscular_dystrophy|genetic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0957114	neurological muscular channelopathy due to a genetic potassium channel defect	nervous_system_disorder	other	nervous_system_disorder	cardiology|neurology|endocrinology|genetics_and_genomics|renal_medicine	neurological_muscular_channeleopathy|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0957196	diffuse midline glioma, H3 K27M-mutant	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|oncology|neurology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0957197	diffuse glioma, H3 G34 mutant	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	genetics_and_genomics|oncology|neurology	neurodegenerative_disease|cancer	spinal_disorder|brain_disorder	false	true	false	true	very_high
MONDO:0957202	spermatogenic failure, X-linked, 7	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	metabolic_disorder|anemia	reproductive_system_disorder	false	false	false	true	medium
MONDO:0957203	intellectual developmental disorder, X-linked 111	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	high
MONDO:0957204	autoinflammation with pulmonary and cutaneous vasculitis	hereditary_disease	other	hereditary_disease	rheumatology|dermatology|pulmonology	autoimmune_diseases|inflammatory_disease	immune_disorder|lung_disorder|skin_disorder|vascular_disorder	true	false	false	true	high
MONDO:0957208	pituitary hormone deficiency, combined or isolated, 8	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder|nervous_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder|nervous_system_disorder	neurology|endocrinology	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|pituitary_hormone_deficiency_isolated_or_combined	false	false	false	true	high
MONDO:0957210	neurooculorenal syndrome	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|renal_medicine	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	kidney_disorder|brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0957211	neurodegeneration and seizures due to copper transport defect	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	neurodegeneration_and_seizures_due_to_copper_transport_defect|brain_disorder	false	false	false	true	high
MONDO:0957215	congenital myopathy 20	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0957216	premature ovarian failure 21	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrinology|obstetrics_and_gynecology	metabolic_disorder|autoimmune_diseases	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0957217	cortical dysplasia, complex, with other brain malformations 12	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease	brain_disorder	false	false	false	false	very_high
MONDO:0957218	neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|neurodevelopmental_disorder	false	false	false	false	high
MONDO:0957220	oocyte/zygote/embryo maturation arrest 17	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|obstetrics_and_gynecology|pediatric	metabolic_disorder|reproductive_endocrine_disorder	oocyte_zygote_embryo_maturation_arrest_is_closely_related_to_reproductive_processes_and_can_be_categorized_under_the_following_____reproductive_system_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0957221	spastic paraplegia 70, autosomal recessive	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0957224	congenital myopathy 21 with early respiratory failure	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|pulmonology	metabolic_disorder|neurodegenerative_disease	lung_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0957225	neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|neurodegeneration_with_developmental_delay_is_not_in_the_list__however_based_on_given_symptoms__brain_disorder|muscle_disorder	true	false	false	true	very_high
MONDO:0957228	intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0957229	hatipoglu immunodeficiency syndrome	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	genetics_and_genomics|allergy_and_immunology|pediatric	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder|liver_disorder	false	false	false	false	very_high
MONDO:0957230	oocyte/zygote/embryo maturation arrest 18	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|ovarian_disorder|maternal_disorder	false	false	false	false	medium
MONDO:0957231	oocyte/zygote/embryo maturation arrest 19	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	reproductive_system_disorder	false	false	false	false	medium
MONDO:0957240	cone-rod dystrophy 24	hereditary_disease|nervous_system_disorder|disorder_of_visual_system|psychiatric_disorder	psychiatric_disorder	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease|inflammatory_disease	eye_disorder	false	false	false	false	low
MONDO:0957247	congenital myopathy 22A, classic	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	high
MONDO:0957248	developmental and epileptic encephalopathy, 31B	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|neurology	epileptic_disease|encephalopathy|neurodegenerative_disease|developmental_disorder	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0957249	spermatogenic failure 82	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	metabolic_disorder|anemia	reproductive_system_disorder	false	false	false	true	high
MONDO:0957250	spermatogenic failure 83	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	metabolic_disorder|anemia|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0957252	ciliary dyskinesia, primary, 50	hereditary_disease|respiratory_system_disorder|syndromic_disease	other	hereditary_disease|syndromic_disease|respiratory_system_disorder	pediatric|pulmonology	metabolic_disorder|neurodegenerative_disease	eye_disorder|lung_disorder	false	false	false	true	high
MONDO:0957253	diarrhea 13	hereditary_disease|digestive_system_disorder	other	hereditary_disease|digestive_system_disorder	gastroenterology|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:0957254	mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0957255	mitochondrial complex V (ATP synthase) deficiency, nuclear type 7	hereditary_disease|metabolic_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease	disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	genetics_and_genomics|pediatrics|neurology	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	false	high
MONDO:0957260	combined low LDL and fibrinogen	hereditary_disease	other	hereditary_disease	endocrinology|cardiology|hepatology|hematology	cardiovascular_disorder|metabolic_disorder	vascular_disorder|liver_disorder	false	false	false	false	low
MONDO:0957261	pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7	respiratory_system_disorder|premature_aging_syndrome|hereditary_disease	other	respiratory_system_disorder|hereditary_disease|premature_aging_syndrome	genetics_and_genomics|pulmonology|hematology	anemia|cancer|telomere_related_conditions_often_involve_bone_marrow_failure__so_this_category_fits_well	blood_bone_marrow_disorder|lung_disorder	false	false	false	true	very_high
MONDO:0957262	osteopetrosis, autosomal recessive 9	musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	pediatric|orthopaedic|genetics_and_genomics|rheumatology	metabolic_disorder|autosomal_recessive_disorders	blood_bone_marrow_disorder|bone_disorder	false	false	false	true	high
MONDO:0957263	pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8	respiratory_system_disorder|premature_aging_syndrome|hereditary_disease	other	respiratory_system_disorder|hereditary_disease|premature_aging_syndrome	genetics_and_genomics|pulmonology|hematology	metabolic_disorder|inflammatory_disease|anemia|cancer	blood_bone_marrow_disorder|lung_disorder	false	false	false	false	very_high
MONDO:0957264	cerebroretinal microangiopathy with calcifications and cysts 3	nervous_system_disorder|premature_aging_syndrome|disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|premature_aging_syndrome|nervous_system_disorder	ophthalmology|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	vascular_disorder|eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0957265	congenital myopathy 22B, severe fetal	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	very_high
MONDO:0957266	RECON progeroid syndrome	premature_aging_syndrome|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|premature_aging_syndrome	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|bone_disorder	false	false	false	true	very_high
MONDO:0957267	neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|psychiatry|neurology	cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	muscle_disorder|vascular_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0957268	hypersulfaturia	hereditary_disease	other	hereditary_disease	gastroenterology|renal_medicine	adrenal_gland_disease|metabolic_disorder	kidney_disorder|liver_disorder	false	false	false	false	high
MONDO:0957270	muscular dystrophy, limb-girdle, autosomal recessive 28	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	orthopaedic|genetics_and_genomics|neurology	metabolic_disorder|inflammatory_disease|neurodegenerative_disease	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0957271	autoinflammatory disease, systemic, with vasculitis	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	syndromic_disease|hereditary_disease|connective_tissue_disorder	rheumatology|hematology	autoimmune_diseases|inflammatory_disease	vascular_disorder|immune_disorder|systemic	false	false	false	true	high
MONDO:0957273	Charcot-Marie-Tooth disease, dominant intermediate A	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	orthopaedic|genetics_and_genomics|neurology	metabolic_disorder|autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0957274	spastic paraplegia 89, autosomal recessive	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0957278	oocyte/zygote/embryo maturation arrest 20	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	pediatric|genetics_and_genomics|obstetrics_and_gynecology	developmental_disorder|metabolic_disorder|reproductive_disorder	reproductive_system_disorder	false	false	false	false	medium
MONDO:0957279	auditory neuropathy, autosomal dominant 2	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	genetics_and_genomics|otolaryngology|neurology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	spinal_disorder|ear_disorder|brain_disorder	false	false	false	false	medium
MONDO:0957281	nemaline myopathy 5B, autosomal recessive, childhood-onset	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0957284	nemaline myopathy 5C, autosomal dominant	hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autosomal_dominant_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0957288	intellectual developmental disorder, autosomal recessive 79	hereditary_disease|nervous_system_disorder|metabolic_disease|psychiatric_disorder	psychiatric_disorder|metabolic_disease	hereditary_disease|metabolic_disease|psychiatric_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	brain_disorder|autosomal_recessive	false	false	false	false	high
MONDO:0957294	pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9	respiratory_system_disorder|premature_aging_syndrome|hereditary_disease	other	respiratory_system_disorder|hereditary_disease|premature_aging_syndrome	genetic|pediatric|oncology|immunology|hematologic|urology|genetics|ophthalmology|orthopaedic|gastroenterology|renal_medicine|cardiology|endocrinology|genetics_and_genomics|hematogenetics_and_genomics|otolaryngology|pulmonology|obstetrics_and_gynecology|rheumatology|genomics|hematology|neurology|dermatology	bone_marrow_failure_syndrome__telomere_related|anemia|cancer	blood_bone_marrow_disorder|lung_disorder	false	false	false	true	high
MONDO:0957301	spermatogenic failure 84	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	metabolic_disorder|inflammation____corrected_to___anemia|anemia|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0957303	palmoplantar keratoderma, epidermolytic, 2	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases	skin_disorder	false	false	false	false	high
MONDO:0957307	woolly hair-skin fragility syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|dermatology	metabolic_disorder|autoimmune_diseases	joint_disorder|hair_disorder|skin_disorder	false	false	false	false	high
MONDO:0957308	spastic paraplegia 90A, autosomal dominant	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0957309	spastic paraplegia 90B, autosomal recessive	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autosomal_recessive	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0957314	retinitis pigmentosa 97	psychiatric_disorder|metabolic_disease|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	metabolic_disease|nervous_system_disorder|psychiatric_disorder|disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	ophthalmology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|adrenal_gland_disease	eye_disorder|blindness_disorder	false	false	false	false	high
MONDO:0957317	hematuria, benign familial	hereditary_disease	other	hereditary_disease	hematology|urology	metabolic_disorder|adrenal_gland_disease|cancer|anemia	urinary_tract_disorder|kidney_disorder	false	false	false	false	low
MONDO:0957318	nephrolithiasis, calcium oxalate	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	urology|renal_medicine	metabolic_disorder|kidney_disease	urinary_tract_disorder|kidney_disorder	false	false	false	true	medium
MONDO:0957337	isolated chorioretinal dystrophy	disorder_of_visual_system|nervous_system_disorder	other	nervous_system_disorder|disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|genetics_and_genomics	neurodegenerative_disease|ocular_disorder	eye_disorder	false	false	false	false	medium
MONDO:0957341	secondary early-onset glaucoma	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|otolaryngology|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|spinal_disorder	false	false	false	true	high
MONDO:0957382	multiple mitochondrial dysfunctions syndrome 7	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	metabolic_disease	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|muscle_disorder	false	false	false	true	very_high
MONDO:0957385	dystonia 37, early-onset, with striatal lesions	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|adrenal_gland_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0957386	neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0957388	autoimmune disease, multisystem, infantile-onset, 3	hereditary_disease|immune_system_disorder	autoimmune_disease	immune_system_disorder|hereditary_disease	immunology|neurology|rheumatology|pediatric	autoimmune_diseases|multisystem___or___autoimmune_diseases|inflammatory_disease	multisystem_____edited_again___note_that_multisystem_is_a_characteristic_rather_than_a_disease_category__and_while_it_does_fit__i_will_not_list_it_as_such_here____immune_disorder_____edited_once_more_for_precision_____immune_disorder|multisystem_____edited_to_replace_the_extra_category_____immune_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0957396	ciliary dyskinesia, primary, 51	hereditary_disease|respiratory_system_disorder|syndromic_disease	other	respiratory_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pulmonology	neurodegenerative_disease|metabolic_disorder	lung_disorder|eye_disorder	false	false	false	true	high
MONDO:0957397	intellectual developmental disorder, autosomal dominant 72	psychiatric_disorder|hereditary_disease|nervous_system_disorder	psychiatric_disorder	hereditary_disease|nervous_system_disorder|psychiatric_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0957400	cataracts, hearing impairment, nephrotic syndrome, and enterocolitis	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	ophthalmology|gastroenterology|otolaryngology|neurology|renal_medicine|pediatric	autoimmune_diseases|allergy___or_inflammatory_disease|metabolic_disorder|neurodegenerative_disease|inflammatory_disease	ear_disorder|kidney_disorder|eye_disorder	false	false	false	true	low
MONDO:0957403	periodic fever syndrome of childhood	syndromic_disease|connective_tissue_disorder	other	syndromic_disease|connective_tissue_disorder	rheumatology|hematology|pediatric	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|liver_disorder	false	false	false	true	medium
MONDO:0957405	granulomatous autoinflammatory syndrome of childhood	syndromic_disease|connective_tissue_disorder	other	syndromic_disease|connective_tissue_disorder	rheumatology|pediatric	autoimmune_diseases|inflammatory_disease	joint_disorder|lung_disorder|immune_disorder	false	false	false	true	high
MONDO:0957408	type 1 interferonopathy of childhood	syndromic_disease|connective_tissue_disorder	other	syndromic_disease|connective_tissue_disorder	allergy_and_immunology|immunology|pediatric	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0957421	borna virus encephalitis	inflammatory_disease|infectious_disease|nervous_system_disorder	infectious_disease	infectious_disease|nervous_system_disorder|acute_disease|inflammatory_disease	neurology|pediatric	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	immune_disorder|brain_disorder	true	false	false	false	high
MONDO:0957423	immunotherapy induced hypophysitis	inflammatory_disease|endocrine_system_disorder|nervous_system_disorder|reproductive_system_disorder	endocrine_system_disorder	nervous_system_disorder|reproductive_system_disorder|endocrine_system_disorder|inflammatory_disease	allergy_and_immunology|endocrinology	autoimmune_diseases|adrenal_gland_disease|inflammatory_disease	immune_disorder|endocrine_disorder	false	false	false	true	medium
MONDO:0957427	B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2)	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|acute_disease|cancer_or_benign_tumor	hematology|genetics_and_genomics|oncology	leukemia|cancer|lymphoma	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0957428	B-lymphoblastic leukemia/lymphoma with t(17;19)	cancer_or_benign_tumor|hematologic_disorder|immune_system_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|acute_disease|cancer_or_benign_tumor	hematology|oncology|pediatric	cancer	blood_bone_marrow_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0957430	childhood-onset schizophrenia	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	psychiatry|pediatric	mental_health_disorder|neurodegenerative_disease	childhood_onset_schizophrenia|brain_disorder	false	false	false	false	very_high
MONDO:0957431	endogenous Cushing syndrome	syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	syndromic_disease|endocrine_system_disorder	genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:0957432	neonatal compartment syndrome	syndromic_disease	other	syndromic_disease	neonatology|obstetrics_and_gynecology|pediatric	metabolic_disorder|inflammatory_disease	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0957433	primary pulmonary vein stenosis	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiothoracic|cardiology|pulmonology	autoimmune_diseases|cardiovascular_disorder	vascular_disorder|lung_disorder|heart_disorder	false	false	false	false	high
MONDO:0957442	autosomal recessive ataxia due to PEX16 deficiency	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0957443	autosomal recessive ataxia due to PEX2 deficiency	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0957451	non-terminal myelocystocele	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|oncology|hematology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	muscle_disorder|spinal_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0957452	segmental arterial mediolysis	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiology|renal_medicine	anemia|metabolic_disorder|cardiovascular_disorder	vascular_disorder|kidney_disorder	false	false	false	false	high
MONDO:0957453	true myelomeningocele	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatric|neurology	neurodegenerative_disease|adrenal_gland_disease|cancer	brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0957454	hemi-myelomeningocele	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|neurology|oncology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0957456	classical dermatomyositis	musculoskeletal_system_disorder|integumentary_system_disorder|connective_tissue_disorder|inflammatory_disease	other	idiopathic_disease|inflammatory_disease|integumentary_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|muscle_disorder|skin_disorder	true	false	false	true	high
MONDO:0957458	adermatopathic dermatomyositis	musculoskeletal_system_disorder|integumentary_system_disorder|connective_tissue_disorder|inflammatory_disease	other	idiopathic_disease|inflammatory_disease|integumentary_system_disorder|musculoskeletal_system_disorder|connective_tissue_disorder	dermatology|rheumatology	inflammatory_disease|autoimmune_diseases	immune_disorder|muscle_disorder|skin_disorder	false	false	false	false	high
MONDO:0957459	congenital esophageal stenosis	digestive_system_disorder|upper_digestive_tract_disorder	other	digestive_system_disorder|upper_digestive_tract_disorder	pediatric|gastroenterology	esophageal_disorder|congenital_esophageal_stenosis_fits_into__congenital_condition	throat_disorder|lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	true	high
MONDO:0957460	spontaneous intestinal perforation	digestive_system_disorder	other	digestive_system_disorder	surgery|pediatric|gastroenterology	inflammatory_disease|gastrointestinal_disorder	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0957461	primary tuberculous lymphadenitis	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases|cancer	lymphatic_disorder|immune_disorder	true	false	false	true	high
MONDO:0957462	primary pulmonary tuberculosis	respiratory_system_disorder|infectious_disease	infectious_disease	respiratory_system_disorder|infectious_disease	pulmonology|cardiology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0957463	primary bone and joint tuberculosis	infectious_disease	infectious_disease	infectious_disease	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	bone_disorder|joint_disorder	true	false	false	true	high
MONDO:0957464	primary cutaneous tuberculosis	infectious_disease|integumentary_system_disorder	infectious_disease	integumentary_system_disorder|infectious_disease	dermatology	inflammatory_disease|autoimmune_diseases|cancer	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0957465	multifocal tuberculosis	infectious_disease	infectious_disease	infectious_disease	pulmonology	inflammatory_disease|autoimmune_diseases	lung_disorder|immune_disorder	true	false	false	true	high
MONDO:0957466	primary tuberculosis of the digestive system	infectious_disease	infectious_disease	infectious_disease	pulmonology|gastroenterology	inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|lung_disorder	true	false	false	true	high
MONDO:0957467	primary genito-urinary tuberculosis	infectious_disease	infectious_disease	infectious_disease	renal_medicine|urology	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|urinary_tract_disorder|kidney_disorder	true	false	false	true	high
MONDO:0957473	craniosynostosis-facial dysmorphism-chiari-1 malformation-developmental and language delay syndrome	syndromic_disease	other	syndromic_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|developmental_delay_syndrome	brain_disorder|spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0957476	isolated persistent urogenital sinus	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	pediatric|urology	congenital_condition|rare_disease|urogenital_disorder|genitourinary_disorder|congenital_anomaly|birth_defect	reproductive_system_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0957477	MYT1L-related developmental delay-intellectual disability-obesity syndrome	syndromic_disease	other	syndromic_disease	pediatric|neurology|genetics_and_genomics|endocrinology	neurodegenerative_disease|metabolic_disorder	brain_disorder|intellectual_disability|endocrine_disorder|developmental_disability	false	false	false	true	high
MONDO:0957481	idiopathic pregnancy-associated osteoporosis	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|obstetric_disorder	other	obstetric_disorder|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	endocrinology|orthopaedic|obstetrics_and_gynecology	inflammatory_disease|metabolic_disorder|autoimmune_diseases	reproductive_system_disorder|bone_disorder	false	false	false	true	medium
MONDO:0957487	idiopathic catatonia	psychiatric_disorder	psychiatric_disorder	psychiatric_disorder	neurology|psychiatry	neurodegenerative_disease|mental_health_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0957494	autoinflammatory disease, multisystem, with immune dysregulation, X-linked	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	syndromic_disease|hereditary_disease|connective_tissue_disorder	pediatric|genetics_and_genomics|rheumatology|immunology	inflammatory_disease|autoimmune_diseases	immune_disorder|multisystem|multisystem___or___immune_disorder|joint_disorder	false	false	false	true	very_high
MONDO:0957495	hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	pediatric|renal_medicine|hematology	anemia|metabolic_disorder	kidney_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0957496	intellectual developmental disorder, X-linked 112	hereditary_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	pediatric|neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	reproductive_system_disorder|brain_disorder	false	false	false	false	high
MONDO:0957497	disabling pansclerotic morphea of childhood	hereditary_disease	other	hereditary_disease	pediatric|dermatology|rheumatology	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	muscle_disorder|skin_disorder|joint_disorder	true	false	false	false	high
MONDO:0957519	diffuse gastric cancer	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	digestive_system_disorder|cancer_or_benign_tumor	oncology|gastroenterology	oncology|cancer|gastrointestinal_cancer	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	true	false	false	high
MONDO:0957524	COX deficiency, benign infantile mitochondrial myopathy	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease|metabolic_disease	metabolic_disease	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder	pediatric|neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_myopathy	false	false	false	false	high
MONDO:0957531	neurodevelopmental disorder with microcephaly and movement abnormalities	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0957533	megalencephalic leukoencephalopathy with subcortical cysts 3	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	spinal_disorder|lymphatic_disorder|brain_disorder	false	false	false	false	high
MONDO:0957534	megalencephalic leukoencephalopathy with subcortical cysts 4, remitting	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|metabolic_disorder	brain_disorder	false	false	false	false	high
MONDO:0957535	immunodeficiency 112	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	pediatrics|allergy_and_immunology|immunology	inflammatory_disease|autoimmune_diseases|immunodeficiency	lymphatic_disorder|immune_disorder	true	false	false	true	low
MONDO:0957536	intellectual developmental disorder, autosomal dominant 73	nervous_system_disorder|psychiatric_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|hereditary_disease|psychiatric_disorder	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	intellectual_developmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0957537	combined oxidative phosphorylation deficiency 58	hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease|metabolic_disease	metabolic_disease	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	muscle_disorder|liver_disorder	false	false	false	false	high
MONDO:0957538	amyotrophic lateral sclerosis 28	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0957539	dystonia 22, juvenile-onset	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	autoimmune_diseases|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0957540	congenital disorder of glycosylation, type IIaa	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	metabolism_is_not_an_option__so_the_closest_category_would_be_genetics_and_genomics|pediatric|genetics_and_genomics	congenital_disorder|metabolic_disorder	liver_disorder|skin_disorder|joint_disorder|eye_disorder	false	false	true	false	high
MONDO:0957541	neurodevelopmental disorder with hypotonia and speech delay, with or without seizures	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|neurology|genetics_and_genomics	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases|metabolic_disorder	muscle_disorder|neurodevelopmental_disorder|speech_delay|brain_disorder	false	false	false	true	medium
MONDO:0957542	dystonia 22, adult-onset	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:0957543	auriculocondylar syndrome 4	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	ear_disorder|joint_disorder	false	false	false	false	low
MONDO:0957544	auriculocondylar syndrome 2B	hereditary_disease	other	hereditary_disease	genetics_and_genomics|orthopaedic	neurodegenerative_disease|autoimmune_diseases	ear_disorder|joint_disorder	false	false	false	false	high
MONDO:0957545	cardiomyopathy, dilated, 2I	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiology|cardiothoracic	cardiovascular_disorder|metabolic_disorder	muscle_disorder|heart_disorder|vascular_disorder	false	false	false	false	high
MONDO:0957553	Houge-Janssens syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|neurology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	immune_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0957556	congenital pulmonary vein atresia	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|pediatric|pulmonology	cardiovascular_disorder|congenital_heart_defect	lung_disorder|heart_disorder	false	false	false	false	high
MONDO:0957560	hearing loss, noise-induced, susceptibility to	hereditary_disease	other	hereditary_disease	neurology|otolaryngology	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	ear_disorder|noise_induced_hearing_loss_susceptibility_is_not_a_direct_category_so_it_is_not_listed_in_the_categories	false	false	false	true	high
MONDO:0957561	encephalitis, acute, infection-induced, susceptibility to, 12	hereditary_disease	other	hereditary_disease	pediatric|neurology	inflammatory_disease|autoimmune_diseases	infection_induced|immune_disorder|brain_disorder	true	false	false	true	high
MONDO:0957563	cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay	hereditary_disease	other	hereditary_disease	pediatric|neurology|genetics_and_genomics	congenital_disorder|developmental_disorder|metabolic_disorder|neurodegenerative_disease	developmental_delay|brain_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0957564	congenital smooth muscle hamartoma, with or without hemihypertrophy	hereditary_disease	other	hereditary_disease	pediatric|genetics_and_genomics	cardiovascular_disorder|metabolic_disorder	liver_disorder|kidney_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0957572	thrombocytopenia 9	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|cardiology	anemia|inflammatory_disease|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0957575	amegakaryocytic thrombocytopenia, congenital, 2	hereditary_disease	other	hereditary_disease	pediatric|hematology|genetics_and_genomics	metabolic_disorder|anemia|inflammatory_disease|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0957576	Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0957577	variegate porphyria, childhood-onset	metabolic_disease|hereditary_disease|integumentary_system_disorder|digestive_system_disorder|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder|integumentary_system_disorder|digestive_system_disorder|hereditary_disease	pediatric|hematology|genetics_and_genomics|dermatology	metabolic_disorder|anemia|autoimmune_diseases	liver_disorder|skin_disorder	false	false	false	false	high
MONDO:0957578	thrombocytopenia 10	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	oncology|hematology|renal_medicine|cardiology	thrombocytopenia|anemia	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	medium
MONDO:0957580	bleeding disorder, platelet-type, 25	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics	platelet_type_disease|bleeding_disorder|anemia|inflammatory_disease|autoimmune_diseases	vascular_disorder|blood_bone_marrow_disorder	false	false	false	true	high
MONDO:0957583	neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|psychiatry|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder|neurodevelopmental_disorder	false	false	false	true	high
MONDO:0957584	spermatogenic failure 85	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|endocrinology|urology	metabolic_disorder|anemia	urinary_tract_disorder|reproductive_system_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0957588	neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	brain_disorder	false	false	false	true	high
MONDO:0957593	spermatogenic failure 86	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	metabolic_disorder|genetic_disorder|endocrine_disorder	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0957594	spermatogenic failure 87	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	metabolic_disorder|anemia|autoimmune_diseases	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0957595	Ziegler-Huang syndrome	hereditary_disease|immune_system_disorder|hematologic_disorder|musculoskeletal_system_disorder	other	hematologic_disorder|immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0957599	epilepsy, early-onset	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	mental_health_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	true	high
MONDO:0957779	neurodevelopmental disorder with language delay and variable cognitive abnormalities	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	medium
MONDO:0957780	developmental and epileptic encephalopathy 111	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	epileptic_disorder|developmental_disorder|neurodegenerative_disease	developmental_disorder|epileptic_disorder|brain_disorder|spinal_disorder	false	false	false	true	very_high
MONDO:0957783	ichthyosis with erythrokeratoderma	hereditary_disease|integumentary_system_disorder	other	hereditary_disease|integumentary_system_disorder	genetics_and_genomics|dermatology|pediatric	metabolic_disorder|inflammatory_disease|autoimmune_diseases	immune_disorder|skin_disorder|genetic_disorder	false	false	false	false	medium
MONDO:0957786	xerosis and growth failure with immune and pulmonary dysfunction syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	immunology|pulmonology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lung_disorder	true	false	false	true	high
MONDO:0957787	Fliedner-Zweier syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0957788	spastic paraplegia 18a, autosomal dominant	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0957790	immune dysregulation, autoimmunity, and autoinflammation	hereditary_disease	other	hereditary_disease	immunology|rheumatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	autoinflammation|immune_disorder|autoimmunity|immune_dysregulation	true	false	false	true	high
MONDO:0957791	neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0957795	arrhythmogenic cardiomyopathy with variable ectodermal abnormalities	hereditary_disease	other	hereditary_disease	genetics_and_genomics|cardiology	metabolic_disorder|autoimmune_diseases|cardiovascular_disorder	heart_disorder|muscle_disorder	false	false	false	false	high
MONDO:0957807	hyper-IgE syndrome 6, autosomal dominant, with recurrent infections	hereditary_disease|immune_system_disorder|hematologic_disorder	other	hematologic_disorder|immune_system_disorder|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics|allergy_and_immunology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	true	false	false	true	high
MONDO:0957809	neutropenia, severe congenital, 10, autosomal recessive	hereditary_disease|immune_system_disorder|hematologic_disorder	other	hematologic_disorder|immune_system_disorder|hereditary_disease	hematology|genetics_and_genomics|pediatric	severe_congenital|metabolic_disorder	immune_disorder|blood_bone_marrow_disorder	false	false	false	true	very_high
MONDO:0957810	developmental delay, dysmorphic facies, and brain anomalies	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease|mental_health_disorder|inflammatory_disease	brain_disorder|developmental_delay|brain_anomalies	false	false	false	false	high
MONDO:0957811	Alport syndrome 3b, autosomal recessive	syndromic_disease|urinary_system_disorder|hereditary_disease|inflammatory_disease	other	urinary_system_disorder|inflammatory_disease|hereditary_disease|syndromic_disease	renal_medicine|genetics_and_genomics	renal_disease|metabolic_disorder	ear_disorder|kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0957812	developmental and epileptic encephalopathy 112	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology	epileptic_encephalopathy|developmental_disorder|neurodegenerative_disease	developmental_disorder|brain_disorder|epileptic_disorder	false	false	false	true	very_high
MONDO:0957813	spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0957815	developmental delay with or without epilepsy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|developmental_disorder|neurodegenerative_disease|inflammatory_disease	brain_disorder|developmental_delay	false	false	false	true	high
MONDO:0957819	arthrogryposis, distal, type 12	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	joint_disorder|muscle_disorder|bone_disorder	false	false	false	false	medium
MONDO:0957820	congenital disorder of glycosylation, type IIbb	metabolic_disease|hereditary_disease	metabolic_disease	metabolic_disease|hereditary_disease	genetics_and_genomics|pediatric	metabolic_disorder|congenital_disorder	liver_disorder|bone_disorder	false	false	true	false	high
MONDO:0957821	spermatogenic failure 88	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	urology|genetics_and_genomics	metabolic_disorder|endocrine_disorder|autoimmune_diseases|anemia___note__i_removed_the_category__inflammatory_disease__because_it_is_a_more_general_term_that_includes_autoimmune_diseases__however__given_that_spermatogenic_failure_has_been_linked_to_hormonal_imbalances_and_autoimmune_factors__all_four_categories_provided_above_are_relevant_to_this_condition	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0957822	premature ovarian failure 22	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	obstetrics_and_gynecology|endocrinology	metabolic_disorder|inflammatory_disease|autoimmune_diseases	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0957824	optic atrophy 14	hereditary_disease|nervous_system_disorder|disorder_of_visual_system	neurodegenerative_disease	nervous_system_disorder|disorder_of_visual_system|hereditary_disease	ophthalmology|neurology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0957825	hearing loss, autosomal recessive 121	auditory_system_disorder|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|nervous_system_disorder|hereditary_disease|psychiatric_disorder	genetics_and_genomics|otolaryngology|pediatric	metabolic_disorder|neurodegenerative_disease	ear_disorder|autosomal_recessive_disease__note__i_corrected_the_disease_name_to_its_actual_category	false	false	false	false	low
MONDO:0957832	craniometadiaphyseal osteosclerosis with hip dysplasia	hereditary_disease	other	hereditary_disease	orthopaedic|genetics_and_genomics|pediatric	metabolic_disorder|autoimmune_diseases|inflammatory_disease	spinal_disorder|joint_disorder|bone_disorder|muscle_disorder	false	false	false	false	high
MONDO:0957870	leukoencephalopathy with vanishing white matter 2	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	hematology|genetics_and_genomics|neurology	neurodegenerative_disease|inflammatory_disease	immune_disorder|brain_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0957871	leukoencephalopathy with vanishing white matter 3	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	hematology|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0957872	leukoencephalopathy with vanishing white matter 4	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	hematology|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0957873	leukoencephalopathy with vanishing white matter 5	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	hematology|genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	brain_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0957874	neuronopathy, distal hereditary motor, autosomal recessive 9	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0957875	neuronopathy, distal hereditary motor, autosomal dominant 11	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autosomal_dominant	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0957876	neuronopathy, distal hereditary motor, autosomal recessive 10	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	muscle_disorder|brain_disorder	false	false	false	false	medium
MONDO:0957896	metabolic dysfunction and alcohol associated liver disease	endocrine_system_disorder|digestive_system_disorder	endocrine_system_disorder	digestive_system_disorder|endocrine_system_disorder	gastroenterology|hepatology	metabolic_disorder|inflammatory_disease	endocrine_disorder|liver_disorder	false	false	false	true	high
MONDO:0957912	organophosphate-induced delayed polyneuropathy	nervous_system_disorder	other	nervous_system_disorder	neurology|pediatric	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	muscle_disorder|nerve_disorder	false	false	false	false	high
MONDO:0957919	Lui-Jee-Baron syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	neurology|genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	bone_disorder|joint_disorder	false	false	false	false	none
MONDO:0957920	immunodeficiency 113 with autoimmunity and autoinflammation	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	allergy_and_immunology|immunodeficiency_is_most_closely_related_to_the_field_of_genetics_and_genomics|rheumatology	inflammatory_disease|immunodeficiency|autoimmune_diseases	inflammation_disorder|autoimmune_disorder|immune_disorder	true	false	false	true	high
MONDO:0957921	Cornelia de Lange syndrome 6	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|syndromic_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|mental_health_disorder	immunodeficiency|skeletal_disorder|developmental_disorder|joint_disorder	false	false	false	false	medium
MONDO:0957922	ciliary dyskinesia, primary, 52	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	hereditary_disease|respiratory_system_disorder|syndromic_disease	neurology|pulmonology|pediatric	metabolic_disorder|neurodegenerative_disease	lung_disorder|eye_disorder	false	false	false	false	high
MONDO:0957928	otosclerosis 11	auditory_system_disorder|hereditary_disease|otorhinolaryngologic_disease	other	hereditary_disease|otorhinolaryngologic_disease|auditory_system_disorder	genetics_and_genomics|otolaryngology	neurodegenerative_disease|inflammatory_disease|autoimmune_diseases	bone_disorder|ear_disorder	false	false	false	true	medium
MONDO:0957935	optic atrophy 15	hereditary_disease|nervous_system_disorder|disorder_of_visual_system	neurodegenerative_disease	hereditary_disease|disorder_of_visual_system|nervous_system_disorder	neurology|ophthalmology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0957953	Garg-Mishra progeroid syndrome	premature_aging_syndrome|disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|premature_aging_syndrome|disorder_of_development_or_morphogenesis	endocrinology|genetics_and_genomics|pediatric|dermatology	metabolic_disorder|neurodegenerative_disease	endocrine_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0957954	lymphatic malformation 14	cardiovascular_disorder|hereditary_disease|immune_system_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|immune_system_disorder	pediatric|hematology|oncology	cancer|lymphatic_disorder	lymphatic_malformation_falls_under_this_category_as_it_is_related_to_the_abnormal_development_of_lymph_vessels|lymphatic_disorder	false	false	false	false	medium
MONDO:0957955	immunodeficiency 114, folate-responsive	hereditary_disease|immune_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|immune_system_disorder|metabolic_disease	allergy_and_immunology|genetics_and_genomics|immunology|pediatric	autoimmune_diseases|metabolic_disorder|anemia	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0957958	spastic paraplegia 72b, autosomal recessive	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0957960	Long-Olsen-Distelmaier syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	dermatology|gastroenterology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	immune_disorder|eye_disorder|skin_disorder|liver_disorder	false	false	false	false	low
MONDO:0957961	oocyte/zygote/embryo maturation arrest 21	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|obstetrics_and_gynecology	metabolic_disorder|developmental_disorder	reproductive_system_disorder	false	false	false	false	medium
MONDO:0957978	optic atrophy 16	nervous_system_disorder|disorder_of_visual_system|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|disorder_of_visual_system|hereditary_disease	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0957981	immunodeficiency 115 with autoinflammation	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|genetics_and_genomics|immunodeficiency_115_is_likely_related_to_a_genetic_condition_affecting_the_immune_system	immunodeficiency_disease|inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0957984	cardiomyopathy, dilated, 2j	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	cardiology|cardiothoracic	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	muscle_disorder|heart_disorder	false	false	false	false	high
MONDO:0957985	neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	childhood_onset|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0957988	osteogenesis imperfecta, type 23	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0957990	Tan-Almurshedi syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|psychiatry|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	liver_disorder|kidney_disorder	false	false	false	as_of_my_last_knowledge_update_in_october_2023__there_are_no_known_efficacious_treatments_that_specifically_cure_or_effectively_manage_tan_almurshedi_syndrome__this_condition_is_very_rare__and_research_on_treatment_options_is_limited__therefore__i_would_return_false	none
MONDO:0957991	ciliary dyskinesia, primary, 53	hereditary_disease|syndromic_disease|respiratory_system_disorder	other	respiratory_system_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|pulmonology|neurology	neurodegenerative_disease|metabolic_disorder	lung_disorder|eye_disorder	false	false	false	false	high
MONDO:0957992	combined oxidative phosphorylation deficiency 59	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	metabolic_disease	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0957993	progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6	metabolic_disease|hereditary_disease|mitochondrial_disease|musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_development_or_morphogenesis	metabolic_disease	nervous_system_disorder|mitochondrial_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0957997	diabetes, deafness, developmental delay, and short stature syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|endocrinology|pediatric	developmental_delay_and_short_stature_syndrome_seems_to_be_closest_match_but_not_exact_category|metabolic_disorder_seems_to_be_most_fitting|autoimmune_diseases|metabolic_disorder	endocrine_disorder|developmental_delay	false	false	false	false	high
MONDO:0957999	intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	metabolic_disease|psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	intellectual_developmental_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0958000	thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies	hereditary_disease|hematologic_disorder	other	hematologic_disorder|hereditary_disease	hematology|genetics_and_genomics|pediatric	metabolic_disorder|anemia	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	very_high
MONDO:0958001	Alfadhel syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|gastroenterology|hepatology	metabolic_disorder|neurodegenerative_disease	liver_disorder|kidney_disorder	false	false	false	false	high
MONDO:0958005	Hoxha-Aliu syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	genetics_and_genomics|pediatrics	autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0958006	spondyloepimetaphyseal dysplasia, Guo-Campeau type	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|orthopaedic|rheumatology	metabolic_disorder|autoimmune_diseases|inflammatory_disease	spinal_disorder|bone_disorder|joint_disorder	false	false	false	false	medium
MONDO:0958009	spastic ataxia 10, autosomal recessive	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0958011	immunodeficiency 117	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	immunology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0958012	neurodegeneration with brain iron accumulation 9	metabolic_disease|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|metabolic_disease|neurodegenerative_disease	nervous_system_disorder|metabolic_disease|psychiatric_disorder|hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0958013	immunodeficiency, common variable, 15	cancer_or_benign_tumor|hereditary_disease|immune_system_disorder|hematologic_disorder|syndromic_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease|hematologic_disorder|immune_system_disorder|hereditary_disease	immunology|genetics_and_genomics|pediatric|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	true	medium
MONDO:0958017	neutropenia, severe congenital, 11, autosomal dominant	hereditary_disease|immune_system_disorder|hematologic_disorder	other	hematologic_disorder|immune_system_disorder|hereditary_disease	hematology|genetics_and_genomics	metabolic_disorder|autoimmune_diseases|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	very_high
MONDO:0958018	leukodystrophy, hypomyelinating, 27	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	hematology|genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|brain_disorder	false	false	false	false	high
MONDO:0958022	lipodystrophy, familial partial, type 8	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|integumentary_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics	metabolic_disorder|genetic_disorders	endocrine_disorder|skin_disorder	false	false	true	false	high
MONDO:0958023	lipodystrophy, congenital generalized, type 5	integumentary_system_disorder|hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|integumentary_system_disorder|hereditary_disease	endocrinology|pediatric|dermatology|genetics_and_genomics	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|skin_disorder	false	false	true	false	high
MONDO:0958030	immunodeficiency 118	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|immunodeficiency	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	true	none
MONDO:0958034	lipodystrophy, familial partial, type 9	hereditary_disease|integumentary_system_disorder|metabolic_disease	metabolic_disease	integumentary_system_disorder|metabolic_disease|hereditary_disease	endocrinology|dermatology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	skin_disorder|endocrine_disorder	false	false	true	false	high
MONDO:0958035	premature ovarian failure 23	endocrine_system_disorder|reproductive_system_disorder|hereditary_disease	endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	obstetrics_and_gynecology|endocrinology	autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0958037	developmental dysplasia of the hip 3	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|orthopaedic	developmental_disorder|neurodegenerative_disease	joint_disorder|bone_disorder	false	false	false	true	high
MONDO:0958071	Hao-Fountain syndrome due to USP7 mutation	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|dermatology|oncology|genetics_and_genomics|pediatrics	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0958075	intramedullary non-dysraphic spinal cord lipoma	nervous_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder|nervous_system_disorder	neurology|pediatric|oncology	cancer|neurodegenerative_disease|spinal_cord_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0958076	myeloschisis	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	oncology|genetics_and_genomics|hematology	anemia|cancer	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	true	false	false	false	very_high
MONDO:0958077	collagen 6-related congenital muscular dystrophy	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	neurology|orthopaedic|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|muscle_disorder	false	false	false	true	high
MONDO:0958083	conjoined twins	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	obstetrics_and_gynecology|pediatric|genetics_and_genomics	cardiovascular_disorder|inflammatory_disease|neurodegenerative_disease	joint_disorder|spinal_disorder	false	false	false	false	high
MONDO:0958085	digenic hemochromatosis	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|hepatology|hematology	anemia|metabolic_disorder	liver_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0958091	cleft palate-congenital heart defect-intellectual disability syndrome	disorder_of_development_or_morphogenesis|syndromic_disease	other	syndromic_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|cardiology	cardiovascular_disorder|metabolic_disorder	upper_gastrointestinal_disorder|kidney_disorder|ear_disorder|brain_disorder|joint_disorder|heart_disorder|teeth_disorder|immune_disorder|vascular_disorder	false	false	false	false	high
MONDO:0958093	non-syndromic supernumerary kidneys	urinary_system_disorder	other	urinary_system_disorder	renal_medicine|urology|genetics_and_genomics	metabolic_disorder|anatomic_anomaly	kidney_disorder|urinary_tract_disorder|bone_disorder	false	false	false	false	medium
MONDO:0958094	adult-onset progressive leukoencephalopathy-early-onset deafness	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|otolaryngology	adrenal_gland_disease|autoimmune_diseases|neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0958095	Nodal T-follicular helper cell lymphoma, follicular type	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	cancer|autoimmune_diseases	lymphatic_disorder|immune_disorder	false	true	false	false	high
MONDO:0958096	monomorphic epitheliotropic intestinal T-cell lymphoma	hematologic_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|hematologic_disorder	oncology|hematology	cancer|autoimmune_diseases	lower_gastrointestinal_disorder|lymphatic_disorder|immune_disorder	false	true	false	false	high
MONDO:0958097	primary superior vena cava aneurysm	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	pulmonology|cardiothoracic|hematology|cardiology	cardiovascular_disorder|vascular_disorder	lymphatic_disorder|vascular_disorder	false	false	false	false	high
MONDO:0958098	primary inferior vena cava aneurysm	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	vascular__removed_since_it_was_not_provided|hepatology|hematology|cardiology	cardiovascular_disorder|vascular_disease	liver_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0958099	idiopathic subglottic stenosis	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|otolaryngology	adrenal_gland_disease|autoimmune_diseases|inflammatory_disease	respiratory_disorder|throat_disorder	false	false	false	false	high
MONDO:0958101	lymphocytic mastitis	cancer_or_benign_tumor|breast_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|breast_disorder	hematolpgy|immunology|pediatrics|allergy_and_immunology|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder_lymphatic_disorder	false	false	false	false	medium
MONDO:0958104	digenic Alport syndrome	inflammatory_disease|urinary_system_disorder|hereditary_disease|syndromic_disease	other	urinary_system_disorder|syndromic_disease|inflammatory_disease|hereditary_disease	renal_medicine|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	high
MONDO:0958106	congenital insensitivity to pain syndrome, Marsili type	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|skin_disorder|eye_disorder	false	false	false	false	medium
MONDO:0958110	atrophic papulosis	cardiovascular_disorder|integumentary_system_disorder	cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder	dermatology	autoimmune_diseases|inflammatory_disease	eye_disorder|skin_disorder	false	false	false	false	medium
MONDO:0958115	autosomal recessive combined immunodeficiency due to complete IL6ST deficiency	hematologic_disorder|immune_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	hematologic_disorder|immune_system_disorder|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|allergy_and_immunology|pediatric	autoimmune_diseases|inflammatory_disease|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0958116	autosomal recessive combined immunodeficiency due to partial IL6ST deficiency	hematologic_disorder|immune_system_disorder|hereditary_disease	other	hematologic_disorder|immune_system_disorder|hereditary_disease	genetics_and_genomics|allergy_and_immunology|immunology|pediatric	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0958117	autosomal dominant combined immunodeficiency due to partial IL6ST deficiency	hematologic_disorder|immune_system_disorder|hereditary_disease	other	hematologic_disorder|immune_system_disorder|hereditary_disease	genetics_and_genomics|immunology|pediatric	autoimmune_diseases|inflammatory_disease|anemia	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0958118	autosomal recessive combined immunodeficiency due to IL6R deficiency	hematologic_disorder|immune_system_disorder|hereditary_disease	other	hematologic_disorder|immune_system_disorder|hereditary_disease	genetics_and_genomics|immunology|pediatric	autoimmune_diseases|inflammatory_disease|anemia	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0958119	embryonal tumor with multilayered rosettes	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|nervous_system_disorder	oncology|neurology|pediatric	neurodegenerative_disease|adrenal_gland_disease|cancer	spinal_disorder|brain_disorder	false	true	false	false	very_high
MONDO:0958120	autosomal dominant combined immunodeficiency due to ERBIN deficiency	hematologic_disorder|immune_system_disorder|hereditary_disease	other	hematologic_disorder|immune_system_disorder|hereditary_disease	genetics_and_genomics|immunology|pediatric	autoimmune_diseases|inflammatory_disease|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0958122	idiopathic small fibers neuropathy	nervous_system_disorder	other	nervous_system_disorder	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0958123	isolated pulmonary artery sling	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	pulmonology|cardiothoracic	cardiovascular_disorder|congenital_heart_disease	vascular_disorder|lung_disorder	false	false	false	false	high
MONDO:0958127	transplant-related bronchiolitis obliterans	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|transplant_related_conditions_would_also_fit_into_pediatric_and_immunology_but_those_categories_aren_t_listed	autoimmune_diseases|inflammatory_disease	vascular_disorder|lung_disorder|immune_disorder	false	false	false	true	high
MONDO:0958128	non-transplant-related bronchiolitis obliterans	respiratory_system_disorder	other	respiratory_system_disorder	renal_medicine|hematology|pulmonology|cardiology|cardiothoracic	autoimmune_diseases|inflammatory_disease	vascular_disorder|lung_disorder|immune_disorder	false	false	false	false	high
MONDO:0958129	COQ7-related distal hereditary motor neuropathy	disorder_of_development_or_morphogenesis|metabolic_disease|nervous_system_disorder|hereditary_disease|mitochondrial_disease	neurodegenerative_disease|metabolic_disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|metabolic_disease|hereditary_disease|mitochondrial_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0958130	Greig cephalopolysyndactyly-contiguous gene syndrome	syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease|musculoskeletal_system_disorder|hereditary_disease	genetics_and_genomics|pediatric	genetic_disorder|metabolic_disorder	lymphatic_disorder|ear_disorder|skin_disorder|upper_gastrointestinal_disorder|eye_disorder|bone_disorder|lower_gastrointestinal_disorder|joint_disorder	false	false	false	false	high
MONDO:0958137	early-onset autoimmune disorder due to DOCK11 partial deficiency	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	connective_tissue_disorder|syndromic_disease|hereditary_disease	immunology|genetics_and_genomics|pediatric	autoimmune_diseases|inflammatory_disease	blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0958138	early-onset immune dysregulation due to DOCK11 complete deficiency	syndromic_disease|connective_tissue_disorder|hereditary_disease	other	connective_tissue_disorder|syndromic_disease|hereditary_disease	genetics_and_genomics|allergy_and_immunology|pediatric	autoimmune_diseases|allergy|inflammatory_disease	lymphatic_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	high
MONDO:0958150	Borrelia miyamotoi disease	infectious_disease	infectious_disease	infectious_disease	neurology|dermatology	inflammatory_disease|autoimmune_diseases	lymphatic_disorder|skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:0958151	cepacia syndrome	infectious_disease	infectious_disease	infectious_disease	allergy_and_immunology|pediatric	adrenal_gland_disease|inflammatory_disease|autoimmune_diseases	upper_gastrointestinal_disorder|lung_disorder|immune_disorder	true	false	false	false	high
MONDO:0958159	sarcoma with BCOR genetic alterations	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|genetics_and_genomics|oncology	adrenal_gland_disease|cancer	blood_bone_marrow_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0958160	round cell sarcoma with EWSR1-non-ETS fusion	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	hematology|pediatric|genetics_and_genomics|oncology	adrenal_gland_disease|cancer	blood_bone_marrow_disorder|muscle_disorder	false	true	false	false	very_high
MONDO:0958161	B acute lymphoblastic leukemia with PAX5 P80R mutation	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|acute_disease	hematology|pediatric|genetics_and_genomics|oncology	cancer|allergy	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0958162	B acute lymphoblastic leukemia with DUX4 rearrangement	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder|acute_disease	hematology|pediatric|genetics_and_genomics|oncology	cancer|leukemia	lymphatic_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0958164	poorly differentiated chordoma	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder	orthopaedic|genetics_and_genomics|oncology	cancer	bone_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:0958165	anaplastic sarcoma of the kidney	cancer_or_benign_tumor|urinary_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|urinary_system_disorder	oncology|urology	kidney_cancer|cancer	kidney_disorder|blood_bone_marrow_disorder	false	true	false	false	very_high
MONDO:0958174	basal cell nevus syndrome 1	nervous_system_disorder|cancer_or_benign_tumor|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	syndromic_disease|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|dermatology|oncology	skin_disorder|cancer|genetic_disorder|nevoid_syndrome	eye_disorder|skin_disorder|brain_disorder	false	false	false	true	medium
MONDO:0958175	craniofacial microsomia 1	musculoskeletal_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	orthopaedic|otolaryngology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder	teeth_disorder|bone_disorder|craniofacial_disorder	false	false	false	false	medium
MONDO:0958176	oculopharyngeal muscular dystrophy 1	musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	other	musculoskeletal_system_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease|disorder_of_orbital_region	genetics_and_genomics|neurology	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	eye_disorder|throat_disorder|muscle_disorder	false	false	false	false	high
MONDO:0958177	chronic recurrent multifocal osteomyelitis 3	connective_tissue_disorder|musculoskeletal_system_disorder|hematologic_disorder|immune_system_disorder|hereditary_disease|syndromic_disease	other	musculoskeletal_system_disorder|immune_system_disorder|syndromic_disease|hereditary_disease|connective_tissue_disorder|hematologic_disorder	orthopaedic|rheumatology	inflammatory_disease|autoimmune_diseases	bone_disorder|spinal_disorder|joint_disorder|immune_disorder|muscle_disorder	false	false	false	false	high
MONDO:0958178	cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	renal_medicine|ophthalmology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|kidney_disorder|lower_gastrointestinal_disorder|ear_disorder	false	false	false	true	high
MONDO:0958179	glycine encephalopathy 1	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	liver_disorder|kidney_disorder|spinal_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0958180	prolonged electroretinal response suppression 1	nervous_system_disorder|disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region|hereditary_disease	ophthalmology|neurology	inflammatory_disease|autoimmune_diseases|neurodegenerative_disease	eye_disorder|muscle_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0958181	mitochondrial trifunctional protein deficiency 1	metabolic_disease|musculoskeletal_system_disorder|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	metabolic_disorder_is_a_subcategory_of_genetics_and_genomics|genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|metabolic_disorder	liver_disorder|muscle_disorder	false	false	false	false	high
MONDO:0958182	C1Q deficiency 1	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|genetics_and_genomics|rheumatology	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|lymphatic_disorder|immune_disorder	false	false	false	true	medium
MONDO:0958183	Leber-like hereditary optic neuropathy, autosomal recessive 1	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0958184	epidermolytic hyperkeratosis 2	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	other	integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|dermatology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	epidermal_disorder|skin_disorder	false	false	false	false	medium
MONDO:0958185	mitochondrial trifunctional protein deficiency 2	disorder_of_development_or_morphogenesis|metabolic_disease|musculoskeletal_system_disorder|mitochondrial_disease|hereditary_disease	metabolic_disease	musculoskeletal_system_disorder|metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	liver_disorder|mitochondrial_disease	false	false	false	false	high
MONDO:0958186	hematuria, benign familial, 2	hereditary_disease	other	hereditary_disease	renal_medicine|genetics_and_genomics|urology|hematology	inflammatory_disease|anemia|metabolic_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	false	medium
MONDO:0958187	C1Q deficiency 2	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|rheumatology	inflammatory_disease|autoimmune_diseases	kidney_disorder|blood_bone_marrow_disorder|immune_disorder	false	false	false	false	medium
MONDO:0958188	C1Q deficiency 3	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|pediatric|genetics_and_genomics|rheumatology	inflammatory_disease|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0958189	basal cell nevus syndrome 2	disorder_of_development_or_morphogenesis|nervous_system_disorder|cancer_or_benign_tumor|hereditary_disease|syndromic_disease	cancer_or_benign_tumor	syndromic_disease|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder|hereditary_disease	genetics_and_genomics|dermatology|oncology	cancer|neurodegenerative_disease	eye_disorder|skin_disorder|brain_disorder	false	false	false	true	low
MONDO:0958190	prolonged electroretinal response suppression 2	nervous_system_disorder|disorder_of_visual_system|hereditary_disease	other	disorder_of_visual_system|nervous_system_disorder|hereditary_disease|disorder_of_orbital_region	neurology|ophthalmology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	eye_disorder	false	false	false	false	high
MONDO:0958191	nephrolithiasis, calcium oxalate, 2, with or without nephrocalcinosis	urinary_system_disorder|hereditary_disease	other	urinary_system_disorder|hereditary_disease	renal_medicine|urology	anemia|cardiovascular_disorder|neurodegenerative_disease|metabolic_disorder	kidney_disorder|urinary_tract_disorder|bone_disorder	false	false	false	true	medium
MONDO:0958192	glycine encephalopathy 2	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	inflammatory_disease|neurodegenerative_disease|metabolic_disorder	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0958193	cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	neurology|renal_medicine|otolaryngology|ophthalmology|urology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	eye_disorder|kidney_disorder|ear_disorder	false	false	false	true	low
MONDO:0958194	craniofacial microsomia 2	syndromic_disease|musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|syndromic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	otolaryngology|genetics_and_genomics|pediatric	congenital_disorder|metabolic_disorder	bone_disorder|teeth_disorder	false	false	false	false	high
MONDO:0958195	oculopharyngeal muscular dystrophy 2	nervous_system_disorder|musculoskeletal_system_disorder|disorder_of_visual_system|hereditary_disease	other	musculoskeletal_system_disorder|nervous_system_disorder|disorder_of_orbital_region|hereditary_disease|disorder_of_visual_system	ophthalmology|genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	throat_disorder|muscle_disorder|eye_disorder	false	false	false	false	high
MONDO:0958196	epilepsy, early-onset, 3, with or without developmental delay	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|neurology	inflammatory_disease|neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder|developmental_delay	false	false	false	true	high
MONDO:0958197	Leber-like hereditary optic neuropathy, autosomal recessive 2	metabolic_disease|mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease|mitochondrial_disease	ophthalmology|genetics_and_genomics|neurology	autoimmune_diseases|neurodegenerative_disease|metabolic_disorder	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0958199	myoclonic epilepsy of Lafora 1	metabolic_disease|nervous_system_disorder|hereditary_disease	metabolic_disease	metabolic_disease|nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0958200	intellectual developmental disorder, X-linked 113	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	true	high
MONDO:0958202	moyamoya disease 7	hereditary_disease|cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|nervous_system_disorder	vascular__as_cardiology_is_closest|neurology	neurodegenerative_disease|inflammatory_disease	brain_disorder|vascular_disorder	false	false	false	false	high
MONDO:0958203	intellectual developmental disorder, autosomal dominant 74	hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|pediatric|neurology	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:0958204	intellectual developmental disorder, autosomal recessive 81	hereditary_disease|psychiatric_disorder|metabolic_disease|nervous_system_disorder	metabolic_disease|psychiatric_disorder	hereditary_disease|metabolic_disease|psychiatric_disorder|nervous_system_disorder	genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder|metabolic_disorder	brain_disorder|intellectual_developmental_disorder	false	false	false	false	high
MONDO:0958205	Yuksel-Vogel-Bauer syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder|autoimmune_diseases|inflammatory_disease	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0958206	spermatogenic failure 89	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	endocrinology|genetics_and_genomics|urology	cancer|anemia|adrenal_gland_disease|metabolic_disorder	blood_bone_marrow_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0958224	encephalopathy, porphyria-related	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|hematology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|allergic_disease_is_not_present_but_its_close_relative__anemia|neurodegenerative_disease	brain_disorder|liver_disorder	false	false	false	true	high
MONDO:0958226	leukoencephalopathy, porphyria-related	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|hematology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	blood_bone_marrow_disorder|brain_disorder	false	false	false	false	medium
MONDO:0958227	polydactyly-macrocephaly syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	genetics_and_genomics|pediatric|neurology	metabolic_disorder|neurodegenerative_disease	other___note__polydactyly_macrocephaly_syndrome_is_a_rare_genetic_disorder_characterized_by_an_enlarged_head_size__macrocephaly__and_extra_fingers__polydactyly___among_other_features__the_exact_categorization_of_this_condition_can_be_complex__but_it_primarily_relates_to_brain_development_and_abnormalities|brain_disorder	false	false	false	false	medium
MONDO:0958228	hearing loss, autosomal recessive 122	auditory_system_disorder|hereditary_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	genetics_and_genomics|pediatric|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder|autosomal_recessive_disorders	false	false	false	true	medium
MONDO:0958229	bleeding disorder, vascular-type	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	genetics_and_genomics|hematology|cardiology	vascular_type|cardiovascular_disorder|bleeding_disorder	blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0958230	orofaciodigital syndrome 20	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	joint_disorder|teeth_disorder|ear_disorder	false	false	false	false	high
MONDO:0958231	neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism	hereditary_disease|psychiatric_disorder|nervous_system_disorder	neurodegenerative_disease|psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0958232	hearing loss, autosomal dominant 90	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder|auditory_system_disorder	genetics_and_genomics|otolaryngology	metabolic_disorder|autosomal_dominant_disorder|neurodegenerative_disease	brain_disorder|ear_disorder	false	false	false	false	medium
MONDO:0958233	Bethlem myopathy 1B	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|neurology	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	high
MONDO:0958234	Bethlem myopathy 1C	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	genetic_disorder|muscle_disorder|hereditary_disorder	false	false	false	false	high
MONDO:0958235	Ullrich congenital muscular dystrophy 1B	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder	false	false	false	false	high
MONDO:0958236	Ullrich congenital muscular dystrophy 1C	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0958237	isolated hyperferritinemia	hereditary_disease	other	hereditary_disease	genetics_and_genomics|hematology	autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|liver_disorder	false	false	false	false	low
MONDO:0958239	microphthalmia/coloboma 11	hereditary_disease|disorder_of_visual_system	other	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system	pediatric|genetics_and_genomics|ophthalmology	cancer|autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0958240	neurodevelopmental disorder with hyperkinetic movements, seizures, and structural brain abnormalities	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|pediatric|neurology|neurodevelopmental_disorders	inflammatory_disease|neurodevelopmental_disorder|neurodegenerative_disease	brain_disorder|neurological_disorder|structural_abnormalities	false	false	false	true	very_high
MONDO:0958241	cardiomyopathy, familial hypertrophic, 30, atrial	cardiovascular_disorder|musculoskeletal_system_disorder|hereditary_disease	cardiovascular_disorder	musculoskeletal_system_disorder|cardiovascular_disorder|hereditary_disease	genetics_and_genomics|pediatric|cardiology	familial_hypertrophic_cardiomyopathy_is_a_subset_of_cardiovascular_disorder_but_it_was_specifically_mentioned_so_i_ll_keep_it_in_the_answer__atrial_is_also_related_to_heart_disease_which_makes_it_fit_into_this_category|cardiovascular_disorder	heart_disorder|vascular_disorder|muscle_disorder	false	false	false	true	high
MONDO:0958242	spermatogenic failure 90	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	anemia|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|male_reproductive_system_disorder	false	false	false	false	high
MONDO:0958256	pyoderma gangrenosum-acne-hidradenitis suppurativa-ankylosing spondylitis syndrome	syndromic_disease	other	syndromic_disease	rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|joint_disorder|skin_disorder	false	false	false	false	high
MONDO:0958257	psoriatic arthritis-pyoderma gangrenosum-acne-hidradenitis suppurativa syndrome	syndromic_disease	other	syndromic_disease	pediatric|rheumatology|dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|joint_disorder|skin_disorder	false	false	false	true	high
MONDO:0958258	Cushing syndrome due to cortisol-producing adrenocortical adenoma	syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|syndromic_disease	endocrinology|oncology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|vascular_disorder	false	false	false	true	high
MONDO:0958259	dysraphism with stalk	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0958260	dysraphic spinal cord lipoma	disorder_of_development_or_morphogenesis|connective_tissue_disorder|musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_development_or_morphogenesis|connective_tissue_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	genetics_and_genomics|pediatric|neurology	spinal_cord_condition|developmental_disorder|neurological_disease|congenital_anomaly	spinal_disorder	false	false	false	false	medium
MONDO:0958262	isolated primary pigmented nodular adrenocortical disease	hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder|hereditary_disease	endocrinology|oncology|dermatology	cancer|metabolic_disorder|adrenal_gland_disease	endocrine_disorder	false	false	false	false	high
MONDO:0958263	isolated micronodular adrenocortical disease	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	nephrology|endocrinology	metabolic_disorder|adrenal_gland_disease	endocrine_disorder|adrenal_cortical_disease	false	false	false	false	medium
MONDO:0958264	infectious scleritis	disorder_of_visual_system|infectious_disease	infectious_disease	disorder_of_orbital_region|infectious_disease|disorder_of_visual_system	ophthalmology|infectious_diseases|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|eye_disorder	true	false	false	false	medium
MONDO:0958265	idiopathic scleritis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	neurology|ophthalmology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|eye_disorder	false	false	false	false	medium
MONDO:0958266	immune-mediated scleritis	disorder_of_visual_system	other	disorder_of_orbital_region|disorder_of_visual_system	ophthalmology|rheumatology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|eye_disorder	false	false	false	true	high
MONDO:0958267	non-syndromic bridging bronchus	respiratory_system_disorder	other	respiratory_system_disorder	pulmonology|cardiothoracic	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	throat_disorder|upper_gastrointestinal_disorder|lung_disorder	false	false	false	false	high
MONDO:0958268	non-syndromic congenital bronchial atresia	respiratory_system_disorder	other	respiratory_system_disorder	pediatric|pulmonology	respiratory_disease|cardiovascular_disorder|neurodegenerative_disease	throat_disorder|lung_disorder	false	false	false	false	high
MONDO:0958269	isolated left bronchial isomerism	respiratory_system_disorder	other	respiratory_system_disorder	genetics_and_genomics|pulmonology|cardiothoracic	metabolic_disorder|cardiovascular_disorder	vascular_disorder|lung_disorder	false	false	false	false	high
MONDO:0958270	central precocious puberty in male	reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|endocrinology	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0958273	cleft palate-congenital heart defect-intellectual disability syndrome due to MEIS2 mutation	disorder_of_development_or_morphogenesis|syndromic_disease	other	disorder_of_development_or_morphogenesis|syndromic_disease	pediatric|genetics_and_genomics|otolaryngology	congenital_heart_defect|metabolic_disorder|intellectual_disability|cardiovascular_disorder	genetic_disorder___since__other__wasn_t_present_in_the_list__i_have_used__congenital_abnormality__and__genetic_disorder|heart_disorder|congenital_abnormality__assuming_intellectual_disability_is_a_correct_substitute_for_this_category|oral_disorder__assuming_teeth_disorder_is_a_correct_substitute_for_oral_disorder	false	false	false	false	very_high
MONDO:0958274	benign atrophic papulosis	integumentary_system_disorder|cardiovascular_disorder	cardiovascular_disorder	integumentary_system_disorder|cardiovascular_disorder	dermatology	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	false	medium
MONDO:0958275	segmental spinal dysgenesis	nervous_system_disorder	other	nervous_system_disorder	pediatric|genetics_and_genomics|neurology|orthopaedic	segmental_spinal_dyssgenesis|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0958277	hearing loss, autosomal recessive 123	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|auditory_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|otolaryngology	metabolic_disorder|neurodegenerative_disease	ear_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0958278	neurodevelopmental disorder with hypotonia and characteristic brain abnormalities	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	true	high
MONDO:0958279	megalencephaly-polydactyly syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|polydactyly_often_associated_with_musculoskeletal_issue_is_removed__however__the_primary_category_remains__brain_disorder	false	false	false	false	high
MONDO:0958295	BCOR ITD sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|oncology|hematology	sarcoma|cancer|adrenal_gland_disease	sarcoma|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0958296	BCOR-CCNB3 sarcoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|oncology|pediatric	cancer|adrenal_gland_disease	muscle_disorder|blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0958297	childhood sarcoma with BCOR genetic alterations	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|oncology|pediatric	cancer|adrenal_gland_disease	bone_disorder|lymphatic_disorder	false	true	false	true	high
MONDO:0958298	childhood round cell sarcoma with EWSR1-non-ETS fusion	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|oncology|pediatric	cancer	muscle_disorder|bone_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0958299	round cell sarcoma with EWSR1-NFATC2 gene fusion	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	genetics_and_genomics|oncology|pediatric	cancer|adrenal_gland_disease	muscle_disorder|bone_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0958300	round cell sarcoma with EWSR1-PATZ1 gene fusion	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|hematology|oncology|genetics_and_genomics	cancer|adrenal_gland_disease	blood_bone_marrow_disorder|muscle_disorder	false	true	false	false	high
MONDO:0958301	round cell sarcoma with FUS-NFATC2 gene fusion	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	pediatric|oncology|genetics_and_genomics	cancer|adrenal_gland_disease	blood_bone_marrow_disorder|muscle_disorder	false	true	false	false	high
MONDO:0958302	TFEB-rearranged renal cell carcinoma	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|oncology|genetics_and_genomics	cancer|renal_cell_carcinoma|kidney_disease	kidney_disorder|renal_cell_carcinoma	false	true	false	false	high
MONDO:0958303	childhood renal cell carcinoma with MiT translocations	urinary_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	urinary_system_disorder|cancer_or_benign_tumor	urology|pediatric|oncology	cancer|adrenal_gland_disease	blood_bone_marrow_disorder|kidney_disorder	false	true	false	true	high
MONDO:0958322	intellectual developmental disorder, X-linked, syndromic 37	psychiatric_disorder|nervous_system_disorder|syndromic_disease|hereditary_disease	psychiatric_disorder	hereditary_disease|syndromic_disease|psychiatric_disorder|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|developmental_disorder|nervous_system_disorder	false	false	false	false	high
MONDO:0958323	neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	mental_health_disorder|neurodevelopmental_disorder|neurodegenerative_disease	brain_disorder|neurodevelopmental_disorder	false	false	false	false	very_high
MONDO:0958324	generalized epilepsy with febrile seizures plus, type 12	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder	false	false	false	false	medium
MONDO:0958325	thrombocytopenia 12 with or without myopathy	hematologic_disorder|hereditary_disease	other	hematologic_disorder|hereditary_disease	hematology	anemia|autoimmune_diseases|metabolic_disorder	muscle_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0958326	macular dystrophy with or without cone dysfunction	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	hereditary_disease|disorder_of_orbital_region|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	ophthalmology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:0958328	Seckel syndrome 11	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	upper_gastrointestinal_disorder|eye_disorder|brain_disorder|joint_disorder	false	false	false	false	high
MONDO:0958329	Jeffries-Lakhani neurodevelopmental syndrome	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0958330	developmental and epileptic encephalopathy 113	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	developmental_disorder|epilepsy|neurodegenerative_disease	brain_disorder|developmental_disorder|spinal_disorder|epileptic_disorder	false	false	false	true	high
MONDO:0958331	developmental and epileptic encephalopathy 114	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	developmental_disorder|epilepsy|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0958332	neuromuscular disorder, congenital, with dysmorphic facies	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	neurodegenerative_disease|congenital_diseases_are_not_in_the_list_so_ignore_them|metabolic_disorder	congenital_disorder|neuromuscular_disorder|muscle_disorder	false	false	false	false	high
MONDO:0958333	thrombocytopenia 13, syndromic	hematologic_disorder|hereditary_disease	other	hereditary_disease|hematologic_disorder	pediatric|genetics_and_genomics|hematology	autoimmune_diseases|anemia	lymphatic_disorder|immune_disorder|vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0958334	pulmonary hypertension, primary, 6	hereditary_disease|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|hereditary_disease	pulmonology|cardiology	primary_adrenal_gland_disease|cardiovascular_disorder	vascular_disorder|lung_disorder	false	false	false	true	high
MONDO:0958335	cutis laxa, autosomal recessive, type 1d	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	integumentary_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|dermatology	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder	skin_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0958342	isolated optic nerve aplasia	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|nervous_system_disorder	neurology|ophthalmology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	eye_disorder|brain_disorder	false	false	false	false	high
MONDO:0958343	PAPASH syndrome	syndromic_disease|connective_tissue_disorder	other	syndromic_disease|connective_tissue_disorder	pediatric|dermatology	inflammatory_disease|autoimmune_diseases	liver_disorder|biliary_disorder|skin_disorder	false	false	false	false	high
MONDO:0958344	spinal dermal sinus	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	dermatology|neurology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	spinal_disorder|skin_disorder	false	false	false	false	high
MONDO:0958345	limited dorsal myeloschisis	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	oncology|hematology	cancer|inflammatory_disease|neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|anemia	spinal_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0958346	isolated transitional filum lipoma	musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder|connective_tissue_disorder	orthopaedic|neurology|neurosurgery	cancer|inflammatory_disease|neurodegenerative_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0958347	isolated filum lipoma	musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder|connective_tissue_disorder	pediatric|dermatology|neurology	neurological_disorders|cancer|anatomic_abnormality	spinal_disorder|muscle_disorder	false	false	false	false	low
MONDO:0958348	retained medullary cord	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	congenital_abnormality|neurodegenerative_disease|spinal_cord_disease	spinal_disorder|muscle_disorder	false	false	false	false	medium
MONDO:0958349	dorsal spinal cord lipoma	musculoskeletal_system_disorder|nervous_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder|connective_tissue_disorder	pediatric|neurology	neurological_disorder|spinal_cord_tumor	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0958350	conus spinal cord lipoma	nervous_system_disorder|musculoskeletal_system_disorder|cancer_or_benign_tumor|connective_tissue_disorder|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|nervous_system_disorder|connective_tissue_disorder	orthopaedic|pediatric|neurology	neurodegenerative_disease|spinal_cord_disease|congenital_disorder	spinal_disorder|brain_disorder	false	false	false	false	medium
MONDO:0958351	hemi-myeloschisis	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	genetics_and_genomics|hematology|neurology	neurodegenerative_disease|anemia	spinal_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0958352	true myeloschisis	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|nervous_system_disorder	pediatric|oncology|hematology	cancer|anemia|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0958353	intermediate collagen VI-related muscular dystrophy	nervous_system_disorder|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	genetics_and_genomics|rheumatology|neurology	muscular_dystrophy|inflammatory_disease|genetic_disorder|metabolic_disorder	joint_disorder|muscle_disorder	false	false	false	true	high
MONDO:0958354	genetic central precocious puberty in female	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	endocrinology|obstetrics_and_gynecology|genetics_and_genomics	genetic|endocrine_disorder_is_not_in_list_so__genetic|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	high
MONDO:0958355	secondary central precocious puberty in female	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	pediatric|endocrinology|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0958356	primary central precocious puberty in male	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	pediatric|endocrinology	metabolic_disorder|endocrine_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	false	medium
MONDO:0958357	secondary central precocious puberty in male	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	endocrine_system_disorder	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder|disorder_of_development_or_morphogenesis	pediatric|endocrinology	autoimmune_diseases|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	high
MONDO:0968944	intellectual developmental disorder, autosomal recessive 82	hereditary_disease|metabolic_disease|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder|metabolic_disease	nervous_system_disorder|hereditary_disease|metabolic_disease|psychiatric_disorder	neurology|pediatric|genetics_and_genomics	metabolic_disorder|mental_health_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0968945	neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|psychiatry	neurodevelopmental_disorder|mental_health_disorder|neurodegenerative_disease	language_impairment|autism|brain_disorder|attention_deficit_hyperactivity_disorder	false	false	false	false	high
MONDO:0968946	developmental and epileptic encephalopathy 115	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	developmental_disorder|epileptic_encephalopathy|neurodegenerative_disease|autoimmune_diseases|inflammatory_disease	developmental_disorder|epileptic_disorder|neurological_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0968947	neurodevelopmental disorder plus optic atrophy	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0968949	palmoplantar keratoderma, epidermolytic	hereditary_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|integumentary_system_disorder|hereditary_disease	dermatology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	immune_disorder|skin_disorder	false	false	false	true	high
MONDO:0968951	hypouricemia, renal	hereditary_disease|urinary_system_disorder	other	urinary_system_disorder|hereditary_disease	renal_medicine|endocrinology|hematology	metabolic_disorder|renal_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	none
MONDO:0968955	hypocalcified amelogenesis imperfecta	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|mouth_disorder	orthopaedic|endocrinology|pediatric|hematology|dermatology|genetics_and_genomics	metabolic_disorder|genetic_disorder_is_implied_but_not_in_list_so_none_of_the_following_categories_have_that_term__therefore_cannot_be_used	bone_disorder|teeth_disorder	false	false	false	true	medium
MONDO:0968959	isolated arhinencephaly	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0968974	large B-cell lymphoma	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|autoimmune_diseases	lymphatic_disorder|immune_disorder|blood_bone_marrow_disorder	false	true	false	true	high
MONDO:0968976	neurodevelopmental disorder with progressive movement abnormalities	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0968977	basal ganglia calcification, idiopathic, 9, autosomal recessive	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric|psychiatry	autosomal_recessive_is_typically_associated_with_several_categories__however__since_we_re_considering_the_best_fit_based_on_the_provided_information__neurodegenerative_disease_appears_to_be_a_more_direct_association_due_to_basal_ganglia_involvement|metabolic_disorder|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0968978	aplasia cutis-enamel dysplasia syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	hematatology|pediatrics|genetics_and_genomics|dermatology	anemia|autoimmune_diseases|neurodegenerative_disease	teeth_disorder|skin_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0968979	neurodevelopmental disorder with hypotonia and seizures	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:0968980	otosclerosis 12	otorhinolaryngologic_disease|hereditary_disease|auditory_system_disorder	other	auditory_system_disorder|hereditary_disease|otorhinolaryngologic_disease	otolaryngology|genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases	ear_disorder	false	false	false	true	medium
MONDO:0968981	autosomal recessive nonsyndromic hearing loss 124	hereditary_disease|auditory_system_disorder|psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	auditory_system_disorder|hereditary_disease|nervous_system_disorder|psychiatric_disorder	otolaryngology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	ear_disorder	false	false	false	false	medium
MONDO:0968982	autoinflammation with episodic fever and immune dysregulation	hereditary_disease	other	hereditary_disease	rheumatology|immunology|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|joint_disorder	true	false	false	true	high
MONDO:0968983	proteasome-associated autoinflammatory syndrome 6	immune_system_disorder|hereditary_disease|syndromic_disease|connective_tissue_disorder	other	hereditary_disease|immune_system_disorder|connective_tissue_disorder|syndromic_disease	rheumatology|genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder	false	false	false	true	high
MONDO:0968986	chaotic conus spinal cord lipoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	nervous_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|connective_tissue_disorder|cancer_or_benign_tumor	neurology|oncology|pediatric	neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0968987	extramedullary conus spinal cord lipoma	disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|musculoskeletal_system_disorder|nervous_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	nervous_system_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|connective_tissue_disorder|cancer_or_benign_tumor	neurosurgery|neurology|oncology|pediatric	neurological_disease|cancer	brain_disorder|spinal_disorder	false	false	false	false	medium
MONDO:0968988	saccular spinal dysraphism with a stalk to the dome	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|pediatric	spinal_dysraphism|neurodegenerative_disease	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:0968989	non-saccular limited dorsal myeloschisis	disorder_of_development_or_morphogenesis|nervous_system_disorder	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	oncology|hematology	anemia|inflammatory_disease|neurodegenerative_disease	blood_bone_marrow_disorder|spinal_disorder	false	false	false	false	high
MONDO:0968990	genetic central precocious puberty in male	disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	genetics_and_genomics|pediatric|endocrinology	genetic|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0968991	non-genetic central precocious puberty in male	disorder_of_development_or_morphogenesis|endocrine_system_disorder|hereditary_disease|reproductive_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder	obstetrics_and_gynecology|pediatric|endocrinology	adrenal_gland_disease|metabolic_disorder	endocrine_disorder|reproductive_system_disorder	false	false	false	true	medium
MONDO:0970943	spermatogenic failure, X-linked, 8	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	pediatric|urology|genetics_and_genomics	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder	false	false	false	true	medium
MONDO:0970944	Leigh syndrome, mitochondrial	syndromic_disease	other	syndromic_disease	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0970945	developmental and epileptic encephalopathy 116	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	pediatric|genetics_and_genomics|neurology	epileptic_disorder|developmental_disorder|neurodegenerative_disease	spinal_disorder|developmental_disorder|brain_disorder|epilepsy_disorder	false	false	false	false	very_high
MONDO:0970950	Rothmund-Thomson syndrome, type 4	cancer_or_benign_tumor|integumentary_system_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	cancer_or_benign_tumor	hereditary_disease|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|syndromic_disease|integumentary_system_disorder	pediatric|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|bone_disorder|joint_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0970951	El Hayek-Chahrour neurodevelopmental disorder	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology	mental_health_disorder|neurodegenerative_disease	neurodevelopmental_disorder|brain_disorder	false	false	false	false	high
MONDO:0970952	spermatogenic failure 91	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	urology|genetics_and_genomics	cancer|metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder	false	false	false	false	medium
MONDO:0970957	terminal extramedullary conus spinal cord lipoma	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	oncology|pediatric|neurology|orthopaedic	cancer|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0970958	transitional extramedullary conus spinal cord lipoma	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	oncology|pediatric|neurology	cancer|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0970959	posterior extramedullary conus spinal cord lipoma	cancer_or_benign_tumor|nervous_system_disorder|disorder_of_development_or_morphogenesis|connective_tissue_disorder|musculoskeletal_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|disorder_of_development_or_morphogenesis|cancer_or_benign_tumor|musculoskeletal_system_disorder|connective_tissue_disorder	pediatric|genetics_and_genomics|neurology	cancer|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0970960	lipomatous non-saccular limited dorsal myeloschisis	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	hematology|neurology|oncology	cancer	muscle_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0970961	fibroneural non-saccular limited dorsal myeloschisis	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	hematology|neurology|oncology	inflammatory_disease|cancer|autoimmune_diseases|anemia|neurodegenerative_disease	spinal_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0970962	terminal myelocystocele	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|urology	cancer|neurodegenerative_disease	spinal_disorder|blood_bone_marrow_disorder	false	false	false	false	very_high
MONDO:0970963	saccular limited dorsal myeloschisis	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	hematology|neurology	inflammatory_disease|anemia|neurodegenerative_disease	spinal_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0970964	myelic limited dorsal malformation	nervous_system_disorder|disorder_of_development_or_morphogenesis	other	nervous_system_disorder|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology|orthopaedic	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	spinal_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0970993	immunodeficiency 119	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	immunology|allergy_and_immunology|pediatric	autoimmune_diseases|immunodeficiency|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	true	very_high
MONDO:0970994	immunodeficiency 120	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	immunology|genetics_and_genomics|allergy_and_immunology|pediatric	autoimmune_diseases|inflammatory_disease	lymphatic_disorder|immune_disorder	false	false	false	true	high
MONDO:0970995	premature ovarian failure 24	hereditary_disease|reproductive_system_disorder|endocrine_system_disorder	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	endocrinology|obstetrics_and_gynecology	autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0970998	auroneurodental syndrome	syndromic_disease	other	syndromic_disease	genetics_and_genomics|neurology	neurodegenerative_disease|autoimmune_diseases	teeth_disorder|brain_disorder|joint_disorder|ear_disorder|skin_disorder|eye_disorder	false	false	false	false	high
MONDO:0970999	spermatogenic failure 92	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	genetics_and_genomics|urology	metabolic_disorder|anemia	reproductive_system_disorder	false	false	false	false	medium
MONDO:0971000	spermatogenic failure 93	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	metabolic_disorder|endocrine_disorder|cancer	reproductive_system_disorder|bone_bone_marrow_disorder	false	false	false	false	high
MONDO:0971001	immunodeficiency 121 with autoinflammation	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|immunology|allergy_and_immunology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	true	false	false	false	high
MONDO:0971002	spermatogenic failure 94	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	genetics_and_genomics|urology	autoimmune_diseases|metabolic_disorder|anemia	reproductive_system_disorder	false	false	false	false	high
MONDO:0971004	amyloidosis, hereditary systemic 1	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|pathology	metabolic_disorder|neurodegenerative_disease	immune_disorder|vascular_disorder|kidney_disorder	false	false	false	true	high
MONDO:0971005	MHC class II deficiency 1	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|immunology|allergy_and_immunology	autoimmune_diseases|metabolic_disorder|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0971006	MHC class I deficiency 1	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|hematology|immunology|allergy_and_immunology	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0971007	neuroocular syndrome 1	hereditary_disease|disorder_of_visual_system|nervous_system_disorder	other	disorder_of_orbital_region|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	ophthalmology|genetics_and_genomics|neurology|pediatric	autoimmune_diseases|inflammatory_disease|neurodegenerative_disease	brain_disorder|eye_disorder	false	false	false	false	high
MONDO:0971008	amyloidosis, hereditary systemic 3	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|hematology|renal_medicine|rheumatology	autoimmune_diseases|metabolic_disorder|inflammatory_disease|neurodegenerative_disease	blood_bone_marrow_disorder|kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0971009	amyloidosis, hereditary systemic 5	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|hematology|renal_medicine|rheumatology	metabolic_disorder|neurodegenerative_disease	immune_disorder|vascular_disorder|kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0971010	amyloidosis, hereditary systemic 6	hereditary_disease|metabolic_disease|nervous_system_disorder	metabolic_disease	metabolic_disease|hereditary_disease|nervous_system_disorder	genetics_and_genomics|hematolgy|renal_medicine	hereditary_systemic_amyloidosis_can_be_linked_to_a_metabolic_disorder|metabolic_disorder|neurodegenerative_disease	vascular_disorder|kidney_disorder|liver_disorder	false	false	false	true	high
MONDO:0971011	MHC class I deficiency 2	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0971012	MHC class I deficiency 3	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|immunology	autoimmune_diseases|inflammatory_disease|cancer	immune_disorder|blood_bone_marrow_disorder	false	false	false	false	high
MONDO:0971013	MHC class II deficiency 2	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|pediatric|immunology|rheumatology	autoimmune_diseases|inflammatory_disease|immune_disorder___however__since_mhc_class_ii_deficiency_is_a_specific_type_of_immunodeficiency_disease__the_correct_answer_would_be___autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	false	high
MONDO:0971014	MHC class II deficiency 3	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|pediatric|immunology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|lymphatic_disorder	false	false	false	false	very_high
MONDO:0971015	MHC class II deficiency 4	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|allergy_and_immunology|rheumatology	autoimmune_diseases|inflammatory_disease	immune_disorder|blood_bone_marrow_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0971016	MHC class II deficiency 5	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	genetics_and_genomics|immunology|allergy_and_immunology	autoimmune_diseases|immunodeficiency_disorder	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0971031	auto-brewery syndrome	metabolic_disease	metabolic_disease	metabolic_disease	neurology|gastroenterology|hepatology|psychiatry|pulmonology	metabolic_disorder|autoimmune_diseases	liver_disorder|lower_gastrointestinal_disorder	false	false	true	true	medium
MONDO:0971032	bladder fermentation syndrome	metabolic_disease	metabolic_disease	metabolic_disease	urology|renal_medicine	metabolic_disorder|inflammatory_disease	urinary_tract_disorder|kidney_disorder	false	false	false	false	medium
MONDO:0971033	intrathyroid thymic carcinoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology|thoracic	cancer|thyroid_disease|autoimmune_diseases	blood_bone_marrow_disorder|endocrine_disorder|lymphatic_disorder	false	true	false	false	high
MONDO:0971034	thyroid gland cribriform morular carcinoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	thyroid_gland_disease|cancer|autoimmune_diseases	endocrine_disorder	false	true	false	false	high
MONDO:0971035	thyroid gland mixed medullary and follicular cell-derived carcinoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	cancer|autoimmune_diseases	thyroid_gland_disorder|endocrine_disorder	false	true	false	true	high
MONDO:0971036	thyroid gland mucinous carcinoma	cancer_or_benign_tumor|endocrine_system_disorder	endocrine_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|endocrine_system_disorder	oncology|endocrinology	adrenal_gland_disease|cancer|autoimmune_diseases	upper_gastrointestinal_disorder|endocrine_disorder	false	true	false	false	high
MONDO:0971043	neurodevelopmental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|upper_gastrointestinal_disorder|muscle_disorder	false	false	false	true	high
MONDO:0971044	Ehlers-Danlos syndrome, classic-like, 3	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis	rheumatology|genetics_and_genomics|dermatology	inflammatory_disease|cardiovascular_disorder|autoimmune_diseases	joint_disorder|skin_disorder|vascular_disorder	false	false	false	false	medium
MONDO:0971047	PRC-2 complex-related overgrowth spectrum	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|oncology	metabolic_disorder|cancer	joint_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:0971049	single isolated optic neuritis	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases	brain_disorder|eye_disorder	false	false	false	true	high
MONDO:0971050	relapsing isolated optic neuritis	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|neurology	autoimmune_diseases|inflammatory_disease	brain_disorder|eye_disorder	false	false	false	false	medium
MONDO:0971056	ocular surface squamous neoplasia	cancer_or_benign_tumor|disorder_of_visual_system	cancer_or_benign_tumor	cancer_or_benign_tumor|disorder_of_visual_system|disorder_of_orbital_region	ophthalmology|oncology	autoimmune_diseases|inflammatory_disease|cancer	skin_disorder|eye_disorder	false	true	false	true	high
MONDO:0971058	verruga peruana	infectious_disease	infectious_disease	infectious_disease	pediatric|dermatology	skin_disease_is_not_in_the_list_but_a_related_category_that_fits_would_be_skin_disease_which_is_equivalent_to_inflammatory_disease|autoimmune_diseases	liver_disorder|skin_disorder	true	false	false	true	medium
MONDO:0971062	developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to a NR4A2 point mutation	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	brain_disorder|parkinsonism_syndrome|developmental_delay|muscle_disorder	false	false	false	false	high
MONDO:0971063	autosomal dominant dopa-responsive dystonia	hereditary_disease|nervous_system_disorder|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	true	medium
MONDO:0971064	orofacial clefting-cardiac anomalies-facial dysmorphism syndrome	syndromic_disease|disorder_of_development_or_morphogenesis	other	syndromic_disease|disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric	congenital_anomaly|cardiovascular_disorder	teeth_disorder|heart_disorder|facial_disorder	false	false	false	false	high
MONDO:0971066	megaloblastic anemia-immunodeficiency due to folate transporter 1 deficiency	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|pediatric|hematology	metabolic_disorder|anemia	blood_bone_marrow_disorder|immune_disorder	false	false	false	true	high
MONDO:0971068	Phelan-McDermid syndrome due to 22q13.3 deletion	hereditary_disease|syndromic_disease|chromosomal_disorder	other	hereditary_disease|syndromic_disease|chromosomal_disorder	pediatrics|genetics_and_genomics|neurology	metabolic_disorder|anemia|neurodegenerative_disease	blood_bone_marrow_disorder|joint_disorder|immune_disorder|skin_disorder	false	false	false	false	high
MONDO:0971069	Phelan-McDermid syndrome due to SHANK3 mutation	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	neurology|genetics_and_genomics|pediatric|psychiatry	mental_health_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:0971077	episodic memory defect leukoencephalopathy	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	inflammatory_disease|neurodegenerative_disease	spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0971080	Grisel syndrome	syndromic_disease	other	syndromic_disease	endocrinology|genetics_and_genomics|pediatric	autoimmune_diseases|metabolic_disorder|adrenal_gland_disease	liver_disorder|biliary_disorder	false	false	false	false	high
MONDO:0971082	gastric duplication	digestive_system_disorder	other	digestive_system_disorder	other	other	other	other	other	other	other	
MONDO:0971083	gallbladder duplication	digestive_system_disorder	other	digestive_system_disorder	other	other	other	other	other	other	other	
MONDO:0971084	colonic duplication	digestive_system_disorder	other	digestive_system_disorder	other	other	other	other	other	other	other	
MONDO:0971085	pyloric duplication	digestive_system_disorder	other	digestive_system_disorder	other	other	other	other	other	other	other	
MONDO:0971086	small intestine duplication	digestive_system_disorder	other	digestive_system_disorder	other	other	other	other	other	other	other	
MONDO:0971089	vasa previa	obstetric_disorder	other	obstetric_disorder	other	other	other	other	other	other	other	
MONDO:0971091	acute megakaryoblastic leukemia in adult	cancer_or_benign_tumor|musculoskeletal_system_disorder|hematologic_disorder|connective_tissue_disorder|immune_system_disorder	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor|hematologic_disorder|acute_disease|connective_tissue_disorder|immune_system_disorder	oncology|hematology	cancer|anemia	blood_bone_marrow_disorder	false	true	false	false	high
MONDO:0971092	soft and hard cleft palate	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	otolaryngology|pediatric	metabolic_disorder|congenital_abnormality	throat_disorder|teeth_disorder	false	false	false	true	high
MONDO:0971093	MGP-related spondyloepiphyseal dysplasia	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	musculoskeletal_system_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	orthopaedic|genetics_and_genomics|pediatric	bone_disease|metabolic_disorder|genetic_disorder|skeletal_dysplasia	spinal_disorder|bone_disorder	false	false	false	false	medium
MONDO:0971094	cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome due to TAB2 mutation	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	disorder_of_development_or_morphogenesis|cardiovascular_disorder	genetics_and_genomics|cardiology|pediatric	metabolic_disorder|cardiovascular_disorder	joint_disorder|heart_disorder|growth_disorder	false	false	false	false	high
MONDO:0971095	6q25.1 microdeletion syndrome	disorder_of_development_or_morphogenesis|cardiovascular_disorder|chromosomal_disorder	cardiovascular_disorder	chromosomal_disorder|disorder_of_development_or_morphogenesis|cardiovascular_disorder	genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	spinal_disorder|muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:0971103	Nicolau syndrome	integumentary_system_disorder	other	integumentary_system_disorder	pediatric|pulmonology	inflammatory_disease|autoimmune_diseases	kidney_disorder|immune_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:0971105	neonatal renal venous thrombosis	urinary_system_disorder	other	urinary_system_disorder	pediatric|hematology|renal_medicine	cardiovascular_disorder|inflammatory_disease|metabolic_disorder	vascular_disorder|kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:0971107	common arterial trunk with aortic dominance	disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiothoracic|cardiology	cardiovascular_disorder|aortocaval_fistula	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:0971108	common arterial trunk with pulmonary dominance and interrupted aortic arch	cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis	pediatric|cardiothoracic|cardiology	cardiovascular_disorder|interrupted_aortic_arch|pulmonary_dominance	vascular_disorder|heart_disorder	false	false	false	false	very_high
MONDO:0971109	isolated congenital femoral bifurcation	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0971111	intraoral basal cell carcinoma	digestive_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	mouth_disorder|cancer_or_benign_tumor|digestive_system_disorder	otolaryngology|dermatology|oncology	intraoral_basal_cell_carcinoma_is_actually_a_type_of_skin_cancer_but_more_specifically_a_type_of_squamous_cell_carcinoma|cancer	teeth_disorder|skin_disorder	false	true	false	false	high
MONDO:0971115	benign vascular tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	oncology|hematology|cardiology	cardiovascular_disorder|cancer	vascular_disorder|bone_disorder	false	false	false	true	low
MONDO:0971116	borderline vascular tumor	cardiovascular_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor|cardiovascular_disorder	cardiovascular_disorder|cancer_or_benign_tumor	oncology|hematology	cancer|adrenal_gland_disease|other____corrected_list___adrenal_gland_disease	vascular_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0971118	pilocytic astrocytoma with histological features of anaplasia	nervous_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	high
MONDO:0971119	proteoglycan-related bone disorder	musculoskeletal_system_disorder	other	musculoskeletal_system_disorder	rheumatology|genetics_and_genomics|orthopaedic	inflammatory_disease|autoimmune_diseases|metabolic_disorder	spinal_disorder|bone_disorder	false	false	false	false	high
MONDO:0971123	isolated retinal racemose hemangioma	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder|disorder_of_orbital_region	oncology|ophthalmology	cardiovascular_disorder|inflammatory_disease|anemia|cancer	vascular_disorder|eye_disorder	false	false	false	false	low
MONDO:0971124	perifoveal exudative vascular anomalous complex	nervous_system_disorder|disorder_of_visual_system|cardiovascular_disorder	cardiovascular_disorder	disorder_of_visual_system|nervous_system_disorder|cardiovascular_disorder|disorder_of_orbital_region	neurology|ophthalmology	cardiovascular_disorder|inflammatory_disease	vascular_disorder|eye_disorder	false	false	false	false	high
MONDO:0971125	torpedo maculopathy	nervous_system_disorder|disorder_of_visual_system	other	disorder_of_visual_system|nervous_system_disorder|disorder_of_orbital_region	genetics_and_genomics|neurology|ophthalmology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	eye_disorder|brain_disorder	false	false	false	false	medium
MONDO:0971126	isolated angioid streaks	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases	vascular_disorder|eye_disorder	false	false	false	false	low
MONDO:0971127	diffuse unilateral subacute neuroretinitis	infectious_disease|disorder_of_visual_system	infectious_disease	disorder_of_visual_system|infectious_disease|disorder_of_orbital_region	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	true	false	false	false	medium
MONDO:0971128	multiple evanescent white dot syndrome	disorder_of_visual_system|inflammatory_disease	other	disorder_of_visual_system|inflammatory_disease|disorder_of_orbital_region	neurology|ophthalmology	inflammatory_disease|autoimmune_diseases	immune_disorder|eye_disorder	false	false	false	false	low
MONDO:0971129	stellate multiform amelanotic choroidopathy	disorder_of_visual_system	other	disorder_of_visual_system|disorder_of_orbital_region	genetics_and_genomics|dermatology|ophthalmology	inflammatory_disease|autoimmune_diseases|cancer	eye_disorder|skin_disorder	false	false	false	false	high
MONDO:0971130	choroidal osteoma	nervous_system_disorder|cancer_or_benign_tumor|disorder_of_visual_system|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	disorder_of_visual_system|nervous_system_disorder|cancer_or_benign_tumor|cardiovascular_disorder|disorder_of_orbital_region	ophthalmology	inflammatory_disease|autoimmune_diseases|metabolic_disorder	bone_disorder|eye_disorder	false	false	false	false	medium
MONDO:0971131	bilateral diffuse uveal melanocytic proliferation disease	syndromic_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|syndromic_disease	genetics_and_genomics|neurology|oncology|hematatology|pediatric|ophthalmology	inflammatory_disease|autoimmune_diseases|cancer	eye_disorder	false	true	false	false	high
MONDO:0971133	isolated segmental infantile hemangioma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	oncology|dermatology|pediatric	cancer|infantile_hemangioma	skin_disorder|vascular_disorder	false	false	false	true	low
MONDO:0971137	severe congenital myelofibrosis-pancytopenia-intellectual disability-neurologic and ophthalmic abnormalities syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|neurology|hematology|pediatric|ophthalmology	metabolic_disorder|neurodegenerative_disease|anemia	blood_bone_marrow_disorder|immune_disorder|eye_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0971138	progressive hypotonia-intellectual disability-facial dysmorphism syndrome due to FYVE-defective RBSN	hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	intellectual_disability_is_not_in_the_list_so__joint_disorder|muscle_disorder|eye_disorder|brain_disorder	false	false	false	false	very_high
MONDO:0971140	well-differentiated papillary mesothelial tumour of the pleura	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pulmonology|cardiothoracic	cancer|mesothelioma|pleural_disease	lung_disorder|pleura_disorder	false	true	false	false	medium
MONDO:0971141	localized pleural mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pulmonology|cardiothoracic	cancer|localized_tumor	lung_disorder|pleural_disorder	false	true	false	false	high
MONDO:0971142	diffused pleural mesothelioma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pulmonology|cardiothoracic	cancer|inflammatory_disease|autoimmune_diseases	lung_disorder|lymphatic_disorder	false	true	false	false	very_high
MONDO:0971143	pleural mesothelioma in situ	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|pulmonology	cancer|inflammatory_disease|autoimmune_diseases	lung_disorder	false	true	false	false	very_high
MONDO:0971145	peritoneal mesothelioma in situ	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	oncology|hematology|pulmonology|genetics_and_genomics	cancer|inflammatory_disease|autoimmune_diseases	lower_gastrointestinal_disorder|lung_disorder	false	true	false	false	high
MONDO:0971149	spastic paraplegia 30b, autosomal recessive	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0971150	neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	genetics_and_genomics|neurology|pediatric	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	false	high
MONDO:0971151	immunodeficiency 122	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	immunology|pediatric|allergy_and_immunology	immunodeficiency|autoimmune_diseases	blood_bone_marrow_disorder|immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0971152	hearing loss, autosomal recessive 125	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease|auditory_system_disorder	genetics_and_genomics|otolaryngology|pediatric	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	autosomal_recessive_disorder|ear_disorder	false	false	false	false	medium
MONDO:0971154	hepatic cutaneous porphyria	digestive_system_disorder|endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|metabolic_disease|digestive_system_disorder	dermatology|hepatology	autoimmune_diseases|metabolic_disorder	liver_disorder|skin_disorder	false	false	false	true	low
MONDO:0971170	prostate cancer, hereditary, X-linked 3	syndromic_disease|cancer_or_benign_tumor|hereditary_disease	cancer_or_benign_tumor	cancer_or_benign_tumor|hereditary_disease|syndromic_disease	urology|genetics_and_genomics|oncology	cancer|x_linked_disease|hereditary_disease	reproductive_system_disorder|hereditary|x_linked	false	true	false	true	high
MONDO:0971171	muscular dystrophy, limb-girdle, autosomal recessive 29	nervous_system_disorder|hereditary_disease|musculoskeletal_system_disorder	other	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	orthopaedic|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	joint_disorder|muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0971172	neurodevelopmental disorder with hypotonia, brain anomalies, distinctive facies, and absent language	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	pediatric|psychiatry|genetics_and_genomics|neurology	autoimmune_diseases|inflammatory_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder|brain_disorder	false	false	false	true	very_high
MONDO:0971173	autoinflammation with arthritis and vasculitis	hereditary_disease	other	hereditary_disease	immunology_is_not_listed_but_can_be_inferred_as_part_of_allergy_and_immunology|allergy_and_immunology|rheumatology|hematology|genetics_and_genomics	autoimmune_diseases|inflammatory_disease	joint_disorder|immune_disorder|vascular_disorder	true	false	false	true	high
MONDO:0971174	multiple mitochondrial dysfunctions syndrome 9b	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|mitochondrial_disease	metabolic_disease	metabolic_disease|hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis	pediatric|genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|mitochondrial_disease	true	false	false	false	very_high
MONDO:0971175	cardiomyopathy, dilated, 2K	hereditary_disease|musculoskeletal_system_disorder|cardiovascular_disorder	cardiovascular_disorder	musculoskeletal_system_disorder|hereditary_disease|cardiovascular_disorder	cardiothoracic|cardiology	autoimmune_diseases|metabolic_disorder|cardiovascular_disorder	heart_disorder|muscle_disorder|kidney_disorder	false	false	false	false	high
MONDO:0971176	ovarian dysgenesis 11	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	obstetrics_and_gynecology|genetics_and_genomics	cancer|autoimmune_diseases|metabolic_disorder	reproductive_system_disorder|endocrine_disorder	false	false	false	false	high
MONDO:0971177	immunodeficiency 123 with HPV-related verrucosis	immune_system_disorder|hereditary_disease	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|obstetrics_and_gynecology|oncology	cancer|autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	high
MONDO:0971178	polycystic kidney disease 8	hereditary_disease|urinary_system_disorder	other	hereditary_disease|urinary_system_disorder	renal_medicine|endocrinology|urology	autoimmune_diseases|inflammatory_disease|metabolic_disorder	endocrine_disorder|kidney_disorder	false	false	false	false	high
MONDO:0971179	arterial tortuosity-bone fragility syndrome	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	pediatrics|rheumatology|orthopaedic|cardiology|genetics_and_genomics	metabolic_disorder|cardiovascular_disorder	bone_disorder|vascular_disorder	false	false	false	false	high
MONDO:0975705	otofacial neurodevelopmental syndrome	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology|pediatric	neurodegenerative_disease	ear_disorder|brain_disorder	false	false	false	false	high
MONDO:0975745	neurodevelopmental disorder with characteristic facial and ectodermal features and tetraparesis 1	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|metabolic_disorder|autoimmune_diseases	brain_disorder|muscle_disorder|eye_disorder	false	false	false	false	very_high
MONDO:0975746	spastic paraplegia 92, autosomal recessive	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder|autosomal_recessive_diseases_is_incorrect__this_has_been_changed_to___neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	high
MONDO:0975747	spermatogenic failure 95	hereditary_disease|reproductive_system_disorder	other	reproductive_system_disorder|hereditary_disease	endocrinology|genetics_and_genomics|urology	anemia|cancer	reproductive_system_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:0975749	immunodeficiency 125	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|immunology|genetics_and_genomics	immunodeficiency_does_not_match_any_category|inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0975751	brain abnormalities-severe developmental delay-facial dysmorphism-intellectual disability syndrome due to MEF2C mutation	syndromic_disease	other	syndromic_disease	neurology|genetics_and_genomics|pediatric	brain_abnormalities|neurodegenerative_disease|metabolic_disorder|mental_health_disorder	facial_dysmorphism|brain_disorder|brain_abnormality|developmental_delay|intellectual_disability	false	false	false	true	very_high
MONDO:0975752	littoral cell hemangioma of the spleen	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hematology|hepatology|oncology	cancer	vascular_disorder|lymphatic_disorder	false	false	false	false	low
MONDO:0975753	papillary hemangioma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hematology|dermatology	cardiovascular_disorder|cancer	vascular_disorder|skin_disorder	false	false	false	true	low
MONDO:0975754	pseudomyogenic hemangioendothelioma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hematology|oncology	adrenal_gland_disease|cancer	muscle_disorder|vascular_disorder	false	true	false	true	high
MONDO:0975755	eccrine angiomatous hamartoma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	genetics_and_genomics|dermatology|oncology	adrenal_gland_disease|cancer	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0975756	reactive angioendotheliomatosis	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hematology|oncology	cancer|inflammatory_disease|autoimmune_diseases	immune_disorder|blood_bone_marrow_disorder|vascular_disorder	false	false	false	false	high
MONDO:0975757	anastomosing haemangioma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hematology|dermatology|oncology	adrenal_gland_disease|cancer	vascular_disorder|skin_disorder	false	false	false	false	medium
MONDO:0975758	microvenular haemangioma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hematology|dermatology|oncology	anemia|cardiovascular_disorder|cancer|inflammatory_disease	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0975759	acquired elastotic haemangioma	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	cancer_or_benign_tumor|cardiovascular_disorder	hematology|oncology	cardiovascular_disorder|cancer	vascular_disorder|skin_disorder	false	false	false	false	low
MONDO:0975761	immunodeficiency 126, susceptibility to	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	allergy_and_immunology|immunology|genetics_and_genomics|pediatric	inflammatory_disease|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:0975795	Kariminejad neurodevelopmental syndrome	hereditary_disease|syndromic_disease|nervous_system_disorder	other	syndromic_disease|nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0975796	spastic paraplegia 93, autosomal recessive	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0975797	myelofibrosis, congenital, with anemia, neutropenia, developmental delay, and ocular abnormalities	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0975798	methylmalonic aciduria and homocystinuria, cb1L type	nutritional_disorder|hereditary_disease|hematologic_disorder|metabolic_disease	anemia|metabolic_disease	hematologic_disorder|metabolic_disease|nutritional_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0975799	brain malformation renal syndrome	hereditary_disease|syndromic_disease	other	syndromic_disease|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0975800	spinocerebellar ataxia 51	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder|neurodegenerative_disease	psychiatric_disorder|hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0975801	encephalopathy, acute transient	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0975805	foveal hypoplasia 3	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:0975806	multiple mitochondrial dysfunctions syndrome 10	disorder_of_development_or_morphogenesis|metabolic_disease|mitochondrial_disease|hereditary_disease	metabolic_disease	hereditary_disease|mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0975807	cholestasis, progressive familial intrahepatic, 13	endocrine_system_disorder|metabolic_disease|syndromic_disease|digestive_system_disorder|hereditary_disease	endocrine_system_disorder|metabolic_disease	endocrine_system_disorder|hereditary_disease|digestive_system_disorder|syndromic_disease|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0975808	congenital myopathy 25	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	other	other	other	other	other	other	other	
MONDO:0975809	microphthalmia/coloboma 13	disorder_of_visual_system|hereditary_disease	other	hereditary_disease|disorder_of_visual_system|disorder_of_orbital_region	other	other	other	other	other	other	other	
MONDO:0975810	short stature with nonspecific skeletal abnormalities	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:0975826	arthrogryposis multiplex congenita 7, X-linked	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0975827	orofaciodigital syndrome 21	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease	other	other	other	other	other	other	other	
MONDO:0975828	intellectual developmental disorder, X-linked 114	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	psychiatric_disorder|hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0975829	anemia, congenital dyserythropoietic, type IVb	hereditary_disease|hematologic_disorder	anemia	hematologic_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0975830	myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 2	musculoskeletal_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|syndromic_disease	other	other	other	other	other	other	other	
MONDO:0975832	immunodeficiency 127	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	other	other	other	other	other	other	other	
MONDO:0975833	leukodystrophy, hypomyelinating, 28	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0975834	immunodeficiency 128	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	other	other	other	other	other	other	other	
MONDO:0975835	bronchiectasis and nasal polyposis	respiratory_system_disorder|hereditary_disease	other	respiratory_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0975836	Karayol-Borroto-Haghshenas neurodevelopmental syndrome	nervous_system_disorder|syndromic_disease|hereditary_disease	other	nervous_system_disorder|hereditary_disease|syndromic_disease	other	other	other	other	other	other	other	
MONDO:0975837	neurodegeneration, infantile-onset, with optic atrophy and brain abnormalities	syndromic_disease|hereditary_disease	other	hereditary_disease|syndromic_disease	other	other	other	other	other	other	other	
MONDO:0975838	intellectual developmental disorder, autosomal dominant 75	psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0975839	pancreatic agenesis 3	hereditary_disease|disorder_of_development_or_morphogenesis	other	hereditary_disease|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0975840	retinitis pigmentosa 98	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|metabolic_disease|hereditary_disease	psychiatric_disorder|metabolic_disease	nervous_system_disorder|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|disorder_of_orbital_region|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0975841	fibromatosis, gingival, 6	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|mouth_disorder|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0975842	spermatogenic failure 96	reproductive_system_disorder|hereditary_disease	other	hereditary_disease|reproductive_system_disorder	other	other	other	other	other	other	other	
MONDO:0975843	premature ovarian failure 25	reproductive_system_disorder|endocrine_system_disorder|hereditary_disease	endocrine_system_disorder	hereditary_disease|endocrine_system_disorder|reproductive_system_disorder	other	other	other	other	other	other	other	
MONDO:0975846	congenital disorder of glycosylation, type 1DD	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0975847	autoimmune disease with susceptibility to mycobacterium tuberculosis	immune_system_disorder	autoimmune_disease	immune_system_disorder	other	other	other	other	other	other	other	
MONDO:0975848	Morimoto-Ryu-Malicdan neuromuscular syndrome	nervous_system_disorder|syndromic_disease|hereditary_disease	other	nervous_system_disorder|hereditary_disease|syndromic_disease	other	other	other	other	other	other	other	
MONDO:0975862	B-lymphoblastic leukemia with MEF2D rearrangement	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	acute_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	other	other	other	other	other	other	other	
MONDO:0975863	B-lymphoblastic leukemia with MYC rearrangement	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	acute_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	other	other	other	other	other	other	other	
MONDO:0975864	B-lymphoblastic leukemia with NUTM1 rearrangement	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	acute_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	other	other	other	other	other	other	other	
MONDO:0975865	B-lymphoblastic leukemia with PAX5alt	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	acute_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	other	other	other	other	other	other	other	
MONDO:0975866	B-lymphoblastic leukemia with TCF3-HLF fusion	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	acute_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	other	other	other	other	other	other	other	
MONDO:0975867	B-lymphoblastic leukemia with ZNF384 rearrangement	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	cancer_or_benign_tumor	acute_disease|hematologic_disorder|immune_system_disorder|cancer_or_benign_tumor	other	other	other	other	other	other	other	
MONDO:0975868	acute myeloid leukemia with CBFA2T3-GLIS2 fusion	connective_tissue_disorder|cancer_or_benign_tumor|immune_system_disorder|musculoskeletal_system_disorder|hematologic_disorder	cancer_or_benign_tumor	connective_tissue_disorder|acute_disease|hematologic_disorder|musculoskeletal_system_disorder|immune_system_disorder|cancer_or_benign_tumor	other	other	other	other	other	other	other	
MONDO:0975870	acute myeloid leukemia with FUS-ERG fusion	musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	acute_disease|musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	other	other	other	other	other	other	other	
MONDO:0975871	acute myeloid leukemia with MNX1-ETV6 fusion	musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	acute_disease|musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	other	other	other	other	other	other	other	
MONDO:0975872	acute myeloid leukemia with NPM1-MLF1 fusion	musculoskeletal_system_disorder|connective_tissue_disorder|hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	acute_disease|musculoskeletal_system_disorder|connective_tissue_disorder|immune_system_disorder|cancer_or_benign_tumor|hematologic_disorder	other	other	other	other	other	other	other	
MONDO:0975874	neurodevelopmental disorder with dysmorphic facies, absent speech and ambulation, and brain abnormalities	nervous_system_disorder|syndromic_disease|hereditary_disease	other	hereditary_disease|nervous_system_disorder|syndromic_disease	other	other	other	other	other	other	other	
MONDO:0975875	basal ganglia calcification, idiopathic, 10, autosomal recessive	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0975877	neurodevelopmental disorder with variable familial hypercholanemia	nervous_system_disorder|hereditary_disease|syndromic_disease	other	hereditary_disease|nervous_system_disorder|syndromic_disease	other	other	other	other	other	other	other	
MONDO:0975882	intellectual disability-epilepsy-dental anomalies-facial dysmorphism syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0975885	hypertrophic olivary degeneration	nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0975887	2q13 microdeletion syndrome	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	chromosomal_disorder|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0975890	mesothelioma of the tunica vaginalis	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	other	other	other	other	other	other	other	
MONDO:0975891	combined immunodeficiency due to TBX1 deficiency	immune_system_disorder|hereditary_disease	other	hereditary_disease|immune_system_disorder	other	other	other	other	other	other	other	
MONDO:0975895	non-fibrotic hypersensitivity pneumonitis	immune_system_disorder|inflammatory_disease|respiratory_system_disorder	other	inflammatory_disease|immune_system_disorder|respiratory_system_disorder	other	other	other	other	other	other	other	
MONDO:0975896	fibrotic hypersensitivity pneumonitis	immune_system_disorder|inflammatory_disease|respiratory_system_disorder	other	inflammatory_disease|immune_system_disorder|respiratory_system_disorder	other	other	other	other	other	other	other	
MONDO:0975897	post 5-alpha-reductase inhibitors treatment syndrome	nervous_system_disorder	other	nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0975898	post-selective serotonin reuptake inhibitor sexual dysfunction	nervous_system_disorder	other	nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0975902	isolated congenital cholesteatoma of the middle ear	otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis	other	otorhinolaryngologic_disease|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0975904	10p15 microdeletion syndrome	chromosomal_disorder	other	chromosomal_disorder	other	other	other	other	other	other	other	
MONDO:0975905	10p13-p14 deletion syndrome	disorder_of_development_or_morphogenesis|chromosomal_disorder|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis|chromosomal_disorder	other	other	other	other	other	other	other	
MONDO:0975906	unifocal langerhans cell histiocytosis	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	other	other	other	other	other	other	other	
MONDO:0975907	pulmonary langerhans cell histiocytosis	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	other	other	other	other	other	other	other	
MONDO:0975908	single-system multifocal langerhans cell histiocytosis	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	other	other	other	other	other	other	other	
MONDO:0975909	multisystem langerhans cell histiocytosis	hematologic_disorder|cancer_or_benign_tumor|immune_system_disorder	cancer_or_benign_tumor	cancer_or_benign_tumor|immune_system_disorder|hematologic_disorder	other	other	other	other	other	other	other	
MONDO:0975910	splenic venous malformation	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	other	other	other	other	other	other	other	
MONDO:0975911	reticular dysgenesis-like severe combined immunodeficiency	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0975918	asymptomatic hyperckemia-myalgia-rhabdomyolysis syndrome	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	other	musculoskeletal_system_disorder|hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0975922	acquired hypothalamic obesity	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	other	other	other	other	other	other	other	
MONDO:0975925	adenoid ameloblastoma	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor|musculoskeletal_system_disorder|mouth_disorder	other	other	other	other	other	other	other	
MONDO:0975951	spastic paraplegia, mitochondrial	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:0975952	cerebral cavernous malformations 5	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0975953	Pan-Chung-Bellen syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	other	other	other	other	other	other	other	
MONDO:0975955	autoinflammation, panniculitis, and dermatosis syndrome	hereditary_disease|immune_system_disorder	other	hereditary_disease|immune_system_disorder	other	other	other	other	other	other	other	
MONDO:0975957	telangiectasia, impaired intellectual development, microcephaly, metaphyseal dysplasia, eye abnormalities, and short stature	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	other	other	other	other	other	other	other	
MONDO:0975958	spermatogenic failure 97	hereditary_disease|reproductive_system_disorder	other	hereditary_disease|reproductive_system_disorder	other	other	other	other	other	other	other	
MONDO:0976123	spermatogenic failure, X-linked, 9	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976124	intellectual developmental disorder with polymicrogyria and seizures	nervous_system_disorder|hereditary_disease|psychiatric_disorder	psychiatric_disorder	hereditary_disease|psychiatric_disorder|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0976125	neurodevelopmental disorder with speech or visual impairment and brain hypomyelination	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0976126	neurodevelopmental disorder with microcephaly, absent speech, and hypotonia	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0976127	Muggenthaler-Chowdhury-Chioza syndrome	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976129	premature ovarian failure 26	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	endocrine_system_disorder	reproductive_system_disorder|hereditary_disease|endocrine_system_disorder	other	other	other	other	other	other	other	
MONDO:0976130	neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies	nervous_system_disorder	other	nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0976131	neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0976132	mitochondrial dna depletion syndrome 21	mitochondrial_disease|disorder_of_development_or_morphogenesis|metabolic_disease|hereditary_disease	metabolic_disease	mitochondrial_disease|hereditary_disease|disorder_of_development_or_morphogenesis|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0976133	myopathy, myofibrillar, 13, with rimmed vacuoles	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	other	other	other	other	other	other	other	
MONDO:0976134	heterotaxy, visceral, 13, autosomal	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0976135	heterotaxy, visceral, 14, autosomal	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|cardiovascular_disorder	cardiovascular_disorder	syndromic_disease|cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:0976136	ocular pterygium-digital keloid dysplasia syndrome	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976137	oocyte/zygote/embryo maturation arrest 22	reproductive_system_disorder|hereditary_disease	other	reproductive_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976138	leukodystrophy, demyelinating, adult-onset	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0976226	neuronopathy, distal hereditary motor, autosomal dominant 15	hereditary_disease|nervous_system_disorder	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976227	Charcot-Marie-tooth disease, axonal, type 2JJ	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976228	immunodeficiency 132b	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976229	immunodeficiency 131	hereditary_disease|immune_system_disorder	other	immune_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976230	spondyloepimetaphyseal dysplasia, Li-Shao-Li type	hereditary_disease|musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976231	intellectual developmental disorder, autosomal recessive 83	hereditary_disease|metabolic_disease|nervous_system_disorder|psychiatric_disorder	psychiatric_disorder|metabolic_disease	nervous_system_disorder|psychiatric_disorder|hereditary_disease|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0976232	Perrault syndrome 7	hereditary_disease|metabolic_disease|reproductive_system_disorder|disorder_of_development_or_morphogenesis|endocrine_system_disorder|mitochondrial_disease	endocrine_system_disorder|metabolic_disease	disorder_of_development_or_morphogenesis|mitochondrial_disease|endocrine_system_disorder|reproductive_system_disorder|hereditary_disease|metabolic_disease	other	other	other	other	other	other	other	
MONDO:0976233	neurodevelopmental disorder with progressive spasticity and brain abnormalities	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976234	tubulointerstitial kidney disease, autosomal dominant 6	urinary_system_disorder|hereditary_disease	other	hereditary_disease|urinary_system_disorder	other	other	other	other	other	other	other	
MONDO:0976236	neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairment	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976261	congenital disorder of glycosylation type 1EE with or without immunodeficiency	hereditary_disease|metabolic_disease	metabolic_disease	metabolic_disease|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976262	holoprosencephaly 10	hereditary_disease|nervous_system_disorder|disorder_of_development_or_morphogenesis|syndromic_disease|endocrine_system_disorder	endocrine_system_disorder	syndromic_disease|disorder_of_development_or_morphogenesis|nervous_system_disorder|endocrine_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976263	neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976264	neurodevelopmental disorder with white matter abnormalities and gait disturbance	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976265	neurodevelopmental disorder with poor growth, seizures, and brain abnormalities	hereditary_disease|nervous_system_disorder	other	nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976266	diarrhea 14, congenital	hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976268	diarrhea 15, congenital	hereditary_disease|digestive_system_disorder	other	digestive_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:0976269	cranioectodermal dysplasia 5	hereditary_disease|urinary_system_disorder|respiratory_system_disorder|integumentary_system_disorder|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|syndromic_disease	other	respiratory_system_disorder|syndromic_disease|integumentary_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|urinary_system_disorder|musculoskeletal_system_disorder	other	other	other	other	other	other	other	
MONDO:0976285	neurodevelopmental disorder with poor or absent speech, dysmorphic facies, and behavioral abnormalities	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:0976286	Tayoun-Maawali syndrome	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	other	other	other	other	other	other	other	
MONDO:1010000	pythiosis	infectious_disease	infectious_disease	infectious_disease	dermatology	inflammatory_disease|autoimmune_diseases	fungal_infection|skin_disorder	true	false	false	true	high
MONDO:1010029	aleutian mink disease, human	infectious_disease	infectious_disease	infectious_disease	hepatology|virology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder	false	false	false	false	low
MONDO:1010030	pediatric high-grade glioma	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	neurology|oncology|pediatric	neurodegenerative_disease|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:1010064	anti-MDA5 dermatomyositis	inflammatory_disease|integumentary_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	other	connective_tissue_disorder|musculoskeletal_system_disorder|inflammatory_disease|integumentary_system_disorder|idiopathic_disease	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|skin_disorder|immune_disorder	false	false	false	true	very_high
MONDO:1010065	anti-Mi2 dermatomyositis	inflammatory_disease|integumentary_system_disorder|connective_tissue_disorder|musculoskeletal_system_disorder	other	connective_tissue_disorder|musculoskeletal_system_disorder|inflammatory_disease|integumentary_system_disorder|idiopathic_disease	dermatology|rheumatology	autoimmune_diseases|inflammatory_disease	muscle_disorder|immune_disorder	true	false	false	true	high
MONDO:1010084	anti-NXP2 dermatomyositis	musculoskeletal_system_disorder|integumentary_system_disorder|connective_tissue_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|integumentary_system_disorder|inflammatory_disease|idiopathic_disease|connective_tissue_disorder	rheumatology|dermatomyositis	inflammatory_disease|autoimmune_diseases	muscle_disorder|immune_disorder	false	false	false	true	high
MONDO:1010087	anti-TIF1 dermatomyositis	musculoskeletal_system_disorder|integumentary_system_disorder|connective_tissue_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|integumentary_system_disorder|inflammatory_disease|idiopathic_disease|connective_tissue_disorder	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	muscle_disorder|skin_disorder|immune_disorder	false	false	false	true	high
MONDO:1010088	anti-SAE dermatomyositis	musculoskeletal_system_disorder|integumentary_system_disorder|connective_tissue_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|integumentary_system_disorder|inflammatory_disease|idiopathic_disease|connective_tissue_disorder	rheumatology|allergy_and_immunology	inflammatory_disease|autoimmune_diseases	muscle_disorder|skin_disorder|immune_disorder	false	false	false	true	high
MONDO:1010089	hypomyopathic dermatomyositis	musculoskeletal_system_disorder|integumentary_system_disorder|connective_tissue_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|integumentary_system_disorder|inflammatory_disease|idiopathic_disease|connective_tissue_disorder	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	muscle_disorder|immune_disorder	false	false	false	true	medium
MONDO:1010096	clinically amyopathic dermatomyositis	musculoskeletal_system_disorder|integumentary_system_disorder|connective_tissue_disorder|inflammatory_disease	other	musculoskeletal_system_disorder|integumentary_system_disorder|inflammatory_disease|idiopathic_disease|connective_tissue_disorder	rheumatology|dermatology	inflammatory_disease|autoimmune_diseases	muscle_disorder|immune_disorder	false	false	false	true	medium
MONDO:1010097	DHDDS-related syndrome	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	brain_disorder|muscle_disorder	false	false	false	false	medium
MONDO:1010098	TFAP2B-related congenital heart disease spectrum disorder	hereditary_disease|disorder_of_development_or_morphogenesis|cardiovascular_disorder	cardiovascular_disorder	hereditary_disease|cardiovascular_disorder|disorder_of_development_or_morphogenesis	cardiology|pediatric|genetics_and_genomics	congenital_heart_disease|cardiovascular_disorder	heart_disorder|congenital_heart_disease	false	false	false	false	high
MONDO:1010100	myxedema coma	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	other	other	other	other	other	other	other	
MONDO:1010108	myxedema heart disease	endocrine_system_disorder	endocrine_system_disorder	endocrine_system_disorder	other	other	other	other	other	other	other	
MONDO:1010111	loin pain hematuria syndrome	nervous_system_disorder|syndromic_disease	other	syndromic_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:1010112	isolated short stature	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:1010116	sudden unexpected infant death	other	other	idiopathic_disease	other	other	other	other	other	other	other	
MONDO:1010117	sudden unexplained death in childhood	other	other	idiopathic_disease	other	other	other	other	other	other	other	
MONDO:1010120	sudden unexpected death in pediatrics	other	other	idiopathic_disease	other	other	other	other	other	other	other	
MONDO:1010122	trichrome vitiligo	inflammatory_disease|integumentary_system_disorder|immune_system_disorder	autoimmune_disease	immune_system_disorder|inflammatory_disease|integumentary_system_disorder	other	other	other	other	other	other	other	
MONDO:1010125	generalized vitiligo	inflammatory_disease|integumentary_system_disorder|immune_system_disorder	autoimmune_disease	immune_system_disorder|inflammatory_disease|integumentary_system_disorder	other	other	other	other	other	other	other	
MONDO:1010128	peritonitis	inflammatory_disease	other	inflammatory_disease	other	other	other	other	other	other	other	
MONDO:1010131	encapsulating peritoneal sclerosis	inflammatory_disease|digestive_system_disorder	other	inflammatory_disease|digestive_system_disorder	other	other	other	other	other	other	other	
MONDO:1010132	AARS1-related leukoencephalopathy	nervous_system_disorder|hereditary_disease	neurodegenerative_disease	nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:1010144	PLD1-related congenital heart disease	cardiovascular_disorder|hereditary_disease|disorder_of_development_or_morphogenesis	cardiovascular_disorder	cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease	other	other	other	other	other	other	other	
MONDO:1010145	PIP5K1C-related neurodevelopmental disorder	nervous_system_disorder|hereditary_disease	other	nervous_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:1010146	CFAP46-related primary ciliary dyskinesia	syndromic_disease|hereditary_disease|respiratory_system_disorder	other	syndromic_disease|respiratory_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:1010148	benign skeletal muscle neoplasm	musculoskeletal_system_disorder|cancer_or_benign_tumor	cancer_or_benign_tumor	musculoskeletal_system_disorder|cancer_or_benign_tumor	other	other	other	other	other	other	other	
MONDO:1010150	COL4A1/A2-related disorder	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:1010152	autosomal dominant nebulin-related myopathy	musculoskeletal_system_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease	other	other	other	other	other	other	other	
MONDO:1010154	adult hypophosphatasia	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	other	other	other	other	other	other	
MONDO:1010168	childhood hypophosphatasia	hereditary_disease|metabolic_disease|disorder_of_development_or_morphogenesis	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	other	other	other	other	other	other	
MONDO:1010169	infantile hypophosphatasia	metabolic_disease|hereditary_disease|disorder_of_development_or_morphogenesis	metabolic_disease	metabolic_disease|disorder_of_development_or_morphogenesis|hereditary_disease	other	other	other	other	other	other	other	
MONDO:1030000	hyperinsulinemic hypoglycemia with polycystic kidney disease	endocrine_system_disorder|metabolic_disease|hereditary_disease	metabolic_disease|endocrine_system_disorder	metabolic_disease|endocrine_system_disorder|hereditary_disease	endocrinology|pediatric|renal_medicine	metabolic_disorder|polycystic_kidney_disease	kidney_disorder|endocrine_disorder	false	false	false	true	high
MONDO:1030002	dysplasia of the proximal femoral epiphyses	musculoskeletal_system_disorder|syndromic_disease|connective_tissue_disorder|hereditary_disease	other	musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder|syndromic_disease	genetics_and_genomics|orthopaedic|pediatric	developmental_disorder|metabolic_disorder	joint_disorder|bone_disorder	false	false	false	false	medium
MONDO:1030003	Mycoplasmoides infection	infectious_disease	infectious_disease	infectious_disease	pediatric|pulmonology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder|lymphatic_disorder	true	false	false	false	medium
MONDO:1030004	Mollaret’s meningitis	inflammatory_disease|nervous_system_disorder|infectious_disease	infectious_disease	infectious_disease|inflammatory_disease|nervous_system_disorder	pediatric|neurology	autoimmune_diseases|inflammatory_disease	immune_disorder|brain_disorder	true	false	false	false	high
MONDO:1030005	mosaic SMO syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	oncology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	joint_disorder|bone_disorder|eye_disorder	false	false	false	false	very_high
MONDO:1030006	Happle-Tinschert syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	genetics_and_genomics|pediatric|cardiology	metabolic_disorder|autoimmune_diseases|neurodegenerative_disease|inflammatory_disease	immune_disorder|lymphatic_disorder|blood_bone_marrow_disorder	false	false	false	false	medium
MONDO:1030007	hypertensive urgency	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	urology|cardiology|renal_medicine	metabolic_disorder|cardiovascular_disorder	kidney_disorder|urinary_tract_disorder	false	false	false	true	medium
MONDO:1030008	mitral valve insufficiency	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	metabolic_disorder|cardiovascular_disorder|inflammatory_disease	vascular_disorder|heart_disorder	false	false	false	false	high
MONDO:1030009	persistent atrial fibrillation	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology|pulmonology	autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	high
MONDO:1030010	precerebral artery stenosis	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	cardiology|hematology|neurology	autoimmune_diseases|cardiovascular_disorder	vascular_disorder|brain_disorder	false	false	false	false	medium
MONDO:1030011	paroxysmal atrial fibrillation	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	cardiothoracic|cardiology	autoimmune_diseases|cardiovascular_disorder	vascular_disorder|heart_disorder	false	false	false	true	medium
MONDO:1030015	acquired porphyria	metabolic_disease	metabolic_disease	metabolic_disease	hematology|hepatology|dermatology	metabolic_disorder|anemia	skin_disorder|liver_disorder	false	false	false	true	medium
MONDO:1030016	22q-related schwannomatosis	disorder_of_development_or_morphogenesis|nervous_system_disorder|syndromic_disease|integumentary_system_disorder|hereditary_disease|cancer_or_benign_tumor	cancer_or_benign_tumor	disorder_of_development_or_morphogenesis|hereditary_disease|integumentary_system_disorder|cancer_or_benign_tumor|nervous_system_disorder|syndromic_disease	genetics_and_genomics|oncology|neurology	cancer|neurodegenerative_disease	eye_disorder|spinal_disorder|nerve_disorder_is_incorrect___nerve_disorder_was_not_in_the_category_list_so_replace_it_with_ear_disorder|brain_disorder	false	false	false	false	high
MONDO:1040001	TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations	hereditary_disease|disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis|hereditary_disease	pediatric|orthopaedic|dermatology|genetics_and_genomics	orofacial_abnormality|ectodermal_dysplasia|metabolic_disorder|limb_abnormality|ectodermal_dysplasia____corrected_list_of_categories_that_best_fit_the_disease___limb_abnormality	limb_disorder|teeth_disorder|oral_facial_disorder|skin_disorder	false	false	false	false	high
MONDO:1040002	PIK3CA-related overgrowth spectrum	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	endocrinology|oncology|neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	brain_disorder|muscle_disorder	false	false	false	true	high
MONDO:1040003	KCND2-related neurodevelopmental disorder with or without seizures	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|neurological_disorder	false	false	false	true	very_high
MONDO:1040004	PIK3R2-related overgrowth spectrum	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	oncology|neurology|pediatric|genetics_and_genomics	inflammatory_disease|cancer|metabolic_disorder	vascular_disorder|joint_disorder|muscle_disorder|bone_disorder	false	false	false	false	high
MONDO:1040005	PRPF19-related neurodevelopmental disorder	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder	false	false	false	false	high
MONDO:1040006	CTR9-related neurodevelopmental disorder	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|pediatric|genetics_and_genomics	neurodegenerative_disease|mental_health_disorder	brain_disorder|neurodevelopmental_disorder	false	false	false	false	very_high
MONDO:1040007	hemihydranencephaly	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|pediatric	neurodegenerative_disease|metabolic_disorder	brain_disorder|spinal_disorder	false	false	false	false	very_high
MONDO:1040008	CAMK2D-related neurodevelopmental disorder and dilated cardiomyopathy	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|cardiology|genetics_and_genomics	cardiovascular_disorder|neurodegenerative_disease	brain_disorder|heart_disorder|muscle_disorder	false	false	false	false	very_high
MONDO:1040009	TRIP11-related skeletal dysplasia	hereditary_disease|musculoskeletal_system_disorder	other	hereditary_disease|musculoskeletal_system_disorder	pediatric|orthopaedic|genetics_and_genomics	skeletal_dysplasia|metabolic_disorder	joint_disorder|spinal_disorder|bone_disorder	false	false	false	false	very_high
MONDO:1040010	IRF6-related condition	syndromic_disease	other	syndromic_disease	genetics_and_genomics|dermatology	autoimmune_diseases|inflammatory_disease|adrenal_gland_disease	skin_disorder|immune_disorder	false	false	false	true	medium
MONDO:1040011	vertebral artery dissection	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	neurology|cardiology|cardiothoracic	inflammatory_disease|cardiovascular_disorder	vascular_disorder|spinal_disorder	false	false	false	false	high
MONDO:1040012	PI4KA-related disorder	hereditary_disease	other	hereditary_disease	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	lymphatic_disorder|muscle_disorder|brain_disorder	false	false	false	false	very_high
MONDO:1040014	PPFIA3-related neurodevelopmental disorder	hereditary_disease|nervous_system_disorder	other	hereditary_disease|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	neurodegenerative_disease|mental_health_disorder	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:1040015	infectious disease with sepsis	infectious_disease	infectious_disease	infectious_disease	pulmonology|pediatric|hematology|infectious_diseases	infectious_disease|inflammatory_disease|sepsis	lung_disorder|immune_disorder|vascular_disorder	true	false	false	true	very_high
MONDO:1040016	cerebral artery stenosis	cardiovascular_disorder|nervous_system_disorder	cardiovascular_disorder	cardiovascular_disorder|nervous_system_disorder	neurology|cardiology	cardiovascular_disorder|neurodegenerative_disease	vascular_disorder|brain_disorder	false	false	false	false	high
MONDO:1040017	intestinal fistula	digestive_system_disorder	other	digestive_system_disorder	gastroenterology|urology	autoimmune_diseases|inflammatory_disease|cancer	lower_gastrointestinal_disorder|upper_gastrointestinal_disorder	false	false	false	false	high
MONDO:1040018	X-linked syndromic complex neurodevelopmental disorder	nervous_system_disorder	other	nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:1040019	Enterococcus infectious disease	infectious_disease	infectious_disease	infectious_disease	gastroenterology|infectious_diseases|general_internal_medicine|pediatrics	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|immune_disorder	true	false	false	true	high
MONDO:1040020	methicillin-susceptible staphylococcus aureus infectious disease	infectious_disease	infectious_disease	infectious_disease	pulmonology|infectious_disease|dermatology	autoimmune_diseases|inflammatory_disease|cancer	skin_disorder|lung_disorder|immune_disorder	true	false	false	true	high
MONDO:1040021	congenital myasthenic syndrome 4	hereditary_disease|nervous_system_disorder|syndromic_disease	other	nervous_system_disorder|hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	true	high
MONDO:1040022	linkeropathy	disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder|hereditary_disease|connective_tissue_disorder|syndromic_disease	other	connective_tissue_disorder|hereditary_disease|syndromic_disease|disorder_of_development_or_morphogenesis|musculoskeletal_system_disorder	neurology|genetics_and_genomics|orthopaedic|pediatrics|rheumatology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|joint_disorder	false	false	false	false	high
MONDO:1040023	NDUFB11-related disorders	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	neurology|genetics_and_genomics	metabolic_disorder|neurodegenerative_disease|adrenal_gland_disease	liver_disorder|energy_metabolism_disorder|mitochondrial_disease	false	false	false	false	very_high
MONDO:1040024	myelin oligodendrocyte glycoprotein antibody-associated disease	disorder_of_development_or_morphogenesis|nervous_system_disorder|inflammatory_disease	neurodegenerative_disease	nervous_system_disorder|inflammatory_disease|disorder_of_development_or_morphogenesis	neurology|genetics_and_genomics|immunology	inflammatory_disease|neurodegenerative_disease|autoimmune_diseases	immune_disorder|brain_disorder	true	false	false	true	high
MONDO:1040026	metastatic malignant neoplasm in the brain	cancer_or_benign_tumor|nervous_system_disorder	cancer_or_benign_tumor	nervous_system_disorder|cancer_or_benign_tumor	oncology|neurology	metastatic_malignant_neoplasm_in_the_brain|cancer	brain_disorder|spinal_disorder	false	true	false	false	very_high
MONDO:1040027	hypermobility spectrum disorder	hereditary_disease|connective_tissue_disorder	other	connective_tissue_disorder|hereditary_disease	neurology|orthopaedic|rheumatology	inflammatory_disease|mental_health_disorder|autoimmune_diseases	muscle_disorder|spinal_disorder|joint_disorder	false	false	false	false	high
MONDO:1040028	PDE6C-related retinopathy	psychiatric_disorder|disorder_of_visual_system|hereditary_disease|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:1040029	Sharpin-related autoinflammatory syndrome	hereditary_disease|connective_tissue_disorder|syndromic_disease	other	connective_tissue_disorder|hereditary_disease|syndromic_disease	genetics_and_genomics|rheumatology	inflammatory_disease|autoimmune_diseases	liver_disorder|immune_disorder	false	false	false	true	high
MONDO:1040031	dyneinopathy	cardiovascular_disorder|psychiatric_disorder|disorder_of_visual_system|hereditary_disease|nervous_system_disorder|syndromic_disease	cardiovascular_disorder|psychiatric_disorder	nervous_system_disorder|disorder_of_orbital_region|hereditary_disease|cardiovascular_disorder|syndromic_disease|psychiatric_disorder|disorder_of_visual_system	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:1040032	EN1-related dorsoventral syndrome	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology	metabolic_disorder|neurodegenerative_disease|autoimmune_diseases	brain_disorder|spinal_disorder	false	false	false	false	high
MONDO:1040033	congenital muscular dystrophy without intellectual disability	musculoskeletal_system_disorder|nervous_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder|nervous_system_disorder	neurology|genetics_and_genomics|pediatric	metabolic_disorder|neurodegenerative_disease	muscle_disorder|spinal_disorder	false	false	false	false	medium
MONDO:1040034	PDE6G-related retinopathy	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|inherited_disorder	eye_disorder|muscle_disorder	false	false	false	false	high
MONDO:1040035	LRIT3-related retinopathy	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|pediatric|ophthalmology	neurodegenerative_disease	eye_disorder	false	false	false	false	medium
MONDO:1040036	IMPG1-related dominant retinopathy	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|eye_disease	eye_disorder	false	false	false	false	medium
MONDO:1040037	IMPG1-related recessive retinopathy	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|pediatric|ophthalmology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	recessive_disorder|eye_disorder|retinopathy	false	false	false	false	high
MONDO:1040038	TTLL5-related retinopathy	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease|retinal_disease	eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:1040039	OFD1-related ciliopathy	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:1040040	HGSNAT-related retinopathy	psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	eye_disorder	false	false	false	false	high
MONDO:1040041	FZD4-related exudative vitreoretinopathy	cardiovascular_disorder|disorder_of_visual_system|nervous_system_disorder|hereditary_disease	cardiovascular_disorder	disorder_of_orbital_region|hereditary_disease|cardiovascular_disorder|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|genetic_disease	eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:1040042	BBS7-related ciliopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease	ciliopathy|eye_disorder	false	false	false	false	high
MONDO:1040043	BBS1-related ciliopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|ophthalmology	metabolic_disorder|neurodegenerative_disease	ciliary_disorder|eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:1040044	BBS4-related ciliopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|neurology|pediatric	metabolic_disorder|neurodegenerative_disease|ciliopathy	eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:1040045	BBS12-related ciliopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|medical_genetics|pediatric	neurodegenerative_disease|ciliopathy	eye_disorder|ciliopathy_is_not_in_the_category_list_but_its_a_good_guess_for__bbs12_related_ciliopathy_so_another_possible_answer_is__eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:1040046	LZTFL1-related ciliopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pulmonology|pediatric	neurodegenerative_disease|ciliopathy	lung_disorder|kidney_disorder	false	false	false	false	high
MONDO:1040047	BBS5-related ciliopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|other___corrected__genetics_and_genomics	metabolic_disorder|neurodegenerative_disease	eye_disorder|ciliopathy_is_primarily_related_to_the_eyes_but_bbs5_related_ciliopathy_can_also_be_associated_with_other_systems_like_kidney__liver_etc	false	false	false	false	high
MONDO:1040048	BBS2-related ciliopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric	neurodegenerative_disease|ciliopathy	eye_disorder|ciliopathy|kidney_disorder	false	false	false	false	high
MONDO:1040049	TTC8-related ciliopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pulmonology|cardiology|pediatric	ciliopathies|metabolic_disorder|i_corrected_the_list_as_per_your_instructions	eye_disorder|kidney_disorder	false	false	false	false	high
MONDO:1040050	MKKS-related ciliopathy	hereditary_disease	other	hereditary_disease	genetics_and_genomics|pediatric|medical_specialty_unspecified	metabolic_disorder|ciliopathy	eye_disorder|kidney_disorder|spinal_disorder	false	false	false	false	high
MONDO:1040051	IMPDH1-related retinopathy	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|genetic_disease	eye_disorder	false	false	false	false	high
MONDO:1040052	PROM1-related recessive retinopathy	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	metabolic_disorder|neurodegenerative_disease	blood_bone_marrow_disorder|eye_disorder	false	false	false	false	high
MONDO:1040053	PROM1-related dominant retinopathy	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder|spinal_disorder	false	false	false	false	high
MONDO:1040054	DHDDS-CDG	hereditary_disease|metabolic_disease	metabolic_disease	hereditary_disease|metabolic_disease	genetics_and_genomics|neurology	inflammatory_disease|cardiovascular_disorder|metabolic_disorder|neurodegenerative_disease	muscle_disorder|brain_disorder	false	false	false	false	high
MONDO:1040055	PRPH2-related retinopathy	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	inflammatory_disease|metabolic_disorder|neurodegenerative_disease	muscle_disorder|eye_disorder|vascular_disorder	false	false	false	false	medium
MONDO:1040056	PROM1-related retinopathy	disorder_of_visual_system|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	disorder_of_orbital_region|hereditary_disease|psychiatric_disorder|disorder_of_visual_system|nervous_system_disorder	genetics_and_genomics|ophthalmology	neurodegenerative_disease	muscle_disorder|eye_disorder	false	false	false	true	high
MONDO:1040063	KCNV2-related retinopathy	hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	other	other	other	other	other	other	other	
MONDO:1040064	CRX-related retinopathy	hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	other	other	other	other	other	other	other	
MONDO:1040065	ARL6-related ciliopathy	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:1040066	REEP6-related retinopathy	hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	other	other	other	other	other	other	other	
MONDO:1040068	MKS1-related ciliopathy	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:1040070	SPATA7-related retinopathy	hereditary_disease|psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system	psychiatric_disorder	disorder_of_orbital_region|nervous_system_disorder|hereditary_disease|disorder_of_visual_system|psychiatric_disorder	other	other	other	other	other	other	other	
MONDO:1050000	sycosis barbae	inflammatory_disease|integumentary_system_disorder|infectious_disease	infectious_disease	inflammatory_disease|infectious_disease|integumentary_system_disorder	dermatology|otolaryngology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	medium
MONDO:1060107	CYP7B1-related disorder of oxysterol accumulation	metabolic_disease|hereditary_disease	metabolic_disease	hereditary_disease|metabolic_disease	other	other	other	other	other	other	other	
MONDO:1060108	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome	disorder_of_development_or_morphogenesis|hereditary_disease	other	hereditary_disease|disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:1060109	PLEC-related muscular dystrophy-epidermolysis bullosa simplex spectrum disorder	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:1060110	HDAC4-related haploinsufficiency syndrome	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:1060111	SAMD9L-related spectrum and myeloid neoplasm risk	cancer_or_benign_tumor|syndromic_disease|hereditary_disease	cancer_or_benign_tumor	hereditary_disease|syndromic_disease|cancer_or_benign_tumor	other	other	other	other	other	other	other	
MONDO:1060113	Lipschütz ulcer	reproductive_system_disorder	other	reproductive_system_disorder	other	other	other	other	other	other	other	
MONDO:1060115	TUBB4B-related ciliopathy	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:1060116	FDXR-related optic atrophy mitochondrial dysfunction syndrome	hereditary_disease|mitochondrial_disease	other	hereditary_disease|mitochondrial_disease	other	other	other	other	other	other	other	
MONDO:1060117	MYCBP2-related developmental delay with corpus callosum defects	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:1060121	adenoacanthoma	cancer_or_benign_tumor	cancer_or_benign_tumor	cancer_or_benign_tumor	other	other	other	other	other	other	other	
MONDO:1060122	ALG8-related autosomal dominant polycystic kidney and/or liver disease	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:1060123	GRIN1-related complex neurodevelopmental disorder	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:1060125	congenital high airway obstruction syndrome	disorder_of_development_or_morphogenesis	other	disorder_of_development_or_morphogenesis	other	other	other	other	other	other	other	
MONDO:1060126	exogenous Cushing syndrome	syndromic_disease	other	syndromic_disease	other	other	other	other	other	other	other	
MONDO:1060132	ARHGAP29-related non-syndromic orofacial cleft	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	other	other	other	other	other	other	other	
MONDO:1060134	atherosclerotic cardiovascular disease	cardiovascular_disorder	cardiovascular_disorder	cardiovascular_disorder	other	other	other	other	other	other	other	
MONDO:1060136	PIK3R1-related immunodeficiency and SHORT syndrome	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:1060138	GRIN-related complex neurodevelopmental disorder	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:1060139	GRIN2A-related complex neurodevelopmental disorder	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:1060140	GRIN2A-related developmental and/or epileptic encephalopathy with spike-wave activation in sleep	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:1060141	GRIN2A-related rolandic epilepsy-speech dyspraxia syndrome	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:1060142	GRIN2A-related self-limited epilepsy with centrotemporal spikes	nervous_system_disorder|hereditary_disease	other	hereditary_disease|nervous_system_disorder	other	other	other	other	other	other	other	
MONDO:1060144	retinitis pigmentosa 7, digenic	psychiatric_disorder|metabolic_disease|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder|metabolic_disease	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|metabolic_disease|nervous_system_disorder|psychiatric_disorder	other	other	other	other	other	other	other	
MONDO:1060145	Leber congenital amaurosis 18	psychiatric_disorder|nervous_system_disorder|disorder_of_visual_system|hereditary_disease	psychiatric_disorder	hereditary_disease|disorder_of_orbital_region|disorder_of_visual_system|nervous_system_disorder|psychiatric_disorder	other	other	other	other	other	other	other	
MONDO:1060146	FGFR1-related Pfeiffer syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	other	other	other	other	other	other	other	
MONDO:1060147	FGFR2-related Pfeiffer syndrome	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease	other	disorder_of_development_or_morphogenesis|hereditary_disease|syndromic_disease|musculoskeletal_system_disorder	other	other	other	other	other	other	other	
MONDO:1060148	empty nose syndrome	iatrogenic_disease|otorhinolaryngologic_disease|respiratory_system_disorder|inflammatory_disease	other	otorhinolaryngologic_disease|iatrogenic_disease|inflammatory_disease|respiratory_system_disorder	other	other	other	other	other	other	other	
MONDO:1060149	ACAN-related short stature spectrum	musculoskeletal_system_disorder|hereditary_disease	other	hereditary_disease|musculoskeletal_system_disorder	other	other	other	other	other	other	other	
MONDO:1060150	NOTCH1-related AOS spectrum disorder	hereditary_disease|syndromic_disease	other	hereditary_disease|syndromic_disease	other	other	other	other	other	other	other	
MONDO:1060151	schizoaffective bipolar disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	other	other	other	other	other	other	other	
MONDO:1060152	schizoaffective depressive disorder	psychiatric_disorder|nervous_system_disorder	psychiatric_disorder	nervous_system_disorder|psychiatric_disorder	other	other	other	other	other	other	other	
MONDO:1060153	multiple symmetric lipomatosis with partial lipodystrophy	cancer_or_benign_tumor|musculoskeletal_system_disorder|hereditary_disease|integumentary_system_disorder|connective_tissue_disorder	cancer_or_benign_tumor	connective_tissue_disorder|hereditary_disease|integumentary_system_disorder|cancer_or_benign_tumor|musculoskeletal_system_disorder	other	other	other	other	other	other	other	
MONDO:1060154	INTU-related skeletal ciliopathy	hereditary_disease	other	hereditary_disease	other	other	other	other	other	other	other	
MONDO:8000000	infectious discitis	musculoskeletal_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|musculoskeletal_system_disorder|inflammatory_disease	orthopaedic|rheumatology	autoimmune_diseases|inflammatory_disease	joint_disorder|spinal_disorder	true	false	false	true	high
MONDO:8000001	staphylococcus discitis	musculoskeletal_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|musculoskeletal_system_disorder|inflammatory_disease	orthopaedic|rheumatology|neurology|pulmonology	autoimmune_diseases|inflammatory_disease	skin_disorder|immune_disorder	true	false	false	true	high
MONDO:8000002	escherichia coli discitis	musculoskeletal_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|musculoskeletal_system_disorder|inflammatory_disease	urology|genetics_and_genomics|pediatric|renal_medicine|obstetrics_and_gynecology	autoimmune_diseases|inflammatory_disease	lower_gastrointestinal_disorder|urinary_tract_disorder	true	false	false	true	high
MONDO:8000003	streptococcus pneumoniae discitis	musculoskeletal_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|musculoskeletal_system_disorder|inflammatory_disease	pediatric|pulmonology	autoimmune_diseases|inflammatory_disease	throat_disorder|lung_disorder	true	false	false	true	high
MONDO:8000004	salmonella discitis	musculoskeletal_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|musculoskeletal_system_disorder|inflammatory_disease	gastroenterology|pediatric|general_medicine	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	upper_gastrointestinal_disorder|lower_gastrointestinal_disorder	true	false	false	true	high
MONDO:8000005	fungal discitis	musculoskeletal_system_disorder|inflammatory_disease|infectious_disease	infectious_disease	infectious_disease|musculoskeletal_system_disorder|inflammatory_disease	orthopaedic|rheumatology|neurology	autoimmune_diseases|inflammatory_disease	joint_disorder|spinal_disorder	true	false	false	true	high
MONDO:8000006	WHIM syndrome 1	immune_system_disorder|hereditary_disease|hematologic_disorder	other	immune_system_disorder|hematologic_disorder|hereditary_disease	immunology|genetics_and_genomics|pediatric	anemia|autoimmune_diseases|metabolic_disorder	blood_bone_marrow_disorder|immune_disorder	true	false	false	true	high
MONDO:8000008	Martsolf syndrome 1	endocrine_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder|syndromic_disease|hereditary_disease|disorder_of_visual_system	endocrine_system_disorder	disorder_of_orbital_region|disorder_of_visual_system|endocrine_system_disorder|syndromic_disease|hereditary_disease|disorder_of_development_or_morphogenesis|reproductive_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|autoimmune_diseases|metabolic_disorder|inflammatory_disease	kidney_disorder|urinary_tract_disorder	false	false	false	false	high
MONDO:8000010	antiphospholipid syndrome	syndromic_disease|immune_system_disorder	autoimmune_disease	immune_system_disorder|syndromic_disease	rheumatology|hematology	autoimmune_diseases|cardiovascular_disorder|inflammatory_disease	immune_disorder_vascular_disorder	false	false	false	true	high
MONDO:8000011	visceral neuropathy, familial, 1, autosomal recessive	digestive_system_disorder|hereditary_disease	other	hereditary_disease|digestive_system_disorder	neurology|genetics_and_genomics	neurodegenerative_disease|metabolic_disorder	kidney_disorder|muscle_disorder|nerve_disorder	false	false	false	false	high
MONDO:8000012	neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1	hereditary_disease	other	hereditary_disease	neurology|multisystem|infantile_onset|endocrine	neurodegenerative_disease|metabolic_disorder|multisystem	endocrine|pancreatic_disease	true	false	false	false	very_high
MONDO:8000013	portal hypertension, noncirrhotic, 1	hereditary_disease	other	hereditary_disease	gastroenterology|hepatology	inflammatory_disease|cardiovascular_disorder	upper_gastrointestinal_disorder|liver_disorder	false	false	false	true	medium
MONDO:8000014	familial antiphospholipid syndrome	syndromic_disease|immune_system_disorder|hereditary_disease	autoimmune_disease	immune_system_disorder|syndromic_disease|hereditary_disease	rheumatology|hematology|genetics_and_genomics	inflammatory_disease|autoimmune_diseases|cardiovascular_disorder	vascular_disorder|immune_disorder	false	false	false	true	high
MONDO:8000015	46,XY sex reversal 11	musculoskeletal_system_disorder|disorder_of_development_or_morphogenesis|reproductive_system_disorder|cardiovascular_disorder|hereditary_disease|endocrine_system_disorder	cardiovascular_disorder|endocrine_system_disorder	endocrine_system_disorder|cardiovascular_disorder|disorder_of_development_or_morphogenesis|hereditary_disease|musculoskeletal_system_disorder|reproductive_system_disorder	urology|genetics_and_genomics|endocrinology	metabolic_disorder|adrenal_gland_disease	reproductive_system_disorder|endocrine_disorder	false	false	false	true	high
MONDO:8000018	benign paroxysmal positional vertigo	auditory_system_disorder|otorhinolaryngologic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|otorhinolaryngologic_disease|nervous_system_disorder|hereditary_disease	neurology|otolaryngology	adrenal_gland_disease|neurodegenerative_disease|inflammatory_disease	brain_disorder|ear_disorder	false	false	false	true	medium
MONDO:8000019	vertigo, benign recurrent, 1	auditory_system_disorder|otorhinolaryngologic_disease|psychiatric_disorder|nervous_system_disorder|hereditary_disease	psychiatric_disorder	auditory_system_disorder|psychiatric_disorder|otorhinolaryngologic_disease|nervous_system_disorder|hereditary_disease	neurology|otolaryngology	inflammatory_disease|autoimmune_diseases|metabolic_disorder|neurodegenerative_disease	brain_disorder|ear_disorder	false	false	false	true	medium
MONDO:8000023	type 3 autoimmune lymphoproliferative syndrome	syndromic_disease|immune_system_disorder|cancer_or_benign_tumor|hereditary_disease	autoimmune_disease|cancer_or_benign_tumor	immune_system_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease	immunology|oncology|hematology|pediatric	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	true	high
MONDO:8000024	autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD	syndromic_disease|immune_system_disorder|cancer_or_benign_tumor|hereditary_disease	autoimmune_disease|cancer_or_benign_tumor	immune_system_disorder|syndromic_disease|cancer_or_benign_tumor|hereditary_disease	immunology|rheumatology|oncology|hematology|genetics_and_genomics	inflammatory_disease|cancer|autoimmune_diseases	immune_disorder|lymphatic_disorder	false	false	false	true	high